TY - JOUR
T1 - Studies of CTNNBL1 and FDFT1 variants and measures of obesity
T2 - Analyses of quantitative traits and case-control studies in 18,014 Danes
AU - Andreasen, Camilla Helene
AU - Mogensen, Mette Sloth
AU - Borch-Johnsen, Knut
AU - Sandbæk, Annelli
AU - Lauritzen, Torsten
AU - Almind, Katrine
AU - Hansen, Lars
AU - Jørgensen, Torben
AU - Pedersen, Oluf
AU - Hansen, Torben
PY - 2009/2/26
Y1 - 2009/2/26
N2 - Background: A genome-wide scan in unrelated US Caucasians identified rs7001819 upstream of farnesyl-diphosphate farnesyltransferase 1 (FDFT1) and multiple variants within catenin (cadherin-associated protein), β-like 1 (CTNNBL1) to associate strongly with body mass index (BMI). The most significantly associating variants within CTNNBL1 including rs6013029 and rs6020846 were additionally confirmed to associate with morbid obesity in a French Caucasian case-control sample. The aim of this study was to investigate the impact of these three variants on obesity, through analyses of obesity-related quantitative traits, and case-control studies in large study samples of Danes. Methods: The FDFT1 rs7001819, CTNNBL1 rs6013029 and rs6020846 were genotyped, using TaqMan allelic discrimination, in a combined study sample comprising 18,014 participants ascertained from; the population-based Inter99 cohort (n = 6,514), the ADDITION Denmark screening study cohort (n = 8,662), and a population-based sample (n = 680) and a type 2 diabetic patients group (n = 2,158) from Steno Diabetes Center. Results: Both CTNNBL1 variants associated with body weight and height with per allele effect sizes of 1.0 [0.3-0.8] kg and 0.6 [0.2-0.9] cm, respectively, for the rs6020846 G-allele. No association was observed with BMI and waist circumference. In case-control studies neither of the CTNNBL1 variants showed association with overweight, obesity or morbid obesity (rs6013029: Odds Ratio (OR)overweight = 1.02 [0.90-1.16], ORobesity = 1.09 [0.95-1.25], ORmorbidobesity = 1.26 [0.91-1.74]; rs6020846: ORoverweight = 1.05 [0.93-1.18], ORobesity= 1.13 [1.00-1.28], ORmorbidobesity = 1.17 [0.86-1.61]). However, in meta-analyses of the present and the previous study, both the rs6013029 T-allele and the rs6020846 G-allele increased the risk of developing morbid obesity (rs6013029: ORcombined = 1.36 [1.12-1.64], p = 0.002; rs6020846: ORcombined = 1.26 [1.06-1.51], p = 0.01), and obesity (rs6013029: ORcombined = 1.17 [1.04-1.31], p = 0.007; rs6020846: ORcombined = 1.17 [1.05-1.30], p = 0.004). The FDFT1 rs7001819 C-allele showed no association with obesity-related quantitative measures or dichotomous measures of overweight, obesity and morbid obesity. Conclusion: CTNNBL1 variants associated with body weight and height, and confer the risk of developing obesity in meta-analyses combining the present and a previous study. FDFT1 rs7001819 showed no association with obesity, neither when analysing quantitative traits nor when performing case-control studies of obesity.
AB - Background: A genome-wide scan in unrelated US Caucasians identified rs7001819 upstream of farnesyl-diphosphate farnesyltransferase 1 (FDFT1) and multiple variants within catenin (cadherin-associated protein), β-like 1 (CTNNBL1) to associate strongly with body mass index (BMI). The most significantly associating variants within CTNNBL1 including rs6013029 and rs6020846 were additionally confirmed to associate with morbid obesity in a French Caucasian case-control sample. The aim of this study was to investigate the impact of these three variants on obesity, through analyses of obesity-related quantitative traits, and case-control studies in large study samples of Danes. Methods: The FDFT1 rs7001819, CTNNBL1 rs6013029 and rs6020846 were genotyped, using TaqMan allelic discrimination, in a combined study sample comprising 18,014 participants ascertained from; the population-based Inter99 cohort (n = 6,514), the ADDITION Denmark screening study cohort (n = 8,662), and a population-based sample (n = 680) and a type 2 diabetic patients group (n = 2,158) from Steno Diabetes Center. Results: Both CTNNBL1 variants associated with body weight and height with per allele effect sizes of 1.0 [0.3-0.8] kg and 0.6 [0.2-0.9] cm, respectively, for the rs6020846 G-allele. No association was observed with BMI and waist circumference. In case-control studies neither of the CTNNBL1 variants showed association with overweight, obesity or morbid obesity (rs6013029: Odds Ratio (OR)overweight = 1.02 [0.90-1.16], ORobesity = 1.09 [0.95-1.25], ORmorbidobesity = 1.26 [0.91-1.74]; rs6020846: ORoverweight = 1.05 [0.93-1.18], ORobesity= 1.13 [1.00-1.28], ORmorbidobesity = 1.17 [0.86-1.61]). However, in meta-analyses of the present and the previous study, both the rs6013029 T-allele and the rs6020846 G-allele increased the risk of developing morbid obesity (rs6013029: ORcombined = 1.36 [1.12-1.64], p = 0.002; rs6020846: ORcombined = 1.26 [1.06-1.51], p = 0.01), and obesity (rs6013029: ORcombined = 1.17 [1.04-1.31], p = 0.007; rs6020846: ORcombined = 1.17 [1.05-1.30], p = 0.004). The FDFT1 rs7001819 C-allele showed no association with obesity-related quantitative measures or dichotomous measures of overweight, obesity and morbid obesity. Conclusion: CTNNBL1 variants associated with body weight and height, and confer the risk of developing obesity in meta-analyses combining the present and a previous study. FDFT1 rs7001819 showed no association with obesity, neither when analysing quantitative traits nor when performing case-control studies of obesity.
UR - http://www.scopus.com/inward/record.url?scp=64549153501&partnerID=8YFLogxK
U2 - 10.1186/1471-2350-10-17
DO - 10.1186/1471-2350-10-17
M3 - Article
C2 - 19245693
AN - SCOPUS:64549153501
SN - 1471-2350
VL - 10
JO - BMC Medical Genetics
JF - BMC Medical Genetics
M1 - 17
ER -