Assessment Of The Association Of Periodontal Disease Among Diabetic And Non Diabetic Patients - A Retrospective Study
Gokul Gunasekaran1, Deepika Rajendran2*, Sri Rengalakshmi3
1 Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Chennai – 600 077, TN, India.
2 Senior Lecturer, Department of Oral Medicine and Radiology, Saveetha Dental College, Saveetha Institute of Medical and Technical Sciences, Saveetha University, 162, Poonamallee High Road, Chennai - 600077, Tamil Nadu, India.
3 Senior Lecturer, Department of Department of Orthodontics, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences (SIMATS) Saveetha University, Chennai, India.
*Corresponding Author
Deepika Rajendran,
Senior Lecturer, Department of Oral Medicine and Radiology, Saveetha Dental College, Saveetha Institute of Medical and Technical Sciences, Saveetha University, 162, Poonamallee
High Road, Chennai - 600077, Tamil Nadu, India.
Tel: +91 7397176665
E-mail: deepikar.sdc@saveetha.com
Received: May 28, 2021; Accepted: June 16, 2021; Published: July 04, 2021
Citation:Gokul Gunasekaran, Deepika Rajendran, Sri Rengalakshmi. Assessment Of The Association Of Periodontal Disease Among Diabetic And Non Diabetic Patients - A Retrospective Study. Int J Dentistry Oral Sci. 2021;8(7):3040-3044.doi: dx.doi.org/10.19070/2377-8075-21000619
Copyright: Deepika Rajendran©2021. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
Abstract
Chronic periodontitis is a common cause of poor oral health globally. Diabetes has been unequivocally confirmed as a major risk factor for periodontitis. The risk of periodontitis is increased by approximately threefold in diabetic individuals compared with non-diabetic individuals. Those at higher risk of this preventable and easily treatable condition need to be identified so that efforts can be taken to decrease disease burden and subsequent consequences. The aim of the study was to compare the prevalence of chronic periodontitis among patients with and without diabetes visiting a private dental institution. Data was collected from 86,000 patient case sheets who visited a private dental college from June 2019 to March 2020 of the patients visiting OP. The data was tabulated and the statistics were done using Chi-square test in SPSS software. Prevalence of chronic periodontitis was high among diabetic patients when compared to individuals without diabetes among the Chennai population and showed a female predilection and more occurrence in older age (36-52 years) (Chi-square test, p=0.000 <0.05). Individuals with diabetes have a higher prevalence for periodontitis especially females. As diabetes mellitus is a strong risk factor for periodontitis, there is a need for targeted education regarding dental hygiene and proper management of diabetic conditions to reduce this preventable condition.
2.Introduction
6.Conclusion
8.References
Keywords
Association; Chronic Periodontitis; Diabetes; Prevalence.
Introduction
Anatomical variations impose certain limitations to the chemicom
Diabetes mellitus is a complicated metabolic disorder characterized
by hypofunction or lack of function of the beta cells of
the islets of Langerhans in the pancreas, leading to high blood
glucose levels and excretion of sugar in the urine [1]. Diabetes is
the commonest among metabolic disorders and its incidence is on
the increase all over the world [2]. Diabetes is an important public
health problem, affecting 245 million people worldwide. Each
year, seven million individuals develop diabetes and the projection
for the year 2030 expects that 366 million people will have the
disease worldwide [3]. Periodontitis is a slowly progressing disease
but the tissue destruction that occurs is largely irreversible. In the
early stages, the condition is typically asymptomatic; it is not usually
painful, and many patients are unaware until the condition
has progressed enough to result in tooth mobility. Periodontitis
is one of the main oral health problems, which is predominantly
a Gram-negative infection resulting in severe inflammation, with
potential for vascular dissemination (via the sulcular epithelium)
of microorganisms and their products such as Lipopolysaccharides
(LPS) throughout the body [4]. Other lifestyle factors such
as obesity, physical activity and diet are also likely to affect the
risk of periodontitis. The worldwide prevalence of periodontal
disease varies from 5 to 20% of the adult population [5]. By far,
it is the most common oral infection in India, with a prevalence
rate of 66.2% among individuals of age 15 years and about 89.2%
among adults in the age group of 35-44 years [6]. The association
between diabetes and periodontal diseases has been recognised in
dental literature for many years. [7] Periodontitis is considered one of the main, oral health problems encountered in patients with diabetes.
