Major adverse events in life such as divorce or death of a family member can accelerate aging in the brain of middle-aged men.

‘Midlife adverse fateful life events (FLEs), especially divorce or death of a family member is linked to advanced brain aging.’

Writing in the journal Neurobiology of Aging, a research team, led by senior author William S. Kremen, PhD, professor of psychiatry and co-director of the Center for Behavior Genetics of Aging at UC San Diego School of Medicine, found that major adverse events in life, such as divorce, separation, miscarriage or death of a family member or friend, can measurably accelerate agingin the brains of older men, even when controlling for such factors as cardiovascular risk , alcohol consumption, ethnicity and socioeconomic status, which are all associated with aging risk.




Specifically, they found that on average, one FLE was associated with an increase in predicted brain age difference (PBAD) of 0.37 years.
In other words, a single adverse event caused the brain to appear physiologically older by approximately one-third of a year than the person's chronological age, based upon magnetic resonance imaging (MRI).
The research team studied 359 men, ages 57 to 66 years old, participating in the Vietnam Era Twin Study of Aging (VETSA).
Scientists asked participants to tally a list of life-changing events over the past two years, which were compared to a similar measure collected five years previously when they joined VETSA. The summaries encapsulated stressful midlife events that had occurred in the first two and last two years of the past seven years.
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The MRIs assessed physiological aspects of the brain, such as volume and cortical thickness, a measure of the cerebral cortex or outer layer of the brain linked to consciousness, memory, attention, thought and other key elements of cognition. These neuroanatomical measurements were then analyzed using advanced software to predict brain age.
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Hatton said exposure to chronic stress has long been associated with biological weathering and premature aging, linked, for example, to oxidative and mitochondrial damage in cells, impaired immune system response and genomic changes.
The study's authors said their findings provide a possible link between molecular aging and brain structure changes in response to major stressful life events.
They do note that the study was a snapshot of a narrow demographic: older, predominantly white, males. It is not known whether females or other ethnicities would show similar findings.
The authors said additional, broader studies involving greater and more diverse numbers of participants were needed to further validate their findings.
But they suggest that using tools to predict brain age could be clinically useful in helping patients understand their brain health relative to their age and in clinical trials where it might improve study design and recruitment.
Source-Eurekalert