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Dyslipidemia, diabetes and periodontal disease, a cross-sectional study in Rafsanjan, a region in southeast Iran

Abstract

The objectives

The association between dyslipidemia, diabetes and alterations in periodontal health are inconsistent. The aim of this study was to determine the association between dyslipidemia, diabetes and periodontal disease in the Oral Health Branch of Rafsanjan Cohort Study (OHBRCS).

Methods

Rafsanjan Cohort Study (RCS) was launched in 2015 in Rafsanjan City a region in the southeast of Iran. A total of 8682 participants aged 35–70 years of both gender were recruited into the OHBRCS as a part of RCS. Bleeding on probing (BOP), probing pocket depth (PPD) and Clinical attachment loss (CAL) were used to assess periodontal health status. When CAL progression was ≥ 1 mm and PPD was > 3 mm, it was defined as periodontitis.

Results

The final sample consisted of 6751 individuals with mean age of 47.67 ± 8.79 years. Among this population, 73.32% (n = 4949), 13.75% (n = 928), 59.67% (n = 4028) and 11.76% (n = 794) had BOP, PPD > 3 mm, CAL ≥ 1 mm and periodontitis respectively. The odds of CAL ≥ 1 mm increased 14% in subjects with high LDL cholesterol (OR: 1.14; 95% CI: 1.01–1.30), 17% in subjects with diabetes (OR: 1.17; 95% CI: 1.01–1.36) and 23% in subjects with both dyslipidemia and diabetes (OR: 1.23; 95% CI: 1.05–1.44). Also, the odds of PPD > 3 mm in the group with high total cholesterol (TC) was 16% higher compared to those with normal TC (OR: 1.16; 95% CI: 1.01–1.34).

Conclusions

There was an increased odds in periodontal disease in association with high TC, high LDL cholesterol, diabetes and having both dyslipidemia and diabetes. This suggests that high TC, high LDL cholesterol, diabetes and having both dyslipidemia and diabetes might be potential indicators for the presence of periodontal disease.

Peer Review reports

Introduction

Gingivitis is an inflammatory process confined to the gingival caused by microorganisms that accumulate on the tooth surface. If gingivitis left untreated, may develop to periodontitis, which is diagnosed by destruction of tooth supporting structures, eventually leading to tooth mobility and loss [1]. An epidemiological study found that among adults, the prevalence of total periodontitis (including mild, moderate and severe forms of periodontitis) was 47.7% and the percentage of severe periodontitis was 8.5% [2, 3]. According to previous reports, 80% of the population of the United States and 51% of the UK population will develop periodontitis in their lifetime [4]. Also, the prevalence of periodontitis in Iranian adolescents and adults was reported to be 30% and 53% respectively [5]. Periodontitis is caused by a large number of bacterial biofilm, but the immune response of the host can affect the progression of this disease [6]. Thus, systemic diseases affecting host response may be risk factors for periodontitis [7].

Diabetes is a metabolic disease characterized by hyperglycemia which caused by the defects in insulin action and/or secretion [8]. Periodontal disease is considered the sixth complication of diabetes [9]. Evidence suggests that diabetes can initiate or promote the periodontal disease [10]. A previous study reported a relationship between increased severity of periodontitis and type 2 diabetes mellitus [11]. Also, another study showed that 83% of people with diabetes suffer from periodontitis [12]. On the contrary, in study of Ueno et al. no significant association was found between periodontitis and diabetes [13].

Dyslipidemia, which is one of the concerns of modern societies, has known as one of the most important risk factors for cardiovascular diseases. According to recent researches, the prevalence of dyslipidemia was 73–83% among Iranian adults [14, 15]. Recent studies indicated an association between dyslipidemia and alterations in periodontal health [16]. Fentoglu and colleagues concluded that patients with hyperlipidemia manifested higher levels of periodontal parameters compared to healthy individuals [16]. However, other studies not found this relationship [11, 17, 18]. These associations may differ based on some risk factors including race, dietary habits, and lifestyle. So, more studies are necessary to conclude definitive results.

Considering the high prevalence of dyslipidemia and diabetes in Iran [19, 20], the likely effects of these two risk factors on the progression of periodontal disease and the discrepancy of results between different studies, this study was conducted to determine the association between dyslipidemia, diabetes and periodontal disease with a larger sample size in the population of OHBRCS.

