Are neuropsychiatric symptoms a marker of small vessel disease progression in older adults? Evidence from the Lothian Birth Cohort 1936.

Abstract

Neuropsychiatric symptoms could form part of an early cerebral small vessel disease prodrome that is detectable before stroke or dementia onset. We aimed to identify whether apathy, depression, anxiety, and subjective memory complaints associate with longitudinal white matter hyperintensity (WMH) progression. Community-dwelling older adults from the observational Lothian Birth Cohort 1936 attended three visits at mean ages 73, 76, and 79years, repeating MRI, Mini-Mental State Examination, neuropsychiatric (Dimensional Apathy Scale, Hospital Anxiety and Depression Scale), and subjective memory symptoms. We ran regression and mixed-effects models for symptoms and normalised WMH volumes (cube root of WMH:ICV×10). At age 73, 76, and 79, m=672, n=476, and n=382 participants attended MRI respectively. Worse apathy at age 79 was associated with WMH volume increase (β=0.27, p=0.04) in the preceding 6years. A 1SD increase in apathy score at age 79 associated with a 0.17 increase in WMH (β=0.17 normalised WMH percent ICV, p=0.009). In apathy subscales, executive (β=0.13, p=0.05) and emotional (β=0.13, p=0.04) scores associated with increasing WMH more than initiation scores (β=0.11, p=0.08). Increasing WMH also associated with age (β=0.40, p=0.002) but not higher depression (β=-0.01, p=0.78), anxiety (β=0.05, p=0.13) scores, or subjective memory complaints (β=1.12, p=0.75). Apathy independently associates with preceding longitudinal WMH progression, while depression, anxiety, and subjective memory complaints do not. Patients with apathy should be considered for enrolment to small vessel disease trials.