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Strokes, falls and dementias are the leading causes for functional deterioration, loss of independence and institutionalization of elderly people. Motor and cognitive brain disorders can be attributed to many known risk factors that can be modified. Falls risk can be modified by better pre-vention of cardiac embolism, slowing atherosclerosis or treating carotid stenosis.
Strokes, falls and dementias are the leading causes for functional deterioration, loss of independence and institutionalization of elderly people. Motor and cognitive brain disorders can be attributed to many known risk factors that can be modified. Falls risk can be modified by better pre-vention of cardiac embolism, slowing atherosclerosis or treating carotid stenosis.
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Strokes, falls and dementias are the leading causes for functional deterioration, loss of independence and institutionalization of elderly people. Motor and cognitive brain disorders can be attributed to many known risk factors that can be modified. Falls risk can be modified by better pre-vention of cardiac embolism, slowing atherosclerosis or treating carotid stenosis.
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DOI 10.1007/s00415-005-0986-6 ORI GI NAL COMMUNI CATI ON
Nir Giladi Michael Mordechovich Leor Gruendlinger Herzel Shabtai Doron Merims Simona Naor Rositsa Baltadzhieva Jeffrey M. Hausdorff Alexander Y. Gur Natan M. Bornstein Brain Screen A self-referral, screening program for strokes, falls and dementia risk factors Introduction Strokes, falls and dementias are the leading causes for functional deterioration, loss of independence and in- stitutionalization of elderly people. Those common dis- orders are the end results of slowly progressive brain dysfunction after a long pre-clinical phase. Motor and cognitive brain disorders can be attributed to many known risk factors that can be modified. Early detection of risk factors for strokes, falls and dementia is justified only if interventional program can modify the natural history of the screened disturbances. Stroke risk has been shown to be modified by better pre- vention of cardiac embolism, slowing atherosclerosis or treating carotid stenosis [6]. Falls risk can be modified J O N
1 9 8 6 Received: 16 March 2005 Received in revised form: 29 June 2005 Accepted: 13 July 2005 Published online: 10 October 2005 N. Giladi, MD () M. Mordechovich, MD L. Gruendlinger, BSc H. Shabtai, MD D. Merims, MD R. Baltadzhieva, MD J. M. Hausdorff, PhD A. Y. Gur, MD, PhD N. M. Bornstein, MD Movement Disorders Unit Department of Neurology Tel-Aviv Sourasky Medical Center 6 Weizman Street Tel-Aviv 64239, Israel Tel.: +972-3/6974912 Fax: +972-3/6974911 E-Mail: ngiladi@ tasmc.health.gov.il N. Giladi, MD D. Merims, MD J. M. Hausdorff, PhD A. Y. Gur, MD, PhD N. M. Bornstein, MD Sackler Faculty of Medicine Tel-Aviv University Tel-Aviv, Israel S. Naor, MD Outpatient Psychiatric Clinic Kaplan Medical Center Rehovot Hadassa School of Medicine Hebrew University Jerusalem, Israel Abstract Background Falls, strokes and dementia can be predicted and their occurrence can be delayed or even prevented by treatment of risk factors. The value of screening self-referred adults is unknown. Objectives To assess whether a screening pro- gram of self-referred adults pro- vides new and valuable medical information on risk factors for falls, stroke and dementia. Method We examined 514 self-referred people (59% women, mean age 688 years (range 4489) and 143 years of education) in our Brain Screen program. Partici- pants completed detailed question- naires and underwent a neurologi- cal examination, computerized gait analysis, carotid Duplex, serum lipid and homocysteine levels, a computerized neuropsychological battery (NeuroTrax) and the Mini-Mental State Exam. Informa- tion that was detected by Brain Screen was compared with the self-reported data. Results Un- known vascular risk factors de- tected by Brain Screen included: high cholesterol in 44%, homocys- teine >10 mol/L in 20%, >1mm carotid intima-media thickness in 13%, and carotid narrowing (>30%) in 2.2%. Unknown risk factors for falls were detected in 66% of the subjects who never fell. Of the 205 subjects (44%) who complained of memory decline, 28% had objective memory disturbances compared with their age group. Mild cognitive impairment (amnestic MCI) was clinically diagnosed in 17% of the population and dementia in 5%. Conclusion Screening self-referred adults for falls, strokes and demen- tia risk factors detected significant unknown risk factors that can be treated in more than one-third of the participants. A national Brain Screen program can have signifi- cant impact on the health of the aging population. Key words risk factor prevention stroke dementia fall 307_315_Giladi_JON_1986 28.02.2006 13:56 Uhr Seite 307 308 by increasing the awareness, adjusting home conditions as well as by maintaining physical fitness, visual acuity, decreasing the number of medications taken, or im- proving alertness and mood [12]. The onset of demen- tia can be delayed by intellectual stimulation and in- creasing leisure activity [39], better control of risk factors for atherosclerosis [37], and possibly by lowering the homocystein level [32], treating depression and de- creasing inflammatory process reflected by high level of C-reactive protein (CRP) [30]. On 1 February 2003, the Department of Neurology of Tel-Aviv Sourasky Medical Center initiated a unique screening program called Brain Screen for the general elderly population. This program provides information on risk factors for stroke, falls and dementia to the gen- eral elderly population of the entire country. Individuals receive questionnaires to fill out at home and are sched- uled for assessment at the Medical Center. A summary of the results, the risk factor profile and practical recom- mendations how to decrease their risk are given at the return visit. We now report on the first 514 consecutive people who participated in Brain Screen. In addition, we assessed whether the information imparted to the screened population was of any significance in terms of new findings which could either be modified or affect the persons life style. Methods General setup Brain Screenis a self-referral, self paid, screening program available to the general population over 50 years of age. It has been advertised in the countrys electronic and print media, and most of the people who enlisted had learned about it from national newspapers. Those who approach Brain Screen and have not been diagnosed with Alzheimers disease, Parkinsons disease, or have a history of major stroke with significant motor or cognitive deficit, major head trauma or any chronic neurological disorders, receive by mail a questionnaire to be self-answered with the help of family members and the family physician. The self-reported questionnaires include: General information: This section covers demographic and de- tailed past and present medical information as well as a detailed family history for neurological disorders and atherosclerotic car- diovascular diseases. Other questions concern past and present depression, sleep problems and change in body weight. A signifi- cant part of the questionnaire contains a set of questions about general cognitive performance, the presence of memory disturb- ances, language and reading difficulties, orientation in space, and the use of household appliances. Finally, there are specific questions for assessing the time course of any difficulty and its effect on daily activities. Fall history questionnaire for assessing fall frequency over the past week and 1, 6, 12 and 24 months. Instrumental Activities of Daily Living (IADL) questionnaire [21]. Questionnaire about leisure time activities during the last month. Short Geriatric Depression Scale (GDS) questionnaire [33]. Spielberger Anxiety Scale questionnaire [34]. First Visit Agenda Checking the self-answered questionnaires and completing any missing information. Full neurological examination by a certified neurologist, includ- ing detailed assessment of mental and cognitive activities of daily life. Measuring supine (after 3 minutes) and standing (after 2 minutes) blood pressure. Calculating body mass index (BMI; in kg/m 2 ) Performing the Mini-Mental State Exam [10] (MMSE) by a neu- rologist. Assessment of balance and postural control: Measured (seconds) tandem stand for up to 30 seconds Timed Up-and Go test (getting up from a chair, walking for 3 meters, turning around, walking back and sitting on the same chair) [25] Pull test [9] Gait speed walking for 20 meters at a self-determined, comfor- table pace. Gait dynamics: walking for 2 minutes in a corridor of 25 meters length and 2 meters width, while wearing