The Prognostic Value of Soluble ST2 in Maintenance Hemodialysis Patients: A Meta-Analysis

被引:8
作者
Wang, Shuang [1 ]
Wei, Fang [1 ]
Chen, Haiyan [1 ]
Wang, Zhe [1 ]
Zhang, Ruining [1 ]
Jiang, Aili [1 ]
机构
[1] Tianjin Med Univ, Dept Kidney Dis & Blood Purificat, Hosp 2, 23rd,Pingiiang Rd, Tianjin 300211, Peoples R China
关键词
Meta-analysis; Kidney dialysis; Soluble ST2; sST2; Mortality; STAGE RENAL-DISEASE; TUMORIGENICITY; 2-LEVEL; CARDIOVASCULAR EVENTS; NATRIURETIC PEPTIDE; SERUM CONCENTRATION; HEART-FAILURE; NT-PROBNP; ALL-CAUSE; MORTALITY; SUPPRESSION;
D O I
10.1159/000503601
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Much controversy remains in the literature with respect to whether soluble suppression of tumorigenicity 2 (sST2) can serve to predict all-cause death in patients undergoing maintenance hemodialysis (MHD). This meta-analysis therefore sought to analyze extant datasets exploring the association between these 2 variables in MHD patients in order to draw relevant conclusions. Methods: Articles published through December 2018 in PubMed and Embase were independently reviewed by 2 authors to identify relevant articles, and STATA 12.0 was used for statistical analyses of relevant results and study parameters. Results: In total, we identified 4 relevant studies that were incorporated into this meta-analysis. These studies included a total of 1,924 participants (60% male, mean follow-up 911 days). The combined study results suggested that increased levels of sST2 were significantly linked to a 2.23 fold rise in all-cause mortality (hazard ratio [HR] 2.23, 95% CI 1.81-2.75). Subgroup analyses confirmed that this same association was true in patients undergoing hemodialysis (HR 2.17, 95% CI 1.74-2.71), which indicated that the increased levels of sST2 were significantly linked to a 2.17 fold rise in all-cause mortality. Conclusions: This analysis suggests that there is a significant link between elevated levels of sST2 and death in patients undergoing MHD. Further large-scale trials, however, will be needed to fully validate these findings and their clinical relevance.
引用
收藏
页码:114 / 120
页数:7
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