Xia Yiyuan, Xia Chunlei, Wu Lida, Li Zheng, Li Hui, Zhang Junxia
Department of Cardiology, Nanjing First Hospital, Nanjing Medical University, Nanjing 210006, China.
Department of Intensive Medicine, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing 211166, China.
J Clin Med. 2023 Jan 31;12(3):1128. doi: 10.3390/jcm12031128.
Chronic low-grade inflammation is associated with various health outcomes, including cardiovascular diseases (CVDs) and cancers. Systemic immune inflammation index (SII) and system inflammation response index (SIRI) have lately been explored as novel prognostic markers for all-cause mortality and cardiovascular mortality. However, studies on prediction value in nationwide representative population are scarce, which limit their generalization. To bridge the knowledge gap, this study aims to prospectively assess the association of SII, SIRI with all-cause mortality and cardiovascular mortality in the National Health and Nutrition Examination Survey (NHANES).
From 1999 to 2018, 42,875 adults who were free of pregnancy, CVDs (stroke, acute coronary syndrome), cancers, and had follow-up records and participated in the NHANES were included in this study. SII and SIRI were quantified by calculating the composite inflammation indicators from the blood routine. To explore the characteristics of the population in different SII or SIRI levels, we divided them according to the quartile of SII or SIRI. The associations between SII, SIRI, and all-cause mortality and cardiovascular mortality events were examined using a Cox regression model. To investigate whether there was a reliable relationship between these two indices and mortalities, we performed subgroup analysis based on sex and age.
A total of 42,875 eligible individuals were enrolled, with a mean age of 44 ± 18 years old. During the follow-up period of up to 20 years, 4250 deaths occurred, including 998 deaths from CVDs. Cox proportional hazards modeling showed that adults with SII levels of >655.56 had higher all-cause mortality (hazard ratio [HR], 1.29; 95% confidence interval [CI], 1.18-1.41) and cardiovascular mortality (HR, 1.33; 95% CI, 1.11-1.59) than those with SII levels of <335.36. Adults with SIRI levels of >1.43 had higher risk of all-cause (HR, 1.39; 95% CI, 1.26-1.52) and cardiovascular death (HR, 1.39; 95% CI, 1.14-1.68) than those with SIRI levels of <0.68. In general population older than 60 years, the elevation of SII or SIRI was associated with the risk of all-cause death.
Two novel inflammatory composite indices, SII and SIRI, were closely associated with cardiovascular death and all-cause death, and more attention should be paid to systemic inflammation to provide better preventive strategies.
慢性低度炎症与多种健康结局相关,包括心血管疾病(CVD)和癌症。全身免疫炎症指数(SII)和全身炎症反应指数(SIRI)最近被探索作为全因死亡率和心血管死亡率的新型预后标志物。然而,关于其在全国代表性人群中的预测价值的研究较少,这限制了它们的推广。为填补这一知识空白,本研究旨在前瞻性评估美国国家健康与营养检查调查(NHANES)中SII、SIRI与全因死亡率和心血管死亡率之间的关联。
1999年至2018年期间,本研究纳入了42875名非妊娠、无CVD(中风、急性冠状动脉综合征)、无癌症且有随访记录并参与NHANES的成年人。通过计算血常规中的综合炎症指标来量化SII和SIRI。为探究不同SII或SIRI水平人群的特征,我们根据SII或SIRI的四分位数对他们进行划分。使用Cox回归模型检验SII、SIRI与全因死亡率和心血管死亡率事件之间的关联。为研究这两个指标与死亡率之间是否存在可靠关系,我们基于性别和年龄进行了亚组分析。
共纳入42875名符合条件的个体,平均年龄为44±18岁。在长达20年的随访期内,发生了4250例死亡,其中包括998例CVD死亡。Cox比例风险模型显示,SII水平>655.56的成年人的全因死亡率(风险比[HR],1.29;95%置信区间[CI],1.18 - 1.41)和心血管死亡率(HR,1.33;95%CI,1.11 - 1.59)高于SII水平<335.36的成年人。SIRI水平>1.43的成年人的全因(HR,1.39;95%CI,1.26 - 1.52)和心血管死亡风险(HR,1.39;95%CI,1.14 - 1.68)高于SIRI水平<0.68的成年人。在60岁以上的普通人群中,SII或SIRI的升高与全因死亡风险相关。
两个新型炎症综合指标SII和SIRI与心血管死亡和全因死亡密切相关,应更加关注全身炎症以提供更好的预防策略。