2014
DOI: 10.1016/j.jpeds.2013.09.044
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Obstetric Risk Factors and Autism Spectrum Disorders in Finland

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Cited by 78 publications
(71 citation statements)
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“…[44] Furthermore, older mothers had a higher prevalence of chronic diseases, which also would lead to an increased risk of adverse birth outcomes. [43,45] These have been observed in serval previous studies, which demonstrated a high risk of obstetric complications among older mothers. [4345] …”
Section: Discussionmentioning
confidence: 74%
See 1 more Smart Citation
“…[44] Furthermore, older mothers had a higher prevalence of chronic diseases, which also would lead to an increased risk of adverse birth outcomes. [43,45] These have been observed in serval previous studies, which demonstrated a high risk of obstetric complications among older mothers. [4345] …”
Section: Discussionmentioning
confidence: 74%
“…[43,45] These have been observed in serval previous studies, which demonstrated a high risk of obstetric complications among older mothers. [4345] …”
Section: Discussionmentioning
confidence: 78%
“…Studies of population attributable fractions (PAFs) in US populations include an assessment of the Georgia Pregnancy Risk Assessment Monitoring System which estimated 42% of CP cases and 13% of ID cases were attributable to LBW [24], an assessment of North Dakota registry data which estimated 8% of ASD cases were attributable to low gestation and 8% were attributable to LBW [25], and an assessment of the Autism and Developmental Disabilities Monitoring Network which estimated 12% of ASD cases were attributable to PTB, LBW, and Cesarean delivery [26]. Studies from other countries of the impacts of various pregnancy complications and/or outcomes on ASD [27], ADHD [20], and developmental delays [28] reported moderate PAFs for the various perinatal factors studied. These past studies had notable limitations.…”
Section: Introductionmentioning
confidence: 99%
“…In a study of autism in the same Finnish birth cohort investigated in the present study, we showed accelerated growth of HC in autism cases at postnatal months 2–4, adjusting for growth velocity of height and weight (McKeague et al, 2015). We and other groups have shown that several early developmental risk factors (Abel et al, 2013; Brown et al, 2004; Lampi et al, 2013; Malaspina et al, 2001; Polo-Kantola et al, 2014; Reichenberg et al, 2006) are shared between the two disorders and certain copy number variants (Grayton et al, 2012) are also found at higher frequencies in both disorders. While schizophrenia is more often characterized as a disorder of reduced overall volume(s) of total brain and several specific brain regions, it is conceivable that disrupted cortical development due to overactive brain growth during the fetal and early postnatal period, a time during which rapid synapse development occurs, alters the trajectory of brain growth and connectivity (Gilmore et al, 2010).…”
Section: Discussionmentioning
confidence: 86%