Department of Bone & Joint Surgery, Peking University Shenzhen Hospital, Shenzhen, 518036, People's Republic of China.
National & Local Joint Engineering Research Center of Orthopaedic Biomaterials, Peking University Shenzhen Hospital, Shenzhen, 518036, People's Republic of China.
Arthritis Res Ther. 2023 Jan 6;25(1):3. doi: 10.1186/s13075-022-02981-w.
Osteoarthritis (OA) is a common and prevalent degenerative joint disease characterized by degradation of the articular cartilage. However, none of disease-modifying OA drugs is approved currently. Teriparatide (PTH (1-34)) might stimulate chondrocyte proliferation and cartilage regeneration via some uncertain mechanisms. Relevant therapies of PTH (1-34) on OA with such effects have recently gained increasing interest, but have not become widespread practice. Thus, we launch this systematic review (SR) to update the latest evidence accordingly. A comprehensive literature search was conducted in PubMed, Web of Science, MEDLINE, the Cochrane Library, and Embase from their inception to February 2022. Studies investigating the effects of the PTH (1-34) on OA were obtained. The quality assessment and descriptive summary were made of all included studies. Overall, 307 records were identified, and 33 studies were included. In vivo studies (n = 22) concluded that PTH (1-34) slowed progression of OA by alleviating cartilage degeneration and aberrant remodeling of subchondral bone (SCB). Moreover, PTH (1-34) exhibited repair of cartilage and SCB, analgesic, and anti-inflammatory effects. In vitro studies (n = 11) concluded that PTH (1-34) was important for chondrocytes via increasing the proliferation and matrix synthesis but preventing apoptosis or hypertrophy. All included studies were assessed with low or unclear risk of bias in methodological quality. The SR demonstrated that PTH (1-34) could alleviate the progression of OA. Moreover, PTH (1-34) had beneficial effects on osteoporotic OA (OPOA) models, which might be a therapeutic option for OA and OPOA treatment.
骨关节炎(OA)是一种常见且普遍的退行性关节疾病,其特征是关节软骨退化。然而,目前尚无任何一种改变疾病进程的 OA 药物获得批准。甲状旁腺素(PTH(1-34))可能通过一些不确定的机制刺激软骨细胞增殖和软骨再生。最近,PTH(1-34)对 OA 的这种治疗作用引起了越来越多的关注,但尚未广泛应用。因此,我们开展了这项系统评价(SR),以更新最新的证据。我们在 PubMed、Web of Science、MEDLINE、Cochrane 图书馆和 Embase 中进行了全面的文献检索,检索时间从建库开始至 2022 年 2 月。获取了研究 PTH(1-34)对 OA 影响的研究。对所有纳入研究进行了质量评估和描述性总结。总的来说,共确定了 307 条记录,纳入了 33 项研究。体内研究(n=22)得出结论,PTH(1-34)通过缓解软骨退化和软骨下骨(SCB)异常重塑来减缓 OA 的进展。此外,PTH(1-34)表现出修复软骨和 SCB、镇痛和抗炎作用。体外研究(n=11)得出结论,PTH(1-34)通过增加增殖和基质合成但防止凋亡或肥大对软骨细胞很重要。所有纳入的研究在方法学质量方面均被评估为低风险或不确定风险。该 SR 表明,PTH(1-34)可以缓解 OA 的进展。此外,PTH(1-34)对骨质疏松性 OA(OPOA)模型有有益作用,这可能是 OA 和 OPOA 治疗的一种治疗选择。