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PMID: 11528401 Published · ppublish English Journal Article

Paternal transmission of the very common class I INS VNTR alleles predisposes to childhood obesity.

Nature genetics ·Vol. 29 ·No. 1 ·2001-09-00 ·Pages 96-9

Le Stunff C, Fallin D, Bougnères P

Abstract

To identify some of the genetic factors that contribute to obesity in children of Central European and North African descent, we studied the parental transmission of alleles at the insulin locus to offspring with early-onset obesity. A variable nucleotide tandem repeat (VNTR) polymorphism upstream of the insulin gene (INS) is associated with variations in the expression of INS and the nearby gene encoding insulin-like growth factor 2 (IGF2). We found an excess of paternal transmission of class I VNTR alleles to obese children: children who inherited a class I allele from their father (but not those inheriting it from their mother) had a relative risk of early-onset obesity of 1.8. Due to the frequency of class I alleles in this population, this risk concerns 65-70% of all infants. These results suggest that increased in utero expression of paternal INS or IGF2 due to the class I INS VNTR allele may predispose offspring to postnatal fat deposition.

MeSH Terms
Adolescent Alleles Child Cohort Studies Female Genetic Predisposition to Disease Genomic Imprinting Humans Insulin/genetics Male Minisatellite Repeats Obesity/genetics
Chemicals
Insulin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Le Stunff C
Department of Pediatric Endocrinology, Hôpital St Vincent de Paul, Paris, France.
Fallin D
Bougnères P
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
Published
2001-09-00
Pages
96-9
Language
English
Region
United States
NLM ID
9216904
Subset
IM
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