Materials and methods

Study design and data collection

Rafsanjan Cohort Study (RCS) included in the Prospective Epidemiological Research Studies in IrAN (PERSIAN) [21] was launched in 2015 in the Rafsanjan, a region in the southeast of Iran. This study was designed to recruit a total of 10,000 participants of both genders aged 35–70 years. All participants signed the informed written consent letter [22].

Selected individuals were interviewed using a standardized and detailed questionnaire validated in the PERSIAN [21]. The questionnaires contain demographic data, socioeconomic status, medication and medical history, life style and anthropometric measurements. Alcohol consumption, smoking and opium usage were self-reported. Smoking was defined as having smoked more than 100 cigarettes in lifetime. Alcohol drinker considered as someone who had consumed 200 ml of beer or 45 ml of liquor, once a week for at least six months during his/her lifetime [21]. A participant was defined as opium user if he/she reported consumption of opium for at least once per week for 6 months during his/her lifetime [23]. Physical activity was assessed based on a 22- item questionnaire and the daily physical activity. Wealth score index (WSI) was used to determine Socio-Economic Status (SES) of individuals.

Oral Health Branch of Rafsanjan Cohort Study (OHBRCS) as part of the RCS was established aiming to investigate the most important aspects of dental and oral health of the participants. All recruited individuals of the adult RCS were also invited to participate in the OHBRCS. Finally, a total of 8682 subjects of the adult cohort study entered the OHBRCS. The questionnaires included factors related to oral health and a full-mouth examination were undertaken by trained oral health professionals. A trained assistant who accompanied the dental specialists recorded the data. Three oral medicine specialist, one periodontist and one general dentist were trained and calibrated with each other and everyone with himself/herself during 2 training sessions for proper diagnosis of oral and periodontal diseases. Instruments were unified for all examiners and included dental mirror and dental probe. The periodontal status was determined by clinical attachment loss (CAL), pocket depth (PPD), and bleeding on probing (BOP). Walking probing method by the Williams Probe (Willliams coded, Hu-Friedy, USA, Michigan ”o” probe) was used for measurements. All permanent, fully erupted teeth except all the erupted third were considered for clinical examination. The obtained CAL included the probing depth plus gingival recession.

This study was approved by the Ethics Committee of Rafsanjan University of Medical Sciences (Ethical codes: ID: IR.RUMS.REC.1399.197). In addition, this study was performed in accordance with the guidelines for the report of observational studies in epidemiology (STROBE).

Definition of terms

Fasting blood glucose (FBG), total cholesterol (TC), low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol and triglycerides (TG) were measured using a biotecnica analyzer (BT 1500, Italy) at the laboratory of Cohort center. Diabetes was described as FBS ≥ 126 mg/dL or receiving the antidiabetic drugs [24]. According to the Third Report of the National Cholesterol Education Program (NCEP-Adult Treatment Panel III), dyslipidemia was defined as LDL ≥ 130 mg/dL, or TC ≥ 200 mg/dL, or HDL ≤ 40 mg/dL in men, and 50 mg/dl in women or TG ≥ 150 mg/dL and or using lipid-lowering medications [25]. High LDL and high TC were considered as LDL ≥ 130 mg/dL or use of lipid-lowering medications for high LDL and TC ≥ 200 mg/dL or use of lipid-lowering medications for high TC. Furthermore, TG ≥ 150 mg/dL or use of lipid-lowering medications for high TG and HDL ≤ 40 mg/dL in men, and 50 mg/dl in women were defined as high TG and low HDL respectively.

Periodontal health indexes were determined in a population with at least 2 teeth (n: 6751). The thresholds for Pocket and CAL were > 3 mm and ≥ 1 mm respectively [26]. When CAL progression was ≥ 1 mm and PPD was > 3 mm, it was defined as periodontitis [27]. However, observed CAL related to causes unrelated to periodontitis was not considered as CAL such as: (1) gingival recession with traumatic origin; (2) dental caries extending in the cervical area of the tooth; (3) the presence of CAL on the distal aspect of a second molar and associated with malposition or extraction of a third molar, (4) an endodontic lesion draining through the marginal periodontium; and (5) the occurrence of vertical root fracture.