force-sensitive insoles that en- able the determination of gait cycle timing (e. g.: stride time) on a stride-to-stride basis [15]. The coefficient of variation (CV) of the stride time was determined by a method that quantifies the dy- namics of walking and filters outliers(due to turns) [16, 19]. The CV of locomotion assesses stride-to-stride variability or gait dys- rhythmicity, a measure associated with fall risk [16]. Computerized neuropsychological test, which takes about 40 minutes (NeuroTrax Inc) [7, 8, 31]. The battery includes tests for memory, ex- ecutive functions, spatial orientation, concentration and motor skills. The memory battery includes accuracy assessment of verbal memory, delayed verbal memory, non-verbal memory and delayed non-verbal memory. All scores are normalized, 100 is the mean and 1 SD is 15 points for matched ages and education levels. This computerized bat- tery has recently been reported to be practical for neuropsychologi- cal assessment of non-demented older adults [17]. Carotid Duplex (Acuson 128 XP Flash/10) measuring Intima- media wall thickness (IMT) and the presence of atherosclerotic plaques or stenosis of the internal carotid arteries. Blood tests are done after fasting for 12 hours: Total cholesterol, high-density lipoprotein cholesterol (HDL-c), low-density lipoprotein cholesterol (LDL-c), triglycerides, urea Homocysteine High sensitive C-reactive protein (CRP) Complete blood count (CBC) Second Visit Agenda At this visit a certified neurologist or psychogeriatrician discusses with the subject any risk factors for stroke, falls or cognitive decline that had been revealed. The session ends with a detailed explanation of the Brain Screens recommendations what should be done in or- der to prevent or delay stroke, falls or dementia. All results and rec- ommendations are given in writing in order to be discussed with the primary family doctor. Fig. 1 displays the general setup (Brain Screen protocol) Discovery of new and unknown risk factors Risk factors for stroke Known risk factors were taken from the history as given by the indi- vidual. Unknown high total cholesterol (>200mg%), high LDL-c (>130mg%), high plasma homocysteine (10mol/L), high CRP (>3mg/L), carotid stenosis (>30%) or a thickened IMT (1mm) were considered as significant vascular risk factors discovered by Brain Screen. 307_315_Giladi_JON_1986 28.02.2006 13:56 Uhr Seite 308 309 Risk factors for falls A subject was considered as having a positive history of falls and, therefore, to have a known risk of future falling if he/she reported at least one fall during the last previous year [12]. An increased risk of fall was defined by the observation of any of the following: 1. Timed Up-and-Go time >13.5 seconds, 2. tandem stance <20 seconds, 3. in- ability to maintain balance in response to the pull test [9] (pull test 2), 4. stride time coefficient of variation (CV) 2.5%, 5. >5 points on the short Geriatric Depression Scale (GDS) questionnaire, 6. MMSE<25, or 7. signs of parkinsonism, i. e., if a subject had rest tremor and either rigidity or abnormal postural response (pull test 2). New risk factors for falls were considered to be discovered by Brain Screen if a risk factor was detected and the subject did not have a history of falls, or known and treated parkinsonism. Risk factors for dementia We considered a risk factor for dementia as being newly discovered only if a person was diagnosed as having amnestic MCI (see below) or the MMSE score was <25/30. Patients with known dementia when entering the Brain Screen program or with dementia diagnosed by Brain Screenwere excluded from the statistical assessment. Amnes- tic MCI was diagnosed if a person had a low memory score (<85); more than 1 standard deviation from the expected performance ad- justed to age, on the age adjusted NeuroTrax memory subscore and if he/she self-reported functionally significant memory decline, pro- gressing over the last year, in the home completed questionnaire. In addition, the screened diagnosis of amnestic MCI had to be con- firmed clinically by an experienced neurologist based on the initial interview, the neurological exam and the objective cognitive assess- ment. Dementia was diagnosed according to the DSM IV criteria [2]. Even though it is known as a risk factor for stroke and dementia [13], obesity as measured by body mass index (BMI) was not consid- ered as a newly discovered