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Vitamin D is associated with blood lead exposure through bone turnover in type 2 diabetes patients

BACKGROUND: Bone is thought to be the reservoir of the human lead burden, and vitamin D is associated with bone turnover. We aimed to explore whether exposure to lower 25-hydroxy vitamin D (25(OH)D) levels was associated with higher blood lead levels (BLLs) by increasing the bone turnover rate in in...

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Autores principales: Zhang, Haojie, Cui, Yuke, Dong, Ruihua, Zhang, Wen, Chen, Shihan, Wan, Heng, Chen, Chi, Chen, Yi, Wang, Yuying, Zhu, Chunfang, Chen, Bo, Wang, Ningjian, Lu, Yingli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133370/
https://www.ncbi.nlm.nih.gov/pubmed/33666568
http://dx.doi.org/10.1530/EC-21-0006
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author Zhang, Haojie
Cui, Yuke
Dong, Ruihua
Zhang, Wen
Chen, Shihan
Wan, Heng
Chen, Chi
Chen, Yi
Wang, Yuying
Zhu, Chunfang
Chen, Bo
Wang, Ningjian
Lu, Yingli
author_facet Zhang, Haojie
Cui, Yuke
Dong, Ruihua
Zhang, Wen
Chen, Shihan
Wan, Heng
Chen, Chi
Chen, Yi
Wang, Yuying
Zhu, Chunfang
Chen, Bo
Wang, Ningjian
Lu, Yingli
author_sort Zhang, Haojie
collection PubMed
description BACKGROUND: Bone is thought to be the reservoir of the human lead burden, and vitamin D is associated with bone turnover. We aimed to explore whether exposure to lower 25-hydroxy vitamin D (25(OH)D) levels was associated with higher blood lead levels (BLLs) by increasing the bone turnover rate in individuals with type 2 diabetes. METHODS: A total of 4103 type 2 diabetic men and postmenopausal women in Shanghai, China, were enrolled in 2018. Their 25(OH)D, β-C-terminal telopeptide (β-CTX), N-MID osteocalcin and procollagen type 1 N-peptide (P1NP) levels were detected. Their BLLs were determined by atomic absorption spectrometry. Mediation analyses were performed to identify the possible role that bone turnover played in the underlying mechanisms. RESULTS: In both the men and postmenopausal women, all three bone turnover markers were inversely associated with 25(OH)D and positively associated with the BLL (all P < 0.01) after adjusting for age, current smoking habits, metabolic parameters, duration of diabetes, vitamin D intake, and use of anti-osteoporosis medication. In the mediation analyses, none of the direct associations between 25(OH)D and BLL was significant for the three bone turnover markers, but all three bone turnover markers were found to be significant mediators of the indirect associations between 25(OH)D and BLL. CONCLUSION: The association between vitamin D and BLL was fully mediated by bone turnover markers in type 2 diabetic patients (mediation effect). This finding suggested that vitamin D may protect against blood lead exposure from the bone reservoir by decreasing bone turnover in individuals with type 2 diabetes.
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spelling pubmed-81333702021-05-21 Vitamin D is associated with blood lead exposure through bone turnover in type 2 diabetes patients Zhang, Haojie Cui, Yuke Dong, Ruihua Zhang, Wen Chen, Shihan Wan, Heng Chen, Chi Chen, Yi Wang, Yuying Zhu, Chunfang Chen, Bo Wang, Ningjian Lu, Yingli Endocr Connect Research BACKGROUND: Bone is thought to be the reservoir of the human lead burden, and vitamin D is associated with bone turnover. We aimed to explore whether exposure to lower 25-hydroxy vitamin D (25(OH)D) levels was associated with higher blood lead levels (BLLs) by increasing the bone turnover rate in individuals with type 2 diabetes. METHODS: A total of 4103 type 2 diabetic men and postmenopausal women in Shanghai, China, were enrolled in 2018. Their 25(OH)D, β-C-terminal telopeptide (β-CTX), N-MID osteocalcin and procollagen type 1 N-peptide (P1NP) levels were detected. Their BLLs were determined by atomic absorption spectrometry. Mediation analyses were performed to identify the possible role that bone turnover played in the underlying mechanisms. RESULTS: In both the men and postmenopausal women, all three bone turnover markers were inversely associated with 25(OH)D and positively associated with the BLL (all P < 0.01) after adjusting for age, current smoking habits, metabolic parameters, duration of diabetes, vitamin D intake, and use of anti-osteoporosis medication. In the mediation analyses, none of the direct associations between 25(OH)D and BLL was significant for the three bone turnover markers, but all three bone turnover markers were found to be significant mediators of the indirect associations between 25(OH)D and BLL. CONCLUSION: The association between vitamin D and BLL was fully mediated by bone turnover markers in type 2 diabetic patients (mediation effect). This finding suggested that vitamin D may protect against blood lead exposure from the bone reservoir by decreasing bone turnover in individuals with type 2 diabetes. Bioscientifica Ltd 2021-03-03 /pmc/articles/PMC8133370/ /pubmed/33666568 http://dx.doi.org/10.1530/EC-21-0006 Text en © 2021 The authors https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Research
Zhang, Haojie
Cui, Yuke
Dong, Ruihua
Zhang, Wen
Chen, Shihan
Wan, Heng
Chen, Chi
Chen, Yi
Wang, Yuying
Zhu, Chunfang
Chen, Bo
Wang, Ningjian
Lu, Yingli
Vitamin D is associated with blood lead exposure through bone turnover in type 2 diabetes patients
title Vitamin D is associated with blood lead exposure through bone turnover in type 2 diabetes patients
title_full Vitamin D is associated with blood lead exposure through bone turnover in type 2 diabetes patients
title_fullStr Vitamin D is associated with blood lead exposure through bone turnover in type 2 diabetes patients
title_full_unstemmed Vitamin D is associated with blood lead exposure through bone turnover in type 2 diabetes patients
title_short Vitamin D is associated with blood lead exposure through bone turnover in type 2 diabetes patients
title_sort vitamin d is associated with blood lead exposure through bone turnover in type 2 diabetes patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133370/
https://www.ncbi.nlm.nih.gov/pubmed/33666568
http://dx.doi.org/10.1530/EC-21-0006
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