Plasma 24S-hydroxycholesterol correlation with markers of Huntington disease progression

24S-hydroxycholesterol (24OHC) is involved in the conversion of excess cholesterol in the brain, and its level in plasma is related to the number of metabolically active neuronal cells. Previous research suggests that plasma 24OHC is substantially reduced in the presence of neurodegenerative disease...

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Main Authors: Valerio Leoni, Jeffrey D. Long, James A. Mills, Stefano Di Donato, Jane S. Paulsen
Format: Article
Language:English
Published: Elsevier 2013-07-01
Series:Neurobiology of Disease
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996113001010
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spelling doaj-284a4736cde64341ac700068556abcf62021-03-22T12:39:49ZengElsevierNeurobiology of Disease1095-953X2013-07-01553743Plasma 24S-hydroxycholesterol correlation with markers of Huntington disease progressionValerio Leoni0Jeffrey D. Long1James A. Mills2Stefano Di Donato3Jane S. Paulsen4Laboratory of Clinical Pathology and Medical Genetics, Fondazione IRCCS Institute of Neurology ‘Carlo Besta’, Milano, ItalyDepartment of Psychiatry, Carver College of Medicine, University of Iowa, USADepartment of Psychiatry, Carver College of Medicine, University of Iowa, USAFondazione IRCCS Institute of Neurology ‘C. Besta’, Milano, ItalyDepartment of Psychiatry, Carver College of Medicine, University of Iowa, USA; Department of Neurology, Carver College of Medicine, University of Iowa, USA; Corresponding author at: Department of Psychiatry, Carver College of Medicine, University of Iowa, USA. Fax: +1 3193533003.24S-hydroxycholesterol (24OHC) is involved in the conversion of excess cholesterol in the brain, and its level in plasma is related to the number of metabolically active neuronal cells. Previous research suggests that plasma 24OHC is substantially reduced in the presence of neurodegenerative disease. Huntington disease (HD) is an inherited autosomal dominant neurodegenerative disorder caused by a cytosine–adenine–guanine (CAG) triplet repeat expansion in the coding region of the huntingtin (HTT) gene. The current study focused on the relative importance of 24OHC as a marker of HD progression. Using mass spectrometry methods, we examined plasma 24OHC levels in three groups of gene-expanded individuals (Low, Medium, High) characterized by their progression at entry into the parent PREDICT-HD study, along with a group of non-gene-expanded controls (total N = 150). In addition, the correlation of 24OHC with a number of motor, cognitive, and imagining markers was examined, and effect sizes for group differences among the markers were computed for comparison with 24OHC. Results show a progression gradient as 24OHC levels decreased as the progression group increased (Low to High). The effect size of group differences for 24OHC was larger than all the other variables, except striatal volume. 24OHC was significantly correlated with many of the other key variables. The results are interpreted in terms of cholesterol synthesis and neuronal degeneration. This study provides evidence that 24OHC is a relatively important marker of HD progression.http://www.sciencedirect.com/science/article/pii/S0969996113001010CholesterolNeurodegenerative diseaseBiomarkersHuntington disease
collection DOAJ
language English
format Article
sources DOAJ
author Valerio Leoni
Jeffrey D. Long
James A. Mills
Stefano Di Donato
Jane S. Paulsen
spellingShingle Valerio Leoni
Jeffrey D. Long
James A. Mills
Stefano Di Donato
Jane S. Paulsen
Plasma 24S-hydroxycholesterol correlation with markers of Huntington disease progression
Neurobiology of Disease
Cholesterol
Neurodegenerative disease
Biomarkers
Huntington disease
author_facet Valerio Leoni
Jeffrey D. Long
James A. Mills
Stefano Di Donato
Jane S. Paulsen
author_sort Valerio Leoni
title Plasma 24S-hydroxycholesterol correlation with markers of Huntington disease progression
title_short Plasma 24S-hydroxycholesterol correlation with markers of Huntington disease progression
title_full Plasma 24S-hydroxycholesterol correlation with markers of Huntington disease progression
title_fullStr Plasma 24S-hydroxycholesterol correlation with markers of Huntington disease progression
title_full_unstemmed Plasma 24S-hydroxycholesterol correlation with markers of Huntington disease progression
title_sort plasma 24s-hydroxycholesterol correlation with markers of huntington disease progression
publisher Elsevier
series Neurobiology of Disease
issn 1095-953X
publishDate 2013-07-01
description 24S-hydroxycholesterol (24OHC) is involved in the conversion of excess cholesterol in the brain, and its level in plasma is related to the number of metabolically active neuronal cells. Previous research suggests that plasma 24OHC is substantially reduced in the presence of neurodegenerative disease. Huntington disease (HD) is an inherited autosomal dominant neurodegenerative disorder caused by a cytosine–adenine–guanine (CAG) triplet repeat expansion in the coding region of the huntingtin (HTT) gene. The current study focused on the relative importance of 24OHC as a marker of HD progression. Using mass spectrometry methods, we examined plasma 24OHC levels in three groups of gene-expanded individuals (Low, Medium, High) characterized by their progression at entry into the parent PREDICT-HD study, along with a group of non-gene-expanded controls (total N = 150). In addition, the correlation of 24OHC with a number of motor, cognitive, and imagining markers was examined, and effect sizes for group differences among the markers were computed for comparison with 24OHC. Results show a progression gradient as 24OHC levels decreased as the progression group increased (Low to High). The effect size of group differences for 24OHC was larger than all the other variables, except striatal volume. 24OHC was significantly correlated with many of the other key variables. The results are interpreted in terms of cholesterol synthesis and neuronal degeneration. This study provides evidence that 24OHC is a relatively important marker of HD progression.
topic Cholesterol
Neurodegenerative disease
Biomarkers
Huntington disease
url http://www.sciencedirect.com/science/article/pii/S0969996113001010
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