Вы находитесь на странице: 1из 13

See

discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/251235271

Bridging Intimate Partner Violence and the


Human Brain: A Literature Review

Article in Trauma Violence & Abuse July 2013


DOI: 10.1177/1524838013496333 Source: PubMed

CITATIONS READS

9 228

4 authors:

Janet Yuen-Ha Wong Daniel YT Fong


The University of Hong Kong The University of Hong Kong
41 PUBLICATIONS 98 CITATIONS 246 PUBLICATIONS 6,703 CITATIONS

SEE PROFILE SEE PROFILE

Vincent Lai Agnes Tiwari


Hong Kong Baptist Hospital The University of Hong Kong
38 PUBLICATIONS 314 CITATIONS 101 PUBLICATIONS 1,309 CITATIONS

SEE PROFILE SEE PROFILE

Some of the authors of this publication are also working on these related projects:

thalassemia View project

All content following this page was uploaded by Agnes Tiwari on 11 May 2015.

The user has requested enhancement of the downloaded file. All in-text references underlined in blue are added to the original document
and are linked to publications on ResearchGate, letting you access and read them immediately.
Article
TRAUMA, VIOLENCE, & ABUSE
2014, Vol 15(1) 22-33
Bridging Intimate Partner Violence and The Author(s) 2013
Reprints and permission:
sagepub.com/journalsPermissions.nav
the Human Brain: A Literature Review DOI: 10.1177/1524838013496333
tva.sagepub.com

Janet Yuen-Ha Wong1, Daniel Yee-Tak Fong1, Vincent Lai2, and


Agnes Tiwari1

Abstract
Past studies mainly focused on the physical and structural brain injuries in women survivors with a history of intimate partner
violence (IPV), but little attention has been given to the biological impact and cognitive dysfunction resulting from such psy-
chological stress. In this article, we aim to establish the connection between IPV and the brain by reviewing current literature
examining (1) the biological mechanisms linking IPV, stress, and the brain; (2) the functional and anatomical considerations of the
brain in abused women; and (3) the abused womens behavioral responses to IPV, including fear, pain, and emotion regulation, by
utilizing functional neuroimaging. The major significance of this study is in highlighting the need to advance beyond self-reports and
to obtain scientific evidence of the neurological impact and cognitive dysfunction in abused women with a history of IPV, an area in
which current literature remains at a descriptive level.

Keywords
intimate partner violence, psychological stress, human brain, neurological impact, functional neuroimaging

Background to the U.S. CDC, mild TBI (MTBI) is defined as traumatically


induced physiological disruption of brain function, as mani-
Intimate Partner Violence and Related Physical Injuries fested by at least one of the symptoms of loss of consciousness,
Intimate partner violence (IPV) has been recognized as an loss of memory, alteration in mental state, and neurological
important human rights issue for many decades. It is also a glo- deficit; loss of consciousness does not exceed 30 min, posttrau-
bal public health problem, significantly contributing to the hid- matic amnesia does not exceed 24 hr, and the Glasgow coma
den costs in health care utilization. According to the Centers for scale is at least 13 after 30 min (National Center for Injury Pre-
Disease Control and Preventions (CDC) Web-based Injury vention and Control, 2003). MTBI is commonly reported in
Statistics Query and Reporting System, the direct medical care abused women with a history of anoxic or hypoxic brain injury
cost of IPV against women was around US$4.2 billion in 2005. from choking or attempted strangulation (Kwako et al., 2011;
In the United States, the total health care cost burden of IPV Smith, Mills, & Taliaferro, 2001; Wilbur et al., 2001). Pro-
against women within the first 12 months after victimization longed TBI or MTBI may cause devastating long-term conse-
ranged between $2.3 and $7.0 billion in 2003 (Brown, Finkel- quences. One of the consequences is postconcussive syndrome,
stein, & Mercy, 2008). defined as the presence of three or more of the following symp-
Physical injuries are among the most costly health condi- toms: (1) headache, (2) dizziness, (3) fatigue, (4) irritability, (5)
tions in abused women, with more than 90% of all injuries insomnia, (6) difficulty in concentration, (7) memory difficulty,
being found on the head, face, or neck regions (Dolezal, and (8) intolerance of stress, emotion, or alcohol for more than
McCollum, & Callahan, 2009; Monahan & OLeary, 1999; 3 months (World Health Organization, 1992). In addition, other
Wu, Huff, & Bhandari, 2010). In particular, traumatic brain
injuries (TBI) have been examined in a significant number of
studies (Banks, 2007; Jackson, Philp, Nuttall, & Diller, 2002; 1
School of Nursing, LKS Faculty of Medicine, The University of Hong Kong,
Kwako et al., 2011; Valera & Berenbaum, 2003). TBI can be Hong Kong
caused by external forces, such as blunt trauma to the face, 2
Department of Diagnostic Radiology, The University of Hong Kong, Hong
or during rapid acceleration and deceleration or rotation (see Kong
Figure 1), resulting in neurological deficits, loss of conscious-
ness, brain damage, and even death (Thurman, Sniezek, John- Corresponding Author:
Janet Yuen-Ha Wong, School of Nursing, LKS Faculty of Medicine, The Uni-
son, Greenspan, & Smith, 1995). The severity of TBI can be versity of Hong Kong, 4/F, William M.W. Mong Block, 21 Sassoon Road,
categorized to be mild, moderate, and severe according to the Pokfulam, Hong Kong S.A.R.
duration of unconsciousness and loss of memory. According Email: janetyh@hku.hk

Downloaded from tva.sagepub.com at University of Hong Kong Libraries on December 14, 2014
Wong et al. 23

Figure 1. A figure showing the mechanisms of accelerationdeceleration and rotational head injury.

studies have revealed the development of poor quality of life health disorders such as anxiety and depression (Drevets, Price,
(Marcel, 2004) and depression (Kreutzer, Seel, & Gourley, & Furey, 2008).
2001) after TBI.
Aim of the Review
IPV and Related Psychological Stress This literature review aims to describe the connections among
In addition to physical injuries, a significant portion of the IPV, neurophysiology, neurochemistry, and neuroanatomy by
health care resource utilization is attributed to the chronic ill- reviewing the current literature on (1) the biological mechan-
nesses of abused women, including chronic pain (Humphreys, isms linking IPV, stress, and the brain; (2) the functional and
Cooper, & Miaskowski, 2011; Koopman et al., 2007; Wuest anatomical considerations of the brain in abused women; and
et al., 2010), immune dysfunction (Inslicht et al., 2006), (3) the abused womens behavioral responses to IPV, including
inflammation, cardiovascular diseases, metabolic symptoms fear, pain, and emotion regulation, using functional neuroima-
(Kendall-Tackett, 2007), posttraumatic stress disorder (PTSD), ging studies.
and depression (Golding, 1999; Mechanic, Weaver, & Resick,
2008). Indeed, some studies revealed that abused women may
have complaints of diminished cognitive abilities, difficulties The Physiological Mechanism Linking IPV,
with memorization, and concentration problems. However, it Stress, and the Brain
is unclear whether such cognitive dysfunction is directly
related to structural/physical brain injury or functional brain
The HypothalamicPituitaryAdrenal Axis
damage as a consequence of psychological stress and trauma Figure 2 shows the hypothalamicpituitaryadrenal (HPA)
exposure (Valera & Berenbaum, 2003). axis. This is a complex union consisting of the hypothalamus,
The chronic nature of IPV has been recognized as a causa- the pituitary gland, and the adrenal glands. In the physiological
tive factor of psychological stress due to the fear of violent regulation of our body, stressors trigger the sympathetic arousal
attack or the actual experience of violence (Coker, Smith, in the autonomic nervous system for the fight-or-flight
Bethea, King, & McKeown, 2000; Walker & Browne, 1985). response to maintain homeostasis (Cannon, 1929). In response
In fact, psychological stress may be further developed into to a threatening stimulation, the paraventricular nucleus (PVN)
autonomic, hormonal, immunological, neurological, and neu- of the hypothalamus excretes corticotropin-releasing hormone
ropsychological alterations relating to thoughts and feelings. (CRH), which stimulates the release of adrenocorticotropic
These alterations may lead to poor decision making about leav- hormones (ACTH) from the anterior pituitary gland. This fur-
ing or staying in abusive relationships (Southwick, Rasmusson, ther stimulates the adrenal cortex to release glucocorticoid hor-
Barron, & Arnsten, 2005), as well as memorization and con- mones, mainly cortisol, into the blood circulation. Cortisol is a
centration problems (Roozendaal, McEwen, & Chattarji, stress hormone that shuts down glucose metabolism, forcing
2009), behavioral responses to pain such as somatization , i.e. cells to operate on stored glycogen (i.e., gluconeogenesis).
bodily pain without a biological cause (Crofford, 2007; Fayed Thus, cortisol mobilizes the energy from the storage site or
et al., 2011), negative emotions or feelings, and even mental from nonessential organs to exercising muscles for the

