Daniels Teresa E, Hjelm Brooke E, Lewis-de Los Angeles William W, Smith Eric, Omidsalar Audrey A, Rollins Brandi L, Sherman Anna, Parade Stephanie, Vawter Marquis P, Tyrka Audrey R
Initiative on Stress, Trauma, and Resilience, Department of Psychiatry and Human Behavior, Warren Alpert Medical School, Brown University, Providence, Rhode Island.
Mood Disorders Research Program and Laboratory for Clinical and Translational Neuroscience, Butler Hospital, Providence, Rhode Island.
Biol Psychiatry Glob Open Sci. 2024 Nov 26;5(2):100422. doi: 10.1016/j.bpsgos.2024.100422. eCollection 2025 Mar.
Mounting evidence suggests that mitochondria respond to psychosocial stress. Recent studies suggest mitochondrial DNA (mtDNA) deletions may be increased in some psychiatric disorders, but no studies have examined early-life stress (ELS) and mtDNA deletions. In this study, we assessed mtDNA deletions in peripheral blood mononuclear cells of medically healthy young adults with and without ELS.
Participants ( = 181; 69% female), ages 18 to 40 years, were recruited from the community. Participants with ELS ( = 108) had moderate to severe childhood maltreatment; 83 also had parental loss, and 59 had psychiatric disorders. Participants in the control group ( = 73) had no maltreatment, parental loss, or psychiatric disorders. Standardized interviews and self-report measures assessed demographic variables, stress, and mental health. mtDNA from peripheral blood mononuclear cells was amplified via long-range polymerase chain reaction; mtDNA deletions were quantified via Seq-Well, next-generation sequencing, and the Splice-Break pipeline. Linear regression models were used to assess relationships of mtDNA deletion metrics with ELS, adult stressors, psychiatric disorders, and demographics.
Participants with ELS had significantly greater rates of unique mtDNA deletion breakpoints per 10,000 coverage than participants without ELS ( < .001), correcting for age, sex, and sequencing depth. Cumulative mtDNA deletion read percentage was not significantly different between groups. Psychiatric disorders and adult stressors were associated with greater unique mtDNA deletion breakpoints (s < .05) but did not account for associations of ELS with mtDNA deletions.
The increased number of unique mtDNA deletion breakpoints in participants with ELS suggests that mitochondrial genomes undergo observable alterations in the context of early stress. Future studies will examine mtDNA deletions with metabolic health measures.
越来越多的证据表明线粒体对心理社会压力有反应。最近的研究表明,线粒体DNA(mtDNA)缺失在某些精神疾病中可能会增加,但尚无研究探讨早期生活压力(ELS)与mtDNA缺失之间的关系。在本研究中,我们评估了有或没有ELS的医学健康年轻成年人外周血单核细胞中的mtDNA缺失情况。
从社区招募了年龄在18至40岁之间的参与者(n = 181;69%为女性)。有ELS的参与者(n = 108)经历过中度至重度童年虐待;83人还经历过父母丧亡,59人患有精神疾病。对照组的参与者(n = 73)没有遭受过虐待、父母丧亡或精神疾病。通过标准化访谈和自我报告测量来评估人口统计学变量、压力和心理健康状况。通过长程聚合酶链反应扩增外周血单核细胞中的mtDNA;通过Seq-Well、下一代测序和Splice-Break管道对mtDNA缺失进行定量。使用线性回归模型评估mtDNA缺失指标与ELS、成人应激源、精神疾病和人口统计学之间的关系。
校正年龄、性别和测序深度后,有ELS的参与者每10,000覆盖度的独特mtDNA缺失断点率显著高于没有ELS的参与者(P < .001)。两组之间的累积mtDNA缺失读数百分比没有显著差异。精神疾病和成人应激源与更多的独特mtDNA缺失断点相关(P < .05),但不能解释ELS与mtDNA缺失之间的关联。
有ELS的参与者中独特mtDNA缺失断点数量增加,表明线粒体基因组在早期压力的背景下发生了可观察到的改变。未来的研究将探讨mtDNA缺失与代谢健康指标之间的关系。