Department of Public Health, University of Helsinki, P.O. Box 20, FI-00014, Helsinki, Finland; Department of Neurosurgery, University of Helsinki and Helsinki University Hospital, P.O. Box 266, FI-00029, Helsinki, Finland.
Department of Neurosurgery, University of Helsinki and Helsinki University Hospital, P.O. Box 266, FI-00029, Helsinki, Finland.
Atherosclerosis. 2018 Jul;274:112-119. doi: 10.1016/j.atherosclerosis.2018.05.011. Epub 2018 May 5.
Studies report that both high and low total cholesterol (TC) elevates SAH risk. There are few prospective studies on high-density lipoproteins (HDL-C) and low-density lipoproteins (LDL-C), and apparently none concerns apolipoproteins A and B. We aimed to clarify the association between lipid profile and SAH risk.
The National FINRISK study provided risk-factor data recorded at enrolment between 1972 and 2007. During 1.52 million person-years of follow-up until 2014, 543 individuals suffered from incident hospitalized SAH or outside-hospital-fatal SAH. Cox proportional hazards model was used to calculate the hazard ratios and multiple imputation predicted ApoA1, ApoB, and LDL-C values for cohorts from a time before apolipoprotein-measurement methods were available.
One SD elevation (1.28 mmol/l) in TC elevated SAH risk in men (hazard ratio (HR) 1.15 (95% CIs 1.00-1.32)). Low HDL-C levels increased SAH risk, as each SD decrease (0.37 mmol/l) in HDL-C raised the risk in women (HR 1.29 (95% CIs 1.07-1.55)) and men (HR 1.20 (95% CIs 1.14-1.27)). Each SD increase (0.29 g/l) in ApoA1 decreased SAH risk in women (HR 0.85 (95% CIs 0.74-0.97)) and men (HR 0.88 (95% CIs 0.76-1.02)). LDL-C (SD 1.07 mmol/l) and ApoB (SD 0.28 g/l) elevated SAH risk in men with HR 1.15 (95% CIs 1.01-1.31) and HR 1.26 (95% CIs 1.10-1.44) per one SD increase. Age did not change these findings.
An adverse lipid profile seems to elevate SAH risk similar to its effect in other cardiovascular diseases, especially in men. Whether SAH incidence diminishes with increasing statin use remains to be studied.
研究报告称,总胆固醇(TC)升高和降低都会增加蛛网膜下腔出血(SAH)的风险。关于高密度脂蛋白胆固醇(HDL-C)和低密度脂蛋白胆固醇(LDL-C)的前瞻性研究较少,显然没有关于载脂蛋白 A 和 B 的研究。我们旨在阐明血脂谱与 SAH 风险之间的关系。
国家 FINRISK 研究提供了 1972 年至 2007 年登记期间记录的危险因素数据。在 152 万人年的随访期间,直到 2014 年,有 543 人患有住院性 SAH 或院外致命性 SAH。使用 Cox 比例风险模型计算风险比,并对可获得载脂蛋白测量方法之前的队列进行多重插补预测载脂蛋白 A1、载脂蛋白 B 和 LDL-C 值。
男性 TC 升高 1 个标准差(1.28mmol/L)会增加 SAH 风险(危险比(HR)1.15(95%置信区间 1.00-1.32))。低 HDL-C 水平增加 SAH 风险,因为每降低 0.37mmol/L(SD)的 HDL-C 会增加女性(HR 1.29(95%置信区间 1.07-1.55))和男性(HR 1.20(95%置信区间 1.14-1.27))的风险。女性每增加 0.29g/L(SD)的载脂蛋白 A1 会降低 SAH 风险(HR 0.85(95%置信区间 0.74-0.97))和男性(HR 0.88(95%置信区间 0.76-1.02))。LDL-C(SD 1.07mmol/L)和载脂蛋白 B(SD 0.28g/L)增加了男性的 SAH 风险,HR 分别为 1.15(95%置信区间 1.01-1.31)和 1.26(95%置信区间 1.10-1.44)。每增加一个 SD,风险增加。年龄并没有改变这些发现。
不良的血脂谱似乎会增加 SAH 风险,其作用类似于其他心血管疾病,尤其是在男性中。SAH 发病率是否会随着他汀类药物使用的增加而降低仍有待研究。