Cardiac Biomarkers, Subclinical Brain Vascular Changes, and Cognitive Decline: Post Hoc Analysis of the SPRINT Trial

Wenxin Zhang1, Simon B Ascher2,3, Sudipto Dolui4

  • 1Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

Insights

Subclinical cardiovascular disease in hypertensive adults is linked to faster cognitive decline and white matter lesions. Intensive blood pressure treatment did not alter this association, suggesting CVD impacts brain health independently.

Area of Science:

  • Cardiology
  • Neurology
  • Gerontology

Background:

  • Subclinical cardiovascular disease (CVD) and its impact on cognitive decline in hypertensive individuals are not fully understood.
  • The role of underlying brain pathologies and the effect of intensified blood pressure (BP) treatment on cognitive decline in this population remain unclear.

Purpose of the Study:

  • To investigate the association between subclinical CVD markers and cognitive decline in hypertensive adults.
  • To determine if intensive BP treatment influences cognitive decline in the presence of subclinical CVD.

Main Methods:

  • Post hoc analysis of the Systolic Blood Pressure Intervention Trial involving 2,733 participants.
  • Subclinical CVD identified by elevated high-sensitivity cardiac troponin T (hs-cTnT) and N-terminal pro-B-type natriuretic peptide (NT-proBNP).
  • Cognitive function assessed at baseline and follow-up; brain imaging (MRI) performed on a subset.

Main Results:

  • Elevated hs-cTnT and NT-proBNP were associated with accelerated cognitive decline across all domains.
  • Individuals with both elevated biomarkers exhibited the most rapid decline in global cognitive function.
  • Elevated biomarkers correlated with increased white matter lesions but not with changes in brain volume or blood flow.

Conclusions:

  • Subclinical CVD may accelerate cognitive decline and white matter lesion progression in hypertensive patients.
  • Intensive BP treatment did not mitigate the negative effects of subclinical CVD on cognitive function.
Abstract