Statistical analyses

Frequency (%) for categorical variables and mean (SD: standard deviation) for the quantitative variables were used and baseline characteristics were compared across the groups of our study using chi-square (χ²) and t-test for categorical and continuous variables, respectively. In addition, we used univariate and multivariate dichotomous logistics regression analysis to determine the odds ratios (ORs) and the corresponding 95% confidence intervals (CI) for the relation of dyslipidemia and diabetes with BOP, PPD, CAL and periodontitis. We used two models in the regression analysis. Potential confounding variables were sequentially entered into multivariate model according to their hypothesized strengths of association with dyslipidemia, diabetes and periodontal health indexes. Variables with a p-value < 0.25 were selected as confounders. Univariate model (crude model) has been stratified on the condition of dyslipidemia and diabetes. Moreover, multivariate adjusted model is adjusted for confounding variables including age (continuous variable), gender (male/ female), education years (continuous variable) and wealth status index, cigarette smoking, opium using, alcohol drinking, body mass index (continuous variable), physical activity level (continuous variable), hypertension (yes/no), CVD history (yes/no), and brushing frequency (categorical variable). As periodontitis prevalence increases significantly after the age of 40 years, this age was selected as cutoff for subgroup analysis [28, 29]. Also, a sub-analysis by category of the number of teeth was done. All analyses were performed through State V.14. All p-values are two-sided.

Results

The final sample consisted of 6751 individuals, both gender with mean age ± standard deviation (SD) 47.67 ± 8.79 years that 44.07% were men and 55.93% were women. Table 1 compares sociodemographic characteristics, general health status, habits and laboratory tests of the study population between periodontal health indexes (BOP, PPD, CAL and periodontitis). Of the 6751 study patients, 73.32% (n = 4949), 13.75% (n = 928), 59.67% (n = 4028) and 11.76% (n = 794) were diagnosed as presenting with BOP, PPD > 3 mm, CAL ≥ 1 mm and periodontitis respectively. Among this population, the prevalence of high TC, high LDL, low HDL and high TG was 52.07%, 31.15%, 11.54% and 47.42% respectively. Additionally, 19.84% and 72.22% of the study patients diagnosed having diabetes and dyslipidemia respectively. A significant difference was found between periodontal status and physical activity, sociodemographic characteristics, general health status, habits and laboratory tests. Among participants with BOP, PPD > 3 mm, CAL ≥ 1 mm and periodontitis, 18.64%, 26.29%, 21.95% and 28.22% were smokers, respectively. Also, among those who had BOP, PPD > 3 mm, CAL ≥ 1 mm and periodontitis 16.32%, 24.32%, 19.45% and 25.54% were opium user. The frequency of BOP, pocket, CAL and periodontitis was higher in people who brushed more than once a day than in other people and showed a significant difference (p < 0.001).

Table 1 Characteristics of the study population, overall and according to the periodontal health indexes (n: 6751).

Table 2 shows the associations of dyslipidemia and diabetes with periodontal health indexes according to age group in multivariate logistic regression models. In the crude model the odds of BOP decreased in subject with high TC (OR: 0.82; 95% CI: 0.73–0.91), diabetes (OR: 0.83; 95% CI: 0.73–0.95) and in subject with both dyslipidemia and diabetes (OR: 0.84; 95% CI: 0.73–0.97). The odds of CAL in the crude model increased in subjects with dyslipidemia (OR: 1.22; 95% CI: 1.10–1.36), high TC (OR: 1.20; 95% CI: 1.09–1.32), high LDL (OR: 1.38; 95% CI: 1.24–1.54), high TG (OR: 1.15; 95% CI: 1.04–1.27), diabetes (OR: 1.45; 95% CI: 1.28–1.64) and in group with both dyslipidemia and diabetes (OR: 1.49; 95% CI: 1.31–1.71). Also, subjects with Low HDL had lower odds of CAL (OR: 0.80; 95% CI: 0.69–0.93). (Table 2).

Table 2 Association of dyslipidemia and diabetes with BOP, PPD > 3 mm, CAL ≥ 1 mm and periodontitis in total and for age group (n = 6749).