Downloaded from tva.sagepub.com at University of Hong Kong Libraries on December 14, 2014
24 TRAUMA, VIOLENCE, & ABUSE 15(1)

tumor necrosis factor-alpha, interleukin-1 (IL-1), and IL-6, as


well as Type I interferons-a/b; it also promotes the production
of IL-4, which is a kind of Th2 cytokine (Wong, 2002). Thus,
hyperactivity of the HPA axis in abused women, especially
those with chronic stress, should result in a high level of corti-
sol, leading to suppression of the immune system (Elzinga,
Schmahl, Vermetten, van Dyck, & Bremner, 2003). However,
the immunosuppressive effect of cortisol is still debatable.
Abused women with PTSD have been found to have higher
numbers of leukocytes and lymphocytes, which enhance their
immune responses (Woods, Wineman, et al., 2005). Moreover,
there is increasing evidence that cortisol should be more
accurately conceptualized as an immunomodulatory hormone,
rather than an immunosuppressive hormone (Silverman,
Pearce, Biron, & Miller, 2005).
Indeed, the relationship between HPA axis alterations and
the immune system is complex. For instance, cytokines have
also been found to have direct interactions at all HPA axis lev-
els, including the pituitary and adrenal glands, to stimulate the
production of glucocorticoids, ACTH, and CRH, which could
further explain the complexity of the HPA axis (Arzt et al.,
1999; Dallman et al., 2004).

Amygdala Involvement in the HPA Axis


The amygdala is a region in the brain located in the limbic sys-
tem, which is responsible for emotions. It is commonly activated
by fear and anxiety. The amygdala also plays a role in the HPA
axis. In response to a stressful or threatening condition, signals
are transmitted to the PVN of the hypothalamus. This results
Figure 2. The hypothalamicpituitaryadrenal (HPA) axis.
in HPA axis activation, and hence enhances the release of CRH
and glucocorticoids, which activate the amygdala (Figure 2;
fight-or-flight response. However, prolonged stimulation Aggleton, 1992; Weidenfeld, Newman, Itzik, Gur, & Feldman,
may cause either cell death or shutdown of the neurogenesis 2002). Unlike other brain regions, the amygdala has glucocorti-
processes in the amygdala and hippocampus because they are coid and mineralocorticoid receptors (de Kloet, 2000), indicating
recognized as nonessential brain regions during the fight-or- that direct activation of the amygdala via elevated levels of glu-
flight response (Joels, Karst, Krugers, & Lucassen, 2007; cocorticoids results in chronic HPA axis alteration (Akana, Chu,
Warner-Schmidt & Duman, 2006). Soriano, & Dallman, 2001). In addition, many studies have
The experience of IPV often induces chronic psychological reported that the amygdala is substantially involved in regulating
stress. While acute environmental stress would activate the stress effects on memory, so that individuals can remember the
HPA axis, prolonged stress may result in HPA axis dysfunction stressful experience, which contributes to the long-term conse-
(Crofford, 2007; McEwen, 1998). Indeed, emerging evidence quences of anxiety if the individual is exposed to repeated stress
has demonstrated that any history of abuse would be associated (McEwen, 2005; Roozendaal et al., 2009). The involvement of
with hyperreactivity of the HPA axis (Bremner et al., 2003; the amygdala in the HPA axis helps explain why IPV-related
Heim et al., 2000; Inslicht et al., 2006; Woods, 2005). The stress contributes to mental health problems, and it is also closely
effect has been found to be accumulative in women survivors linked to the thinking and emotional processes of abused women
of IPV or childhood maltreatment (Heim et al., 2002; Shea, (Heim, Ehlert, Hanker, & Hellhammer, 1998; Woods, Page,
Walsh, Macmillan, & Steiner, 2005). et al., 2005).

The Relationship Between the HPA Axis and the


Functional and Anatomical Considerations of
Immune System
the Brain in Abused Women
Stress-induced cortisol, produced via the HPA axis, not only
protects the human body against the stressor but also protects
The Anatomical Structure of a Human Brain
against overreaction of the immune system by suppressing the Our brain is basically structured into four parts, namely the cer-
production of proinflammatory cytokines (Figure 2), such as ebrum, cerebellum, limbic system, and brain stem (Figure 3).

Downloaded from tva.sagepub.com at University of Hong Kong Libraries on December 14, 2014
Wong et al. 25

Anterior cingulate cortex (ACC)

Hypothalamus CEREBRUM Prefrontal cortex (PFC)

Hippocampus
CEREBELLUM Amygdala

BRAIN STEM

Figure 3. A figure showing the anatomical structure of a human brain.

The cerebrum consists of cortexes responsible for cognitive depressive symptoms (Kiy et al., 2011), and poor treatment
and higher thinking skills. The cerebellum is similar to the cer- response in depression (Frodl et al., 2008).
ebrum in structure, but is smaller and is mainly responsible for Many neuroimaging studies have found a reduced hippocam-
balance, coordination, posture, and movements. The limbic pal volume in trauma-exposed individuals, with or without
system is often referred to as the emotional brain and com- PTSD, when compared with healthy controls who have not been
prises the thalamus, hypothalamus, amygdala, hippocampus, exposed to trauma (Karl et al., 2006; Smith, 2005; Woon, Sood,
anterior cingulate cortex (ACC), insula, and several nearby & Hedges, 2010). However, all these studies included both par-
areas. The brain stem, which is located underneath the limbic ticipants who had experienced abuse-related trauma, and also
system, is responsible for vital function control, such as breath- those who had been exposed to other trauma, such as wars, com-
ing, blood pressure, heart rate, sensation, and consciousness. bat, accidents, and disasters. Neuroimaging studies conducted
In the past, neuroscientists studied the human brain through in abused women showed no significant difference in the
structural brain lesions or operations on brain-damaged hippocampal volume between abused and nonabused women
patients. Nowadays, advanced technology has enabled func- (Fennema-Notestine, Stein, Kennedy, Archibald, & Jernigan,
tional and structural analysis of the brain using noninvasive 2002; Flegar et al., 2011), rendering the findings on the effect
imaging modalities, including magnetic resonance imaging of IPV on womens hippocampal volume inconclusive. There
(MRI), functional magnetic resonance imaging (fMRI), posi- are two explanations for such inconsistent findings. First, comor-
tron emission tomography (PET), and single-photon emission bid conditions, such as depression and alcohol dependence, may
computed tomography. Also, structural alterations or volu- affect the results of hippocampal pathology (Davidson, Pizza-
metric changes can be studied using region of interest analysis. galli, Nitschke, & Putnam, 2002; Hedges & Woon, 2010; Shin,
The following sections will first provide basic information Rauch, & Pitman, 2006). From the demographical data of both
about the structure and functions of the hippocampus, amyg- Fennema-Notestine, Stein, Kennedy, Archibald, and Jernigan
dala, ACC, and prefrontal cortex (PFC). Then, we will outline (2002) and Flegar et al.s (2011) studies, abused women had
some of their key anatomical alterations, which are highly sus- more depressive symptoms than nonabused women. Also,
ceptible to be found in women survivors of IPV. abused women in Flegar et al.s study were recruited from a pro-
gram to change drinking behavior and thus were highly alcohol-
dependent. Another potential explanation is related to the meth-
odological considerations. As the age at which traumatic stress is
Hippocampus encountered and aging might both contribute to hippocampal
The hippocampus, which is a small seahorse-shaped structure atrophy, data analysis with adjustment for age and timing of the
in the limbic system, is responsible for learning and memory, traumatic stress is important (Bremner & Narayan, 1998;
including the encoding of context during fear conditioning Resnick, Pham, Kraut, Zonderman, & Davatzikos, 2003). How-
(Figure 3). Also, it releases stress-evoked CRH to stimulate ever, neither Fennema-Notestine et al. nor Flegar et al.s study
ACTH production (Chen et al., 2004; Stern, 2011). The hippo- conducted their data analysis with adjustment for age. Perhaps
campus is sensitive and malleable (McEwen, 2007). Reduced replicating the studies with assessment and data adjustment for
hippocampal volume has been shown to have a positive corre- age, as well as other potential confounding factors such as drink-
lation with memory impairment (Bremner, 1999; Ystad et al., ing habits and depression, is necessary to verify the impact of
2009), executive dysfunction (Frodl et al., 2006), more severe IPV on hippocampal volume.

