Salivary Transcriptome Biomarkers for Early Diabetes Detection

Sponsor
PeriRx (Industry)
Overall Status
Unknown status
CT.gov ID
NCT02673762
Collaborator
(none)
180
1
37
4.9

Study Details

Study Description

Brief Summary

A PRoBE design study will be used to obtain saliva from patients before undergoing blood study evaluation for screening at risk patients for the presence of undiagnosed pre-diabetes of type II diabetes. Pre-specified saliva biomarkers will be evaluated along with multi-marker models for their discriminatory value for distinguishing patients with normal glucose metabolism from those with disease. Appropriate housekeeping genes will also be incorporated to allow for the measurement of relative gene expression.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Prospective-specimen-collection, retrospective-blinded-evaluation (PRoBE) methods will be employed to collect saliva and evaluate transcriptome markers for early pre-diabetes and type II diabetes identification. At risk patients will have fasting blood glucose and insulin levels measured along with hemoglobin A1c and 2 hour post-prandial glucose levels. Saliva samples will be stored and will be analyzed after pre-specifying a panel of mRNAs and a multi marker model for validation. The pre-specified mRNAs and multi-marker model will be determined after analysis of data from a currently ongoing case-control study. After analyzing the data from this prior trial a validation plan will be locked before analysis of the prospectively collected specimens. Pre-diabetes will be defined based on abnormal glucose tolerance tests. Insulin resistance will be calculated as HOMA IR. The diagnostic value of the salivary transcriptome for will be compared with that of hemoglobin A1c and fasting blood glucose for the detection of pre-diabetes, insulin resistance and type II diabetes.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    180 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    Salivary Transcriptome Biomarkers for Early Diabetes Detection
    Actual Study Start Date :
    Jan 1, 2016
    Anticipated Primary Completion Date :
    Dec 1, 2018
    Anticipated Study Completion Date :
    Feb 1, 2019

    Arms and Interventions

    Arm Intervention/Treatment
    Normal glucose metabolism

    Normal fasting blood glucose, 2 hour post prandial glucose, hemoglobin A1c and HOMA IR

    Pre-diabetes

    Abnormal glucose tolerance tests and/or insulin resistance with fating blood glucose and hemoglobin A1c below type II diabetes levels

    Type II diabetes

    Hemoglobin A1c 6.5% or greater, fasting blood glucose >125 mg/dl or 2 hour post-prandial blood glucose 200 mg/ml or greater

    Outcome Measures

    Primary Outcome Measures

    1. A multi marker test score based on a pre-specified model is measured in each patient. The test score is on a scale of 0 to 1.0 and relates to the probability of disease. [At study entry]

      The area under the ROC curve is used to determine the overall performance of the model at the completion of the study. An area over 0.7 is considered clincially significant.

    Secondary Outcome Measures

    1. Pre-specified mRNA marker Ct values from PCR analysis will be measured in individual patients [At study entry]

      The performance of each individual marker will be determined at study completion my comparing median values between groups by nonparametric analysis. A p value of less than or equal to 0.05 is considered significant.

    2. Housekeeping gene Ct values on PCR analysis will be measured in individual patients [At study entry]

      The performance of these genes will be determined based on stability within and between groups utilizing the NormFinder program. Stability values of < 0.2 will be considered significant.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Adult patients with unknown glucose metabolism status and

    • Requiring clinically driven screening for abnormal glucose metabolism and

    • Outpatient status

    Exclusion Criteria:
    • Patients on treatment for abnormal glucose metabolism including diet and drug therapy

    • Patients with a prior diagnosis of abnormal glucose metabolism

    • Patients on treatment with corticosteroids

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 San Antonio Endovascular and Heart Institute San Antonio Texas United States 78258

    Sponsors and Collaborators

    • PeriRx

    Investigators

    • Principal Investigator: Jack L Martin, MD, San Antonio Endovascular and Heart Institute

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    PeriRx
    ClinicalTrials.gov Identifier:
    NCT02673762
    Other Study ID Numbers:
    • PeriRx003
    First Posted:
    Feb 4, 2016
    Last Update Posted:
    Apr 12, 2018
    Last Verified:
    Apr 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 12, 2018