Sensitivity of Volumetric Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy to Progression of Spinocerebellar Ataxia Type 1.

biomarker effect size magnetic resonance spectroscopy volumetry

Journal

Movement disorders clinical practice
ISSN: 2330-1619
Titre abrégé: Mov Disord Clin Pract
Pays: United States
ID NLM: 101630279

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 29 04 2019
accepted: 29 05 2019
entrez: 21 9 2019
pubmed: 21 9 2019
medline: 21 9 2019
Statut: epublish

Résumé

Spinocerebellar ataxia type 1 (SCA1) causes progressive degeneration of the cerebellum and brainstem. Volumetric magnetic resonance imaging (MRI) was shown to be more sensitive to disease progression than the most sensitive clinical measure, the Scale for the Assessment and Rating of Ataxia (SARA), in longitudinal studies, and magnetic resonance spectroscopy (MRS) was shown to detect neurochemical abnormalities with high sensitivity cross-sectionally in SCA1. The objectives of this study were to compare the sensitivities to change of volumetric MRI, MRS, and SARA in a 3-year longitudinal study in SCA1. A total of 16 early-to-moderate stage patients with SCA1 (SARA 0-14) and 21 matched healthy participants were scanned up to 3 times with 1.5-year intervals. Ataxia severity was assessed with SARA. T The pontine total Both MRI and MRS were more sensitive to disease progression than SARA in SCA1. Pontine volume was most sensitive to change, whereas MRS may have more sensitivity at the premanifest stage and predictive value for disease progression.

Sections du résumé

BACKGROUND BACKGROUND
Spinocerebellar ataxia type 1 (SCA1) causes progressive degeneration of the cerebellum and brainstem. Volumetric magnetic resonance imaging (MRI) was shown to be more sensitive to disease progression than the most sensitive clinical measure, the Scale for the Assessment and Rating of Ataxia (SARA), in longitudinal studies, and magnetic resonance spectroscopy (MRS) was shown to detect neurochemical abnormalities with high sensitivity cross-sectionally in SCA1.
OBJECTIVES OBJECTIVE
The objectives of this study were to compare the sensitivities to change of volumetric MRI, MRS, and SARA in a 3-year longitudinal study in SCA1.
METHODS METHODS
A total of 16 early-to-moderate stage patients with SCA1 (SARA 0-14) and 21 matched healthy participants were scanned up to 3 times with 1.5-year intervals. Ataxia severity was assessed with SARA. T
RESULTS RESULTS
The pontine total
CONCLUSION CONCLUSIONS
Both MRI and MRS were more sensitive to disease progression than SARA in SCA1. Pontine volume was most sensitive to change, whereas MRS may have more sensitivity at the premanifest stage and predictive value for disease progression.

Identifiants

pubmed: 31538089
doi: 10.1002/mdc3.12804
pii: MDC312804
pmc: PMC6749810
doi:

Types de publication

Journal Article

Langues

eng

Pagination

549-558

Subventions

Organisme : NIBIB NIH HHS
ID : P41 EB015894
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS080816
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000114
Pays : United States
Organisme : NINDS NIH HHS
ID : P30 NS076408
Pays : United States
Organisme : NINDS NIH HHS
ID : U01 NS104326
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS070815
Pays : United States

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Auteurs

Dinesh K Deelchand (DK)

Center for Magnetic Resonance Research University of Minnesota Minneapolis MN USA.

James M Joers (JM)

Center for Magnetic Resonance Research University of Minnesota Minneapolis MN USA.

Adarsh Ravishankar (A)

University of Minnesota Medical School Minneapolis MN USA.

Tianmeng Lyu (T)

Division of Biostatistics University of Minnesota Minneapolis MN USA.

Uzay E Emir (UE)

Center for Magnetic Resonance Research University of Minnesota Minneapolis MN USA.

Diane Hutter (D)

Center for Magnetic Resonance Research University of Minnesota Minneapolis MN USA.

Christopher M Gomez (CM)

Department of Neurology University of Chicago Chicago IL USA.

Khalaf O Bushara (KO)

Department of Neurology University of Minnesota Minneapolis MN USA.

Christophe Lenglet (C)

Center for Magnetic Resonance Research University of Minnesota Minneapolis MN USA.

Lynn E Eberly (LE)

Division of Biostatistics University of Minnesota Minneapolis MN USA.

Gülin Öz (G)

Center for Magnetic Resonance Research University of Minnesota Minneapolis MN USA.

Classifications MeSH