With the increase in the incidence of diabetes worldwide,
its negative impact on oral health should be considered. Scientific
evidence has shown for some time that diabetes is a risk factor for
the development of periodontitis. Recent revisions confirm that
type 2 diabetes can be considered a risk factor for periodontitis
[8]. Moreover, the increased severity of periodontal disease in diabetes
mellitus may reflect an alteration in the pathogenic potential
of bacteria, enhancing the breakdown of periodontal tissues, resulting
in more frequent and severe periodontal-tissue destruction
[9]. Previously our team has a rich experience in working on various
research projects across multiple disciplines [10-24]. The link
between periodontitis and diabetes is stemmed from the increased
number of diabetic patients with other infections and conditions
but these are to be researched upon. The aim of the present study
was to investigate the association of periodontal diseases among
diabetic and non diabetic patients in the Chennai population and
evaluate the prevalence of diabetes among different age groups
and gender.
Materials And Methods
This retrospective study was conducted in the university setting .
Data chosen for evaluation were patients who reported to a private
dental college for any dental treatment. The details of the patients
were obtained from analysis of 86,000 patients from June 2019
to March 2020 from private dental records for the purpose of
preservation and efficient analysis of the patients details including
intraoral and extra oral pictures and treatments done, which
is maintained in a confidential manner. These served as records
for the retrospective study. The study was conducted after getting
ethical approval from the Institutional Ethical Committee (Ethical
approval number: SDC/SIHEC/2020/DIASDATA/0619-0320).
Cross verification was done with the help of dental records data.
To minimise sampling bias all data were included. Inclusion criteria:
Individuals with diabetes Both Type 1 and 2, on medication/
diagnosed with medical history), aged between 18–82 years were
included in the study. Control group for comparison included individuals
without diabetes or any other systemic diseases with the
same age group. Exclusion criteria: Participants who had less than
10 teeth currently, or those who had undergone any periodontal
treatment within the past 1 year, or patients with any other
systemic condition apart from diabetes were excluded from the
study. A total number of 1090 patients were randomly selected
with 545 diabetic patients and 545 non diabetic patients. The data
was tabulated in MS-Excel and descriptive statistics analysis was
performed on the data and the results were obtained.
Results And Discussion
The study on the association of diabetes mellitus with periodontitis
on 1090 patients, with 545 patients who were diabetic and
545 were non diabetic. Among the non diabetic patients (Figure
1), 60.73% of non diabetic patients were affected with gingivitis
while 21.83% were affected with periodontitis and 17.83%
were having healthy gingiva. Among the diabetic patients (Figure
2), 61.36 % of diabetic patients were affected with periodontitis
while 25.27% were affected with gingivitis and 13.37% were
having healthy gingiva. This reveals an association between diabetes
and chronic periodontitis among the population of Chennai.
In (Figure 3), the percentage of diabetic patients were found
to be higher in the age group of 36-53 years (23.6%), followed
by 54-71 years (20.29%), 71-89 years (4.41%) and lower in 18-35
years (5.79%). The Chi-square test showed p value: 0.000(<0.05).
Hence statistically significant, which on interpretation reveals
that older age influences the presence of diabetes among patients.
From Figure 4, diabetes was found to be more prevalent
in females (20.55%) when compared males (29.54%). Chi-square
value: p value: 0.007(<0.05). Hence statistically significant , proving
gender influences the presence of diabetes among patients
and is found to be prevalent among females rather than males. In
Figure 5, the percentage of diabetic patients who were found to
be affected with periodontitis was (30.73%), gingivitis (12.66%)
and patients who had healthy gingiva (6.70%). The Chi-square
test showed p value: 0.000(<0.05). Hence, statistically significant,
which on interpretation reveals that the presence of diabetes influences
the occurrence of periodontitis among patients which is
similar to other studies [25].
