Urinary elementomic analysis indicates aluminum as a potential urinary biomarker of sarcopenia in the older adults

Sarcopenia is characterized by aging-related progressive loss of muscle mass and function; however, the specific and sensitive biomarkers are still limited. Biometals and trace elements provide a potential connection linking the environment and lifestyle to pathological processes of sarcopenia. The...

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Published inExperimental gerontology Vol. 209; p. 112865
Main Authors Li, Mei-Lin, Li, Yi-Min, Huang, Jing-Jing, Wang, Zhi-Yue, Wang, Quan, Zhao, Can, Lu, Xiang, Xu, Jin-Shui, Shen, Zheng-Kai, Gao, Wei
Format Journal Article
LanguageEnglish
Published England Elsevier Inc 01.10.2025
Elsevier
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ISSN0531-5565
1873-6815
1873-6815
DOI10.1016/j.exger.2025.112865

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Abstract Sarcopenia is characterized by aging-related progressive loss of muscle mass and function; however, the specific and sensitive biomarkers are still limited. Biometals and trace elements provide a potential connection linking the environment and lifestyle to pathological processes of sarcopenia. The aim of the present study was to investigate the relationship between urinary trace elements levels and the presence of sarcopenia. A total of 100 older adults aged ≥65 years consisting of 50 patients with sarcopenia and 50 subjects without sarcopenia were enrolled. The urinary concentrations of 35 elements were examined by using inductively coupled plasma mass spectrometry. We found that a panel of 11 urinary elements including Ti, B, Na, Al, K, Ca, V, Rb, Sr, Cs, and Tl were decreased in patients with sarcopenia. Partial correlation analysis showed that urinary levels of Na (r = 0.242, P = 0.017) and Al (r = 0.303, P = 0.002) were positively correlated with gait speed. Multivariate logistic regression analysis showed that urinary Al level (adjusted OR = 0.986, 95 %CI =0.978–0.996, P = 0.004) was negatively associated with the risk of sarcopenia in older adults even after adjustment for potential confounding factors. ROC curve analysis indicated that the optimal cut-off value of urinary Al level for the prediction of sarcopenia was 46.53 μg/mL with a sensitivity of 58 % and a specificity of 78 % (AUC =0.691, 95 % CI =0.587–0.796, P < 0.001). Taken together, our data indicate that urinary Al level shows potential as a biomarker associated with sarcopenia status in older adults. Further studies are needed to confirm the results of our study and elucidate the underlying mechanism by which Al participates in the pathogenesis of sarcopenia. •A panel of 11 urinary elements were decreased in patients with sarcopenia.•Urinary levels of Na and Al were positively correlated with gait speed.•Urinary Al level was negatively associated with the risk of sarcopenia.
AbstractList Sarcopenia is characterized by aging-related progressive loss of muscle mass and function; however, the specific and sensitive biomarkers are still limited. Biometals and trace elements provide a potential connection linking the environment and lifestyle to pathological processes of sarcopenia. The aim of the present study was to investigate the relationship between urinary trace elements levels and the presence of sarcopenia. A total of 100 older adults aged ≥65 years consisting of 50 patients with sarcopenia and 50 subjects without sarcopenia were enrolled. The urinary concentrations of 35 elements were examined by using inductively coupled plasma mass spectrometry. We found that a panel of 11 urinary elements including Ti, B, Na, Al, K, Ca, V, Rb, Sr, Cs, and Tl were decreased in patients with sarcopenia. Partial correlation analysis showed that urinary levels of Na (r = 0.242, P = 0.017) and Al (r = 0.303, P = 0.002) were positively correlated with gait speed. Multivariate logistic regression analysis showed that urinary Al level (adjusted OR = 0.986, 95 %CI =0.978-0.996, P = 0.004) was negatively associated with the risk of sarcopenia in older adults even after adjustment for potential confounding factors. ROC curve analysis indicated that the optimal cut-off value of urinary Al level for the prediction of sarcopenia was 46.53 μg/mL with a sensitivity of 58 % and a specificity of 78 % (AUC =0.691, 95 % CI =0.587-0.796, P < 0.001). Taken together, our data indicate that urinary Al level shows potential as a biomarker associated with sarcopenia status in older adults. Further studies are needed to confirm the results of our study and elucidate the underlying mechanism by which Al participates in the pathogenesis of sarcopenia.Sarcopenia is characterized by aging-related progressive loss of muscle mass and function; however, the specific and sensitive biomarkers are still limited. Biometals and trace elements provide a potential connection linking the environment and lifestyle to pathological processes of sarcopenia. The aim of the present study was to investigate the relationship between urinary trace elements levels and the presence of sarcopenia. A total of 100 older adults aged ≥65 years consisting of 50 patients with sarcopenia and 50 subjects without sarcopenia were enrolled. The urinary concentrations of 35 elements were examined by using inductively coupled plasma mass spectrometry. We found that a panel of 11 urinary elements including Ti, B, Na, Al, K, Ca, V, Rb, Sr, Cs, and Tl were decreased in patients with sarcopenia. Partial correlation analysis showed that urinary levels of