The risks for major psychiatric disorders in the siblings of probands with major depressive disorder

IF 9.6 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Psychiatry Pub Date : 2024-07-07 DOI:10.1038/s41380-024-02650-1
Sang Jin Rhee, Linda Abrahamsson, Jan Sundquist, Kristina Sundquist, Kenneth S. Kendler
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Abstract

Using a case-controlled study including siblings of major depression (MD) and control probands, born 1970–1990 and followed through 2018, we sought to clarify the degree to which the familial liability to MD is reflected in its clinical features, and the pattern of psychiatric disorders at elevated risk in the siblings of MD probands. The study population included full-siblings of 197,309 MD and matched 197,309 control probands. The proband-sibling tetrachoric correlation of for MD was +0.20. Both linear and quadratic effects of younger AAO and number of episodes significantly increased the risk of MD in siblings. Male sex, anxiety disorder, alcohol use disorder (AUD), inpatient treatment, psychotic symptoms, severity, and antidepressant prescription in MD probands increased the risk of MD in siblings. Cox proportional hazard models (hazard ratios, 95% CI) revealed a significantly increased risk of attention deficit hyperactivity disorder (1.82, 1.76–1.88), generalized anxiety disorder (1.79, 1.74–1.85), bipolar disorder (1.78, 1.70–1.85), MD (1.74, 1.72–1.76), obsessive-compulsive disorder (1.72, 1.65–1.80), phobic anxiety disorder (1.71, 1.65–1.76), and panic disorder (1.68, 1.64–1.72) in MD co-siblings. The HRs for AUD (1.64, 1.60–1.68), post-traumatic stress disorder (1.62, 1.59–1.66) were modestly lower, and the lowest was seen for schizophrenia (1.42, 1.30–1.54). The overall pattern of increased risk of these disorders was similar in reared-apart half-siblings and cousins of MD probands. Our findings suggest that MD is familial, and a range of important clinical factors predict its familial liability. The familial liability to MD, mostly due to genetic factors, is shared with a broad range of psychiatric disorders.

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重度抑郁障碍患者兄弟姐妹罹患重性精神病的风险
通过一项病例对照研究(包括 1970-1990 年出生并随访至 2018 年的重度抑郁症(MD)疑似患者和对照疑似患者的兄弟姐妹),我们试图弄清重度抑郁症的家族责任在其临床特征中的反映程度,以及重度抑郁症疑似患者兄弟姐妹中风险升高的精神疾病的模式。研究对象包括 197,309 名 MD 疑似者的同胞兄弟姐妹和 197,309 名匹配的对照疑似者。多发性硬化症的概率-同胞四项相关性为+0.20。年龄较小的 AAO 和发作次数的线性和二次效应都会显著增加兄弟姐妹患 MD 的风险。男性性别、焦虑症、酒精使用障碍(AUD)、住院治疗、精神病性症状、严重程度以及MD探查者的抗抑郁药处方都会增加兄弟姐妹患MD的风险。Cox 比例危险模型(危险比,95% CI)显示,注意力缺陷多动障碍(1.82,1.76-1.88)、广泛性焦虑症(1.79,1.74-1.85)、双相情感障碍(1.79,1.76-1.88)、多动障碍(1.82,1.76-1.88)、躁郁症(1.79,1.74-1.85)的风险显著增加。85)、双相情感障碍(1.78,1.70-1.85)、多发性硬化症(1.74,1.72-1.76)、强迫症(1.72,1.65-1.80)、恐惧症(1.71,1.65-1.76)和惊恐障碍(1.68,1.64-1.72)。AUD(1.64,1.60-1.68)和创伤后应激障碍(1.62,1.59-1.66)的HR值略低,精神分裂症的HR值最低(1.42,1.30-1.54)。这些疾病风险增加的总体模式在与 MD 疑似患者同父异母的兄弟姐妹和表兄弟姐妹中相似。我们的研究结果表明,MD 具有家族性,一系列重要的临床因素可预测其家族性。多发性硬化症的家族遗传倾向主要是由遗传因素造成的,这与多种精神疾病的家族遗传倾向相同。
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来源期刊
Molecular Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
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