Patients with bipolar disorder showed an accelerated epigenetic aging compared to healthy controls.
Bipolar disorder may be associated with accelerated epigenetic aging, suggests a research team from The University of Texas Health Science Center at Houston (UTHealth). This could explain why persons with the disorder are more likely to have and die from age-related diseases. The study findings were published in Translational Psychiatry, a Nature Publishing Group journal. While chronological age is measured in the amount of time that a person has been alive, epigenetic age measures molecular markers of chemical modifications to DNA.
‘The cross-talk between the nucleus and the mitochondria might be underlying the premature aging in bipolar disorder.’
"Bipolar disorder has been previously associated with accelerated aging but the mechanisms are largely unknown," said Gabriel R. Fries, Ph.D., first author and post-doctoral research fellow in the Department of Psychiatry and Behavioral Sciences at McGovern Medical School at UTHealth. "We aimed to understand from our study the biology of what's driving the accelerated aging. What we found is that patients with bipolar disorder showed an accelerated epigenetic aging compared to healthy controls." The chemical modifications could be precipitated by the disorder itself or by poor lifestyle habits in diet, exercise, tobacco use and illegal substance use.
"Controlling these factors is just as important as taking medications," Fries said.
Senior author of the study was Joao L. de Quevedo, M.D., Ph.D., professor and director of the Translational Psychiatry Program in the Department of Psychiatry and Behavioral Sciences at McGovern Medical School.
Using blood samples, the researchers compared 22 patients with bipolar disorder, 16 siblings of bipolar patients and 20 healthy controls. They also found that while older bipolar disorder patients had significantly accelerated epigenetic aging compared to controls, no difference was found in younger patients.
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Along with the epigenetic clock, the study included two other biologic clocks: telomere length and mitochondrial DNA copy numbers.
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Source-Eurekalert