risk factor by Brain Screen based on the assumption that everyone knows if he/she is overweight. We did, how- ever, relay the information to 347 (68.2%) people and some subjects were surprised to know that they have a BMI >25. Similarly, in spite of measuring high blood pressure (>130/>85), we did not consider it as newly diagnosed risk factor in 329 people, based on the published criteria, which required more than a single measurement in order to diagnose high blood pressure [5]. Those whose blood pressure values were high during Brain Screen and were not aware of their possible risk (unknown and untreated BP n=169) did, however, benefit from receiving the information. Statistics Results are reported as mean standard deviation. Out- come, dependent variables were checked for normality and outliers. Initially, scatter plots and box plots were to visualize the association between dependent and inde- pendent variables. Subjects groups were compared us- ing Fishers exact test and Chi square analysis for cate- gorical data. For continuous data, the two-sample, Students t-test was used to compare two groups. A p- value less than 0.05 (two-tailed) was considered statisti- cally significant. Statistical analysis was performed us- ing SPSS for Windows (version 10.1). Results The general characteristics of the first consecutive 514 subjects assessed in Brain Screen are presented in Table 1. In general, the typical screened person was a woman, around 70 years of age, with 14 years of educa- tion, overweight, and concerned about memory. Vascular risk factors (Table 2) The most significant new finding in terms of vascular risk factors for stroke was hypercholesterolemia discov- ered in 203 people (43.8%). Overall, 72.2% of the screened subjects had hypercholesterolemia, making it the most common vascular risk factor. Ninety people Pre-visit one SeIf reported questionnaires: GeneraI medicaI & IADL FaIIs history Short Geriatric Depression ScaIe SpieIberger anxiety scaIe Leisure activities Visit one - tests NeuroIogicaI exam Measuring BMI Supine and standing bIood pressure MMSE BaIance and posturaI controI Computerized gait dynamics Computerized neuropsychoIogicaI test Carotid DoppIer (fIow and IMT) BIood tests Last visit Report on aII tests done GeneraI risk for: stroke faIIs dementia PracticaI recommendations Fig. 1 Brain Screen Protocol (MMSE Mini-Mental State Exam; IADL Instrumental Activities of daily liv- ing; BMI Body Mass Index; IMT Intima-media thick- ness) 307_315_Giladi_JON_1986 28.02.2006 13:56 Uhr Seite 309 310 (19.9%) were found to have relatively high homocys- teine (>10mol/L) levels. Interestingly, none of the peo- ple assessed had reported about hyper-homocystinemia when they enrolled in Brain Screen, even though this test is available in all primary care programs in Israel. We did not find a single person with >50% narrowing of the carotid arteries and no one in the study cohort had carotid-related symptoms. IMT measurements of the carotid artery were not available elsewhere in Israel; so all-60 persons (13%) with1mm of IMT in one com- mon carotid artery could not have these data prior to Brain Screen assessment. CRP is not measured rou- tinely in Israel, so all-76/218 people with CRP>3mg/L (34.9%) were not likely to have this information prior to Brain Screen. Risk factors for falls (Table 3) Over one-fifth (105, 22.6%) of the screened population not including 7 treated parkinsonian patients, reported at least one fall over the last year. Among them, 82 (78.1%) had at least a second objective risk factor for falls, 50 (47.6%) had at least two additional risk factors and 29 (27.6%) had at least three additional risk factors. Among the 360 people with no history of falls, 239 (66.4%) had at least one objective risk factor for future falls, 92 (25.6%) had 2 risk factors and 31 (8.6%) had three risk factors. Among the subjects with no history of falls, the most common fall risk factors were depressive signs, poor tandem stance, increased stride CV, and poor response to the pull test. One-hundred and two people (22.6%) not including Table 1 General characteristics of 514 people screened by the Brain Screen pro- gram Male/Female (%) 209/305 (40.7/59.3) Mean age (years) 688 (4489) Mean years of education 14.03.4 People with body mass index 25 (%) 347 (68.2%) History of hypertension 198 (42.2%) History of hypercholesterolemia 183 (39.0%) History of ischemic heart