Neuroendocrine disturbances in Huntington's disease.

BACKGROUND: Huntington's disease (HD) is a severe inherited neurodegenerative disorder characterized, in addition to neurological impairment, by weight loss suggesting endocrine disturbances. The aims of this study were to look for neuroendocrine disturbances in patients with Huntington's...

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Main Authors: Nadine Saleh, Stéphane Moutereau, Alexandra Durr, Pierre Krystkowiak, Jean-Philippe Azulay, Christine Tranchant, Emmanuel Broussolle, Françoise Morin, Anne-Catherine Bachoud-Lévi, Patrick Maison
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2655649?pdf=render
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spelling doaj-eaeac266ac574cb79351e5aeb6e7d7692020-11-24T21:55:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-01-0143e496210.1371/journal.pone.0004962Neuroendocrine disturbances in Huntington's disease.Nadine SalehStéphane MoutereauAlexandra DurrPierre KrystkowiakJean-Philippe AzulayChristine TranchantEmmanuel BroussolleFrançoise MorinAnne-Catherine Bachoud-LéviPatrick MaisonBACKGROUND: Huntington's disease (HD) is a severe inherited neurodegenerative disorder characterized, in addition to neurological impairment, by weight loss suggesting endocrine disturbances. The aims of this study were to look for neuroendocrine disturbances in patients with Huntington's disease (HD) and to determine the relationship with weight loss seen in HD METHODS AND FINDING: We compared plasma levels of hormones from the five pituitary axes in 219 patients with genetically documented HD and in 71 sex- and age-matched controls. Relationships between hormone levels and disease severity, including weight-loss severity, were evaluated. Growth hormone (GH) and standard deviation score of insulin-like growth factor 1 (SDS IGF-1) were significantly higher in patients than in controls (0.25 (0.01-5.89) vs. 0.15 (0.005-4.89) ng/ml, p = 0.013 and 0.16+/-1.02 vs. 0.06+/-0.91, p = 0.039; respectively). Cortisol was higher (p = 0.002) in patients (399.14+/-160.5 nmol/L vs. 279.8+/-130.1 nmol/L), whereas no differences were found for other hormone axes. In patients, elevations in GH and IGF-1 and decreases in thyroid-stimulating hormone, free triiodothyronine and testosterone (in men) were associated with severity of impairments (Independence scale, Functional score, Total Functional Capacity, Total Motor score, Behavioral score). Only GH was independently associated with body mass index (beta = -0.26, p = 0.001). CONCLUSION: Our data suggest that the thyrotropic and in men gonadotropic axes are altered in HD according to the severity of the disease. The somatotropic axis is overactive even in patients with early disease, and could be related to the weight loss seen in HD patients.http://europepmc.org/articles/PMC2655649?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Nadine Saleh
Stéphane Moutereau
Alexandra Durr
Pierre Krystkowiak
Jean-Philippe Azulay
Christine Tranchant
Emmanuel Broussolle
Françoise Morin
Anne-Catherine Bachoud-Lévi
Patrick Maison
spellingShingle Nadine Saleh
Stéphane Moutereau
Alexandra Durr
Pierre Krystkowiak
Jean-Philippe Azulay
Christine Tranchant
Emmanuel Broussolle
Françoise Morin
Anne-Catherine Bachoud-Lévi
Patrick Maison
Neuroendocrine disturbances in Huntington's disease.
PLoS ONE
author_facet Nadine Saleh
Stéphane Moutereau
Alexandra Durr
Pierre Krystkowiak
Jean-Philippe Azulay
Christine Tranchant
Emmanuel Broussolle
Françoise Morin
Anne-Catherine Bachoud-Lévi
Patrick Maison
author_sort Nadine Saleh
title Neuroendocrine disturbances in Huntington's disease.
title_short Neuroendocrine disturbances in Huntington's disease.
title_full Neuroendocrine disturbances in Huntington's disease.
title_fullStr Neuroendocrine disturbances in Huntington's disease.
title_full_unstemmed Neuroendocrine disturbances in Huntington's disease.
title_sort neuroendocrine disturbances in huntington's disease.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-01-01
description BACKGROUND: Huntington's disease (HD) is a severe inherited neurodegenerative disorder characterized, in addition to neurological impairment, by weight loss suggesting endocrine disturbances. The aims of this study were to look for neuroendocrine disturbances in patients with Huntington's disease (HD) and to determine the relationship with weight loss seen in HD METHODS AND FINDING: We compared plasma levels of hormones from the five pituitary axes in 219 patients with genetically documented HD and in 71 sex- and age-matched controls. Relationships between hormone levels and disease severity, including weight-loss severity, were evaluated. Growth hormone (GH) and standard deviation score of insulin-like growth factor 1 (SDS IGF-1) were significantly higher in patients than in controls (0.25 (0.01-5.89) vs. 0.15 (0.005-4.89) ng/ml, p = 0.013 and 0.16+/-1.02 vs. 0.06+/-0.91, p = 0.039; respectively). Cortisol was higher (p = 0.002) in patients (399.14+/-160.5 nmol/L vs. 279.8+/-130.1 nmol/L), whereas no differences were found for other hormone axes. In patients, elevations in GH and IGF-1 and decreases in thyroid-stimulating hormone, free triiodothyronine and testosterone (in men) were associated with severity of impairments (Independence scale, Functional score, Total Functional Capacity, Total Motor score, Behavioral score). Only GH was independently associated with body mass index (beta = -0.26, p = 0.001). CONCLUSION: Our data suggest that the thyrotropic and in men gonadotropic axes are altered in HD according to the severity of the disease. The somatotropic axis is overactive even in patients with early disease, and could be related to the weight loss seen in HD patients.
url http://europepmc.org/articles/PMC2655649?pdf=render
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