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November 2, 2006Journal of Hypertension29 citations

QT interval in patients with primary aldosteronism and low-renin essential hypertension

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SMSimona MaulePMPaolo MulateroAMAlberto Milan

Structured PICO

Is the corrected QT interval prolonged in patients with primary aldosteronism and low-renin essential hypertension compared to those with essential hypertension or healthy controls?

P
Population
186 individuals including 27 with primary aldosteronism, 17 with low-renin essential hypertension (LREH), 117 with essential hypertension, and 25 healthy controls.
I
Intervention
Primary aldosteronism and low-renin essential hypertension (LREH)
C
Comparator
Essential hypertension and healthy controls
O
Outcome
Corrected QT interval (QTc) measured from a 12-lead electrocardiogramsurrogate

Patients with primary aldosteronism and low-renin essential hypertension have significantly longer QTc intervals compared to those with normal-renin essential hypertension and healthy controls, potentially contributing to increased cardiovascular risk.

Abstract

INTRODUCTION: QT interval prolongation increases the risk of sudden death in several medical conditions. Patients with primary aldosteronism and salt-sensitive hypertension experience more cardiovascular events than those with normal-renin essential hypertension. QT interval prolongation might represent one of the risk factors for cardiovascular events in these patients. The aim of the present study was to evaluate the QT interval in patients with primary aldosteronism and low-renin essential hypertension (LREH). METHODS: Twenty-seven patients with primary aldosteronism, 17 patients with LREH, 117 patients with essential hypertension and 25 healthy individuals were studied. Plasma aldosterone, plasma renin activity, and aldosterone to plasma renin activity ratio (ARR) were determined. Corrected QT intervals (QTcs) were measured from a 12-lead electrocardiogram. RESULTS: The QTc was longer in primary aldosteronism (434 +/- 23 ms) and LREH (430 +/- 18 ms) compared with essential hypertension (419 +/- 22 ms) and healthy controls (412 +/- 19 ms) (P = 0.0004). The prevalence of QTc longer than 440 ms was higher in primary aldosteronism (48%) and LREH (23%) compared with essential hypertension (11%) and healthy controls (4%) (P < 0.0001). QTc correlated with plasma aldosterone (P = 0.01), ARR (P = 0.02), and diastolic blood pressure (P = 0.01). ARR (P = 0.01) and systolic blood pressure (P = 0.01) were identified as independent predictors of QTc. CONCLUSIONS: We postulate that the elevated aldosterone secretion contributes to the prolongation of the QT interval in patients with primary aldosteronism and LREH through both a depletion of intracellular potassium concentration and higher blood pressure values. QTc measurement might represent one simple, non-invasive and reproducible index to characterize the cardiovascular risk in patients with primary aldosteronism and LREH.

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Cite This Study

Maule et al. (2006) studied this question.

synapsesocial.com/papers/6a208e2cfdf8ac6477c63dcfhttps://doi.org/10.1097/01.hjh.0000251908.93298.a0
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