کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
335777 547025 2014 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Linking genetic variants of the mineralocorticoid receptor and negative memory bias: Interaction with prior life adversity
ترجمه فارسی عنوان
پیوند دادن انواع ژنتیکی گیرنده کانالکورتیکوئید و تعصب حافظه منفی: درگیری با پیشداوریهای زندگی گذشته
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی علوم غدد
چکیده انگلیسی

SummarySubstantial research has been conducted investigating the association between life adversity and genetic vulnerability for depression, but clear mechanistic links are rarely identified and investigation often focused on single genetic variants. Complex phenotypes like depression, however, are likely determined by multiple variants in interaction with environmental factors. As variations in the mineralocorticoid receptor gene (NR3C2) have been related to a higher risk for depression, we investigated whether NR3C2 variance is related to negative memory bias, an established endophenotype for depression, in healthy participants. Furthermore, we explored the influence of life adversity on this association.We used a set-based analysis to simultaneously test all measured variation in NR3C2 for an association with negative memory bias in 483 participants and an interaction with life adversity. To further specify this interaction, we split the sample into low and high live adversity groups and repeated the analyses in both groups separately.NR3C2 variance was associated with negative memory bias, especially in the high life adversity group. Additionally, we identified a functional polymorphism (rs5534) related to negative memory bias and demonstrating a gene × life adversity interaction.Variations in NR3C2 are associated with negative memory bias and this relationship appears to be influenced by life adversity. As negative memory bias is implicated in the susceptibility to depression, our findings provide mechanistic support for the notion that variations in NR3C2 – which could compromise the proper function of this receptor – are a risk factor for the development of mood disorders.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Psychoneuroendocrinology - Volume 40, February 2014, Pages 181–190
نویسندگان
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