Research on Potential Biomarkers of Prediabetes and Diabetes Based on MALDI-TOF MS Platform.

Sponsor
Zhujiang Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT06097065
Collaborator
(none)
2,860
1
55.4
51.6

Study Details

Study Description

Brief Summary

Through the MALDI-TOF MS platform, explore the proteomics and peptidomics differences of fasting serum/plasma and urine between non pregnant people with normal glucose tolerance test and prediabetes /diabetes patients, pregnant people with normal glucose tolerance test and pregnant diabetes patients respectively; To explore the role of its proteomics and peptidomics differences in the diagnosis of prediabetes and diabetes, and to establish a new method of differential diagnosis by using the omics data and key characteristic peaks to find potential new diagnostic markers.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Oral Glucose Tolerance Test

Detailed Description

Prediabetes is a stage of abnormal glucose metabolism between normal blood glucose level and diabetes, which is a "gray zone" between normal and abnormal, including impaired fasting glucose (IFG), impaired glucose tolerance (IGT) or both. It is a very important high-risk group of diabetes. Diabetes is a group of metabolic diseases characterized by hyperglycemia caused by a variety of causes. Gestational diabetes mellitus refers to varying degrees of abnormal glucose metabolism that occur during pregnancy. This project aims to detect differential feature peaks through MALDI-TOF MS technology between non pregnant people with normal glucose tolerance test and prediabetes/diabetes patients, pregnant people with normal glucose tolerance test and pregnant diabetes patients respectively and to establish a clinical predictive diagnostic model based on differences, and to evaluate the model.

Study Design

Study Type:
Observational
Anticipated Enrollment :
2860 participants
Observational Model:
Case-Control
Time Perspective:
Other
Official Title:
Research on Potential Biomarkers of Prediabetes and Diabetes Based on MALDI-TOF MS Platform.
Actual Study Start Date :
May 20, 2022
Anticipated Primary Completion Date :
Dec 31, 2025
Anticipated Study Completion Date :
Dec 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Non pregnant people with prediabetes or diabetes

Non pregnancy meeting the diagnosis of prediabetes or diabetes.

Diagnostic Test: Oral Glucose Tolerance Test
Grouping based on detected oral glucose tolerance test results without any other intervention.

Non pregnant people with normal glucose tolerance

Non pregnant population with normal Oral Glucose Tolerance Test results.

Diagnostic Test: Oral Glucose Tolerance Test
Grouping based on detected oral glucose tolerance test results without any other intervention.

pregnant people with gestational diabetes mellitus

Pregnant people who meet the diagnosis of gestational diabetes.

Diagnostic Test: Oral Glucose Tolerance Test
Grouping based on detected oral glucose tolerance test results without any other intervention.

pregnant people with normal glucose tolerance

Pregnant people with normal Oral Glucose Tolerance Test results.

Diagnostic Test: Oral Glucose Tolerance Test
Grouping based on detected oral glucose tolerance test results without any other intervention.

Outcome Measures

Primary Outcome Measures

  1. Number and types of proteins/peptides differential characteristic peaks [one year]

    Obtain the number and types of proteins/peptides differential characteristic peaks between the case group and the control group through data analysis.

Secondary Outcome Measures

  1. ROC curve and area under curve AUC of clinical predictive diagnostic model [one year]

    Construct a clinical predictive diagnostic model based on the obtained proteins/peptides differential feature peaks and calculate the area under the ROC curve AUC to evaluate the predictive effect of the model.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Inclusion criteria for cases:

Non pregnant people: the remaining fasting serum/plasma and urine samples of prediabetes/diabetes patients (prediabetes: IFG: FPG 6.1-6.9mmol/L, Blood glucose 2h after meal<7.8mmol/L(WHO); IGT: FPG<7.0mmol/L, Blood glucose 2h after meal 7.8-11.1mmol/L(WHO); diabetes: Typical symptoms of diabetes, FPG >= 7.0mmol/L or 75g OGTT 2h blood glucose >= 11.1mmol/L).

Pregnant people: the remaining fasting serum/plasma and urine samples of gestational diabetes patients (75g OGTT test FPG >= 5.1mmol/L or 1h blood glucose >= 10.0mmol/L or 2h blood glucose >= 8.5mmol/L(IADPSG; ADA)).

  1. Inclusion criteria of the controls were as follows:

Non pregnant people: the remaining fasting serum/plasma and urine samples of normal population for glucose tolerance test (FPG 3.9-6.1mmol/L,75g OGTT test 1h blood glucose 6.7-11.1mmol/L,75g OGTT test 2h blood glucose 3.6-7.8mmol/L).

Pregnant people: the remaining fasting serum/plasma and urine samples of people who do not meet the diagnostic criteria for gestational diabetes (3.9<=75g OGTT test FPG<5.1mmol/L,6.7 <= 1h blood glucose<10.0mmol/L,3.6<=2h blood glucose<8.5mmol/L).

-

Exclusion Criteria:

Common exclusion criteria for cases and control were as follows: The sample volume of serum/plasma/urine is less than 300ul; Improper storage of samples or repeated freezing and thawing; The serum /plasma has obvious hemolysis, lipemia or jaundice.

-

Contacts and Locations

Locations

Site City State Country Postal Code
1 Zhujiang Hospital of Southern Medical University Guangzhou Guangdong China 510000

Sponsors and Collaborators

  • Zhujiang Hospital

Investigators

  • Study Chair: Hongwei Zhou, Professor, Zhujiang Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Zhujiang Hospital
ClinicalTrials.gov Identifier:
NCT06097065
Other Study ID Numbers:
  • Zhujiangzx
First Posted:
Oct 24, 2023
Last Update Posted:
Oct 24, 2023
Last Verified:
Feb 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 24, 2023