Cardiovascular effects of depot long-acting somatostatin analog sandostatin LAR in acromegaly

被引:94
作者
Colao, A
Marzullo, P
Ferone, D
Spinelli, L
Cuocolo, A
Bonaduce, D
Salvatore, M
Boerlin, V
Lancranjan, I
Lombardi, G
机构
[1] Univ Naples Federico II, Dept Mol & Clin Endocrinol & Oncol, I-80131 Naples, Italy
[2] Univ Naples Federico II, Dept Internal Med, I-80131 Naples, Italy
[3] Univ Naples Federico II, Dept Biomorphol & Funct Sci, Natl Council Res Nucl Med, I-80131 Naples, Italy
[4] Sci Inst Res & Care Neuromed, Pozzilli, Italy
[5] Novartis Pharma AG, CH-4002 Basel, Switzerland
关键词
D O I
10.1210/jc.85.9.3132
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiovascular disease is the most severe complication of acromegaly accounting for the increased mortality of these patients. Recently, the slow-release form of octreotide (OCT; Sandostatin LAR, OCT-LAR), for im injection every 28 days, was reported to induce suppression of GH levels below 7.5 mU/L (2.5 mu g/L) in 39-75% of patients, and normalization of insulin-like growth factor (IGF)-I levels for age in 64-88% of patients, with an excellent patients' compliance. The aim of the present study was to investigate the early effect of OCT-LAR treatment on the left ventricular (LV) structure and performance in 15 somatostatin analog-naive patients with acromegaly (GH, 94.8 +/- 24.9 mU/L; IGF-I, 757.9 +/- 66.6 mu g/L), focusing on the early effect of GH and IGF-I suppression on the heart. Cardiac structure was investigated by echocardiography, whereas LV performance was investigated by gated-blood-pool scintigraphy, before and after 3 and 6 months of treatment with OCT-LAR. OCT-LAR was initially administered im, at a dose of 20 mg every 28 days, for 3 months. In six patients, the dose was then increased to 30 mg every 28 days to achieve disease control, which was considered when fasting and/or glucose-suppressed GH values were below 7.5 and 3.0 mU/L, respectively, together with IGF-I values within the normal range for age. The treatment with OCT-LAR for 6 months induced a significant decrease of GH (to 12.9 +/- 3.0 mU/L) and IGF-I levels (to 340.3 +/- 40.2 mu g/L) in all 15 patients. After 6 months of treatment, the percent IGF-I suppression was 52.8 +/- 4.4%, and serum GH/IGF-I levels were normalized in 9 patients. A significant decrease of LV mass index (LVMi), interventricular septum thickness, and LV posterior wall thickness was observed in all 15 patients after 3 and 6 months of OCT-LAR treatment: LVMi was decreased by 19.1 +/- 2.0% without any difference in patients with (19.9 +/- 2.7%) or without disease control (17.8 +/- 3.3%). Among the 11 patients with LV hypertrophy, 6 normalized their LVMi aRer treatment. At study entry, an inadequate LV ejection fraction (LVEF) at rest (<50%) was found in 5 patients (33.3%), whereas an impaired response of LVEF at peak exercise (<5% increase of basal value) was found in 9 patients (60%). A significant increase in LVEF, both at rest (from 51.6 +/- 2.6 to 58.1 +/- 1.7%, P < 0.01) and at peak exercise (from 51.6 +/- 2.3 to 60.2 +/- 2.4%, P < 0.001) was found in patients with las compared with those without) disease control (from 55.2 +/- 3.8 to 58.0 +/- 4% and from 61.8 +/- 4.6 to 61.8 +/- 3.4%, respectively). Among the 5 patients with inadequate LVEF at rest, all but 1 regained a normal LVEF after 6 months of treatment; whereas, among the 9 patients with an impaired response of the LVEF at