骨转换标志物在绝经后骨质疏松症诊断中的应用综述

S. Mada, S. Ibrahim, M. Abarshi, B. Sanusi, P. Abaya, N. Garba, Kabiru Usman, A. Hamza, M. Umar, Muttaka Auwalu, A. Jabbi, Kabiru Samaila
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引用次数: 0

摘要

绝经后骨质疏松症是一种与年龄相关的骨骼代谢紊乱,影响全球大多数老年妇女,其原因是雌激素活性降低、骨转换率增加和骨转换标志物循环水平升高。虽然骨钙素、骨特异性碱性磷酸酶、I型前胶原N端和c端前肽被认为是骨形成最敏感的标志物,但它们也有一定的局限性。因此,骨膜蛋白、硬化蛋白和dickkopf-1蛋白(Dkk-1)是新兴的骨病理诊断标志物,并监测绝经后骨质疏松症的治疗干预和管理。这些标志物可作为诊断骨骼疾病的有效工具,预测骨折风险的降低,反映骨重塑过程中药物的代谢作用,并可用于确定引起骨密度所需变化的最低剂量。来自不同来源的生物变异,包括可控和不可控因素,可能是这些已建立的骨形成标志物(BFMs)的主要限制。因此,本文将重点介绍骨转换标志物在绝经后骨质疏松症早期诊断中的应用。
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Bone Turnover Markers for Diagnosis of postmenopausal osteoporosis – A review
Postmenopausal osteoporosis is an age related skeletal metabolic disorder that affects most elderly women worldwide owing to the loss of estrogen activity, increase in bone turnover rate and circulating level of bone turnover markers. Although osteocalcin, bone specific alkaline phosphatase, and pro-collagen type I N- and C-terminal pro-peptides are considered as the most sensitive markers of bone formation however, they suffer some limitations. Consequently, periostin, sclerostin and dickkopf-1 protein (Dkk-1) are emerging diagnosis markers of bone pathologies and monitoring therapeutic interventions and management of postmenopausal osteoporosis. These markers serve as effective tools for diagnosis of bone disorders, predict reduction in fracture risk, reflect metabolic effect of drugs during bone remodeling and could be used to establish the lowest dose that elicit the required change in bone mineral density. Biological variability from different sources including controllable and uncontrollable factors could serve as the major limitations of these established markers of bone formation (BFMs). This review, therefore focus on the therapeutic applications of selected bone turnover markers for early diagnosis of postmenopausal osteoporosis.
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