4.5 Article

Structural changes in small resistance arteries and left ventricular geometry in patients with primary and secondary hypertension

Journal

JOURNAL OF HYPERTENSION
Volume 20, Issue 7, Pages 1439-1444

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/00004872-200207000-00032

Keywords

essential hypertension; left ventricular geometry; secondary hypertension; small resistance arteries

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Objective To prospectively evaluate the interrelationships between left ventricular (LV) geometry and structural characteristics of the vessel wall in small resistance arteries in patients with consecutive primary and secondary hypertension. Methods In 14 patients with phaeochromocytoma, 12 with primary aldosteronism, 25 with renovascular, 25 with essential hypertension and 12 normotensive controls, an echocardiographic study for the measurement of LV mass index and relative wall thickness (RWT) was performed. Morphological characteristics of small resistance arteries (relaxed diameter < 300 pm) were directly evaluated by a micromyographic technique. Results A total of 25 patients had normal LV mass and geometry, 28 patients had normal RWT (< 0.45) and 23 patients had a RWT greater than or equal to 0.45; all normotensive subjects had normal LV mass and geometry. Media to lumen ratio (M/L) in subcutaneous small arteries was greater in hypertensive patients with concentric LV hypertrophy in respect to normotensives (ANOVA P = 0.01) and hypertensives with normal LV geometry (ANOVA P = 0.05). In the whole group of hypertensive patients the correlation coefficient between M/L and LV mass index was 0.33 (P < 0.05); the correlation coefficient between M/L and RWT was 0.46 (P < 0.01) and it was higher in primary aldosteronism (r = 0.67) and renovascular hypertension patients (r = 0.46). Conclusions A close relation between morphology of subcutaneous small resistance arteries and LV geometric patterns may be observed in hypertensive patients; this relationship is more evident when the renin-angiotensin-aldosterone system is activated. (C) 2002 Lippincott Williams Wilkins.

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