Brain Vascular Age Prediction Using Cerebral Blood Flow Velocity and Machine Learning Algorithms

TL;DR

This study develops a machine learning approach using transcranial Doppler features to estimate brain vascular age and identify accelerated aging in individuals with brain diseases.

Contribution

It introduces a novel method combining TCD-derived features and machine learning to assess cerebrovascular aging and disease-related age acceleration.

Findings

Healthy subjects' cerebrovascular age predicted to be 3.69 years above chronological age.

Subjects with brain diseases show varying levels of age acceleration.

Imbalanced datasets impact the accuracy of brain age prediction models.

Abstract

Defining vascular age in terms of physiological function has become one focal point of the extensive studies to categorize and track chronological age. Transcranial Doppler (TCD) is a method by which cerebral blood flow velocity is measured along the major arteries feeding the human brain. This study aims to use features extracted from TCD to estimate chronological age and assess accelerated aging in subjects with various brain diseases. We predict subjects with various brain diseases to present with accelerated cerebrovascular aging when tested on various regression models trained by healthy subjects. 168 healthy subjects and 277 diseased subjects with bilateral TCD recordings of the middle cerebral artery were analyzed using the Morphological Analysis and Clustering of Intracranial Pressure (MOCAIP) algorithm. MOCAIP-generated features and heart rate variability features were used as input features for regression models to predict the brain vascular age. 66 subjects with acute stroke, 27 subjects with post stroke, 26 subjects with Alzheimer's disease, 23 subjects with mild cognitive impairment, and 135 established subjects were tested against the machine learning model to assess for accelerated cerebrovascular age. The trained model, on average, predicted healthy subjects' cerebrovascular age to be 3.69 years above their chronological age. Subjects with different disease conditions exhibited varying levels of age acceleration. The differences in healthy and diseased subjects' performances suggest that features generated using TCD may be relevant when evaluating accelerated cerebrovascular aging. Moreover, imbalanced datasets have been observed to affect the performance of machine-learning-based brain age prediction models.