The number of older patients affected were much higher than the
younger groups which is similar to other studies which reveals a
higher incidence among the older age group [26], another study
had clinical attachment loss significantly higher among individuals
aged 60-69 years compared with groups of adults 40-50 years
[27]. In another study , males were found to be more prone to
diabetes and chronic periodontitis when compared to females
[28] but our study showed a predominance among females.This
maybe due to hormonal changes in women increase the likelihood
of periodontal disease [29]. Females may experience gingival inflammation
before menstruation and during ovulation due to a high level of progesterone which blocks the repair of collagen
fibers and causes the dilation of blood vessels [30]. Saito et al. [31]
conducted a retrospective cohort study identifying the increased
likelihood of periodontal pocket development in patients with
impaired glucose tolerance which is a hallmark of type 2 diabetes
mellitus. An increase in pocket formation perpetuates the progression
of periodontitis by providing greater surface area for the
proliferation of the bacterial biofilm responsible for clinical attachment
and bone loss. It also increases periodontal inflamed
surface area (PISA), which in turn can provide systemic access to
microorganisms and their products [32]. Periodontitis or pyorrhea
is a Gram-negative infection which may lead to severe inflammation
with potential intravascular dissemination of micro-organisms
and their products throughout the body. However, periodontitis
tends to be an inconspicuous disease until destruction
results in acute symptoms. Most patients, as well as many medical
professionals do not recognize this potential source of infection
that may exist within the oral cavity [33]. There is a worldwide
increase in incidence and prevalence of diabetes mellitus, which
is prevalent. This has been attributed to westernization, urbanization,
and mechanization with a risk resulting from lifestyle change.
[34] Among 1090 patients ,545 were diabetic and 545 were non
diabetic. A significant number of diabetic patients were found in
the age group 36-53 years and the number of patients affected by periodontitis in diabetic patients were higher than non diabetic
patients. Although many studies support the prevalence of periodontitis
among diabetic patients [6, 35, 36] many studies have
also shown to have had the opposite results [37-39]. According to
them the cause of periodontitis is due to accumulation of local
irritants in the oral cavity such a smoking, poor oral hygiene etc
which increases the risk of periodontitis. All levels of treatment
needs were found to be lower in diabetics than in non-diabetics in
another study, which shows less correlation between periodontitis
and diabetes which may be due to other factors such as genetics
in the study population and lifestyle changes [40]. In another few
study ,there were no significant differences between the whole
diabetic group and the control group as regards the frequency of
pockets and alveolar bone level. A comparison between the controls
and the diabetic subgroups revealed that the well-controlled
diabetic patients had better periodontal health than the controls.
[41]When the diabetic patient suffered periodontitis it was due
to factors (such as genetic predisposition) other than impaired
glucose metabolism [39]. The socioeconomic status of patients
may also play an important role in oral hygiene, a relatively low socioeconomic
status may be a factor for chronic periodontitis [42].
This may be related to poor oral hygiene as well as poor access to
dental care. Smoking was also found to be associated with chronic
periodontitis in this study, similar to the results from previous
studies, indicating the need to target this modifiable risk factor for
promoting oral health [43, 44]. A review article, examining the relationship
between diabetes and chronic periodontitis, concluded
that the relationship is bidirectional, and more understanding is
required regarding the impact of periodontal diseases on diabetes.
[45] This study shows the prevalence of periodontitis among the
population of Chennai with diabetes which doesn’t mean there
isn’t a correlation between diabetes and periodontitis but maybe
said to be a lower incidence of such manifestations. It must be
clearly stated that the variations among the different studies on
diabetes and periodontitis may be attributed to different study
population around the world. These differences may be linked to
genetic background, dietary consistency, diverse criteria and subjective
interexaminer disparity. There is an absolute necessity for
adopting preventive dental health care. Our institution is passionate
about high quality evidence based research and has excelled in
various fields [46-56].
