胰高血糖素样肽-1 受体激动剂与糖尿病骨病:促泌剂的另一种积极作用?一项为期 12 个月的纵向研究。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-08-01 Epub Date: 2024-06-12 DOI:10.1007/s00223-024-01240-1
Antonella Al Refaie, Leonardo Baldassini, Caterina Mondillo, Elena Ceccarelli, Roberto Tarquini, Luigi Gennari, Stefano Gonnelli, Carla Caffarelli
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引用次数: 0

摘要

糖尿病骨病是 2 型糖尿病(T2DM)患者的常见并发症。T2DM 与骨折风险增加之间的关联促使人们研究新型抗糖尿病药物对骨代谢的影响。胰高血糖素样肽-1受体激动剂(GLP-1RAs)是一种增量蛋白模拟药物,具有多种生物效应特性。GLP-1RAs 与骨骼之间的关系非常复杂:虽然体外和动物研究已证明其对骨骼有保护作用,但人体研究却很少。我们领导了一项为期 12 个月的纵向研究,对 65 名计划接受 GLP-1RAs 治疗的 T2DM 患者的骨骼变化进行评估。54 名 T2DM 患者完成了为期 12 个月的研究,其中 30 人接受了每周一次的度拉鲁肽治疗,24 人接受了每周一次的赛马鲁肽治疗。使用 GLP-1RA 治疗一年后,体重和体重指数显著下降。在接受 GLP-1RAs 治疗 12 个月之前和之后,对骨质密度 (BMD)、骨代谢、骨小梁评分 (TBS)、脂肪连素和肌生成素进行了评估。治疗 12 个月后,骨转换标志物和脂肪连蛋白显著增加,而肌生成素值则略有下降,但幅度很大。通过 DXA 测定的 BMD-LS 值明显下降,而通过 REMS 测定的 BMD-LS 值下降不明显,TBS 值略有上升。DXA 和 REMS 技术都显示股骨 BMD 有轻微但明显的下降。总之,使用 GLP-1RA 12 个月可保持骨质并重新激活骨转换。GLP-1RA 是否能成为 T2DM 和骨质疏松症患者的有效治疗选择,还需要进一步研究证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Glucagon-like Peptide-1 Receptor Agonists and Diabetic Osteopathy: Another Positive Effect of Incretines? A 12 Months Longitudinal Study.

Glucagon-like Peptide-1 Receptor Agonists and Diabetic Osteopathy: Another Positive Effect of Incretines? A 12 Months Longitudinal Study.

Diabetic osteopathy is a frequent complication in patients with type 2 diabetes mellitus (T2DM). The association between T2DM and increased fracture risk has led to study the impact of new antidiabetic drugs on bone metabolism. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are incretin mimetic drugs which have many pleiotropic properties. The relationship between GLP-1RAs and bone is very complex: while in vitro and animal studies have demonstrated a protective effect on bone, human studies are scarce. We led a 12 months longitudinal study evaluating bone changes in 65 patients withT2DM for whom a therapy with GLP-1RAs had been planned. Fifty-four T2DM patients completed the 12-month study period; of them, 30 had been treated with weekly dulaglutide and 24 with weekly semaglutide. One-year therapy with GLP-1RAs resulted in a significant reduction in weight and BMI. Bone mineral density (BMD), bone metabolism, trabecular bone score (TBS), adiponectin, and myostatin were evaluated before and after 12 months of GLP-1RAs therapy. After 12 months of therapy bone turnover markers and adiponectin showed a significant increase, while myostatin values showed a modest but significant reduction. BMD-LS by DXA presented a significant reduction while the reduction in BMD-LS by REMS was not significant and TBS values showed a marginal increase. Both DXA and REMS techniques showed a modest but significant reduction in femoral BMD. In conclusion, the use of GLP-1RAs for 12 months preserves bone quality and reactivates bone turnover. Further studies are needed to confirm whether GLP-1RAs could represent a useful therapeutic option for patients with T2DM and osteoporosis.

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