Document Detail


The long-term cardiovascular outcome of different GH-lowering treatments in acromegaly.
MedLine Citation:
PMID:  17987389     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The aim of this longitudinal study was to evaluate the echocardiographic outcome of acromegalic heart disease in patients undergoing different therapeutic approaches, in order to investigate whether SSA could provide therapeutic advantages as compared with neurosurgery. In total of 36, consecutive patients undergoing SSA treatment after neurosurgery were enrolled in this study (Gr.Surg.-SSA). After 12 months of treatment, 21 patients had a controlled disease, while the remaining 15 patients displayed uncontrolled disease. Twelve acromegalic patients who did not undergo SSA treatment due to controlled disease after neurosurgery were enrolled as control group (Gr.Surg). The echocardiographic-Doppler study was performed before neurosurgery and after 12-months of follow-up. After follow-up, a significant reduction in serum GH and IGF-I values, Left Ventricular Mass index (LVMi) and LVH rate with an improvement in diastolic function was observed in both groups of patients. We found a significant reduction of LVMi either in patients with controlled disease or in those with poorly controlled disease undergoing SSA treatment. Diastolic function and of LVH percentage improved in all groups, but significantly so only in controlled patients, no significant difference in any echocardiographic parameters and in the prevalence of the LVH rate were observed between the three groups of patients at the end of follow-up. Therefore, our data appear to show that for echographic parameters medical treatment additive beneficial effects is compared to neurosurgery alone. SSA also appears to contribute to the improvement of acromegalic cardiomyopathy also in patients who did not achieve biochemical control of the disease.
Authors:
Laura De Marinis; Antonio Bianchi; Gherardo Mazziotti; Marco Mettimano; Domenico Milardi; Alessandra Fusco; Vincenzo Cimino; Giulio Maira; Alfredo Pontecorvi; Andrea Giustina
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Pituitary     Volume:  11     ISSN:  1573-7403     ISO Abbreviation:  Pituitary     Publication Date:  2008  
Date Detail:
Created Date:  2008-01-28     Completed Date:  2009-06-11     Revised Date:  2009-06-26    
Medline Journal Info:
Nlm Unique ID:  9814578     Medline TA:  Pituitary     Country:  United States    
Other Details:
Languages:  eng     Pagination:  13-20     Citation Subset:  IM    
Affiliation:
Department of Endocrinology, School of Medicine, Catholic University, Via Cassia 901, Rome 00189, Italy. laurademarinis@yahoo.it
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MeSH Terms
Descriptor/Qualifier:
Acromegaly / blood,  complications,  therapy*
Biological Markers / blood
Cardiomyopathies / etiology,  physiopathology,  prevention & control*,  ultrasonography
Combined Modality Therapy
Echocardiography, Doppler
Female
Human Growth Hormone / blood*
Humans
Hypertrophy, Left Ventricular / etiology,  physiopathology,  prevention & control*,  ultrasonography
Insulin-Like Growth Factor I / metabolism
Longitudinal Studies
Male
Middle Aged
Neurosurgical Procedures*
Octreotide / therapeutic use*
Somatostatin / analogs & derivatives,  therapeutic use*
Time Factors
Treatment Outcome
Ventricular Function, Left / drug effects
Chemical
Reg. No./Substance:
0/Biological Markers; 12629-01-5/Human Growth Hormone; 51110-01-1/Somatostatin; 67763-96-6/Insulin-Like Growth Factor I; 83150-76-9/Octreotide

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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