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大屠杀创伤暴露导致 FKBP5 甲基化的代际效应。

Holocaust Exposure Induced Intergenerational Effects on FKBP5 Methylation.

机构信息

Traumatic Stress Studies Division, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York; Mental Health Care Center, PTSD Clinical Research Program & Laboratory of Clinical Neuroendocrinology and Neurochemistry, James J. Peters Veterans Affairs Medical Center, Bronx, New York.

Traumatic Stress Studies Division, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York; Mental Health Care Center, PTSD Clinical Research Program & Laboratory of Clinical Neuroendocrinology and Neurochemistry, James J. Peters Veterans Affairs Medical Center, Bronx, New York.

出版信息

Biol Psychiatry. 2016 Sep 1;80(5):372-80. doi: 10.1016/j.biopsych.2015.08.005. Epub 2015 Aug 12.

Abstract

BACKGROUND

The involvement of epigenetic mechanisms in intergenerational transmission of stress effects has been demonstrated in animals but not in humans.

METHODS

Cytosine methylation within the gene encoding for FK506 binding protein 5 (FKBP5) was measured in Holocaust survivors (n = 32), their adult offspring (n = 22), and demographically comparable parent (n = 8) and offspring (n = 9) control subjects, respectively. Cytosine-phosphate-guanine sites for analysis were chosen based on their spatial proximity to the intron 7 glucocorticoid response elements.

RESULTS

Holocaust exposure had an effect on FKBP5 methylation that was observed in exposed parents as well in their offspring. These effects were observed at bin 3/site 6. Interestingly, in Holocaust survivors, methylation at this site was higher in comparison with control subjects, whereas in Holocaust offspring, methylation was lower. Methylation levels for exposed parents and their offspring were significantly correlated. In contrast to the findings at bin 3/site 6, offspring methylation at bin 2/sites 3 to 5 was associated with childhood physical and sexual abuse in interaction with an FKBP5 risk allele previously associated with vulnerability to psychological consequences of childhood adversity. The findings suggest the possibility of site specificity to environmental influences, as sites in bins 3 and 2 were differentially associated with parental trauma and the offspring's own childhood trauma, respectively. FKBP5 methylation averaged across the three bins examined was associated with wake-up cortisol levels, indicating functional relevance of the methylation measures.

CONCLUSIONS

This is the first demonstration of an association of preconception parental trauma with epigenetic alterations that is evident in both exposed parent and offspring, providing potential insight into how severe psychophysiological trauma can have intergenerational effects.

摘要

背景

已在动物中证明,表观遗传机制参与了应激效应的代际传递,但在人类中尚未证明。

方法

分别在大屠杀幸存者(n=32)、其成年子女(n=22)以及在人口统计学上可比的父母(n=8)和子女(n=9)对照组中测量编码 FK506 结合蛋白 5(FKBP5)的基因中的胞嘧啶甲基化。选择分析的胞嘧啶-磷酸-鸟嘌呤位点基于它们与内含子 7 糖皮质激素反应元件的空间接近度。

结果

大屠杀暴露对 FKBP5 甲基化有影响,在暴露的父母及其子女中均观察到这种影响。这些影响在 bin3/site6 处观察到。有趣的是,在大屠杀幸存者中,与对照相比,该位点的甲基化水平更高,而在大屠杀后代中,甲基化水平较低。暴露父母及其后代的甲基化水平呈显著相关性。与 bin3/site6 的发现相反,在 bin2/sites3 到 5 处的后代甲基化与童年期身体和性虐待有关,与先前与童年逆境心理后果易感性相关的 FKBP5 风险等位基因相互作用。这些发现表明环境影响存在特定部位的可能性,因为 bin3 和 bin2 中的位点分别与父母创伤和后代自身的童年创伤相关。所检查的三个 bin 中平均的 FKBP5 甲基化与醒来时的皮质醇水平相关,表明了甲基化测量的功能相关性。

结论

这是首次证明,亲代创伤在暴露的父母和子女中都存在与表观遗传改变相关的关联,这为严重心理生理创伤如何产生代际影响提供了潜在的见解。

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