Thyroid Disease and Chronic Periodontitis

Thyroid Insufficiency as a Modifying Factor for Chronic Periodontitis

Currently, the investigators are unaware of any previous studies that have analyzed the relationship between the prevalence of thyroid disease and chronic periodontitis among adults utilizing a retrospective, cross-sectional design. This study will review approximately 2000 patient records and compare the prevalence of thyroid disease in three groups with increasing severity of chronic periodontitis.

Study Overview

• Status: Completed
• Conditions: Thyroid Diseases; Chronic Periodontitis
• Intervention / Treatment: Other: NO intervention, patient records review only

Detailed Description

This is a retrospective, cross-sectional patient records review study. Only records with subjects that were 35 years or older and have been active patients of the School of Dental Medicine, University at Buffalo will be included. Three individual searches with three distinct patient criteria will be conducted to obtain records from subjects in three populations with different degrees of periodontal disease. All subjects that qualify the eligibility criteria will be selected. The IT Department has access to select the subjects according to the eligibility criteria without requiring access to the physical patient record. The three subject groups are:

1. Periodontally healthy patients: Patients with a D1110 or D1111 (adult prophylaxis including those with 6 or fewer teeth) treatment code, seen by a 3rd or 4th year pre-doctoral dental student. Excludes all charts that have ever had a U4990 (Perio case) treatment code. Patient is 35 years or older relative to 1/1/2016.
2. Patients with a history of advanced periodontal treatment, group 1: All patients treated in the Postgraduate Periodontics department by a periodontics resident between 1/1/2000 - 12/31/2017. Patients presenting for treatment of chronic periodontitis will be included while those patients presenting to the clinic for other reasons, such as crown lengthening procedures, will be labeled as such. All patients selected will be 35 years or older at time of initial exam.
3. Patients with history of advanced periodontal treatment, group 2: All patients ever treated in the private faculty practice of one periodontist, that were still active patients during between 1/1/16 - 12/31/16. Only those 35 years and older were included. Patients presenting for treatment of chronic periodontitis will be included while those patients presenting to the clinic for other reasons, such as crown lengthening procedures, will be labeled as such.

All duplicates within a group will be excluded (e.g. patients may have had a D1110 code more than once per year). These 3 subject search criteria should yield a sufficient number of patient records for statistical analysis.

All patient records will be reviewed and data will be collected and recorded in an electronic Microsoft Excel database file that is saved on an encrypted flash drive. The only patient identifier recorded will be the patient records number. Once data collection is complete, or at a maximum of 3 years from the start of the study, all identifying information will be deleted and only de-identified data saved on a separate electronic file will be analyzed. No code key will be required.

Data will be analyzed using ANOVA (F-test). If multiple variables are used, analysis will be by using generalized estimating equations (GEE).

• Study Type: Observational
• Enrollment (Actual): 4965

Contacts and Locations

Study Locations

• United States
  • New York
    • Buffalo, New York, United States, 14214
      • School of Dental Medicine, University at Buffalo

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 35 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes

• Sampling Method: Non-Probability Sample

Study Population

The study population is sampled from the patient records available at the School of Dental Medicine, University at Buffalo, State University of New York. The patient records reviewed will be of patients seen in the predoctoral as well as postgraduate clinics.

The third group population is sampled from the patient records available from the faculty practice of one provider located at the University of Buffalo, State University of New York

Description

Inclusion Criteria:

• Active patient of the School of Dental Medicine, University at Buffalo.

• The remaining eligibility criteria varies between the three distinct subject populations, which are noted below. All eligibility criteria is selected for by an electronic search of patient records performed by the IT Department at the School of Dental Medicine, University at Buffalo.

  1. Periodontally healthy patients:

     1. A treatment code of D1110 or D111 was processed at least once but excluding patients that were ever assigned a treatment code of U4990
     2. A 3rd or 4th year pre-doctoral dental student provider
     3. 35 years or older as of 1/1/2016
     4. Patient presented to clinic between 1/1/2016-12/31/2016

  2. Patients with history of advanced periodontal treatment, group 1:

     1. All patients presenting to the Postgraduate Periodontics Department at UB and being seen by a periodontics resident
     2. Time period between 1/1/2000-12/31/2017
     3. Patients will be 35 years or older at time of initial exam
     4. Patients presenting for reasons other than chronic periodontitis treatment (e.g. crown lengthening) will be labeled as such.

  3. Patients with history of advanced periodontal treatment, group 2:

     1. All patients treated in the faculty practice of one periodontist that remained active patients during the time period 1/1/2016-12/31-2016
     2. All patients were 35 years or older at time of initial exam

Duplicates within groups are eliminated.

