Effect of Genetic Variation in the Human Fatty Acid Synthase Gene (FASN) on Obesity and Fat Depot-Specific mRNA Expression

• Published in: Obesity (Silver Spring, Md.) Vol. 18; no. 6; pp. 1218 - 1225
• Main Authors: Schleinitz, Dorit, Klöting, Nora, Körner, Antje, Berndt, Janin, Reichenbächer, Marlene, Tönjes, Anke, Ruschke, Karen, Böttcher, Yvonne, Dietrich, Kerstin, Enigk, Beate, Filz, Matthias, Schön, Michael R, Jenkner, Jost, Kiess, Wieland, Stumvoll, Michael, Blüher, Matthias
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.06.2010
• Subjects: adipose tissue; Adipose Tissue - metabolism; Adipose Tissue - pathology; Adolescent; Adult; adults; Aged; Aged, 80 and over; Body fat; body mass index; Case-Control Studies; Child; childhood; childhood obesity; Diabetes; energy; Enzymes; fasting; Fatty Acid Synthases - genetics; Fatty Acid Synthases - metabolism; Fatty acids; fatty-acid synthase; Female; Gene Expression; genes; genetic variation; Genetic Variation - physiology; genotyping; Glucose; homeostasis; Humans; insulin; Insulin resistance; linkage disequilibrium; Male; messenger RNA; mice; Middle Aged; noninsulin-dependent diabetes mellitus; Obesity; Obesity - genetics; Obesity - metabolism; Organ Specificity; Oxidation; pathophysiology; RNA, Messenger - metabolism; school children; single nucleotide polymorphism; Surgery; waist-to-hip ratio; Weight control; Whites; Young Adult; Germany
• ISSN: 1930-7381; 1930-739X; 1930-739X
• DOI: 10.1038/oby.2009.392

Inhibition of fatty acid synthase (FASN) induces a rapid decline in fat stores in mice, suggesting a role for this enzyme in energy homeostasis. To investigate the potential role of FASN in the pathophysiology of human obesity, the FASN gene was sequenced in 48 German whites. Thirty-five single-nucleotide polymorphisms (SNPs) were identified. Eight SNPs representative for their linkage disequilibrium groups and the Val1483Ile (rs2228305) substitution were genotyped for subsequent association analyses in 1,311 adults from Germany. Further, the tagging SNPs were genotyped also in German childhood cohorts (738 schoolchildren, 205 obese children). Effects of genetic variation on FASN mRNA expression in visceral and subcutaneous adipose tissue from a subgroup of 172 subjects were analyzed. Several polymorphisms in the FASN (rs62078748, rs2229422, rs2229425, and rs17848939) were nominally associated with obesity in case–control studies including 446 obese subjects (BMI ≥30 kg/m2) and 389 lean controls (BMI ≤25 kg/m2) (adjusted P < 0.05). The strongest significant effect was found for rs2229422 (P = 1.3 × 10−5 adjusted for age, sex, type 2 diabetes status), which was supported by associations with BMI, waist-to-hip ratio (WHR), fasting plasma insulin and glucose infusion rate (adjusted P < 0.05). Subjects with the Val1483Ile substitution appeared to be protected against obesity. In addition, rs17848939 was nominally significantly associated with the ratio of visceral/subcutaneous FASN mRNA expression (adjusted P = 0.04). No effect of genetic variation in FASN on obesity was found in children. In conclusion, our data indicate a role of FASN genetic variation in susceptibility to obesity in adults.