Davin Annalisa, Monti Maria Cristina, Polito Letizia, Vaccaro Roberta, Abbondanza Simona, Gnesi Marco, Villani Simona, Guaita Antonio
"Golgi Cenci" Foundation, Abbiategrasso, Italy.
Section of Biostatistics and Clinical Epidemiology, Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.
PLoS One. 2015 Nov 23;10(11):e0143395. doi: 10.1371/journal.pone.0143395. eCollection 2015.
Depression is common in the elderly. The role of genetic and environmental factors in modulating depressive symptoms is not clear.
We evaluated the influence of serotonin transporter gene polymorphisms and recent adverse life events on depressive symptoms in an elderly Italian population. We used data from "InveCe.Ab", a population-based study of 1321 subjects aged 70-74 years. We used the 15-item Geriatric Depression Scale (GDS) to assess depressive symptoms-a GDS score ≥5 points (GDS≥5) indicated the presence of clinically relevant symptoms-and performed 5-HTTLPR and rs25531 genotyping to obtain the triallelic polymorphism of the serotonin transporter. We used the Geriatric Adverse Life Events Scale to measure adverse life events, and logistic regression models to evaluate the role of genotype and recent adverse life events in depressive symptoms, controlling for potential confounders and independent predictors.
Two hundred subjects (15.76%) had a GDS≥5. The 5-HTTLPR triallelic polymorphism was significantly associated with GDS≥5. Only S'S' carriers showed an increased risk of depressive symptoms (ORadj = 1.81, p = .022); one extra adverse life event increased this risk by 14% (p = .061) independently of genotype. Other factors significantly related to GDS≥5 were: female gender (ORadj = 2.49, p < .001), age (ORadj = 1.19, p = .007), a history of depression (ORadj = 4.73, p < .001), and comorbidity (ORadj = 1.23, p = .001). One extra adverse life event increased the risk of depressive symptoms by 57% (p = .005) only in the L'L' carriers, while antidepressant intake was directly related to GDS≥5 in the L'S' carriers (ORadj = 2.46, p = .036) and borderline significant in the S'S' carriers (ORadj = 2.41, p = .081).
The S'S' genotype and recent exposure to adverse life events were independently associated with depressive symptoms. The S'S' genotype, compared with the environment, exerted a predominant effect on depressive symptoms, suggesting that it reduces the efficacy of antidepressant therapy. We conclude that genetics may be an important risk factor for depressive symptoms in late adulthood.
抑郁症在老年人中很常见。基因和环境因素在调节抑郁症状方面的作用尚不清楚。
我们评估了血清素转运体基因多态性和近期不良生活事件对意大利老年人群抑郁症状的影响。我们使用了来自“InveCe.Ab”的数据,这是一项基于人群的研究,涉及1321名70 - 74岁的受试者。我们使用15项老年抑郁量表(GDS)来评估抑郁症状——GDS得分≥5分(GDS≥5)表明存在临床相关症状——并进行5 - HTTLPR和rs25531基因分型以获得血清素转运体的三等位基因多态性。我们使用老年不良生活事件量表来测量不良生活事件,并使用逻辑回归模型来评估基因型和近期不良生活事件在抑郁症状中的作用,同时控制潜在的混杂因素和独立预测因素。
200名受试者(15.76%)的GDS≥5。5 - HTTLPR三等位基因多态性与GDS≥5显著相关。只有S'S'携带者出现抑郁症状的风险增加(校正后比值比 = 1.81,p = 0.022);每增加一次不良生活事件,无论基因型如何,该风险独立增加14%(p = 0.061)。与GDS≥5显著相关的其他因素包括:女性(校正后比值比 = 2.49,p < 0.001)、年龄(校正后比值比 = 1.19,p = 0.007)、抑郁症病史(校正后比值比 = 4.73,p < 0.001)和合并症(校正后比值比 = 1.23,p = 0.001)。仅在L'L'携带者中,每增加一次不良生活事件,抑郁症状风险增加57%(p = 0.005),而在L'S'携带者中,抗抑郁药的使用与GDS≥5直接相关(校正后比值比 = 2.46,p = 0.036),在S'S'携带者中接近显著(校正后比值比 = 2.41,p = 0.081)。
S'S'基因型和近期暴露于不良生活事件与抑郁症状独立相关。与环境相比,S'S'基因型对抑郁症状产生了主要影响,表明它降低了抗抑郁治疗的疗效。我们得出结论,基因可能是成年后期抑郁症状的一个重要风险因素。