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 in | Experimental gerontology Vol. 209; p. 112865 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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England
Elsevier Inc
01.10.2025
Elsevier |
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ISSN | 0531-5565 1873-6815 1873-6815 |
DOI | 10.1016/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. |
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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 |
Author_xml | – sequence: 1 givenname: Mei-Lin surname: Li fullname: Li, Mei-Lin organization: Department of Geriatrics, The Third People's Hospital of Chengdu, Affiliated Hospital of Southwest Jiaotong University, Chengdu, China – sequence: 2 givenname: Yi-Min surname: Li fullname: Li, Yi-Min organization: Department of Cardiology, Sir Run Run Hospital, Nanjing Medical University, Nanjing, China – sequence: 3 givenname: Jing-Jing surname: Huang fullname: Huang, Jing-Jing organization: Department of Geriatrics, The Fourth Affiliated Hospital of Nanjing Medical University, Nanjing, China – sequence: 4 givenname: Zhi-Yue surname: Wang fullname: Wang, Zhi-Yue organization: Department of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, China – sequence: 5 givenname: Quan surname: Wang fullname: Wang, Quan organization: Department of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, China – sequence: 6 givenname: Can surname: Zhao fullname: Zhao, Can organization: Department of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, China – sequence: 7 givenname: Xiang surname: Lu fullname: Lu, Xiang organization: Department of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, China – sequence: 8 givenname: Jin-Shui surname: Xu fullname: Xu, Jin-Shui organization: Jiangsu Province Center for Disease Control and Prevention, Nanjing, China – sequence: 9 givenname: Zheng-Kai surname: Shen fullname: Shen, Zheng-Kai email: shenzhengkai@jscdc.cn organization: Jiangsu Province Center for Disease Control and Prevention, Nanjing, China – sequence: 10 givenname: Wei surname: Gao fullname: Gao, Wei email: drweig1984@outlook.com organization: Department of Geriatrics, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40819771$$D View this record in MEDLINE/PubMed |
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Keywords | Elementomics Urine Sarcopenia Aluminum Older adults |
Language | English |
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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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