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Association of mineral metabolism biomarkers with chronic kidney disease in Chinese adults
BACKGROUND: We aimed to examine the association of three mineral metabolism markers, including serum calcium, inorganic phosphorus, and intact parathyroid hormone with the risk of chronic kidney disease (CKD) at all stages. METHODS: This retrospective cohort study involved 3563 participants, includi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8154768/ https://www.ncbi.nlm.nih.gov/pubmed/33725210 http://dx.doi.org/10.1007/s10157-021-02037-4 |
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author | Li, Jialin He, Danni Zhao, Wenjing Wu, Xi’ai Luo, Minjing Wang, Ying Yan, Meihua Niu, Wenquan Li, Ping |
author_facet | Li, Jialin He, Danni Zhao, Wenjing Wu, Xi’ai Luo, Minjing Wang, Ying Yan, Meihua Niu, Wenquan Li, Ping |
author_sort | Li, Jialin |
collection | PubMed |
description | BACKGROUND: We aimed to examine the association of three mineral metabolism markers, including serum calcium, inorganic phosphorus, and intact parathyroid hormone with the risk of chronic kidney disease (CKD) at all stages. METHODS: This retrospective cohort study involved 3563 participants, including 3274 CKD patients and 289 healthy controls. CKD is diagnosed according to clinical guidelines from the 2012 KDIGO. Effect sizes are expressed odds ratio (OR) and 95 confidence interval (CI). RESULTS: After propensity score matching, per 0.5 mg/dL increment of inorganic phosphorus was significantly associated with 1.33-, 1.61-, and 2.85-fold increased risk of CKD at stages 1–2, 4, and 5, respectively. Regarding per 8 pg/mL increment of intact parathyroid hormone, significance was only noted for stage 5. In subsidiary analyses, the risk prediction of mineral metabolism markers under study was more evident in males and hypertensive subjects. A nomogram prediction model was constructed based on age, sex, and three mineral metabolism markers for CKD, with decent accuracy. CONCLUSIONS: Our findings indicate that serum calcium was associated with all-stage CKD risk, whereas the association for inorganic phosphorus and intact parathyroid hormone was significant at advanced stages. |
format | Online Article Text |
id | pubmed-8154768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-81547682021-06-01 Association of mineral metabolism biomarkers with chronic kidney disease in Chinese adults Li, Jialin He, Danni Zhao, Wenjing Wu, Xi’ai Luo, Minjing Wang, Ying Yan, Meihua Niu, Wenquan Li, Ping Clin Exp Nephrol Original Article BACKGROUND: We aimed to examine the association of three mineral metabolism markers, including serum calcium, inorganic phosphorus, and intact parathyroid hormone with the risk of chronic kidney disease (CKD) at all stages. METHODS: This retrospective cohort study involved 3563 participants, including 3274 CKD patients and 289 healthy controls. CKD is diagnosed according to clinical guidelines from the 2012 KDIGO. Effect sizes are expressed odds ratio (OR) and 95 confidence interval (CI). RESULTS: After propensity score matching, per 0.5 mg/dL increment of inorganic phosphorus was significantly associated with 1.33-, 1.61-, and 2.85-fold increased risk of CKD at stages 1–2, 4, and 5, respectively. Regarding per 8 pg/mL increment of intact parathyroid hormone, significance was only noted for stage 5. In subsidiary analyses, the risk prediction of mineral metabolism markers under study was more evident in males and hypertensive subjects. A nomogram prediction model was constructed based on age, sex, and three mineral metabolism markers for CKD, with decent accuracy. CONCLUSIONS: Our findings indicate that serum calcium was associated with all-stage CKD risk, whereas the association for inorganic phosphorus and intact parathyroid hormone was significant at advanced stages. Springer Singapore 2021-03-16 2021 /pmc/articles/PMC8154768/ /pubmed/33725210 http://dx.doi.org/10.1007/s10157-021-02037-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Li, Jialin He, Danni Zhao, Wenjing Wu, Xi’ai Luo, Minjing Wang, Ying Yan, Meihua Niu, Wenquan Li, Ping Association of mineral metabolism biomarkers with chronic kidney disease in Chinese adults |
title | Association of mineral metabolism biomarkers with chronic kidney disease in Chinese adults |
title_full | Association of mineral metabolism biomarkers with chronic kidney disease in Chinese adults |
title_fullStr | Association of mineral metabolism biomarkers with chronic kidney disease in Chinese adults |
title_full_unstemmed | Association of mineral metabolism biomarkers with chronic kidney disease in Chinese adults |
title_short | Association of mineral metabolism biomarkers with chronic kidney disease in Chinese adults |
title_sort | association of mineral metabolism biomarkers with chronic kidney disease in chinese adults |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8154768/ https://www.ncbi.nlm.nih.gov/pubmed/33725210 http://dx.doi.org/10.1007/s10157-021-02037-4 |
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