In adjusted OR, the association measurement estimated that in participants aged over 40 years, the odds of BOP decreased 15% in individuals with high TC (OR: 0.85; 95% CI: 0.74–0.97) and the odds of CAL increased 14% in subjects with High LDL (OR: 1.14; 95% CI: 1.01–1.30), 17% in subjects with diabetes (OR: 1.17; 95% CI: 1.01–1.36) and 23% in subjects with both dyslipidemia and diabetes (OR: 1.23; 95% CI: 1.05–1.44) (Table 2).

The adjusted results showed that in 35–39 years old group, frequency of CAL in those with high LDL was higher than in participants with normal LDL (OR: 1.42; 95% CI: 1.05–1.90). In total papulation the odds of Pocket in the group with high TC was 16% higher compared to those with normal TC (OR: 1.16; 95% CI: 1.01–1.34) in fully adjusted model (Table 2).

Table 3 shows the associations of dyslipidemia and diabetes with periodontal health indexes according to the number of teeth in multivariate logistic regression models. In fully adjusted model, in participants > 8 teeth, the odds of PPD increased about 31% in individuals with dyslipidemia (OR: 1.31; 95% CI: 1.03–1.66) and 28% in individuals with high TC 1.28 (OR: 1.28; 95% CI: 1.04–1.58).

Table 3 Association of dyslipidemia and diabetes with BOP, PPD > 3 mm and CAL ≥ 1 mm and periodontitis based on the number of teeth (n = 6751).

Discussion

The present study is a population-based study aimed to evaluate the prevalence of periodontal health indexes in relation to diabetes and dyslipidemia in the participants of Oral Health Branch of Rafsanjan Cohort Study (OHBRCS). The number of study patients involved in the present study (n = 8682) represents the largest population in an oral health cohort study in Iran. Of the 6751 study participants, 73.32%, 13.75%, 59.67% and 11.76% were diagnosed as presenting with BOP, PPD > 3 mm, CAL ≥ 1 mm and periodontitis respectively. Among this population, the prevalence of high TC, high LDL, low HDL and high TG was 52.07%, 31.15%, 11.54% and 47.42% respectively. Additionally, 19.84% and 72.22% of the study patients diagnosed having diabetes and dyslipidemia respectively. One of the main findings of this study was that there was a direct association between having high TC and increased odds of PPD > 3 mm even after adjusting for potential confounding variables such as those related to demographic, lifestyle, history of CVD, history of hypertension and brushing frequency. Also, the odds of CAL ≥ 1 mm increased in subjects with high LDL cholesterol, diabetes and subjects with both dyslipidemia and diabetes showing that high TC, high LDL, diabetes and having both dyslipidemia and diabetes may be associated with periodontal disease.

Although there are some studies regarding the association between periodontal disease and dyslipidemia, the results are inconsistent. Some studies reported an association between periodontitis with total cholesterol [30, 31] or TG [32] or LDL [31] while other studies reported an association between periodontal disease with both total cholesterol and TG [33,34,35]. Another study reported that TG and LDL levels were higher and HDL level was lower in the group with periodontitis [36, 37]. On the other hand some studies with relatively small sample sizes of 52 to 261 participants did not find any association [11, 17]. This discrepancy may be due to differences in study design, sample size, characteristics of the participants, methodology, variety in diagnostic criteria for periodontal parameters and various definitions of lipid disorders.

In the present study, we observed a positive relation between high TC and increased odds of Pocket. In accordance with this finding, in a similar large cohort study, a significant positive association was found between periodontal Pockets with total cholesterol and also LDL levels [31]. In another study, Pocket and CAL had significant associations with serum levels of LDL, TG and TC [38].

Our study also showed that high levels of LDL increased the odds of CAL about 42% and 14% in the participants of less than 40 and over 40 years respectively. Therefore, health professionals should emphasize the management of high LDL levels even for young people like those with older ages for preventing periodontal disease. In the study of Fentoglu, TG, TC and LDL levels were significantly and positively associated with Pocket, BOP, and CAL. In that study, HDL-C was significantly, but negatively associated with CAL. After multiple regression analyses, TG level was significantly associated with Pocket and BOP [16]. The study of Fatin et al. showed higher values of BOP, Pocket and CAL in the hyperlipidemia group compared to the control group. There was a positive association between TC, LDL, and the value of CAL. Also, an association between TG and both Pocket and CAL was noticed [39]. In study of Su-Jin et al. low HDL in both age groups (under 40 years and over 40 years groups) and high LDL in the over 40 years group were related with periodontitis [28]. Consistent with our study, Machado et al. [18], Su-Jin et al. [28] and katz et al. [30], did not mention a significant association between periodontal status and TG levels.

