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Received: 6 February 2018    Revised: 31 May 2018    Accepted: 10 June 2018

DOI: 10.1111/jcpe.12959

E PIDE MIOLOGY (COHORT STUDY


OR C A SE– CONTROL STUDY )

Prevalence of self-­reported gingival bleeding in a


representative sample of the Brazilian adolescent population

Paulo Nadanovsky1,2  | Ana Paula Pires dos Santos3 | Katia Vergetti Bloch4

1
Department of Epidemiology, National
School of Public Health, Oswaldo Cruz Abstract
Foundation (Fiocruz), Rio de Janeiro, Brazil Aim: To estimate the prevalence of self-­reported gingival bleeding in a representative
2
Department of Epidemiology, Institute
sample of 12-­to 17-­year-­old Brazilian adolescents.
of Social Medicine, Rio de Janeiro State
University, Rio de Janeiro, Brazil Materials and Methods: Sociodemographic and oral health information were ob-
3
Department of Community and Preventive tained through a self-­administered questionnaire of the Study of Cardiovascular Risk
Dentistry, Faculty of Dentistry, Rio de
Factors in Adolescents. The adolescents answered “yes” or “no” to the question “Do
Janeiro State University, Rio de Janeiro,
Brazil your gums bleed?”
4
Instituto de Estudos em Saúde Results: 74,589 of the 102,327 eligible adolescents answered the questionnaire and
Coletiva, Universidade Federal do Rio de
Janeiro, Rio de Janeiro, Brazil 18.4% (95% CI 17.5–19.3) reported having bleeding gums. The prevalence of self-­
reported gingival bleeding varied as following: 21.4% (95% CI 20.3–22.6) in girls and
Correspondence
Paulo Nadanovsky, Department of 15.3% (95% CI 14.3–16.4) in boys; 20.5% (95% CI 19.2–21.8) in older and 17.5% (95%
Epidemiology, National School of Public CI 16.4–18.6) in younger adolescents; 20.6% (95% CI 18.5–22.9) in Black people and
Health, Oswaldo Cruz Foundation (Fiocruz),
Rua Leopoldo Bulhões, 1480, CEP 21041- 17.1% (95% CI 16.1–18.1) in White people. Regarding mother’s level of education, the
210 Rio de Janeiro – RJ, Brazil. prevalences were 18.1% (95% CI 16.2–20.3), 17.6% (95% CI 16.4–18.9) and 19.3%
Emails: nadanovsky@ensp.fiocruz.br;
nadanovsky@ims.uerj.br (95% CI 17.9–20.9) for high, middle and low levels, respectively. For socioeconomic
status, the equivalent figures were 16.4% (95% CI 14.3–18.7), 18.4% (95% CI 17.5–
Funding information
The ERICA study was supported by the 19.4) and 23.0% (95% CI 17.3–29.9).
Brazilian Ministry of Health (Science and
Conclusion: Nearly one in five Brazilian adolescents reported having gingival bleed-
Technology Department) and the Brazilian
Ministry of Science and Technology ing, which might not be a serious condition, but reflect the disease and the adoles-
(Financiadora de Estudos e Projetos/
cents’ perception of oral health status.
FINEP and Conselho Nacional de Pesquisa/
CNPq) (grants FINEP: 01090421, CNPq:
565037/2010-2 and 405009/2012-7) KEYWORDS
adolescent, epidemiology, gingivitis, prevalence, self-report

1 | I NTRO D U C TI O N process. Although most gingivitis lesions do not progress to peri-
odontitis (Kinane & Attström, 2005), managing gingivitis is a primary
Gingivitis is a gingival inflammation caused by the accumulation of preventive strategy for periodontitis (Chapple et al., 2015).
dental plaque. It can be influenced by several factors, such as sys- Children and adolescents with higher levels of dental plaque had
temic disorders, blood dyscrasias, malnutrition and medications higher risk of presenting gingivitis and periodontitis at the age of 32
(Armitage, 1999). It is characterised by inflammation of the marginal (Broadbent, Thomson, Boyens, & Poulton, 2011). However, there is
gingiva without detectable loss of connective tissue attachment or scarce prospective evidence of the amount of plaque accumulation
bone resorption. Clinically, there is redness and swelling of marginal necessary to cause periodontitis and that signs of gingivitis in child-
gingiva and bleeding on probing (Oh, Eber, & Wang, 2002). Gingivitis hood predicts risk of periodontitis. Thus, the extent to which gin-
and periodontitis (i.e., loss of connective tissue attachment or bone gival inflammation and plaque accumulation can accurately predict
resorption) are seen as a continuum of the same inflammatory the individuals who will develop periodontitis is not well established.

