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

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Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey : heritabilities. / Souren, N Y; Paulussen, A D C; Loos, R J F; Gielen, M; Beunen, G; Fagard, R; Derom, C; Vlietinck, R; Zeegers, M P.

In: Diabetologia, Vol. 50, No. 10, 10.2007, p. 2107-16.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Souren, NY, Paulussen, ADC, Loos, RJF, Gielen, M, Beunen, G, Fagard, R, Derom, C, Vlietinck, R & Zeegers, MP 2007, 'Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: heritabilities', Diabetologia, vol. 50, no. 10, pp. 2107-16. https://doi.org/10.1007/s00125-007-0784-z

APA

Souren, N. Y., Paulussen, A. D. C., Loos, R. J. F., Gielen, M., Beunen, G., Fagard, R., Derom, C., Vlietinck, R., & Zeegers, M. P. (2007). Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: heritabilities. Diabetologia, 50(10), 2107-16. https://doi.org/10.1007/s00125-007-0784-z

Vancouver

Souren NY, Paulussen ADC, Loos RJF, Gielen M, Beunen G, Fagard R et al. Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: heritabilities. Diabetologia. 2007 Oct;50(10):2107-16. https://doi.org/10.1007/s00125-007-0784-z

Author

Souren, N Y ; Paulussen, A D C ; Loos, R J F ; Gielen, M ; Beunen, G ; Fagard, R ; Derom, C ; Vlietinck, R ; Zeegers, M P. / Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey : heritabilities. In: Diabetologia. 2007 ; Vol. 50, No. 10. pp. 2107-16.

Bibtex

@article{87a3f273972c424bb1b9375edc637ef3,
title = "Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: heritabilities",
abstract = "AIMS/HYPOTHESIS: We determined the genetic contribution of 18 anthropometric and metabolic risk factors of type 2 diabetes using a young healthy twin population.METHODS: 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.RESULTS: 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.CONCLUSIONS/INTERPRETATION: Genetic factors explain the greater part of the variation in traits related to obesity, glucose intolerance/insulin resistance and dyslipidaemia.",
keywords = "Adipose Tissue/anatomy & histology, Adolescent, Adult, Analysis of Variance, Anthropometry, Belgium, Body Mass Index, Body Size, Dietary Carbohydrates/metabolism, Dietary Fats/metabolism, Female, Genetic Variation, Humans, Lipids/blood, Male, Skinfold Thickness, Triglycerides/blood, Twins, Dizygotic, Twins, Monozygotic",
author = "Souren, {N Y} and Paulussen, {A D C} and Loos, {R J F} and M Gielen and G Beunen and R Fagard and C Derom and R Vlietinck and Zeegers, {M P}",
year = "2007",
month = oct,
doi = "10.1007/s00125-007-0784-z",
language = "English",
volume = "50",
pages = "2107--16",
journal = "Diabetologia",
issn = "0012-186X",
publisher = "Springer",
number = "10",

}

RIS

TY - JOUR

T1 - Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey

T2 - heritabilities

AU - Souren, N Y

AU - Paulussen, A D C

AU - Loos, R J F

AU - Gielen, M

AU - Beunen, G

AU - Fagard, R

AU - Derom, C

AU - Vlietinck, R

AU - Zeegers, M P

PY - 2007/10

Y1 - 2007/10

N2 - AIMS/HYPOTHESIS: We determined the genetic contribution of 18 anthropometric and metabolic risk factors of type 2 diabetes using a young healthy twin population.METHODS: 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.RESULTS: 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.CONCLUSIONS/INTERPRETATION: Genetic factors explain the greater part of the variation in traits related to obesity, glucose intolerance/insulin resistance and dyslipidaemia.

AB - AIMS/HYPOTHESIS: We determined the genetic contribution of 18 anthropometric and metabolic risk factors of type 2 diabetes using a young healthy twin population.METHODS: 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.RESULTS: 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.CONCLUSIONS/INTERPRETATION: Genetic factors explain the greater part of the variation in traits related to obesity, glucose intolerance/insulin resistance and dyslipidaemia.

KW - Adipose Tissue/anatomy & histology

KW - Adolescent

KW - Adult

KW - Analysis of Variance

KW - Anthropometry

KW - Belgium

KW - Body Mass Index

KW - Body Size

KW - Dietary Carbohydrates/metabolism

KW - Dietary Fats/metabolism

KW - Female

KW - Genetic Variation

KW - Humans

KW - Lipids/blood

KW - Male

KW - Skinfold Thickness

KW - Triglycerides/blood

KW - Twins, Dizygotic

KW - Twins, Monozygotic

U2 - 10.1007/s00125-007-0784-z

DO - 10.1007/s00125-007-0784-z

M3 - Journal article

C2 - 17694296

VL - 50

SP - 2107

EP - 2116

JO - Diabetologia

JF - Diabetologia

SN - 0012-186X

IS - 10

ER -

ID: 258453819