Journal Article Research Support, Non-U.S. Gov't Epublish 1 citation
PubMed: 37904138 DOI: 10.1186/s12873-023-00896-6
Elevated circulating PCSK9 level is associated with 28-day mortality in patients with sepsis: a prospective cohort study.
BMC Emerg Med 23(1):127
Authors: Yuanlu Shu, Ziwei Deng, Ye Deng, Jianliang Zhou, Jin Wang, Zhenxing Duan, Tao Jiang, Xiang Zhao, Zhihua Shi, Chengfeng Qiu
Affiliations
- Evidence-based Medicine and Clinical Center, The First People's Hospital of Huaihua, Huaihua, 418000, P.R. China.
- Clinical Pharmacy Department, The First People's Hospital of Huaihua, Huaihua, 418000, P.R. China.
- Emergency Department, The First People's Hospital of Huaihua, Huaihua, 418000, P.R. China.
- Evidence-based Medicine and Clinical Center, The First People's Hospital of Huaihua, Huaihua, 418000, P.R. China. Clinical Pharmacy Department, The First People's Hospital of Huaihua, Huaihua, 418000, P.R. China. School of Basic Medical Sciences, University of South China, Hengyang, 421000, P.R. China.
Abstract
OBJECTIVES
Pro-protein convertase subtilisin/kexin 9 (PCSK9) decreases the clearance of the pathogenic lipids, supporting the potential role of PCSK9 in the prognosis of sepsis.
METHODS
In this prospective cohort study, patients with sepsis were consecutively recruited from 1 to 2020 to 30 September 2021 at the First People's Hospital of Huaihua, China. All the eligible patients were categorized into low-PCSK9 and high-PCSK9 groups, based on their PCSK9 levels at admission. Time-dependent receiver operating characteristic curves and Cox proportional hazards regression were used to evaluate the association between PCSK9 level and 28-day mortality of sepsis.
RESULTS
Of the 203 enrolled patients, 56 (27.59%) died during the 28-day follow-up. The PCSK9 level was positively related to the C-reactive protein level. The cut-off point of PCSK9 levels for 28-day mortality risk was 370 ng/ml. Through comparison between high-PCSK9 (> 370 ng/ml) with low-PCSK9 (≤ 370 ng/ml) groups, the adjusted HR for mortality was 2.56 (95% CI: 1.25-5.23, p = 0.01).
CONCLUSIONS
The 28-day mortality of sepsis increased significantly as the baseline circulating PCSK9 level exceeded 370 ng/ml, indicating circulating PCSK9 levels may be a potential biomarker to predict the prognosis of sepsis.
MeSH
Mortality, Cohort Studies, Sepsis, Emergency Treatment, Prognosis