Hyperglycemia and Adverse Pregnancy Outcome Follow-up Study (HAPO FUS): Maternal Gestational Diabetes Mellitus and Childhood Glucose Metabolism

Author:

Lowe William L.1ORCID,Scholtens Denise M.1,Kuang Alan1,Linder Barbara2,Lawrence Jean M.3,Lebenthal Yael4,McCance David5ORCID,Hamilton Jill6ORCID,Nodzenski Michael1,Talbot Octavious1,Brickman Wendy J.17,Clayton Peter8,Ma Ronald C.9ORCID,Tam Wing Hung9ORCID,Dyer Alan R.1,Catalano Patrick M.10,Lowe Lynn P.1,Metzger Boyd E.1ORCID,Deerochanawong Chaicharn,Tanaphonpoonsuk Thadchanan,Chotigeat Sukeeta Binratkaew Uraiwan,Manyam Wanee,Forde Martinette,Greenidge Andre,Neblett Kathleen,Lashley Paula Michele,Walcott Desiree,Corry Katie,Francis Loraine,Irwin Jo-anne,Langan Anne,McCance David R.,Mousavi Maureen,Young Ian,Gutierrez Jennifer,Jimenez Jennifer,Lawrence Jean M.,Sacks David A.,Takhar Harpreet S.,Tanton Elizabeth,Brickman Wendy J.,Howard Jennifer,Josefson Jami L.,Miller Lauren,Bjaloncik Jacqui,Catalano Patrick M.,Davis Ajuah,Koontz Michaela,Presley Larraine,Smith Shoi,Tyhulski Amanda,Li Albert Martin,Ma Ronald C.,Ozaki Risa,Tam Wing Hung,Wong Michelle,Yuen Cindy Siu Man,Clayton Peter E.,Khan Aysha,Vyas Avni,Maresh Michael,Benzaquen Hadasse,Glickman Naama,Hamou Alona,Hermon Orna,Horesh Orit,Keren Yael,Lebenthal Yael,Shalitin Shlomit,Cordeiro Kristina,Hamilton Jill,Nguyen Hahn Y.,Steele Shawna,Chen Fei,Dyer Alan R.,Huang Wenyu,Kuang Alan,Jimenez Maria,Lowe Lynn P.,Lowe William L.,Metzger Boyd E.,Nodzenski Michael,Reisetter Anna,Scholtens Denise,Talbot Octavious,Yim Paul,Dunger David,Thomas Alicia,Horlick Mary,Linder Barbara,Unalp-Arida Aynur,Grave Gilman,

Affiliation:

1. Northwestern University Feinberg School of Medicine, Chicago, IL

2. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD

3. Kaiser Permanente Southern California, Pasadena, CA

4. Schneider Children’s Medical Center of Israel, Petah Tiqva, Israel, and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

5. Royal Victoria Hospital, Belfast, U.K.

6. The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

7. Ann and Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL

8. Royal Manchester Children’s Hospital, Manchester University Hospitals NHS Foundation Trust, Manchester Academic Healthy Sciences Centre, School of Medical Sciences, Faculty of Biology, Medicine, and Health, University of Manchester, Manchester, U.K.

9. The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China

10. MetroHealth Medical Center, Case Western Reserve University, Cleveland, OH

Abstract

OBJECTIVE Whether hyperglycemia in utero less than overt diabetes is associated with altered childhood glucose metabolism is unknown. We examined associations of gestational diabetes mellitus (GDM) not confounded by treatment with childhood glycemia in the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) cohort. RESEARCH DESIGN AND METHODS HAPO Follow-up Study (FUS) included 4,160 children ages 10–14 years who completed all or part of an oral glucose tolerance test (OGTT) and whose mothers had a 75-g OGTT at ∼28 weeks of gestation with blinded glucose values. The primary predictor was GDM by World Health Organization criteria. Child outcomes were impaired fasting glucose (IFG), impaired glucose tolerance (IGT), and type 2 diabetes. Additional measures included insulin sensitivity and secretion and oral disposition index. RESULTS For mothers with GDM, 10.6% of children had IGT compared with 5.0% of children of mothers without GDM; IFG frequencies were 9.2% and 7.4%, respectively. Type 2 diabetes cases were too few for analysis. Odds ratios (95% CI) adjusted for family history of diabetes, maternal BMI, and child BMI z score were 1.09 (0.78–1.52) for IFG and 1.96 (1.41–2.73) for IGT. GDM was positively associated with child’s 30-min, 1-h, and 2-h but not fasting glucose and inversely associated with insulin sensitivity and oral disposition index (adjusted mean difference −76.3 [95% CI −130.3 to −22.4] and −0.12 [−0.17 to −0.064]), respectively, but not insulinogenic index. CONCLUSIONS Offspring exposed to untreated GDM in utero are insulin resistant with limited β-cell compensation compared with offspring of mothers without GDM. GDM is significantly and independently associated with childhood IGT.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases and the Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

American Diabetes Association

Subject

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

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