Drexel University School of Public Health, Philadelphia, Pennsylvania.
Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
JAMA Netw Open. 2019 Mar 1;2(3):e190154. doi: 10.1001/jamanetworkopen.2019.0154.
Familial aggregation of mental and neurological disorders is often observed in autism spectrum disorders (ASD), but reports have generally focused on single disorders and are limited to first-degree relatives.
To examine family history of mental and neurological disorders among first- to fourth-degree relatives and risk of ASD with and without intellectual disability (ID) in index persons.
DESIGN, SETTING, AND PARTICIPANTS: In this population-based cohort study, 567 436 index persons were identified from the Stockholm Youth Cohort, an ongoing longitudinal register-linkage cohort study of the total population aged 0 to 17 years residing in Stockholm County, Sweden. Index persons were nonadopted singleton births born between 1984 and 2009 who were at least 2 years of age at the end of follow-up on December 31, 2011, had resided in Stockholm County for at least 2 years since birth, and could be linked to both biological parents. Data analysis was conducted from May 2017 to December 2018.
Mental and neurological diagnoses of relatives of the index persons.
Diagnosis of ASD, with or without co-occurring ID, in the index persons.
The cohort included 567 436 index persons (291 191 [51.3%] male; mean [SD] age at the end of follow-up, 14.3 [7.5] years). The prevalence of ASD with and without ID was 0.4% and 1.5%, respectively. Positive family history of mental and neurological disorders was associated with higher odds of ASD in index persons; 6895 (63.1%) of index persons with ASD had a parent with history of mental and/or neurological disorders, compared with 252 454 (45.4%) of index persons without ASD. Family history of multiple disorders was associated with higher odds of ASD in index persons, including history of ASD (odds ratio among first-degree relatives for ASD with and without ID: 14.2, 9.0), intellectual disability (7.6, 2.3), attention-deficit/hyperactivity disorder (3.3, 4.7), obsessive compulsive disorder (1.9, 2.1), schizophrenia and other nonaffective psychotic disorders (2.1, 1.8), depression (1.4, 2.0), bipolar disorder (1.4, 2.2), personality disorder (2.1, 2.6), cerebral palsy (2.2, 1.5), and epilepsy (2.0, 1.3). The more closely related the affected family member was, the higher the odds was of ASD for the index person. ASD without intellectual disability was associated with more disorders compared to ASD with intellectual disability. ASD with intellectual disability exhibited a weaker familial association with other mental disorder diagnoses but a stronger familial association with some neurological diagnoses as compared to ASD without intellectual disability.
This study suggests that family history of mental and neurological disorders is associated with increased risk of ASD. The familial component of ASD etiology may differ by presence or absence of co-occurring ID.
在自闭症谱系障碍(ASD)中,经常观察到精神和神经障碍的家族聚集,但报告通常集中在单一疾病上,并且仅限于一级亲属。
检查一级至四级亲属的精神和神经障碍家族史,以及索引个体中伴有和不伴有智力障碍(ID)的 ASD 的风险。
设计、设置和参与者:在这项基于人群的队列研究中,从斯德哥尔摩青年队列中确定了 567436 名索引个体,这是一项正在进行的、针对居住在瑞典斯德哥尔摩县的 0 至 17 岁全部人群的纵向登记-链接队列研究。索引个体是非收养的单胎出生,出生于 1984 年至 2009 年之间,在 2011 年 12 月 31 日随访结束时至少 2 岁,在出生后至少 2 年居住在斯德哥尔摩县,并可与亲生父母建立联系。数据分析于 2017 年 5 月至 2018 年 12 月进行。
索引个体亲属的精神和神经诊断。
索引个体的 ASD 诊断,伴有或不伴有共病 ID。
该队列包括 567436 名索引个体(291191 [51.3%] 为男性;随访结束时的平均[SD]年龄,14.3[7.5]岁)。ASD 伴或不伴 ID 的患病率分别为 0.4%和 1.5%。阳性精神和神经障碍家族史与索引个体 ASD 发病风险增加相关;在患有 ASD 的索引个体中,有 6895 名(63.1%)的父母有精神和/或神经障碍史,而在没有 ASD 的索引个体中,有 252454 名(45.4%)。家族史中多种疾病与索引个体 ASD 发病风险增加有关,包括 ASD 病史(一级亲属 ASD 伴或不伴 ID 的比值比:14.2、9.0)、智力障碍(7.6、2.3)、注意力缺陷/多动障碍(3.3、4.7)、强迫症(1.9、2.1)、精神分裂症和其他非情感性精神病障碍(2.1、1.8)、抑郁(1.4、2.0)、双相障碍(1.4、2.2)、人格障碍(2.1、2.6)、脑瘫(2.2、1.5)和癫痫(2.0、1.3)。受影响的家族成员越近,索引个体患 ASD 的可能性就越高。与智力障碍相关的 ASD 相比,无智力障碍的 ASD 与更多的疾病相关。与 ASD 伴智力障碍相比,ASD 不伴智力障碍与其他精神障碍诊断的家族关联性较弱,但与某些神经障碍诊断的家族关联性较强。
这项研究表明,精神和神经障碍的家族史与 ASD 风险增加有关。ASD 病因的家族成分可能因是否伴有共病 ID 而有所不同。