4.7 Article

Independent Relations of Left Ventricular Structure With the 24-Hour Urinary Excretion of Sodium and Aldosterone

Journal

HYPERTENSION
Volume 54, Issue 3, Pages 489-U95

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/HYPERTENSIONAHA.109.130492

Keywords

aldosterone; left ventricle; plasma renin activity; population science; renal sodium handling

Funding

  1. European Union [IC15-CT98-0329-EPOGH, LSHM-CT-2006-037093, HEALTH-2007-2.1.1-2]
  2. Fonds voor Wetenschappelijk Onderzoek Vlaanderen, Brussels, Belgium [G.25056.05, G.0575.06]
  3. Katholieke Universiteit Leuven, Leuven, Belgium [OT/04/34, OT/05/49]
  4. Swiss National Science Foundation [PROSPER 3200BO-111361/2]

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Previous studies reported on the association of left ventricular mass index (LVMI) with urinary sodium or with circulating or urinary aldosterone. We investigated the independent associations of LVMI with the urinary excretion of both sodium and aldosterone. We randomly recruited 317 untreated subjects from a white population (45.1% women; mean age 48.2 years). Measurements included echocardiographic left ventricular (LV) properties, the 24-hour urinary excretion of sodium and aldosterone, plasma renin activity (PRA), and proximal (RNaprox) and distal (RNadist) renal sodium reabsorption, assessed from the endogenous lithium clearance. In multivariable-adjusted models, we expressed changes in LVMI per 1-SD increase in the explanatory variables, while accounting for sex, age, systolic blood pressure, and the waist-to-hip ratio. LVMI increased independently with the urinary excretion of both sodium (+ 2.48 g/m(2); P=0.005) and aldosterone (+ 2.63 g/m(2); P=0.004). Higher sodium excretion was associated with increased mean wall thickness (MWT:+ 0.126 mm, P=0.054), but with no change in LV end-diastolic diameter (LVID:+0.12 mm, P=0.64). In contrast, higher aldosterone excretion was associated with higher LVID (+0.54 mm; P=0.017), but with no change in MWT (+0.070 mm; P=0.28). Higher RNadist was associated with lower relative wall thickness (=0.81x10(-2), P=0.017), because of opposite trends in LVID (+0.33 mm; P=0.13) and MWT (-0.130 mm; P=0.040). LVMI was not associated with PRA or RNaprox. In conclusion, LVMI independently increased with both urinary sodium and aldosterone excretion. Increased MWT explained the association of LVMI with urinary sodium and increased LVID the association of LVMI with urinary aldosterone. (Hypertension. 2009; 54: 489-495.)

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