Mechanisms Underlying Normal Fracture Healing and Risk Factors for Delayed Healing

被引:44
作者
Cheng, Cheng [1 ,2 ]
Shoback, Dolores [1 ,2 ]
机构
[1] San Francisco VA Med Ctr, Dept Med, Endocrine Res Unit, 1700 Owens St,Room 369, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Dept Med, Div Endocrinol & Metab, San Francisco, CA 94143 USA
关键词
Fracture healing; Risk factors; Osteoporosis; Bisphosphonates; Denosumab; Estrogen; Raloxifene; Parathyroid hormone (PTH); PTH-related peptide; Atypical femoral fracture; Sclerostin; Dickkopf-1; ATYPICAL FEMORAL FRACTURES; IMPROVES SCREW FIXATION; SCLEROSTIN ANTIBODY; POSTMENOPAUSAL WOMEN; BONE-FORMATION; DISTAL RADIUS; NONENZYMATIC GLYCATION; SYSTEMIC TREATMENT; BISPHOSPHONATE USE; DIABETES-MELLITUS;
D O I
10.1007/s11914-019-00501-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of ReviewSubstantial advances have been made in understanding the biological basis of fracture healing. Yet, it is unclear whether the presence of osteoporosis or prior or current osteoporosis therapy influences the healing process or is associated with impaired healing. This review discusses the normal process of fracture healing and the role of osteoporosis and patient-specific factors in relation to fracture repair.Recent FindingsThe definitive association of osteoporosis to impaired fracture healing remains inconclusive because of limited evidence addressing this point. eStudies testing anabolic agents in preclinical models of ovariectomized animals with induced fractures have produced mostly positive findings showing enhanced fracture repair. Prospective human clinical trials, although few in number and limited in design and to testing only one anabolic agent, have similarly yielded modestly favorable results.SummaryInterest is high for exploring currently available osteoporosis therapies for efficacy in fracture repair. Definitive data supporting their efficacy are essential in achieving approval for this indication.
引用
收藏
页码:36 / 47
页数:12
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