<scp>DXA</scp> ‐Measured Visceral Adipose Tissue and Accelerated Biological Aging in Middle‐Aged Adults

OBJECTIVE: Obesity, particularly excess visceral adipose tissue (VAT), may accelerate biological aging; however, few studies have examined this in middle-aged adults. We investigated associations between dual-energy X-ray absorptiometry (DXA)-derived VAT and two biomarkers of biological aging-phenotypic age acceleration (PhenoAgeAccel) and leukocyte telomere length (LTL)-in 4799 participants (2614 females, aged 45-69 years) from the Busselton Healthy Ageing Study. METHODS: Whole-body DXA (GE Lunar) quantified VAT mass. Phenotypic age was estimated from chronological age and nine biomarkers. In a subsample of 1221 participants, LTL was measured as the telomeric DNA to single-copy gene (T/S) ratio. Sex-stratified linear regressions assessed associations, adjusting for chronological age and lifestyle factors. RESULTS: Mean ± SD VAT mass was 1677 ± 873 g in males and 882 ± 598 g in females. Higher VAT was associated with greater PhenoAgeAccel in both sexes; each 1-SD increase in VAT corresponds to 1.397 (95% CI 1.197, 1.596) and 1.919 (1.738, 2.099) years higher PhenoAgeAccel in males and females, respectively. In females only, higher VAT was associated with shorter LTL (-0.041 [-0.069, -0.013] per 1 SD). Associations mostly remained significant after adjustment for anthropometric and other DXA-derived adiposity measures. CONCLUSIONS: VAT may represent a specific marker of accelerated biological aging, independent of lifestyle and adiposity measures.

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Publication Details

Journal
Obesity
Published
2026-06-28
DOI
https://doi.org/10.1002/oby.70239
Primary Topic
Telomeres, Telomerase, and Senescence
Type
article
Field-Weighted Citation Impact
0.00

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article

DXA ‐Measured Visceral Adipose Tissue and Accelerated Biological Aging in Middle‐Aged Adults

Jennie Hui, Chrianna Bharat, Kevin Murray, Michael Hunter et al.
Obesity
Telomeres, Telomerase, and Senescence
article

DXA ‐Measured Visceral Adipose Tissue and Accelerated Biological Aging in Middle‐Aged Adults

Jennie Hui, Chrianna Bharat, Kevin Murray, Michael Hunter, Kun Zhu, John Walsh, Gillian Arscott, Riorden O'Shea
article en

Abstract

OBJECTIVE: Obesity, particularly excess visceral adipose tissue (VAT), may accelerate biological aging; however, few studies have examined this in middle-aged adults. We investigated associations between dual-energy X-ray absorptiometry (DXA)-derived VAT and two biomarkers of biological aging-phenotypic age acceleration (PhenoAgeAccel) and leukocyte telomere length (LTL)-in 4799 participants (2614 females, aged 45-69 years) from the Busselton Healthy Ageing Study. METHODS: Whole-body DXA (GE Lunar) quantified VAT mass. Phenotypic age was estimated from chronological age and nine biomarkers. In a subsample of 1221 participants, LTL was measured as the telomeric DNA to single-copy gene (T/S) ratio. Sex-stratified linear regressions assessed associations, adjusting for chronological age and lifestyle factors. RESULTS: Mean ± SD VAT mass was 1677 ± 873 g in males and 882 ± 598 g in females. Higher VAT was associated with greater PhenoAgeAccel in both sexes; each 1-SD increase in VAT corresponds to 1.397 (95% CI 1.197, 1.596) and 1.919 (1.738, 2.099) years higher PhenoAgeAccel in males and females, respectively. In females only, higher VAT was associated with shorter LTL (-0.041 [-0.069, -0.013] per 1 SD). Associations mostly remained significant after adjustment for anthropometric and other DXA-derived adiposity measures. CONCLUSIONS: VAT may represent a specific marker of accelerated biological aging, independent of lifestyle and adiposity measures.

Obesity
The University of Western Australia (AU), Sir Charles Gairdner Hospital (AU), WA Country Health Service (AU), Pathwest Laboratory Medicine (AU), Bushehr University of Medical Sciences (IR)
National Health and Medical Research Council, Department of Jobs, Tourism, Science and Innovation, Government of Western Australia, Department of Health, Government of Western Australia
Openalex Percentile: Top 8%
Telomeres, Telomerase, and Senescence
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