Predominantly L-shaped association between hemoglobin glycation index and all-cause mortality in hospitalized patients with heart failure.

IF 3
Diabetes & vascular disease research Pub Date : 2026-09-01 Epub Date: 2026-09-07 DOI:10.1177/14791641261474039
Rui-Yun Wu, Jia-Hao Dou, Chen Guo, Jin Wei
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Abstract

BackgroundHeart failure (HF) is closely associated with abnormalities in glucose metabolism, which substantially influence clinical outcomes. The hemoglobin glycation index (HGI), reflecting the discrepancy between observed and predicted glycated hemoglobin, has emerged as a marker of interindividual variation in glycation beyond conventional HbA1c. However, the prognostic significance of HGI in hospitalized patients with HF remains unclear.MethodsIn this retrospective cohort study, we analyzed data from the MIMIC-IV database and included 3,470 adult patients hospitalized with HF. HGI was calculated as the difference between measured HbA1c and predicted HbA1c derived from fasting plasma glucose, and participants were categorized into quartiles. The primary outcome was 365-day all-cause mortality, and the secondary outcome was 30-day all-cause mortality. Kaplan-Meier survival analysis, restricted cubic spline modeling, multivariable Cox regression, and subgroup analyses were performed to evaluate the association between HGI and mortality.ResultsAmong the 3,470 included patients, 837 (24.1%) died within 365 days after discharge. Restricted cubic spline analysis demonstrated a predominantly L-shaped association between HGI and both 30-day and 365-day all-cause mortality, with excess mortality risk mainly concentrated at low HGI values. In multivariable Cox models, compared with the lowest quartile, higher HGI quartiles were associated with significantly lower risks of both short-term and long-term mortality, supporting the particular vulnerability of patients with extremely low HGI. Subgroup analyses generally supported the robustness of these findings, although a significant interaction with diabetes status was observed for 365-day mortality.ConclusionsHGI was independently associated with short-term and long-term all-cause mortality in hospitalized patients with HF, with a predominantly L-shaped pattern observed. Excess mortality risk was mainly concentrated at low HGI values. HGI may serve as a simple and accessible marker for risk stratification in this population.

住院心力衰竭患者血红蛋白糖化指数与全因死亡率呈l型相关。
心衰(HF)与糖代谢异常密切相关,糖代谢异常对临床结果有很大影响。血红蛋白糖化指数(HGI)反映了观察到的糖化血红蛋白与预测的糖化血红蛋白之间的差异,已经成为糖化个体间差异的标志,而不仅仅是常规的HbA1c。然而,HGI在住院心衰患者中的预后意义尚不清楚。方法在这项回顾性队列研究中,我们分析了MIMIC-IV数据库的数据,纳入了3470例HF住院成人患者。HGI是根据空腹血糖测量的HbA1c与预测的HbA1c之间的差异来计算的,参与者被分为四分位数。主要结局是365天全因死亡率,次要结局是30天全因死亡率。采用Kaplan-Meier生存分析、受限三次样条模型、多变量Cox回归和亚组分析来评估HGI与死亡率之间的关系。结果3470例患者中,837例(24.1%)在出院后365天内死亡。限制性三次样条分析显示,HGI与30天和365天全因死亡率之间存在l型相关性,超额死亡率风险主要集中在低HGI值。在多变量Cox模型中,与最低四分位数相比,高HGI四分位数与短期和长期死亡风险显著降低相关,支持极低HGI患者的特殊脆弱性。亚组分析总体上支持这些发现的稳健性,尽管观察到365天死亡率与糖尿病状态有显著的相互作用。结论shgi与HF住院患者的短期和长期全因死亡率独立相关,并以l型模式为主。超额死亡风险主要集中在低HGI值。HGI可作为这一人群中简单易行的风险分层指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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