952  |  wileyonlinelibrary.com/journal/jcpe


© 2018 John Wiley & Sons A/S. J Clin Periodontol. 2018;45:952–958.
Published by John Wiley & Sons Ltd
NADANOVSKY et al. |
      953

Periodontitis is consistently associated with negative impacts


on oral health-­related quality of life, and the greater the severity of
Clinical Relevance
the disease the greater the impact (Buset et al., 2016; Ferreira, Dias-­
Pereira, Branco-­de-­Almeida, Martins, & Paiva, 2017). The impact of Scientific rationale for the study: First study that assessed
gingivitis on oral health-­related quality of life is not as significant as the prevalence of self-­reported gingival bleeding on a na-
the impact of periodontitis. However, gingivitis has been linked to tional basis. Gingival inflammation might influence the indi-
pain as well as with difficulties related to toothbrushing and wear- vidual perception of her own oral health status.
ing dentures, which points to an association between gingivitis and Principal findings: Nearly one in five Brazilian adolescents
oral discomfort (Ferreira et al., 2017). In children, there might be a reported that their gums bled.
negative impact of gingival bleeding on both social interactions and Practical implications: Future research should investigate
self-­esteem (Machado, Tomazoni, Ortiz, Ardenghi, & Zanatta, 2017). the specific socio-­psychological and behaviour impact of
Despite the cross-­sectional nature of these associations, which are self-­reported gingival bleeding in adolescents, including
prone to reverse causation, it is difficult to think how oral health-­ their care-­seeking behaviour.
related quality of life could affect gingivitis and periodontitis rather
than gingivitis and periodontitis affect oral health-­related quality of
life.
There are different ways of measuring gingivitis, one of which activities, physical activity, eating habits, smoking, alcohol use, re-
is to clinically assess the presence of gingival bleeding on prob- productive health, oral health, sleep duration, physical morbidity
ing (BOP). In Brazil, the prevalence of gingivitis was 27% for and mental health.
12-­year-­olds and 34% for 15-­to 19-­year-­olds, according to the Information on sociodemographic characteristics and oral health-­
community periodontal index (CPI) (Brasil, 2011). A similar prev- directed behaviours were obtained through a self-­
administered
alence (33%) was found in 16-­to 19-­year-­olds in Albania (Laganà questionnaire using an electronic device. Gingival bleeding was self-­
et al., 2015). An alternative to clinical periodontal assessment is reported and the adolescents answered “yes” or “no” to the question
self-­report, which is a method widely used to assess the preva- “Do your gums bleed?”
lence of many medical conditions and health-­related behaviours In this study, we analysed the following sociodemographic
(Taylor & Borgnakke, 2007). It is advantageous as it is less time and variables: sex (girls or boys), age (12, 13, 14, 15, 16 or 17), mother’s
resource consuming and reflects the individual’s perception of her level of education (illiterate, 1–3 years of schooling, 4–7 years of
own oral health status. schooling, complete primary school, incomplete high school, com-
While clinically assessed gingival bleeding defines the condition plete high school, incomplete university, complete university or
of the gum, self-­report is important because it expresses an illness do not know), socioeconomic status (A—the highest, B, C, D or
dimension related to the disease (Locker, 1988; Tsakos, Allen, Steele, E; these Brazilian criteria consider ownership of goods, presence
& Locker, 2012). We should expect that there is some association of housemaid and level of education of the head of the house-
between self-­reported and clinically assessed gingival bleeding, as hold), skin colour (white, black, brown, yellow, indigenous or not
both are roughly measuring the same condition. These are two truly reported), school type (public or private), school region (rural or
complementary approaches, and, currently, it is not yet possible to urban) and Brazilian macro-­regions (North, Northeast, Midwest,
elect which one is more relevant. Southeast or South). We categorised age into two groups (younger
We found no study of the prevalence of self-­reported gingival 12–15 and older 16–17), mother’s level of education into four
bleeding in a national representative sample of any country. Thus, groups (high—incomplete or complete university, middle—incom-
the aim of this study was to estimate the prevalence of self-­reported plete or complete high school, low—illiterate to incomplete or
gingival bleeding in a representative sample of Brazilian adolescents. complete primary school and do not know) and socioeconomic
status (SES) into four groups (high—A, middle—B and C, low—D
and E and do not know).
2 | M ATE R I A L S A N D M E TH O DS The oral health-­directed behaviours were as follows: last visit to
the dentist (never, 6 months or more, less than 6 months or do not
The Study of Cardiovascular Risk Factors in Adolescents know), daily toothbrushing frequency (none, once, twice, three times
(Portuguese acronym, ERICA) is a school-­b ased cross-­sectional or more than three times), use of toothbrush (yes or no), use of dental
multi-­center study which aimed to estimate the prevalence of car- floss (yes or no) and use of toothpaste (yes or no).
diovascular risk factors in a random sample of adolescents aged All participating students signed an assent form and brought
12–17 years enrolled in private and public schools located in the the informed consent form signed by their legal guardians (when
273 Brazilian municipalities with more than 100,000 inhabitants required by the local Research Ethics Committee). The study was
(Bloch et al., 2015). Data were collected between March 2013 and approved by the Research Ethics Committee of the Institution of the
December 2014 and the questionnaire consisted of 105 questions Study Coordination Center (IESC/UFRJ – Process 45/2008) and by
divided into 11 blocks: sociodemographic aspects, occupational each Brazilian state involved.
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954       NADANOVSKY et al.

