Department of Psychiatry, School of Medicine, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.
Eur Arch Psychiatry Clin Neurosci. 2013 Mar;263(2):105-18. doi: 10.1007/s00406-012-0337-4. Epub 2012 Jul 3.
The serotonin 1A receptor gene (HTR1A) has been associated with mood disorders (MDs), including major depressive disorder (MDD) and bipolar disorder (BP). Therefore, we conducted a systematic review and meta-analysis between rs6295 (C-1019G) as well as rs878567 in HTR1A and MDs. Searching PubMed through May 2012, 15 studies, including our own, previously unpublished association study (135 MDD patients and 107 healthy controls), met inclusion criteria for the meta-analysis of rs6295 (4,297 MDs patients and 5,435 controls). Five association studies met criteria for the meta-analysis of rs878567 (2041MDs patients and 2,734 controls). rs6295 was associated with combined MDs (P allele model = 0.007 and P recessive model = 0.01). When divided by diagnostic subgroup (MDD = 3,119 patients and 4,380 controls or BP = 1,170 patients and 2,252 controls), rs6295 was associated with each MDs separately (MDD: P allele model = 0.006, P recessive model = 0.01; BP: P dominant model = 0.003). Likewise, rs878567 was associated with combined MDs (2,041 patients and 2,734 controls (P allele model = 0.0002, P dominant model = 0.0008, and P recessive model = 0.01). When divided by diagnostic subgroup (MDD = 1,013 patients and 1,728 controls or BP = 1,051 patients and 2,099 controls), rs878567 was associated with MDD (P allele model = 0.0007 and P dominant model = 0.01), while only one BP study had such data, precluding a meta-analysis. All of these significances survived correction for multiple comparisons. Results from this expanded meta-analysis, which included our own new study, suggest that rs6295 (C-1019G) and rs878567 in HTR1A are related to the pathophysiology of MDs, with overlap between MDD and BP. Findings provide additional clues to the underlying biology and treatment targets in MDs.
5-羟色胺 1A 受体基因(HTR1A)与心境障碍(MDs)有关,包括重性抑郁障碍(MDD)和双相障碍(BP)。因此,我们进行了一项系统综述和荟萃分析,以研究 HTR1A 中的 rs6295(C-1019G)和 rs878567 与 MDs 的关系。通过 2012 年 5 月之前的 PubMed 检索,有 15 项研究符合荟萃分析的纳入标准,其中包括我们自己的先前未发表的关联研究(135 例 MDD 患者和 107 例健康对照),以及 rs6295(4297 例 MDs 患者和 5435 例对照)。有 5 项关联研究符合 rs878567 的荟萃分析标准(2041 例 MDs 患者和 2734 例对照)。rs6295 与合并 MDs 相关(P 等位基因模型 P = 0.007,P 隐性模型 P = 0.01)。按诊断亚组(MDD = 3119 例患者和 4380 例对照或 BP = 1170 例患者和 2252 例对照)进一步分析,rs6295 与每个 MDs 分别相关(MDD:P 等位基因模型 P = 0.006,P 隐性模型 P = 0.01;BP:P 显性模型 P = 0.003)。同样,rs878567 与合并 MDs 相关(2041 例患者和 2734 例对照(P 等位基因模型 P = 0.0002,P 显性模型 P = 0.0008,P 隐性模型 P = 0.01)。按诊断亚组(MDD = 1013 例患者和 1728 例对照或 BP = 1051 例患者和 2099 例对照)进一步分析,rs878567 与 MDD 相关(P 等位基因模型 P = 0.0007,P 显性模型 P = 0.01),而只有一项 BP 研究有此类数据,因此无法进行荟萃分析。所有这些显著性均通过多重比较校正。此次扩大的荟萃分析结果,包括我们自己的新研究,表明 HTR1A 中的 rs6295(C-1019G)和 rs878567 与 MDs 的病理生理学有关,与 MDD 和 BP 重叠。这些发现为 MDs 的潜在生物学和治疗靶点提供了更多线索。