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Spinal cord damage in Friedreich’s ataxia: Results from the ENIGMA-Ataxia

Authors :
Thiago JR Rezende
Isaac M Adanyeguh
Filippo Arrigoni
Benjamin Bender
Fernando Cendes
Louise A Corben
Andreas Deistung
Martin Delatycki
Imis Dogan
Gary F Egan
Sophia L Göricke
Nellie Georgiou-Karistianis
Pierre-Gilles Henry
Diane Hutter
Neda Jahanshad
James M Joers
Christophe Lenglet
Tobias Lindig
Alberto RM Martinez
Andrea Martinuzzi
Gabriella Paparella
Denis Peruzzo
Kathrin Reetz
Sandro Romanzetti
Ludger Schöls
Jörg B Schulz
Matthis Synofzik
Sophia I Thomopoulos
Paul M Thompson
Dagmar Timmann
Ian H Harding
Marcondes C. França
Publication Year :
2022
Publisher :
Cold Spring Harbor Laboratory, 2022.

Abstract

ObjectiveSpinal cord damage is a hallmark of Friedreich ataxia (FRDA), but its progression and clinical correlates remain unclear. Here we performed a characterization of cervical spinal cord structural abnormalities in a large multisite FRDA cohort.MethodsWe performed a cross-sectional analysis of cervical spinal cord (C1 to C4) cross-sectional area (CSA) and eccentricity using MRI data from eight sites within the ENIGMA-Ataxia initiative, including 256 individuals with FRDA and 223 age- and sex-matched controls. Correlations and subgroup analyses within the FRDA cohort were undertaken based on disease duration, ataxia severity, and onset age.ResultsIndividuals with FRDA, relative to controls, had significantly reduced CSA at all examined levels, with large effect sizes (d>2.1) and significant correlations with disease severity (rd>1.2), but without significant clinical correlations. Subgroup analyses showed that CSA and eccentricity are abnormal at all disease stages. However, while CSA appears to decrease progressively, eccentricity remains stable over time.InterpretationPrevious research has shown that increased eccentricity reflects dorsal column (DC) damage, while decreased CSA reflects either DC or corticospinal tract (CST) damage or both. Hence, our data support the hypothesis that damage to DC and CST follow distinct courses in FRDA: developmental abnormalities likely define the DC, whereas CST alterations may be both developmental and degenerative. These results provide new insights about FRDA pathogenesis and indicate that CSA of the cervical spinal cord should be investigated further as a potential biomarker of disease progression.

Details

Database :
OpenAIRE
Accession number :
edsair.doi...........d3726442601dfb55b984094b072ecc4a