Association of Appendicular Lean Mass, and Subcutaneous and Visceral Adipose Tissue With Mortality in Older Brazilians: The São Paulo Ageing & Health Study

ABSTRACT Body composition changes as a result of ageing may impact the survival of older adults. However, its influence on mortality risk is uncertain. Currently, the best method for body composition analysis in clinical practice is DXA. Nonetheless, the few studies on body composition by DXA and mo...

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Veröffentlicht in:Journal of bone and mineral research 2019-07, Vol.34 (7), p.1264-1274
Hauptverfasser: Santana, Felipe M, Domiciano, Diogo S, Gonçalves, Michel A, Machado, Luana G, Figueiredo, Camille P, Lopes, Jaqueline B, Caparbo, Valéria F, Takayama, Lilliam, Menezes, Paulo R, Pereira, Rosa MR
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Sprache:eng
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Zusammenfassung:ABSTRACT Body composition changes as a result of ageing may impact the survival of older adults. However, its influence on mortality risk is uncertain. Currently, the best method for body composition analysis in clinical practice is DXA. Nonetheless, the few studies on body composition by DXA and mortality risk in the elderly have some limitations. We investigated the association between body composition by DXA and mortality in a cohort of elderly subjects. Eight hundred thirty‐nine community‐dwelling subjects (516 women, 323 men) ≥ 65 years of age were assessed by a questionnaire, clinical data, laboratory exams, and body composition by DXA at baseline. Total fat and its components (eg, visceral adipose tissue [VAT]) were estimated. Appendicular lean mass (ALM) adjusted for fat and ALM divided by height² was used to ascertain the presence of low muscle mass (LMM). Mortality was recorded during follow‐up. Multivariate logistic regression was used to compute ORs for all‐cause and cardiovascular mortality. Over a mean follow‐up of 4.06 ± 1.07 years, there were 132 (15.7%) deaths. In men, after adjustment for relevant variables, the presence of LMM (OR, 11.36, 95% CI, 2.21 to 58.37, P = 0.004) and VAT (OR, 1.99, 95% CI, 1.38 to 2.87, P
ISSN:0884-0431
1523-4681
DOI:10.1002/jbmr.3710