FKBP5基因型与中国地震幸存者ptsd -抑郁合并症状相关

Gen Li, Li Wang, Kunlin Zhang, Chengqi Cao, Xing Cao, Ruojiao Fang, Ping Liu, Shu Luo, Xiangyang Zhang
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引用次数: 8

摘要

背景:创伤后应激障碍(PTSD)和抑郁症是经历创伤性事件的个体常见的精神障碍。迄今为止,很少有研究研究创伤个体的遗传基础与表型异质性之间的关系。本研究检测了4个FKBP5 snp (rs1360780、rs3800373、rs9296158和rs9470080)在4个灾后组(低症状组、以抑郁为主组、以PTSD为主组和PTSD-抑郁联合症状组)中的作用。方法:共有1140名经历过2008年汶川地震的成年人参与了我们的研究。使用标准心理测量仪器测量地震相关创伤、创伤后应激障碍和抑郁症状。使用定制设计的2 × 48-Plex SNP scan™Kit对四个FKBP5 SNP进行基因分型。结果:经协变量调整后,PTSD-抑郁联合组与低症状组、抑郁为主组和PTSD为主组相比,rs9470080的主交互效应和基因-环境交互效应均显著。rs9470080 TT基因型携带者发生高并发PTSD和抑郁症状的风险高于C等位基因携带者。然而,当创伤暴露严重时,TT基因型携带者和C等位基因携带者在发生高并发PTSD和抑郁症状的风险方面没有差异。其他三个snp没有明显的影响。此外,发现rs3800373-rs9296158-rs1360780-rs9470080单倍型A-G-C-T与合并ptsd -抑郁症状显著相关。结论:我们的研究结果支持创伤暴露人群表型异质性的遗传基础。此外,研究结果还揭示了FKBP5基因变异可能与抑郁症- ptsd共病有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FKBP5 Genotype Linked to Combined PTSD-Depression Symptom in Chinese Earthquake Survivors
Background: Post-traumatic stress disorder (PTSD) and depression are common mental disorders in individuals experiencing traumatic events. To date, few studies have studied the relationship between genetic basis and phenotypic heterogeneity of traumatized individuals. The present study examined the effects of four FKBP5 SNPs (rs1360780, rs3800373, rs9296158, and rs9470080) in four postdisaster groups (low symptom, predominantly depressive, predominantly PTSD, and combined PTSD-depression symptom groups) as identified by latent profile analysis. Methods: A total of 1,140 adults who experienced the 2008 Wenchuan earthquake participated in our study. Earthquake-related trauma, PTSD, and depressive symptoms were measured using standard psychometric instruments. The four FKBP5 SNPs were genotyped using a custom-by-design 2 × 48-Plex SNP scan™ Kit. Results: After adjusting for covariates, the main and gene–environment interaction effects of rs9470080 were all significant when the combined PTSD-depression group was compared with the low symptoms, predominantly depression and predominantly PTSD groups. rs9470080 TT genotype carriers had a higher risk of developing high co-occurring PTSD and depression symptoms than the C allele carriers. However, when trauma exposure was severe, the TT genotype carriers and C allele carriers did not differ in the risk of developing high co-occurring PTSD and depressive symptoms. The other three SNPs demonstrated no significant effects. Moreover, the rs3800373-rs9296158-rs1360780-rs9470080 haplotype A-G-C-T was found significantly associated with combined PTSD-depression symptoms. Conclusion: Our findings support the genetic basis of phenotypic heterogeneity in people exposed to trauma. Furthermore, the results reveal the possibility that the variants of FKBP5 gene may be associated with depression-PTSD comorbidity.
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