Literature DB >> 20884675

Growth hormone response to arginine test differentiates between two subgroups of Huntington's disease patients.

Elena Salvatore1, Carlo Rinaldi, Tecla Tucci, Luigi Di Maio, Carolina Di Somma, Silvia Savastano, Gaetano Lombardi, Alessandro Filla, Annamaria Colao, Giuseppe De Michele.   

Abstract

OBJECTIVE: Huntington's disease (HD) is an autosomal dominant disorder characterised by motor, cognitive and psychiatric disturbances. Several studies have demonstrated that hypothalamic dysfunction is part of the phenotypic spectrum. The aim of the study was to evaluate the growth hormone (GH) response to arginine infusion in a cohort of HD patients, to search for an in vivo biomarker of hypothalamic dysfunction.
METHODS: The authors investigated 17 HD patients and 17 age-, sex- and BMI-matched healthy controls. Clinical assessment of patients was performed using the Unified Huntington's Disease Rating Scale motor section and total function capacity. Metabolic and endocrine investigations included total, LDL and HDL cholesterol, basal insulin, GH, insulin-like growth factor 1 (IGF-1), SD Score IGF-1 (SDS IGF-1) and the GH response to arginine stimulation.
RESULTS: HD patients showed lower plasma IGF-1 and SDS IGF-1 levels and a higher baseline GH in comparison with control subjects. The arginine test induced a normal GH peak in nine patients (53%; Arg+), whereas the response was absent in the remaining eight (47%; Arg-). Arg+ and Arg- also showed two distinct endocrine/metabolic profiles with differences in insulin and lipid metabolism.
CONCLUSION: It remains to be clarified if these two subgroups of patients, according to the GH response to arginine, correspond to different disease stages or to different patterns of neurodegeneration.

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Year:  2010        PMID: 20884675     DOI: 10.1136/jnnp.2010.208553

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  5 in total

1.  A randomized controlled clinical trial of growth hormone in amyotrophic lateral sclerosis: clinical, neuroimaging, and hormonal results.

Authors:  Francesco Saccà; Mario Quarantelli; Carlo Rinaldi; Tecla Tucci; Raffaele Piro; Gaetano Perrotta; Barbara Carotenuto; Angela Marsili; Vincenzo Palma; Giuseppe De Michele; Arturo Brunetti; Vincenzo Brescia Morra; Alessandro Filla; Marco Salvatore
Journal:  J Neurol       Date:  2011-06-25       Impact factor: 4.849

2.  Altered hypothalamic protein expression in a rat model of Huntington's disease.

Authors:  Wei-na Cong; Huan Cai; Rui Wang; Caitlin M Daimon; Stuart Maudsley; Kerstin Raber; Fabio Canneva; Stephan von Hörsten; Bronwen Martin
Journal:  PLoS One       Date:  2012-10-18       Impact factor: 3.240

3.  Integration of targeted metabolomics and transcriptomics identifies deregulation of phosphatidylcholine metabolism in Huntington's disease peripheral blood samples.

Authors:  Anastasios Mastrokolias; Rene Pool; Eleni Mina; Kristina M Hettne; Erik van Duijn; Roos C van der Mast; GertJan van Ommen; Peter A C 't Hoen; Cornelia Prehn; Jerzy Adamski; Willeke van Roon-Mom
Journal:  Metabolomics       Date:  2016-07-27       Impact factor: 4.290

4.  Blood Oxidative Stress Marker Aberrations in Patients with Huntington's Disease: A Meta-Analysis Study.

Authors:  Quan Tang; Hua Liu; Xiao-Jie Shi; Yong Cheng
Journal:  Oxid Med Cell Longev       Date:  2020-09-08       Impact factor: 6.543

Review 5.  A Critical Evaluation of Wet Biomarkers for Huntington's Disease: Current Status and Ways Forward.

Authors:  Edina Silajdžić; Maria Björkqvist
Journal:  J Huntingtons Dis       Date:  2018
  5 in total

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