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

Denise Scholtens(Northwestern University), Alan Kuang(Northwestern University), Lynn P. Lowe(Northwestern University), Jill Hamilton(University of Toronto), Jean M. Lawrence(Kaiser Permanente), Yael Lebenthal(Tel Aviv University), Wendy J. Brickman(Northwestern University), Peter Clayton(Manchester Academic Health Science Centre), Ronald C.W.(Chinese University of Hong Kong), David R. McCance(University of Ulster), Wing Hung Tam(Chinese University of Hong Kong), Patrick M. Catalano(MetroHealth Medical Center), Barbara Linder(National Institutes of Health), Alan R. Dyer(Northwestern University), William L. Lowe(Northwestern University), Boyd E. Metzger(Northwestern University), Chaicharn Deerochanawong, Thadchanan Tanaphonpoonsuk, Sukeeta Binratkaew Uraiwan Chotigeat, Wanee Manyam, Martinette Forde, André Greenidge, Kathleen Neblett, Paula Michele Lashley, Desiree Walcott, Katie Corry, Loraine Francis, Jo-anne Irwin, Anne Langan, David R. McCance(University of Ulster), Maureen Mousavi, Ian Young, Jennifer Gutierrez, Jennifer Jimenez, Jean M. Lawrence(Kaiser Permanente), David A. Sacks(University of Ulster), Harpreet S. Takhar, Elizabeth Tanton, Wendy J. Brickman(Northwestern University), Jennifer Howard, Jami L. Josefson, Lauren A. Miller, Jacqui Bjaloncik, Patrick M. Catalano(MetroHealth Medical Center), Ajuah Davis, Michaela B. Koontz, Larraine Presley, Shoi Smith, Amanda Tyhulski, Albert Martin Li(National Institutes of Health), Ronald C.W.(Chinese University of Hong Kong), Risa Ozaki, Wing Hung Tam(Chinese University of Hong Kong), Michelle S. Wong, Cindy Siu Man Yuen, Peter Clayton(Manchester Academic Health Science Centre), Aysha Habib Khan, Avni Vyas, Michael Maresh(Northwestern University), Hadasse Benzaquen, Naama Glickman, Alona Hamou, Orna Hermon, Orit Horesh, Yael Keren(Tel Aviv University), Yael Lebenthal(Tel Aviv University), Shlomit Shalitin, Kristina Cordeiro, Jill Hamilton(University of Toronto), Hahn Y. Nguyen, Shawna Steele, Fei Chen, Alan R. Dyer(Northwestern University), Wenyu Huang, Alan Kuang(Northwestern University), M. Ángeles Jiménez, Lynn P. Lowe(Northwestern University), William L. Lowe(Northwestern University), Boyd E. Metzger(Northwestern University), Michael Nodzenski(Northwestern University), Anna C. Reisetter, Denise Scholtens(Northwestern University), Octavious Talbot(Northwestern University), Paul Yim, David B. Dunger(University of Ulster), Alicia Thomas, Mary Horlick, Barbara Linder(National Institutes of Health), Aynur Ünalp–Arida, Gilman D. Grave
Diabetes Care
January 7, 2019
Cited by 306Open Access
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Abstract

OBJECTIVE: This study examined associations of maternal glycemia during pregnancy with childhood glucose outcomes in the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) cohort. RESEARCH DESIGN AND METHODS: HAPO was an observational international investigation that established associations of maternal glucose with adverse perinatal outcomes. The HAPO Follow-up Study included 4,832 children ages 10-14 years whose mothers had a 75-g oral glucose tolerance test (OGTT) at ∼28 weeks of gestation. Of these, 4,160 children were evaluated for glucose outcomes. Primary outcomes were child impaired glucose tolerance (IGT) and impaired fasting glucose (IFG). Additional outcomes were glucose-related measures using plasma glucose (PG), A1C, and C-peptide from the child OGTT. RESULTS: Maternal fasting plasma glucose (FPG) was positively associated with child FPG and A1C; maternal 1-h and 2-h PG were positively associated with child fasting, 30 min, 1-h, and 2-h PG, and A1C. Maternal FPG, 1-h, and 2-h PG were inversely associated with insulin sensitivity, whereas 1-h and 2-h PG were inversely associated with disposition index. Maternal FPG, but not 1-h or 2-h PG, was associated with child IFG, and maternal 1-h and 2-h PG, but not FPG, were associated with child IGT. All associations were independent of maternal and child BMI. Across increasing categories of maternal glucose, frequencies of child IFG and IGT, and timed PG measures and A1C were higher, whereas insulin sensitivity and disposition index decreased. CONCLUSIONS: Across the maternal glucose spectrum, exposure to higher levels in utero is significantly associated with childhood glucose and insulin resistance independent of maternal and childhood BMI and family history of diabetes.


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