述情障碍与维生素D水平降低有关,但与维生素D结合蛋白基因多态性无关。

IF 1.5 4区 医学 Q4 GENETICS & HEREDITY
Jan Terock, Anke Hannemann, Antoine Weihs, Deborah Janowitz, Hans J Grabe
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引用次数: 2

摘要

目的:述情障碍是一种以难以识别和描述情绪为特征的人格特征,与各种精神障碍有关,包括抑郁症和创伤后应激障碍(PTSD)。其发病机制尚不完全清楚,但先前的研究表明,遗传和代谢因素也参与其中。然而,到目前为止,还没有关于维生素D的作用以及维生素D结合蛋白(VDBP)的多态性rs4588和rs7041的结果发表。方法:在波美拉尼亚健康研究(SHIP)的两个普通人群样本(总n=5733)中测量血清总25(OH)D水平。多伦多述情障碍量表-20(TAS-20)用于述情障碍的测量。研究参与者进行了rs4588和rs7041的基因分型。对性别、年龄、腰围、体力活动、季节和研究进行了线性和逻辑回归分析,并在适用的情况下对一批基因分型和前三个遗传主成分进行了调整。在敏感性分析中,对模型进行了额外的抑郁症状调整。结果:25(OH)D水平与TAS-20评分(β=-0.002;P<0.001)和述情障碍呈负相关,根据TAS-20>60的共同界限(β=-0.103;P=0.001)。这些结果在调整抑郁症状后保持稳定。测试的遗传多态性与述情障碍没有显著相关性。结论:我们的研究结果表明,低维生素D水平可能与述情障碍的病理生理学有关。鉴于未观察到述情障碍与rs4588以及rs7041之间的关联,表明述情障碍受试者的行为或营养特征也可以解释这种关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alexithymia is associated with reduced vitamin D levels, but not polymorphisms of the vitamin D binding-protein gene.

Objective: Alexithymia is a personality trait characterized by difficulties in identifying and describing emotions, which is associated with various psychiatric disorders, including depression and posttraumatic stress disorder (PTSD). Its pathogenesis is incompletely understood but previous studies suggested that genetic as well as metabolic factors, are involved. However, no results on the role of vitamin D and the polymorphisms rs4588 and rs7041 of the vitamin D binding protein (VDBP) have been published so far.

Methods: Serum levels of total 25(OH)D were measured in two general-population samples (total n = 5733) of the Study of Health in Pomerania (SHIP). The Toronto Alexithymia Scale-20 (TAS-20) was applied to measure alexithymia. Study participants were genotyped for rs4588 and rs7041. Linear and logistic regression analyses adjusted for sex, age, waist circumference, physical activity, season and study and, when applicable, for the batch of genotyping and the first three genetic principal components, were performed. In sensitivity analyses, the models were additionally adjusted for depressive symptoms.

Results: 25(OH)D levels were negatively associated with TAS-20 scores (β = -0.002; P < 0.001) and alexithymia according to the common cutoff of TAS-20>60 (β = -0.103; P < 0.001). These results remained stable after adjusting for depressive symptoms. The tested genetic polymorphisms were not significantly associated with alexithymia.

Conclusions: Our results suggest that low vitamin D levels may be involved in the pathophysiology of alexithymia. Given that no associations between alexithymia and rs4588 as well as rs7041 were observed, indicates that behavioral or nutritional features of alexithymic subjects could also explain this association.

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来源期刊
Psychiatric Genetics
Psychiatric Genetics 医学-神经科学
CiteScore
2.30
自引率
0.00%
发文量
39
审稿时长
3 months
期刊介绍: ​​​​​​The journal aims to publish papers which bring together clinical observations, psychological and behavioural abnormalities and genetic data. All papers are fully refereed. Psychiatric Genetics is also a forum for reporting new approaches to genetic research in psychiatry and neurology utilizing novel techniques or methodologies. Psychiatric Genetics publishes original Research Reports dealing with inherited factors involved in psychiatric and neurological disorders. This encompasses gene localization and chromosome markers, changes in neuronal gene expression related to psychiatric disease, linkage genetics analyses, family, twin and adoption studies, and genetically based animal models of neuropsychiatric disease. The journal covers areas such as molecular neurobiology and molecular genetics relevant to mental illness. Reviews of the literature and Commentaries in areas of current interest will be considered for publication. Reviews and Commentaries in areas outside psychiatric genetics, but of interest and importance to Psychiatric Genetics, will also be considered. Psychiatric Genetics also publishes Book Reviews, Brief Reports and Conference Reports.
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