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雷美替胺使用与脆性骨折风险之间的关联:一项回顾性队列研究。

Association between ramelteon use and risk of fragility fractures: A retrospective cohort study.

作者信息

Tange Hitoshi, Miyamoto Yoshihisa, Sasabuchi Yusuke, Yasunaga Hideo

机构信息

Department of Clinical Epidemiology and Health Economics, School of Public Health, The University of Tokyo, 7-3-1, Hongo, Bunkyo-Ku, Tokyo, 1130033, Japan.

Department of Real-World Evidence, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

出版信息

Arch Osteoporos. 2025 Jul 15;20(1):95. doi: 10.1007/s11657-025-01582-9.

Abstract

UNLABELLED

The effect of melatonin receptor agonists on bone remains unclear. This retrospective cohort study provides the first evidence that the short- to mid-term use of ramelteon is not associated with the risk of fracture. Further research with longer follow-up is needed to clarify the effects of ramelteon on bone health.

BACKGROUND

Recent studies have suggested that melatonin may have the potential to treat osteoporosis. However, few studies have examined the effects of melatonin receptor agonists on bone health. This study aimed to evaluate the association between ramelteon use and the risk of fragility fractures.

METHODS

We conducted a retrospective cohort study from April 2014 to November 2022 using the DeSC database, a large healthcare claims database in Japan, employing an active comparator and new-user design. Female participants aged ≥ 50 years were included in the study. Exposure was defined as the first dispensation of ramelteon or orexin receptor antagonists. The outcome was a composite of major fragility fractures, including hip, vertebral, wrist, proximal humeral, and ankle fractures. To adjust for potential confounders, we used overlap weighting analysis with propensity scores. Cox regression analyses were performed both before and after applying overlap weighting.

RESULTS

A total of 106,511 individuals were identified, including 23,312 new ramelteon users and 83,199 new orexin receptor antagonist users. The overall fracture incidence was 9,429 per 100,000 person-years in the ramelteon group and 7,330 per 100,000 person-years in the orexin receptor antagonist group. The adjusted hazard ratio for overall fractures associated with ramelteon use was 1.07 (95% confidence interval: 0.99-1.17). The results were consistent across fracture types, age groups, and landmark analyses.

CONCLUSIONS

In a real-world setting, short- to mid-term ramelteon use was not associated with an increased risk of fractures. Future studies should consider longer follow-up periods to further investigate the effects of ramelteon on bone health.

摘要

未标注

褪黑素受体激动剂对骨骼的影响尚不清楚。这项回顾性队列研究首次证明,短期至中期使用雷美替胺与骨折风险无关。需要进行更长时间随访的进一步研究,以阐明雷美替胺对骨骼健康的影响。

背景

最近的研究表明,褪黑素可能具有治疗骨质疏松症的潜力。然而,很少有研究探讨褪黑素受体激动剂对骨骼健康的影响。本研究旨在评估雷美替胺的使用与脆性骨折风险之间的关联。

方法

我们使用日本一个大型医疗保健理赔数据库DeSC数据库,于2014年4月至2022年11月进行了一项回顾性队列研究,采用活性对照和新用户设计。纳入研究的女性参与者年龄≥50岁。暴露定义为首次配发雷美替胺或食欲素受体拮抗剂。结局为主要脆性骨折的复合情况,包括髋部、脊椎、腕部、肱骨近端和踝部骨折。为了调整潜在的混杂因素,我们使用倾向评分重叠加权分析。在应用重叠加权前后均进行了Cox回归分析。

结果

共识别出106,511人,包括23,312名新的雷美替胺使用者和83,199名新的食欲素受体拮抗剂使用者。雷美替胺组的总体骨折发生率为每十万人年9,429例,食欲素受体拮抗剂组为每十万人年7,330例。与使用雷美替胺相关联的总体骨折调整后风险比为1.07(95%置信区间:0.99 - 1.17)。在骨折类型、年龄组和标志性分析中结果一致。

结论

在现实环境中,短期至中期使用雷美替胺与骨折风险增加无关。未来的研究应考虑更长时间随访,以进一步研究雷美替胺对骨骼健康产生的影响。

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