Acromegalic cardiomyopathy. An echocardiography study
- 1 March 1988
- journal article
- research article
- Published by Springer Nature in Journal of Endocrinological Investigation
- Vol. 11 (3) , 159-164
- https://doi.org/10.1007/bf03350125
Abstract
Eighteen acromegalic patients (A) and 18 controls without clinical evidence of cardiac involvement and/or endocrine disease (C), matched for sex, age, body surface area, and blood pressure (BP), were investigated by M-mode (2-D derived) echocardiography, to clarify the prevalence and the possible determinants of left ventricular hypertrophy (LVH). Seven patients in each group were hypertensive (BP > 160/95 mmHg). Left ventricular mass (LVM) was 183.1 ± 60.0 g/m2 in A and 130 ± 25.9 g/m2 in C. ALVM above 140 g/m2 (that is the upper normal range in our laboratory) was found in 15/18 A and 2/18 C. The LVH was concentric (h/r > 0.45) in 12/15 A and 1/2 C. Systolic function indexes (% FS, end-systolic stress/end-systolic volume), cardiac index and total peripheral resistance index (as determined by echo) were within the normal range and similar in both groups. No correlationwas found between LVM and BP, LVM and GH plasma levels, LVM and Sm-C levels. A significant correlation was found between LVM and duration of the disease (r 0.44; p<0.05). Our data confirm that LVH is an early and frequent finding in acromegaly. Its prevalence is not entirely accounted for by such factors as body size, BP or increased cardiac output. Metabolic factors may play a major role, and a long lasting exposition to increased GH levels seems the most relevant determinant of LVH.This publication has 24 references indexed in Scilit:
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