Evidence map›Paper›PMID 40074311›Full record

Observational studyZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences2024

Cystatin C is associated with osteoporosis and fractures: An observational study based on Mendelian randomization analysis.

Wenhui Wang, Han Wang, Shufeng Lei, Pei He

Abstract readObservational Study
In one paragraph

Observational study in Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Wenhui WangResearch for Genetic Epidemiology and Genomics, School of Public Health, Suzhou Medical College of Soochow University, Suzhou Jiangsu 215123, China. wwenhui99@163.com.
Han WangResearch for Genetic Epidemiology and Genomics, School of Public Health, Suzhou Medical College of Soochow University, Suzhou Jiangsu 215123, China. 1271383513@qq.com.
Shufeng LeiResearch for Genetic Epidemiology and Genomics, School of Public Health, Suzhou Medical College of Soochow University, Suzhou Jiangsu 215123, China.
Pei HeResearch for Genetic Epidemiology and Genomics, School of Public Health, Suzhou Medical College of Soochow University, Suzhou Jiangsu 215123, China. peihe@suda.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesOsteoporosis is characterized by decreased bone mass and damaged bone microstructure, often leading to fragility fractures. Low bone mineral density is a key risk factor for fractures. Serum cystatin C (CysC), an endogenous marker of glomerular filtration rate, is negatively correlated with bone mineral density and may be a potential risk factor for osteoporosis. This study aims to investigate the association and potential pathogenic mechanisms between CysC and osteoporosis and fractures in the general population by combining cohort analysis and Mendelian randomization (MR) analysis.

methodsLarge-scale prospective cohort data from the UK Biobank and summary statistics from genome-wide association study (GWAS) in European populations were utilized, with strict exclusion criteria applied (excluding non-white individuals, those with thyroid diseases, gastrointestinal dysfunction, kidney diseases, rheumatoid diseases, malignant tumors, chronic infections or inflammatory diseases, diabetes, hypertension, and individuals taking medications that affect bone metabolism). Multivariable linear regression, logistic regression, and Cox proportional hazards models were used to analyze the relationship between CysC and bone mineral density, osteoporosis, and fracture risk. All analyses were performed using three sequential models to adjust for confounding factors: Model 1 adjusted for demographic characteristics and lifestyle factors; Model 2 further adjusted for renal function based on Model 1; and Model 3 further adjusted for physical activity based on Model 2. Restricted cubic spline models were used to explore non-linear relationships, and MR analysis was conducted to assess the causal associations between CysC and osteoporosis and fractures.

resultsMultivariate analysis showed that after adjusting for basic variables (Model 1), there was no correlation between CysC and estimated bone mineral density (eBMD) in the overall study population; however, when stratified by gender, both males and females exhibited a significant negative correlation (

conclusionsElevated levels of CysC are significantly associated with an increased risk of osteoporosis and fractures, and this association is more pronounced in females. Renal function and physical activity levels may be important factors influencing this relationship. The link between CysC and osteoporosis and fractures may be mediated by several mechanisms: Eelevated CysC may lead to abnormalities in vitamin D and mineral metabolism, thereby inhibiting bone formation; renal dysfunction may exacerbate inflammation, affecting bone resorption; or in the osteoporosis state, increased osteoclast differentiation may result in elevated CysC levels. These findings support the potential use of CysC as a biomarker for predicting the risk of osteoporosis.

Indexed as

Cystatin CFractures, BoneMendelian Randomization AnalysisOsteoporosisOsteoporotic FracturesAgedBone DensityFemaleGenome-Wide Association StudyHumansMaleMiddle AgedProportional Hazards ModelsProspective StudiesRisk FactorsCystatin Ccystatin Cmendelian randomization analysisosteoporosis, fracturesprospective cohort study

Identifiers

PMID40074311
PMCPMC11897978

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