A study led by Dr. Alan Brown, professor of epidemiology at Columbia University’s Mailman School of Public Health, reveals a new link between low levels of the thyroid hormone thyroxine during pregnancy and risk of schizophrenia in the offspring. Low levels of free thyroxine in pregnant women, referred to as hypothyroxinemia, are associated with abnormalities in cognitive development similar to those in schizophrenia, a neurodevelopmental disorder. Hypothyroxinemia is also associated with preterm birth, a risk factor for schizophrenia. Findings are published in Biological Psychiatry.
[Photo: Dr. Alan Brown]
To determine if hypothyroxinemia is associated with schizophrenia, Dr. Brown and colleagues examined thyroxine levels in archived serum samples from 1010 mothers of children with schizophrenia and 1010 matched control mothers. The sera were collected during the first and early second trimesters of pregnancy as part of the Finnish Maternity Cohort. Comprehensive Finnish registries of the population and psychiatric diagnoses provided information on case status (schizophrenia or control) among offspring of mothers corresponding to the prenatal serum samples.
The authors found that 12 percent of people with schizophrenia had a mother with hypothyroxinemia, compared with 9 percent of people without schizophrenia. The finding was statistically significant. This suggests that children of mothers with hypothyroxinemia during pregnancy have an increased odds of developing schizophrenia. The association remained even after adjusting for variables strongly related to schizophrenia such as maternal psychiatric history and smoking.
According to Dr. David Gyllenberg of the University of Turku and first author of the study, the importance of this paper is that it “links the finding to an extensive literature on maternal hypothyroxinemia during gestation altering offspring brain development.” Dr. Gyllenberg was a visiting scholar at Columbia University when much of the research was conducted.
Dr. Brown, who is also professor of Psychiatry Epidemiology at Columbia University Medical Center, and the New York State Psychiatric Institute, emphasized that “this work adds to a body of literature suggesting that maternal influences, both environmental and genetic, contribute to the risk of schizophrenia. Although replication in independent studies is required before firm conclusions can be drawn, the study was based on a national birth cohort with a large sample size, increasing the plausibility of the findings.”
This study did not address the cause of this association, but did find that adjusting for preterm birth lessened the association between hypothyroxinemia and schizophrenia, suggesting that preterm birth may mediate some of the increased risk.
The authors note in the paper that the finding may not be specific to schizophrenia, but could be a risk factor for other neurodevelopmental disorders as well, such as bipolar disorder, autism, and mental retardation. The finding is expected to stimulate further studies examining how hypothyroxinemia causes neurodevelopmental abnormalities and ultimately contributes to risk of mental illnesses that arise during development.
Dr. John Krystal, editor of Biological Psychiatry, thinks the association has clinical potential for reducing risk in the offspring of mothers with low thyroxine levels. “This study identifies a preventable potential contributor to the risk for schizophrenia. Maternal hypothyroidism can be easily diagnosed and effectively treated,” said Krystal, who is chairman of the department of psychiatry at the Yale University School of Medicine and chief of Psychiatry at Yale-New Haven Hospital.