Yin Li, Zhang Xu, Huang Yi, Sun XueLi
Department of Psychiatry, West China Hospital of Sichuan University, Chengdu, Sichuan Province, China.
Sichuan Forensic Expertise Center in Southwest China, Chengdu, Sichuan Province, China.
Asia Pac Psychiatry. 2016 Jun;8(2):109-17. doi: 10.1111/appy.12180. Epub 2015 Apr 8.
Genes that regulate the catecholamine metabolism pathways are potential targets for research in the antidepressant treatment response. This study was intended to determine whether antidepressant responses to selective serotonin reuptake inhibitors (SSRIs) are associated with genetic polymorphisms of the tyrosine or tryptophan gene in Chinese major depressive disorder (MDD) patients.
A total of 290 MDD patients were recruited and received a 6-week SSRIs randomized double-blinded treatment. Allele, genotype, and haplotype frequencies were compared between responders and nonresponders in catecholamine genes.
Genotype frequency of the rs1800544 polymorphism in the DRD4 gene was significantly different between responders and nonresponders after false discovery rate correction (P = 0.042). The frequency of the DRD4 rs1800544 CG genotype was significantly higher (P = 0.003) in responders (51.4%) than in nonresponders (35.8%), and patients with the CG genotype showed an 81.7% response rate. In comparison, the response rates were 73.9% and 52.2% in patients with the GG genotype and the CC genotype, respectively. The frequencies of the DRD4 rs1800544 CC and GG genotypes were significantly lower (P = 0.003) in responders (7.7%, 40.9%) than in the nonresponders (19.4%, 44.8%). No significant difference was found between two groups either in genotype or allele frequencies of single nucleotide polymorphisms in the TPH, SLC6A2, SLC6A3, or DRD2 genes. No significant difference was found between two groups in TPH, SLC6A2, SLC6A3, DRD2, orDRD4 gene haplotypes.
Polymorphisms of the DRD4 gene appear to be associated with SSRI treatment response in Chinese MDD patients.
调节儿茶酚胺代谢途径的基因是抗抑郁治疗反应研究的潜在靶点。本研究旨在确定中国重度抑郁症(MDD)患者对选择性5-羟色胺再摄取抑制剂(SSRI)的抗抑郁反应是否与酪氨酸或色氨酸基因的遗传多态性相关。
共招募290例MDD患者,接受为期6周的SSRI随机双盲治疗。比较儿茶酚胺基因中反应者和无反应者之间的等位基因、基因型和单倍型频率。
经错误发现率校正后,反应者和无反应者之间DRD4基因rs1800544多态性的基因型频率存在显著差异(P = 0.042)。反应者(51.4%)中DRD4 rs1800544 CG基因型的频率显著高于无反应者(35.8%)(P = 0.003),CG基因型患者的反应率为81.7%。相比之下,GG基因型和CC基因型患者的反应率分别为73.9%和52.2%。反应者(7.7%,40.9%)中DRD4 rs1800544 CC和GG基因型的频率显著低于无反应者(19.4%,44.8%)(P = 0.003)。在TPH、SLC6A2、SLC6A3或DRD2基因的单核苷酸多态性的基因型或等位基因频率方面,两组之间未发现显著差异。在TPH、SLC6A2、SLC6A3、DRD2或DRD4基因单倍型方面,两组之间未发现显著差异。
DRD4基因多态性似乎与中国MDD患者的SSRI治疗反应相关。