Hyperlipidemia has a dysregulatory effect on immune system cells and on wound healing; as a result, it increases the susceptibility to periodontitis and other infections. Hyperlipidemia leads to functional abnormalities in polymorphonuclear leukocytes (PMNs), that have a protective role in the early response to periodontal infection [16]. Hyperlipidemia can increase monocyte differentiation process, which results in a change of macrophage subsets and cytokine release at the wound site, impairing the wound-healing processes [39]. It has been demonstrated that hyperlipidemia leads to hyperactivity of white blood cells (WBC) ,which it turn, leads to increased production of oxygen radicals that had been associated with progressive periodontitis in adults [16].

The relationship between diabetes and periodontal disease is applied in both directions that called bilateral relationship [40]. Previous evidence suggests that the risk of periodontitis in health people is approximately 3 to 4 times lower than in subjects with diabetes [10]. Also, Popławska showed that 83% of people with diabetes suffer from periodontitis, which shows a direct link between the two diseases [12]. According to the results of our study and in consistent with some previous studies [11, 41, 42], the odds of CAL increased in diabetes. While, some studies did not find any association between diabetes mellitus and periodontal disease [13, 43]. Differences in methodological approaches and definitions of diabetes may explain the contradictory findings. In the present study, diabetes and having both diabetes and dyslipidemia were related to CAL among the over 40 years group. Therefore, control of these systemic diseases is important for periodontal disease management particularly among people aged over 40 years.

Studies have shown that diabetes and systemic and inflammatory diseases cause periodontitis in such a way that these diseases promote formation and activation of osteoclasts [44] and poor control of blood sugar leads to increased bone loss [45]. Disruption of the homeostatic balance between the host and bacterial responses causes inflammation near the bone and periodontal ligament [45, 46]. Another postulated mechanism for diabetic effects on periodontal disease is that diabetes-enhanced inflammation and apoptosis specifically affect periodontal tissues and change expression of genes related to periodontal destruction [47]. Since the prevalence of diabetes in the Iranian population is increasing [20], it shows the importance of controlling this disease to prevent periodontal disease among other risk factors.

A large number of participants and population-based research are the major strengths of this study. Extensive data collection for potential confounders (demographic, lifestyle, medical history and etc.) is other strength of this study. However, there are some methodological limitations when interpreting our results. First, because this study had a cross-sectional design, it is difficult to make causal inferences based on its findings. Therefore, a cohort study with follow-up in the future will be helpful to determine the causal association between periodontal disease and these systemic diseases. Diagnostic criteria with FBS alone (not in combination with 2hBG and HbA1c) was another limitation of our study. Finally, the information about the severity levels of periodontal indexes (mild, moderate and severe) was not available in the present study.

Conclusion

The present study found that there was an increased odds in periodontal disease in association with high TC, high LDL, diabetes and having both dyslipidemia and diabetes. This suggests that high LDL, high TC, diabetes and having both dyslipidemia and diabetes might be potential indicators for the presence of periodontal disease.

Data Availability

The data is not available publicly. However, upon a reasonable request, the data can be obtained from the corresponding author.

References

  1. Hujoel PP, Kotsakis G, Hujoel IA. Dental Morbidities, Smoking, oral hygiene, and inflammatory bowel diseases. Clin Gastroenterol Hepatol. 2016;14(12):1840–1.

    Article  PubMed  Google Scholar 

  2. Papapanou PN, Susin C. Periodontitis epidemiology: is periodontitis under-recognized, over‐diagnosed, or both? Periodontology 2000. 2017;75(1):45–51.

  3. Eke PI, Thornton-Evans G, Dye B, Genco R. Advances in surveillance of periodontitis: the Centers for Disease Control and Prevention periodontal disease surveillance project. J Periodontol. 2012;83(11):1337–42.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Sculley DV, Langley-Evans SC. Salivary antioxidants and periodontal disease status. Proc Nutr Soc. 2002;61(1):137–43.

