Abstracts
Introduction
Smoking is a risk factor for prevalence, severity and progression of periodontal disease and appears to suppress marginal periodontium inflammatory response.
Purpose
To correlate Visible Plaque Index (VPI) and Gingival Bleeding Index (GBI) in smokers and never-smokers, as well as GBI and bleeding on probing (BOP ) in these groups.
Material and method
We used baseline data of one quasi-experimental study in which 11 smokers and 14 subjects who never smoked were submitted to clinical periodontal examinations between September 2010 and October 2011.
Result
The correlation between VPI and GBI was positive for both groups, it was strong and statistically significant in subjects who had never smoked and moderate in smokers. Regarding GBI and BOP correlations were moderate for smokers and weaker for individuals who had never smoked.
Conclusion
Smokers have lower strength correlation between VPI and GBI compared to individuals who had never smoked resulting in a less pronounced marginal gingival bleeding.
Tobacco; periodontal index; inflammation; periodontitis; gingivitis
Introdução
O hábito de fumar é um fator de risco importante na prevalência, progressão e gravidade das doenças periodontais e parece suprimir a resposta inflamatória marginal no periodonto.
Objetivo
Correlacionar Índice de Placa visível (IPV) e Índice de Sangramento Gengival (ISG) em fumantes e indivíduos que nunca fumaram, bem como correlacionar ISG e o sangramento à sondagem (SS) nesses dois grupos.
Material e método
Foram utilizados dados de baseline de um estudo quasi-experimental, no qual 11 pacientes fumantes e 14 indivíduos que nunca fumaram foram submetidos a exames clínicos periodontais no período de setembro de 2010 e outubro de 2011.
Resultado
A correlação entre IPV e ISG foi positiva para ambos os grupos, sendo forte e estatisticamente significante nos indivíduos que nunca fumaram e moderada nos fumantes. Com relação ao ISG e SS houve moderada correlação para os fumantes e fraca para os indivíduos que nunca fumaram.
Conclusão
Fumantes apresentam uma correlação entre IPV e ISG de menor força em relação aos indivíduos que nunca fumaram resultando em um sangramento gengival marginal menos pronunciado.
Tabaco; índice periodontal; inflamação; periodontite; gengivite
INTRODUCTION
Gingivitis, which refers to inflammation of the protective tissues of the teeth
caused by the presence of supragingival biofilm, develops prior to the establishment
of subgingival biofilm, which can initiate periodontitis11 American Academy of Periodontology – AAP. Glossary of periodontal
terms. 4th ed. Chicago: AAP; 2001.,22 Schätzle M, Löe H, Bürgin W, Anerud A, Boysen H, Lang NP. Clinical
course of chronic periodontitis. I. Role of gingivitis. J Clin Periodontol. 2003
Oct;30(10):887-901. http://dx.doi.org/10.1034/j.1600-051X.2003.00414.x.
PMid:14710769
http://dx.doi.org/10.1034/j.1600-051X.20...
. There is high prevalence of gingivitis and
periodontitis in both developed and developing countries, with differences in
periodontitis prevalence being observed among different age groups33 Albandar JM, Rams TE. Global epidemiology of periodontal diseases:
an overview. Periodontol 2000. 2002; 29(1):7-10.
http://dx.doi.org/10.1034/j.1600-0757.2002.290101.x.
PMid:12102700
http://dx.doi.org/10.1034/j.1600-0757.20...
.
The correct clinical diagnosis of periodontal diseases is directly related to the
presence of inflammatory signs in response to the accumulation of microbial
biofilms44 Armitage GC. Periodontal diagnoses and classification of periodontal
diseases. Periodontol 2000. 2004; 34(1):9-21.
http://dx.doi.org/10.1046/j.0906-6713.2002.003421.x.
PMid:14717852
http://dx.doi.org/10.1046/j.0906-6713.20...
. Factors, such as
the smoking habit, seem suppress the marginal inflammatory response in the
periodontium55 Dietrich T, Bernimoulin JP, Glynn RJ. The effect of cigarette
smoking on gingival bleeding. J Periodontol. 2004 Jan;75(1):16-22.
http://dx.doi.org/10.1902/jop.2004.75.1.16. PMid:15025212
http://dx.doi.org/10.1902/jop.2004.75.1....
