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Further exploration of the possible influence of polymorphisms in HTR2C and 5HTT on body weight

Jessica BahaCorresponding Author Informationemail address, Lars Westberga, Fariba Baghaeib, Susanne Henningssona, Roland Rosmondb, Jonas Melkea, Göran Holmb, Elias Erikssona

Received 27 March 2009; accepted 5 November 2009. published online 21 January 2010.
Corrected Proof

Abstract 

Receptors of the 5-HT2C subtype are of importance for the influence of serotonin on food intake, and 2 single nucleotide polymorphisms in this gene (HTR2C)—Cys23Ser (rs6318) and −759C>T (rs3813929)—have been reported to be associated with weight and/or antipsychotic-induced weight gain. The present study aimed to replicate these associations; in addition, the 5-HTTLPR polymorphism in the promoter region of the serotonin transporter gene (SLC6A4) was assessed. The polymorphisms were genotyped in subjects recruited from the normal population (n = 510), and possible associations between genotype and body mass index (BMI) were assessed. The Ser23 allele was more common in underweight subjects (BMI <20) than in normal- and overweight (BMI ≥20) subjects (P = .006). The T allele of the −759C/T polymorphism was less common in the overweight group (BMI ≥25) (P = .007). Homozygosity for the short allele of 5-HTTLPR was more frequent in underweight subjects (P = .015). Our results are in agreement with previous studies, suggesting polymorphisms in HTR2C to be associated with body weight, particularly in women; and they also suggest that 5-HTTLPR may influence this phenotype. Further studies on the importance of the investigated genes for eating disorders and drug-induced weight gain are warranted.

a Department of Pharmacology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at Göteborg University, Box 431, SE- 405 30 Göteborg, Sweden

b The Cardiovascular Institute, The Sahlgrenska Academy at Göteborg University, Göteborg, Sweden

Corresponding Author InformationCorresponding author. Tel.: +46 31 786 34 48; fax: +46 31 82 10 85.

PII: S0026-0495(09)00482-X

doi:10.1016/j.metabol.2009.11.007

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