Association of stress hyperglycemia ratio with in‐hospital new‐onset atrial fibrillation and long‐term outcomes in patients with acute myocardial infarction

Author:

Luo Jiachen1ORCID,Li Zhiqiang1,Qin Xiaoming1,Zhang Xingxu1,Liu Xiangdong1,Zhang Wenming1,Xu Wei1,Liu Baoxin1,Wei Yidong1,

Affiliation:

1. Department of Cardiology Shanghai Tenth People's Hospital Tongji University School of Medicine Shanghai China

Abstract

AbstractAimsTo investigate the predictive value and prognostic impact of stress hyperglycemia ratio (SHR) for new‐onset atrial fibrillation (NOAF) complicating acute myocardial infarction (AMI).Materials and MethodsThis retrospective study included 2145 AMI patients without AF history between February 2014 and March 2018. SHR was calculated using fasting blood glucose (mmol/L)/[1.59*HbA1c (%)‐2.59]. The association between SHR and post‐MI NOAF was assessed with multivariable logistic regression analyses. The primary outcome was a composite of cardiac death, heart failure hospitalisation, recurrent MI, and ischaemic stroke (MACE). Cox regression‐adjusted hazard ratios with 95% confidence intervals (CI) were estimated for MACE.ResultsA total of 245 (11.4%) patients developed NOAF. In the multivariable logistic regression analyses, SHR (each 10% increase) was significantly associated with increased risks of NOAF in the whole population (OR: 1.05, 95% CI: 1.01–1.10), particularly in non‐diabetic individuals (OR:1.08, 95% CI: 1.01–1.17). During a median follow‐up of 2.7 years, 370 (18.5%) MACEs were recorded. The optimal cut‐off value of SHR for MACE prediction was 1.119. Patients with both high SHR (≥1.119) and NOAF possessed the highest risk of MACE compared to those with neither high SHR nor NOAF after multivariable adjustment (HR: 2.18, 95% CI: 1.39–3.42), especially for diabetics (HR: 2.63, 95% CI: 1.41–4.91). Similar findings were observed using competing‐risk models.ConclusionsSHR is an independent predictor of post‐MI NOAF in non‐diabetic individuals. Diabetic patients with both high SHR and NOAF had the highest risk of MACE, suggesting that therapies targeting SHR may be considered in these patients.Trial registrationClinicalTrials.gov, NCT03533543.

Funder

Natural Science Foundation of Shanghai

National Natural Science Foundation of China

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

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