. However, it
remains unclear as to whether bleeding in the base of the periodontal pockets during
probing is suppressed in smokers.
The smoking habit is the most important behavioral risk factor to impact the
prevalence, progression, and severity of periodontitis. Smoking is associated with
other chronic diseases, such as lung and oral cancers and cardiovascular
diseases66 Doll R. Uncovering the effects of smoking: historical perspective.
Stat Methods Med Res. 1998 June;7(2):87-117.
http://dx.doi.org/10.1191/096228098668199908. PMid:9654637
http://dx.doi.org/10.1191/09622809866819...
. This habit
compromises periodontal health77 Bergström J. Periodontitis and smoking: an evidence-based appraisal.
J Evid Based Dent Pract. 2006 Mar;6(1):33-41.
http://dx.doi.org/10.1016/j.jebdp.2005.12.018. PMid:17138394
http://dx.doi.org/10.1016/j.jebdp.2005.1...
due to the negative impact of tobacco on the patient’s responses to biofilm,
periodontal treatment, and healing, leading to higher risk in those patients who
have more severe periodontal disease88 Bergström J. Tobacco smoking and risk for periodontal disease. J
Clin Periodontol. 2003 Feb;30(2):107-13.
http://dx.doi.org/10.1034/j.1600-051X.2003.00272.x.
PMid:12622851
http://dx.doi.org/10.1034/j.1600-051X.20...
.
Inflammation of the periodontal tissues can be evaluated by the presence of bleeding
as an objective and easy-to-evaluate sign. Together with other clinical data,
interpretation of bleeding, either by the gingival bleeding index (GBI) or bleeding
on probing (BOP), can permit an accurate diagnosis of periodontal diseases and aid
in treatment planning. The GBI reflects inflammatory changes in the gingival margin
caused by supragingival biofilm, whereas BOP reflects inflammation in the base of
the periodontal pocket caused by subgingival biofilm99 Lie MA, Timmerman MF, Van der Velden U, van der Weijden GA.
Evaluation of 2 methods to assess gingival bleeding in smokers and non-smokers
in natural and experimental gingivitis. J Clin Periodontol. 1998
Sept;25(9):695-700. http://dx.doi.org/10.1111/j.1600-051X.1998.tb02509.x.
PMid:9763323
http://dx.doi.org/10.1111/j.1600-051X.19...
. Studies have shown that GBI is the main clinical
parameter of marginal gingival inflammation. However, inflammatory indicators are
suppressed, bleeding of the gingival margin is less pronounced1010 Bergström J, Preber H. The influence of cigarette smoking on the
development of experimental gingivitis. J Periodontal Res. 1986
Nov;21(6):668-76. http://dx.doi.org/10.1111/j.1600-0765.1986.tb01504.x.
PMid:2948000
http://dx.doi.org/10.1111/j.1600-0765.19...
11 Danielsen B, Manji F, Nagelkerke N, Fejerskov O, Baelum V. Effect of
cigarette smoking on the transition dynamics in experimental gingivitis. J Clin
Periodontol. 1990 Mar;17(3):159-64.
http://dx.doi.org/10.1111/j.1600-051X.1990.tb01080.x.
PMid:2319002
http://dx.doi.org/10.1111/j.1600-051X.19...
-1212 Bergström J, Floderus-Myrhed B. Co-twin control study of the
relationship between smoking and some periodontal disease factors. Community
Dent Oral Epidemiol. 1983 Apr;11(2):113-6.
http://dx.doi.org/10.1111/j.1600-0528.1983.tb01367.x.
PMid:6573237
http://dx.doi.org/10.1111/j.1600-0528.19...
, and inflammatory signs, such as erythema and
swelling, are less evident in smokers compared to individuals who have never
smoked1313 Bergström J. Tobacco smoking and chronic destructive periodontal
disease. Odontology. 2004 Sept;92(1):1-8.
http://dx.doi.org/10.1007/s10266-004-0043-4. PMid:15490298
http://dx.doi.org/10.1007/s10266-004-004...
. These conditions
can make it difficult to diagnose periodontal disease in smokers. Moreover, some
studies have not found reduced gingival blood flow in smokers1414 Mavropoulos A, Brodin P, Rösing CK, Aass AM, Aars H. Gingival blood
flow in periodontitis patients before and after periodontal surgery assessed in
smokers and non-smokers. J Periodontol. 2007 Sept;78(9):1774-82.
http://dx.doi.org/10.1902/jop.2007.060472. PMid:17760548
http://dx.doi.org/10.1902/jop.2007.06047...
