Conventional and Metabolomic Predictors of Prediabetes & Insulin Resistance

NCT ID: NCT05055219

Last Updated: 2021-09-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

772 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-06-30

Study Completion Date

2020-02-19

Brief Summary

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The purpose of this study is to evaluate the longitudinal test performance of an array of conventional biomarkers of glycemia, including Hemoglobin A1c (HbA1c), and novel metabolomic biomarkers for identifying progression of glucose tolerance (normal to prediabetes or prediabetes to diabetes) in an overweight and obese pediatric cohort.

Detailed Description

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Conditions

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PreDiabetes Obesity, Childhood

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Group 1: Overweight or Obese Group (visits #1-4)

Children and young adults who are 8 to 22 years of age, who have risk factors for diabetes such as being overweight. Overweight or obese, as defined by a BMI ≥ 85th percentile \& \<95th percentile or BMI ≥ 95th percentile, respectively. Study participants cannot be pregnant or currently take medications known to affect glucose metabolism including, metformin, oral steroids, sulfonylureas, and insulin.

No interventions assigned to this group

Group 2: Overweight or Obese Group (visits #3-4)

Children and young adults who are 8 to 22 years of age, who have risk factors for diabetes such as being overweight, or children and young adults who previously participated in the study (completed visits #1-2 in previous study phase). Overweight or obese, as defined by a BMI ≥ 85th percentile \& \<95th percentile or BMI ≥ 95th percentile, respectively. Study participants cannot be pregnant or currently take medications known to affect glucose metabolism including, metformin, oral steroids, sulfonylureas, and insulin.

No interventions assigned to this group

Group 3: Normal Weight Control Group

Children and adolescents who are 8 to 17 years of age, who have do not have risk factors for diabetes such as being overweight or a history of type 2 diabetes in the family. Healthy weight, as defined by a BMI ≥ 5th percentile \& \< 85th percentile. Study participants cannot be pregnant or currently take medications known to affect glucose metabolism including, metformin, oral steroids, sulfonylureas, and insulin.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Groups 1 and 2 (overweight and obese groups):
* Age 8-17 years for the visits #1 and #2, individuals can be as old as 22 years for follow-up visits #3 and 4
* Overweight or obese, as defined by a BMI ≥ 85th% \& \<95th% or BMI ≥ 95th%, respectively by age and sex, and for those 16 years and older, BMI ≥25 and \<30 and BMI ≥30
* For Group 2 only: previously completed visits 1-2 in 2007-2013 and formally agreed to be re-contacted for study purposes
* Group 3 (Normal weight controls):
* Age 8-17 years
* Healthy weight, as defined by a BMI ≥ 5th percentile \& \< 85th percentile, respectively by age and sex

Exclusion Criteria

* Previous diagnosis of type 1 diabetes
* Use of concurrent medications known to affect glucose metabolism (metformin, oral steroids, sulfonylureas, insulin)
* Verbal report of Pregnancy
Minimum Eligible Age

8 Years

Maximum Eligible Age

22 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

NIH

Sponsor Role collaborator

University of Michigan

OTHER

Sponsor Role lead

Responsible Party

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Joyce Lee

MD, MPH

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Joyce Lee, MD, MPH

Role: PRINCIPAL_INVESTIGATOR

University of Michigan

Locations

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University of Michigan

Ann Arbor, Michigan, United States

Site Status

Countries

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United States

Other Identifiers

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5R01HD074559-05

Identifier Type: NIH

Identifier Source: secondary_id

View Link

HUM00006955

Identifier Type: -

Identifier Source: org_study_id

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