Downloaded from tva.sagepub.com at University of Hong Kong Libraries on December 14, 2014
26 TRAUMA, VIOLENCE, & ABUSE 15(1)

Amygdala showing that the ACC has separate cognitive and affective
divisions to handle both cognitive and emotional processing
The amygdala interacts with the hippocampus and PFC in
(Bush, Luu, & Posner, 2000). Any structural alteration or dys-
responses to emotions and feelings (Aggleton, 1992). It is also
function of the ACC may potentially affect an individuals
involved in the process of memory encoding, consolidation,
emotional self-control and problem-solving capacity (Allman,
storage, and retrieval at various stages of information process-
Hakeem, Erwin, Nimchinsky, & Hof, 2001).
ing (Phelps, 2004). The memorized emotional reactions can
Many studies have reported a significant reduction in the
thus be retrieved for future use (LaBar & Cabeza, 2006; Phelps,
ACC volume of PTSD individuals who had been victims of the
2004; Richardson, Strange, & Dolan, 2004). When there is
subway sarin attack (Araki et al., 2005) or had been involved in
stress, the amygdala triggers the release of stress hormones
combat (Rauch et al., 2003; Woodward et al., 2006). Using
through the HPA axis, which enhances memory consolidation
volumetric analyses and the technology of voxel-based mor-
for stressful conditions (LaBar & Cabeza, 2006). In addition,
phometry, it was found that acute PTSD individuals had no sig-
in the situation of conditioned fear, the amygdala plays a vital
nificant volumetric differences but significant shape
role in mediating the states of increased arousal as well as phy-
differences in the ACC when compared with normal individu-
siologic and behavioral fear responses (LeDoux, 2000).
als (Corbo, Clement, Armony, Pruessner, & Brunet, 2005).
IPV is known to be strongly associated with prolonged and
Moreover, diminished volume of the dorsal ACC (dACC) has
repeated stress, PTSD, and depression (Golding, 1999). These
been consistently found to be associated with emotion dysregu-
emotions and feelings have a suspected link to functional or
lation (Giuliani, Drabant, & Gross, 2011), depression, anxiety,
anatomical changes in the amygdala. In the 1990s, volumetric
and panic disorders (Asami et al., 2008; van Tol et al., 2010).
change in the amygdala was found to be rare in humans, except
However, there remains insufficient evidence regarding the
in those who had operations due to epilepsy or behavioral dis-
effects of IPV, through both physical and psychological path-
turbances (Aggleton, 2000). Indeed, this fits with the recent
ways, on the ACC volume.
evidence that there is no significant difference of amygdala
volume in individuals with PTSD (Woon & Hedges, 2009) or
depression (Hamilton, Siemer, & Gotlib, 2008), or in those PFC
experiencing stressful conditions (Holzel et al., 2010). Never-
The PFC is the most anterior part of the brain (Figure 3) and is
theless, chronic and repeated stress was found to produce den-
responsible for executive and cognitive functions, such as per-
dritic growth in amygdala neurons, the basic cellular unit of the
ception, judgment, reasoning, problem solving, and choice
brain (Vyas, Mitra, Rao, & Chattarji, 2002). This indicates the
making (Roberts, Robbins, & Weiskrantz, 1998). Unlike the
silent anatomical alteration in the amygdala during stress. Also,
autonomic responses, the PFC performs complex top down
it explains the hypersensitivity of the amygdala demonstrated
processing by mapping between sensory stimuli and thoughts
by functional neuroimaging studies in individuals who have
to yield corresponding responses (Miller & Cohen, 2001).
experienced different types of trauma (Bryant et al., 2008;
Therefore, any damage to the PFC can result in impairment
Fonzo et al., 2010).
of various kinds of cognitive functioning and behavioral
Unfortunately, no study has compared the anatomical
responses. Indeed, there has been evidence showing that pre-
changes in the amygdala between abused women and nona-
frontal damage resulted in defective social and moral reasoning
bused women. Thus, there is still inadequate understanding
(Anderson, Bechara, Damasio, Tranel, & Damasio, 1999) as
of the anatomical changes of the amygdala in abused women.
well as moral judgments (Koenigs et al., 2007).
Nevertheless, the work of Vyas, Mitra, Rao, and Chattarji
Many interventions and rehabilitations of abused women
(2002) has shown that there may not be volumetric changes
comprise an empowerment or educational component to help
in the amygdala in abused women, but there may be cellular
the women to manage the abusive relationship (Wathen &
level changes. It is crucial to set up a research hypothesis to
MacMillan, 2003). PFC damage may result in executive and
understand the impact of IPV on the structure of the amygdala
cognitive dysfunction and significantly diminish the effective-
at both the brain region level and the cellular level.
ness of interventions or rehabilitations for abused women. The
damage may be assessed by the volume of gray matter in the
PFC region, and neuroimaging studies have revealed a reduc-
ACC tion in gray matter volume in the PFC region in abused women
The ACC is located at the frontal part of the cingulate cortex, with PTSD (Fennema-Notestine et al., 2002). As the PFC is
which is anatomically connected to the PFC at the dorsal part, responsible for executive and cognitive functions, these abused
and also to the amygdala, hypothalamus, and anterior insula at women may have an impaired ability to make decisions when it
the ventral part (Figure 3). The ACC is particularly important comes to choosing between leaving and staying in the abusive
in conflict monitoring and error processing among the brain relationships. Fennema-Notestine et al.s (2002) study, how-
regions (van Veen, Cohen, Botvinick, Stenger, & Carter, ever, focused on a specific group of abused women with PTSD.
2001). It calls for further processing to the PFC to guide beha- Further studies are recommended to test for the association
vioral responses and decision making. The ACC is also between PFC volume and the planning and decision making
involved in emotions. There has been substantial evidence of abused women in general.

Downloaded from tva.sagepub.com at University of Hong Kong Libraries on December 14, 2014
Wong et al. 27

