ClinicalTrials.Veeva

Menu

Investigation of the Relationship Between Periodontitis and Alzheimer's Disease in Terms of Blood Parameters

U

Uskudar University

Status

Completed

Conditions

Periodontitis
Alzheimer Disease
Blood Cell Count
Biomarkers / Blood
Periodontal Disease
Periodontal Inflammation

Treatments

Diagnostic Test: Standardized Mini-Mental Test
Diagnostic Test: Clinical Dementia Rating scale
Diagnostic Test: Complete Blood Count Test
Diagnostic Test: Periodontal examinations

Study type

Observational

Funder types

Other

Identifiers

NCT07069244
KKARADURAN

Details and patient eligibility

About

The aim of this study was to analyse the possible relationship between periodontal inflammation and Alzheimer's disease and to investigate the role of blood parameters in this relationship.

Full description

This retrospective case-control study will include individuals who were clinically and radiographically examined, diagnosed with periodontal disease, read and signed informed consent forms between March 2022 and July 2025 at the Periodontology Departments of Bezmialem Vakif University, Uskudar University and Bolu Abant Izzet Baysal University Faculty of Dentistry.

In this study, two groups will be formed as a case group consisting of individuals with periodontitis diagnosed with probable Alzheimer's disease according to NINCDS-ADRDA and DSM-V diagnostic criteria and a control group consisting of individuals with periodontitis only.

Patients who underwent periodontal evaluations at six sites per tooth, with the following parameters recorded-plaque percentage, probing pocket depth, percentage of bleeding on probing, clinical attachment level, number of teeth, and periodontal inflamed surface area (PISA)-will be included in the study.

Compliance with the inclusion and exclusion criteria will be verified through patient files and digital records. In individuals with a probable diagnosis of Alzheimer's disease according to NINCDS-ADRDA and DSM-V diagnostic criteria, disease stage as determined by the Clinical Dementia Rating scale and Standardized Mini-Mental Test (SMMT) scores will also be recorded.

Hematological data will be obtained from patients' recorded complete blood count test results and the following parameters will be utilized:

  • White blood cell count, neutrophil, lymphocyte, monocyte, eosinophil, basophil counts and percentages, neutrophil/lymphocyte ratio (NLR), monocyte/lymphocyte ratio (MLR)
  • Platelet count, platelet/lymphocyte ratio (PLR), platelet distribution width (PDW), mean platelet volume (MPV), plateletcrit (PCT)
  • Erythrocyte count, hemoglobin (HGB), hematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH), mean corpuscular haemoglobin concentration (MCHC), red blood cell distribution width (RDW)
  • In addition, inflammation indicators such as pan-immune inflammation value (PIV), systemic immune-inflammation index (SII) and hemoglobin/erythrocyte ratio (HRR), which are formulated from the above parameters, will also be recorded.

Enrollment

100 patients

Sex

All

Ages

50 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Between March 2022 and July 2025, those who applied to the Periodontics Departments of the Dentistry Faculties of Uskudar University, Bezmialem Vakif University and Bolu Abant Izzet Baysal University,
  • Informed consent form was obtained during the examination,
  • Over 50 years of age,
  • Non-smoker and non-alcoholic,
  • No psychiatric disorders affecting cognitive status and no medication affecting cognitive status,
  • Complete blood count was performed within the 6 months prior to the date of inclusion in the study,
  • No dental treatment within the last 1 year,
  • Periodontal examination was performed by expert periodontologists who calibrated the inter- and intra-examination,
  • Individuals diagnosed with periodontitis as a result of periodontal examination and radiographic examination, and
  • For individuals diagnosed with Alzheimer's disease: Recording their stage according to the Clinical Dementia Rating (CDR) and Standardized Mini-Mental Test (SMMT) scores

Exclusion criteria

  • Individuals with fewer than 10 teeth,
  • Individuals with uncontrolled systemic disease,
  • Individuals who regularly use anti-inflammatories or corticosteroids

Trial design

100 participants in 2 patient groups

Case group
Description:
Periodontitis with Alzheimer's disease
Treatment:
Diagnostic Test: Periodontal examinations
Diagnostic Test: Complete Blood Count Test
Diagnostic Test: Clinical Dementia Rating scale
Diagnostic Test: Standardized Mini-Mental Test
Control group
Description:
Periodontitis without Alzheimer's disease
Treatment:
Diagnostic Test: Periodontal examinations
Diagnostic Test: Complete Blood Count Test

Trial contacts and locations

3

Loading...

Central trial contact

KUBRA KARADURAN

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems