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Maternal infection exacerbates genes’ effect on autism

by  /  23 February 2015
Julia Yellow

 

Children with too many or too few copies of certain genes are more likely to have autism, as are children born to women who battled a severe infection while pregnant. These seemingly disparate risk factors work together to worsen autism symptoms, suggests a new study1.

The study, published 27 January in the Journal of Developmental and Behavioral Pediatrics, is one of the first to look at the combined effects of genetic and environmental risk factors for autism.

“The interactions between genetics and exposure in the intrauterine environment sort of bump up the symptoms,” says lead researcher Raphael Bernier, associate professor of psychiatry and behavioral science at the University of Washington in Seattle.

Epidemiological studies indicate that having a serious infection while pregnant raises the risk of having a child with autism. Animal studies support this theory, showing that mimicking infection during pregnancy in rodents and monkeys can alter social behavior in their young2, 3. But only a small proportion of women who have infections during pregnancy have children with autism, suggesting that genetic factors are also at play.

Bernier and his colleagues sought to tease out these factors by looking closely at children with autism who have both risk factors: exposure to maternal infection, as well as at least one large duplication or deletion of DNA, known as a copy number variation, (CNV), linked to the disorder4.

They found that children with autism who have both risk factors have more severe symptoms, such as repetitive behaviors and social deficits, than children with autism who have only one or neither of the risk factors.

“Many studies suggest a role for both gene and environmental factors in autism risk,” says Elizabeth Thomas, associate professor of molecular and cellular neuroscience at The Scripps Research Institute in La Jolla, California, who was not involved in the study. “But to see real data supporting this hypothesis is exciting.”

Infection connection:

The finding comes on the heels of several epidemiological studies looking at maternal infection and autism risk. Last year, a study of more than 2 million people in Sweden found that having an infection during pregnancy raises the risk of having a child with autism by 37 percent5, and a 2012 study of nearly 100,000 Danish children found that a weeklong fever can triple the odds6.

To explore this further, the researchers looked at genetic data, detailed descriptions of autism symptoms and the mother’s history of infection or fever during pregnancy for 1,971 children with autism from the Simons Simplex Collection. (The collection contains data from families that have one child with autism and unaffected parents and siblings, and is funded by the Simons Foundation, SFARI.org’s parent organization.)

They found patterns showing how genes and environmental exposures can interact to affect specific facets of autism.

The parents filled out three assessments that evaluate patterns of repetitive behavior, social awareness, anxiety and social communication, among other measures. The children also took age-appropriate tests to assess verbal and nonverbal intelligence quotients (IQs) and adaptive functioning, a measure of how well they can handle day-to-day activities.

As expected, children with autism-associated CNVs score lower on measures of adaptive functioning and IQ. By contrast, children exposed to maternal infection but who don’t have any autism-linked CNVs show slightly more severe autism-related symptoms on one of the three tests. They also have no significant differences in cognitive ability compared with children who have neither risk factor.

The most significant effects emerge in children who have both risk factors: These children have more severe autism symptoms according to all three tests.

“We were surprised that the findings were specifically tied to autism symptomology and not just broader neurodevelopment,” says Bernier.

Access to the detailed genetic and clinical data allowed the researchers to parse the interaction of genetic and environmental risk factors in a way that previous epidemiological studies have not been able to do, says Brian Lee, assistant professor of epidemiology and biostatistics at Drexel University in Philadelphia, who was not involved in the study. “This is one of the few demonstrated examples in a human sample where [the gene-environment interaction] paradigm seems to be apparent,” says Lee.

These interactions may be involved in only a small proportion of autism cases. Of the 395 mothers who reported an infection or fever during pregnancy, 29 have children who carry an autism-linked CNV. This means only 1.5 percent of the 1,971 children in the study have both risk factors.

Researchers must explore exactly how exposure to maternal infection can affect genes in the developing brain. Several previous studies offer hints. For example, Thomas and her colleagues have shown that activating a pregnant mouse’s immune system produces inflammatory compounds in her pups. These compounds, called cytokines, can alter the expression of genes, including those involved in brain development and immune regulation7.

It’s possible that similar mechanisms are at work in people, says Alan S. Brown, professor of psychiatry and epidemiology at Columbia University, who was not involved in the study. Elevated levels of the cytokine interleukin-8 during pregnancy have been shown to alter the size of brain regions in people, for instance.

CNVs that affect immune-related genes might make some children more sensitive to their mother’s immune response. Alternatively, Brown says, “it is possible that the microbial infection, not the immune response, might alter brain development.”

In the meantime, Bernier’s team plans to look at the effect of maternal infection on children with a deletion in the chromosomal region 16p11.2 — one of the most common CNVs seen in people with autism. “This is the first foray,” Bernier says. “Both sides of the scale need to be further specified to get a clear answer.”