The frontal lobe of the brain was found to be one of the most concentration leads to changes in magnetic susceptibility. The
affected structural regions in abused women with TBI (Ken- BOLD signals are then generated according to the degree of
nedy et al., 2007), which often involves damage to the PFC due reduced deoxyhemoglobin concentration in the activated area
to the shearing or tearing of brain tissue and neuronal damage of eloquent cortex, which provides an indirect measure of brain
in the frontal regions against the inner skull (Bryant, 2008). activity (Harris, Reynell, & Attwell, 2011; Savoy, 2001). The
However, almost none of the current neuroimaging studies con- BOLD signal will be stronger with a higher degree of activation.
ducted in abused women have measured the presence of head In fMRI studies, neuroscientists often use specific stimuli,
injury or TBI. such as pictures, tone, colors, light, scripts, video, pain, or tem-
perature to test their research hypothesis. Many fMRI studies
Does IPV Alter the Neuroanatomy of Abused Women? are beginning to show consistent findings in functional activa-
tion and deactivation of certain areas of eloquent cortex, such
In summary, our review has identified three main themes in as the limbic structures, in abused women. The following sec-
regard to the functional and anatomical alteration of abused tion summarizes the pattern and distribution of activated elo-
women. The first theme is the scarcity of research on the altera- quent cortex in the brain, and how they may lead to certain
tions in brain anatomy in abused women. Most work was con- behavioral responses, in particular the fear response, pain
ducted on PTSD or depressed survivors. Hence, it is unclear response, and emotion regulation, which are often found in
whether the identified anatomical alterations were due to the abused women suffering from IPV.
IPV exposure or the sequelae of IPV exposure via PTSD or
depression. The second theme depicts the uncertainty about the
anatomical alterations in abused women as a result of psycho- Fear Response
logical stress, physical brain injury, or both. In particular, the Fear has been consistently reported by women experiencing
reviewed studies did not report whether the abused women had IPV, and it has been found to be associated with the severity
experienced head injury or TBI, making it difficult to assess the and frequency of IPV (Kernsmith, 2006; Van Hightower, Gor-
impact of brain injury on anatomical alterations in abused ton, & DeMoss, 2000). In addition, for those abused women
women. Further research should measure the types of abuse who experienced forced sex, the fear level may be even higher
and the presence of brain injury. The third theme relates to the (DeMaris & Swinford, 1996). Ross (2012) summarized the
doseresponse relationship. None of the above studies reported findings of 10 existing IPV research studies that evaluated fear.
the duration of abuse, which is essential for understanding the The majority of them (7 of the 10) used a single item with a
long-term effect of IPV on the human brain. Future studies Likert-type scale to quantify fear (Capaldi & Owen, 2001;
should measure the duration of abuse, so that the impact of IPV DeMaris & Swinford, 1996; Follingstad, Wright, Lloyd, &
on the anatomy of the brain can be analyzed in accordance with Sebastian, 1991; Graham-Kevan & Archer, 2005; Kernsmith,
different levels of IPV exposure in abused women. 2006; Olson et al., 2008; Van Hightower et al., 2000), while the
remainder (3 of the 10; Fergusson, Horwood, & Ridder, 2005;
Understanding Behavioral Responses of Hamberger & Guse, 2002, 2005) used multiple items to quan-
tify fear. However, none of them used a validated measurement
Abused Women Using Functional
tool to evaluate fear, making the findings noncomparable
Neuroimaging among the studies.
The development of noninvasive fMRI using the blood oxygen Our brain can learn to manage fear, a process known as fear
level dependent (BOLD) technique has provided an effective conditioning. Fear conditioning is a conditioned fear response
and safe means to study human brain activity. The BOLD tech- induced by linking certain objects/situations to unrelated
nique indirectly measures brain activity by detecting the objects/situations. This is vital for the detection of danger,
change of oxygen concentration in the blood. Specifically, a self-protection, and survival. However, a hyperresponsive per-
protein molecule in red blood cells, called hemoglobin, is son may be misguided by the fear conditioning and has unne-
responsible for transferring oxygen from the lungs to other cessary fear responses eventually leading to anxiety disorder,
organs, including the brain. Due to its iron-containing structure, panic disorder, or PTSD. For example, there is a notable asso-
hemoglobin can be magnetized. The BOLD technique makes ciation between fear conditioning and anxiety in children with
use of the fact that the magnetic field of hemoglobin varies with early childhood adversity (Anda et al., 2006; Grillon & Mor-
the degree of oxygen saturation. If the hemoglobin is highly gan, 1999; LeDoux & Phelps, 2008; Pine, 1999).
saturated with oxygen (oxyhemoglobin), it becomes a diamag- There is an expanding body of evidence of hyperresponsive
netic substance (weakly repulses a magnetic field); whereas, if limbic structures in women with a history of abuse or PTSD.
oxygen has been used up (deoxyhemoglobin), it becomes para- Using threat-related emotional face stimuli, two fMRI studies
magnetic (attracts and distorts a magnetic field). Once a specific found that abused women with PTSD had significantly ele-
part of eloquent cortex is activated, there will be an increase in vated activation in the left anterior insula, amygdala, and
local cerebral blood flow which causes a reduction in deoxyhe- dACC during matching of fearful versus happy faces, when
moglobin concentration in the activated cortex. As deoxyhemo- compared to women in the control group (Bryant et al., 2008;
globin is paramagnetic, the decrease in deoxyhemoglobin Fonzo et al., 2010). A similar pattern resulted when matching

Downloaded from tva.sagepub.com at University of Hong Kong Libraries on December 14, 2014
28 TRAUMA, VIOLENCE, & ABUSE 15(1)

of angry versus happy faces was performed (Fonzo et al., Emotion Regulation
2010). These results demonstrated that abused women with
Depression and anxiety are both common mental health disor-
PTSD had hyperresponsiveness in the anterior insula, amyg-
ders in abused women (Golding, 1999; Pico-Alfonso et al.,
dala, and dACC. Therefore, the fearful faces, which were orig-
2006), and they are widely considered to be the consequences
inally a nonspecific stimulus of threat, triggered strong
of emotion dysregulation (Berking & Wupperman, 2012). Emo-
activation of the limbic system. Another significant finding
tion dysregulation refers to the loss of control of emotions, which
of Fonzos study was that there was significantly greater acti-
includes decreasing, maintaining, or increasing positive/negative
vation of the dACC in the abused group with PTSD when com-
emotional reactions (Gross, 2002). Therefore, a good under-
paring male faces with female faces. The authors suggested that
standing of emotion regulation is highly relevant to the develop-
the hyperactivity of the dACC while matching male faces
ment of interventions for reducing depression and anxiety. A
might reflect hypervigilance, a core symptom of PTSD, due
recent meta-analysis investigated the relationships between six
to the dysregulated appraisal of the stimulus related to past
emotion regulation strategies (acceptance, avoidance, problem
trauma (Bryant et al., 2008). Both fMRI studies clearly showed
solving, reappraisal, rumination, and suppression) and mental
that abused women learned fear from their IPV experience. The
health problems (depression, anxiety, eating disorders, and sub-
fear response to fearful faces was unconscious, which helped in
stance abuse; Aldao, Nolen-Hoeksema, & Schweizer, 2010).
explaining why women can develop hyperactivation of danger
Rumination was found to be highly associated with poor mental
perception in the emotion-related circuitry of the brain after
health, while avoidance and suppression had a moderate associ-
being abused.
ation with poor mental health. Problem solving was found to
have a moderate to high association with good mental health,
Pain Response while reappraisal was noted to have a moderate to low associa-
tion with good mental health. Unexpectedly, acceptance, which
Pain is associated with more health care utilization (Plichta,
has been long perceived as one of the methods for healing
2004; Wong, Wester, Mol, Romkens, & Lagro-Janssen,
depression, was not observed to be significantly associated with
2007). Chronic pain is often reported in abused women (Hum-
mental health. These relationship patterns provided relevant
phreys et al., 2011; Kendall-Tackett, Marshall, & Ness, 2003;
information about emotion regulation strategies in the preven-
Wuest et al., 2010). This can be chronic low back pain, chronic
tion or treatment of mental health problems. However, the
headache (Humphreys et al., 2011), chronic pelvic pain (Tho-
cross-sectional nature of this study and the subjective self-
mas, Moss-Morris, & Faquhar, 2006), or fibromyalgia (Rubin,
assessment of emotion regulation were the major limitations.
2005).
Neuroimaging studies, on the contrary, examined emotion
Pain response in abused women has not yet been clearly
regulation in a more objective domain. For instance, deficits
explained using neuroimaging studies. Only two fMRI studies
of ACC function were determined by both an fMRI study (New
investigated the pain response of women with a history of
et al., 2009) and a PET study (Bremner et al., 2004) in women
abuse. Noll-Hussong et al. (2010) performed a pilot study on
with a history of sexual abuse. The ACC is responsible for
women suffering from chronic pain with or without a history
emotion regulation. Both studies found that there was less acti-
of childhood sexual abuse. By viewing 120 pictures with four
vation in the ACC during downregulation of emotions to a neg-
levels of pain (no, low, medium, and high pain), the partici-
ative stimulus in abused women compared with healthy
pants were instructed to rate the pain intensity during fMRI
controls. Therefore, it is suggested that IPV may impede
scanning. Women who were sexually abused during their child-
womens ability to decrease emotional responses to negative
hood were found to have higher activation in the left medial
stimuli.
and lateral PFC than women without a history of childhood
A cognitive emotional regulation strategy was found to be
sexual abuse. Given the involvement in memory retrieval of the
helpful for women to regulate their emotions in an fMRI study
left frontal areas, the study concluded that sexually abused
when women were shown threat-related and neutral pictures
women were much more sensitive in their response to pain.
(Eippert et al., 2007). The findings showed that the activation
In contrast, another fMRI study did not show higher activation
of the amygdala, which is known to be involved in the response
of the brain regions related to pain in response to experimental
to a threat-related picture, diminished when the participants
pain perception (i.e., nonpainful temperatures, slightly painful
were asked to downregulate emotions. In contrast, the frontal
temperatures, and moderately painful temperatures) in abused
regions, including the ACC, dorsal PFC, and orbitofrontal cor-
women (Strigo et al., 2010). Instead, with repeated exposure
tex, were much more reactive, when compared with the base-
to painful temperatures, abused women experienced a reduced
line. In other words, the emotional responses in the amygdala
subjective pain intensity compared with nonabused women.
were susceptible to top-down control from the frontal region.
The authors explained the findings in terms of avoidance,
These results indicated the potential effective use of cognitive
which is a PTSD symptom. However, this argument cannot
strategies in emotion regulation as a treatment for mental health
explain the experience of chronic pain in abused women. It
problems. However, the study did not measure the abuse his-
may be that the pain experienced by abused women is psycho-
tory of the participants, making the results inconclusive in
somatic or social, which is different from the physical pain
abused women.
tested in Strigo et al.s (2010) experimental fMRI study.

