The relationship between neighborhood disadvantage and the brain age gap

Abstract Background Accelerated aging is strongly linked to adverse social exposome and accelerated aging of the brain may be a dementia risk factor. Machine‐learning can estimate the biological “brain age” from neuroimages, which provides complementary information to the chronological/calendar age. The difference between biological and chronological age is referred to as the “brain age gap.” The Area Deprivation Index is a metric representing 17 indicators of neighborhood level poverty, education, employment, and physical environment, and provides a robust measure of the social exposome. The purpose of this work was to test the relationship between neighborhood‐level disadvantage and accelerated brain aging using brain age gap estimates in a Wisconsin cohort. Method Brain age was estimated using T1‐weighted MR images from 1052 participants enrolled in the Wisconsin Registry for Alzheimer’s Prevention or Wisconsin Alzheimer’s Disease Research Center studies. Brain age was estimated using a publicly available deep learning model called the two‐stage‐age‐network (TSAN) that was pre‐trained on >4000 scans from OASIS, ADNI‐I, and PAC‐2019 datasets. Average brain age was used when multiple images were available at the same time point. Participants’ addresses were geolinked to their statewide ranking of neighborhood disadvantage using a time‐concordant ADI. Participants were binned by quintile based on state ADI rank, where Quintile 5 comprised of participants with highest ADI (Table 1). In the analyses, Quintile 5 was compared to a grouped category of Quintiles 1‐4. A marginal means test was conducted on a fitted one‐way ANOVA model to assess differences in mean brain age gaps between Quintile 5 and Quintiles 1‐4. The ANOVA model used quintile as a fixed effect predictor variable of brain age gap and a random effect of participant ID to account for participants with multiple visits. Result The mean brain age gap for Quintile 5 was 0.96 years (‐0.79, 2.71), and for Quintiles 1‐4 was 0.27 years (‐0.12, 0.66) (Figure 1). Conclusion This analysis found that the mean brain age gap does not significantly differ between Quintile 5 and Quintiles 1‐4 (p≤0.45), however statistical power was low given very broad confidence intervals. Future work will test for longitudinal effects and incorporate a larger sample.

Authors

Institutions

Publication Details

Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.092973
Primary Topic
Urban Transport and Accessibility
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The relationship between neighborhood disadvantage and the brain age gap

Nagesh Adluru, Barbara B. Bendlin, W. Ryan Powell, Andrew L. Alexander et al.
Alzheimer s & Dementia
Urban Transport and Accessibility
article

The relationship between neighborhood disadvantage and the brain age gap

Nagesh Adluru, Barbara B. Bendlin, W. Ryan Powell, Andrew L. Alexander, Vivek Prabhakaran, Veena A. Nair, Amy Kind, Sanjay Asthana, Sterling C. Johnson, Yolana C Martin
article en

Abstract

Abstract Background Accelerated aging is strongly linked to adverse social exposome and accelerated aging of the brain may be a dementia risk factor. Machine‐learning can estimate the biological “brain age” from neuroimages, which provides complementary information to the chronological/calendar age. The difference between biological and chronological age is referred to as the “brain age gap.” The Area Deprivation Index is a metric representing 17 indicators of neighborhood level poverty, education, employment, and physical environment, and provides a robust measure of the social exposome. The purpose of this work was to test the relationship between neighborhood‐level disadvantage and accelerated brain aging using brain age gap estimates in a Wisconsin cohort. Method Brain age was estimated using T1‐weighted MR images from 1052 participants enrolled in the Wisconsin Registry for Alzheimer’s Prevention or Wisconsin Alzheimer’s Disease Research Center studies. Brain age was estimated using a publicly available deep learning model called the two‐stage‐age‐network (TSAN) that was pre‐trained on >4000 scans from OASIS, ADNI‐I, and PAC‐2019 datasets. Average brain age was used when multiple images were available at the same time point. Participants’ addresses were geolinked to their statewide ranking of neighborhood disadvantage using a time‐concordant ADI. Participants were binned by quintile based on state ADI rank, where Quintile 5 comprised of participants with highest ADI (Table 1). In the analyses, Quintile 5 was compared to a grouped category of Quintiles 1‐4. A marginal means test was conducted on a fitted one‐way ANOVA model to assess differences in mean brain age gaps between Quintile 5 and Quintiles 1‐4. The ANOVA model used quintile as a fixed effect predictor variable of brain age gap and a random effect of participant ID to account for participants with multiple visits. Result The mean brain age gap for Quintile 5 was 0.96 years (‐0.79, 2.71), and for Quintiles 1‐4 was 0.27 years (‐0.12, 0.66) (Figure 1). Conclusion This analysis found that the mean brain age gap does not significantly differ between Quintile 5 and Quintiles 1‐4 (p≤0.45), however statistical power was low given very broad confidence intervals. Future work will test for longitudinal effects and incorporate a larger sample.

Alzheimer s & DementiaVol. 20(S2)
University of Wisconsin–Madison (US)
Openalex Percentile: Top 77%
Urban Transport and Accessibility
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.