CMC Ambroise Paré, Critical Care Medicine Department, Neuilly-sur-Seine, France; Sorbonne Université, INSERM CIC Paris-Est, AP-HP, ICAN, Pitié-Salpêtrière Hospital, Department of Pharmacology, F-75013 Paris, France.
CMC Ambroise Paré, Critical Care Medicine Department, Neuilly-sur-Seine, France.
Int J Cardiol. 2019 Jul 1;286:159-161. doi: 10.1016/j.ijcard.2019.01.048. Epub 2019 Jan 15.
Patients at increased cardiovascular (CV) risk, noticeably hypertensive patients, have multiple CV risk factors which may be treatment targets. LDL-cholesterol is one of such targets. Using the SPRINT cohort, studying the cardiovascular outcomes of hypertensive patients at increased CV risk, this post-hoc study aimed to assess the association of LDL-C with CV outcomes.
Clinical outcomes were those defined in SPRINT: a composite of various CV outcomes, all-cause mortality, and CV mortality. Association between LDL-C and the primary outcome was analyzed using survival regression adjusted on confounding factors (age, sex, body-mass index, active smoking status, eGFR-estimated kidney function, history of CV disease, Framingham risk score, SPRINT treatment arm (intensive or control), baseline high-density-lipoprotein-bound cholesterol, and co-treatments by aspirin and statins).
LDL-C was not associated with the primary outcome in the overall cohort (n = 9631). Among patients in secondary prevention (i.e. with a previous history of CV disease) (n = 1562), LDL-C was marginally associated with the incidence of the primary outcome (adjusted hazard-ratio 1.005 (95% CI = 1.002-1.009), p = 0.005 (per 1 mg/dl increase)) however, discrimination was poor with a ROC AUC of 0.54, p = 0.087. There was no association between LDL-C and the primary outcome in other subgroup analyses (those under statin or not, and those in primary prevention).
This post-hoc analysis of SPRINT indicates that LDL-C levels do not influence cardiovascular events over a period of 3 years in a large cohort of hypertensive patients at increased risk of cardiovascular events but without previous history of clinical cardiovascular disease other than stroke.
心血管风险增加的患者,尤其是高血压患者,存在多种心血管风险因素,这些因素可能是治疗靶点。LDL-胆固醇就是其中一个靶点。本研究利用 SPRINT 队列,研究了心血管风险增加的高血压患者的心血管结局,旨在评估 LDL-C 与心血管结局的相关性。
临床结局为 SPRINT 中定义的各种心血管结局、全因死亡率和心血管死亡率的复合结局。使用调整混杂因素(年龄、性别、体重指数、吸烟状态、估计的肾小球滤过率、心血管疾病史、Framingham 风险评分、SPRINT 治疗组(强化或常规)、基线高密度脂蛋白结合胆固醇以及阿司匹林和他汀类药物的联合治疗)的生存回归分析 LDL-C 与主要结局之间的关系。
在整个队列(n=9631)中,LDL-C 与主要结局无关。在二级预防患者(即有心血管疾病史)(n=1562)中,LDL-C 与主要结局的发生率呈边缘相关(调整后的危险比 1.005(95%CI=1.002-1.009),p=0.005(每增加 1mg/dl)),但区分能力较差,ROC 曲线下面积为 0.54,p=0.087。在其他亚组分析中(他汀类药物治疗或不治疗以及一级预防患者),LDL-C 与主要结局之间没有关联。
SPRINT 的这项事后分析表明,在没有除中风以外的临床心血管疾病史的心血管风险增加的高血压患者中,LDL-C 水平在 3 年内不会影响心血管事件。