Association between the-2548G/A polymorphism of the leptin gene and antipsychotic-induced weight gain: Analysis of the CATIE sample and meta-analysis

被引:6
|
作者
Yoshida, Kazunari [1 ,2 ]
Maciukiewicz, Malgorzata [1 ,3 ]
Zai, Clement C. [1 ,4 ,5 ,6 ]
Goncalves, Vanessa F. [1 ,4 ]
Brandl, Eva J. [7 ]
Lieberman, Jeffrey A. [8 ]
Meltzer, Herbert Y. [9 ]
Tiwari, Arun K. [1 ,4 ]
Kennedy, James L. [1 ,4 ,5 ]
Mueller, Daniel J. [1 ,4 ,5 ]
机构
[1] Ctr Addict & Mental Hlth, Campbell Family Mental Hlth Res Inst, Pharmacogenet Res Clin, 250 Coll St, Toronto, ON M5T 1R8, Canada
[2] Keio Univ, Dept Neuropsychiat, Sch Med, Tokyo, Japan
[3] Univ Hosp Zurich, Ctr Expt Rheumatol, Dept Rheumatol, Zurich, Switzerland
[4] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[5] Univ Toronto, Inst Med Sci, Toronto, ON, Canada
[6] Univ Toronto, Lab Med & Pathobiol, Toronto, ON, Canada
[7] Charite Univ Med Berlin, Dept Psychiat & Psychotherapy, Campus Mitte, Berlin, Germany
[8] Columbia Univ, Coll Phys & Surg, New York State Psychiat Inst, Dept Psychiat, New York, NY USA
[9] Northwestern Feinberg Sch Med, Dept Psychiat & Behav Sci, Evanston, IL USA
来源
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY | 2020年 / 102卷
基金
加拿大健康研究院;
关键词
Antipsychotic-induced weight gain (AIWG); Clinical antipsychotic trials of intervention effectiveness (CATIE); Leptin; Meta-analysis; Schizophrenia; LEPR GENE; OBESITY; SCHIZOPHRENIA; RECEPTOR; HTR2C; CHILDREN; BMI; PHARMACOGENETICS; INSIG2; RISK;
D O I
10.1016/j.pnpbp.2020.109952
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Antipsychotics, especially most of the second-generation antipsychotics, have a high risk for metabolic syndrome and antipsychotic-induced weight gain (AIWG). A promoter variant of the leptin (LEP) gene, -2548G/A (rs7799039), has been associated with AIWG in several studies. The aim of this study was to evaluate this association in the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) sample, followed by meta-analysis. Methods: We investigated the association between rs7799039 and AIWG in a sub-sample of European (N = 164) individuals from the CATIE study. Body mass index (BMI) change and weight gain (presence or absence) was analyzed using ANCOVA and logistic regression, respectively. For the meta-analysis, a literature search was conducted using MEDLINE, Embase, and PsycINFO up to October 2019. The pooled odds ratio was calculated for presence or absence of weight gain (>= 7% weight change) using a random effects model. Results: We did not detect an association between rs7799039 and BMI change or weight gain (presence or absence) in the CATIE sample. As for the meta-analysis, we included 12 studies. No significant associations between the LEP rs7799039 polymorphism and AIWG were observed under the allelic genetic model (allele A vs. allele G) (OR = 1.10 [0.71, 1.70], p = .68). In the subgroup analyses of first-episode schizophrenia patients, a significant association between the A-allele and weight gain was observed, respectively (OR = 2.32 [1.41, 3.82], p = .0009). Conclusions: The present meta-analysis showed no significant effect of rs7799039 on AIWG. However, this variant may influence AIWG in first-episode schizophrenia patients. Further investigation of a larger and more homogenous sample is required to elucidate the role of the LEP gene in AIWG.
引用
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页数:9
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