D14 Plasma levels of 24S-hydroxycholesterol are reduced in Huntington disease subjects: preliminary results of a 2-year longitudinal study
ObjectivesBrain cholesterol is produced in situ and its turn-over is ensured by the conversion into 24S-hydroxycholesterol (24-OHC) which can cross the blood-brain barrier. Brain biosynthesis was shown to be reduced in murine models of Huntington’s disease (HD) and 24-OHC plasma concentrations were...
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Published in | Journal of neurology, neurosurgery and psychiatry Vol. 93; no. Suppl 1; p. A25 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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London
BMJ Publishing Group Ltd
01.09.2022
BMJ Publishing Group LTD |
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Abstract | ObjectivesBrain cholesterol is produced in situ and its turn-over is ensured by the conversion into 24S-hydroxycholesterol (24-OHC) which can cross the blood-brain barrier. Brain biosynthesis was shown to be reduced in murine models of Huntington’s disease (HD) and 24-OHC plasma concentrations were found reduced in HD patients. We aimed to investigate 24-OHC longitudinal changes and correlate the plasma levels with disease progression, basal ganglia MRI volumes, and neurofilament concentrations.Participants and MethodsWe conducted a 2-year observational study in 78 HD subjects and 64 healthy controls. Cholesterol and its metabolites were measured using two different in-house developed and validated methods based on liquid chromatography and mass spectrometry. Fifty-eight subjects underwent 3T-MRI for brain morphometry. Neurofilament plasma measures are ongoing. HD subjects were classified using the novel Huntington Disease Integrated Staging System (HD-ISS).ResultsTwenty-one subjects were in stage 0-1; 11 in stage 2; and 46 in stage 3(a-c). Preliminary analyses of baseline data showed 24-OHC significantly reduced in stage 3b and 3c patients in comparison with controls (p=0.03; p<0.02 respectively). We also observed a trend of reduction of 24-OHC from prodromal disease stages (0-1) to the late manifest disease stages. 24-OHC levels were 40.+/-1.9 ng/ml (mean +/- SEM) in controls; 33.6+/-3.8 in HD-stage 0-1; 34.3+/-5.5 in HD-stage 2; 30.9+/-3.9 in HD-stage 3a; 29.3+/-2.5 in HD-stage 3b; and 23.3+/-1.9 in HD-stage 3c.ConclusionsMonitoring 24-OHC plasma concentrations may contribute in following disease progression and may represent a valuable outcome measure in clinical trials testing cholesterol as a candidate drug in HD. |
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AbstractList | ObjectivesBrain cholesterol is produced in situ and its turn-over is ensured by the conversion into 24S-hydroxycholesterol (24-OHC) which can cross the blood-brain barrier. Brain biosynthesis was shown to be reduced in murine models of Huntington’s disease (HD) and 24-OHC plasma concentrations were found reduced in HD patients. We aimed to investigate 24-OHC longitudinal changes and correlate the plasma levels with disease progression, basal ganglia MRI volumes, and neurofilament concentrations.Participants and MethodsWe conducted a 2-year observational study in 78 HD subjects and 64 healthy controls. Cholesterol and its metabolites were measured using two different in-house developed and validated methods based on liquid chromatography and mass spectrometry. Fifty-eight subjects underwent 3T-MRI for brain morphometry. Neurofilament plasma measures are ongoing. HD subjects were classified using the novel Huntington Disease Integrated Staging System (HD-ISS).ResultsTwenty-one subjects were in stage 0-1; 11 in stage 2; and 46 in stage 3(a-c). Preliminary analyses of baseline data showed 24-OHC significantly reduced in stage 3b and 3c patients in comparison with controls (p=0.03; p<0.02 respectively). We also observed a trend of reduction of 24-OHC from prodromal disease stages (0-1) to the late manifest disease stages. 24-OHC levels were 40.+/-1.9 ng/ml (mean +/- SEM) in controls; 33.6+/-3.8 in HD-stage 0-1; 34.3+/-5.5 in HD-stage 2; 30.9+/-3.9 in HD-stage 3a; 29.3+/-2.5 in HD-stage 3b; and 23.3+/-1.9 in HD-stage 3c.ConclusionsMonitoring 24-OHC plasma concentrations may contribute in following disease progression and may represent a valuable outcome measure in clinical trials testing cholesterol as a candidate drug in HD. |
Author | Marchini, Gloria Mariotti, Caterina Grisoli, Marina Favagrossa, Monica Colombo, Laura Nanetti, Lorenzo Gellera, Cinzia Birolini, Giulia Valenza, Marta Bagnati, Renzo Cattaneo, Elena Salmona, Mario Nigri, Anna Mongelli, Alessia Castaldo, Anna Passoni, Alice Fichera, Mario |
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Copyright | Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. 2022 Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. |
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Snippet | ObjectivesBrain cholesterol is produced in situ and its turn-over is ensured by the conversion into 24S-hydroxycholesterol (24-OHC) which can cross the... |
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SubjectTerms | 24-OHC Basal ganglia MRI volumes Biomarker Cholesterol D: Wet biomarkers Huntingtons disease Longitudinal studies Longitudinal study Plasma |
Title | D14 Plasma levels of 24S-hydroxycholesterol are reduced in Huntington disease subjects: preliminary results of a 2-year longitudinal study |
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