    Article  PubMed  Google Scholar 

  5. Nazir M, Al-Ansari A, Al-Khalifa K, Alhareky M, Gaffar B, Almas K. Global prevalence of periodontal disease and lack of its surveillance. The Scientific World Journal. 2020;2020.

  6. Socransky S, Haffajee A, Cugini M, Smith C, Kent R Jr. Microbial complexes in subgingival plaque. J Clin Periodontol. 1998;25(2):134–44.

    Article  PubMed  Google Scholar 

  7. Friedewald VE, Kornman KS, Beck JD, Genco R, Goldfine A, Libby P, et al. The American Journal of Cardiology and Journal of Periodontology editors’ consensus: periodontitis and atherosclerotic cardiovascular disease. J Periodontol. 2009;80(7):1021–32.

    Article  PubMed  Google Scholar 

  8. Wu Y-Y, Xiao E, Graves DT. Diabetes mellitus related bone metabolism and periodontal disease. Int J Oral Sci. 2015;7(2):63–72.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Bascones-Martinez A, Gonzalez-Febles J, Sanz-Esporrin J. Diabetes and periodontal disease. Review of the literature. Am J Dent. 2014;27(2):63–7.

    PubMed  Google Scholar 

  10. Mealey BL, Oates TW. Diabetes mellitus and periodontal diseases. J Periodontol. 2006;77(8):1289–303.

    Article  PubMed  Google Scholar 

  11. Almeida Abdo J, Cirano FR, Casati MZ, Ribeiro FV, Giampaoli V, Viana Casarin RC, et al. Influence of dyslipidemia and diabetes mellitus on chronic periodontal disease. J Periodontol. 2013;84(10):1401–8.

    Article  PubMed  Google Scholar 

  12. Popławska-Kita A, Siewko K, Szpak P, Król B, Telejko B, Klimiuk P et al. Relationship between type 2 diabetes and periodontal disease. Progress in Health Sciences. 2013;3(2).

  13. Ueno M, Takeuchi S, Oshiro A, Shinada K, Ohara S, Kawaguchi Y. Association between diabetes mellitus and oral health status in japanese adults. Int J Oral Sci. 2010;2(2):82–9.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Darroudi S, Saberi-Karimian M, Tayefi M, Arekhi S, Motamedzadeh Torghabeh A, Seyedzadeh Sani SMR, et al. Prevalence of combined and noncombined dyslipidemia in an iranian population. J Clin Lab Anal. 2018;32(8):e22579.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Jamali Z, Noroozi Karimabad M, Khalili P, Sadeghi T, Sayadi A, Mohammadakbari Rostamabadi F, et al. Prevalence of dyslipidemia and its association with opium consumption in the Rafsanjan cohort study. Sci Rep. 2022;12(1):11504.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Fentoğlu Ö, Öz G, Taşdelen P, Uskun E, Aykaç Y, Bozkurt FY. Periodontal status in subjects with hyperlipidemia. J Periodontol. 2009;80(2):267–73.

    Article  PubMed  Google Scholar 

  17. Banihashemrad SA, Moeintaghavi A, Rafighdoost A. Relationship between cholesterol and triglyceride blood values and periodontal parameters in patients of Mashhad health center. NY State Dent J. 2008;74(5):65.

    Google Scholar 

  18. Machado ACP, Quirino MRdS, Nascimento LFC. Relation between chronic periodontal disease and plasmatic levels of triglycerides, total cholesterol and fractions. Brazilian oral research. 2005;19:284–9.

    Article  PubMed  Google Scholar 

  19. Sadeghi M, Talaei M, Oveisgharan S, Rabiei K, Dianatkhah M, Bahonar A et al. The cumulative incidence of conventional risk factors of cardiovascular disease and their population attributable risk in an iranian population: the Isfahan Cohort Study. Adv biomedical Res. 2014;3.

  20. Khamseh ME, Sepanlou SG, Hashemi-Madani N, Joukar F, Mehrparvar AH, Faramarzi E, et al. Nationwide prevalence of diabetes and prediabetes and associated risk factors among iranian adults: analysis of data from PERSIAN cohort study. Diabetes Therapy. 2021;12(11):2921–38.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Poustchi H, Eghtesad S, Kamangar F, Etemadi A, Keshtkar AA, Hekmatdoost A, et al. Prospective Epidemiological Research Studies in Iran (the PERSIAN Cohort Study): Rationale, objectives, and design. Am J Epidemiol. 2018;187(4):647–55.

