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The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment response

机译:国际SSRI药物基因组学联盟(ISPC):抗抑郁药治疗反应的全基因组关联研究

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摘要

Response to treatment with selective serotonin reuptake inhibitors (SSRIs) varies considerably between patients. The International SSRI Pharmacogenomics Consortium (ISPC) was formed with the primary goal of identifying genetic variation that may contribute to response to SSRI treatment of major depressive disorder. A genome-wide association study of 4-week treatment outcomes, measured using the 17-item Hamilton Rating Scale for Depression (HRSD-17), was performed using data from 865 subjects from seven sites. The primary outcomes were percent change in HRSD-17 score and response, defined as at least 50% reduction in HRSD-17. Data from two prior studies, the Pharmacogenomics Research Network Antidepressant Medication Pharmacogenomics Study (PGRN-AMPS) and the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study, were used for replication, and a meta-analysis of the three studies was performed (N=2394). Although many top association signals in the ISPC analysis map to interesting candidate genes, none were significant at the genome-wide level and the associations were not replicated using PGRN-AMPS and STAR*D data. Top association results in the meta-analysis of response included single-nucleotide polymorphisms (SNPs) in the HPRTP4 (hypoxanthine phosphoribosyltransferase pseudogene 4)/VSTM5 (V-set and transmembrane domain containing 5) region, which approached genome-wide significance (P=5.03E−08) and SNPs 5' upstream of the neuregulin-1 gene, NRG1 (P=1.20E−06). NRG1 is involved in many aspects of brain development, including neuronal maturation and variations in this gene have been shown to be associated with increased risk for mental disorders, particularly schizophrenia. Replication and functional studies of these findings are warranted.
机译:不同患者对选择性5-羟色胺再摄取抑制剂(SSRI)的治疗反应差异很大。成立国际SSRI药物基因组学协会(ISPC)的主要目标是确定可能对SSRI治疗重度抑郁症作出反应的遗传变异。使用来自七个地点的865名受试者的数据,使用17个项目的汉密尔顿抑郁量表(HRSD-17)进行了4周治疗结果的全基因组关联研究。主要结果是HRSD-17得分和反应的百分比变化,定义为HRSD-17降低至少50%。重复使用两项先前的研究数据:药物基因组学研究网络抗抑郁药物药物基因组学研究(PGRN-AMPS)和缓解抑郁症的测序治疗替代方案(STAR * D)研究,并对这三项研究进行了荟萃分析(N = 2394)。尽管ISPC分析中许多顶级关联信号都映射到有趣的候选基因,但在全基因组水平上都没有明显的关联,并且使用PGRN-AMPS和STAR * D数据也无法复制关联。最高关联性导致对响应的荟萃分析,其中包括HPRTP4(次黄嘌呤磷酸核糖转移酶假基因4)/ VSTM5(V集合和跨膜结构域包含5个)区域中的单核苷酸多态性(SNP),接近全基因组意义(P = 5.03E-08)和神经调节蛋白1基因NRG1上游的SNP 5'(P = 1.20E-06)。 NRG1参与大脑发育的许多方面,包括神经元成熟和该基因的变异与精神疾病,特别是精神分裂症的风险增加相关。必须对这些发现进行复制和功能研究。

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