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Dietary Selenium Intake and Sarcopenia in American Adults

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Journal Front Nutr
Date 2024 Sep 27
PMID 39328467
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Abstract

Background: The relationship between dietary selenium intake and sarcopenia remains poorly understood. Therefore, this study investigates the associations between dietary selenium intake and sarcopenia among American adults.

Methods: This cross-sectional study analyzed data from 19,696 participants in the National Health and Nutrition Examination Survey (NHANES) for the periods 1999-2006 and 2011-2018. Appendicular muscle mass, assessed using dual-energy x-ray absorptiometry and adjusted for body mass index, was used as a marker for sarcopenia. Dietary selenium intake was evaluated using the 24-h dietary recall system, and the study accounted for the complex sampling methodology and incorporated dietary sample weights in the analysis.

Results: Among the 19,696 participants, the prevalence of sarcopenia was found to be 8.46%. When compared to the lowest quintile of dietary selenium intake (Q1, < 80.10 μg/day), the odds ratios for sarcopenia in the second quintile (Q2, 80.10-124.61 μg/day) and the third quintile (Q3, >124.61 μg/day) were 0.80 [95% confidence interval (CI): 0.70-0.92, = 0.002] and 0.61 (95% CI: 0.51-0.73, < 0.001), respectively. A negative relationship was observed between dietary selenium intake and sarcopenia (non-linear: = 0.285). Furthermore, sensitivity analyses revealed a robust association between selenium intake and the prevalence of sarcopenia after further adjusting for blood selenium levels.

Conclusion: The results suggest an inverse association between dietary selenium intake and the prevalence of sarcopenia among American adults.

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References
1.
Han S, Lee B, Yim S, Gladyshev V, Lee S . Characterization of mammalian selenoprotein o: a redox-active mitochondrial protein. PLoS One. 2014; 9(4):e95518. PMC: 3994087. DOI: 10.1371/journal.pone.0095518. View

2.
Bubenik J, Miniard A, Driscoll D . Characterization of the UGA-recoding and SECIS-binding activities of SECIS-binding protein 2. RNA Biol. 2015; 11(11):1402-13. PMC: 4615290. DOI: 10.1080/15476286.2014.996472. View

3.
Burk R, Hill K . Regulation of Selenium Metabolism and Transport. Annu Rev Nutr. 2015; 35:109-34. DOI: 10.1146/annurev-nutr-071714-034250. View

4.
Cruz-Jentoft A, Sayer A . Sarcopenia. Lancet. 2019; 393(10191):2636-2646. DOI: 10.1016/S0140-6736(19)31138-9. View

5.
Gomes M, Martinez P, Pagan L, Damatto R, Cezar M, Lima A . Skeletal muscle aging: influence of oxidative stress and physical exercise. Oncotarget. 2017; 8(12):20428-20440. PMC: 5386774. DOI: 10.18632/oncotarget.14670. View