,1515 Baab DA, Oberg PA. The effect of cigarette smoking on gingival blood
flow in humans. J Clin Periodontol. 1987 Aug;14(7):418-24.
http://dx.doi.org/10.1111/j.1600-051X.1987.tb01547.x.
PMid:2957396
http://dx.doi.org/10.1111/j.1600-051X.19...
. Thus, the literature is not consistent with regard to
whether smokers and never-smokers differ in terms of their gingival bleeding
parameters. The aim of this study was to correlate the visible plaque index (VPI)
and BOP with GBI in smokers and in never-smokers.
MATERIAL AND METHOD
Study Population
This study refers to the baseline examination of patients participating in a
quasi-experimental study1616 Ardais R, Mário TG, Boligon J, Kantorski KZ, Moreira CH. The effect
of smoking on bleeding on probing after nonsurgical periodontal therapy: a
quasi-experimental study. Braz Oral Res. 2014 Jan-Feb;28(1):1-7.; published
online October 21, 2014. http://dx.doi.org/10.1590/1807-3107BOR-2014.vol28.0058.
PMid:25337935
http://dx.doi.org/10.1590/1807-3107BOR-2...
.
The sample consisted of individuals diagnosed with chronic periodontitis1717 Tonetti MS, Claffey N, and the European Workshop in Periodontology
group C. Advances in the progression of periodontitis and proposal of
definitions of a periodontitis case and disease progression for use in risk
factor research. Group C consensus report of the 5th European Workshop in
Periodontology. J Clin Periodontol. 2005; 32(6 Suppl):210-3.
http://dx.doi.org/10.1111/j.1600-051X.2005.00822.x.
PMid:16128839
http://dx.doi.org/10.1111/j.1600-051X.20...
who requested treatment at
the Dentistry Course of the Federal University of Santa Maria (UFSM) in southern
Brazil between September 2010 and October 2011. Eligible individuals had at
least 12 teeth in their mouth and a probing pocket depth (PPD) of 5 mm or more
in at least four teeth, with no indication of extraction or
periodontal-endodontic lesions, and had no contraindications to dental
treatment. Individuals reported either a minimal consumption of 10 cigarettes
per day for the past 6 months (smoker/test group) or a history of never smoking
(never-smoker/control group). Individuals with any of the following conditions
were excluded: 1) a history of diabetes or hormone replacement therapy, 2)
pregnancy, 3) regular use of antibiotics or anti-inflammatory drugs in the past
6 and 3 months, respectively, 4) use of medications that cause increased
gingival volume, and 5) any periodontal treatment in the last 12 months.
Ethical Considerations
Eligible subjects were informed about the purpose of the study and were invited to participate. All included patients agreed to participate and signed an informed consent form. This study was conducted in accordance with the Declaration of Helsinki and was approved by the Research Ethics Committee of the UFSM.
Evaluation Methods and Reproducibility
Participants were interviewed to obtain demographic, socioeconomic, behavioral,
and medical data. Two calibrated and trained examiners collected clinical
parameters, including the VPI, GBI, PPD, plaque retentive factors (PRFs), and
clinical attachment level (CAL), at six sites per tooth (distobuccal, buccal,
mesiobuccal, mesiolingual, lingual, and distolingual). Clinical parameters were
not measured on the third molars, teeth indicated for extraction, or teeth with
periodontal-endodontic lesions. BOP results were categorized as BOP1 (small
point bleeding), BOP2 (blood flowing through the groove area), and total BOP
(BOP1 + BOP2)99 Lie MA, Timmerman MF, Van der Velden U, van der Weijden GA.
Evaluation of 2 methods to assess gingival bleeding in smokers and non-smokers
in natural and experimental gingivitis. J Clin Periodontol. 1998
Sept;25(9):695-700. http://dx.doi.org/10.1111/j.1600-051X.1998.tb02509.x.
PMid:9763323
http://dx.doi.org/10.1111/j.1600-051X.19...
. All tests
were performed with a manual periodontal probe (CP 15 UNC, Neumar, Brazil) at a
dental unit in the Periodontics Clinic of the UFSM.
