Menzies Institute for Medical Research, Hobart, TAS, Australia.
Murdoch Children's Research Institute, Melbourne, VIC, Australia.
Mult Scler. 2019 May;25(6):848-855. doi: 10.1177/1352458518770021. Epub 2018 Apr 23.
In the general population, variation in the serotonin-transporter-linked polymorphic region ( 5-HTTLPR) has been shown to modify the association between stressful events and depression/anxiety. This has not been examined in people with multiple sclerosis (MS).
We examined the interaction between significant life events (SLE), 5-HTTLPR and depression/anxiety.
A population-based longitudinal cohort of 198 people with MS was followed biannually for 2.5 years. Depression and anxiety symptoms were measured at each review using the Hospital Anxiety and Depression Scale (HADS). SLEs were assessed using a questionnaire based on the Social Readjustment Rating Scale.
We found an interaction between SLE load in the previous 12 months and functional variation in the 5-HTTLPR allele type in predicting depression, with the association between SLE load and depression being stronger for those with S/S allele type (β = 0.21 (95% confidence interval (CI): 0.09-0.33) per 10-unit increase) and S/L (β = 0.14 (95% CI: 0.05-0.24)) compared to L/L allele type (β = 0.04 (95% CI: -0.05 to 0.24); p < 0.001). No convincing evidence of an interaction was found with anxiety.
We found that the association between SLE load and MS depression severity was stronger among those with one or two copies of the short allele of the 5-HTTLPR. The identification of a gene-environment interaction between SLEs and depression in a population where depression is partly disease-driven is novel.
在普通人群中,5-羟色胺转运体相关多态性区域(5-HTTLPR)的变异被证明可以调节应激事件与抑郁/焦虑之间的关系。这在多发性硬化症(MS)患者中尚未得到检验。
我们研究了重大生活事件(SLE)、5-HTTLPR 与抑郁/焦虑之间的相互作用。
对 198 名多发性硬化症患者进行了基于人群的纵向队列研究,随访时间为 2.5 年,每 6 个月进行一次评估。使用医院焦虑和抑郁量表(HADS)在每次评估时测量抑郁和焦虑症状。使用基于社会再适应评定量表的问卷评估 SLE。
我们发现,在过去 12 个月内 SLE 负荷与 5-HTTLPR 等位基因类型的功能变异之间存在交互作用,SLE 负荷与抑郁之间的相关性在 S/S 等位基因类型(β=0.21(95%置信区间(CI):0.09-0.33),每增加 10 个单位)和 S/L(β=0.14(95%CI:0.05-0.24))患者中比 L/L 等位基因类型(β=0.04(95%CI:-0.05 至 0.24))更强(p<0.001)。没有发现焦虑存在交互作用的证据。
我们发现,在 5-HTTLPR 短等位基因有一个或两个拷贝的患者中,SLE 负荷与多发性硬化症患者抑郁严重程度之间的关联更强。在部分由疾病驱动的人群中,发现 SLE 与抑郁之间存在基因-环境相互作用是新颖的。