Systematic Review on the Role of IL-6 and IL-1β in Cardiovascular Diseases

被引:10
作者
Katkenov, Nurlubek [1 ]
Mukhatayev, Zhussipbek [1 ]
Kozhakhmetov, Samat [1 ]
Sailybayeva, Aliya [2 ]
Bekbossynova, Makhabbat [2 ]
Kushugulova, Almagul [1 ,2 ]
机构
[1] Nazarbayev Univ, Natl Lab Astana, Lab Microbiome, Astana 010000, Kazakhstan
[2] CF Univ Med Ctr, Heart Ctr, Astana 010000, Kazakhstan
关键词
cardiovascular diseases; IL-6; IL-1; beta; inflammation; biomarkers; INFLAMMATORY MARKERS; RISK; INTERLEUKIN-6; INHIBITION; BIOMARKERS; PREDICTOR; THERAPY;
D O I
10.3390/jcdd11070206
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiovascular diseases (CVDs) are a leading cause of global morbidity and mortality, significantly driven by chronic inflammation. Interleukin-6 (IL-6) and interleukin-1 beta (IL-1 beta) are critical inflammatory cytokines implicated in CVD progression. This systematic review evaluates the roles of IL-6 and IL-1 beta in CVDs by synthesizing data from relevant studies to understand their impact on cardiovascular outcomes and identify potential therapeutic interventions. A comprehensive literature search was conducted using PubMed and Embase, covering studies from January 2014 to December 2024. Inclusion criteria encompassed studies investigating IL-6 and/or IL-1 beta in CVDs, including human and relevant animal models, and reporting clinical outcomes, molecular mechanisms, or therapeutic interventions. Data extraction and quality assessment were performed independently by two reviewers. Our review included 12 studies focusing on the roles of IL-6 and IL-1 beta in various CVDs. Elevated IL-6 levels were significantly associated with peripheral artery disease, myocardial infarction, and heart failure, while IL-1 beta levels were linked to worse outcomes in coronary artery disease and heart failure. Meta-analyses indicated a significant association between higher IL-6 and IL-1 beta levels and increased risk of adverse cardiovascular events. These findings suggest that targeting IL-6 and IL-1 beta could offer promising therapeutic strategies for reducing inflammation and improving cardiovascular outcomes.
引用
收藏
页数:14
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