Association of Adiposity Trajectories With Insulin Sensitivity and Glycemic Deterioration

Author:

Liu Rong1,Brickman Wendy J.2,Christoffel Katherine K.1,Liu Xin1,Wang Guoying1,Arguelles Lester1,Zhang Shanchun3,Zimmerman Donald2,Wang Binyan1,Xu Xiping4,Li Zhiping5,Xing Houxun5,Wang Xiaobin16

Affiliation:

1. Mary Ann and J. Milburn Smith Child Health Research Program, Department of Pediatrics, Northwestern University Feinberg School of Medicine, and Children's Memorial Hospital and Children's Memorial Research Center, Chicago, Illinois

2. Division of Endocrinology, Department of Pediatrics, Northwestern University Feinberg School of Medicine, and Children's Memorial Hospital and Children's Memorial Research Center, Chicago, Illinois

3. Department of Epidemiology and Health Statistics, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China

4. Center for Population Genetics, University of Illinois at Chicago School of Public Health, Chicago, Illinois

5. Anhui Medical University Institute of Biomedicine, Hefei, China

6. Department of Population, Family and Reproductive Health, Center on the Childhood Origins of Disease, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland

Abstract

OBJECTIVE To evaluate associations between adiposity trajectories over time and insulin sensitivity and glucose deterioration in a Chinese twin cohort. RESEARCH DESIGN AND METHODS This study focused on 341 males and 292 females aged 20–50 years at baseline who had physical clinical examinations and oral glucose tolerance test at two time points with an average of 6 years apart. BMI, waist circumference, percent body fat (PBF), and percent trunk fat (PTF) trajectories were classified into five track groups based on age- and sex-specific tertiles at each visit. We calculated the odds of the insulin sensitivity index(0,120) [ISI(0,120)] or glycemic deterioration at follow-up among five defined trajectories (tertilebaseline → tertilefollow-up) using generalized estimate equation models. Additionally, we applied structural equation models to examine genetic and environmental influences on adiposity, adiposity change over time (ACO), ISI(0,120), and the interrelationships among them. RESULTS Participants with stable adiposity (BMI, waist circumference, PBF, and PTF) in the highest tertile or shifting to the highest tertile tended to have the lowest ISI(0,120) at follow-up or experience glycemic deterioration. Genetic factors exerted the major influence on adiposity, but environmental factors unique to each twin contributed more strongly to ISI and ACO. Correlations between adiposity/ACO and insulin sensitivity were mainly due to environmental influences. CONCLUSIONS When adiposity stays or becomes high, insulin sensitivity falls and risk of glycemic deterioration rises. Additionally, we found that genetic factors exerted the major influence on adiposity, while environmental factors played the principal role for ACO and insulin sensitivity.

Publisher

American Diabetes Association

Subject

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

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