Variation in extracellular matrix genes is associated with weight regain after weight loss in a sex-specific manner

被引:0
作者
Nadia J. T. Roumans
Roel G. Vink
Marij Gielen
Maurice P. Zeegers
Claus Holst
Ping Wang
Arne Astrup
Wim H. Saris
Armand Valsesia
Jörg Hager
Marleen A. van Baak
Edwin C. M. Mariman
机构
[1] Maastricht University,Department of Human Biology, NUTRIM School of Nutrition and Translational Research in Metabolism
[2] Maastricht University,Department of Complex Genetics, NUTRIM School of Nutrition and Translational Research in Metabolism
[3] Copenhagen University Hospital,Centre for Health and Society, Institute of Preventive Medicine
[4] University Hospital Maastricht,Laboratory of Biochemical Genetics, Department of Clinical Genetics, Maastricht University Medical Centre
[5] University of Copenhagen,Department of Nutrition, Exercise and Sports, Faculty of Science
[6] Nestlé Institute of Health Sciences,undefined
来源
Genes & Nutrition | 2015年 / 10卷
关键词
Weight regain; Extracellular matrix; SNPs; Adipocytes;
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摘要
The extracellular matrix (ECM) of adipocytes is important for body weight regulation. Here, we investigated whether genetic variation in ECM-related genes is associated with weight regain among participants of the European DiOGenes study. Overweight and obese subjects (n = 469, 310 females, 159 males) were on an 8-week low-calorie diet with a 6-month follow-up. Body weight was measured before and after the diet, and after follow-up. Weight maintenance scores (WMS, regained weight as percentage of lost weight) were calculated based on the weight data. Genotype data were retrieved for 2903 SNPs corresponding to 124 ECM-related genes. Regression analyses provided us with six significant SNPs associated with the WMS in males: 3 SNPs in the POSTN gene and a SNP in the LAMB1, COL23A1, and FBLN5 genes. For females, 1 SNP was found in the FN1 gene. The risk of weight regain was increased by: the C/C genotype for POSTN in a co-dominant model (OR 8.25, 95 % CI 2.85–23.88) and the T/C–C/C genotype in a dominant model (OR 4.88, 95 % CI 2.35–10.16); the A/A genotype for LAMB1 both in a co-dominant model (OR 18.43, 95 % CI 2.35–144.63) and in a recessive model (OR 16.36, 95 % CI 2.14–124.9); the G/A genotype for COL23A1 in a co-dominant model (OR 3.94, 95 % CI 1.28–12.10), or the A-allele in a dominant model (OR 2.86, 95 % CI 1.10–7.49); the A/A genotype for FBLN5 in a co-dominant model (OR 13.00, 95 % CI 1.61–104.81); and the A/A genotype for FN1 in a recessive model (OR 2.81, 95 % CI 1.40–5.63). Concluding, variants of ECM genes are associated with weight regain after weight loss in a sex-specific manner.
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