Figure 1. This bar graph represents the association between the periodontal status and non diabetic patients. X-axis represents the periodontal status and Y-axis represents the number of non diabetic patients.The percentage of patients with gingivitis(60.73%) (pink) was found to be more than the patients with healthy gingiva(17.83%) (orange) or with periodontitis( 21.83%) (yellow).
Figure 2. This bar graph represents the association between the periodontal status and diabetic patients. X-axis represents the periodontal status and Y-axis represents the number of diabetic patients.The percentage of patients with periodontitis( 61.36%) (yellow) was found to be more than the patients with gingivitis(25.27) (pink) or healthy gingiva (13.37%)(orange).
Figure 3. This bar graph represents the association between age groups and the number of patients. X-axis represents the age distribution and Y-axis represents the total number of patients (Presences of diabetes-YES-Green, NO-Blue). From the graph, diabetics were found to be higher among the older age groups when compared to the younger age group. Chi-square test was done and association was found to be statistically significant. Pearson’s Chi square value: p value: 0.000(<0.05) Hence it was found to be statistically significant.
Figure 4. This bar graph represents the association between gender and diabetic patients. X-axis represents the gender distribution and Y-axis represents the total number of patients(Presences of diabetes-YES-Green,NO-Blue). From the graph, the presence of diabetes was found to be prevalent among females rather than males. Chi-square test was done and association was found to be statistically significant. Pearson’s Chi square value: p value: 0.007(<0.05). Hence statistically significant.
Figure 5. This bar graph represents the association between periodontal status and the number of patients. X-axis represents the periodontal status and Y-axis represents the total number of patients (Presences of diabetes-YES-Green,NOBlue). From the graph, the presence of periodontitis was found to be prevalent among diabetic patients rather than non daibetic patients.Chi-square test was done and association was found to be statistically significant . Pearson’s Chi square value: p value: 0.000(<0.05). Hence, it is statistically significant.
Conclusion
Within the limits of the study,we can conclude that diabetes is
more favorable to occur in the older age group most commonly
in the age range of (36-52 years) and females were found to be
predominantly affected by diabetes and were found to have a
higher association with periodontitis compared to males. In future
studies, larger sample size with multicentered and multiple ethnic
groups should be involved to get reasonable and relevant results.
Acknowledgement
The authors thank Saveetha Dental College for constant support
in providing the data for analysis.
References
- Wild S, Roglic G, Green A, Sicree R, King H. Global prevalence of diabetes: estimates for the year 2000 and projections for 2030. Diabetes care. 2004 May 1;27(5):1047-53.
- Mealy BL, Klokkevold Perry R. Periodontal Medicine: Carranza's Clinical Periodontology. New Delhi: Elsevier; 2004.
- WHO. Basic methods for assessment of renal fluoride excretion in community prevention programmes for oral health.WHO. 2014:83.
- Kharbanda OP, Wadhawan N, Dhingra K, Tewari N, Grover A. Oral health in India: Researchers’ Perspective Part 2-Periodontal Diseases, Geriatric Dentistry and Special Health Care Needs. J Pierre Fauchard Acad (India Section). 2018 Dec 14;32(3-4):48-56.
- Taylor GW. Bidirectional interrelationships between diabetes and periodontal diseases: an epidemiologic perspective. Ann Periodontol. 2001 Dec;6(1):99-112.Pubmed PMID: 11887478.
- Chávarry NG, Vettore MV, Sansone C, Sheiham A. The relationship between diabetes mellitus and destructive periodontal disease: a meta-analysis. Oral Health Prev Dent. 2009 Jun 1;7(2):107–27.
- Nishimura F, Iwamoto Y, Soga Y. The periodontal host response with diabetes. Periodontol. 2000. 2007 Feb;43(1):245-53.
- Cockram CS. The epidemiology of diabetes mellitus in the Asia-Pacific region. Hong Kong Med J. 2000 Mar 1;6(1):43-52.
- Nand KY, Oommen AM, Chacko RK, Abraham VJ. Chronic periodontitis among diabetics and nondiabetics aged 35-65 years, in a rural block in Vellore, Tamil Nadu: A cross-sectional study. J Indian Soc Periodontol. 2017 Jul-Aug;21(4):309-314.Pubmed PMID: 29456306.
