Exploring the Relationship of Bone Turnover Markers and Bone Mineral Density in Community-Dwelling Postmenopausal Women

Author:

Wei Xu12ORCID,Zhang Yili13ORCID,Xiang Xinghua4,Sun Menghua5,Sun Kai1,Han Tao1,Qi Baoyu1,Xie Yanming5,Zhang Ranxing6ORCID,Zhu Liguo12ORCID

Affiliation:

1. Wangjing Hospital, China Academy of Chinese Medical Sciences, Beijing, China

2. Institute of Orthopaedics of Beijing Integrative Medicine, Beijing, China

3. Beijing University of Chinese Medicine, Beijing, China

4. Hunan University of Science and Technology, Xiangtan, China

5. Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, China

6. Department of Clinical Laboratory, Eye Hospital, China Academy of Chinese Medical Sciences, Beijing, China

Abstract

Aims. To explore the relationships of procollagen type 1 N-terminal propeptide (P1NP) and β cross-linked C-telopeptide of type 1 collagen (β-CTX) with bone mineral density (BMD) in postmenopausal women. Methods. All postmenopausal women were selected from a community-based case-control study. The anteroposterior L1-L4 and left proximal femur BMD were measured. P1NP and β-CTX were also collected and tested. The main correlation analysis was applied to explore the relationships of BMD, P1NP, and β-CTX. Results. The total 1055 postmenopausal women were enrolled. The BMD at all sites kept a decrease continually with age ( P < 0.01 ). In addition, the level of β-CTX increased significantly from 45 to 50 years old and remained at a high level in the later stage, while the level of P1NP changed little or even decreased with age. Logistic regression model showed that β-CTX has better ability to predict BMD than P1NP, as demonstrated by an area under the curve (AUC) of 0.63. Conclusion. P1NP and β-CTX are important markers to monitor bone metabolism. This trial is registered with ChiCTR-SOC-17013090. The date of registration is Oct. 23, 2017.

Funder

Fundamental Research Funds for the Central Public Welfare Research Institutes

Publisher

Hindawi Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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