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Impact of serum calcium levels on local and total body bone mineral density: A Mendelian randomization study and an age stratum analysis

Jing-yi Sun, Haihua Zhang, Yan Zhang, Longcai Wang, Jin Rok Oh, Bao-liang Sun, Guiyou Liu
doi: https://doi.org/10.1101/737585
Jing-yi Sun
aDepartment of orthopedics Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine, Wonju, Gangwon 220-701, Republic of Korea
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Haihua Zhang
bSchool of Economics, Nankai University, Tianjin 300071, Tianjin, China
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Yan Zhang
cDepartment of Pathology, The Affiliated Hospital of Weifang Medical University, Weifang 261053, China
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Longcai Wang
dDepartment of Anesthesiology, The Affiliated Hospital of Weifang Medical University, Weifang 261053, China
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Jin Rok Oh
aDepartment of orthopedics Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine, Wonju, Gangwon 220-701, Republic of Korea
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Bao-liang Sun
eKey Laboratory of Cerebral Microcirculation in Universities of Shandong; Department of Neurology, Second Affiliated Hospital; Shandong First Medical University & Shandong Academy of Medical Sciences, Taian 271000, Shandong, China
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  • For correspondence: liu_gy@tib.cas.cn blsun88@163.com
Guiyou Liu
fDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing 100053, China
gBeijing Institute for Brain Disorders, Capital Medical University, Beijing, China
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  • For correspondence: liu_gy@tib.cas.cn blsun88@163.com
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Abstract

Objectives Until recently, randomized controlled trials and meta-analyses have not demonstrated convincing conclusions regarding the association of calcium intake with bone mineral density (BMD). Until now, it remains unclear whether high serum calcium levels are causally associated with BMD. This study aimed to investigate the genetic association between serum calcium levels and BMD using a large-scale serum calcium GWAS dataset and four large-scale BMD GWAS datasets in individuals of European descent.

Methods We performed a Mendelian randomization study to investigate the association of increased serum calcium levels with BMD using a large-scale serum calcium genome-wide association study (GWAS) dataset (including up to 61,079 individuals) and four large-scale BMD GWAS datasets (including minimum 4,180 individuals and maximum 142,487 individuals) regarding the total body, forearm, femoral neck, lumbar spine, and heel BMD. Here, we selected three Mendelian randomization methods including inverse-variance weighted meta-analysis (IVW), weighted median, and MR-Egger.

Results In specific site analysis, we found that increased serum calcium levels could reduce BMD at forearm (OR=0.59, 95% CI: 0.36-0.95, P=0.029) and lumbar spine (OR=0.65, 95% CI: 0.49-0.86, P=0.002). We did not identify any suggestive association of genetically increased serum calcium levels with BMD of total body, femoral neck, and heel BMD. In specific age stratum analysis, we found that genetically increased serum calcium levels were statistically significantly associated with reduced total body BMD in age stratum 60 or more years (OR=0.58, 95% CI: 0.41-0.82, P=0.002).

Conclusions We provide genetic evidence that increased serum calcium levels could not improve BMD in the general population. The elevated serum calcium levels in generally healthy populations, especially adults older than 60 years, may even reduce the BMD, and further cause osteoporosis.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted August 16, 2019.
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Impact of serum calcium levels on local and total body bone mineral density: A Mendelian randomization study and an age stratum analysis
Jing-yi Sun, Haihua Zhang, Yan Zhang, Longcai Wang, Jin Rok Oh, Bao-liang Sun, Guiyou Liu
bioRxiv 737585; doi: https://doi.org/10.1101/737585
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Impact of serum calcium levels on local and total body bone mineral density: A Mendelian randomization study and an age stratum analysis
Jing-yi Sun, Haihua Zhang, Yan Zhang, Longcai Wang, Jin Rok Oh, Bao-liang Sun, Guiyou Liu
bioRxiv 737585; doi: https://doi.org/10.1101/737585

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