Downloaded from tva.sagepub.com at University of Hong Kong Libraries on December 14, 2014
Wong et al. 29

To our knowledge, no study to date has investigated the Akana, S. F., Chu, A., Soriano, L., & Dallman, M. F. (2001). Corticos-
effectiveness of different coping strategies in abused women terone exerts site-specific and state-dependent effects in prefrontal
to regulate emotions using an fMRI study. However, it is likely cortex and amygdala on regulation of adrenocorticotropic hor-
that the interplay between the affective and cognitive division mone, insulin and fat depots. Journal of Neuroendocrinology,
of the brain underlies the emotion regulation in women experi- 13, 625637.
encing IPV. It is recommended, specifically, that future studies Aldao, A., Nolen-Hoeksema, S., & Schweizer, S. (2010). Emotion-
should assess the emotion regulation strategies and enable the regulation strategies across psychopathology: A meta-analytic
comparison of ACC and amygdala activation or deactivation review. Clinical Psychology Review, 30, 217237.
among IPV survivors using different emotion regulation strate- Allman, J. M., Hakeem, A., Erwin, J. M., Nimchinsky, E., & Hof, P.
gies by advanced neuroimaging studies. The findings are (2001). The anterior cingulate cortex. The evolution of an interface
expected to be helpful in developing interventions to improve between emotion and cognition. Annals of the New York Academy
abused womens mental health outcomes. of Sciences, 935, 107117.
Anda, R. F., Felitti, V. J., Bremner, J. D., Walker, J. D., Whitfield, C.,
Perry, B. D., . . . Giles, W. H. (2006). The enduring effects of
Implications for Research, Practice,
abuse and related adverse experiences in childhood. A conver-
and Policy gence of evidence from neurobiology and epidemiology. European
 Research on neurological damage and neuropsychologi- Archives of Psychiatry and Clinical Neuroscience, 256, 174186.
cal damage in women survivors of IPV is seriously lack- Anderson, S. W., Bechara, A., Damasio, H., Tranel, D., & Damasio,
ing. Existing studies mainly focused on the target A. R. (1999). Impairment of social and moral behavior related to
population of women with PTSD. However, there is a early damage in human prefrontal cortex. Nature Neurosciences,
possibility that abused women might suffer from neuro- 2, 10321037.
physiological changes associated with cognitive dys- Araki, T., Kasai, K., Yamasue, H., Kato, N., Kudo, N., Ohtani, T., . . .
function but without PTSD symptoms. Iwanami, A. (2005). Association between lower P300 amplitude
 Research on the impact of IPV on abused women, such and smaller anterior cingulate cortex volume in patients with post-
as depression, anxiety, poor memory, and inability in traumatic stress disorder: A study of victims of Tokyo subway
decision making remains at a descriptive level. Current sarin attack. NeuroImage, 25, 4350.
studies are still unable to explain why some abused Arzt, E., Pereda, M. P., Castro, C. P., Pagotto, U., Renner, U., & Stalla,
women develop mental health problems, while some G. K. (1999). Pathophysiological role of the cytokine network in
do not. Therefore, future research should aim to gain sci- the anterior pituitary gland. Frontiers in Neuroendocrinology,
entific evidence for the explanations of these phenom- 20, 7195.
ena through neuroimaging studies. Asami, T., Hayano, F., Nakamura, M., Yamasue, H., Uehara, K.,
 Through the evidence of neuroimaging studies, we can Otsuka, T., . . . Hirayasu, Y. (2008). Anterior cingulate cortex vol-
further understand the neurological damage in abused ume reduction in patients with panic disorder. Psychiatry and Clin-
women. This can provide relevant information to ical Neurosciences, 62, 322330.
develop efficient and cost-effective interventions for Banks, M. E. (2007). Overlooked but critical: Traumatic brain injury
women survivors of IPV. as a consequence of interpersonal violence. Trauma Violence
 Health care professionals or case workers of IPV victims Abuse, 8, 290298.
should receive training about brain function and assess- Berking, M., & Wupperman, P. (2012). Emotion regulation and men-
ment of neurological functioning, and acquire the skills tal health: Recent findings, current challenges, and future direc-
of caring for women with neurological or neuropsycholo- tions. Current Opinion in Psychiatry, 25, 128134.
gical damage. Bremner, J. D. (1999). Does stress damage the brain? Biological Psy-
chiatry, 45, 797805.
Bremner, J. D., & Narayan, M. (1998). The effects of stress on mem-
Declaration of Conflicting Interests ory and the hippocampus throughout the life cycle: Implications
The author(s) declared no potential conflicts of interest with respect to for childhood development and aging. Development and Psycho-
the research, authorship, and/or publication of this article. pathology, 10, 871885.
Bremner, J. D., Vermetten, E., Vythilingam, M., Afzal, N., Schmahl,
Funding C., Elzinga, B., & Charney, D. S. (2004). Neural correlates of the
The author(s) received no financial support for the research, author- classic color and emotional stroop in women with abuse-related
ship, and/or publication of this article. posttraumatic stress disorder. Biological Psychiatry, 55, 612620.
Bremner, J. D., Vythilingam, M., Anderson, G., Vermetten, E.,
References McGlashan, T., Heninger, G., . . . Charney, D. S. (2003). Assess-
Aggleton, J. P. (1992). The amygdala: Neurobiological aspects of emo- ment of the hypothalamic-pituitary-adrenal axis over a 24-hour
tion, memory, and mental dysfunction. New York, NY: Wiley-Liss. diurnal period and in response to neuroendocrine challenges in
Aggleton, J. P. (2000). Amygdala: A functional analysis. New York, women with and without childhood sexual abuse and posttraumatic
NY: Oxford University Press. stress disorder. Biological Psychiatry, 54, 710718.

Downloaded from tva.sagepub.com at University of Hong Kong Libraries on December 14, 2014
30 TRAUMA, VIOLENCE, & ABUSE 15(1)

