Children with autism spectrum disorder (ASD) were more than twice as likely to have been exposed in utero to preeclampsia, and the likelihood of an autism diagnosis was even greater if the mother experienced more severe disease, a large study by researchers with the UC Davis MIND Institute has found.
Women with preeclampsia experience hypertension during the latter half of their pregnancies, and may have increased levels of protein in their urine and edema, or fluid retention. Preeclampsia can develop into eclampsia, a life-threatening condition in which seizures may occur.
The study was conducted in more than 1,000 children between the ages of two and three years enrolled in the Childhood Risks of Autism from Genetics and the Environment (CHARGE) Study in Northern California. It is published online today in JAMA Pediatrics.
“We found significant associations between preeclampsia and ASD that increased with severity. We also observed a significant association between severe preeclampsia and developmental delay,” said Cheryl Walker, study senior author, assistant professor, Department of Obstetrics and Gynecology Division of Maternal Fetal Medicine and a researcher affiliated with the UC Davis MIND Institute.
While preeclampsia has previously been examined as a risk factor for autism, the literature has been inconsistent. The current study provides a robust population-based, case-controlled examination of the association between autism and preeclampsia and whether risk was associated with preeclampsia severity.
The research was conducted in more than 500 male and female children diagnosed with autism; nearly 200 diagnosed with developmental delay; and 350 children who were developing typically. All of the mothers had confirmed diagnoses of preeclampsia.
It found that the mothers of children with autism were more than twice as likely to have had pregnancies complicated by preeclampsia. Mothers of children with autism and children with developmental delay also were significantly more likely to have had placental insufficiency, severe preeclampsia or both, when compared to the mothers of children who were developing typically. The children with autism of mothers with preeclampsia also were more likely to be cognitively lower functioning.
The large, population-based study also found a correlation between preeclampsia and developmental delay without autism, primarily in instances involving placental insufficiency.
Preeclampsia during mother’s pregnancy associated with greater autism risk
There are several mechanisms by which preeclampsia may affect the developing brain, Walker said.
For the fetus, limitations in nutrient and oxygen availability cause progressive oxidative stress which prompt the release of proteins into the maternal bloodstream in an effort to improve circulation.
“The level of detail obtained by the CHARGE Study on predictors, confounders, and outcomes enabled a comprehensive exploration of this topic,” Walker said. “While single studies cannot establish causality, the cumulative evidence supports efforts to reduce preeclampsia and diminish severity, to improve neonatal outcomes.”
About this autism research
Other study authors include Paula Krakowiak, Alice Baker, Robin Hansen, Sally Ozonoff, all of UC Davis and the UC Davis MIND Institute.
The study was funded by grants from the National Institute of Environmental Health Sciences P01 ES11269, R01 ES 015359, the Eunice Kennedy Shriver National Institute of Child Health and Human Development 1U54 HD079125, the U.S. Environmental Protection Agency through Science to Achieve Results (STAR) Program R829388 and R833292 and the UC Davis MIND Institute.
Contact: Phyllis Brown – UC Davis Source:UC Davis press release Image Source: The image is credited to Greyerbaby and is in the public domain Video Source: The video is available at the UC Davis Health System YouTube page Original Research:Abstract for “Preeclampsia and Autism” by Cheryl K. Walker, MD; Paula Krakowiak, PhD; Alice Baker, MPH; Robin L. Hansen, MD2,4; Sally Ozonoff, PhD; and Irva Hertz-Picciotto, PhD in JAMA Pediatrics. Published online December 8 2014 doi:10.1001/jamapediatrics.2014.2645