    Article  PubMed  Google Scholar 

  22. Hakimi H, Ahmadi J, Vakilian A, Jamalizadeh A, Kamyab Z, Mehran M et al. The profile of Rafsanjan Cohort Study. Eur J Epidemiol. 2020:1–10.

  23. Khalili P, Ayoobi F, Mohamadi M, Jamalizadeh A, La Vecchia C, Esmaeili-Nadimi A. Effect of opium consumption on cardiovascular diseases–a cross-sectional study based on data of Rafsanjan cohort study. BMC Cardiovasc Disord. 2021;21(1):1–11.

    Article  Google Scholar 

  24. Association AD. Standards of medical care in diabetes—2019 abridged for primary care providers. Clin diabetes: publication Am Diabetes Association. 2019;37(1):11.

    Article  Google Scholar 

  25. Kazemi M, Bazyar M, Naghizadeh MM, Dehghan A, Rahimabadi MS, Chijan MR, et al. Lipid profile dysregulation in opium users based on Fasa PERSIAN cohort study results. Sci Rep. 2021;11(1):1–9.

    Article  Google Scholar 

  26. Lang NP, Lindhe J. Clinical periodontology and implant dentistry. 2 ed. Volume Set: John Wiley & Sons; 2015.

    Google Scholar 

  27. Papapanou PN, Sanz M, Buduneli N, Dietrich T, Feres M, Fine DH, et al. Periodontitis: Consensus report of workgroup 2 of the 2017 World workshop on the classification of Periodontal and Peri-Implant Diseases and Conditions. J Periodontol. 2018;89:173–S82.

    Google Scholar 

  28. Su-Jin Han R, Yi Y-J. The association between dyslipidemia, oral health behavior, and periodontal disease: the Korea National Health and Nutrition Examination Survey. Quintessence Int. 2019;50(5):394–401.

    PubMed  Google Scholar 

  29. Schätzle M, Löe H, Bürgin W, Ånerud Ã, Boysen H, Lang NP. Clinical course of chronic periodontitis: I. Role of gingivitis. J Clin Periodontol. 2003;30(10):887–901.

    Article  PubMed  Google Scholar 

  30. Katz J, Chaushu G, Sharabi Y. On the association between hypercholesterolemia, cardiovascular disease and severe periodontal disease. J Clin Periodontol. 2001;28(9):865–8.

    Article  PubMed  Google Scholar 

  31. Katz J, Flugelman MY, Goldberg A, Heft M. Association between periodontal pockets and elevated cholesterol and low density lipoprotein cholesterol levels. J Periodontol. 2002;73(5):494–500.

    Article  PubMed  Google Scholar 

  32. Morita M, Horiuchi M, Kinoshita Y, Yamamoto T, Watanabe T. Relationship between blood triglyceride levels and periodontal status. Community Dent Health. 2004;21(1):32–6.

    PubMed  Google Scholar 

  33. Lösche W, Karapetow F, Pohl A, Pohl C, Kocher T. Plasma lipid and blood glucose levels in patients with destructive periodontal disease. J Clin Periodontol. 2000;27(8):537–41.

    Article  PubMed  Google Scholar 

  34. Hagh LG, Zakavi F, Hajizadeh F, Saleki M. The association between hyperlipidemia and periodontal infection. Iran Red Crescent Med J. 2014;16(12).

  35. Taleghani F, Shamaei M, Shamaei M. Association between chronic periodontitis and serum lipid levels. 2010.

  36. Penumarthy S, Penmetsa GS, Mannem S. Assessment of serum levels of triglycerides, total cholesterol, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol in periodontitis patients. J Indian Soc periodontology. 2013;17(1):30.

    Article  Google Scholar 

  37. Nepomuceno R, Pigossi SC, Finoti LS, Orrico SR, Cirelli JA, Barros SP, et al. Serum lipid levels in patients with periodontal disease: a meta-analysis and meta‐regression. J Clin Periodontol. 2017;44(12):1192–207.