Na (r = 0.242, P = 0.017) and Al (r = 0.303, P = 0.002) were positively correlated with gait speed. Multivariate logistic regression analysis showed that urinary Al level (adjusted OR = 0.986, 95 %CI =0.978-0.996, P = 0.004) was negatively associated with the risk of sarcopenia in older adults even after adjustment for potential confounding factors. ROC curve analysis indicated that the optimal cut-off value of urinary Al level for the prediction of sarcopenia was 46.53 μg/mL with a sensitivity of 58 % and a specificity of 78 % (AUC =0.691, 95 % CI =0.587-0.796, P < 0.001). Taken together, our data indicate that urinary Al level shows potential as a biomarker associated with sarcopenia status in older adults. Further studies are needed to confirm the results of our study and elucidate the underlying mechanism by which Al participates in the pathogenesis of sarcopenia.
Sarcopenia is characterized by aging-related progressive loss of muscle mass and function; however, the specific and sensitive biomarkers are still limited. Biometals and trace elements provide a potential connection linking the environment and lifestyle to pathological processes of sarcopenia. The aim of the present study was to investigate the relationship between urinary trace elements levels and the presence of sarcopenia. A total of 100 older adults aged ≥65 years consisting of 50 patients with sarcopenia and 50 subjects without sarcopenia were enrolled. The urinary concentrations of 35 elements were examined by using inductively coupled plasma mass spectrometry. We found that a panel of 11 urinary elements including Ti, B, Na, Al, K, Ca, V, Rb, Sr, Cs, and Tl were decreased in patients with sarcopenia. Partial correlation analysis showed that urinary levels of Na (r = 0.242, P = 0.017) and Al (r = 0.303, P = 0.002) were positively correlated with gait speed. Multivariate logistic regression analysis showed that urinary Al level (adjusted OR = 0.986, 95 %CI =0.978–0.996, P = 0.004) was negatively associated with the risk of sarcopenia in older adults even after adjustment for potential confounding factors. ROC curve analysis indicated that the optimal cut-off value of urinary Al level for the prediction of sarcopenia was 46.53 μg/mL with a sensitivity of 58 % and a specificity of 78 % (AUC =0.691, 95 % CI =0.587–0.796, P < 0.001). Taken together, our data indicate that urinary Al level shows potential as a biomarker associated with sarcopenia status in older adults. Further studies are needed to confirm the results of our study and elucidate the underlying mechanism by which Al participates in the pathogenesis of sarcopenia.
Sarcopenia is characterized by aging-related progressive loss of muscle mass and function; however, the specific and sensitive biomarkers are still limited. Biometals and trace elements provide a potential connection linking the environment and lifestyle to pathological processes of sarcopenia. The aim of the present study was to investigate the relationship between urinary trace elements levels and the presence of sarcopenia. A total of 100 older adults aged ≥65 years consisting of 50 patients with sarcopenia and 50 subjects without sarcopenia were enrolled. The urinary concentrations of 35 elements were examined by using inductively coupled plasma mass spectrometry. We found that a panel of 11 urinary elements including Ti, B, Na, Al, K, Ca, V, Rb, Sr, Cs, and Tl were decreased in patients with sarcopenia. Partial correlation analysis showed that urinary levels of Na (r = 0.242, P = 0.017) and Al (r = 0.303, P = 0.002) were positively correlated with gait speed. Multivariate logistic regression analysis showed that urinary Al level (adjusted OR = 0.986, 95 %CI =0.978–0.996, P = 0.004) was negatively associated with the risk of sarcopenia in older adults even after adjustment for potential confounding factors. ROC curve analysis indicated that the optimal cut-off value of urinary Al level for the prediction of sarcopenia was 46.53 μg/mL with a sensitivity of 58 % and a specificity of 78 % (AUC =0.691, 95 % CI =0.587–0.796, P < 0.001). Taken together, our data indicate that urinary Al level shows potential as a biomarker associated with sarcopenia status in older adults. Further studies are needed to confirm the results of our study and elucidate the underlying mechanism by which Al participates in the pathogenesis of sarcopenia. •A panel of 11 urinary elements were decreased in patients with sarcopenia.•Urinary levels of Na and Al were positively correlated with gait speed.•Urinary Al level was negatively associated with the risk of sarcopenia.
ArticleNumber 112865
Author Li, Yi-Min
Huang, Jing-Jing
Shen, Zheng-Kai
Li, Mei-Lin
Wang, Zhi-Yue
Xu, Jin-Shui
Gao, Wei
Zhao, Can
Wang, Quan
Lu, Xiang
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Keywords Elementomics
Urine
Sarcopenia
Aluminum
Older adults
Language English
License This is an open access article under the CC BY license.
Copyright © 2025 The Authors. Published by Elsevier Inc. All rights reserved.
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SubjectTerms Aged
Aged, 80 and over
Aluminum
Aluminum - urine
Biomarkers - urine
Case-Control Studies
Elementomics
Female
Humans
Male
Older adults
ROC Curve
Sarcopenia
Sarcopenia - diagnosis
Sarcopenia - urine
Trace Elements - urine
Urine
Walking Speed
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Title Urinary elementomic analysis indicates aluminum as a potential urinary biomarker of sarcopenia in the older adults
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