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Inverse association between fasting plasma glucose and risk of ventricular arrhythmias
Francesco Zaccardi1, David R Webb, Sudhir Kurl
1Diabetes Research Centre, University of Leicester, Leicester General Hospital, Leicester, LE5 4PW, UK, frazac@fastwebnet.it.
Insights
In nondiabetic men, lower fasting plasma glucose (FPG) levels were linked to a reduced risk of ventricular arrhythmias. This suggests a potential connection between glucose regulation and heart rhythm disturbances.
Area of Science:
- Cardiology
- Endocrinology
- Epidemiology
Background:
- Low fasting plasma glucose (FPG) is linked to increased cardiovascular event risk in nondiabetics.
- Understanding mechanisms is crucial for clarifying the glycaemia-cardiovascular disease relationship.
Purpose of the Study:
- To investigate the association between FPG levels and the incidence of ventricular arrhythmias in nondiabetic men.
Main Methods:
- A population-based cohort of 2,482 nondiabetic men had FPG and cardiometabolic risk factors measured.
- Incident ventricular arrhythmias were tracked, and Cox regression analysis was used to estimate associations.
Main Results:
- During a median follow-up of 23.3 years, 74 incident ventricular arrhythmia events occurred.
- A multivariable analysis revealed an inverse association between FPG and ventricular arrhythmia risk (HR 0.58 per 1 mmol/l higher FPG).
- This inverse association persisted after adjusting for multiple confounders.
Conclusions:
- Fasting plasma glucose was inversely associated with the risk of ventricular arrhythmias in this cohort of nondiabetic men.
- These findings may contribute to understanding the link between lower glucose levels and cardiovascular risk.
- Further research is needed to validate these results in diverse populations.
Aims/Hypothesis:
In nondiabetic individuals, low values of fasting plasma glucose (FPG) have been associated with an increased risk of cardiovascular events. Identification of the potential mechanisms behind this association could help to elucidate the relationship between glycaemia and cardiovascular disease. We aimed to determine the association between FPG and ventricular arrhythmias.
Methods:
FPG and other cardiometabolic risk factors were measured in a population-based cohort of 2,482 men without a known history of type 2 diabetes mellitus at baseline. Associations between FPG levels and incident cases of ventricular arrhythmias (ventricular tachycardia or fibrillation events ascertained using the National Hospital Discharge Register) were estimated using Cox regression analysis adjusted for potential confounders.
Results:
During a median follow-up of 23.3 (interquartile range 18.5-25.3) years, 74 (2.9%) incident events were recorded. In a multivariable analysis adjusted for age, systolic BP, smoking status, LDL- and HDL-cholesterol, and C-reactive protein, the HR for ventricular arrhythmia per 1 mmol/l higher baseline FPG was 0.58 (95% CI 0.34, 0.98); this estimate did not materially change after further adjustment for BMI, alcohol consumption, triacylglycerols and history of ischaemic heart disease (0.50 [95% CI 0.28, 0.89]).
Conclusions/Interpretation:
In this nondiabetic male population, FPG was inversely associated with incident risk of ventricular arrhythmias. While our results could help clarify the relationship between low glucose levels and cardiovascular risk, further studies are required to confirm these findings in other populations.
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