Metabolism - Clinical and Experimental
Volume 58, Issue 9 , Pages 1263-1269, September 2009

Genetic variation of FTO and TCF7L2 in premature adrenarche

  • Saila Lappalainen

      Affiliations

    • Department of Pediatrics, University of Kuopio and Kuopio University Hospital, FI-70211 Kuopio, Finland
    • Corresponding Author InformationCorresponding author. Department of Pediatrics, Clinical Research Centre, University of Kuopio, PO Box 1627, FI-70211 Kuopio, Finland. Tel.: +358 50 3722400; fax: +358 17 172410.
  • ,
  • Raimo Voutilainen

      Affiliations

    • Department of Pediatrics, University of Kuopio and Kuopio University Hospital, FI-70211 Kuopio, Finland
  • ,
  • Pauliina Utriainen

      Affiliations

    • Department of Pediatrics, University of Kuopio and Kuopio University Hospital, FI-70211 Kuopio, Finland
  • ,
  • Markku Laakso

      Affiliations

    • Department of Medicine, University of Kuopio and Kuopio University Hospital, FI-70211 Kuopio, Finland
  • ,
  • Jarmo Jääskeläinen

      Affiliations

    • Department of Pediatrics, University of Kuopio and Kuopio University Hospital, FI-70211 Kuopio, Finland

Received 25 November 2008; accepted 18 March 2009. published online 04 June 2009.

Abstract 

Premature adrenarche (PA) has been associated with increased body mass index. Our aim was to determine whether the obesity-associated variant at fat mass and obesity gene (FTO) is more frequent in PA subjects. Furthermore, we hypothesized that altered Wnt signaling due to genetic variants at transcription factor 7–like 2 (TCF7L2) could play a role in the polygenic pathogenesis of PA. We genotyped polymorphisms at FTO rs9939609 and at TCF7L2 rs7903146 and rs12255372 in 73 Finnish white prepubertal children with PA and in 97 age- and sex-matched healthy controls. In addition, we investigated the associations of these genetic variations with weight, height, circulating adrenocortical hormone levels, glucose metabolism, lipid profile, and blood pressure. The differences in the minor allele frequencies (MAFs) of rs9939609, rs7903146, and rs12255372 were not statistically significant between the PA and control groups (difference in MAFs [95% confidence interval]: −0.06 [−0.18, 0.05], 0.04 [−0.05, 0.12], and 0.01 [−0.07, 0.10]; P = .3, .4, and .8, respectively). However, the risk allele at TCF7L2 rs7903146 was more frequent in PA subjects than in controls when we restricted the analysis to the subjects with lower weight-for-height than the median of the PA subjects (weight-for-height <108%, corresponding body mass index SD score <0.79; difference in MAFs [95% confidence interval]: 0.12 [−0.001, 0.23]; P = .038). Risk variant at FTO rs9939609 associated with higher weight-for-height in the healthy children (P = .001). In conclusion, the minor variant at FTO rs9939609 seems to play no major role in the increased weight-for-height of PA subjects; but the risk allele at TCF7L2 rs7903146 may have a role in the pathogenesis of PA in lean subjects.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 The study protocol was approved by the Research Ethics Committee of Kuopio University Hospital.

PII: S0026-0495(09)00136-X

doi:10.1016/j.metabol.2009.03.025

Metabolism - Clinical and Experimental
Volume 58, Issue 9 , Pages 1263-1269, September 2009