作者
Daniel E Adkins, Karolina Åberg, Joseph L McClay, József Bukszár, Zhongming Zhao, Peilin Jia, T Scott Stroup, Diana Perkins, Joseph Patrick McEvoy, Jeffrey A Lieberman, Patrick F Sullivan, Edwin JCG van den Oord
发表日期
2011/3
期刊
Molecular psychiatry
卷号
16
期号
3
页码范围
321-332
出版商
Nature Publishing Group
简介
Understanding individual differences in the susceptibility to metabolic side effects as a response to antipsychotic therapy is essential to optimize the treatment of schizophrenia. Here, we perform genomewide association studies (GWAS) to search for genetic variation affecting the susceptibility to metabolic side effects. The analysis sample consisted of 738 schizophrenia patients, successfully genotyped for 492K single nucleotide polymorphisms (SNPs), from the genomic subsample of the Clinical Antipsychotic Trial of Intervention Effectiveness study. Outcomes included 12 indicators of metabolic side effects, quantifying antipsychotic-induced change in weight, blood lipids, glucose and hemoglobin A1c, blood pressure and heart rate. Our criterion for genomewide significance was a pre-specified threshold that ensures, on average, only 10% of the significant findings are false discoveries. A total of 21 SNPs satisfied …
引用总数
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