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Inverse association of total testosterone with central haemodynamics and left ventricular mass in hypertensive men
Charalambos Vlachopoulos1, Panagiota Pietri1, Nikolaos Ioakeimidis1
1Hypertension Unit and Peripheral Vessels Units, 1st Cardiology Department, Hippokration Hospital, Athens Medical School, Athens, Greece.
Insights
Low total testosterone (TT) in hypertensive men is independently linked to higher central blood pressure and left ventricular mass. This finding may help explain increased cardiovascular risk in men with low testosterone levels.
Area of Science:
- Cardiovascular endocrinology
- Hypertension research
- Men's health
Background:
- Low plasma testosterone is linked to increased cardiovascular event risk in hypertensive men.
- Central blood pressure is a key determinant of left ventricular hypertrophy and cardiovascular mortality.
- Understanding the relationship between testosterone and cardiovascular parameters in hypertension is crucial.
Purpose of the Study:
- To investigate the association between total testosterone (TT) and central hemodynamics.
- To assess the relationship between TT and left ventricular mass in hypertensive men.
- To explore the role of TT in cardiovascular risk stratification in hypertensive males.
Main Methods:
- Study included 134 hypertensive men and 60 normotensive controls.
- Central hemodynamics (aortic systolic pressure, aortic pulse pressure, augmentation index) measured using pulse wave analysis.
- Left ventricular mass calculated via echocardiography; plasma TT measured by enzyme immunoassay.
Main Results:
- Significant inverse correlations found between TT and aortic systolic pressure, aortic pulse pressure, augmentation index, and left ventricular mass in hypertensive men.
- Multivariate analysis confirmed independent inverse associations of TT with aortic pulse pressure, augmentation index, and left ventricular mass.
- These associations remained significant even after adjusting for multiple cardiovascular risk factors and including normotensive subjects.
Conclusions:
- Total testosterone is independently and inversely associated with central pulse pressure, wave reflections, and left ventricular mass in hypertensive men.
- These findings suggest low testosterone may contribute to increased cardiovascular risk in hypertensive patients.
- Further research is needed to determine if assessing central hemodynamics can improve risk stratification in hypertensive men with low testosterone.
Background:
There is evidence for inverse association between endogenous testosterone and blood pressure. Furthermore, low plasma testosterone is associated with increased risk of major cardiovascular events in middle-aged hypertensive men. Central (aortic) blood pressures determine left ventricular hypertrophy and predict cardiovascular mortality. The aim of the present study was to assess the relationship of total testosterone (TT) with central haemodynamics and left ventricular mass in hypertensive men.
Methods:
We investigated 134 non-diabetic, middle-aged, hypertensive men and 60 age-matched normotensive males. All participants were subject to measurement of aortic systolic (aoSBP) and pulse pressure (aoPP) by pulse wave analysis using the SphygmoCor device. Wave reflections were assessed by the measurement of heart rate corrected augmentation index (AIx75). Echocardiography was performed in all individuals and left ventricular mass (LVM) was calculated using the Devereux's formula. Plasma TT was measured by enzyme immunoassay.
Results:
In hypertensive men, univariate analysis showed an inverse, significant correlation between TT and aoSBP (r = -20, p = 0.02), aoPP (r = -0.21, p = 0.01), AIx75 (r = -0.22, p = 0.01) and LVM (r = -0.19, p = 0.008). Multivariate regression analysis demonstrated an independent inverse association of TT with aoPP (b = -0.21, p = 0.02), AIx75 (b = -0.19, p = 0.03) and LVM (b = -0.28, p = 0.005) after adjustment for age, BMI, smoking, total cholesterol, triglycerides, fasting glucose, mean arterial pressure, antihypertensive treatment and statin use. Independent associations were retained even after inclusion of normotensive subjects in the analysis.
Conclusions:
In hypertensive men, TT is independently and inversely associated with central pulse pressure, wave reflections and left ventricular mass. Considering the adverse prognostic role of central blood pressures and LV hypertrophy on cardiovascular outcomes in hypertensive patients, the present findings might explain part of the increased cardiovascular risk associated with low testosterone. Whether measurement of central haemodynamics may improve risk stratification in hypertensive men with low testosterone warrants further investigation.
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