The statistical analysis was performed using Stata 13.1®. The TA B L E   1   Prevalence (%) and 95% confidence intervals (CI) of
command svy (survey) was used to estimate the prevalences and self-­reported gingival bleeding by demographic, social and
their 95% confidence intervals (CI). All analyses were weighted con- geographic variables. ERICA, Brazil, 2013–2014

sidering the complex sampling plan that includes stratification and Self-­reported gingival bleeding
conglomeration.
% (95% CI) Total

All 18.4 (17.5–19.3) 74,589

3 |   R E S U LT S Sex
Female 21.4 (20.3–22.6) 41,225
According to the Brazilian Institute of Geography and Statistics Male 15.3 (14.3–16.4) 33,364
(http://www.ibge.gov.br/home/estatistica/populacao/projecao_ Age group (years)
da_populacao/2013/default.shtm), the estimated total population 12–15 17.5 (16.4–18.6) 48,460
of 12-­to 17-­year-­old Brazilians is 10,147,700. In the ERICA study, 16–17 20.5 (19.2–21.8) 26,129
74,589 of the 102,327 eligible adolescents answered the question
Mother’s level of education
on gingival bleeding (response rate = 72.9%). Among these, 18.4%
High 18.1 (16.2–20.3) 17,671
(95% CI 17.5–19.3) reported that their gums bled. The prevalence of
Middle 17.6 (16.4–18.9) 20,981
self-­reported gingival bleeding was significantly higher among girls
Low 19.3 (17.9–20.9) 18,163
(21.4%, 95% CI 20.3–22.6) than among boys (15.3%, 95% CI 14.3–
Do not know 18.3 (16.8–19.9) 17,774
16.4). There was also a statistically significant difference when older
adolescents (20.5%, 95% CI 19.2–21.8) were compared to younger SES

adolescents (17.5%, 95% CI 16.4–18.6). Adolescents from low SES High 16.4 (14.3–18.7) 6,336

and whose mother’s level of education was low had higher preva- Middle 18.4 (17.5–19.4) 43,597
lence of self-­reported gingival bleeding, but the differences were not Low 23.0 (17.3–29.9) 936
statistically significant, nor were the differences regarding skin col- Do not know 18.5 (17.2–20.0) 23,720
our, except when White people (17.1%, 95% CI 16.1–18.1) were com- Skin colour
pared to Black people (20.6%, 95% CI 18.5–22.9). The prevalence of White 17.1 (16.1–18.1) 26,477
self-­reported gingival bleeding was almost identical between adoles- Black 20.6 (18.5–22.9) 5,654
cents from private or public schools. However, this prevalence was
Brown 19.2 (17.8–20.7) 37,984
significantly higher among those attending schools in urban (18.7%,
Yellow 18.6 (15.0–22.9) 1,881
95% CI 18.0–19.5) than rural (9.7%, 95% CI 6.2–15.0) areas. At last,
Indigenous 15.6 (10.5–22.0) 561
we detected a statistically significant difference in the prevalence of
Not reported 16.2 (13.6–19.2) 2,032
self-­reported gingival bleeding between the macro-­region Midwest,
School type
which showed the lowest prevalence (15.9%, 95% CI 14.6–17.3) and
the macro-­region Southeast, which showed the highest prevalence State 18.3 (17.3–19.4) 58,707

(19.2%, 95% CI 17.6–21.0). Private 18.8 (17.3–20.4) 15,882


Table 1 shows the prevalence and 95% CI of self-­reported gingi- School region
val bleeding by sex, age group, mother’s level of education, SES, skin Rural 9.7 (6.2–15.0) 1,340
colour, school type, school region and Brazilian macro-­regions. The Urban 18.7 (18.0–19.5) 73,249
prevalence and 95% CI of self-­reported gingival bleeding stratified Macro-­region
by age and sex is depicted in Figure 1. North 17.1 (16.2–18.1) 15,073
Self-­reported gingival bleeding was higher among adolescents
Northeast 17.4 (16.3–18.5) 23,167
who had never visited the dentist (22.7%, 95% CI 19.9–25.6) and
Midwest 15.9 (14.6–17.3) 9,727
did not use dental floss (20.7%, 95% CI 19.7–21.8). The higher the
Southeast 19.2 (17.6–21.0) 17,080
toothbrushing frequency, the lower the prevalence of self-­reported
South 19.0 (17.3–20.8) 9,542
gingival bleeding. Use of toothbrush and toothpaste was almost uni-
versal (Table 2). Note. SES, socioeconomic status.

