New research that involved the examination of thousands of genes from nearly 150 human brains shows the circadian rhythm of gene activity changes with aging.
The findings from researchers at the University of Pittsburgh School of Medicine suggest that a biological clock begins ticking in the older brain.
A 24-hour circadian rhythm controls nearly all brain and body processes, such as the sleep/wake cycle, metabolism, alertness and cognition, explained senior investigator Colleen McClung, Ph.D., associate professor of psychiatry, Pitt School of Medicine.
“Studies have reported that older adults tend to perform complex cognitive tasks better in the morning and get worse through the day,” McClung said. “We know also that the circadian rhythm changes with aging, leading to awakening earlier in the morning, fewer hours of sleep and less robust body temperature rhythms.”
In addition, the presence of gene changes or “molecular aging” in the brain had been previously shown by senior co-investigator Etienne Sibille, Ph.D., formerly a professor of psychiatry at Pitt School of Medicine and now the Campbell Family Chair in Clinical Neuroscience at the Centre for Addiction and Mental Health at the University of Toronto.
For the new study, researchers at both schools decided to look at the effects of normal aging on molecular rhythms in the prefrontal cortex, an area of the brain involved in learning, memory, and other aspects of cognitive performance.
Researchers examined brain samples from 146 people with no history of mental health or neurological problems whose families had donated their remains for medical research and for whom the time of death was known.
They categorized the brains depending on whether they had come from a person younger than 40 or older than 60, and used a newly developed statistical technique to analyze two tissue samples from the prefrontal cortex for rhythmic activity, or expression, of thousands of genes.
Using the information they had about the time of death, they identified 235 core genes that make up the molecular clock in this part of the brain.
“As we expected, younger people had that daily rhythm in all the classic ‘clock’ genes,” McClung said. “But there was a loss of rhythm in many of these genes in older people, which might explain some of the alterations that occur in sleep, cognition, and mood in later life.”
To their surprise, the researchers also found a set of genes that gained rhythmicity in older individuals.
This information could ultimately be useful in the development of treatments for cognitive and sleep problems that can occur with aging, as well as a possible treatment for “sundowning,” a condition in which older individuals with dementia become agitated, confused and anxious in the evening, the researchers said.
“Since depression is associated with accelerated molecular aging, and with disruptions in daily routines, these results also may shed light on molecular changes occurring in adults with depression,” said Sibille.
The researchers next plan to explore the function of the brain’s circadian-rhythm genes in lab and animal models, as well as see if they are altered in people who have psychiatric or neurological illnesses.
The study was published in the Proceedings of the National Academy of Sciences.