Section of Endocrinology, Diabetes and Metabolism, University and Azienda Ospedaliera Universitaria Integrata of Verona, Verona, Italy.
Division of Cardiology, ''IRCCS Sacro Cuore - Don Calabria'' Hospital, Negrar, Verona, Italy.
J Clin Lipidol. 2020 Mar-Apr;14(2):176-185. doi: 10.1016/j.jacl.2020.01.005. Epub 2020 Jan 23.
Recent cohort studies evaluated the association between some previously identified high-risk ceramides [Cer(d18:1/16:0), Cer(d18:1/18:0), Cer(d18:1/22:0), Cer(d18:1/24:0) and Cer(d18:1/24:1)] and risk of major adverse cardiovascular events in adult population.
The objective of this meta-analysis was to investigate the magnitude of such associations.
We searched publication databases using appropriate keywords to identify cohort studies (published up to July 30, 2019), in which association between previously identified high-risk ceramides and major adverse cardiovascular events was reported. Data from eligible studies were extracted and meta-analysis was performed using random-effects modeling.
Seven cohort studies with aggregate data on 29,818 individuals (2736 new cases of cardiovascular events over a median follow-up of 6 years) were included. Higher plasma levels of Cer(d18:1/16:0) (random effects hazard ratio [HR] per standard deviation 1.21, 95% confidence interval [CI] 1.11-1.32, I = 88%), Cer(d18:1/18:0) (HR 1.19, 95% CI 1.10-1.27, I = 68%), and Cer(d18:1/24:1) (HR 1.17, 95% CI 1.08-1.27, I = 83%) were associated with major adverse cardiovascular events. Conversely, no association with plasma levels of Cer(d18:1/22:0) (HR 1.14 95% CI 0.88-1.47, I = 88%) and Cer(d18:1/24:0) (HR 0.97, 95% CI 0.89-1.05, I = 73%) was found. Subgroup analyses did not substantially modify the findings.
Higher plasma levels of Cer(d18:1/16:0), Cer(d18:1/18:0) and Cer(d18:1/24:1) were associated with major adverse cardiovascular events, whereas plasma levels of Cer(d18:1/22:0) and Cer(d18:1/24:0) were not. Additional research is required to elucidate the different role of ceramides on pathways involved in cardiovascular disease.
最近的队列研究评估了一些先前确定的高危神经酰胺[Cer(d18:1/16:0)、Cer(d18:1/18:0)、Cer(d18:1/22:0)、Cer(d18:1/24:0)和 Cer(d18:1/24:1)]与成年人群重大不良心血管事件风险之间的关联。
本荟萃分析的目的是研究这种关联的程度。
我们使用适当的关键词搜索出版数据库,以确定队列研究(截至 2019 年 7 月 30 日发表),其中报告了先前确定的高危神经酰胺与重大不良心血管事件之间的关联。提取合格研究的数据,并使用随机效应模型进行荟萃分析。
纳入了 7 项队列研究,共有 29818 名个体的汇总数据(中位随访 6 年期间有 2736 例新发生心血管事件)。更高的血浆 Cer(d18:1/16:0)水平[每标准偏差的随机效应危险比(HR)为 1.21,95%置信区间(CI)为 1.11-1.32,I=88%]、Cer(d18:1/18:0)(HR 1.19,95%CI 1.10-1.27,I=68%)和 Cer(d18:1/24:1)(HR 1.17,95%CI 1.08-1.27,I=83%)与重大不良心血管事件相关。相反,没有发现与血浆 Cer(d18:1/22:0)(HR 1.14,95%CI 0.88-1.47,I=88%)和 Cer(d18:1/24:0)(HR 0.97,95%CI 0.89-1.05,I=73%)水平之间存在关联。亚组分析并未实质性改变研究结果。
更高的血浆 Cer(d18:1/16:0)、Cer(d18:1/18:0)和 Cer(d18:1/24:1)水平与重大不良心血管事件相关,而 Cer(d18:1/22:0)和 Cer(d18:1/24:0)水平则没有。需要进一步的研究来阐明神经酰胺在涉及心血管疾病的途径中的不同作用。