Exposure to Gestational Diabetes Mellitus: Impact on the Development of Early-Onset Type 2 Diabetes in Canadian First Nations and Non–First Nations Offspring

Author:

Sellers Elizabeth A.C.12,Dean Heather J.12,Shafer Leigh Anne3,Martens Patricia J.45,Phillips-Beck Wanda67,Heaman Maureen248,Prior Heather J.45,Dart Allison B.12,McGavock Jonathan12,Morris Margaret9,Torshizi Ali A.3,Ludwig Sora3,Shen Garry X.3

Affiliation:

1. Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, Manitoba, Canada

2. Children’s Hospital Research Institute of Manitoba, Winnipeg, Manitoba, Canada

3. Department of Internal Medicine, University of Manitoba, Winnipeg, Manitoba, Canada

4. Manitoba Centre for Health Policy, University of Manitoba, Winnipeg, Manitoba, Canada

5. Department of Community Health Science, University of Manitoba, Winnipeg, Manitoba, Canada

6. University of Manitoba, Winnipeg, Manitoba, Canada

7. Assembly of Manitoba Chiefs, Winnipeg, Manitoba, Canada

8. Faculty of Nursing, University of Manitoba, Winnipeg, Manitoba, Canada

9. Department of Obstetrics and Gynecology, University of Manitoba, Winnipeg, Manitoba, Canada

Abstract

OBJECTIVE Type 2 diabetes is increasing in children worldwide, with Canadian First Nations (FN) children disproportionally affected. The prevalence of gestational diabetes mellitus (GDM) also is increasing. The objective of this study was to evaluate the impact of GDM exposure in utero and FN status on the subsequent risk of type 2 diabetes in offspring in the first 30 years of life. RESEARCH DESIGN AND METHODS In this population-based historical prospective cohort study, we used administrative databases linked to a clinical database to explore the independent association and interaction between GDM and FN status on the subsequent development of type 2 diabetes in offspring. RESULTS Among 321,008 births with a median follow-up of 15.1 years, both maternal GDM and FN status were independently associated with subsequent risk of type 2 diabetes in offspring in the first 30 years of life (hazard ratio 3.03 [95% CI 2.44–3.76; P < 0.0001] vs. 4.86 [95% CI 4.08–5.79; P < 0.0001], respectively). No interaction between GDM and FN status on type 2 diabetes risk was observed. FN status had a stronger impact on the development of type 2 diabetes in offspring than GDM. CONCLUSIONS GDM is an important modifiable risk factor for type 2 diabetes, and its prevention may reduce the prevalence of subsequent type 2 diabetes in offspring. This study adds unique and rigorous evidence to the global public health debate about the impact of GDM on the long-term health of offspring.

Funder

Canadian Institutes for Health Research

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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