Examiners were trained to perform all clinical examinations and calibrated for PPD and CAL. Weighted Kappa coefficients (± 1 mm) for examiners 1 and 2 were 0.97 and 0.96, respectively, for PPD and 0.88 and 0.70, respectively, for CAL. Interexaminer values were 0.94 for PPD and 0.84 for CAL.
Measured Outcomes
The primary outcome was the correlation between the GBI and VPI values. The correlation between the GBI and BOP was considered the secondary outcome.
Statistical Analysis
Data were analyzed with the Statistical Package for Social Sciences (SPSS for Windows, version 21.0, SPSS Inc., Chicago, IL, USA). Means were obtained for all data. Standard deviations were obtained for continuous variables and frequency distributions for categorical variables. Pearson’s correlation coefficient (r) was used to determine the correlations of GBI with BOP1, BOP2, and VPI in the two groups. The significance level was 5%.
RESULT
The sample comprised 25 subjects, including 11 smokers and 14 never-smokers (Figure 1). The groups were similar with respect to income, age, and gender (P > 0.05). The mean duration of the smoking habit among smokers was 25 years, with an average consumption of 20 cigarettes per day. Compared to never-smokers, smokers had four times less bleeding in the gingival margin, despite presenting twice as many PRFs and one-third more visible plaque. Smokers showed almost twice as much suppuration on probing and increased clinical attachment loss. There were no statistically significant differences in PPD, total BOP, BOP1, or BOP2 between the two groups (Table 1).
Demographic, socioeconomic, behavioral and clinical variables of sample (%, mean ± standard deviation)
All observed correlations were positive (Table 2). The correlation between VPI and GBI was moderate in smokers (r = 0.35) but strong in never-smokers (P < 0.05). Correlations of GBI with BOP1 and BOP2 were moderate in smokers (both r = 0.35) and low in never-smokers (r = 0.18 and r = 0.03, respectively).
DISCUSSION
Smokers presented a moderate correlation between VPI and GBI, whereas a strong correlation was observed among never-smokers. Thus, despite their higher rates of visible plaque, smokers had fewer signs of marginal inflammation compared to individuals who had never smoked. The higher correlations of GBI with BOP1 and BOP2 in smokers compared to never-smokers may indicate that the marginal bleeding in smokers is more reflective of subgingival inflammation than it is in individuals who have never smoked.
Limitations of this study include the fact that the number of cigarettes smoked and
the duration of the smoking habit were self-reported. Biochemical markers, such as
cotinine, may be a reliable alternative to determining tobacco use1818 González YM, De Nardin A, Grossi SG, Machtei EE, Genco RJ, De Nardin
E. Serum cotinine levels, smoking, and periodontal attachment loss. J Dent Res.
1996 Feb;75(2):796-802. http://dx.doi.org/10.1177/00220345960750021001.
PMid:8655777
http://dx.doi.org/10.1177/00220345960750...
. Furthermore, it was not
possible for the investigators to be blinded, due to the presence of smoking-related
features (e.g., halitosis and dental staining) in patients.
Several studies have investigated the effect of smoking on the suppression of
inflammatory indicators, because the biological mechanisms that lead to increased
periodontitis in these patients have not been well elucidated. Bergström et al.1919 Bergström J, Persson L, Preber H. Influence of cigarette smoking on
vascular reaction during experimental gingivitis. Scand J Dent Res. 1988
Feb;96(1):34-9. PMid:3422504. induced gingivitis in dental
students with similar plaque index values. The vascular response was less pronounced
in smokers when compared to those who had never smoked. Photographic evaluation of
the vascular changes demonstrated that smoking led to a reduction in the number of
blood vessels. This finding can explain the masking of inflammatory signs and,
therefore, the reduction in the average GBI in smokers. Dietrich et al.55 Dietrich T, Bernimoulin JP, Glynn RJ. The effect of cigarette
smoking on gingival bleeding. J Periodontol. 2004 Jan;75(1):16-22.
http://dx.doi.org/10.1902/jop.2004.75.1.16. PMid:15025212
http://dx.doi.org/10.1902/jop.2004.75.1....
reported that smoking caused a
strong, chronic, and dose-dependent effect in the suppression of gingival bleeding.
In the present study, the moderate correlation between VPI and GBI in smokers and
strong correlation in never-smokers corroborate the results of the aforementioned
studies.