1996; Kallio & Murtomaa, 1997), most examined the participants


4 |  D I S CU S S I O N clinically, but did not ask whether they perceived that their gums
bled (Abuhaloob & Petersen, 2017; Antunes, Peres, Frias, Crosato, &
We found that approximately one in five Brazilian adolescents re- Biazevic, 2008; Brasil, 2011; Campus et al., 2007; Fonseca, Ferreira,
ported bleeding gums. There were previous reports on the preva- Abreu, Palmier, & Vargas, 2015; Funieru et al., 2017; Gao et al.,
lence of gingival bleeding. However, with few exceptions (Kallio, 2014; Laganà et al., 2015; Nicolau, Marcenes, Bartley, & Sheiham,
NADANOVSKY et al. |
      955

F I G U R E   1   Prevalence (%) and 95%


confidence intervals (CI) of self-­reported
gingival bleeding by age and sex. ERICA,
Brazil, 2013–2014

TA B L E   2   Prevalence (%) and 95% confidence intervals (CI) of adolescents (Ayo-­Yusuf, Reddy, & van den Borne, 2008; Mattila
self-­reported gingival bleeding by oral health-­directed behaviours. et al., 2016) and in adults (Lintula et al., 2014), but none (at least to
ERICA, Brazil, 2013–2014
our knowledge) assessed it on a representative sample of any na-
Self-­reported gingival bleeding tion. Our study population was representative of the Brazilian ado-
lescent population who lived in the 273 cities of at least 100,000
% (95% CI) Total
inhabitants.
Last visit to the dentist
The prevalence of gingival bleeding in Brazil was assessed in a
Never 22.7 (19.9–25.8) 4,153 previous national survey (Brasil, 2011). However, that survey was
Six months or more 18.7 (17.2–20.2) 15,125 representative only for the 27 Brazilian capitals and assessed the
Less than 6 months 18.2 (16.9–19.6) 34,791 prevalence of clinical gingival bleeding. In that survey, 27% and
Do not know 17.5 (16.3–18.7) 20,520 34% of 12 and 15-­to 19-­year-­olds, respectively, presented gin-
Daily toothbrushing frequency gival bleeding. That prevalence was higher than the prevalence
None 23.8 (12.4–40.9) 168 of self-­reported gingival bleeding found in our study, which was

Once 23.1 (20.1–26.3) 2,816 19% for 12-­year-­olds and 17% for 15, 21% for 16 and 20% for
17-­year-­olds. This higher prevalence of clinically assessed when
Twice 21.8 (20.0–23.7) 20,561
compared to self-­reported gingival bleeding might be explained
Three times 17.4 (16.4–18.3) 34,245
by the way gingival bleeding was measured during clinical exam-
More than three 15.3 (13.6–17.2) 16,799
times
ination. The CPI index, used in that survey, evaluates BOP, that
is, the presence of bleeding after inserting a periodontal probe
Use of toothbrush
with standardised force in the gingival margin. This measurement
Yes 18.4 (17.6–19.4) 73,977
may provide higher levels of bleeding than self-­report assessment
No 10.9 (6.6–82.6) 612
of gingival bleeding, which most probably is only salient during
Use of dental floss
self-­p erformed oral hygiene, which should be physically gentler
Yes 16.3 (15.3–17.4) 38,813
to the gum than the hard periodontal probe. The clinical gingival
No 20.7 (19.7–21.8) 35,776 probing by the dentist may provoke too much bleeding, inadver-
Use of toothpaste tently making the CPI index too sensitive (i.e., generating an ex-
Yes 18.4 (17.5–19.3) 74,157 cess of false-­p ositive diagnoses). On the other hand, self-­report
No 12.6 (8.3–18.7) 432 may lack sensitivity (i.e., generating an excess of false-­n egative di-
agnoses). In essence, there is a conceptual problem, as there is no
well-­e stablished gold standard for gingival bleeding. Thus, it is not
2005; Petersen, Hoerup, Poomviset, Prommajan, & Watanapa, possible, in the current state of the art, to infer which prevalence
2001; Pitts, Chadwick, & Anderson, 2015; Rebelo, Lopes, Vieira, of gingival bleeding is more valid; the approximately 18% that we
& Parente, 2009; Tomazoni et al., 2017; Vadiakas, Oulis, Tsinidou, found or the nearly 30% found in the previous national survey.
Mamai-­Homata, & Polychronopoulou, 2012; Zhang, Xu, Liu, Lo, In addition, our question did not distinguish spontaneous bleed-
& Chu, 2015). Others assessed self-­reported gingival bleeding in ing from bleeding on brushing and frequency of bleeding. The
|
956       NADANOVSKY et al.

