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Published on: November 29, 2024
[Prognostic importance of abnormal glucose metabolism in chronic heart failure]
Jing-chuan Guo1, Zhao-ping Li, Wei Gao
1Department of Cardiology, Peking University Third Hospital, Key Laboratory of Ministry of Education on Molecular Cardiology, Beijing 100191, China.
Insights
Diabetes mellitus independently predicts 1-year mortality in chronic heart failure (CHF) patients. Impaired fasting glucose (IFG) and higher fasting plasma glucose (FPG) levels also increase mortality risk in CHF patients without diabetes.
Area of Science:
- Cardiology
- Endocrinology
- Metabolic Syndrome
Context:
- Chronic heart failure (CHF) affects millions globally, with abnormal glucose metabolism being a common comorbidity.
- Understanding the prognostic implications of glucose dysregulation in CHF is crucial for risk stratification and management.
- Previous studies have explored the link between diabetes and adverse outcomes in CHF, but the role of pre-diabetic states like impaired fasting glucose (IFG) requires further elucidation.
Purpose:
- To investigate the prognostic significance of abnormal glucose metabolism, including diabetes mellitus and IFG, on 1-year all-cause mortality in patients with decompensated chronic heart failure (CHF).
- To determine whether IFG and fasting plasma glucose (FPG) levels are associated with increased mortality risk in CHF patients without diagnosed diabetes.
- To identify independent predictors of mortality within the CHF population based on glucose metabolism status.
Summary:
- A cohort of 444 decompensated CHF patients was analyzed, categorized into diabetic (34.5%), IFG (25.4%), and normal glucose (40.1%) groups.
- One-year all-cause mortality was significantly higher in patients with diabetes mellitus and IFG compared to those with normal glucose levels (P < 0.01).
- Diabetes mellitus was identified as an independent predictor of 1-year mortality (OR = 2.383). In non-diabetic CHF patients, IFG (OR = 3.564) and higher FPG levels (OR = 1.791) were associated with increased 1-year mortality.
Impact:
- This study highlights that abnormal glucose metabolism, including both diagnosed diabetes and pre-diabetic states (IFG), significantly impacts mortality risk in patients with chronic heart failure.
- The findings underscore the importance of screening for and managing glucose abnormalities in CHF patients, even in the absence of overt diabetes.
- Identifying IFG as an independent risk factor in non-diabetic CHF patients provides a target for early intervention to potentially improve outcomes.
Objective:
To investigate the importance of abnormal glucose metabolism in a chronic heart failure (CHF) population.
Methods:
A total of 444 patients were enrolled sequentially for decompensated CHF from January 1st, 2005 to December 31st, 2007 at our department. They were divided into diabetic (n = 153, 34.5%) and non-diabetic groups (n = 291, 65.5%). Among the non-diabetics, there were 113 (25.4%) with impaired fasting glucose (IFG) (FPG 5.6-6.9 mmol/L) and 178 (40.1%) with normal glucose levels. All subjects received a follow-up to record their clinical status, biochemical parameters and end-point events (all-cause death in one year). And the correlations of abnormal glucose metabolism and end-point events were analyzed.
Results:
Among these patients, 83 (17.1%) died in 1 year, 31 (7.0%) were lost to follow-up; Among 83 dead patients, 15 (8.4%) were within normal glucose levels, 34 (21.2%) with IFG and 44 (28.8%) with diabetes mellitus. Compared with normal glucose level patients, the mortality rates of diabetes mellitus and IFG patients were higher (P < 0.01). There was no significant difference in mortality rate between diabetes mellitus and IFG patients. After adjustment for other prognostic attributes (age, sex and etc.), diabetes mellitus was a predictor of 1-year all-cause mortality (OR = 2.383, 95% CI: 1.317 to 4.312; P = 0.004). In diabetics, the mortality of the higher glucose level group (FPG > 7.0 mmol/L) was 30.4% and that of the lower glucose level group (FPG < or = 7.0 mmol/L) 27.4%. And there was no significant difference (P > 0.05). The FPG level could not predict the 1-year all-cause mortality. In non-diabetics, the mortality of IFG group (FPG 5.6 - 6.9 mmol/L) was significantly higher than that of normal glucose levels group (21.2% vs 8.4%, P < 0.01). IFG status predicted 1-year all-cause mortality (OR = 3.564, 95%CI: 1.494 - 8.497, P = 0.004). The FPG level was also associated with the 1-year all-cause mortality (OR = 1.791, 95%CI: 1.090 - 2.943, P = 0.021).
Conclusion:
Diabetes mellitus is an independent predictor of 1-year all-cause mortality for CHF. And IFG and a higher FPG level are associated with 1-year all-cause mortality for CHF without diabetes mellitus.
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