Protein associations and protein-metabolite interactions with depressive symptoms and the p-factor.

IF 6.2 1区 医学 Q1 PSYCHIATRY Translational Psychiatry Pub Date : 2025-04-06 DOI:10.1038/s41398-025-03362-y
Alyce M Whipp, Gabin Drouard, Richard J Rose, Lea Pulkkinen, Jaakko Kaprio
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Abstract

Despite increasing mental health problems among young people, few studies have examined associations between plasma proteins and mental health. Interactions between proteins and metabolites in association with mental health problems remain underexplored. In 730 twins, we quantified associations between plasma proteins measured at age 22 with 21 indicators of either depressive symptoms or the p-factor and tested for interactions with metabolites. Symptoms were collected from questionnaires and interviews completed by different raters (e.g., self-report, teachers) through adolescence to young adulthood (12 to 22 years). We found 47 proteins associated with depressive symptoms or the p-factor (FDR < 0.2), 9 being associated with both. Two proteins, contactin-1 and mast/stem cell growth factor receptor kit, positively interacted with valine levels in explaining p-factor variability. Our study demonstrates strong associations between plasma proteins and mental health and provides evidence for proteome-metabolome interactions in explaining higher levels of mental health problems.

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蛋白质关联和蛋白质代谢物与抑郁症状和p因子的相互作用。
尽管年轻人的心理健康问题越来越多,但很少有研究调查血浆蛋白和心理健康之间的关系。与心理健康问题相关的蛋白质和代谢物之间的相互作用仍未得到充分探讨。在730名双胞胎中,我们量化了22岁时血浆蛋白与抑郁症状或p因子的21项指标之间的关联,并测试了与代谢物的相互作用。症状收集自问卷调查和访谈,由不同的评分者(如自我报告,教师)完成,从青春期到青年期(12至22岁)。我们发现了47种与抑郁症状或p因子(FDR)相关的蛋白质
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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