Association Between Salivary Soluble RANKL, OPG Concentration and Mandibular Resorption to Clinically Predict Severe Residual Ridge Resorption Risk

January 29, 2025 updated by: Nguyen Thu Thuy

Background. Affecting all individuals, residual ridge resorption (RRR) is a prevalent, progressive condition developing post tooth loss, often remaining silent until denture instability occurs. The molecular mechanisms and predictive bone biomarkers for severe RRR in edentulous individuals are poorly understood.

Object.This study aimed to investigate:

  1. The association between salivary soluble Receptor activator of nuclear factor-κB ligand (RANKL), osteoprotegerin (OPG) concentration and the extent of mandibular resorption
  2. Propose a way to clinically predict severe RRR risk. Methods.This cross-sectional study, conducted at the Faculty of Dentistry, University of Medicine and Pharmacy at Ho Chi Minh City, Vietnam (November 2021 to April 2024), enrolled 140 systemically healthy, edentulous adults (mean age 69.2 ± 8 years). Participants were stratified into atrophic (n=70) and non-atrophic (n=70) groups based on mandibular height. Demographic data (age, sex), edentulous duration, and denture history were recorded. Unstimulated whole saliva samples (5 mL) were collected, and salivary RANKL and OPG concentrations were quantified by ELISA.

Study Overview

Status

Completed

Detailed Description

This cross-sectional study was approved by the Ethical Committee Board of the University of Medicine and Pharmacy in Ho Chi Minh City (UMP) (No.488/HĐĐĐ-ĐHYD), recruited participants between November 2021 and April 2024. All participants provided informed and written consent before clinical examinations and saliva. A convenience sampling method was employed. Of the 254 potential edentulous participants, 140 participants were included in the study.

Participant grouping: Participants underwent panoramic radiography to assess mandibular ridge height. They were classified into two groups. Atrophic groups have mandibular ridge heights less than 25 mm anteriorly and less than 16 mm posteriorly. In the non-atrophic group, mandibular ridge height is ≥ 25 mm anteriorly and ≥ 16 mm posteriorly.

Clinical factors: The participant's age, sex, duration of edentulism, and past complete denture experience were collected by the patient or patient's relative interview.

To obtain unstimulated whole saliva from each participants, approximately 5 ml was collected. Before the collection, all participants were instructed to refrain from eating and drinking for at least 30 minutes. Between 7:00 and 8:00 a.m., the collection was conducted through expectoration into sterile polypropylene tubes. Immediately after collection, the samples were placed in a cool box containing an ice pack and then hand-delivered to the Center for Molecular Biomedicine at UMP, Ho Chi Minh City, Vietnam.

RANKL and OPG salivary levels were measured using enzyme-linked immunosorbent assay Data analysis, including the relationship between RANKL, OPG and other variables, and the development of a predictive nomogram for high-risk bone resorption, was performed using R language version 3.4.0.

Study Type

Observational

Enrollment (Actual)

140

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Ho Chi Minh, Vietnam
        • Faculty of Dentistry, University of Medicine and Pharmacy Ho Chi Minh City, Viet Nam

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Edentulous participants seeking oral care and treatment at the Faculty of Dentistry Clinic of the University of Medicine and Pharmacy Ho Chi Minh City from November 2021 to April 2024.

Description

Inclusion Criteria:

  • complete edentulism for more than 3 years
  • age > 35 years old
  • no history of bone augmentation or mandibular defects

Exclusion Criteria:

  • systemic diseases known to affect bone metabolism or immune function
  • a history of malignancy
  • salivary gland disease
  • using antibiotics or immunosuppressant medications within 3 months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Atrophic mandibular ridge
Non-Atrophic mandibular ridge

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The concentration level of nuclear factor-κB ligand (RANKL)
Time Frame: within 6 months after sample collection
It is measured using enzyme-linked immunosorbent assay (ELISA) kits (CSBE05125h, Cusabio, China ) mixing with the participant saliva
within 6 months after sample collection
The concentration level of osteoprotegerin (OPG)
Time Frame: within 6 months after sample collection
It is measured using enzyme-linked immunosorbent assay (ELISA) kits (CEHTNFRSF11B, Invitrogen, Massachusetts, USA ) mixing with the participant saliva
within 6 months after sample collection

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 30, 2021

Primary Completion (Actual)

April 1, 2024

Study Completion (Actual)

April 1, 2024

Study Registration Dates

First Submitted

January 29, 2025

First Submitted That Met QC Criteria

January 29, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 29, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 488/HĐĐĐ-DHYD

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Privacy concern

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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