All authors: Centre for Heart Lung Innovation, University of British Columbia, Vancouver, BC, Canada.
Crit Care Med. 2019 Mar;47(3):463-466. doi: 10.1097/CCM.0000000000003551.
Low low-density lipoprotein levels are associated with increased mortality in sepsis. Whether low low-density lipoprotein levels contribute causally to adverse sepsis outcome is unknown.
Retrospective analysis of two sepsis patient cohorts using a Mendelian Randomization strategy.
Sepsis patients enrolled into clinical research cohorts at tertiary care teaching hospitals.
The first cohort included 200 sepsis patients enrolled in an observational study in a hospital Emergency Department. The second cohort included genotyped patients enrolled in the Vasopressin and Septic Shock Trial.
Retrospective analysis of these patient datasets. In 632 patients enrolled in Vasopressin and Septic Shock Trial, Proprotein Convertase Subtilisin/Kexin type 9, and 3-Hydroxy-3-Methylglutaryl-CoA Reductase single nucleotide polymorphisms known to be associated with low-density lipoprotein levels were genotyped, and a genetic score related to low-density lipoprotein levels was calculated.
In the first cohort, we replicated the finding that low low-density lipoprotein levels are associated with increased 28-day mortality. In genotyped patients in the Vasopressin and Septic Shock Trial trial, we found that the 3-Hydroxy-3-Methylglutaryl-CoA Reductase genetic score, known to be directly related to low low-density lipoprotein levels, was not associated with increased mortality. Surprisingly the Proprotein Convertase Subtilisin/Kexin type 9 genetic score, known to be directly related to low low-density lipoprotein levels, was associated with decreased (not increased) mortality.
Both 3-Hydroxy-3-Methylglutaryl-CoA Reductase and Proprotein Convertase Subtilisin/Kexin type 9 genetic scores should have been associated with increased mortality if low low-density lipoprotein levels contributed causally to sepsis mortality. But this was not the case, and the opposite was observed for the Proprotein Convertase Subtilisin/Kexin type 9 genetic score. This suggests that low-density lipoprotein levels, per se, do not contribute causally to adverse sepsis outcomes. The Proprotein Convertase Subtilisin/Kexin type 9 genetic score finding raises the possibility that increased low-density lipoprotein clearance (the effect of these Proprotein Convertase Subtilisin/Kexin type 9 genotypes) may contribute to improved sepsis outcomes.
低低密度脂蛋白水平与脓毒症死亡率增加有关。低低密度脂蛋白水平是否对不良脓毒症结局有因果关系尚不清楚。
使用孟德尔随机化策略对两个脓毒症患者队列进行回顾性分析。
在三级护理教学医院的脓毒症患者纳入临床研究队列。
第一队列纳入了在医院急诊科进行的一项观察性研究中的 200 名脓毒症患者。第二队列纳入了经基因分型的患者参加血管加压素和脓毒性休克试验。
对这些患者数据集进行回顾性分析。在血管加压素和脓毒性休克试验中,纳入了 632 名经基因分型的患者,已知载脂蛋白转化酶枯草溶菌素/激肽释放酶 9 和 3-羟基-3-甲基戊二酰基辅酶 A 还原酶单核苷酸多态性与低密度脂蛋白水平相关,计算了与低密度脂蛋白水平相关的遗传评分。
在第一队列中,我们复制了低低密度脂蛋白水平与 28 天死亡率增加相关的发现。在血管加压素和脓毒性休克试验中,我们发现,与低低密度脂蛋白水平直接相关的 3-羟基-3-甲基戊二酰基辅酶 A 还原酶遗传评分与死亡率增加无关。令人惊讶的是,与低低密度脂蛋白水平直接相关的载脂蛋白转化酶枯草溶菌素/激肽释放酶 9 遗传评分与降低(而非增加)死亡率相关。
如果低低密度脂蛋白水平对脓毒症死亡率有因果关系,那么 3-羟基-3-甲基戊二酰基辅酶 A 还原酶和载脂蛋白转化酶枯草溶菌素/激肽释放酶 9 遗传评分都应该与死亡率增加相关。但事实并非如此,载脂蛋白转化酶枯草溶菌素/激肽释放酶 9 遗传评分则相反。这表明,低密度脂蛋白水平本身不会对不良脓毒症结局产生因果关系。载脂蛋白转化酶枯草溶菌素/激肽释放酶 9 遗传评分的发现提出了这样一种可能性,即增加的低密度脂蛋白清除率(这些载脂蛋白转化酶枯草溶菌素/激肽释放酶 9 基因型的作用)可能有助于改善脓毒症结局。