prevalence of spontaneous and frequent bleeding may be more Questions related to the number of teeth and the use and
relevant than bleeding on brushing or probing only. need of prostheses have shown consistent validity according to
The prevalence of clinically assessed gingival bleeding in Brazil the clinical exam (Buhlin, Gustafsson, Andersson, Håkansson, &
is similar to findings in other countries. In Albania, 33% of adoles- Klinge, 2002; Ramos, Bastos, & Peres, 2013). Self-­reported gingi-
cents aged 16–19 years presented gingival bleeding that is also mea- val bleeding and clinical gingival health appear to correlate in ad-
sured by the CPI index (Laganà et al., 2015). In the United Kingdom, olescents. As expected, this correlation is far from perfect (Kallio
40% of 15-­year-­olds presented gingival bleeding on probing, with & Murtomaa, 1997; Taani & Alhaija, 2003). Self-­reported gingival
no differences among the UK countries (Pitts et al., 2015). When bleeding predicted, to a certain extent, the findings from clini-
clinically assessed, gingival bleeding tends to be more prevalent in cal exams, with values of sensitivity and specificity of the order
boys than in girls (Antunes et al., 2008; Funieru et al., 2017; Jenkins of 35%–42% and 76%–88%, respectively, according to Blicher,
& Papapanou, 2001). On the other hand, the prevalence of self-­ Joshipura, and Eke (2005), and with values of sensitivity and spec-
perceived bleeding gums when brushing teeth among 12-­year-­olds ificity of the order of 75%–100% and 18%–43%, respectively,
in Finland was 23%; 27% in girls and 19% in boys, slightly higher according to Ramos et al. (2013). The differences in the reported
percentages when compared to our findings (Mattila et al., 2016). values of sensitivity and specificity between these two reviews
We found higher prevalences of self-­reported gingival bleeding in are probably due to differences in the self-­reported questions and
girls aged 14, 15, 16 and 17. The higher prevalence of self-­reported, in the clinical gold standard used.
and lower of clinically assessed gingival bleeding in girls might re- Gingival bleeding is not a major health problem. However, it may
flect the fact that they are more concerned with health (Feldman, be a nuisance. It causes bad breath (De Geest, Laleman, Teughels,
Hodgson, Corber, & Quinn, 1986), and brush their teeth more fre- Dekeyser, & Quirynen, 2016) and hampers social well-­
being
quently (Maes, Vereecken, Vanobbergen, & Honkala, 2006; Mattila (Krisdapong, Prasertsom, Rattanarangsima, & Sheiham, 2012). In
et al., 2016; Vettore, Moysés, Sardinha, & Iser, 2012) than boys. This addition, in part it reflects inadequate oral hygiene, which in turn
makes girls more attentive to any signs and symptoms of diseases increases the risk of periodontitis in a proportionally small, but
and provides them with more opportunities to detect an episode of large number of people in the general population. Oral conditions,
gingival bleeding, and at the same time, lowers their risk of gingival including periodontitis, remain a major public health challenge all
inflammation. However, in an adult population, men reported sig- over the world, with severe periodontitis affecting 7.4% of the global
nificantly more often gingival bleeding than women (Lintula et al., population (Kassebaum et al., 2017). There may be an association
2014). between prediabetes and gingival and/or periodontal bleeding on
We did not find differences in the prevalence of self-­reported gentle probing of the periodontal tissues (Andriankaja & Joshipura,
gingivitis related to mothers’ level of education or SES. This con- 2014). Also, self-­reported use of lipid-­lowering agents has shown a
trasts to findings from studies that clinically assessed gingival bleed- potential reduction effect on BOP levels, suggesting a connection
ing and found more gingival bleeding among those with lower SES between these systemic agents and oral inflammation (Andriankaja
(Antunes et al., 2008; Bastos, Boing, Peres, Antunes, & Peres, 2011; et al., 2015). Further large prospective studies should be carried out
Fonseca et al., 2015; Funieru et al., 2017; Tomazoni et al., 2017) and to confirm these findings. It is therefore too early to speculate that
among those whose mothers had fewer years of schooling (Funieru gingival bleeding increases the risk of prediabetes or any other sys-
et al., 2017; Tomazoni et al., 2017). In future studies, we intend to temic disease as this association might be in the opposite direction.
investigate, in this data set, the extent to which self-­reported gingi- Our study discovered that nearly one in five adolescents in Brazil
val bleeding is related to eating and other habits which themselves report gingival bleeding. There is no lack of oral hygiene among ado-
vary according to SES and maternal educational level. It is notewor- lescents in Brazil; almost all of them use toothbrush and toothpaste,
thy, however, that the variables mother’s level of education and SES and report toothbrushing at least twice a day—93% in our study and
had higher proportions of missing data as many adolescents did not 95% in a previous survey—(Vettore et al., 2012). Approximately half
know how to answer these questions, and this may affect their valid- of the adolescents reported flossing. There is some evidence that
ity. In any case, further analyses of these missing data suggested that flossing in addition to toothbrushing reduces the risk of gingivitis
overall nonrespondents seemed to be similar to respondents, with compared to toothbrushing alone (Sambunjak et al., 2011). The pub-
the exception that there were more young adolescents (12–15 years lic health sector in cooperation with schools, industry and the media
old) than old adolescents (16–17 years old) among the nonrespon- need to implement population preventive strategies to improve the
dents compared to the respondents, and the missing information quality of oral hygiene and reduce gingival bleeding in adolescents.
about mother’s level of education and SES seems not to have biased The relevance of this study is in the originality of assessing the
the observed prevalence of gingival bleeding we found (Supporting prevalence of self-­reported gingival bleeding in a representative sam-
Information Tables S1 and S2). Skin colour is closely associated with ple of the adolescent population of a large nation. Future research
SES in Brazil, and we found more self-­reported gingival bleeding in should investigate the specific socio-­psychological and behaviour
Black people than in White people, which is in agreement with previ- impact of self-­reported gingival bleeding in adolescents, including
ous studies that assessed gingival bleeding clinically (Antunes et al., their care-­
seeking behaviour. Furthermore, longitudinal studies
2008; Fonseca et al., 2015). should assess the predictive value of adolescents self-­
reported
NADANOVSKY et al. |
      957

