Unveiling the association between low-density lipoprotein cholesterol lowering and fracture risk : real-world evidence from a target trial emulation study.

IF 5.5 2区 医学 Q2 CELL & TISSUE ENGINEERING
Zeqin Wen, Xiaoxiao Li, Yilun Wang, Yuqing Zhang, Junqing Xie, Houchen Lyu, Changjun Li, Jie Wei, Guanghua Lei, Chao Zeng
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Abstract

Aims: High serum low-density lipoprotein cholesterol (LDL-C) levels are associated with increased risk of fracture; however, it remains unclear whether lowering LDL-C reduces fracture risk, and, if so, whether the magnitude of LDL-C reduction is linearly associated with fracture risk. This study aimed to evaluate the relation between the degree of LDL-C reduction and fracture risk.

Methods: This population-based cohort study included individuals aged 40 to 90 years who initiated statins for hyperlipidaemia from IQVIA Medical Research Data primary care database in the UK (2000 to 2022). The primary outcome was hip fracture. Secondary outcomes included composite fracture and major osteoporotic fracture. A hypothetical target trial was emulated to assess the effect of achieving a LDL-C level of 1.8 to 2.6 mmol/L or < 1.8 mmol/L versus > 2.6 mmol/L induced by statin initiation within one year on the risk of incident and recurrent fractures over five years.

Results: Among 165,242 people with hyperlipidaemia initiating statins (mean age 62.6 years, 51.1% female), the five-year risk of incident hip fracture was lower in the 1.8 to 2.6 mmol/L arm (0.53%) and in the < 1.8 mmol/L arm (0.52%) than the > 2.6 mmol/L LDL-C arm (0.65%). The corresponding hazard ratios (HRs) were 0.77 (95% CI 0.65 to 0.91) and 0.68 (95% CI 0.54 to 0.86), respectively. A similar decreased risk of recurrent hip fracture was observed for the 1.8 to 2.6 mmol/L arm (HR = 0.79, 95% CI 0.39 to 1.58) and < 1.8 mmol/L arm (HR = 0.32, 95% CI 0.15 to 0.66), respectively. Additionally, lowering LDL-C levels reduced the risks of composite fracture and major osteoporotic fracture.

Conclusion: In this population-based cohort study, LDL-C lowering was associated with a decreased risk of fracture in individuals with hyperlipidaemia. This decreased risk appeared to be associated with the extent of LDL-C lowering, suggesting that the therapeutic paradigm of 'lower is better' could be advantageous for fracture prevention in individuals with hyperlipidaemia.

Abstract Image

Abstract Image

揭示低密度脂蛋白胆固醇降低与骨折风险之间的关系:来自目标试验模拟研究的真实世界证据。
目的:高血清低密度脂蛋白胆固醇(LDL-C)水平与骨折风险增加相关;然而,目前尚不清楚降低LDL-C是否能降低骨折风险,如果是这样,LDL-C降低的幅度是否与骨折风险线性相关。本研究旨在评价LDL-C降低程度与骨折风险之间的关系。方法:这项基于人群的队列研究纳入了来自英国IQVIA医学研究数据初级保健数据库(2000年至2022年)的40至90岁开始使用他汀类药物治疗高脂血症的个体。主要结局为髋部骨折。次要结局包括复合骨折和主要骨质疏松性骨折。模拟了一项假设的目标试验,以评估LDL-C水平达到1.8至2.6 mmol/L或< 1.8 mmol/L与他汀类药物在一年内诱导的2.6 mmol/L对五年内发生和复发性骨折风险的影响。结果:在165242名开始服用他汀类药物的高脂血症患者中(平均年龄62.6岁,51.1%为女性),1.8 ~ 2.6 mmol/L组(0.53%)和< 1.8 mmol/L组(0.52%)发生髋部骨折的5年风险低于2.6 mmol/L组(0.65%)。相应的风险比(hr)分别为0.77 (95% CI 0.65 ~ 0.91)和0.68 (95% CI 0.54 ~ 0.86)。在1.8至2.6 mmol/L组(HR = 0.79, 95% CI 0.39至1.58)和< 1.8 mmol/L组(HR = 0.32, 95% CI 0.15至0.66)中观察到类似的髋部骨折复发风险降低。此外,降低LDL-C水平降低了复合骨折和主要骨质疏松性骨折的风险。结论:在这项基于人群的队列研究中,LDL-C降低与高脂血症患者骨折风险降低相关。这种风险的降低似乎与LDL-C降低的程度有关,这表明“越低越好”的治疗模式可能有利于高脂血症患者的骨折预防。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Bone & Joint Research
Bone & Joint Research CELL & TISSUE ENGINEERING-ORTHOPEDICS
CiteScore
7.40
自引率
23.90%
发文量
156
审稿时长
12 weeks
期刊介绍: The gold open access journal for the musculoskeletal sciences. Included in PubMed and available in PubMed Central.
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