| Literature DB >> 27295183 |
Renata S Auriemma1, Ludovica F S Grasso1, Mariano Galdiero1, Maurizio Galderisi2, Claudia Pivonello1, Chiara Simeoli1, Maria Cristina De Martino1, Rosario Ferrigno1, Mariarosaria Negri1, Cristina de Angelis1, Rosario Pivonello3, Annamaria Colao1.
Abstract
To date, no data are available on the effects of long-term combined treatment with somatostatin analogues (SA) and pegvisomant (PEG) on cardiovascular complications in acromegaly. The current study aimed at investigating the effects of long-term SA + PEG on cardiac structure and performance. Thirty-six patients (14 M, 22 F, aged 52.3 ± 10.2 years) entered this study. Weight, BMI, systolic (SBP) and diastolic (DBP) blood pressure, IGF-I, fasting glucose (FG), fasting insulin (FI), HOMA-IR, HbA1c, and lipids were evaluated at baseline (T0), after long-term (median 36 months) SA (T1), after 12 (T12) and 60 (T60) months of SA + PEG, and at last follow-up (LFU, median 78 months). At each time point, all patients underwent echocardiography. At T1, induced a slight but not significant decrease in IGF-I (p = 0.077), whereas FI (p = 0.004), HOMA-IR (p = 0.013), ejection fraction (EF, p = 0.013), early (E) to late (A) ventricular filling velocities (E/A, p = 0.001), and isovolumetric relaxation time (IVRT, p = 0.000) significantly improved. At T12, IGF-I (p = 0.000) significantly reduced compared to T0, and FI (p = 0.001), HOMA-IR (p = 0.000), LVMI (p = 0.000), and E/A (p = 0.006) further improved compared to T1. At T60, FI (p = 0.027), HOMA-IR (p = 0.049), and E/A (p = 0.005) significantly improved as compared to T1. At LFU IGF-I normalized in 83.3 %, FI (p = 0.000), HOMA-IR (p = 0.000), LVMi (p = 0.000), and E/A (p = 0.005) further improved as compared to T1. PEG dose significantly correlated with LVMi at T12 (r = 0.575, p = 0.000) and T60 (r = 0.403, p = 0.037). Long-term PEG addition to SA improves cardiac structure and performance, particularly diastolic dysfunction, in acromegalic patients resistant to SA.Entities:
Keywords: Acromegalic cardiomyopathy; Acromegaly; Cardiac performance; Cardiac structure; Diastolic dysfunction; Ejection fraction; IGF-I; Insulin resistance; Left ventricular hypertrophy; Metabolic syndrome; Pegvisomant; Pituitary tumors; Somatostatin analogues
Mesh:
Substances:
Year: 2016 PMID: 27295183 DOI: 10.1007/s12020-016-0995-5
Source DB: PubMed Journal: Endocrine ISSN: 1355-008X Impact factor: 3.633