Accelerated brain aging predicts impulsivity and symptom severity in depression

• Published in: Neuropsychopharmacology (New York, N.Y.) Vol. 46; no. 5; pp. 911 - 919
• Main Authors: Dunlop, Katharine, Victoria, Lindsay W., Downar, Jonathan, Gunning, Faith M., Liston, Conor
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 01.04.2021; Springer International Publishing
• Subjects: Adult; Age; Aging; Bipolar disorder; Brain - diagnostic imaging; Child, Preschool; Cognitive ability; Depression; Depressive Disorder, Major; Humans; Impulsive Behavior; Impulsivity; Life span; Magnetic fields; Magnetic Resonance Imaging; Male; Mental depression; Neural networks; Neuroimaging; Placebos; Prefrontal cortex; Structure-function relationships; Transcranial magnetic stimulation
• ISSN: 0893-133X; 1740-634X; 1740-634X
• DOI: 10.1038/s41386-021-00967-x

Multiple structural and functional neuroimaging measures vary over the course of the lifespan and can be used to predict chronological age. Accelerated brain aging, as quantified by deviations in the MRI-based predicted age with respect to chronological age, is associated with risk for neurodegenerative conditions, bipolar disorder, and mortality. Whether age-related changes in resting-state functional connectivity are accelerated in major depressive disorder (MDD) is unknown, and, if so, it is unclear if these changes contribute to specific cognitive weaknesses that often occur in MDD. Here, we delineated age-related functional connectivity changes in a large sample of normal control subjects and tested whether brain aging is accelerated in MDD. Furthermore, we tested whether accelerated brain aging predicts individual differences in cognitive function. We trained a support vector regression model predicting age using resting-state functional connectivity in 710 healthy adults aged 18-89. We applied this model trained on normal aging subjects to a sample of actively depressed MDD participants (n = 109). The difference between predicted brain age and chronological age was 2.11 years greater (p = 0.015) in MDD patients compared to control participants. An older MDD brain age was significantly associated with increased impulsivity and, in males, increased depressive severity. Unexpectedly, accelerated brain aging was also associated with increased placebo response in a sham-controlled trial of high-frequency repetitive transcranial magnetic stimulation targeting the dorsomedial prefrontal cortex. Our results indicate that MDD is associated with accelerated brain aging, and that accelerated aging is selectively associated with greater impulsivity and depression severity.