Brown, D. S., Finkelstein, E. A., & Mercy, J. A. (2008). Methods for Elzinga, B. M., Schmahl, C. G., Vermetten, E., van Dyck, R., & Brem-
estimating medical expenditures attributable to intimate partner ner, J. D. (2003). Higher cortisol levels following exposure to
violence. Journal of Interpersonal Violence, 23, 17471766. traumatic reminders in abuse-related PTSD. Neuropsychophar-
Bryant, R. A. (2008). Disentangling mild traumatic brain injury and stress macology, 28, 16561665.
reactions. The New England Journal of Medicine, 358, 525527. Fayed, N., Andres, E., Rojas, G., Moreno, S., Serrano-Blanco, A.,
Bryant, R. A., Kemp, A. H., Felmingham, K. L., Liddell, B., Olivieri, Roca, M., & Garcia-Campayo, J. (2011). Brain dysfunction in
G., Peduto, A., . . . Williams, L. M. (2008). Enhanced amygdala fibromyalgia and somatization disorder using proton magnetic
and medial prefrontal activation during nonconscious processing resonance spectroscopy: A controlled study. Acta Psychiatric
of fear in posttraumatic stress disorder: An fMRI study. Human Scandinavica, 126, 115125.
Brain Mapping, 29, 517523. Fennema-Notestine, C., Stein, M. B., Kennedy, C. M., Archibald, S. L.,
Bush, G., Luu, P., & Posner, M. I. (2000). Cognitive and emotional & Jernigan, T. L. (2002). Brain morphometry in female victims of
influences in anterior cingulate cortex. Trends in Cognitive Sci- intimate partner violence with and without posttraumatic stress dis-
ence, 4, 215222. order. Biological Psychiatry, 52, 10891101.
Cannon, W. B. (1929). Bodily changes in pain, hunger, fear, and rage. Fergusson, D. M., Horwood, L. J., & Ridder, E. M. (2005). Partner
New York, NY: Appleton-Century-Crofts. violence and mental health outcomes in a New Zealand birth
Capaldi, D. M., & Owen, L. D. (2001). Physical aggression in a com- cohort. Journal of Marriage and Family, 67, 11031119.
munity sample of at-risk young couples: Gender comparisons for Flegar, S. J., Fouche, J. P., Jordaan, E., Marais, S., Spottiswoode, B.,
high frequency, injury, and fear. Journal of Family Psychology, Stein, D. J., & Vythilingum, B. (2011). The neural correlates of
15, 425440. intimate partner violence in women. African Journal of Psychiatry
Chen, Y., Brunson, K. L., Adelmann, G., Bender, R. A., Frotscher, M., (Johannesbg), 14, 310314.
& Baram, T. Z. (2004). Hippocampal corticotropin releasing hor- Follingstad, D. R., Wright, S., Lloyd, S., & Sebastian, J. A. (1991).
mone: Pre- and postsynaptic location and release by stress. Neu- Sex differences in motivations and effects in dating violence. Fam-
roscience, 126, 533540. ily Relations, 40, 5157.
Coker, A., Smith, P., Bethea, L., King, M., & McKeown, R. (2000). Fonzo, G. A., Simmons, A. N., Thorp, S. R., Norman, S. B., Paulus,
Physical health consequences of physical and psychological inti- M. P., & Stein, M. B. (2010). Exaggerated and disconnected
mate partner violence. Archives of Family Medicine, 9, 451457. insular-amygdalar blood oxygenation level-dependent response
Corbo, V., Clement, M. H., Armony, J. L., Pruessner, J. C., & Brunet, to threat-related emotional faces in women with intimate-
A. (2005). Size versus shape differences: Contrasting voxel-based partner violence posttraumatic stress disorder. Biological Psy-
and volumetric analyses of the anterior cingulate cortex in individ- chiatry, 68, 433441.
uals with acute posttraumatic stress disorder. Biological Psychia- Frodl, T., Jager, M., Smajstrlova, I., Born, C., Bottlender, R., Palla-
try, 58, 119124. dino, T., . . . Meisenzahl, E. M. (2008). Effect of hippocampal and
Crofford, L. J. (2007). Violence, stress, and somatic syndromes. amygdala volumes on clinical outcomes in major depression: A
Trauma, Violence, & Abuse, 8, 299313. 3-year prospective magnetic resonance imaging study. Journal of
Dallman, M. F., Akana, S. F., Strack, A. M., Scribner, K. S., Pecoraro, Psychiatry & Neuroscience, 33, 423430.
N., La Fleur, S. E., . . . Gomez, F. (2004). Chronic stress-induced Frodl, T., Schaub, A., Banac, S., Charypar, M., Jager, M.,
effects of corticosterone on brain: Direct and indirect. Annals of the Kummler, P., . . . Meisenzahl, E. M. (2006). Reduced hippocam-
New York Academy of Sciences, 1018, 141150. pal volume correlates with executive dysfunctioning in major
Davidson, R. J., Pizzagalli, D., Nitschke, J. B., & Putnam, K. (2002). depression. Journal of Psychiatry & Neuroscience, 31, 316323.
Depression: Perspectives from affective neuroscience. Annual Giuliani, N. R., Drabant, E. M., & Gross, J. J. (2011). Anterior cingu-
Review of Psychology, 53, 545574. late cortex volume and emotion regulation: Is bigger better? Biolo-
de Kloet, E. R. (2000). Stress in the brain. European Journal of Phar- gical Psychology, 86, 379382.
macology, 405, 187198. Golding, J. M. (1999). Intimate partner violence as a risk factor for
DeMaris, A., & Swinford, S. (1996). Female victims of vpousal vio- mental disorders: A meta-analysis. Journal of Family Violence,
lence: Factors influencing their level of fearfulness. Family Rela- 14, 99132.
tions, 45, 98106. Graham-Kevan, N., & Archer, J. (2005). Investigating three explana-
Dolezal, T., McCollum, D., & Callahan, M. (2009). Hidden costs in tions of womens relationship aggression. Psychology of Women
health care: The economic impact of violence and abuse. Eden Quarterly, 29, 270277.
Prairie, MN: The Academy on Violence and Abuse. Grillon, C., & Morgan, C. A. I. (1999). Fearpotentiated startle condi-
Drevets, W. C., Price, J. L., & Furey, M. L. (2008). Brain structural tioning to explicit and contextual cues in Gulf War veterans with
and functional abnormalities in mood disorders: Implications for posttraumatic stress disorder. Journal of Abnormal Psychology,
neurocircuitry models of depression. Brain Structure and Func- 108, 134142.
tion, 213, 93118. Gross, J. J. (2002). Emotion regulation: Affective, cognitive, and
Eippert, F., Veit, R., Weiskopf, N., Erb, M., Birbaumer, N., & Anders, social consequences. Psychophysiology, 39, 281291.
S. (2007). Regulation of emotional responses elicited by threat- Hamberger, L. K., & Guse, C. (2005). Typology of reactions to inti-
related stimuli. [Research Support, Non-U.S. Govt]. Human Brain mate partner violence among men and women arrested for partner
Mapping, 28, 409423. violence. Violence and Victims, 20, 303317.

Downloaded from tva.sagepub.com at University of Hong Kong Libraries on December 14, 2014
Wong et al. 31