disease 61 (13.0%) History of diabetes mellitus 60 (12.8%) Smokers 50 (10.7%) History of depression/non-treated (%) 139 (29.6%)/89 (19.0%) Known and treated parkinsonism 7 (1.4%) Reasons for participating in Brain Screen* Memory problems 270 (57.6%) Stroke concern 23 (4.9%) Gait insecurity fear of falling 77 (16.4%) Family history of Alzheimers disease 96 (20.5%) Other 124 (26.4%) * A person could have more than one reason Vascular risk factors Known by history Found by Newly diagnosed by Brain Screen Brain Screen Hypercholesterolemia 183 (39 %) 335 (72.2%) 203 (43.8%) Carotid stenosis (> 30 %) None 10 (2.2%) 10 (2.2%) IMT 1 mm None 60 (13.0%) 60 (13.0%) High homocysteine ( 10 mol/L) None 90 (19.9%) 90 (19.9%) High CRP (> 3 mg/L) (n = 218) None 76 (34.9%) 76 (34.9%) IMT intima- media thickness; CRP C-reactive protein * % of total population Table 2 Frequency* of vascular risk factors pre- screening and post-Brain Screen Fall risk factors History of 1 fall Found by No history of falls over the last year Brain Screen (n = 360, 77.4%) (n = 105, 22.6%) TUaG > 13.5 sec 11 (10.5%) 23 12 (3.3%) Stride-to-stride variability CV 2.5 % 30 (28.6%) 102 72 (20.0%) Pull test 2 34 (32.4%) 97 63 (17.5%) Tandem stand < 20 sec 39 (37.1%) 143 104 (28.9%) MMSE < 25/30 5 (4.8%) 13 8 (2.2%) Self-reported depression or GDS short > 5 59 (56.2%) 182 123 (34.2%) Undiagnosed parkinsonism 1 (1.0%) 12 11 (3.1%) TUaG Timed Up and Go test; CV Coefficient of Variance; MMSE Mini-Mental State Exam; GDS Geriatric depression scale Table 3 Detection of risk factors for falls pre- and post-Brain Screen program 307_315_Giladi_JON_1986 28.02.2006 13:56 Uhr Seite 310 311 treated parkinsonian patients had increased stride-to- stride variability (stride CV 2.5%) and 72 of them had no history of falls. Interestingly, these 72 subjects with dysrhythmic locomotion (and no history of falls) had higher BMI (28.6 vs. 27.3, P<0.05) and a higher average left common carotid artery IMT (0.65 vs. 0.60, P<0.05) than the rest of the study cohort. The two groups were not different with respect to age, history of high blood pressure, diabetes mellitus, depression (GDS>5) or the global score on the neuropsychological assessment bat- tery. As shown in Table 1, 74 people (16%) not including treated parkinsonian patients, out of 469 who answered a question about a cause of approaching Brain Screen, came because of concerns about gait. Among them, (93%) had at least one objective risk factor for falls, (66.2%) had at least 2 risk factors, and 37.8% had at least 3 factors. Among the remaining subjects, 64.8% had at least one objective risk factor for falls, 24.2% had at least two risk factors, and 8.5% had at least three risk factors. Risk factors for cognitive decline (Table 4) Twenty-two people (4.8%) were diagnosed by Brain Screen as having dementia. Four of those 22 patients had already been diagnosed and treated for AD but did not report about it in the telephone interview. All 22 sub- jects had been encouraged to contact Brain Screen by their family members. Only 12/18 of the patients actu- ally complained about memory loss. Subjective com- plaint of memory impairment was reported by 351 sub- jects out of 457 (79.4%) not including the demented patients. 205 people out of 469 (43.7%) complained about one year or more of progressive decline in mem- ory disturbances. Fifty eight out of 444 people who had reported about their memory and its time course were diagnosed by Brain Screen as having amnestic MCI, based on the neuropsychological assessment and the subjective progressive complaint. Among the 58 Brain Screen diagnosed Amnestic MCI people 12 were later diagnosed for the first time as demented by a neurolo- gist. The subjects with objective memory impairment (NeuroTrax memory score <85, n=122) were older (mean age 71 vs. 66 years, P<0.001) and had higher GDS scores (4.4 vs. 2.5, P<0.02). Among the subjects without objective memory im- pairment (NeuroTrax memory score >85, n=392), complainers of memory decline had a higher score on the GDS (3.8 vs. 2.6, P<0.02). Thus, there may be a rela- tionship between complaining about memory decline and depression as reflected in the GDS. We could not demonstrate any relationships between complaining about memory decline and age to suggest that depres- sion is the leading factor for complaints about memory decline. Discussion Brain Screen is the first screening program in