Estimating Visceral Adiposity from Wrist-Worn Accelerometry

TL;DR

This study develops and compares machine learning models to estimate visceral adiposity using wrist-worn accelerometry data, revealing a strong link between physical activity patterns and VAT levels.

Contribution

It introduces novel deep learning and feature-based methods for non-invasively estimating visceral fat from accelerometry data, enhancing metabolic health risk assessment.

Findings

Deep neural networks achieved high correlation (r=0.86) with actual VAT measurements.

Combining feature-based and neural network approaches improved estimation accuracy.

Adding demographic and body measurements further enhanced model performance.

Abstract

Visceral adipose tissue (VAT) is a key marker of both metabolic health and habitual physical activity (PA). Excess VAT is highly correlated with type 2 diabetes and insulin resistance. The mechanistic basis for this pathophysiology relates to overloading the liver with fatty acids. VAT is also a highly labile fat depot, with increased turnover stimulated by catecholamines during exercise. VAT can be measured with sophisticated imaging technologies, but can also be inferred directly from PA. We tested this relationship using National Health and Nutrition Examination Survey (NHANES) data from 2011-2014, for individuals aged 20-60 years with 7 days of accelerometry data (n=2,456 men; 2,427 women) [1]. Two approaches were used for estimating VAT from activity. The first used engineered features based on movements during gait and sleep, and then ridge regression to map summary statistics of these features into a VAT estimate. The second approach used deep neural networks trained on 24 hours of continuous accelerometry. A foundation model first mapped each 10s frame into a high-dimensional feature vector. A transformer model then mapped each day's feature vector time series into a VAT estimate, which were averaged over multiple days. For both approaches, the most accurate estimates were obtained with the addition of covariate information about subject demographics and body measurements. The best performance was obtained by combining the two approaches, resulting in VAT estimates with correlations of r=0.86. These findings demonstrate a strong relationship between PA and VAT and, by extension, between PA and metabolic health risks.