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Sub-optimal cholesterol response to initiation of statins and future risk of cardiovascular disease

机译:次优的胆固醇回应起始他汀类药物和未来心血管疾病的风险

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Objective To assess low-density lipoprotein cholesterol (LDL-C) response in patients after initiation of statins, and future risk of cardiovascular disease (CVD). Methods Prospective cohort study of 165 411 primary care patients, from the UK Clinical Practice Research Datalink, who were free of CVD before statin initiation, and had at least one pre-treatment LDL-C within 12 months before, and one post-treatment LDL-C within 24 months after, statin initiation. Based on current national guidelines, <40% reduction in baseline LDL-C within 24 months was classified as a sub-optimal statin response. Cox proportional regression and competing-risks survival regression models were used to determine adjusted hazard ratios (HRs) and sub-HRs for incident CVD outcomes for LDL-C response to statins. Results 84 609 (51.2%) patients had a sub-optimal LDL-C response to initiated statin therapy within 24 months. During 1 077 299 person-years of follow-up (median follow-up 6.2 years), there were 22 798 CVD events (12 142 in sub-optimal responders and 10 656 in optimal responders). In sub-optimal responders, compared with optimal responders, the HR for incident CVD was 1.17 (95% CI 1.13 to 1.20) and 1.22 (95% CI 1.19 to 1.25) after adjusting for age and baseline untreated LDL-C. Considering competing risks resulted in lower but similar sub-HRs for both unadjusted (1.13, 95% CI 1.10 to 1.16) and adjusted (1.19, 95% CI 1.16 to 1.23) cumulative incidence function of CVD. Conclusions Optimal lowering of LDL-C is not achieved within 2 years in over half of patients in the general population initiated on statin therapy, and these patients will experience significantly increased risk of future CVD.
机译:摘要目的评估低密度脂蛋白胆固醇(低密度脂蛋白)反应后的病人他汀类药物的起始,和未来的风险心血管疾病(CVD)。165 411名初级护理患者队列研究,来自英国的临床实践研究数据链接,在他汀类药物和无心血管疾病情况下启动,,至少有一个预处理低密度12个月前,一个治疗后的低密度后24个月内,他汀类初始化。对当前国家指导方针,<减少40%基线内低密度划分为24个月次优的他汀类药物的反应。回归和competing-risks生存回归模型来确定调整风险比率(小时)和sub-HRs CVD事件结果的支持对他汀类药物的反应。84年609名(51.2%)患者有一个次优的低密度反应开始他汀类药物治疗在24个月。后续(中位随访6.2年),在那里22 798 CVD事件(12 142次优急救员和10 656年最佳反应)。最优反应者,而最优的反应,发生心血管疾病为1.17(95%的人力资源可信区间1.13 - 1.20)和1.22 (95% CI 1.19 - 1.25)在调整了年龄和基线治疗低密度。但类似的sub-HRs未经调整的低(1.13, 95%可信区间1.10到1.16)和调整(1.19,95%可信区间1.16到1.23)累计发病率化学汽相淀积的函数。低密度不是在2年内达到一半以上的患者在一般人群开始他汀类药物治疗,这些患者体验未来的风险显著增加CVD。

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