Multimorbidity Double Burden: Elevated Refracture Risk Despite High Mortality Following Fractures - A Linked Cohort Study.

IF 6.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Mike Lin, Thach Tran, Dima Alajlouni, Weiwen Chen, Angela Sheu, Robert D Blank, Dana Bliuc, Jacqueline R Center
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引用次数: 0

Abstract

Multimorbidity - defined as the presence of two or more chronic conditions - is highly prevalent among older adults with fractures and is associated with excess mortality; however, its impact on refracture risk remains uncertain. This study aimed to quantify refracture risk across different multimorbidity clusters and fracture sites, in order to identify high-risk individuals. A whole-of-population data linkage cohort study was conducted among adults aged 50 years and above living in New South Wales, Australia with at least one hospital or emergency admission between 1 January 2005 and 30 June 2022. Individuals who sustained a fracture between 1 January 2005 to 30 June 2021 were followed until 30 June 2022 for refracture and mortality outcomes. Latent class analysis (LCA) identified multimorbidity clusters. Fine-Gray subdistribution and Cox proportional hazards models estimated refracture and mortality risk. Among 335,308 individuals with fractures, 31.2% were men (mean [SD] age, 76.3 (10.7) years) and 68.8% were women (77.4 [10.7] years). Six clusters were identified: five multimorbidity clusters (cardiometabolic, cardiovascular, cancer, geriatric and mental health; median comorbidity count: 4-13) and one low multimorbidity cluster (median comorbidity count: 0). When compared to the general NSW population risk of incident fracture and death, all clusters demonstrated substantially higher refracture risk (HR range: 2.39-3.38 in men, 1.62-2.36 in women) despite high competing mortality (HR range: 1.58-4.52 in men, 1.13-3.08 in women). The mental health cluster carried the highest refracture burden, while distal fracture sites were associated with higher refracture risk due to lower mortality. Multimorbidity does not attenuate refracture risk; instead, it heightens vulnerability among older fracture patients, even in the presence of competing mortality. These findings reinforce the need for timely, targeted secondary fracture prevention, particularly following non-hip, non-vertebral fractures.

多病双重负担:骨折后死亡率高,再骨折风险高——一项相关队列研究。
多病——定义为存在两种或两种以上慢性疾病——在老年骨折患者中非常普遍,并与高死亡率相关;然而,其对再破裂风险的影响仍不确定。本研究旨在量化不同多病群和骨折部位的再骨折风险,以确定高危人群。在2005年1月1日至2022年6月30日期间至少住过一家医院或急诊的澳大利亚新南威尔士州50岁及以上成年人中开展了一项全人口数据关联队列研究。对2005年1月1日至2021年6月30日期间发生骨折的患者进行随访,直至2022年6月30日,观察再骨折和死亡率结果。潜在分类分析(LCA)确定了多发病集群。细灰色亚分布和Cox比例风险模型估计了再骨折和死亡风险。在335308例骨折患者中,31.2%为男性(平均[SD]年龄76.3(10.7)岁),68.8%为女性(77.4[10.7]岁)。确定了6个集群:5个多病集群(心脏代谢、心血管、癌症、老年和精神健康;共病中位数:4-13)和1个低多病集群(共病中位数:0)。与新南威尔士州一般人群的意外骨折和死亡风险相比,尽管死亡率很高(男性的风险比范围:2.39-3.38,女性的风险比范围:1.62-2.36),但所有人群的再骨折风险都明显更高(男性的风险比范围:1.58-4.52,女性的风险比范围:1.13-3.08)。精神健康群的再骨折负担最重,而远端骨折部位由于死亡率较低,再骨折风险较高。多重发病不能降低再骨折的风险;相反,它增加了老年骨折患者的脆弱性,即使存在竞争死亡率。这些发现强调了及时、有针对性地预防继发性骨折的必要性,特别是在非髋部、非椎体骨折后。
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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
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