The prognostic value of the stress hyperglycemia ratio for all-cause mortality in stroke patients with diabetes or prediabetes

IF 2.9 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM Journal of diabetes and its complications Pub Date : 2025-03-05 DOI:10.1016/j.jdiacomp.2025.108979
Meng Jin , Ziyi Bao , Xiaqing Hong , Songbin He , Feng Gao
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Abstract

Background

The stress hyperglycemia ratio (SHR), originally proposed in 2015 by Robert et al., is more significantly relevant and predictive of critical illness than absolute hyperglycemia. Several studies have validated the association between stress hyperglycemia ratio and cerebrovascular disease. However, the value of stress hyperglycemia ratio for severe stroke patients admitted to the ICU remains uncertain. The aim of this study was to investigate the relationship between stress hyperglycemia ratio and clinical short- and long-term prognosis of critically ill patients with acute ischemic stroke (AIS).

Methods

Clinical data from 893 critically ill patients with ischemic stroke (IS) were extracted from the Medical Information Marketplace for Intensive Care (MIMIC-IV) database and 793 critically ill IS patients with 1 year of follow-up. The SHR is expressed by the formula: SHR = [(admission glucose (mg/dl)) / (28.7 × HbA1c (%) − 46.7)]. The study population was categorized into quartiles based on SHR level. Outcomes included ICU mortality, hospital mortality, and 1-year mortality. Cox proportional risk regression analysis and restricted cubic spline curves were used to elucidate the association between SHR and clinical prognosis in critically ill patients with AIS.

Results

There were 69 ICU deaths and 100 in-hospital deaths in cohort 1, and 229 patients experienced all-cause mortality during the 1-year follow-up in cohort 2. Multivariate Cox proportional risk analysis showed that elevated SHR was significantly associated with an increased risk of hospital and 1-year all-cause mortality. After adjusting for confounders, patients with elevated SHR were significantly associated with hospital mortality (adjusted risk ratio, 1.870; 95 % confidence interval, 1.180–2.962; P = 0.008) and 1-year mortality (adjusted risk ratio, 2.325; 95 % confidence, 1.729–3.127; P < 0.001). Restricted cubic spline bars showed that a progressively increasing risk of all-cause mortality was associated with an elevated SHR.

Conclusion

Stress hyperglycemia ratios were significantly associated with in-hospital and 1-year all-cause mortality in critically ill IS patients. Moreover, we found that non-diabetic and prediabetic patients showed an increased risk of all-cause mortality. It is suggested that SHR may be useful in identifying ischemic stroke patients at high risk of all-cause mortality and providing personalized interventions as early as possible.
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背景应激性高血糖比值(SHR)最初由罗伯特等人于2015年提出,与绝对高血糖相比,应激性高血糖比值对危重症的相关性和预测性更强。多项研究已经验证了应激性高血糖比值与脑血管疾病之间的关联。然而,应激性高血糖比值对入住重症监护室的严重脑卒中患者的价值仍不确定。方法从重症监护医学信息市场(MIMIC-IV)数据库中提取 893 例缺血性卒中(IS)重症患者的临床数据,以及 793 例随访 1 年的 IS 重症患者的临床数据。SHR 用公式表示:SHR=[(入院血糖(mg/dl))/(28.7 × HbA1c(%)- 46.7)]。根据 SHR 水平将研究对象分为四等分。研究结果包括重症监护室死亡率、住院死亡率和 1 年死亡率。结果队列1中有69例ICU死亡和100例院内死亡,队列2中有229例患者在1年随访期间全因死亡。多变量 Cox 比例风险分析显示,SHR 升高与住院和 1 年全因死亡风险增加显著相关。调整混杂因素后,SHR升高的患者与住院死亡率(调整后风险比为1.870;95%置信区间为1.180-2.962;P = 0.008)和1年死亡率(调整后风险比为2.325;95%置信区间为1.729-3.127;P <0.001)显著相关。结论应激性高血糖比率与重症 IS 患者的院内和 1 年全因死亡率显著相关。此外,我们还发现,非糖尿病和糖尿病前期患者的全因死亡风险增加。这表明,SHR 可能有助于识别全因死亡风险较高的缺血性卒中患者,并尽早提供个性化干预措施。
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来源期刊
Journal of diabetes and its complications
Journal of diabetes and its complications 医学-内分泌学与代谢
CiteScore
5.90
自引率
3.30%
发文量
153
审稿时长
16 days
期刊介绍: Journal of Diabetes and Its Complications (JDC) is a journal for health care practitioners and researchers, that publishes original research about the pathogenesis, diagnosis and management of diabetes mellitus and its complications. JDC also publishes articles on physiological and molecular aspects of glucose homeostasis. The primary purpose of JDC is to act as a source of information usable by diabetes practitioners and researchers to increase their knowledge about mechanisms of diabetes and complications development, and promote better management of people with diabetes who are at risk for those complications. Manuscripts submitted to JDC can report any aspect of basic, translational or clinical research as well as epidemiology. Topics can range broadly from early prediabetes to late-stage complicated diabetes. Topics relevant to basic/translational reports include pancreatic islet dysfunction and insulin resistance, altered adipose tissue function in diabetes, altered neuronal control of glucose homeostasis and mechanisms of drug action. Topics relevant to diabetic complications include diabetic retinopathy, neuropathy and nephropathy; peripheral vascular disease and coronary heart disease; gastrointestinal disorders, renal failure and impotence; and hypertension and hyperlipidemia.
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