Smoking leads to an increase in the thickness of the gingival epithelium by affecting
the proliferation of cells in the basal layer and the stratum corneum (keratin
layer). This increased thickness occurs regardless of periodontal status and can
reduce the signs of gingival inflammation during infection2020 Villar CC, Lima AF. Smoking influences on the thickness of marginal
gingival epithelium. Pesqui Odontol Bras. 2003 Jan-Mar;17(1):41-5.
http://dx.doi.org/10.1590/S1517-74912003000100008.
PMid:12908058
http://dx.doi.org/10.1590/S1517-74912003...
,2121 van Oijen MG, Gilsing MM, Rijksen G, Hordijk GJ, Slootweg PJ.
Increased number of proliferating cells in oral epithelium from smokers and
ex-smokers. Oral Oncol. 1998 July;34(4):297-303.
http://dx.doi.org/10.1016/S1368-8375(98)80011-0. PMid:9813726
http://dx.doi.org/10.1016/S1368-8375(98)...
. However, one study demonstrated that although smoking
has an effect on cell proliferation, the increased epithelial thickness is mostly
associated with the inflammatory condition of the periodontium2222 Gültekin SE, Sengüven B, Karaduman B. The effect of smoking on
epithelial proliferation in healthy and periodontally diseased marginal gingival
epithelium. J Periodontol. 2008 Aug;79(8):1444-50.
http://dx.doi.org/10.1902/jop.2008.070645. PMid:18672994
http://dx.doi.org/10.1902/jop.2008.07064...
.
In this study, the correlation between GBI and BOP (1 and 2) was moderate in smokers
and weak in patients who had never smoked. Thus, unlike in the gingival margin,
smoking does not attenuate bleeding in the base of the periodontal pockets. This
result is in agreement with other studies2323 Müller HP, Stadermann S, Heinecke A. Longitudinal association
between plaque and gingival bleeding in smokers and non-smokers. J Clin
Periodontol. 2002 Apr;29(4):287-94.
http://dx.doi.org/10.1034/j.1600-051X.2002.290403.x.
PMid:11966925
http://dx.doi.org/10.1034/j.1600-051X.20...
24 Müller HP, Stadermann S. Multivariate multilevel models for repeated
measures in the study of smoking effects on the association between plaque and
gingival bleeding. Clin Oral Investig. 2006 Dec;10(4):311-6.
http://dx.doi.org/10.1007/s00784-006-0067-y. PMid:16896834
http://dx.doi.org/10.1007/s00784-006-006...
-2525 Farina R, Tomasi C, Trombelli L. The bleeding site: a multi-level
analysis of associated factors. J Clin Periodontol. 2013 Aug;40(8):735-42.
http://dx.doi.org/10.1111/jcpe.12118. PMid:23713685
http://dx.doi.org/10.1111/jcpe.12118...
. in which smokers had higher BOP values than
never-smokers. Furthermore, the presence of marginal gingival bleeding (GBI) in
smokers may suggest that the inflammatory infiltrate is associated with deeper
regions of the periodontal pockets. Therefore, the likelihood of inflammation in the
base of the periodontal pockets is increased relative to individuals who have never
smoked.
Accordingly, more attention should be given to marginal bleeding in smokers. This condition may suggest the presence of subgingival infection, because the suppressed inflammatory response only seems to occur at the gingival margin and not in the base of the periodontal pockets. Overall, the GBI does not appear to be an accurate clinical marker for detecting gingivitis and monitoring oral hygiene habits in smokers. In these individuals, an assessment of the gingival margin condition must include the VPI, obtained at different times, to determine the patient’s true oral hygiene condition.
CONCLUSION
Compared to individuals who have never smoked, smokers present a lower correlation between VPI and GBI, resulting in less pronounced gingival margin bleeding. Therefore, gingivitis must be carefully diagnosed in these patients. When present in smokers, marginal gingival bleeding may represent a subgingival infection, as indicated by the greater correlation between GBI and BOP (1 and 2) compared to never-smokers.
REFERENCES
-
1American Academy of Periodontology – AAP. Glossary of periodontal terms. 4th ed. Chicago: AAP; 2001.