- Hafeez N. Accessory foramen in the middle cranial fossa. Res J Pharm Technol. 2016;9(11):1880-2.
- Krishnan RP, Ramani P, Sherlin HJ, Sukumaran G, Ramasubramanian A, Jayaraj G, et al. Surgical Specimen Handover from Operation Theater to Laboratory: A Survey. Ann Maxillofac Surg. 2018 Jul-Dec;8(2):234-238. Pubmed PMID: 30693238.
- Somasundaram S, Ravi K, Rajapandian K, Gurunathan D. Fluoride Content of Bottled Drinking Water in Chennai, Tamilnadu. J Clin Diagn Res. 2015 Oct;9(10):ZC32-4.Pubmed PMID: 26557612.
- Felicita AS. Orthodontic extrusion of Ellis Class VIII fracture of maxillary lateral incisor - The sling shot method. Saudi Dent J. 2018 Jul;30(3):265- 269.Pubmed PMID: 29942113.
- . Kumar S, Rahman R. Knowledge, awareness, and practices regarding bio-medical waste management among undergraduate dental students. Asian J Pharm Clin Res. 2017;10(8):341.
- Gurunathan D, Shanmugaavel AK. Dental neglect among children in Chennai. J Indian Soc Pedod Prev Dent. 2016 Oct 1;34(4):364.
- Sneha S. Knowledge and awareness regarding antibiotic prophylaxis for infective endocarditis among undergraduate dental students. Asian J Pharm Clin Res. 2016 Oct 1:154-9.
- Dhinesh B, Lalvani JI, Parthasarathy M, Annamalai K. An assessment on performance, emission and combustion characteristics of single cylinder diesel engine powered by Cymbopogon flexuosus biofuel. Energy Convers Manage. 2016 Jun 1;117:466-74.
- . Choudhari S, Thenmozhi MS. Occurrence and Importance of Posterior Condylar Foramen. Res J Pharm Technol. 2016;9(8):11-43.
- Paramasivam A, Vijayashree Priyadharsini J, Raghunandhakumar S. N6- adenosine methylation (m6A): a promising new molecular target in hypertension and cardiovascular diseases. Hypertens Res. 2020 Feb;43(2):153- 154.Pubmed PMID: 31578458.
- Wu F, Zhu J, Li G, Wang J, Veeraraghavan VP, Krishna Mohan S, et al. Biologically synthesized green gold nanoparticles from Siberian ginseng induce growth-inhibitory effect on melanoma cells (B16). Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):3297-3305.Pubmed PMID: 31379212.
- Palati S, Ramani P, Shrelin HJ, Sukumaran G, Ramasubramanian A, Don KR, et al. Knowledge, Attitude and practice survey on the perspective of oral lesions and dental health in geriatric patients residing in old age homes. Indian J Dent Res. 2020 Jan-Feb;31(1):22-25.Pubmed PMID: 32246676.
- Saravanan M, Arokiyaraj S, Lakshmi T, Pugazhendhi A. Synthesis of silver nanoparticles from Phenerochaete chrysosporium (MTCC-787) and their antibacterial activity against human pathogenic bacteria. Microb Pathog. 2018 Apr;117:68-72.Pubmed PMID: 29427709.
- Govindaraju L, Gurunathan D. Effectiveness of Chewable Tooth Brush in Children-A Prospective Clinical Study. J Clin Diagn Res. 2017 Mar;11(3):ZC31-ZC34.Pubmed PMID: 28511505.
- Vijayakumar Jain S, Muthusekhar MR, Baig MF, Senthilnathan P, Loganathan S, Abdul Wahab PU, et al. Evaluation of Three-Dimensional Changes in Pharyngeal Airway Following Isolated Lefort One Osteotomy for the Correction of Vertical Maxillary Excess: A Prospective Study. J Maxillofac Oral Surg. 2019 Mar;18(1):139-146.Pubmed PMID: 30728705.
