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PMID: 17593304 Published · epublish English Journal Article Research Support, Non-U.S. Gov't

TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population.

BMC medical genetics ·Vol. 8 ·2007-06-25 ·Pages 37

Cauchi S, Meyre D, Choquet H, Deghmoun S, Durand E, Gaget S, Lecoeur C, Froguel P, Levy-Marchal C

Abstract

In adults, the TCF7L2 rs7903146 T allele, commonly associated with type 2 diabetes (T2D), has been also associated with a lower body mass index (BMI) in T2D individuals and with a smaller waist circumference in subjects with impaired glucose tolerance. The present association study aimed at analyzing the contribution of the rs7903146 SNP to smallness for gestational age (SGA) and metabolic profiles in subjects with SGA or appropriate for gestational age birth weight (AGA). Two groups of French Caucasian subjects were selected on birth data: SGA (birth weight < 10th percentile; n = 764), and AGA (25th < birth weight < 75th percentile; n = 627). Family-based association tests were also performed in 3,012 subjects from 628 SGA and AGA pedigrees. The rs7903146 genotypic distributions between AGA (30.7%) and SGA (29.0%) were not statistically different (allelic OR = 0.92 [0.78-1.09], p = 0.34). Family association-based studies did not show a distortion of T allele transmission in SGA subjects (p = 0.52). No significant effect of the T allele was detected on any of the metabolic parameters in the SGA group. However, in the AGA group, trends towards a lower insulin secretion (p = 0.03) and a higher fasting glycaemia (p = 0.002) were detected in carriers of the T allele. The TCF7L2 rs7903146 variant neither increases the risk for SGA nor modulates birth weight and young adulthood glucose homeostasis in French Caucasian subjects born with SGA.

MeSH Terms
Adolescent Adult Alleles Birth Weight/genetics Case-Control Studies Child Cohort Studies Female France Genotype Humans Infant, Newborn Infant, Small for Gestational Age Insulin Resistance/genetics Male Obesity/genetics Polymorphism, Single Nucleotide Quantitative Trait, Heritable TCF Transcription Factors/genetics Transcription Factor 7-Like 2 Protein
Chemicals
TCF Transcription Factors TCF7L2 protein, human Transcription Factor 7-Like 2 Protein
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Cauchi Stéphane
CNRS, 8090-Institute of biology, Pasteur Institute, Lille, 59000 France. [email protected]
Meyre David
Choquet Hélène
Deghmoun Samia
Durand Emmanuelle
Gaget Stefan
Lecoeur Cécile
Froguel Philippe
Levy-Marchal Claire
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Article Info
Journal
BMC medical genetics
Abbr.
BMC Med Genet
ISSN
1471-2350
Published
2007-06-25
Epub
2007-00-25
Pages
37
Language
English
Region
England
NLM ID
100968552
PMCID
PMC1920504
Subset
IM
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