Molecular Imaging and Neuropathology Area, New York State Psychiatric Institute, New York, NY, USA; Department of Psychiatry, Columbia University Irving Medical Center, New York, NY, USA.
Molecular Imaging and Neuropathology Area, New York State Psychiatric Institute, New York, NY, USA; Mailman School of Public Health, Columbia University, New York, USA.
J Psychiatr Res. 2023 Jul;163:262-269. doi: 10.1016/j.jpsychires.2023.05.051. Epub 2023 May 16.
Mood disorders and suicidal behavior have moderate heritability and familial transmission, and are associated with smaller hippocampal volumes. However, it is unclear whether hippocampal alterations reflect heritable risk or epigenetic effects of childhood adversity, compensatory mechanisms, illness-related changes, or treatment effects. We sought to separate the relationships of hippocampal substructure volumes to mood disorder, suicidal behavior, and risk and resilience to both by examining high familial risk individuals (HR) who have passed the age of greatest risk for psychopathology onset. Structural brain imaging and hippocampal substructure segmentation quantified Cornu Ammonis (CA1-4), dentate gyrus, and subiculum gray matter volumes in healthy volunteers (HV, N = 25) and three groups with one or more relatives reporting early-onset mood disorder and suicide attempt: 1. Unaffected HR (N = 20); 2. HR with lifetime mood disorder and no suicide attempt (HR-MOOD, N = 25); and 3. HR with lifetime mood disorder and a previous suicide attempt (HR-MOOD + SA, N = 18). Findings were tested in an independent cohort not selected for family history (HV, N = 47; MOOD, N = 44; and MOOD + SA, N = 21). Lower CA3 volume was found in HR (vs. HV), consistent with the direction of previously published findings in MOOD+SA (vs. HV and MOOD), suggesting the finding reflects a familial biological risk marker, not illness or treatment-related sequelae, of suicidal behavior and mood disorder. Familial suicide risk may be mediated in part by smaller CA3 volume. The structure may serve as a risk indicator and therapeutic target for suicide prevention strategies in high-risk families.
心境障碍和自杀行为具有中度遗传性和家族性传递,与海马体体积较小有关。然而,目前尚不清楚海马体的改变是反映遗传性风险还是儿童逆境的表观遗传效应、代偿机制、与疾病相关的变化,还是治疗效果。我们试图通过检查已经过精神病理学发病最大风险年龄的高家族风险个体(HR),来分离海马亚结构体积与心境障碍、自杀行为以及对两者的风险和适应能力的关系。结构脑成像和海马亚结构分割定量了 Cornu Ammonis(CA1-4)、齿状回和下托灰质体积,研究对象包括健康志愿者(HV,N=25)和三个具有一个或多个报告早发性心境障碍和自杀企图的亲属的组:1. 未受影响的 HR(N=20);2. 有一生心境障碍但无自杀企图的 HR(HR-MOOD,N=25);3. 有一生心境障碍和既往自杀企图的 HR(HR-MOOD+SA,N=18)。在未选择家族史的独立队列中对发现结果进行了测试(HV,N=47;MOOD,N=44;和 MOOD+SA,N=21)。与 HV 相比,HR 的 CA3 体积较低,这与 MOOD+SA(与 HV 和 MOOD 相比)之前发表的发现方向一致,这表明该发现反映了自杀行为和心境障碍的家族生物学风险标志物,而不是疾病或治疗相关的后遗症。家族性自杀风险可能部分通过较小的 CA3 体积来介导。该结构可能作为高危家庭预防自杀策略的风险指标和治疗靶点。