Chen Ming, Lyu Yiming, Zhao Jingwei, Han Xianwei, Huang Tao, Yang Tongtao, Zhou Yong
Department of Orthopedics, Tangdu Hospital, Airforce Medical University (Fourth Military Medical University), Xi'an, Shanxi, China.
Medmotion Clinic, Shanghai, China.
Front Endocrinol (Lausanne). 2025 May 21;16:1586589. doi: 10.3389/fendo.2025.1586589. eCollection 2025.
Type 2 diabetes mellitus (T2DM) is an independent risk factor for osteoporosis, increasing the risk of fractures and poor prognosis. Recent studies suggest that glucagon-like peptide-1 receptor agonists (GLP-1 RAs) may play a protective role in bone metabolism. However, limited evidence exists on their effect on osteoporosis incidence in T2DM patients. This study aimed to evaluate the association between GLP-1 RA use and osteoporosis risk in a real-world cohort of elderly T2DM patients.
This retrospective cohort study utilized electronic medical records (EMRs) from Tangdu Hospital, Xi'an, China, between January 1, 2012, and December 31, 2023. Patients with T2DM who had at least two clinical visits annually and no prior osteoporosis diagnosis (ICD-10: M80-M82) at baseline were included. The primary outcome was the incidence of osteoporosis during follow-up. Cox proportional hazards models were used to evaluate the association between GLP-1 RA use and osteoporosis risk, adjusting for age, sex, BMI, blood pressure, lipid profile, renal function, osteocalcin, vitamin D levels, HbA1c, statin use, antihypertensive medication use, and smoking status. Subgroup analyses were conducted to assess potential effect modifications.
A total of 1,845 patients with T2DM were included, of whom 676 (36.6%) developed osteoporosis during follow-up. Among the 256 patients who received GLP-1 RAs, the incidence of osteoporosis was significantly lower than in those who did not receive GLP-1 RAs (P < 0.01). In the fully adjusted Cox model, GLP-1 RA use was associated with a significantly reduced risk of osteoporosis compared to non-users (hazard ratio [HR] = 0.69, 95% confidence interval [CI] =0.45-0.84, P < 0.05). Subgroup analyses indicated that the protective effect of GLP-1 RAs was consistent across age, sex, BMI, smoking status, and antihypertensive medication use (P for interaction > 0.05).
In patients with T2DM, patients with treatment of GLP-1 RAs resulted in lower risks of osteoporosis than those without treatment of GLP-1 RAs. These findings support the potential bone-protective effects of GLP-1 RAs but further randomized controlled trials (RCTs) or large-scale database analyses are needed to confirm these observations and guide clinical recommendations.
2型糖尿病(T2DM)是骨质疏松症的独立危险因素,会增加骨折风险和不良预后。近期研究表明,胰高血糖素样肽-1受体激动剂(GLP-1 RAs)可能在骨代谢中发挥保护作用。然而,关于其对T2DM患者骨质疏松症发病率影响的证据有限。本研究旨在评估在老年T2DM患者的真实世界队列中,使用GLP-1 RA与骨质疏松症风险之间的关联。
这项回顾性队列研究利用了中国西安唐都医院2012年1月1日至2023年12月31日的电子病历(EMR)。纳入每年至少有两次临床就诊且基线时无骨质疏松症诊断(国际疾病分类第10版:M80-M82)的T2DM患者。主要结局是随访期间骨质疏松症的发病率。使用Cox比例风险模型评估使用GLP-1 RA与骨质疏松症风险之间的关联,并对年龄、性别、体重指数、血压、血脂谱、肾功能、骨钙素、维生素D水平、糖化血红蛋白、他汀类药物使用、抗高血压药物使用和吸烟状况进行校正。进行亚组分析以评估潜在的效应修饰。
共纳入1845例T2DM患者,其中676例(36.6%)在随访期间发生骨质疏松症。在接受GLP-1 RA的256例患者中,骨质疏松症的发病率显著低于未接受GLP-1 RA的患者(P<0.01)。在完全校正的Cox模型中,与未使用者相比,使用GLP-1 RA与骨质疏松症风险显著降低相关(风险比[HR]=0.69,95%置信区间[CI]=0.45-0.84,P<0.05)。亚组分析表明,GLP-1 RA的保护作用在年龄、性别、体重指数、吸烟状况和抗高血压药物使用方面是一致的(交互作用P>0.05)。
在T2DM患者中,接受GLP-1 RA治疗的患者发生骨质疏松症的风险低于未接受GLP-1 RA治疗的患者。这些发现支持了GLP-1 RA潜在的骨保护作用,但需要进一步的随机对照试验(RCT)或大规模数据库分析来证实这些观察结果并指导临床建议。