Susceptibility genes for the side effect of antipsychotics on body weight and obesity

被引:25
作者
Chagnon, Yvon C. [1 ]
机构
[1] Univ Laval, Ctr Rech Robert Giffard, Beauport, PQ G1S 2G3, Canada
关键词
D O I
10.2174/138945006779025400
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Antipsychotic-induced body weight gain is becoming a major health concern since the increasing use of this medication in different mental disorders with a high prevalence in different populations. The percentage of patients gaining weight following antipsychotic medication can reach up to 80% according to the antipsychotic used, with around 30% developing obesity. The origins of this adverse effect of antipsychotics are probably multifactorial with the environment (food and exercise habits, medication) and the genetics coming into play. We have compiled the available genetic results on the antipsychotic-induced body weight gain and obesity. Candidate genes analysis showed that six genes have been associated with this adverse effect of antipsychotics. Among these, the associations with the serotonin receptor 2C and the leptin genes have been observed in more then one study. Thirteen other genes, mainly antipsychotic known receptors, have shown negative results. To find informative gene variations, we have also compared the effects of some polymorphisms of the serotonin receptor 2C and 2A in mental disorders, for antipsychotic therapeutic effect, for antipsychotic neuronal side effects, and for obesity. We have found results for six polymorphisms in each of the two genes. When association was observed for more then one phenotype, the same genotype or allele was generally involved identifying those sensitive to environmental pressures and to genetic background. Animal transgenic models of knockout or overexpressed genes of antipsychotic receptors have been evaluated for changes in obesity-related phenotypes. Seventeen out of the twenty-three antipsychotic receptors with transgenic models showed some effects on obesity-related phenotypes. Ten of these receptors have not been tested yet for antipsychotic-induced body weight gain, while the others have been tested only once with negative results, or is already associated to the effect such as the serotonin receptor 2C. Finally, pharmacogenomic approaches have allowed to detect more then 300 possible candidate genes for antipsychotic-induced body weight gain.
引用
收藏
页码:1681 / 1695
页数:15
相关论文
共 201 条
[61]   COMPARATIVE CONTROLLED TRIAL OF PIMOZIDE AND FLUPHENAZINE DECANOATE IN CONTINUATION THERAPY OF SCHIZOPHRENIA [J].
FALLOON, I ;
WATT, DC ;
SHEPHERD, M .
PSYCHOLOGICAL MEDICINE, 1978, 8 (01) :59-70
[62]   The TNF-alpha gene Nco I polymorphism influences the relationship among insulin resistance, percent body fat, and increased serum leptin levels [J].
FernandezReal, JM ;
Gutierrez, C ;
Ricart, W ;
Casamitjana, R ;
FernandezCastaner, M ;
Vendrell, J ;
Richart, C ;
Soler, J .
DIABETES, 1997, 46 (09) :1468-1472
[63]   Role for M5 muscarinic acetylcholine receptors in cocaine addiction [J].
Fink-Jensen, A ;
Fedorova, I ;
Wörtwein, G ;
Woldbye, DPD ;
Rasmussen, T ;
Thomsen, M ;
Bolwig, TG ;
Knitowski, KM ;
McKinzie, DL ;
Yamada, M ;
Wess, J ;
Basile, A .
JOURNAL OF NEUROSCIENCE RESEARCH, 2003, 74 (01) :91-96
[64]   Loss of vagally mediated bradycardia and bronchoconstriction in mice lacking M2 or M3 muscarinic acetylcholine receptors [J].
Fisher, JT ;
Vincent, SG ;
Gomeza, J ;
Yamada, M ;
Wess, J .
FASEB JOURNAL, 2004, 18 (02) :711-+
[65]   Estimating the consequences of anti-psychotic induced weight gain on health and mortality rate [J].
Fontaine, KR ;
Heo, M ;
Harrigan, EP ;
Shear, CL ;
Lakshminarayanan, M ;
Casey, DE ;
Allison, DB .
PSYCHIATRY RESEARCH, 2001, 101 (03) :277-288
[66]   TARGETED DISRUPTION OF NMDA RECEPTOR-1 GENE ABOLISHES NMDA RESPONSE AND RESULTS IN NEONATAL DEATH [J].
FORREST, D ;
YUZAKI, M ;
SOARES, HD ;
NG, L ;
LUK, DC ;
SHENG, M ;
STEWART, CL ;
MORGAN, JI ;
CONNOR, JA ;
CURRAN, T .
NEURON, 1994, 13 (02) :325-338
[67]   Glutamatergic modulation of hyperactivity in mice lacking the dopamine transporter [J].
Gainetdinov, RR ;
Mohn, AR ;
Bohn, LM ;
Caron, MG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (20) :11047-11054
[68]   A polymorphic CYP19 TTTA repeat influences aromatase activity and estrogen levels in elderly men:: Effects on bone metabolism [J].
Gennari, L ;
Masi, L ;
Merlotti, D ;
Picariello, L ;
Falchetti, A ;
Tanini, A ;
Mavilia, C ;
Del Monte, F ;
Gonnelli, S ;
Lucani, B ;
Gennari, C ;
Brandi, ML .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (06) :2803-2810
[69]   Lymphocytes as a neural probe: potential for studying psychiatric disorders [J].
Gladkevich, A ;
Kauffman, HF ;
Korf, J .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2004, 28 (03) :559-576
[70]   The 5-HT2A-1438G/A polymorphism in anorexia nervosa:: a combined analysis of 316 trios from six European centres [J].
Gorwood, P ;
Adès, J ;
Bellodi, L ;
Cellini, E ;
Collier, DA ;
Di Bella, D ;
Di Bernardo, M ;
Estivill, X ;
Fernandez-Aranda, F ;
Gratacos, M ;
Hebebrand, J ;
Hinney, A ;
Hu, X ;
Karwautz, A ;
Kipman, A ;
Mouren-Siméoni, MC ;
Nacmias, B ;
Ribasés, M ;
Remschmidt, H ;
Ricca, V ;
Rotella, CM ;
Sorbi, S ;
Treasure, J .
MOLECULAR PSYCHIATRY, 2002, 7 (01) :90-94