Your new experience awaits. Try the new design now and help us make it even better

ORIGINAL RESEARCH article

Front. Endocrinol.

Sec. Cardiovascular Endocrinology

Volume 16 - 2025 | doi: 10.3389/fendo.2025.1627821

Aggregate Index of Systemic Inflammation as a Novel Prognostic Biomarker in Chinese Patients with Acute Decompensated Heart Failure: A Population-Based Real-World Study

Provisionally accepted
Lin  HuLin Hu1Yangjie  DengYangjie Deng2Chuanjin  LiuChuanjin Liu2Yinghao  KuangYinghao Kuang1Xinfang  HuangXinfang Huang1Jinyan  ZhangJinyan Zhang1Wanfen  HuangWanfen Huang1Yafei  JianYafei Jian1Guobo  XieGuobo Xie1Yang  ZouYang Zou1Shuhua  ZhangShuhua Zhang1*
  • 1Jiangxi Provincial People's Hospital, Nanchang, China
  • 2Yongfeng County Hospital of Traditional Chinese Medicine, Jian, China

The final, formatted version of the article will be published soon.

Objective: Inflammation is hypothesized as an early trigger for decompensation in heart failure patients. This study aims to evaluate the prognostic value of a novel inflammatory biomarker, the Aggregate Index of Systemic Inflammation (AISI), for predicting 30-day mortality in patients with acute decompensated heart failure (ADHF). Methods: This analysis included 2,765 patients from the Jiangxi-ADHF II registry (2018-2024). Complete blood counts were measured at hospital admission, with 30-day mortality outcomes followed. Multivariable Cox proportional hazards model was employed to analyze the association between AISI and all-cause mortality. Results: During 30-day follow-up, the overall mortality rate was 7.34% (203 deaths), with rates progressively increasing across AISI quartiles (Q1-Q4: 2.32%, 3.33%, 5.21%, 18.50%). Compared with the lowest AISI quartile, the highest quartile was associated with a 210% higher risk of 30-day mortality (Hazard Ratio: 3.10, 1.62-5.94). This association remained robust across multiple sensitivity analyses, including subgroup analysis, temporal sensitivity assessments, and data integrity verification. Further spline regression analysis revealed a U-shaped curve association between AISI (and LnAISI) and 30-day mortality in ADHF patients (P for non-linearity < 0.05). In general, both extremely low and high levels of AISI and its natural logarithm (LnAISI) were associated with an increased risk of 30-day mortality in ADHF patients. Moreover, in predicting 30-day mortality among ADHF patients, the AISI demonstrated significantly superior predictive value compared to white blood cell count, neutrophil count, monocyte count, and lymphocyte count (Area under the curve=0.77; all DeLong tests P <0.05), with an optimal threshold of 925.44. Conclusion: This population-based retrospective cohort study demonstrated the predictive value of AISI for short-term outcomes in Chinese ADHF patients. Compared to conventional inflammatory biomarkers, AISI significantly improved the predictive performance for 30-day mortality in ADHF patients. These findings may facilitate optimized prevention of adverse outcomes in ADHF and enable early risk stratification through targeted assessment of individual ADHF patients.

Keywords: Inflammation, aggregate index of systemic inflammation, Acute decompensated heart failure, Chinese, risk stratification Inflammation, risk stratification

Received: 13 May 2025; Accepted: 28 Jul 2025.

Copyright: © 2025 Hu, Deng, Liu, Kuang, Huang, Zhang, Huang, Jian, Xie, Zou and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Shuhua Zhang, Jiangxi Provincial People's Hospital, Nanchang, China

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.