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PMID: 17003362 Published · ppublish English Journal Article Multicenter Study Research Support, N.I.H., Intramural Research Support, Non-U.S. Gov't

IL6 gene promoter polymorphisms and type 2 diabetes: joint analysis of individual participants' data from 21 studies.

Diabetes ·Vol. 55 ·No. 10 ·2006-10-00 ·Pages 2915-21

Huth C, Heid IM, Vollmert C, Gieger C, Grallert H, Wolford JK, Langer B, Thorand B, Klopp N, Hamid YH, Pedersen O, Hansen T, Lyssenko V, Groop L, Meisinger C, Döring A, Löwel H, Lieb W, Hengstenberg C, Rathmann W, Martin S, Stephens JW, Ireland H, Mather H, Miller GJ, Stringham HM, Boehnke M, Tuomilehto J, Boeing H, Möhlig M, Spranger J, Pfeiffer A, Wernstedt I, Niklason A, López-Bermejo A, Fernández-Real JM, Hanson RL, Gallart L, Vendrell J, Tsiavou A, Hatziagelaki E, Humphries SE, Wichmann HE, Herder C, Illig T

Abstract

Several lines of evidence indicate a causal role of the cytokine interleukin (IL)-6 in the development of type 2 diabetes in humans. Two common polymorphisms in the promoter of the IL-6 encoding gene IL6, -174G>C (rs1800795) and -573G>C (rs1800796), have been investigated for association with type 2 diabetes in numerous studies but with results that have been largely equivocal. To clarify the relationship between the two IL6 variants and type 2 diabetes, we analyzed individual data on >20,000 participants from 21 published and unpublished studies. Collected data represent eight different countries, making this the largest association analysis for type 2 diabetes reported to date. The GC and CC genotypes of IL6 -174G>C were associated with a decreased risk of type 2 diabetes (odds ratio 0.91, P = 0.037), corresponding to a risk modification of nearly 9%. No evidence for association was found between IL6 -573G>C and type 2 diabetes. The observed association of the IL6 -174 C-allele with a reduced risk of type 2 diabetes provides further evidence for the hypothesis that immune mediators are causally related to type 2 diabetes; however, because the association is borderline significant, additional data are still needed to confirm this finding.

MeSH Terms
Case-Control Studies Diabetes Mellitus, Type 2/genetics Genetics, Population Humans Interleukin-6/genetics Odds Ratio Polymorphism, Genetic Promoter Regions, Genetic Risk
Chemicals
Interleukin-6
Authors & Affiliations
45 authors, click to expand affiliations / ORCID
Huth Cornelia
GSF-Institute of Epidemiology, Neuherberg, Germany.
Heid Iris M
Vollmert Caren
Gieger Christian
Grallert Harald
Wolford Johanna K
Langer Birgit
Thorand Barbara
Klopp Norman
Hamid Yasmin H
Pedersen Oluf
Hansen Torben
Lyssenko Valeriya
Groop Leif
Meisinger Christa
Döring Angela
Löwel Hannelore
Lieb Wolfgang
Hengstenberg Christian
Rathmann Wolfgang
Martin Stephan
Stephens Jeffrey W
Ireland Helen
Mather Hugh
Miller George J
Stringham Heather M
Boehnke Michael
Tuomilehto Jaakko
Boeing Heiner
Möhlig Matthias
Spranger Joachim
Pfeiffer Andreas
Wernstedt Ingrid
Niklason Anders
López-Bermejo Abel
Fernández-Real José-Manuel
Hanson Robert L
Gallart Luis
Vendrell Joan
Tsiavou Anastasia
Hatziagelaki Erifili
Humphries Steve E
Wichmann H-Erich
Herder Christian
Illig Thomas
Article Info
Journal
Diabetes
Abbr.
Diabetes
ISSN
0012-1797
Published
2006-10-00
Pages
2915-21
Language
English
Region
United States
NLM ID
0372763
Subset
IM
Grants
NIDDK NIH HHS · R01 DK062370 · United States
NHGRI NIH HHS · T32 HG000040 · United States
Intramural NIH HHS · United States
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