- Marjanovic M, Buhlin K. Periodontal and systemic diseases among Swedish dental school patients - a retrospective register study. Oral Health Prev Dent. 2013;11(1):49-55.Pubmed PMID: 23507681.
- Grodstein F, Colditz GA, Stampfer MJ. Post-menopausal hormone use and tooth loss: a prospective study. J Am Dent Assoc. 1996 Mar;127(3):370-7, quiz 392.Pubmed PMID: 8819784.
- Rheu GB, Ji S, Ryu JJ, Lee JB, Shin C, Lee JY, et al. Risk assessment for clinical attachment loss of periodontal tissue in Korean adults. J Adv Prosthodont. 2011 Mar;3(1):25-32.Pubmed PMID: 21503190.
- Liu Y, Yu Y, Nickel JC, Iwasaki LR, Duan P, Simmer-Beck M, et al. Gender differences in the association of periodontitis and type 2 diabetes. Int Dent J. 2018 Dec 1;68(6):433-40.
- Güncü GN, Tözüm TF, Caglayan F. Effects of endogenous sex hormones on the periodontium--review of literature. Aust Dent J. 2005 Sep;50(3):138- 45.Pubmed PMID: 16238210.
- Markou E, Boura E, Tsalikis L, Deligianidis A, Konstantinidis A. The influence of sex hormones on proinflammatory cytokines in gingiva of periodontally healthy premenopausal women. J Periodontal Res. 2011 Oct;46(5):528- 32.Pubmed PMID: 21501171.
- Saito T, Shimazaki Y, Kiyohara Y, Kato I, Kubo M, Iida M, et al. The severity of periodontal disease is associated with the development of glucose intolerance in non-diabetics: the Hisayama study. J Dent Res. 2004 Jun;83(6):485- 90.Pubmed PMID: 15153457.
- Nesse W, Linde A, Abbas F, Spijkervet FK, Dijkstra PU, de Brabander EC, et al. Dose-response relationship between periodontal inflamed surface area and HbA1c in type 2 diabetics. J Clin Periodontol. 2009 Apr;36(4):295- 300.Pubmed PMID: 19426175.
- Newman MG, Takei H, Klokkevold PR, Carranza FA. Newman and Carranza's Clinical periodontology E-book. Elsevier Health Sciences; 2018 May 29:944.
- Pathak AK, Shakya VK, Chandra A, Goel K. Association between diabetes mellitus and periodontal status in north Indian adults. Eur. J. Gen. Dent. 2013 Jan 1;2(1):58.
- Ogunbodede EO, Fatusi OA, Akintomide A, Kolawole K, Ajayi A. Oral health status in a population of Nigerian diabetics. J Contemp Dent Pract. 2005 Nov 15;6(4):75-84.Pubmed PMID: 16299609.
- Pinducciu G, Micheletti L, Piras V, Songini C, Serra C, Pompei R, et al. Periodontal disease, oral microbial flora and salivary antibacterial factors in diabetes mellitus type 1 patients. Eur J Epidemiol. 1996 Dec;12(6):631-6. Pubmed PMID: 8982624.
- Barnett ML, Baker RL, Yancey JM, MacMillan DR, Kotoyan M. Absence of periodontitis in a population of insulin-dependent diabetes mellitus (IDDM) patients. J Periodontol. 1984 Jul;55(7):402-5.Pubmed PMID: 6589390.
- Ervasti T, Knuuttila M, Pohjamo L, Haukipuro K. Relation between control of diabetes and gingival bleeding. J Periodontol. 1985 Mar;56(3):154-7.
- Hayden P, Buckley LA. Diabetes mellitus and periodontal disease in an Irish population. J Periodontal Res. 1989 Sep;24(5):298-302.Pubmed PMID: 2533253.
- . Bacic M, Plancak D, Granic M. CPITN assessment of periodontal disease in diabetic patients. J Periodontol. 1988 Dec;59(12):816-22.
- Tervonen T, Knuuttila M. Relation of diabetes control to periodontal pocketing and alveolar bone level. Oral Surg Oral Med Oral Pathol. 1986 Apr 1;61(4):346-9.
