Molecular pathway analysis associates alterations in obesity-related genes and antipsychotic-induced weight gain

被引:13
|
作者
Corfitsen, Henrik Thyge [1 ]
Krantz, Betina [2 ]
Larsen, Agnete [3 ]
Drago, Antonio [1 ]
机构
[1] Aarhus Univ, Inst Biomedicin, Psykiatr Forskningsenhed Vest, Herning, Denmark
[2] VIA Univ Coll, Holstebro, Denmark
[3] Aarhus Univ, Inst Biomed, Forskning & Uddannelse, Ost, Denmark
来源
ACTA NEUROPSYCHIATRICA | 2020年 / 32卷 / 02期
关键词
antipsychotic agents; metabolic networks and pathways; pharmacogenetics; polymorphism; single nucleotide; weight gain; ENERGY HOMEOSTASIS GENES; BODY-MASS INDEX; EARLY PSYCHOSIS; THAI CHILDREN; RECEPTOR GENE; LEPTIN GENE; POLYMORPHISMS; FTO; MC4R; RISK;
D O I
10.1017/neu.2019.41
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Objective: Antipsychotics often induce excessive weight gain. We hypothesised that individuals with genetic variations related to known obesity-risk genes have an increased risk of excessive antipsychotic-induced weight gain (AIWG). This hypothesis was tested in a subset of the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) trial data set. Methods: The CATIE trial compared effects and side effects of five different antipsychotics through an 18-month period. Based on the maximum weight gain recorded, excessive weight gain was defined as >7% weight gain. Cytoscape and GeneMANIA were instrumental in composing a molecular pathway from eight selected genes linked to obesity. Genetic information on a total of 495.172 single-nucleotide polymorphisms (SNPs) were available from 765 (556 males) individuals. Enrichment test was conducted through ReactomePA and Bioconductor. A permutation test was performed, testing the generated pathway against 10(5) permutated pathways (p <= 0.05). In addition, a standard genome-wide association study (GWAS) analysis was performed. Result: GWAS analysis did not detect significant differences related to excessive weight gain. The pathway generated contained 28 genes. A total of 2067 SNPs were significantly expressed (p < 0.01) within this pathway when comparing excessive weight gainers to the rest of the sample. Affected genes including PPARG and PCSK1 were not previously related to treatment-induced weight gain. Conclusions: The molecular pathway composed from high-risk obesity genes was shown to overlap with genetics of patients who gained >7% weight gain during the CATIE trial. This suggests that genes related to obesity compose a pathway of increased risk of excessive AIWG. Further independent analyses are warranted that may confirm or clarify the possible reasoning behind.
引用
收藏
页码:72 / 83
页数:12
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