TY - JOUR
T1 - Association between sedentary behavior and dynapenic abdominal obesity among older adults from low- and middle-income countries
AU - Smith, Lee
AU - López Sánchez, Guillermo F.
AU - Rahmati, Masoud
AU - Tully, Mark A.
AU - Pizzol, Damiano
AU - Veronese, Nicola
AU - Soysal, Pinar
AU - Kostev, Karel
AU - Yon, Dong Keon
AU - Butler, Laurie
AU - Shin, Jae Il
AU - Koyanagi, Ai
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/12
Y1 - 2024/12
N2 - Background: Sedentary behavior, or time spent sitting, may increase risk for dynapenic abdominal obesity (DAO), but there are currently no studies on this topic. Aims: Therefore, we investigated the association between sedentary behaviour and DAO in a nationally representative sample of older adults from six low- and middle-income countries. Methods: Cross-sectional data from the Study on Global AGEing and Adult Health were analysed. Dynapenia was defined as handgrip strength < 26 kg for men and < 16 kg for women. Abdominal obesity was defined as waist circumference of > 88 cm (> 80 cm for Asian countries) for women and > 102 cm (> 90 cm) for men. DAO was defined as having both dynapenia and abdominal obesity. Self-reported sedentary behavior was categorized as ≥ 8 h/day (high sedentary behaviour) or < 8 h/day. Multivariable multinomial logistic regression was conducted. Results: Data on 20,198 adults aged ≥ 60 years were analyzed [mean (SD) age 69.3 (13.1) years; 54.1% females]. In the overall sample, ≥ 8 h of sedentary behavior per day (vs. <8 h) was significantly associated with 1.52 (95%CI = 1.11–2.07) times higher odds for DAO (vs. no dynapenia and no abdominal obesity), and this was particularly pronounced among males (OR = 2.27; 95%CI = 1.42–3.62). Highly sedentary behavior was not significantly associated with dynapenia alone or abdominal obesity alone. Discussion: High sedentary behaviour may increase risk for DAO among older adults. Conclusions: Interventions to reduce sedentary behaviour may also lead to reduction of DAO and its adverse health outcomes, especially among males, pending future longitudinal research.
AB - Background: Sedentary behavior, or time spent sitting, may increase risk for dynapenic abdominal obesity (DAO), but there are currently no studies on this topic. Aims: Therefore, we investigated the association between sedentary behaviour and DAO in a nationally representative sample of older adults from six low- and middle-income countries. Methods: Cross-sectional data from the Study on Global AGEing and Adult Health were analysed. Dynapenia was defined as handgrip strength < 26 kg for men and < 16 kg for women. Abdominal obesity was defined as waist circumference of > 88 cm (> 80 cm for Asian countries) for women and > 102 cm (> 90 cm) for men. DAO was defined as having both dynapenia and abdominal obesity. Self-reported sedentary behavior was categorized as ≥ 8 h/day (high sedentary behaviour) or < 8 h/day. Multivariable multinomial logistic regression was conducted. Results: Data on 20,198 adults aged ≥ 60 years were analyzed [mean (SD) age 69.3 (13.1) years; 54.1% females]. In the overall sample, ≥ 8 h of sedentary behavior per day (vs. <8 h) was significantly associated with 1.52 (95%CI = 1.11–2.07) times higher odds for DAO (vs. no dynapenia and no abdominal obesity), and this was particularly pronounced among males (OR = 2.27; 95%CI = 1.42–3.62). Highly sedentary behavior was not significantly associated with dynapenia alone or abdominal obesity alone. Discussion: High sedentary behaviour may increase risk for DAO among older adults. Conclusions: Interventions to reduce sedentary behaviour may also lead to reduction of DAO and its adverse health outcomes, especially among males, pending future longitudinal research.
KW - Dynapenic abdominal obesity
KW - Epidemiology
KW - Low- and middle-income countries
KW - Older adults
KW - Sitting time
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U2 - 10.1007/s40520-024-02763-1
DO - 10.1007/s40520-024-02763-1
M3 - Article
C2 - 38730062
AN - SCOPUS:85192932276
SN - 1594-0667
VL - 36
JO - Aging Clinical and Experimental Research
JF - Aging Clinical and Experimental Research
IS - 1
M1 - 109
ER -