Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

Research output: Contribution to journalJournal articleResearchpeer-review

  • Agnar Helgason
  • Snaebjörn Pálsson
  • Gudmar Thorleifsson
  • Struan F A Grant
  • Valur Emilsson
  • Steinunn Gunnarsdottir
  • Adebowale Adeyemo
  • Yuanxiu Chen
  • Guanjie Chen
  • Inga Reynisdottir
  • Rafn Benediktsson
  • Anke Hinney
  • Gitte Andersen
  • Knut Borch-Johnsen
  • Torben Jorgensen
  • Helmut Schäfer
  • Mezbah Faruque
  • Ayo Doumatey
  • Jie Zhou
  • Robert L Wilensky
  • Muredach P Reilly
  • Daniel J Rader
  • Yu Bagger
  • Claus Christiansen
  • Gunnar Sigurdsson
  • Johannes Hebebrand
  • Unnur Thorsteinsdottir
  • Jeffrey R Gulcher
  • Augustine Kong
  • Charles Rotimi
  • Kári Stefánsson
We recently described an association between risk of type 2diabetes and variants in the transcription factor 7-like 2 gene (TCF7L2; formerly TCF4), with a population attributable risk (PAR) of 17%-28% in three populations of European ancestry. Here, we refine the definition of the TCF7L2 type 2diabetes risk variant, HapB(T2D), to the ancestral T allele of a SNP, rs7903146, through replication in West African and Danish type 2 diabetes case-control studies and an expanded Icelandic study. We also identify another variant of the same gene, HapA, that shows evidence of positive selection in East Asian, European and West African populations. Notably, HapA shows a suggestive association with body mass index and altered concentrations of the hunger-satiety hormones ghrelin and leptin in males, indicating that the selective advantage of HapA may have been mediated through effects on energy metabolism.
Original languageEnglish
JournalNature Genetics
Issue number2
Pages (from-to)218-25
Number of pages8
Publication statusPublished - 2007

    Research areas

  • African Continental Ancestry Group, Asian Continental Ancestry Group, Biological Evolution, Body Mass Index, Case-Control Studies, Diabetes Mellitus, Type 2, European Continental Ancestry Group, Female, Genetic Predisposition to Disease, Genetic Variation, Haplotypes, Humans, Iceland, Male, Polymorphism, Single Nucleotide, Risk, Selection, Genetic, TCF Transcription Factors, Transcription Factor 7-Like 2 Protein

ID: 38336238