Long-term glycemic variability predicts compromised development of heart failure with improved ejection fraction: a cohort study

被引:2
作者
Yang, Chen Die [1 ]
Chen, Jia Wei [2 ]
Quan, Jin Wei [2 ]
Shu, Xin Yi [2 ]
Feng, Shuo [1 ]
Aihemaiti, Muladili [2 ]
Ding, Feng Hua [1 ]
Shen, Wei Feng [1 ,2 ]
Lu, Lin [1 ,2 ]
Zhang, Rui Yan [1 ]
Wang, Xiao Qun [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Dept Cardiovasc Med, Ruijin Hosp, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Inst Cardiovasc Dis, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
glycemic variability; heart failure with improved ejection fraction; heart failure with reduced ejection fraction; myocardial recovery; fasting plasma glucose; VENTRICULAR DIASTOLIC FUNCTION; STRESS HYPERGLYCEMIA RATIO; OXIDATIVE STRESS; CARDIOVASCULAR EVENTS; MYOCARDIAL RECOVERY; GLUCOSE; IMPACT; OUTCOMES; HBA1C; ASSOCIATION;
D O I
10.3389/fendo.2023.1211954
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: A substantial portion of heart failure (HF) patients adherent to guideline-directed medical therapies have experienced improved ejection fraction (EF), termed HFimpEF. Glycemic variability (GV) has emerged as a critical cardiometabolic factor. However, the relation between long-term GV and the incidence of HFimpEF is still unclear. Methods: A total of 591 hospitalized HF patients with reduced EF (HFrEF, EF <= 40%) admitted from January 2013 to December 2020 were consecutively enrolled. Repeat echocardiograms were performed at baseline and after around 12 months. The incidence of HFimpEF, defined as (1) an absolute EF improvement >= 10% and (2) a second EF > 40% and its association with long-term fasting plasma glucose (FPG) variability were analyzed. Results: During a mean follow-up of 12.2 +/- 0.6 months, 218 (42.0%) patients developed HFimpEF. Multivariate analysis showed FPG variability was independently associated with the incidence of HFimpEF after adjustment for baseline HbA1c, mean FPG during follow-up and other traditional risk factors (odds ratio [OR] for highest vs. lowest quartile of CV of FPG: 0.487 [95% CI 0.257 similar to 0.910]). Evaluation of GV by alternative measures yielded similar results. Subgroup analysis revealed that long-term GV was associated with HFimpEF irrespective of glycemic levels and diabetic conditions. Conclusions: This study reveals that greater FPG variability is associated with compromised development of HFimpEF. A more stable control of glycemic levels might provide favorable effects on myocardial functional recovery in HF patients even without diabetes.
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页数:10
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