Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: heritabilities

• DOI: 10.1007/s00125-007-0784-z
• Publication Date: 2007-08-10T13:46:22Z
• Authors: N. Y. Souren; A. D. C. Paulussen; R. J. F. Loos; M. Gielen; G. Beunen; R. Fagard; C. Derom; R. Vlietinck; M. P. Zeegers
• Keywords: Adult; Male; 0301 basic medicine; Adolescent; Endocrinology, Diabetes and Metabolism; Article; Body Mass Index; 03 medical and health sciences; Belgium; Internal Medicine; Dietary Carbohydrates; Twins, Dizygotic; Body Size; Humans; Triglycerides; 2. Zero hunger; Analysis of Variance; 0303 health sciences; Anthropometry; Genetic Variation; Twins, Monozygotic; Dietary Fats; Lipids; 3. Good health; Skinfold Thickness; Adipose Tissue; Female

We determined the genetic contribution of 18 anthropometric and metabolic risk factors of type 2 diabetes using a young healthy twin population.Traits were measured in 240 monozygotic (MZ) and 138 dizygotic (DZ) twin pairs aged 18 to 34 years. Twins were recruited from the Belgian population-based East Flanders Prospective Twin Survey, which is characterised by its accurate zygosity determination and extensive collection of perinatal and placental data, including information on chorionicity. Heritability was estimated using structural equation modelling implemented in the Mx software package.Intra-pair correlations of the anthropometric and metabolic characteristics did not differ between MZ monochorionic and MZ dichorionic pairs; consequently heritabilities were estimated using the classical twin approach. For body mass, BMI and fat mass, quantitative sex differences were observed; genetic variance explained 84, 85 and 81% of the total variation in men and 74, 75 and 70% in women, respectively. Heritability estimates of the waist-to-hip ratio, sum of four skinfold thicknesses and lean body mass were 70, 74 and 81%, respectively. The heritability estimates of fasting glucose, fasting insulin, homeostasis model assessment of insulin resistance and beta cell function, as well as insulin-like growth factor binding protein-1 levels were 67, 49, 48, 62 and 47%, in that order. Finally, for total cholesterol, LDL-cholesterol, HDL-cholesterol, total cholesterol:HDL-cholesterol ratio, triacylglycerol, NEFA and leptin levels, genetic factors explained 75, 78, 76, 79, 58, 37 and 53% of the total variation, respectively.Genetic factors explain the greater part of the variation in traits related to obesity, glucose intolerance/insulin resistance and dyslipidaemia.