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Long-term effects of statin treatment in elderly people: extended follow-up of the PROspective Study of Pravastatin in the Elderly at Risk (PROSPER)

机译:他汀类药物治疗对老年人的长期影响:普伐他汀在高危老年人中的前瞻性研究的扩展随访(PROSPER)

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摘要

Background The PROspective Study of Pravastatin in the Elderly at Risk (PROSPER), a placebo-controlled trial of pravastatin, demonstrated a 19% reduction in coronary outcomes (p = 0.006) after a mean of 3.2 years, with no impact on stroke outcomes or all-cause mortality. However, there was a suggestion of increased cancer risk. Our aim is to determine the long-term benefits and safety of pravastatin treatment in older people using post-trial follow-up of the PROSPER participants. Methods: 5,804 (2,520 Scottish) men and women aged 70–82 years with either pre-existing vascular disease or increased risk of such disease because of smoking, hypertension or diabetes, were randomised to 40 mg pravastatin or matching placebo. Using record linkage to routinely collected health records, all participants (full cohort) were linked to death and cancer registries, and the Scottish cohort additionally to hospital admissions, to provide composite fatal/non-fatal cardiovascular outcomes (total mean follow-up 8.6 years). Results: Pravastatin treatment for 3.2 years reduced CHD death in the full cohort, hazard ratio (HR) 0.80, 95% confidence interval (CI) 0.68–0.95, p = 0.0091 and fatal coronary events or coronary hospitalisations in the Scottish cohort (HR 0.81, 95% CI 0.69–0.95, p = 0.0081) over 8.6 years. There was no reduction in stroke or all-cause mortality. Cancer risk was not increased in the full cohort (HR 1.08, 95% CI 0.96–1.21, p = 0.22). Conclusions: Pravastatin treatment of elderly high-risk subjects for 3.2 years provided long-term protection against CHD events and CHD mortality. However, this was not associated with any increase in life expectancy, possibly due to competing mortality with deaths from other causes. There was no evidence of long-term increased risk of cancer.
机译:背景普伐他汀在危险中的老年人中的前瞻性研究(PROSPER)是普伐他汀的安慰剂对照试验,显示平均3.2年后,冠状动脉预后降低19%(p = 0.006),对卒中预后或全因死亡率。但是,有增加癌症风险的暗示。我们的目的是通过对PROSPER参与者进行试验后的随访,确定普伐他汀对老年人的长期益处和安全性。方法:将5,804名(2,520名苏格兰人)年龄在70-82岁之间的既往存在血管疾病或因吸烟,高血压或糖尿病而患此类疾病的风险增加的男性和女性随机分配至40 mg普伐他汀或与之匹配的安慰剂。使用记录链接到常规收集的健康记录,所有参与者(整个队列)都与死亡和癌症登记处相关联,苏格兰队列与医院入院相关联,以提供致命/非致命的心血管综合结果(平均平均随访8.6年) )。结果:普伐他汀治疗3.2年可降低整个队列中的冠心病死亡,危险比(HR)0.80、95%置信区间(CI)0.68-0.95,p = 0.0091以及苏格兰队列中致命的冠状动脉事件或冠心病住院(HR 0.81 ,95%CI 0.69–0.95,p = 0.0081),为期8.6年。中风或全因死亡率没有降低。在整个队列中,癌症风险没有增加(HR 1.08,95%CI 0.96-1.21,p = 0.22)。结论:普伐他汀治疗老年高危受试者3.2年,可长期预防冠心病事件和冠心病死亡率。但是,这与预期寿命的任何增加均无关,这可能是由于死亡率与其他原因导致的死亡相抵触所致。没有证据表明长期患癌症的风险增加。

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