Israel which provides data on risk factors for stroke, falls and dementia. Such a program is justified if it provides new and valuable information that can be translated into tak- ing steps which will modify disease course. In order to provide new and important data, we performed tests that are not available in any health plan in Israel for screening purposes. This approach has given a signifi- cant number of people important and new information that if treated can modify the risk for stroke, falls or de- mentia. In order to achieve this goal we had to go over a very high bar, because such a self-referral population that took part in the screening program have a high level of awareness about their health in general and brain dis- orders in particular, and providing them with new med- ical information about themselves is not a trivial matter. The relatively high mean years of education (14.13.4) in our assessed population, which was much higher than the mean years of education (9.4) in the general adult population of that age group in Israel [20], supports this point. In spite of the good national health plan in Israel, which covers all Israeli citizens and the relatively well- educated people who approached Brain Screenduring the programs initial phase, we were surprised to iden- tify a high percentage of participants who were com- pletely unaware of some important and treatable risk factors. Cognitive Subjects without subjective Subjects with subjective complaints assessment tools complaints of memory of progressive memory disturbances disturbances over the past year n = 351 (79.4%) n = 205 (43.7%) MMSE < 25/30 6 7 NeuroTrax Memory subscore < 85 64 58* n = 122 * Patients with calculated amnestic-mild cognitive impairment (A-MCI) Table 4 Frequency of mental disturbances and comparison between subjective and objective data 307_315_Giladi_JON_1986 28.02.2006 13:56 Uhr Seite 311 312 Vascular risk factors The most striking and unexpected finding was the high percentage of people who were first informed by Brain Screen about their hypercholesterolemia. Treatment with statins for hypercholesterolemia can significantly decrease the relative and absolute risk for stroke by 21% and 0.9%, respectively [1]. In spite of the fact that today, lowering cholesterol level with statins is not considered as primary but only as secondary stroke prevention, we believe that treating cardio-vascular risk factors is of great importance to brain protection. In addition, we were able to stress the need for follow-up even to those people who were on statins but were not effectively con- trolled. All 58 people who had a 10mg/L concentration of homocysteine in their plasma were instructed to take folic acid >1mg/day. Some but not all clinical trials sug- gest that lowering plasma homocysteine level can de- crease the risk of stroke [3] and myocardial infarction [36]. We think all those participants who were informed that their homocysteine blood level was high, gained significant and valuable knowledge, first by the aware- ness of an existing problem and second by initiating treatment with folic acid, which might have a protective effect. The information on IMT and carotid flow has two major objectives. The first is to increase awareness of the concept of atherosclerosis and giving it a more real and measurable meaning. The second is to track individuals at risk for carotid narrowing and to put them on tighter follow-up program. None of the tested people had a sig- nificant carotid narrowing that required prompt referral to a vascular surgeon. All those with carotid narrowing >30% were invited for follow up test in 6 months. Small doses of aspirin were recommended to all those with high IMT or carotid narrowing >30% if they also had either hypertension, diabetes mellitus or hypercholes- terolemia. This approach was taken in spite of insuffi- cient evidence for its absolute protective effect. Increased level of CRP has been associated with symp- tomatic cardiovascular disease [35] and dementia [22] or stroke [4]. Recently, for the first time, a prospective study demonstrated that treatment with statins can decrease CRP level and the risk for myocardial infarct or death from coronary causes [26] to support the need for CRP assessment. Furthermore, a prospective study recently has shown substantial improvement of survival in pa- tients with severe peripheral artery disease treated with statins [29]. Interestingly, only patients with elevated high sensitive CRP benefited from the treatment with statins.Due to lack of evidence for similar effect on stroke or dementia we did not recommend specific treatment to 35% of our Brain Screen population with high CRP level but referred them to their dentist with suspected gingivitis and a recommendation for follow-up [23]. Brain Screen was developed to detect new and modifiable risk factors by performing tests that are not performed routinely by the Israeli health plans. As a re- sult, we relied on the patients reports about the presence of classical vascular risk factors like arterial hyperten- sion, diabetes mellitus, atrial fibrillation etc. we based our strategy on the quality of the basic medical care in Israel, which is very aware of those risk factors. This is also the reason why we chose not to perform an electro- cardiogram. Risk of falling Only a relatively small percentage (16.4%) of the sub- jects approached Brain Screen because of concerns about their gait. However, we were able to identify an in- creased risk of falls in 65% of the subjects who came to Brain Screenfor other concerns and in 66% of the sub- jects who did not report a history of falling. These sub- jects benefited from a discussion about the danger of falls and the importance of preventive behavior. They also were told about the benefits of exercise and regular walking for falls prevention [14] and were encouraged to carry out these activities. We also advised the subjects who had an increased risk of falls to assess their bone density and, if needed, to obtain treatment for osteo- porosis. Overall, Brain Screen provided critical infor- mation to those with an increased risk of falls and equipped them with guidelines that they could use to de- crease their risk of falls and avoid common fall-related sequelae, such as hip fractures, surgery, and nursing home admission. In addition to the above, Brain Screen was heavily focused on detecting and treating depression and or- thostatic hypotension as well as avoiding benzodi- azepines which are of added value for the effort to de- crease fall risk and severe injuries [12, 18]. Previous studies have called for an increased aware- ness of the risk of falls, improving older adults knowl- edge about falls and the ways to avoid them, and en- couraging older adults to take preventative steps [12, 28]. To a large degree,Brain Screenis a response to this call for action, educating a largely uninformed popula- tion at increased risk of falls. Delaying dementia Memory disturbances might be the initial stage of de- mentia but it is much more frequently a subjective feel- ing associated with fear of Alzheimers disease. The goal of any screening program should be to identify the indi- viduals who are at risk to develop dementia, but no less important is reassuring those who are functioning within the normal range for their age. Because of the 307_315_Giladi_JON_1986 28.02.2006 13:56 Uhr Seite 312 313 multi-factorial nature of cognitive decline, we believe that only a program such as Brain Screen can provide reliable data on the subjects status. All the participants with vascular risk factors or gait disturbances were in- formed that, in addition to their risk for strokes or falls, these problems might be risk markers for future devel- opment of cognitive decline. If we add obesity, which has recently been shown to stand alone as a dementia risk factor [13] similar to depression and anxiety [38, 40], then most of the people who had been screened in the Brain Screen program gained valuable new informa- tion for behavioral modification that could affect their risk for dementia. In other words, participation in Brain Screen and exposure to the modern concepts about the natural course of dementia and the signifi- cance of risk factors to cognitive decline and onset of de- mentia is by itself compelling justification for participa- tion in the program. The other objective of Brain Screen was to identify people with MCI [24] and subjects who were normal from among those who complained about memory dis- turbances. In order to decrease the false positive diag- nosis of MCI we required that the complaint of decline in memory had to have lasted and progressed for at least one year. Our streaked criteria for MCI might have missed several people with amnestic MCI. A screening program such as ours, however, should