gingival bleeding, in addition to BOP, regarding the risk of developing Buset, S. L., Walter, C., Friedmann, A., Weiger, R., Borgnakke, W. S.,
periodontitis in adulthood. & Zitzmann, N. U. (2016). Are periodontal diseases really silent?
A systematic review of their effect on quality of life. Journal of
Clinical Periodontology, 43(4), 333–344. https://doi.org/10.1111/
jcpe.12517
C O N FL I C T O F I N T E R E S T
Campus, G., Solinas, G., Cagetti, M. G., Senna, A., Minelli, L., Majori, S.,
The authors declare they have no conflict of interest. … Strohmenger, L. (2007). National pathfinder survey of 12-­year-­old
children’s oral health in Italy. Caries Research, 41(6), 512–517. https://
doi.org/10.1159/000110884
ORCID Chapple, I. L., Van der Weijden, F., Doerfer, C., Herrera, D., Shapira, L.,
Polak, D., … Graziani, F. (2015). Primary prevention of periodontitis:
Paulo Nadanovsky  http://orcid.org/0000-0003-3345-9873 Managing gingivitis. Journal of Clinical Periodontology, 42(Suppl 16),
S71–S76. https://doi.org/10.1111/jcpe.12366
De Geest, S., Laleman, I., Teughels, W., Dekeyser, C., & Quirynen, M.
(2016). Periodontal diseases as a source of halitosis: A review of the
REFERENCES
evidence and treatment approaches for dentists and dental hygien-
Abuhaloob, L., & Petersen, P. E. (2017). Oral health status among chil- ists. Periodontology 2000, 71(1), 213–227. https://doi.org/10.1111/
dren and adolescents in governmental and private schools of the prd.12111
Palestinian Territories. International Dental Journal, 68, 105-112. Feldman, W., Hodgson, C., Corber, S., & Quinn, A. (1986). Health con-
https://doi.org/10.1111/idj.12345 cerns and health-­related behaviours of adolescents. CMAJ, 134(5),
Andriankaja, O. M., Jiménez, J. J., Muñoz-Torres, F. J., Pérez, C. M., 489–493.
Vergara, J. L., & Joshipura, K. (2015). Lipid lowering agents use and Ferreira, M. C., Dias-Pereira, A. C., Branco-de-Almeida, L. S., Martins,
systemic and oral inflammation in overweight or obese adult Puerto C. C., & Paiva, S. M. (2017). Impact of periodontal disease on qual-
Ricans: The San Juan Overweight Adults Longitudinal Study (SOALS). ity of life: A systematic review. Journal of Periodontal Research, 52,
Journal of Clinical Periodontology, 42(12), 1090–1096. https://doi. 651–665. https://doi.org/10.1111/jre.12436
org/10.1111/jcpe.12461 Fonseca, E. P., Ferreira, E. F., Abreu, M. H., Palmier, A. C., & Vargas,
Andriankaja, O. M., & Joshipura, K. (2014). Potential association be- A. M. (2015). The relationship between gingival condition and
tween prediabetic conditions and gingival and/or periodontal in- socio-­ demographic factors of adolescents living in a Brazilian
flammation. Journal of Diabetes Investigation, 5, 108–114. https://doi. region. Cien Saude Colet, 20(11), 3375–3384. https://doi.
org/10.1111/jdi.12122 org/10.1590/1413-812320152011.00142015
Antunes, J. L., Peres, M. A., Frias, A. C., Crosato, E. M., & Biazevic, M. G. Funieru, C., Klinger, A., Băicuș, C., Funieru, E., Dumitriu, H. T., & Dumitriu,
(2008). Gingival health of adolescents and the utilization of dental A. (2017). Epidemiology of gingivitis in schoolchildren in Bucharest,
services, state of São Paulo, Brazil. Revista de Saude Publica, 42(2), Romania: A cross-­sectional study. Journal of Periodontal Research,
191–199. https://doi.org/10.1590/S0034-89102008000200002 52(2), 225–232. https://doi.org/10.1111/jre.12385
Armitage, G. C. (1999). Development of a classification system for peri- Gao, J., Ruan, J., Zhao, L., Zhou, H., Huang, R., & Tian, J. (2014).
odontal diseases and conditions. Annals of Periodontology, 4(1), 1–6. Oral health status and oral health knowledge, attitudes and
