CHRONIC TREATMENT WITH THE SOMATOSTATIN ANALOG OCTREOTIDE IMPROVES CARDIAC ABNORMALITIES IN ACROMEGALY

Citation
B. Merola et al., CHRONIC TREATMENT WITH THE SOMATOSTATIN ANALOG OCTREOTIDE IMPROVES CARDIAC ABNORMALITIES IN ACROMEGALY, The Journal of clinical endocrinology and metabolism, 77(3), 1993, pp. 790-793
Citations number
18
Categorie Soggetti
Endocrynology & Metabolism
ISSN journal
0021972X
Volume
77
Issue
3
Year of publication
1993
Pages
790 - 793
Database
ISI
SICI code
0021-972X(1993)77:3<790:CTWTSA>2.0.ZU;2-7
Abstract
The aim of this study was to investigate the effects of a 6-month octr eotide treatment on cardiac mass and function by means of Doppler echo cardiography in 11 normotensive patients affected with active acromega ly. The GH and insulin-like growth factor-I levels were normalized dur ing octreotide therapy from 34 +/- 6.5 and 767.4 +/- 72.4 mug/L to 4.6 +/- 0.9 and 235 +/- 10.3 mug/L, respectively (P < 0.001; mean SEM). A fter the 6-month treatment, we observed a significant decrease in the left ventricular mass index from 138 +/- 11 to 116 +/- 13 g/m2 (P < 0. 001) and in the mean wall thickness/internal end-diastolic radius rati o from 0.47 +/- 0.1 to 0.44 +/- 0.1 (P < 0.001). No significant differ ences were found in systolic function indices, whereas diastolic filli ng indices improved over the course of the therapy; the isovolumic rel axation time decreased from 115 +/- 6 to 100 +/- 6 ms (P < 0.05), tric uspid late diastolic filling velocities decreased from 41 +/- 3 to 36 +/- 2 cm/s (P < 0.03), and tricuspid deceleration time decreased from 280 +/- 28 to 198 +/- 15 ms (P < 0.005); the ratio of early to late pe ak velocity of the right ventricular filling significantly increased f rom 1 +/- 0.01 to 1.3 +/- 0.1 (P < 0.03). A significant correlation wa s detected between left ventricular mass regression and increase in th e early to late peak velocity ratio of the left ventricular filling (r = 0.62; P < 0.05). The results of this study show an improvement in c ardiac structural and functional abnormalities during chronic treatmen t with octreotide, thus supporting the hypothesis of a specific heart disease secondary to high circulating GH levels.