-
2Schätzle M, Löe H, Bürgin W, Anerud A, Boysen H, Lang NP. Clinical course of chronic periodontitis. I. Role of gingivitis. J Clin Periodontol. 2003 Oct;30(10):887-901. http://dx.doi.org/10.1034/j.1600-051X.2003.00414.x. PMid:14710769
» http://dx.doi.org/10.1034/j.1600-051X.2003.00414.x -
3Albandar JM, Rams TE. Global epidemiology of periodontal diseases: an overview. Periodontol 2000. 2002; 29(1):7-10. http://dx.doi.org/10.1034/j.1600-0757.2002.290101.x. PMid:12102700
» http://dx.doi.org/10.1034/j.1600-0757.2002.290101.x -
4Armitage GC. Periodontal diagnoses and classification of periodontal diseases. Periodontol 2000. 2004; 34(1):9-21. http://dx.doi.org/10.1046/j.0906-6713.2002.003421.x. PMid:14717852
» http://dx.doi.org/10.1046/j.0906-6713.2002.003421.x -
5Dietrich T, Bernimoulin JP, Glynn RJ. The effect of cigarette smoking on gingival bleeding. J Periodontol. 2004 Jan;75(1):16-22. http://dx.doi.org/10.1902/jop.2004.75.1.16. PMid:15025212
» http://dx.doi.org/10.1902/jop.2004.75.1.16 -
6Doll R. Uncovering the effects of smoking: historical perspective. Stat Methods Med Res. 1998 June;7(2):87-117. http://dx.doi.org/10.1191/096228098668199908. PMid:9654637
» http://dx.doi.org/10.1191/096228098668199908 -
7Bergström J. Periodontitis and smoking: an evidence-based appraisal. J Evid Based Dent Pract. 2006 Mar;6(1):33-41. http://dx.doi.org/10.1016/j.jebdp.2005.12.018. PMid:17138394
» http://dx.doi.org/10.1016/j.jebdp.2005.12.018 -
8Bergström J. Tobacco smoking and risk for periodontal disease. J Clin Periodontol. 2003 Feb;30(2):107-13. http://dx.doi.org/10.1034/j.1600-051X.2003.00272.x. PMid:12622851
» http://dx.doi.org/10.1034/j.1600-051X.2003.00272.x -
9Lie MA, Timmerman MF, Van der Velden U, van der Weijden GA. Evaluation of 2 methods to assess gingival bleeding in smokers and non-smokers in natural and experimental gingivitis. J Clin Periodontol. 1998 Sept;25(9):695-700. http://dx.doi.org/10.1111/j.1600-051X.1998.tb02509.x. PMid:9763323
» http://dx.doi.org/10.1111/j.1600-051X.1998.tb02509.x -
10Bergström J, Preber H. The influence of cigarette smoking on the development of experimental gingivitis. J Periodontal Res. 1986 Nov;21(6):668-76. http://dx.doi.org/10.1111/j.1600-0765.1986.tb01504.x. PMid:2948000
» http://dx.doi.org/10.1111/j.1600-0765.1986.tb01504.x -
11Danielsen B, Manji F, Nagelkerke N, Fejerskov O, Baelum V. Effect of cigarette smoking on the transition dynamics in experimental gingivitis. J Clin Periodontol. 1990 Mar;17(3):159-64. http://dx.doi.org/10.1111/j.1600-051X.1990.tb01080.x. PMid:2319002
» http://dx.doi.org/10.1111/j.1600-051X.1990.tb01080.x -
12Bergström J, Floderus-Myrhed B. Co-twin control study of the relationship between smoking and some periodontal disease factors. Community Dent Oral Epidemiol. 1983 Apr;11(2):113-6. http://dx.doi.org/10.1111/j.1600-0528.1983.tb01367.x. PMid:6573237
» http://dx.doi.org/10.1111/j.1600-0528.1983.tb01367.x -
13Bergström J. Tobacco smoking and chronic destructive periodontal disease. Odontology. 2004 Sept;92(1):1-8. http://dx.doi.org/10.1007/s10266-004-0043-4. PMid:15490298
» http://dx.doi.org/10.1007/s10266-004-0043-4 -
14Mavropoulos A, Brodin P, Rösing CK, Aass AM, Aars H. Gingival blood flow in periodontitis patients before and after periodontal surgery assessed in smokers and non-smokers. J Periodontol. 2007 Sept;78(9):1774-82. http://dx.doi.org/10.1902/jop.2007.060472. PMid:17760548