https://doi.org/10.1902/annals.1999.4.1.1 behavior among rural children in Shaanxi, western China: A
Ayo-Yusuf, O. A., Reddy, P. S., & van den Borne, B. W. (2008). Adolescents’ cross-­s ectional survey. BMC Oral Health, 14, 144. https://doi.
sense of coherence and smoking as longitudinal predictors of self-­ org/10.1186/1472-6831-14-144
reported gingivitis. Journal of Clinical Periodontology, 35(11), 931–937. Jenkins, W. M., & Papapanou, P. N. (2001). Epidemiology of periodontal
https://doi.org/10.1111/j.1600-051X.2008.01319.x disease in children and adolescents. Periodontology 2000, 26, 16–32.
Bastos, J. L., Boing, A. F., Peres, K. G., Antunes, J. L., & Peres, M. A. https://doi.org/10.1034/j.1600-0757.2001.2260102.x
(2011). Periodontal outcomes and social, racial and gender inequali- Kallio, P. (1996). Self-­assessed bleeding in monitoring gingival health
ties in Brazil: A systematic review of the literature between 1999 and among adolescents. Community Dentistry and Oral Epidemiology, 24(2),
2008. Cadernos de Saúde Pública, 27(Suppl 2), S141–S153. https://doi. 128–132. https://doi.org/10.1111/j.1600-0528.1996.tb00829.x
org/10.1590/S0102-311X2011001400003 Kallio, P., & Murtomaa, H. (1997). Determinants of self-­assessed gingi-
Blicher, B., Joshipura, K., & Eke, P. (2005). Validation of self-­reported val health among adolescents. Acta Odontologica Scandinavica, 55(2),
periodontal disease: A systematic review. Journal of Dental Research, 106–110. https://doi.org/10.3109/00016359709115401
84(10), 881–890. https://doi.org/10.1177/154405910508401003 Kassebaum, N. J., Smith, A. G. C., Bernabé, E., Fleming, T. D., Reynolds,
Bloch, K. V., Szklo, M., Kuschnir, M. C., Abreu Gde, A., Barufaldi, L. A., A. E., Vos, T., … GBD 2015 Oral Health Collaborators. (2017). Global,
Klein, C. H., & da Silva, T. L. (2015). The Study of cardiovascular risk regional, and national prevalence, incidence, and disability-­adjusted
in adolescents–ERICA: Rationale, design and sample characteris- life years for oral conditions for 195 countries, 1990-­2015: A sys-
tics of a national survey examining cardiovascular risk factor pro- tematic analysis for the global burden of diseases, injuries, and
file in Brazilian adolescents. BMC Public Health, 15, 94. https://doi. risk factors. Journal of Dental Research, 96(4), 380–387. https://doi.
org/10.1186/s12889-015-1442-x org/10.1177/0022034517693566
Brasil. (2011). Projeto SB Brasil 2010. Resultados principais. Brasília: Kinane, D. F., & Attström, R. (2005). Advances in the pathogenesis of peri-
Ministério da Saúde. odontitis. Group B consensus report of the fifth European Workshop
Broadbent, J. M., Thomson, W. M., Boyens, J. V., & Poulton, R. (2011). in Periodontology. Journal of Clinical Periodontology, 32(Suppl 6),
Dental plaque and oral health during the first 32 years of life. Journal 130–131. https://doi.org/10.1111/j.1600-051X.2005.00823.x
of the American Dental Association, 142(4), 415–426. https://doi. Krisdapong, S., Prasertsom, P., Rattanarangsima, K., & Sheiham,
org/10.14219/jada.archive.2011.0197 A. (2012). Relationships between oral diseases and impacts on
Buhlin, K., Gustafsson, A., Andersson, K., Håkansson, J., & Klinge, B. Thai schoolchildren’s quality of life: Evidence from a Thai na-
(2002). Validity and limitations of self-­reported periodontal health. tional oral health survey of 12-­and 15-­ year-­o lds. Community
Community Dentistry and Oral Epidemiology, 30(6), 431–437. https:// Dentistry and Oral Epidemiology, 40(6), 550–559. https://doi.
doi.org/10.1034/j.1600-0528.2002.00014.x org/10.1111/j.1600-0528.2012.00705.x
|
958       NADANOVSKY et al.