Hamberger, L. K., & Guse, C. E. (2002). Mens and womens use of posttraumatic stress disorder-like symptoms and mild traumatic
intimate partner violence in clinical samples. Violence Against brain injury. Journal of Rehabilitation Research and Development,
Women, 8, 13011331. 44, 895920.
Hamilton, J. P., Siemer, M., & Gotlib, I. H. (2008). Amygdala volume Kernsmith, P. (2006). Gender differences in the impact of family of
in major depressive disorder: A meta-analysis of magnetic reso- origin violence on perpetrators of domestic violence. Journal of
nance imaging studies. Molecular Psychiatry, 13, 9931000. Family Violence, 21, 163171.
Harris, J. J., Reynell, C., & Attwell, D. (2011). The physiology of Kiy, G., Lehmann, P., Hahn, H. K., Eling, P., Kastrup, A., & Hildeb-
developmental changes in BOLD functional imaging signals. randt, H. (2011). Decreased hippocampal volume, indirectly mea-
Developmental Cognitive Neuroscience, 1, 199216. sured, is associated with depressive symptoms and consolidation
Hedges, D. W., & Woon, F. L. (2010). Alcohol use and hippocampal deficits in multiple sclerosis. Multiple Sclerosis Journal, 17,
volume deficits in adults with posttraumatic stress disorder: A 10881097.
meta-analysis. Biological Psychology, 84, 163168. Koenigs, M., Young, L., Adolphs, R., Tranel, D., Cushman, F., Hau-
Heim, C., Ehlert, U., Hanker, J. P., & Hellhammer, D. H. (1998). ser, M., & Damasio, A. (2007). Damage to the prefrontal cortex
Abuse-related posttraumatic stress disorder and alterations of the increases utilitarian moral judgements. Nature, 446, 908911.
hypothalamic-pituitary-adrenal axis in women with chronic pelvic Koopman, C., Ismailji, T., Palesh, O., Gore-Felton, C., Narayanan, A.,
pain. Psychosomatic Medicine, 60, 309318. Saltzman, K. M., . . . McGarvey, E. L. (2007). Relationships of
Heim, C., Newport, D. J., Heit, S., Graham, Y. P., Wilcox, M., Bon- depression to child and adult abuse and bodily pain among women
sall, R., . . . Nemeroff, C. B. (2000). Pituitary-adrenal and auto- who have experienced intimate partner violence. Journal of Inter-
nomic responses to stress in women after sexual and physical personal Violence, 22, 438455.
abuse in childhood. The Journal of the American Medical Associ- Kreutzer, J. S., Seel, R. T., & Gourley, E. (2001). The prevalence and
ation, 284, 592597. symptom rates of depression after traumatic brain injury: A com-
Heim, C., Newport, D. J., Wagner, D., Wilcox, M. M., Miller, A. H., & prehensive examination. Brain Injury, 15, 563576.
Nemeroff, C. B. (2002). The role of early adverse experience and Kwako, L. E., Glass, N., Campbell, J., Melvin, K. C., Barr, T., & Gill,
adulthood stress in the prediction of neuroendocrine stress reactiv- J. M. (2011). Traumatic brain injury in intimate partner violence: A
ity in women: A multiple regression analysis. Depress Anxiety, 15, critical review of outcomes and mechanisms. Trauma, Violence, &
117125. Abuse, 12, 115126.
Holzel, B. K., Carmody, J., Evans, K. C., Hoge, E. A., Dusek, J. A., LaBar, K. S., & Cabeza, R. (2006). Cognitive neuroscience of emo-
Morgan, L., . . . Lazar, S. W. (2010). Stress reduction correlates tional memory. Nature Review Neuroscience, 7, 5464.
with structural changes in the amygdala. Social Cognitive and LeDoux, J. E. (2000). Emotion circuits in the brain. Annual Review of
Affective Neuroscience, 5, 1117. Neuroscience, 23, 155184.
Humphreys, J., Cooper, B. A., & Miaskowski, C. (2011). Occurrence, LeDoux, J. E., & Phelps, E. A. (2008). Emotional networks in the
characteristics, and impact of chronic pain in formerly abused brain. In M. Lewis, J. M. Haviland-Jones, & L. F. Barrett (Eds.),
women. Violence Against Women, 17, 13271343. Handbook of emotions (pp. 159179). New York, NY: Guilford
Inslicht, S. S., Marmar, C. R., Neylan, T. C., Metzler, T. J., Hart, S. L., Press.
Otte, C., . . . Baum, A. (2006). Increased cortisol in women with Marcel, P. D. (2004). Quality of life after traumatic brain injury: A
intimate partner violence-related posttraumatic stress disorder. review of research approaches and findings. Archives of Physical
Psychoneuroendocrinology, 31, 825838. Medicine and Rehabilitation, 85, 2135.
Jackson, H., Philp, E., Nuttall, R. L., & Diller, L. (2002). Traumatic McEwen, B. S. (1998). Protective and damaging effects of stress med-
brain injury: A hidden consequence for battered women. Profes- iators. New England Journal of Medicine, 338, 171179.
sional Psychology: Research and Practice, 33, 3945. McEwen, B. S. (2005). Stressed or stressed out: What is the differ-
Joels, M., Karst, H., Krugers, H. J., & Lucassen, P. J. (2007). Chronic ence? Journal of Psychiatry & Neuroscience, 30, 315318.
stress: Implications for neuronal morphology, function and neuro- McEwen, B. S. (2007). Physiology and neurobiology of stress and
genesis. Frontiers in Neuroendocrinology, 28, 7296. adaptation: Central role of the brain. Physiological Reviews, 87,
Karl, A., Schaefer, M., Malta, L. S., Dorfel, D., Rohleder, N., & 873904.
Werner, A. (2006). A meta-analysis of structural brain abnorm- Mechanic, M. B., Weaver, T. L., & Resick, P. A. (2008). Mental
alities in PTSD. Neuroscience & Biobehavioral Reviews, 30, health consequences of intimate partner abuse: A multidimensional
10041031. assessment of four different forms of abuse. Violence Against
Kendall-Tackett, K. A. (2007). Inflammation, cardiovascular disease, Women, 14, 634654.
and metabolic syndrome as sequelae of violence against women: Miller, E. K., & Cohen, J. D. (2001). An integrative theory of prefron-
The role of depression, hostility, and sleep disturbance. Trauma tal cortex function. Annual Review of Neuroscience, 24, 167202.
Violence Abuse, 8, 117126. Monahan, K., & OLeary, K. D. (1999). Head injury and battered
Kendall-Tackett, K. A., Marshall, R., & Ness, K.E. (2003). Chronic women: An initial inquiry. Health & Social Work, 24, 269278.
pain syndromes and violence against women. Women and Therapy, National Center for Injury Prevention and Control. (2003). Report to
26, 4556. congress on mild traumatic brain injury in the United States: Steps
Kennedy, J. E., Jaffee, M. S., Leskin, G. A., Stokes, J. W., Leal, F. O., & to prevent a serious public health problem. Atlanta, GA: Centers
Fitzpatrick, P. J. (2007). Posttraumatic stress disorder and for Disease Control and Prevention.

Downloaded from tva.sagepub.com at University of Hong Kong Libraries on December 14, 2014
32 TRAUMA, VIOLENCE, & ABUSE 15(1)

New, A. S., Fan, J., Murrough, J. W., Liu, X., Liebman, R. E., Guise, Silverman, M. N., Pearce, B. D., Biron, C. A., & Miller, A. H. (2005).
K. G., . . . Charney, D. S. (2009). A functional magnetic reso- Immune modulation of the hypothalamic-pituitary-adrenal (HPA)
nance imaging study of deliberate emotion regulation in resili- axis during viral infection. Viral Immunology, 18, 4178.
ence and posttraumatic stress disorder. Biological Psychiatry, Smith, D. J., Jr., Mills, T., & Taliaferro, E. H. (2001). Frequency and
66, 656664. relationship of reported symptomology in victims of intimate part-
Noll-Hussong, M., Otti, A., Laeer, L., Wohlschlaeger, A., Zimmer, C., ner violence: The effect of multiple strangulation attacks. The
Lahmann, C., . . . Guendel, H. (2010). Aftermath of sexual abuse Journal of Emergency Medicine, 21, 323329.
history on adult patients suffering from chronic functional pain Smith, M. E. (2005). Bilateral hippocampal volume reduction in adults
syndromes: An fMRI pilot study. Journal of Psychosomatic with post-traumatic stress disorder: A meta-analysis of structural
Research, 68, 483487. MRI studies. Hippocampus, 15, 798807.
Olson, E. C., Kerker, B. D., McVeigh, K. H., Stayton, C., Wye, G. V., Southwick, S. M., Rasmusson, A., Barron, J., & Arnsten, A. (2005).
& Thorpe, L. (2008). Profiling risk of fear of an intimate partner Neurobiological and neurocognitive alterations in PTSD. In J. J.
among men and women. Preventive Medicine, 47, 559564. Vasterling & C. R. Brewin (Eds.), Neuropsychology of PTSD: Bio-
Phelps, E. A. (2004). Human emotion and memory: Interactions of the logical, cognitive, and clinical perspectives (pp. 2758). New
amygdala and hippocampal complex. Current Opinion in Neuro- York, NY: The Guilford Press.
biology, 14, 198202. Stern, C. M. (2011). Corticotropin-releasing factor in the hippocam-
Pico-Alfonso, M. A., Garcia-Linares, M. I., Celda-Navarro, N., pus: Eustress or distress? The Journal of Neuroscience, 31,
Blasco-Ros, C., Echeburua, E., & Martinez, M. (2006). The impact 19351936.
of physical, psychological, and sexual intimate male partner vio- Strigo, I. A., Simmons, A. N., Matthews, S. C., Grimes, E. M., Allard,
lence on womens mental health: Depressive symptoms, posttrau- C. B., Reinhardt, L. E., . . . Stein, M. B. (2010). Neural correlates of
matic stress disorder, state anxiety, and suicide. Journal of Womens altered pain response in women with posttraumatic stress disorder
Health (Larchmt), 15, 599611. from intimate partner violence. Biological Psychiatry, 68, 442450.
Pine, D. S. (1999). Pathophysiology of childhood anxiety disorders. Thomas, E., Moss-Morris, R., & Faquhar, C. (2006). Coping with
Biological Psychiatry, 46, 15551566. emotions and abuse history in women with chronic pelvic pain.
Plichta, S. B. (2004). Intimate partner violence and physical health Journal of Psychosomatic Research, 60, 109112.
consequences. Journal of Interpersonal Violence, 19, 12961323. Thurman, D. J., Sniezek, J. E., Johnson, D., Greenspan, A., & Smith,
Rauch, S. L., Shin, L. M., Segal, E., Pitman, R. K., Carson, M. A., S. M. (1995). Guidelines for surveillance of central nervous system
McMullin, K., . . . Makris, N. (2003). Selectively reduced regional injury. Atlanta, GA: Centers for Disease Control and Prevention.
cortical volumes in post-traumatic stress disorder. NeuroReport, Valera, E. M., & Berenbaum, H. (2003). Brain injury in battered
14, 913916. women. Journal of Consulting and Clinical Psychology, 71,
Resnick, S. M., Pham, D. L., Kraut, M. A., Zonderman, A. B., & 797804.
Davatzikos, C. (2003). Longitudinal magnetic resonance imaging Van Hightower, N. R., Gorton, J., & DeMoss, C. L. (2000). Predictive
studies of older adults: A shrinking brain. The Journal of Neu- models of domestic violence and fear of intimate partners among
roscience, 23, 32953301. migrant and seasonal farm worker women. Journal of Family Vio-
Richardson, M. P., Strange, B. A., & Dolan, R. J. (2004). Encoding of lence, 15, 137154.
emotional memories depends on amygdala and hippocampus and van Tol, M. J., van der Wee, N. J., van den Heuvel, O. A., Nielen, M.
their interactions. Nature Neuroscience, 7, 278285. M., Demenescu, L. R., Aleman, A., . . . Veltman, D. J. (2010).
Roberts, A. C., Robbins, T. W., & Weiskrantz, L. (1998). The prefron- Regional brain volume in depression and anxiety disorders.
tal cortexExecutive and cognitive functions. Oxford, England: Archives of General Psychiatry, 67, 10021011.
Oxford University Press. van Veen, V., Cohen, J. D., Botvinick, M. M., Stenger, V. A., &
Roozendaal, B., McEwen, B. S., & Chattarji, S. (2009). Stress, mem- Carter, C. S. (2001). Anterior cingulate cortex, conflict monitoring,
ory and the amygdala. Nature Reviews Neuroscience, 10, 423433. and levels of processing. NeuroImage, 14, 13021308.
Ross, J. M. (2012). Self-reported fear in partner violent relationships: Vyas, A., Mitra, R., Rao, B. S. S., & Chattarji, S. (2002). Chronic
Findings on gender differences from two samples. Psychology of stress induces contrasting patterns of dendritic remodeling in hip-
Violence, 2, 5874. pocampal and amygdaloid neurons. The Journal of Neuroscience,
Rubin, J. J. (2005). Psychosomatic pain: New insights and manage- 22, 68106818.
ment strategies. Southern Medical Journal, 98, 10991110. Walker, L. E., & Browne, A. (1985). Gender and victimization by inti-
Savoy, R. L. (2001). History and future directions of human brain map- mates. Journal of Personality, 53, 179195.
ping and functional neuroimaging. Acta Psychologica, 107, 942. Warner-Schmidt, J. L., & Duman, R. S. (2006). Hippocampal neuro-
Shea, A., Walsh, C., Macmillan, H., & Steiner, M. (2005). Child mal- genesis: Opposing effects of stress and antidepressant treatment.
treatment and HPA axis dysregulation: Relationship to major Hippocampus, 16, 239249.
depressive disorder and post traumatic stress disorder in females. Wathen, C. N., & MacMillan, H. L. (2003). Interventions for violence
Psychoneuroendocrinology, 30, 162178. against women: Scientific review. The Journal of the American
Shin, L. M., Rauch, S. L., & Pitman, R. K. (2006). Amygdala, medial Medical Association, 289, 589600.
prefrontal cortex, and hippocampal function in PTSD. Annals of Weidenfeld, J., Newman, M. E., Itzik, A., Gur, E., & Feldman, S.
the New York Academy of Sciences, 1071, 6779. (2002). The amygdala regulates the pituitary-adrenocortical

