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地诺单抗治疗骨质疏松症的综述。

A review of denosumab for the treatment of osteoporosis.

作者信息

Miyazaki Tsuyoshi, Tokimura Fumiaki, Tanaka Sakae

机构信息

Department of Orthopedic Surgery, Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology, Itabashi-ku, Tokyo, Japan ; Department of Geriatric Medicine, Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology, Itabashi-ku, Tokyo, Japan.

Department of Orthopedic Surgery, Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology, Itabashi-ku, Tokyo, Japan.

出版信息

Patient Prefer Adherence. 2014 Apr 8;8:463-71. doi: 10.2147/PPA.S46192. eCollection 2014.

Abstract

Osteoporosis is an age-related systemic skeletal disease characterized by low bone mass and microarchitectural deterioration of bone tissue, with a consequent increase in bone fragility. Bone remodeling involves two types of cells: osteoblasts and osteoclasts. Receptor activator of nuclear factor-κB ligand (RANKL) is a key regulator of the formation and function of bone-resorbing osteoclasts, and its cell surface receptor, receptor activator of nuclear factor-κB (RANK), is expressed by both osteoclast precursors and mature osteoclasts. Denosumab is a fully human monoclonal anti-RANKL antibody that inhibits the binding of RANKL to RANK, thereby decreasing osteoclastogenesis and bone-resorbing activity of mature osteoclasts. Although there are many medications available for the treatment of osteoporosis, inhibition of RANKL by denosumab has been shown to significantly affect bone metabolism. Denosumab appears to be a promising, highly effective, and safe parenteral therapy with good adherence for osteoporosis. Moreover, denosumab may be cost-effective therapy compared with existing alternatives. Therefore, in this review, we focus on studies of denosumab and the risks and benefits identified for this type of treatment for osteoporosis.

摘要

骨质疏松症是一种与年龄相关的全身性骨骼疾病,其特征为骨量低和骨组织微结构退化,进而导致骨脆性增加。骨重塑涉及两种类型的细胞:成骨细胞和破骨细胞。核因子κB受体活化因子配体(RANKL)是骨吸收破骨细胞形成和功能的关键调节因子,其细胞表面受体核因子κB受体活化因子(RANK)在破骨细胞前体和成熟破骨细胞中均有表达。地诺单抗是一种全人源单克隆抗RANKL抗体,可抑制RANKL与RANK的结合,从而减少破骨细胞生成和成熟破骨细胞的骨吸收活性。尽管有许多药物可用于治疗骨质疏松症,但地诺单抗抑制RANKL已被证明可显著影响骨代谢。地诺单抗似乎是一种有前景、高效且安全的肠外治疗药物,对骨质疏松症的依从性良好。此外,与现有替代药物相比,地诺单抗可能是具有成本效益的治疗方法。因此,在本综述中,我们重点关注地诺单抗的研究以及这种骨质疏松症治疗方法所确定的风险和益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c36/3986336/8943ad9329cd/ppa-8-463Fig1.jpg

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