TY - JOUR
T1 - Family History of Mental and Neurological Disorders and Risk of Autism
AU - Xie, Sherlly
AU - Karlsson, Håkan
AU - Dalman, Christina
AU - Widman, Linnea
AU - Rai, Dheeraj
AU - Gardner, Renee
AU - Magnusson, Cecilia
AU - Schendel, Diana
AU - Newschaffer, Craig J
AU - Lee, Brian
PY - 2019/3
Y1 - 2019/3
N2 - Importance
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.Objectives
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.Exposure
Mental and neurological diagnoses of relatives of the index persons.Main Outcomes and Measures
Diagnosis of ASD, with or without co-occurring ID, in the index persons.Results
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.Conclusions and Relevance
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.
AB - Importance
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.Objectives
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.Exposure
Mental and neurological diagnoses of relatives of the index persons.Main Outcomes and Measures
Diagnosis of ASD, with or without co-occurring ID, in the index persons.Results
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.Conclusions and Relevance
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.
U2 - 10.1001/jamanetworkopen.2019.0154
DO - 10.1001/jamanetworkopen.2019.0154
M3 - Article (Academic Journal)
C2 - 30821823
SN - 2574-3805
VL - 2
JO - JAMA Network Open
JF - JAMA Network Open
IS - 3
M1 - e190154
ER -