OneinSeven Gestational Diabetes Genetic and Socioeconomic Risk Study

NCT ID: NCT04789473

Last Updated: 2021-06-30

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

UNKNOWN

Total Enrollment

10000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-06-24

Study Completion Date

2022-08-01

Brief Summary

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The objective of the Gestational Diabetes Genetic Socioeconomic Risk Study is to generate genome wide association study data (GWAS) to calculate polygenic risk scores (PRS) for the development of gestational diabetes in pregnant women. Oshun Medical's GWAS study will be conducted by collecting DNA samples alongside medical and socioeconomic data and applying data science methodology to generate a polygenic risk score algorithm for gestational diabetes. Our hypothesis is that key genetic variants linked to gestational diabetes will be identified, and sociodemographic characteristics may impact epigenetic factors which further contribute to this risk of gestational diabetes. The PRS generated through our study will be combined with an analysis of epigenetic factors to produce a new method for predicting risk of developing gestational diabetes during pregnancy.

Detailed Description

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Gestational diabetes is a condition where high blood glucose levels occur during pregnancy and the mother was not diabetic before pregnancy. Between 6-9% of pregnancies are affected by this disorder. Gestational diabetes is usually diagnosed with a glucose challenge test where a blood glucose level of 190mg/dL or above would be indicative of gestational diabetes. This test usually occurs around 24-28 weeks into pregnancy. If a patient has other risk factors such as obesity or family history of diabetes, the assessment may be performed earlier.

Gestational diabetes increases risk of complications in both the mother and the baby. For the child, it may result in excessive weight at birth, a preterm birth, hypoglycemia, Type II diabetes later in life, and potential stillbirth. For the mother, it drastically increases the risk of high blood pressure, preeclampsia, and developing diabetes later in life. Gestational diabetes can also lead to further pregnancy related complications and increased risk of maternal morbidity and mortality events.

Very few genome-wide association studies have been carried out to correlate genetic variants to gestational diabetes, and have identified a small non-exhaustive number of genes linked to the condition. The list comprises genes encoding transcription factors such as TCF7L2 and genes required for glucose processing such as GCK and GCKR. Many of these genes are also associated with the risk of Type II diabetes. A large number of GWAS have identified genes tightly associated with Type II diabetes including CDKALI 1, FOXO1, GCKR and FTO, and the risk of gestational diabetes and type II is strongly correlated. These variants, along with demonstrated non-genetic risk factors such as obesity and high blood pressure, have demonstrated a clear ability to assess risk of different types of diabetes including gestational diabetes . However, there are currently no PRS for gestational diabetes available as a market product in any country. Additionally, the studies mentioned above do not wholly combine genome data with sociodemographic and lifestyle risks. Very few large scale GWAS studies have focused solely on female participants or pregnancy related complications. Further, existing literature and publications lack diversity among female participants and often focus on specific sub-populations. Prenome intends to conduct a large-scale GWAS in conjunction with the additional socioeconomic qualifications to generate a novel PRS to assess the risk of gestational diabetes with focus on inclusion of diverse populations in our samples. With these added quantifications of qualitative data, Prenome's PRS will be more representative of a patient's personal health and risk of developing gestational diabetes.

Conditions

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Gestational Diabetes Pregnancy Complications Pregnancy Related Genetic Predisposition Risk Reduction

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Control Normal Glycemic Pregnancy

Cohort of control adults who are currently pregnant or have been pregnant within the last year, but were not diagnosed with gestational diabetes.

Polygenic Risk Score Generation

Intervention Type GENETIC

PRS will be calculated for gestational diabetes risk using both cohorts, participants wont have results returned to them during the study.

Gestational Diabetic Cohort

Cohort of adults who are currently pregnant or have been pregnant within the last year, but were diagnosed with gestational diabetes.

Polygenic Risk Score Generation

Intervention Type GENETIC

PRS will be calculated for gestational diabetes risk using both cohorts, participants wont have results returned to them during the study.

Interventions

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Polygenic Risk Score Generation

PRS will be calculated for gestational diabetes risk using both cohorts, participants wont have results returned to them during the study.

Intervention Type GENETIC

Eligibility Criteria

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Inclusion Criteria

* Adult females who are currently pregnant
* Adult females who have been pregnant within the last 12 months
* Adult female who is currently diagnosed with gestational diabetes
* Adult female who has been diagnosed with gestational diabetes within the last 12 months

Exclusion Criteria

* Males
* Minors/ Children
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Prenome

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Barbara Levy, MD

Role: PRINCIPAL_INVESTIGATOR

Prenome

Locations

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Illumina Accelerator

Foster City, California, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Sarah Brozio, PHD

Role: CONTACT

6693429253

Stevie Cline, LLM

Role: CONTACT

6148008477

Facility Contacts

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Sarah Brozio, PhD

Role: primary

669-342-9253

Stevie Cline, LLM

Role: backup

6148008477

Provided Documents

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Document Type: Study Protocol

View Document

Related Links

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Other Identifiers

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PRE001

Identifier Type: -

Identifier Source: org_study_id

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