A study conducted by researchers at Columbia University’s Mailman School of Public Health and Harvard T.H. Chan School of Public Health reported elevated odds for attention deficit hyperactivity disorder (ADHD) in the grandchildren of users of diethylstilbestrol, a synthetic estrogen commonly known as DES prescribed between 1938 and 1971 to prevent pregnancy complications. This is the first study to provide evidence of the potential neurodevelopmental consequences of DES use across generations. The findings are published online in JAMA Pediatrics.
DES treatment for pregnant women was phased out after a 1953 study showed no benefit, and was banned in 1971 when DES was linked to vaginal adenocarcinomas in the daughters of women who had used DES during pregnancy. DES, which disrupts the body’s endocrine system, was later also linked to multiple other reproductive problems in DES daughters. Although the exact number of pregnant women that used DES is unknown, in the U.S. it is estimated to be between 5-10 million.
“Our aim was to explore the potential impact of DES use across generations, and specifically on third-generation neurodevelopment,” said Marianthi-Anna Kioumourtzoglou, ScD, assistant professor of Environmental Health Sciences at the Mailman School of Public Health. “To date, and to our knowledge, no epidemiologic study has assessed multigenerational impacts of DES—or any other endocrine disruptors—on neurodevelopment.”
The study was based on self-reported health information from 47,540 participants enrolled in the ongoing Nurses’ Health Study II, approximately 2 percent of whom had mothers who used DES while pregnant, as well as the 106,198 children born to nurses in the study.
Using DES was associated with 36 percent higher odds of ADHD among grandchildren of women who used DES compared to grandchildren women who did not use the drug during pregnancy. These results did not differ by the sex of the children.
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