Correction: This article has been modified from the original. It has been changed to clarify that 1.5 percent of all the children in the study have both risk factors (a CNV and maternal infection).

References:

1. Mazina V. et al. J. Dev. Behav. Pediatr. 36, 61-67 (2015) PubMed

2. Schwartzer J.J. et al. Transl. Psychiatry 3, e240 (2013) PubMed

3. Machado C.J. et al. Biol. Psychiatry Epub ahead of print (2014) PubMed

4. Matsunami N. et al. PLoS One 8, e52239 (2013) PubMed

5. Lee B.K. et al. Brain Behav. Immun. 44, 100-105 (2015) PubMed

6. Atladóttir H.O. et al. Pediatrics 130, e1447-1454 (2012) PubMed

7. Tang B. et al. Brain Behav. Immun. 30, 168-175 (2013) PubMed

 


7 responses to “Maternal infection exacerbates genes’ effect on autism”

  1. RAJensen says:

    CNV’s in CCL3L1 has both risk and resistance properties. A lower copy number is associated with an increased risk of HIV-1 infection, while a higher copy number is associated with reduced risk for acquiring HIV-1. CCL3L1 resides in the 17q11.2 region. This region contains the serotonin transporter gene SLC6A4 an early identified autism candidate gene.
    Regardless of copy number variations HIV infection can only occur after exposure to the HIV-1 virus.
    http://www.ncbi.nlm.nih.gov/pubmed/21209899
    http://www.ncbi.nlm.nih.gov/pubmed/15995945

  2. Only the beginning says:

    Continuing on from RAJensen’s comment, it should be noted that 30-40% of HIV positive children (those who do not receive HAART antiviral therapy) develop symptoms that are absolutely identical to idiopathic autism, and often can be reversed or reduced through antiviral and immunomodulatory therapies.

    The genetic risk of developing NeuroAIDS (language impairments, lack of appropriate social interactions, restricted interests, repetitive actions… aka AUTISM) in those children seems to reside in variations of their immune-related genes, especially cytokine/chemokine receptors.

  3. Planet Autism says:

    I would be interested in the data on what constitutes a “severe” infection. Does flu count? Many women also suffer UTI’s during pregnancy, as we know, the body automatically lowers it’s immunity level to stop the pregnancy being identified as a foreign body.

    • Varvara Mazina says:

      In our study covered above, along with other research that has evaluated the risks associated with infection, the mechanism through which infection impacts development is the systemic response mounted to the pathogen. Specifically, we defined ‘severe’ infection in our study by evaluating parental report of symptoms associated with the illness: fever >101 degrees F, duration of infection, including the flu. Influenza and maternal fever due to any cause have both previously been found to be associated with increased risk of ASD.

      Regarding the note about UTIs, It is true that pregnant women are relatively immunosuppressed; for this reason women are routinely screened for even asymptomatic bacteria in the urine and treated aggressively, so as to prevent the many known complications of pyelonephritis for both the mother and the infant. The data demonstrating both the association of fever in pregnancy with ASD as well as the attenuation of those risks with treatment with antipyretic medication (http://www.ncbi.nlm.nih.gov/pubmed/22562209) give yet another reason for prompt treatment of infection in pregnancy.

      Varvara Mazina
      University of Washington School of Medicine

  4. Autism Parent says:

    My son has mild autism and his behaviors increase and subside day to day based on immune response to allergies, foods, bacteria, viruses. I was completely healthy during pregnancy except given antibiotics for strep B and rhogam. He was born via a scheduled c-section on time with fluid in his lungs and given vaccines while in the NICU. He’s 10 years old now and we manage his immune triggers. It’s a mysterious illness. I feel like his immune system was compromised in utero or when he lacked oxygen and given vax in the NICU. I wish someone could tell me and tell me how to repair his immune system. Chronic strep or high ASO, chronic mycoplasma, environmental allergies, dilated eyes, skin rashes, gastro problems, OCD, tics, foggy brained. But give him Enhansa, Advil, B Vitamins, Enzymes, Probiotics, Allegra….and all of it disappears for a day and his autism becomes almost nil, his eyes are normal, he’s communicative, OCD calms down. Band Aid Effect. (Anecdotal nonsense)

  5. Gertie says:

    My son with ASD has congenital Lyme Disease passed through me. I was a silent carrier. Treating the Lyme and bartonella infection is making the ASD go away. All food sensitivities are also gone on antibiotics. He has PANS/pandas and autoimmune encephalopathy. Everyone with an ASD child should test for Lyme via IgenX.

  6. Steph says:

    I had an operation for an ovarian cyst in the fifth month of pregnancy. My daughter now aged thirty seven, has always displayed autistic like behaviour. Is it likely that the operation was responsible for his? I was kept sedated for several days after the operation. I would be interested in any eplies. Thank you.

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