» http://dx.doi.org/10.1902/jop.2007.060472 -
15Baab DA, Oberg PA. The effect of cigarette smoking on gingival blood flow in humans. J Clin Periodontol. 1987 Aug;14(7):418-24. http://dx.doi.org/10.1111/j.1600-051X.1987.tb01547.x. PMid:2957396
» http://dx.doi.org/10.1111/j.1600-051X.1987.tb01547.x -
16Ardais R, Mário TG, Boligon J, Kantorski KZ, Moreira CH. The effect of smoking on bleeding on probing after nonsurgical periodontal therapy: a quasi-experimental study. Braz Oral Res. 2014 Jan-Feb;28(1):1-7.; published online October 21, 2014. http://dx.doi.org/10.1590/1807-3107BOR-2014.vol28.0058. PMid:25337935
» http://dx.doi.org/10.1590/1807-3107BOR-2014.vol28.0058 -
17Tonetti MS, Claffey N, and the European Workshop in Periodontology group C. Advances in the progression of periodontitis and proposal of definitions of a periodontitis case and disease progression for use in risk factor research. Group C consensus report of the 5th European Workshop in Periodontology. J Clin Periodontol. 2005; 32(6 Suppl):210-3. http://dx.doi.org/10.1111/j.1600-051X.2005.00822.x. PMid:16128839
» http://dx.doi.org/10.1111/j.1600-051X.2005.00822.x -
18González YM, De Nardin A, Grossi SG, Machtei EE, Genco RJ, De Nardin E. Serum cotinine levels, smoking, and periodontal attachment loss. J Dent Res. 1996 Feb;75(2):796-802. http://dx.doi.org/10.1177/00220345960750021001. PMid:8655777
» http://dx.doi.org/10.1177/00220345960750021001 -
19Bergström J, Persson L, Preber H. Influence of cigarette smoking on vascular reaction during experimental gingivitis. Scand J Dent Res. 1988 Feb;96(1):34-9. PMid:3422504.
-
20Villar CC, Lima AF. Smoking influences on the thickness of marginal gingival epithelium. Pesqui Odontol Bras. 2003 Jan-Mar;17(1):41-5. http://dx.doi.org/10.1590/S1517-74912003000100008. PMid:12908058
» http://dx.doi.org/10.1590/S1517-74912003000100008 -
21van Oijen MG, Gilsing MM, Rijksen G, Hordijk GJ, Slootweg PJ. Increased number of proliferating cells in oral epithelium from smokers and ex-smokers. Oral Oncol. 1998 July;34(4):297-303. http://dx.doi.org/10.1016/S1368-8375(98)80011-0. PMid:9813726
» http://dx.doi.org/10.1016/S1368-8375(98)80011-0 -
22Gültekin SE, Sengüven B, Karaduman B. The effect of smoking on epithelial proliferation in healthy and periodontally diseased marginal gingival epithelium. J Periodontol. 2008 Aug;79(8):1444-50. http://dx.doi.org/10.1902/jop.2008.070645. PMid:18672994
» http://dx.doi.org/10.1902/jop.2008.070645 -
23Müller HP, Stadermann S, Heinecke A. Longitudinal association between plaque and gingival bleeding in smokers and non-smokers. J Clin Periodontol. 2002 Apr;29(4):287-94. http://dx.doi.org/10.1034/j.1600-051X.2002.290403.x. PMid:11966925
» http://dx.doi.org/10.1034/j.1600-051X.2002.290403.x -
24Müller HP, Stadermann S. Multivariate multilevel models for repeated measures in the study of smoking effects on the association between plaque and gingival bleeding. Clin Oral Investig. 2006 Dec;10(4):311-6. http://dx.doi.org/10.1007/s00784-006-0067-y. PMid:16896834
» http://dx.doi.org/10.1007/s00784-006-0067-y -
25Farina R, Tomasi C, Trombelli L. The bleeding site: a multi-level analysis of associated factors. J Clin Periodontol. 2013 Aug;40(8):735-42. http://dx.doi.org/10.1111/jcpe.12118. PMid:23713685
» http://dx.doi.org/10.1111/jcpe.12118
Publication Dates
-
Publication in this collection
June 2015
History
-
Received
14 June 2014 -
Accepted
15 Dec 2014