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

被引:21
作者
Bah, Jessica [1 ]
Westberg, Lars [1 ]
Baghaei, Fariba [2 ]
Henningsson, Susanne [1 ]
Rosmond, Roland [2 ]
Melke, Jonas [1 ]
Holm, Goran [2 ]
Eriksson, Elias [1 ]
机构
[1] Univ Gothenburg, Dept Pharmacol, Inst Neurosci & Physiol, Sahlgrenska Acad, SE-40530 Gothenburg, Sweden
[2] Univ Gothenburg, Cardiovasc Inst, Sahlgrenska Acad, Gothenburg, Sweden
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2010年 / 59卷 / 08期
基金
英国医学研究理事会;
关键词
5-HT2C RECEPTOR GENE; ANOREXIA-NERVOSA; EATING DISORDER; MASS INDEX; ASSOCIATION; OBESITY; PROMOTER; SUBSTITUTION; REGION; GAIN;
D O I
10.1016/j.metabol.2009.11.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1156 / 1163
页数:8
相关论文
共 36 条
[1]   Fine-tuning serotonin2c receptor function in the brain: Molecular and functional implications [J].
Berg, Kelly A. ;
Clarke, William R. ;
Cunningham, Kathryn A. ;
Spampinato, Umberto .
NEUROPHARMACOLOGY, 2008, 55 (06) :969-976
[2]   Association study of olanzapine-induced weight gain and therapeutic response with SERT gene polymorphisms in female schizophrenic patients [J].
Bozina, Nada ;
Medved, Vesna ;
Kuzman, Martina Rojnic ;
Sain, Ivica ;
Sertic, Jadranka .
JOURNAL OF PSYCHOPHARMACOLOGY, 2007, 21 (07) :728-734
[3]   Low gene expression conferred by association of an allele of the 5-HT2C receptor gene with antipsychotic-induced weight gain [J].
Buckland, PR ;
Hoogendoorn, B ;
Guy, CA ;
Smith, SK ;
Coleman, SL ;
O'Donovan, MC .
AMERICAN JOURNAL OF PSYCHIATRY, 2005, 162 (03) :613-615
[4]   Moderate dieting causes 5-HT2C receptor supersensitivity [J].
Cowen, PJ ;
Clifford, EM ;
Walsh, AES ;
Williams, C ;
Fairburn, CG .
PSYCHOLOGICAL MEDICINE, 1996, 26 (06) :1155-1159
[5]   Serotonin transporter linked polymorphic region in anorexia nervosa and bulimia nervosa [J].
Di Bella, D ;
Catalano, M ;
Cavallini, MC ;
Riboldi, C ;
Bellodi, L .
MOLECULAR PSYCHIATRY, 2000, 5 (03) :233-234
[6]  
Ebstein RP, 1997, AM J MED GENET, V74, P65, DOI 10.1002/(SICI)1096-8628(19970221)74:1<65::AID-AJMG15>3.0.CO
[7]  
2-P
[8]   Impulsiveness, serotonin genes and repetition of deliberate self-harm (DSH) [J].
Evans, J ;
Reeves, B ;
Platt, H ;
Leibenau, A ;
Goldman, D ;
Jefferson, K ;
Nutt, D .
PSYCHOLOGICAL MEDICINE, 2000, 30 (06) :1327-1334
[9]   Pharmacological properties of the Cys23Ser single nucleotide polymorphism in human 5-HT2C receptor isoforms [J].
Fentress, HM ;
Grinde, E ;
Mazurkiewicz, JE ;
Backstrom, JR ;
Herrick-Davis, K ;
Sanders-Bush, E .
PHARMACOGENOMICS JOURNAL, 2005, 5 (04) :244-254
[10]   5-HT2C receptor gene polymorphisms associated with antipsychotic drug action alter promoter activity [J].
Hill, Matthew J. ;
Reynolds, Gavin P. .
BRAIN RESEARCH, 2007, 1149 :14-17