Biernacka J M, Sangkuhl K, Jenkins G, Whaley R M, Barman P, Batzler A, Altman R B, Arolt V, Brockmöller J, Chen C H, Domschke K, Hall-Flavin D K, Hong C J, Illi A, Ji Y, Kampman O, Kinoshita T, Leinonen E, Liou Y J, Mushiroda T, Nonen S, Skime M K, Wang L, Baune B T, Kato M, Liu Y L, Praphanphoj V, Stingl J C, Tsai S J, Kubo M, Klein T E, Weinshilboum R
1] Department of Psychiatry and Psychology, Mayo Clinic, Rochester, MN, USA [2] Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
Department of Genetics, Stanford University, Stanford, CA, USA.
Transl Psychiatry. 2015 Apr 21;5(4):e553. doi: 10.1038/tp.2015.47.
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 (STARD) 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 STARD data. The top association result in the meta-analysis of response represents 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.
患者对选择性5-羟色胺再摄取抑制剂(SSRI)治疗的反应差异很大。国际SSRI药物基因组学联盟(ISPC)成立的主要目标是识别可能影响重度抑郁症患者对SSRI治疗反应的基因变异。使用来自7个研究点的865名受试者的数据,开展了一项全基因组关联研究,以评估4周治疗效果,采用17项汉密尔顿抑郁量表(HRSD-17)进行测量。主要疗效指标为HRSD-17评分的变化百分比及反应情况,反应定义为HRSD-17评分至少降低50%。两项既往研究的数据,即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)和缓解抑郁的序贯治疗替代方案(STARD)研究,用于重复验证,并对这三项研究进行了荟萃分析(N=2394)。尽管ISPC分析中的许多顶级关联信号映射到了有趣的候选基因,但在全基因组水平上均无显著意义,且这些关联在使用PGRN-AMPS和STARD数据时未得到重复验证。荟萃分析中反应的顶级关联结果代表神经调节蛋白-1基因(NRG1)5′上游的单核苷酸多态性(SNP)(P = 1.20E - 06)。NRG1参与大脑发育的多个方面,包括神经元成熟,并且该基因的变异已被证明与精神障碍风险增加有关,尤其是精神分裂症。有必要对这些发现进行重复验证和功能研究。