» Articles » PMID: 33968284

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

Overview
Journal Dis Markers
Publisher Wiley
Specialty Biochemistry
Date 2021 May 10
PMID 33968284
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Aims: To explore the relationships of procollagen type 1 N-terminal propeptide (P1NP) and cross-linked C-telopeptide of type 1 collagen (-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 -CTX were also collected and tested. The main correlation analysis was applied to explore the relationships of BMD, P1NP, and -CTX.

Results: The total 1055 postmenopausal women were enrolled. The BMD at all sites kept a decrease continually with age ( < 0.01). In addition, the level of -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 -CTX has better ability to predict BMD than P1NP, as demonstrated by an area under the curve (AUC) of 0.63.

Conclusion: P1NP and -CTX are important markers to monitor bone metabolism. This trial is registered with ChiCTR-SOC-17013090. The date of registration is Oct. 23, 2017.

Citing Articles

Plasma levels of anti phosphocholine IgM antibodies are negatively correlated with bone mineral density in humans.

Palmieri M, Maraka S, Spencer H, Thostenson J, Dishongh K, Knox M Sci Rep. 2025; 15(1):2109.

PMID: 39814831 PMC: 11735633. DOI: 10.1038/s41598-025-85624-9.


Regulation of bone homeostasis: signaling pathways and therapeutic targets.

Wu Z, Li W, Jiang K, Lin Z, Qian C, Wu M MedComm (2020). 2024; 5(8):e657.

PMID: 39049966 PMC: 11266958. DOI: 10.1002/mco2.657.


The prevalence and treatment of osteoporosis in patients undergoing total hip arthroplasty and the levels of biochemical markers of bone turnover.

Watanabe N, Miyatake K, Takada R, Ogawa T, Amano Y, Jinno T Bone Joint Res. 2022; 11(12):873-880.

PMID: 36464500 PMC: 9792872. DOI: 10.1302/2046-3758.1112.BJR-2022-0252.R1.


Risk of primary osteoporosis score (RPOPs): an algorithm model for primary osteoporosis risk assessment in grass-roots hospital.

Jiang X, Yan N, Zheng Y, Yang J, Zhao Y BMC Musculoskelet Disord. 2022; 23(1):1041.

PMID: 36456916 PMC: 9713074. DOI: 10.1186/s12891-022-06014-0.


Bone-turnover biomarkers as potential prognostic factors in sudden sensorineural hearing loss: A prospective cohort study.

Chen X, Zheng Z, Xiao L, Liu C, Shen Y, Ma N Front Neurol. 2022; 13:980150.

PMID: 36090873 PMC: 9453032. DOI: 10.3389/fneur.2022.980150.


References
1.
. Assessment of fracture risk and its application to screening for postmenopausal osteoporosis. Report of a WHO Study Group. World Health Organ Tech Rep Ser. 1994; 843:1-129. View

2.
Vasikaran S, Chubb S, Ebeling P, Jenkins N, Jones G, Kotowicz M . Harmonised Australian Reference Intervals for Serum PINP and CTX in Adults. Clin Biochem Rev. 2015; 35(4):237-42. PMC: 4310062. View

3.
Sun X, Yang X, Zhao Y, Li Y, Guo L . Effects of 17β-Estradiol on Mitophagy in the Murine MC3T3-E1 Osteoblast Cell Line is Mediated via G Protein-Coupled Estrogen Receptor and the ERK1/2 Signaling Pathway. Med Sci Monit. 2018; 24:903-911. PMC: 5819311. DOI: 10.12659/msm.908705. View

4.
Awasthi H, Mani D, Singh D, Gupta A . The underlying pathophysiology and therapeutic approaches for osteoporosis. Med Res Rev. 2018; 38(6):2024-2057. DOI: 10.1002/med.21504. View

5.
Cong Q, Jia H, Biswas S, Li P, Qiu S, Deng Q . p38α MAPK Regulates Lineage Commitment and OPG Synthesis of Bone Marrow Stromal Cells to Prevent Bone Loss under Physiological and Pathological Conditions. Stem Cell Reports. 2016; 6(4):566-578. PMC: 4834033. DOI: 10.1016/j.stemcr.2016.02.001. View