TY - JOUR
T1 - Variation in the gene encoding Kruppel-like factor 7 influences body fat: studies of 14,818 Danes
AU - Zobel, Dorit
AU - Andreasen, Camilla
AU - Burgdorf, Kristoffer
AU - Andersson, Ehm
AU - Sandbæk, Annelli
AU - Lauritzen, Torsten
AU - Borch-Johnsen, Knut
AU - Jørgensen, Torben
AU - Maeda, Shiro
AU - Nakamura, Yusuke
AU - Eiberg, Hans
AU - Pedersen, Oluf
AU - Hansen, Torben
PY - 2009
Y1 - 2009
N2 - Objective: KLF7 encodes Kruppel-like factor (KLF) 7, a member of the KLF family of transcription factors, initially shown to play important roles in cellular development and differentiation, and reported to be specifically involved in adipogenesis. Several single nucleotide polymorphisms (SNPs) have been identified in KLF7, of which the A-allele of rs2302870 has been associated with type 2 diabetes in a Japanese population; however, a possible association of KLF7 SNPs with obesity has not been investigated. We aimed to identify variation in the putative promoter region, the coding regions, exon/intron boundaries, and 3'-untranslated region of KLF7, and to examine identified variants in relation to obesity, type 2 diabetes and related quantitative traits in Danish individuals. Methods: Identified variants were investigated for association with type 2 diabetes in 8,777 individuals and with obesity in 14,818 individuals. Results: We identified four common SNPs in low pairwise linkage disequilibrium; three in the putative promoter region (-1119 G>A, -963 C>A [rs7568369], and -614 G>A) and IVS2+35092 A>C (rs2302870). We failed to confirm an association between rs2302870 and type 2 diabetes. Neither were rs7568369 associated with type 2 diabetes; however, the minor A-allele of rs7568369 protected against obesity (OR=0.90 [0.84-0.96], P=0.001) and in studies of quantitative traits (n=5,535) the variant associated with decreased BMI (P=0.002) and waist circumference (P=0.003). The -1119 G>A and -614 G>A variants were not associated with obesity or type 2 diabetes. Conclusion: We identified a novel association between the minor A-allele of KLF7 rs7568369 and protection against obesity in the Danish population.
AB - Objective: KLF7 encodes Kruppel-like factor (KLF) 7, a member of the KLF family of transcription factors, initially shown to play important roles in cellular development and differentiation, and reported to be specifically involved in adipogenesis. Several single nucleotide polymorphisms (SNPs) have been identified in KLF7, of which the A-allele of rs2302870 has been associated with type 2 diabetes in a Japanese population; however, a possible association of KLF7 SNPs with obesity has not been investigated. We aimed to identify variation in the putative promoter region, the coding regions, exon/intron boundaries, and 3'-untranslated region of KLF7, and to examine identified variants in relation to obesity, type 2 diabetes and related quantitative traits in Danish individuals. Methods: Identified variants were investigated for association with type 2 diabetes in 8,777 individuals and with obesity in 14,818 individuals. Results: We identified four common SNPs in low pairwise linkage disequilibrium; three in the putative promoter region (-1119 G>A, -963 C>A [rs7568369], and -614 G>A) and IVS2+35092 A>C (rs2302870). We failed to confirm an association between rs2302870 and type 2 diabetes. Neither were rs7568369 associated with type 2 diabetes; however, the minor A-allele of rs7568369 protected against obesity (OR=0.90 [0.84-0.96], P=0.001) and in studies of quantitative traits (n=5,535) the variant associated with decreased BMI (P=0.002) and waist circumference (P=0.003). The -1119 G>A and -614 G>A variants were not associated with obesity or type 2 diabetes. Conclusion: We identified a novel association between the minor A-allele of KLF7 rs7568369 and protection against obesity in the Danish population.
U2 - 10.1530/EJE-08-0688
DO - 10.1530/EJE-08-0688
M3 - Journal article
C2 - 19147600
VL - 160
SP - 603
EP - 609
JO - European Journal of Endocrinology
JF - European Journal of Endocrinology
SN - 0804-4643
IS - 4
ER -