UC Davis study confirms link between advanced maternal age and autism
February 12, 2010
By Phyllis Brown
Advanced maternal age is linked to a significantly elevated risk of having a child with autism, regardless of the father’s age, according to an exhaustive study of all births in California in the 1990s. The study by the UC Davis Health System found that advanced paternal age is associated with elevated autism risk only when the father is older and the mother is under 30.
“Independent and Dependent Contributions of Advanced Maternal and Paternal Ages to Autism Risk,” published online Feb. 8 by the journal Autism Research, is one of the largest population-based studies to quantify how each parent's age — separately and together — affects the risk of having a child with autism
The study found that the incremental risk of having a child with autism increased by 18 percent for every five-year increase in the mother’s age. A 40-year-old woman’s risk of having a child later diagnosed with autism was 50 percent greater than that of a woman from 25 to 29 years old.
Advanced parental age is a known risk factor for having a child with autism. However, previous research has shown contradictory results regarding whether the mother, the father—or both—contribute most to the increased risk of autism. For example, one study reported that fathers over 40 were six times more likely than fathers under 30 to have a child with autism.
“This study challenges a current theory in autism epidemiology that identifies the father’s age as a key factor in increasing the risk of having a child with autism,” said Janie Shelton, the study’s lead author and a doctoral student in the Department of Public Health Sciences.
“It shows that while maternal age consistently increases the risk of autism, the father's age only contributes an increased risk when the father is older and the mother is under 30 years old. Among mothers over 30, increases in the father's age do not appear to further increase the risk of autism.”
Autism is a pervasive developmental disorder of deficits in social skills and communication, as well as repetitive and restricted behaviors, with onset occurring prior to age 3. Abnormal brain development, probably beginning in the womb, is known to be fundamental to the behaviors that characterize autism.
Estimates place the incidence of autism at between 1 in 100 and 1 in 110 children in the United States.
During the 1990s, the number of California women over 40 giving birth increased by more than 300 percent. But only about 5 percent of the 600-percent increase in the number of autism cases in the state can be attributed to women waiting longer to have children, the study suggests.
To conduct their investigation, the researchers obtained the electronic records for all births in California from Jan. 1, 1990, to Dec. 31, 1999. The records incorporated detailed demographic information, including the ages of both parents. The researchers obtained electronic records identifying the children who had received autism diagnoses from the state Department of Developmental Services. In this study, autism was defined as a diagnosis of full-syndrome autism at a California Regional Center.
The researchers excluded a small number of births for which demographic information about parents, such as their ages and levels of education, was not available. Instances of multiple births were analyzed separately. The exclusions brought the total size of the study sample to approximately 4.9 million births and 12,159 cases of autism.
For older mothers, the step-wise progression in the risk of having a child who later would be diagnosed with autism was apparent among every age group of fathers. When the father was older and the mother was younger — under 30 — the child’s risk for developing autism also was elevated.
For example, among births to mothers under 25, children fathered by a man over 40 were twice as likely to develop autism as those whose father was between 25 and 29. Among mothers over 30, the increased risk associated with older fathers dissipated, the study found.
Because of the large study size, the researchers were able to show how risk for autism was affected by each parent's age. They did this by holding one parent's age constant and then comparing autism incidence across the age of the other parent across five-year increments.
The subtle interaction of how each parent's age affects the risk of autism then became quantifiable, even when the risk was reliant on the other parent's age.
This methodology is more efficacious and requires fewer assumptions than the mathematical modeling used by earlier studies, the researchers said.
The researchers note that understanding the relationship between increased parental age and autism risk is critical to understanding its biological causes. Earlier studies have observed that advanced maternal age is a risk factor for a variety of other birth-related conditions, including infertility, early fetal loss, low birth-weight, chromosomal aberrations and congenital anomalies.
The study's senior author, Irva Hertz-Picciotto, professor of public health sciences and a researcher at the UC Davis MIND Institute, said the reason why having an older parent places a child at risk for autism is not known.
"We still need to figure out what it is about older parents that puts their children at greater risk for autism and other adverse outcomes, so that we can begin to design interventions," Hertz-Picciotto said.
One possible clue comes from a 2008 UC Davis study that found that some mothers of children with autism had antibodies to fetal brain protein, while none of the mothers of typical children did. Advancing age has been associated with an increase in autoantibody production.
Further work investigating advancing age in such findings may be useful, the study authors said.
They added that some persistent environmental chemicals accumulate in the body and also may have a role to play in autism, possibly contributing to the apparent effect of parental age.
The study also suggests that epigenetic changes over time “may enable an older parent to transfer a multitude of molecular functional alterations to a child. ... Thus, epigenetics may be involved in the risks contributed by advancing parental age as a result of changes induced by stresses from environmental chemicals, co-morbidity or assistive reproductive therapy.”
Daniel Tancredi, an assistant professor in the Department of Pediatrics , also contributed to this study.
Funding came from a grant from the National Institute of Environmental Health Sciences; a U.S. Environmental Protection Agency Science to Achieve Results (STAR) grant; the UC Davis School of Medicine; and the Office of Graduate Studies.
Phyllis Brown is a senior public information representative for the UC Davis Health System.
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