Downloaded from tva.sagepub.com at University of Hong Kong Libraries on December 14, 2014
Wong et al. 33

response and release of hypothalamic serotonin following electri- the emergency department: A systematic review and meta-analy-
cal stimulation of the dorsal raphe nucleus in the rat. Neuroendo- sis. Trauma Violence Abuse, 11, 7182.
crinology, 76, 6369. Wuest, J., Ford-Gilboe, M., Merritt-Gray, M., Wilk, P., Campbell, J.
Wilbur, L., Higley, M., Hatfield, J., Surprenant, Z., Taliaferro, E., C., Lent, B., . . . Smye, V. (2010). Pathways of chronic pain in sur-
Smith, D. J., Jr., & Paolo, A. (2001). Survey results of women who vivors of intimate partner violence. The Journal of Womens Health
have been strangled while in an abusive relationship. The Journal (Larchmt), 19, 16651674.
of Emergency Medicine, 21, 297302. Ystad, M., Lundervold, A., Wehling, E., Espeseth, T., Rootwelt, H.,
Woods, A. B., Page, G. G., OCampo, P., Pugh, L. C., Ford, D., & Westlye, L., . . . Lundervold, A. (2009). Hippocampal volumes are
Campbell, J. C. (2005). The mediation effect of posttraumatic important predictors for memory function in elderly women. BMC
stress disorder symptoms on the relationship of intimate partner Medical Imaging, 9, 17.
violence and IFN-gamma levels. Americam Journal of Community
Psychology, 36, 159175.
Woods, S. J. (2005). Intimate partner violence and post-traumatic Author Biographies
stress disorder symptoms in women: What we know and need to
Janet Yuen-Ha Wong, RN, PhD, is an assistant professor at the
know. Journal of Interpersonal Violence, 20, 394402.
School of Nursing of the University of Hong Kong. She received her
Woods, S. J., Wineman, N. M., Page, G. G., Hall, R. J., Alexander, T.
PhD at the University of Hong Kong. Her principal research interest
S., & Campbell, J. C. (2005). Predicting immune status in women lies in intimate partner violence and physical, psychological, and cog-
from PTSD and childhood and adult violence. ANS Advaances in nitive well-being of abused women. During her PhD study, she had
Nursing Science, 28, 306319. been awarded Fulbright visiting scholarship (20102011) affiliated
Wong, C. M. (2002). Post-traumatic stress disorder: Advances in with University of Virginia in the United States.
psychoneuroimmunology. Psychiatric Clinics of North America,
Daniel Yee-Tak Fong, PhD, is an associate professor at the School of
25, 369383.
Nursing of The University of Hong Kong. He received his degrees of
Wong, S. L. F., Wester, F., Mol, S., Romkens, R., & Lagro-Janssen, T.
BSc in mathematics and MPhil in statistics from The University of
(2007). Utilisation of health care by women who have suffered Hong Kong. He then obtained his PhD in statistics from the University
abuse: A descriptive study on medical records in family practice. of Waterloo, Canada. He is an experienced biostatistician in health
The British Journal of General Practice, 57, 396400. research. Specifically, he focuses on the application of the best avail-
Woodward, S. H., Kaloupek, D. G., Streeter, C. C., Martinez, C., able methods to scientific research in health-related fields, and to
Schaer, M., & Eliez, S. (2006). Decreased anterior cingulate develop novel methodologies with applications in health research.
volume in combat-related PTSD. Biologic Psychiatry, 59,
Vincent Lai, MBChB (CUHK), FRCR (UK), FHKCR, FHKAM (Radi-
582587.
ology), is currently a clinical assistant professor at the Department of
Woon, F. L., & Hedges, D. W. (2009). Amygdala volume in adults Diagnostic Radiology of The University of Hong Kong. He obtained his
with posttraumatic stress disorder: A meta-analysis. The Journal medical degree from the Chinese University of Hong Kong and became
of Neuropsychiatry and Clinical Neurosciences, 21, 512. the Fellow of the Hong Kong Academy of Medicine in 2010. He was
Woon, F. L., Sood, S., & Hedges, D. W. (2010). Hippocampal volume awarded the Rohan Williams Medal in the Royal College of Radiologists
deficits associated with exposure to psychological trauma and post- examination. He is a specialist neuroradiologists with main research
traumatic stress disorder in adults: A meta-analysis. Progess in Neu- interest in neuroradiology with use of advanced MR imaging techniques.
ropsychopharmacology & Biolgical Psychiatry, 34, 11811188.
Agnes Tiwari, RN, PhD, FAAN, is a professor and head of School of
World Health Organization. (Ed.). (1992). International statistical Nursing at the University of Hong Kong. She is internationally recog-
classification of diseases and related health problems (10th ed.). nized for her work on interpersonal violence prevention and interven-
Geneva, Switzerland: Author. tion including the validation of the Chinese Abuse Assessment Screen
Wu, V., Huff, H., & Bhandari, M. (2010). Pattern of physical injury and several clinical trials of violence prevention models at primary,
associated with intimate partner violence in women presenting to secondary, and tertiary levels.

Downloaded from tva.sagepub.com at University of Hong Kong Libraries on December 14, 2014
View publication stats