OBJECTIVE:Converging lines of evidence implicate vascular factors in late-life depression, and argue that late-life depression is a distinct entity among the mood disorders. The A1166C polymorphism in the angiotensin II receptor, vascular type 1 (AGTR1) gene has been associated with a range of vascular diseases. This study investigated the association of AGTR1 genotype on 18-month treatment outcome in late-life depression. METHODS:In a large, prospective cohort study, patients with late-life depression received individualized treatment using a standardized algorithm. The authors genotyped participants at the AGTR1 A1166C single nucleotide polymorphism (SNP) using standardized methodology, then used survival analysis to estimate the impact of A1166C and demographic variables on time to remission during 18 months of follow-up. RESULTS:The hazard ratio for AGTR1 homozygous C/C status was 0.37. The A1166C SNP showed evidence for genotypic and allelic association in a comparison of remitted and unremitted/censored subjects. CONCLUSION:Consistent with its association with numerous vascular disorders, AGTR1 is associated with treatment outcome in late-life depression. Further studies are needed to replicate this finding, and to investigate the impact of other genetic markers of vascular disease on late-life depression outcome.

译文

目的:越来越多的证据暗示血管因素与晚发性抑郁症有关,并认为晚发性抑郁症是情绪障碍中的一个独特实体。血管紧张素II受体1型血管(AGTR1)基因的A1166C多态性与一系列血管疾病有关。这项研究调查了AGTR1基因型与晚期抑郁症18个月治疗结局的关系。
方法:在一项大型前瞻性队列研究中,患有晚期抑郁症的患者使用标准化算法接受了个性化治疗。作者使用标准化方法对AGTR1 A1166C单核苷酸多态性(SNP)的参与者进行了基因分型,然后使用生存分析来评估18个月随访期间A1166C和人口统计学变量对缓解时间的影响。
结果:AGTR1纯合C / C状态的危险比为0.37。 A1166C SNP在对缓解和未缓解/检查对象的比较中显示了基因型和等位基因关联的证据。
结论:AGTR1与许多血管疾病有关,与晚期抑郁症的治疗结果有关。需要进一步的研究来重复这一发现,并调查其他血管疾病的遗传标志物对晚期抑郁症结局的影响。

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