peak exercise, 3 patients normalized, 4 improved, and 2 impaired their responses after treatment. The percent of IGF-I suppression was significantly correlated with the percent increase of resting LVEF (r = 0.644, P < 0.01). Exercise duration (from 6.0 +/- 0.7 to 7.3 +/- 0.7 min) and capacity (from 69.0 +/- 8.2 to 80 +/- 7.8 watts) were increased in the 15 patients considered as a whole, but the improvement in the exercise response was significant only in patients with disease control (P < 0.01 and P < 0.05, respectively) who also had an increase in the peak ejection rate (P = 0.03). No change in hemodynamic parameters, either at rest or at peak exercise, was found after treatment with OCT-LAR in the 15 patients. In conclusion, the results of the present study demonstrate that OCT-LAR im injections every 28 days induces a sustained suppression of GH levels and IGF-I levels in all acromegalic patients, allowing achievement of disease control in 60% of patients after 6 months of treatment. The sustained suppression of IGF-I levels was followed by a significant reduction of LVMi in all patients already after 3 months of treatment, with recovery of LV hypertrophy in 6 of 11 patients. In contrast, LV performance was significantly improved only in patients achieving normalization of their hormone levels. These data suggest that the treatment with OCT-LAR, by inducing a rapid suppression of circulating GH and IGF-I levels, could produce an early improvement of the cardiac abnormalities of acromegaly, thus contributing to reversal of the poor prognosis for cardiovascular diseases of these patients.
引用
收藏
页码:3132 / 3140
页数:9
相关论文
共 45 条
[1]  
BACHARACH SL, 1979, J NUCL MED, V20, P1889
[2]   Cardiac effects of slow-release lanreotide, a slow-release somatostatin analog, in acromegalic patients [J].
Baldelli, R ;
Ferretti, E ;
Jaffrain-Rea, ML ;
Iacobellis, G ;
Minniti, G ;
Caracciolo, B ;
Moroni, C ;
Cassone, R ;
Gulino, A ;
Tamburrano, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (02) :527-532
[3]  
BATES AS, 1993, Q J MED, V86, P293
[4]  
BENGTSSON BA, 1988, ACTA MED SCAND, V223, P327
[5]  
BERTONI PD, 1987, ACTA CARDIOL, V42, P1
[6]   IMPAIRED LEFT-VENTRICULAR DIASTOLIC FILLING IN PATIENTS WITH CORONARY-ARTERY DISEASE - ASSESSMENT WITH RADIONUCLIDE ANGIOGRAPHY [J].
BONOW, RO ;
BACHARACH, SL ;
GREEN, MV ;
KENT, KM ;
ROSING, DR ;
LIPSON, LC ;
LEON, MB ;
EPSTEIN, SE .
CIRCULATION, 1981, 64 (02) :315-323
[7]   CARDIOVASCULAR EFFECTS OF THE SOMATOSTATIN ANALOG OCTREOTIDE IN ACROMEGALY [J].
CHANSON, P ;
TIMSIT, J ;
MASQUET, C ;
WARNET, A ;
GUILLAUSSEAU, PJ ;
BIRMAN, P ;
HARRIS, AG ;
LUBETZKI, J .
ANNALS OF INTERNAL MEDICINE, 1990, 113 (12) :921-925
[8]   Acromegaly [J].
Colao, A ;
Merola, B ;
Ferone, D ;
Lombardi, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (09) :2777-2781
[9]   Systemic hypertension and impaired glucose tolerance are independently correlated to the severity of the acromegalic cardiomyopathy [J].
Colao, A ;
Baldelli, R ;
Marzullo, P ;
Ferretti, E ;
Ferone, D ;
Gargiulo, P ;
Petretta, M ;
Tamburrano, G ;
Lombardi, G ;
Liuzzi, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (01) :193-199
[10]   Prediction of efficacy of octreotide therapy in patients with acromegaly [J].
Colao, A ;
Ferone, D ;
Lastoria, S ;
Marzullo, P ;
Cerbone, G ;
DiSarno, A ;
Longobardi, S ;
Merola, B ;
Salvatore, M ;
Lombardi, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (06) :2356-2362