- Gundala R, Chava VK. Effect of lifestyle, education and socioeconomic status on periodontal health. Contemp Clin Dent. 2010 Jan;1(1):23-6.
- Bokhari SA, Suhail AM, Malik AR, Imran MF. Periodontal disease status and associated risk factors in patients attending a Dental Teaching Hospital in Rawalpindi, Pakistan. J Indian Soc Periodontol. 2015 Nov- Dec;19(6):678-82.Pubmed PMID: 26941520.
- Sbaraglia M, Turnbull RS, Locker D. Risk indicators for periodontal disease in a remote Canadian community--a dental practice-based study. J Public Health Dent. 2002 Winter;62(1):51-6.Pubmed PMID: 14700090.
- Chandra A, Yadav OP, Narula S, Dutta A. Epidemiology of periodontal diseases in Indian population since last decade. J Int Soc Prev Community Dent. 2016 Mar-Apr;6(2):91-6.Pubmed PMID: 27114945.
- Vijayashree Priyadharsini J. In silico validation of the non-antibiotic drugs acetaminophen and ibuprofen as antibacterial agents against red complex pathogens. J Periodontol. 2019 Dec;90(12):1441-1448.Pubmed PMID: 31257588.
- Pc J, Marimuthu T, Devadoss P, Kumar SM. Prevalence and measurement of anterior loop of the mandibular canal using CBCT: A cross sectional study. Clin Implant Dent Relat Res. 2018 Apr 6;20(4):531-4.
- Ramesh A, Varghese S, Jayakumar ND, Malaiappan S. Comparative estimation of sulfiredoxin levels between chronic periodontitis and healthy patients - A case-control study. J Periodontol. 2018 Oct;89(10):1241-1248.Pubmed PMID: 30044495.
- Ramadurai N, Gurunathan D, Samuel AV, Subramanian E, Rodrigues SJ. Effectiveness of 2% Articaine as an anesthetic agent in children: randomized controlled trial. Clin Oral Investig. 2019 Sep;23(9):3543-50.
- Sridharan G, Ramani P, Patankar S, Vijayaraghavan R. Evaluation of salivary metabolomics in oral leukoplakia and oral squamous cell carcinoma. J Oral Pathol Med. 2019 Apr;48(4):299-306.
- Ezhilarasan D, Apoorva VS, Ashok Vardhan N. Syzygium cumini extract induced reactive oxygen species-mediated apoptosis in human oral squamous carcinoma cells. J Oral Pathol Med. 2019 Feb;48(2):115-121.Pubmed PMID: 30451321.
- Mathew MG, Samuel SR, Soni AJ, Roopa KB. Evaluation of adhesion of Streptococcus mutans, plaque accumulation on zirconia and stainless steel crowns, and surrounding gingival inflammation in primary molars: randomized controlled trial. Clin Oral Investig. 2020 Sep;24(9):1-6.Pubmed PMID: 31955271.
- Samuel SR. Can 5-year-olds sensibly self-report the impact of developmental enamel defects on their quality of life? Int J Paediatr Dent. 2021 Mar;31(2):285-286.Pubmed PMID: 32416620.
- R H, Ramani P, Ramanathan A, R JM, S G, Ramasubramanian A, et al. CYP2 C9 polymorphism among patients with oral squamous cell carcinoma and its role in altering the metabolism of benzo[a]pyrene. Oral Surg Oral Med Oral Pathol Oral Radiol. 2020 Sep;130(3):306-312.Pubmed PMID: 32773350.
- Chandrasekar R, Chandrasekhar S, Sundari KKS, Ravi P. Development and validation of a formula for objective assessment of cervical vertebral bone age. Prog Orthod. 2020 Oct 12;21(1):38.Pubmed PMID: 33043408.
- Vijayashree Priyadharsini J, Smiline Girija AS, Paramasivam A. In silico analysis of virulence genes in an emerging dental pathogen A. baumannii and related species. Arch Oral Biol. 2018 Oct;94:93-98.Pubmed PMID: 30015217.