Laganà, G., Abazi, Y., Beshiri Nastasi, E., Vinjolli, F., Fabi, F., Divizia, M., management of periodontal diseases and dental caries in adults.
& Cozza, P. (2015). Oral health conditions in an Albanian adoles- Cochrane Database of Systematic Reviews, 12, CD008829. https://doi.
cent population: An epidemiological study. BMC Oral Health, 15, 67. org/10.1002/14651858.CD008829.pub2
https://doi.org/10.1186/s12903-015-0050-6 Taani, D. Q., & Alhaija, E. S. (2003). Self-­ assessed bleeding as
Lintula, T., Laitala, V., Pesonen, P., Sipilä, K., Laitala, M. L., Taanila, A., & an indicator of gingival health among 12-­ 14-­
year-­
old chil-
Anttonen, V. (2014). Self-­reported oral health and associated factors dren. Journal of Oral Rehabilitation, 30(1), 78–81. https://doi.
in the North Finland 1966 birth cohort at the age of 31. BMC Oral org/10.1046/j.1365-2842.2003.01021.x
Health, 14, 155. https://doi.org/10.1186/1472-6831-14-155 Taylor, G. W., & Borgnakke, W. S. (2007). Self-­ reported periodon-
Locker, D. (1988). Measuring oral health: A conceptual framework. tal disease: Validation in an epidemiological survey. Journal of
Community Dental Health, 5(1), 3–18. Periodontology, 78(7 Suppl), 1407–1420. https://doi.org/10.1902/
Machado, M. E., Tomazoni, F., Ortiz, F. R., Ardenghi, T. M., & Zanatta, F. B. jop.2007.060481
(2017). Impact of partial-­mouth periodontal examination protocols Tomazoni, F., Vettore, M. V., Zanatta, F. B., Tuchtenhagen, S., Moreira,
on the association between gingival bleeding and oral health-­related C. H., & Ardenghi, T. M. (2017). The associations of socioeconomic
quality of life in adolescents. Journal of Periodontology, 88, 693–701. status and social capital with gingival bleeding among schoolchil-
https://doi.org/10.1902/jop.2017.160622 dren. Journal of Public Health Dentistry, 77(1), 21–29. https://doi.
Maes, L., Vereecken, C., Vanobbergen, J., & Honkala, S. (2006). Tooth org/10.1111/jphd.12166
brushing and social characteristics of families in 32 countries. Tsakos, G., Allen, P. F., Steele, J. G., & Locker, D. (2012).
International Dental Journal, 56(3), 159–167. https://doi.org/10.1111/ Interpreting oral health-­ related quality of life data. Community
j.1875-595X.2006.tb00089.x Dentistry and Oral Epidemiology, 40(3), 193–200. https://doi.
Mattila, M. L., Tolvanen, M., Kivelä, J., Pienihäkkinen, K., Lahti, S., & org/10.1111/j.1600-0528.2011.00651.x
Merne-Grafström, M. (2016). Oral health-­related knowledge, at- Vadiakas, G., Oulis, C. J., Tsinidou, K., Mamai-Homata, E., &
titudes and habits in relation to perceived oral symptoms among Polychronopoulou, A. (2012). Oral hygiene and periodontal status of
12-­year-­old school children. Acta Odontologica Scandinavica, 74(5), 12 and 15-­year-­old Greek adolescents. A national pathfinder survey.
343–347. https://doi.org/10.3109/00016357.2016.1139177 European Archives of Paediatric Dentistry, 13(1), 11–20. https://doi.
Nicolau, B., Marcenes, W., Bartley, M., & Sheiham, A. (2005). Associations org/10.1007/BF03262835
between socio-­economic circumstances at two stages of life and ad- Vettore, M. V., Moysés, S. J., Sardinha, L. M., & Iser, B. P. (2012).
olescents’ oral health status. Journal of Public Health Dentistry, 65(1), Socioeconomic status, toothbrushing frequency, and health-­
14–20. https://doi.org/10.1111/j.1752-7325.2005.tb02782.x related behaviors in adolescents: An analysis using the PeNSE da-
Oh, T. J., Eber, R., & Wang, H. L. (2002). Periodontal diseases in the child tabase. Cadernos de Saúde Pública, 28(Suppl), s101–s113. https://doi.
and adolescent. Journal of Clinical Periodontology, 29(5), 400–410. org/10.1590/S0102-311X2012001300011
https://doi.org/10.1034/j.1600-051X.2002.290504.x Zhang, S., Xu, B., Liu, J., Lo, E. C., & Chu, C. H. (2015). Dental and peri-
Petersen, P. E., Hoerup, N., Poomviset, N., Prommajan, J., & Watanapa, odontal status of 12-­year-­old Dai school children in Yunnan Province,
A. (2001). Oral health status and oral health behaviour of urban China: A cross-­sectional study. BMC Oral Health, 15(1), 117. https://
and rural schoolchildren in Southern Thailand. International Dental doi.org/10.1186/s12903-015-0106-7
Journal, 51(2), 95–102. https://doi.org/10.1002/j.1875-595X.2001.
tb00829.x
Pitts, N., Chadwick, B., & Anderson, T. (2015). Children’s Dental Health S U P P O R T I N G I N FO R M AT I O N
Survey 2013. Report 2: Dental disease and damage in children.
England, Wales and Northern Ireland. Additional supporting information may be found online in the
Ramos, R. Q., Bastos, J. L., & Peres, M. A. (2013). Diagnostic validity of Supporting Information section at the end of the article. 
self-­reported oral health outcomes in population surveys: Literature
review. Revista Brasileira de Epidemiologia, 16(3), 716–728. https://
doi.org/10.1590/S1415-790X2013000300015 How to cite this article: Nadanovsky P, dos Santos APP, Bloch
Rebelo, M. A., Lopes, M. C., Vieira, J. M., & Parente, R. C. (2009). Dental KV. Prevalence of self-­reported gingival bleeding in a
caries and gingivitis among 15 to 19  year-­old students in Manaus,
representative sample of the Brazilian adolescent population. J
AM, Brazil. Brazilian Oral Research, 23(3), 248–254. https://doi.
org/10.1590/S1806-83242009000300005 Clin Periodontol. 2018;45:952–958. https://doi.org/10.1111/
Sambunjak, D., Nickerson, J. W., Poklepovic, T., Johnson, T. M., Imai, jcpe.12959
P., Tugwell, P., & Worthington, H. V. (2011). Flossing for the

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