under-diagnose and not over-diagnose MCI as long as there is no proven protective treatment for Alzheimers disease. The avai- lability of a detailed and structured neuropsychological testing modality has given us an opportunity to look at other cognitive domains, such as visuo-spatial perform- ance, executive functions and attention. Because of the lack of well-established criteria for non-amnestic MCI and no subjective complaints about those domains by the people who were tested, we neither diagnosed nor discussed the importance of those cognitive domains as risk factors for dementia. People with cognitive decline and depression are al- ways a challenge to diagnose due to the fact that depres- sion could influence cognitive performance. We found a higher percentage of depressed patients among those who were diagnosed with MCI compared to those who complained about memory loss but did not meet the cri- teria for MCI. Brain Screen gave us the opportunity to detect in- dividuals who are on the course towards the develop- ment of dementia. It also gave us the opportunity to re- assure many worried people by ruling out their concern that they were functioning abnormally for their age and not in the early stages of dementia or Alzheimers dis- ease. All participants in the Brain Screen program re- ceived general recommendations to watch their weight, blood pressure and cholesterol level. We also recom- mended and encouraged them to exercise daily for 3045 minutes, actively and purposefully challenge and exercise their cognitive performances as well as main- tain a healthy diet enriched by vitamins E and C. People with amnestic MCI were invited to participate in a computerized cognitive training program Cognifit free of charge as well as to pay extra attention to the control of vascular risk factors, depression and sleep dis- turbances. Recent reports demonstrated that brisk walk- ing and active participation in leisure time activities could slow down or postpone dementia of Alzheimers type [11] to support our recommendations. Moreover, the coexistence of vascular atherosclerotic changes in the Alzheimers brain with its role in the pathogenesis of AD further supports the importance of treating atherosclerotic risks factors. Furthermore, statin treatment has been shown to delay the time of de- mentia onset [41] to support the use of statins in non hy- percholesterolemia people just to delay dementia [27] In spite of the recent reports, we do not recommend statin treatment for prevention of dementia and only the fu- ture will give a clear answer to this possible therapeutic approach. In conclusion, based on the analysis of the first 514 consecutive people who were screened by Brain Screen, we demonstrated that there is a place for such a screening program. We were able to provide new and valuable information to relatively educated individuals who were very much aware of their health and aging and were compliant to a concept of intervention based on a risk factor profile for the delay or prevention of brain disorders in the elderly. We propose that the basic idea behind Brain Screen should be adopted for the general population in the con- viction that early detection and intervention for delay- ing or preventing brain disorders, common among the elderly population, is the only way to decrease the ever- growing burden of those brain disorders on society. Acknowledgment We thank Mrs. Orna Moor, RN MSc, and Liat Ra- zon for all technical support, Mrs. Judith Knaani for superb secretar- ial support, Mrs. Talia Herman MSc for technical support in gait as- sessment, Prof. Shlomo Berliner and Dr. Einor Ben Assiag for support in blood testing and data entry, Roni Zamishlani for data entry and Prof. Amos D. Korczyn for guidance and support in the development of the program. 307_315_Giladi_JON_1986 28.02.2006 13:56 Uhr Seite 313 314 1. Amarenco P, Lavalle P, Touboul PJ (2004) Stroke prevention, blood cho- lesterol, and statins. Lancet Neurol 3(5):271278 2. American Psychiatric Association (1994) Diagnostic and statistical man- ual of Mental disorders. Fourth Edi- tion. American Psychiatric Association 3. Bazzano LA, He J, Ogden LG, et al. (2002) Dietary intake of folate and risk of stroke in US men and women: NHANES I Epidemiologic Follow-up Study. National Health and Nutrition Examination Survey. Stroke 33(5): 11831188 4. 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