Wei Chao, Wang Xiaobin, Mei Zubing, Li Jing
Department of Spine Surgery, The Second Xiangya Hospital, Central South University, Changsha, China.
Department of Spine Surgery, The First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China.
Front Pharmacol. 2025 Mar 10;16:1510968. doi: 10.3389/fphar.2025.1510968. eCollection 2025.
Osteoporosis and diabetes mellitus (DM) are both prevalent chronic conditions associated with significant morbidity, particularly in aging populations. Patients with DM are at increased risk of developing osteoporosis due to complex pathophysiological interactions between glucose metabolism and bone health. Although pharmacological interventions have been used to prevent and manage osteoporosis in individuals with DM, variability in reported outcomes across studies hinders evidence synthesis and meta-analyses. A standardized Core Outcome Set (COS) is required to harmonize outcome reporting in clinical trials, improving comparability and clinical relevance. This paper outlines the protocol for developing a COS for pharmacological interventions targeting osteoporosis among patients with DM.
The development of the COS will follow a five-phase approach. Phase 1 involves a systematic review to identify key outcomes in clinical trials of osteoporosis pharmacotherapy in diabetic populations. Phase 2 consists of a modified Delphi process involving international experts in endocrinology, bone metabolism, and diabetes care, as well as patients and public representatives. This will be followed by Phase 3, where consensus meetings will be held to finalize the essential outcomes for inclusion. Phase 4 will focus on identifying appropriate outcome measurement tools based on a systematic review and additional consensus-building meetings. Finally, Phase 5 will involve dissemination and implementation activities to ensure broad adoption of the COS in future research and clinical trials. Patient and Public Involvement (PPI) will be integrated throughout all phases of the project to ensure the relevance of selected outcomes.
The resulting COS will provide a standardized framework for reporting outcomes in pharmacological intervention studies of osteoporosis in patients with DM. By facilitating meta-analyses and data pooling, this COS will improve the comparability of clinical trials, enhance research efficiency, and reduce outcome reporting bias. Ultimately, the COS will support better clinical decision-making, fostering the development of targeted and effective therapies for osteoporosis in the context of diabetes.
骨质疏松症和糖尿病(DM)都是常见的慢性疾病,会引发严重的发病率,尤其是在老年人群中。由于葡萄糖代谢与骨骼健康之间存在复杂的病理生理相互作用,糖尿病患者患骨质疏松症的风险增加。尽管已采用药物干预措施来预防和管理糖尿病患者的骨质疏松症,但各研究报告结果的差异阻碍了证据综合和荟萃分析。需要一个标准化的核心结局集(COS)来统一临床试验中的结局报告,提高可比性和临床相关性。本文概述了为针对糖尿病患者骨质疏松症的药物干预制定COS的方案。
COS的制定将采用五阶段方法。第1阶段包括系统评价,以确定糖尿病患者骨质疏松症药物治疗临床试验中的关键结局。第2阶段包括一个经过改进的德尔菲法过程,涉及内分泌学、骨代谢和糖尿病护理方面的国际专家,以及患者和公众代表。接下来是第3阶段,将召开共识会议以最终确定纳入的基本结局。第4阶段将专注于根据系统评价和额外的共识建立会议确定合适的结局测量工具。最后,第5阶段将涉及传播和实施活动,以确保COS在未来研究和临床试验中得到广泛采用。患者和公众参与(PPI)将贯穿项目的所有阶段,以确保所选结局的相关性。
最终形成的COS将为糖尿病患者骨质疏松症药物干预研究的结局报告提供一个标准化框架。通过促进荟萃分析和数据合并,该COS将提高临床试验的可比性,提高研究效率,并减少结局报告偏倚。最终,COS将支持更好的临床决策,促进在糖尿病背景下针对骨质疏松症的靶向有效治疗的发展。