Exclusion Criteria:

• inadequate data from records

Note: the majority of patient records selected by the search criteria done electronically by the IT department will be included in the study, since the search criteria very closely overlaps the overall study criteria

Study Plan

How is the study designed?

Design Details

• Observational Models: Other
• Time Perspectives: Retrospective

Number of groups / cohorts

3

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
Periodontally healthy patients; Patients that have no history of periodontal treatment and that have been scheduled for routine prophylaxis appointments in the predoctoral clinics at the School of Dental Medicine, University at Buffalo.	Other: NO intervention, patient records review only; There is no intervention - the three study groups are created by utilizing three unique sets of search criteria for the patient records review.
Periodontitis, group 1; Patients that have been referred from the pre-doctoral dental clinics to the Postgraduate Periodontics clinic for advanced periodontal disease. Clinical attachment loss, pain, mobility, bleeding, suppuration, and probing depths > 4 mm more likely to be prevalent.	Other: NO intervention, patient records review only; There is no intervention - the three study groups are created by utilizing three unique sets of search criteria for the patient records review.
Periodontitis, group 2; Patients referred to a faculty practice periodontist over the course of his clinical career due to chronic periodontitis that could not be treated by the referring general dentist. Clinical attachment loss, pain, mobility, bleeding, suppuration, and probing depths > 4 mm more likely to be prevalent.	Other: NO intervention, patient records review only; There is no intervention - the three study groups are created by utilizing three unique sets of search criteria for the patient records review.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Thyroid disease prevalence	The presence or absence of thyroid medication in the patient record will be used as a surrogate marker for thyroid disease presence or absence.	Assessed at one time point only, during patient's initial exam noted in patient records (cross-sectional study).

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
smoking history	Smoking history will be determined from the Medical Questionnaire form in the patient records.	Assessed at one time point only, during patient's initial exam noted in patient records (cross-sectional study).
diabetes disease prevalence	The Medical Questionnaire and the Medication List in the patient records will be referenced to determine the presence of diabetes.	Assessed at one time point only, during patient's initial exam noted in patient records (cross-sectional study).
Periodontal Probing Depths 5mm or greater	Number of teeth that have one or more sites that contain a 5mm or greater pocket, recorded in periodontal chart	Assessed at one time point only, during patient's initial exam noted in patient records (cross-sectional study).
Periodontal Probing Depths 6mm or greater	Number of teeth that have one or more sites that contain a 6mm or greater pocket, recorded in periodontal chart	Assessed at one time point only, during patient's initial exam noted in patient records (cross-sectional study).
Teeth	Total number of teeth, recorded in periodontal chart	Assessed at one time point only, during patient's initial exam noted in patient records (cross-sectional study).
proton pump inhibitor use	The Medication List in the patient records will be referenced to determine any history of proton pump inhibitor use.	Assessed at one time point only, during patient's initial exam noted in patient records (cross-sectional study).
Plaque Score	Percentage of tooth surfaces positive for plaque out of total tooth surfaces	Assessed at one time point only, during patient's initial exam noted in patient records (cross-sectional study).
Hormone replacement therapy	The presence or absence of hormone supplementation (birth control or hormone replacement therapy included)	Assessed at one time point only, during patient's initial exam noted in patient records (cross-sectional study).
bisphosphonate use	The Medication List in the patient records will be referenced to determine any history of bisphosphonate use.	Assessed at one time point only, during patient's initial exam noted in patient records (cross-sectional study).

Collaborators and Investigators

• Sponsor: University at Buffalo

Study record dates

Study Major Dates

• Study Start (Actual): February 2, 2018
• Primary Completion (Actual): September 1, 2023
• Study Completion (Actual): September 1, 2023

Study Registration Dates

• First Submitted: November 28, 2017
• First Submitted That Met QC Criteria: December 5, 2017
• First Posted (Actual): December 12, 2017

Study Record Updates

• Last Update Posted (Actual): October 2, 2023
• Last Update Submitted That Met QC Criteria: September 28, 2023
• Last Verified: September 1, 2023

More Information

Terms related to this study

• Keywords: periodontitis; hypothyroidism
• Additional Relevant MeSH Terms: Pathologic Processes; Endocrine System Diseases; Disease Attributes; Stomatognathic Diseases; Periodontal Diseases; Mouth Diseases; Chronic Disease; Periodontitis; Thyroid Diseases; Chronic Periodontitis
• Other Study ID Numbers: STUDY00001811

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No