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首页> 外文期刊>Philosophical Transactions of the Royal Society of London, Series B. Biological Sciences >Using the high-risk family design to identify biomarkers for major depression
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Using the high-risk family design to identify biomarkers for major depression

机译:使用高风险家庭设计识别严重抑郁症的生物标志物

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摘要

The familial nature of major depressive disorder (MDD) is now well recognized.We followed children and grandchildren of probands with and without MDD to examine transmission of depression over generations, and to identify early vulnerability markers prior to the onset of disease. The study now includes three generations and five completed assessment waves spanning 25 years, with a sixth wave underway. Beginning with the fourth wave, we collected measures of brain structure (magnetic resonance imaging, MRI) and physiology (electroencephalography, EEG) and DNA in order to examine at a biological level why the offspring of depressed parents were at higher risk. In this paper, we provide an overview of the study design, the main findings, including new data, and the role of the high-risk design in translational research. We demonstrate that offspring of depressed parents ('high-risk'), when compared with those of non-depressed parents ('low-risk'), were at increased risk for depressive and anxiety disorders, with anxiety appearing earlier and being a predisposing factor for MDD. Offspring with two generations previously affected were at greatest risk. Thinning of the cortical mantle (MRI) and reduced resting-state activity (EEG) within the right parieto-temporal hemisphere differentiated high- from low-risk offspring, egardless of whether the offspring had MDD, suggesting that these measures might serve as familial trait markers for depression and related syndromes. The high- and low-risk offspring also differed by serotonin transporter promoter length polymorphism genotypes, even though the same genotypes were not associated with the presence of MDD. The high-risk epidemiological design appears to be a particularly valuable asset in translational research as it allows targeting of biological processes that emerge prior to the onset of disease, and identifies individuals at high risk for the disorder who may carry the trait or marker but not yet be affected.
机译:现在已经充分认识到了严重抑郁症(MDD)的家族性质,我们追踪了患有和不患有MDD的先证者的子女,以检查抑郁症在几代人中的传播情况,并在疾病发作之前确定早期的易感性标志物。现在的研究包括三代人和五个完成了25年的评估浪潮,正在进行第六次浪潮。从第四波开始,我们收集了大脑结构(磁共振成像,MRI)和生理学(脑电图,EEG)和DNA的量度,以便从生物学的角度检查为什么沮丧的父母的后代有更高的风险。在本文中,我们概述了研究设计,主要发现(包括新数据)以及高风险设计在翻译研究中的作用。我们证明,与没有抑郁的父母相比,抑郁的父母(“高风险”)的后代患抑郁症和焦虑症的风险增加,焦虑出现的时间较早且易患MDD的因素。先前受影响的两代后代的风险最高。右顶颞半球内的皮层变薄(MRI)和静息状态活动(EEG)降低,区分了高风险和低风险的后代,无论后代是否患有MDD,表明这些措施可能是家族性抑郁症和相关综合症的标志物。高风险和低风险的后代也具有5-羟色胺转运蛋白启动子长度多态性基因型的差异,即使相同的基因型与MDD的存在无关。高风险的流行病学设计似乎是转化研究中特别有价值的资产,因为它可以针对疾病发作之前出现的生物学过程,并识别出可能携带该性状或标志物但无此特征的高危人群尚未受到影响。

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