Center for Genomic Medicine, Massachusetts General Hospital, Boston.
Department of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston.
JAMA Psychiatry. 2022 Oct 1;79(10):971-980. doi: 10.1001/jamapsychiatry.2022.2379.
Suicide rates have been increasing among youth in the US. While the heritability of suicide risk is well established, there is limited understanding of how genetic risk is associated with suicidal thoughts and behaviors in young children.
To examine whether genetic susceptibility to suicide attempts (SAs) is associated with suicidal thoughts and behaviors in children.
DESIGN, SETTING, AND PARTICIPANTS: This case-control study examined data from the Adolescent Brain Cognitive Development (ABCD) study, a population-based longitudinal study of 11 878 US children enrolled at age 9 and 10 years from September 2016 to November 2018. Youth reports of suicidal ideation (SI) and SAs were obtained from the Kiddie Schedule for Affective Disorder and Schizophrenia at baseline and 2 subsequent years. After conservative quality control of genotype data, this analysis focused on 4344 unrelated individuals of European ancestry. Data analysis was conducted from November 2020 to February 2022.
Children's lifetime experiences of SI and SAs were assessed each year from ages 9 to 10 years to ages 11 to 12 years. Polygenic risk scores (PRSs) for SAs were calculated for ABCD study participants based on the largest genome-wide association study of SA cases and controls of European ancestry (total sample n = 518 612).
Of 4344 children of European ancestry (2045 [47.08%] female; mean [SD] age, 9.93 [0.62] years), significant associations were found between children's SA PRSs and their lifetime SAs with the most robust association in the follow-up year 2 (odds ratio, 1.43 [95% CI, 1.18-1.75]; corrected P = 1.85 × 10-3; Nagelkerke pseudo R2 = 1.51%). These associations remained significant after accounting for children's sociodemographic backgrounds, psychopathology symptoms, parental histories of suicide and mental health, and PRSs for major depression and attention-deficit/hyperactivity disorder (likelihood ratio test P < .05). Children's depressive mood and aggressive behavior were the most significant partial mediators of SA genetic risk on SAs (mediation analysis P < 1 × 10-16). Children's behavioral problems, such as attention problems, rule-breaking behavior, and social problems, also partially mediated the association of SA PRSs with SAs (mediation analysis false discover rate < 0.05).
This study's findings indicate that there may be genetic factors associated with SA risk across the life span and suggest behaviors and conditions through which the risk could be mediated in childhood. Further research is warranted to examine whether incorporating genetic data could improve the identification of children at risk for suicide.
美国青少年的自杀率一直在上升。虽然自杀风险的遗传性已得到充分证实,但人们对遗传风险如何与幼儿的自杀念头和行为相关知之甚少。
研究自杀尝试(SA)的遗传易感性是否与儿童的自杀念头和行为有关。
设计、地点和参与者:这项病例对照研究分析了青少年大脑认知发展(ABCD)研究的数据,该研究是一项基于人群的纵向研究,于 2016 年 9 月至 2018 年 11 月招募了美国 11878 名 9 岁和 10 岁的儿童。基线和随后的 2 年中,通过儿童情绪障碍和精神分裂症时间表(Kiddie Schedule for Affective Disorder and Schizophrenia)获得青少年自杀意念(SI)和 SA 的报告。在对基因型数据进行严格的质量控制后,本分析重点关注了 4344 名无亲缘关系的欧洲血统个体。数据分析于 2020 年 11 月至 2022 年 2 月进行。
从 9 岁到 10 岁到 11 岁到 12 岁,每年评估儿童的 SI 和 SA 终生经历。根据最大的欧洲血统 SA 病例和对照的全基因组关联研究(总样本 n=518612),为 ABCD 研究参与者计算了 SA 的多基因风险评分(PRS)。
在 4344 名欧洲血统的儿童中(2045[47.08%]名女性;平均[SD]年龄,9.93[0.62]岁),发现儿童 SA PRS 与他们的 SA 终生经历之间存在显著关联,在随访年 2 中关联最为显著(优势比,1.43[95%CI,1.18-1.75];校正 P=1.85×10-3;Nagelkerke 伪 R2=1.51%)。在考虑了儿童的社会人口背景、精神病理学症状、自杀和精神健康的父母病史以及主要抑郁和注意缺陷多动障碍的 PRS 后,这些关联仍然显著(似然比检验 P < 0.05)。儿童的抑郁情绪和攻击行为是 SA 遗传风险对 SA 的最显著部分中介(中介分析 P < 1×10-16)。儿童的行为问题,如注意力问题、违反规则行为和社交问题,也部分中介了 SA PRS 与 SA 之间的关联(中介分析错误发现率 < 0.05)。
本研究的结果表明,可能存在与整个生命周期 SA 风险相关的遗传因素,并表明通过儿童时期的行为和条件可以进行中介。需要进一步研究以检验纳入遗传数据是否可以提高识别自杀风险儿童的能力。