    Article  PubMed  Google Scholar 

  38. Sayar F, Fallah S, Akhondi N, Jamshidi S. Association of serum lipid indices and statin consumption with periodontal status. Oral Dis. 2016;22(8):775–80.

    Article  PubMed  Google Scholar 

  39. Fatin Awartani B, Atassi F. Evaluation of periodontal status in subjects with hyperlipidemia. J Contemp Dent Pract. 2010;11(2).

  40. Nazir G, Amin J. Diabetes mellitus and periodontal diseases: a two way relationship. Int J Dentistry Res. 2021;6(2):43–56.

    Article  Google Scholar 

  41. Demmer RT, Holtfreter B, Desvarieux M, Jacobs DR Jr, Kerner W, Nauck M, et al. The influence of type 1 and type 2 diabetes on periodontal disease progression: prospective results from the study of Health in Pomerania (SHIP). Diabetes Care. 2012;35(10):2036–42.

    Article  PubMed  PubMed Central  Google Scholar 

  42. Botero JE, Yepes FL, Roldan N, Castrillón CA, Hincapie JP, Ochoa SP, et al. Tooth and periodontal clinical attachment loss are associated with hyperglycemia in patients with diabetes. J Periodontol. 2012;83(10):1245–50.

    Article  PubMed  Google Scholar 

  43. Ziukaite L, Slot D, Cobb C, Coucke W, Van der Weijden G. Prevalence of diabetes among patients diagnosed with periodontitis: a retrospective cross-sectional study. Int J Dental Hygiene. 2018;16(2):305–11.

    Article  Google Scholar 

  44. Suzuki K, Kurose T, Takizawa M, Maruyama M, Ushikawa K, Kikuyama M, et al. Osteoclastic function is accelerated in male patients with type 2 diabetes mellitus: the preventive role of osteoclastogenesis inhibitory factor/osteoprotegerin (OCIF/OPG) on the decrease of bone mineral density. Diabetes Res Clin Pract. 2005;68(2):117–25.

    Article  PubMed  Google Scholar 

  45. Hajishengallis G, Liang S, Payne MA, Hashim A, Jotwani R, Eskan MA, et al. Low-abundance biofilm species orchestrates inflammatory periodontal disease through the commensal microbiota and complement. Cell Host Microbe. 2011;10(5):497–506.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Graves DT, Oates T, Garlet GP. Review of osteoimmunology and the host response in endodontic and periodontal lesions. J oral Microbiol. 2011;3(1):5304.

    Article  Google Scholar 

  47. Duarte PM, Szeremeske Miranda T, Lima JA, Dias Gonçalves TE, Santos VR, Bastos MF, et al. Expression of immune-inflammatory markers in sites of chronic periodontitis in patients with type 2 diabetes. J Periodontol. 2012;83(4):426–34.

    Article  PubMed  Google Scholar 

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Acknowledgements

We thank the people who participated in the study, the study-site personnel, and members of the Rafsanjan cohort center and Rafsanjan University of Medical Sciences.

Funding

The Iranian Ministry of Health and Medical Education has contributed to the funding used in the PERSIAN Cohort through Grant No. 700/534.

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Authors and Affiliations

Authors

Contributions

Salari Sedigh S and Hakimi H contributed to the study conception and design. Khalili P performed the statistical analysis and interpretation of the data. Jamali Z and Ayoobi F contributed to the interpretation of the data, drafting the manuscript. Sharifi Z and Sardari F contributed to the collection of the data. Hakimi H contributed to critical revision of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Zahra Jamali.

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Competing interests

The authors declare no competing interests.

Ethics approval

Ethical approval for the study was obtained from the Ethical Committee of RUMS (ID: IR.RUMS.REC. 1399.197).

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Informed consent was obtained from all subjects.

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NA.

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The authors declare that there is no conflict of interests.

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Ayoobi, F., Salari Sedigh, S., Khalili, P. et al. Dyslipidemia, diabetes and periodontal disease, a cross-sectional study in Rafsanjan, a region in southeast Iran. BMC Oral Health 23, 549 (2023). https://doi.org/10.1186/s12903-023-03262-x

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  • DOI: https://doi.org/10.1186/s12903-023-03262-x

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