TY - JOUR
T1 - Neuroimaging Biomarkers for Friedreich Ataxia
T2 - A Cross-Sectional Analysis of the TRACK-FA Study
AU - Georgiou-Karistianis, Nellie
AU - Corben, Louise A.
AU - Lock, Eric F.
AU - Bujalka, Helena
AU - Adanyeguh, Isaac
AU - Corti, Manuela
AU - Deelchand, Dinesh K.
AU - Delatycki, Martin B.
AU - Dogan, Imis
AU - Farmer, Jennifer
AU - França, Marcondes C.
AU - Gabay, Anthony S.
AU - Gaetz, William
AU - Harding, Ian H.
AU - Joers, James
AU - Lax, Michelle A.
AU - Li, Jiakun
AU - Lynch, David R.
AU - Mareci, Thomas H.
AU - Martinez, Alberto R.M.
AU - Pandolfo, Massimo
AU - Papoutsi, Marina
AU - Parker, Richard G.
AU - Reetz, Kathrin
AU - Rezende, Thiago J.R.
AU - Roberts, Timothy P.
AU - Romanzetti, Sandro
AU - Rudko, David A.
AU - Saha, Susmita
AU - Schulz, Jörg B.
AU - Subramony, Sub H.
AU - Supramaniam, Veena G.
AU - Lenglet, Christophe
AU - Henry, Pierre Gilles
N1 - Publisher Copyright:
© 2025 The Author(s). Annals of Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.
PY - 2025/8
Y1 - 2025/8
N2 - Objective: We aimed to quantify differences in the brain and spinal cord between Friedreich ataxia and controls, stratified by age and disease stage, including for the first time in young children. Methods: TRACK-FA is the largest prospective, longitudinal, multi-modal neuroimaging study in Friedreich ataxia to date. We assessed individuals with Friedreich ataxia and controls, 5 to 42 years, at 7 sites across 4 continents. The 17 imaging primary outcome measures (POMs) were selected from metrics that showed a significant longitudinal change in previous small-scale studies. These included brain and spinal cord morphometry (structural magnetic resonance imaging [MRI]) and microstructure (diffusion MRI); brain iron levels (quantitative susceptibility mapping); and spinal cord biochemistry (magnetic resonance spectroscopy). This study is registered with ClinicalTrials.gov (NCT04349514). Results: Between February 2021 and August 2023, we assessed 169 individuals with Friedreich ataxia and 95 controls. Compared to controls, individuals with Friedreich ataxia had lower volume of dentate nucleus and superior cerebellar peduncles; smaller cross-sectional area of spinal cord; lower fractional anisotropy and higher diffusivity in spinal cord and superior cerebellar peduncles; and lower total N-acetyl-aspartate/myo-inositol ratio in spinal cord. Morphometric differences in spinal cord and superior cerebellar peduncles increased dramatically with age during childhood, with rapid development in controls, but not in Friedreich ataxia. Many imaging POMs showed significant associations with clinical severity. Interpretation: Our findings provide strong imaging evidence of impaired development of spinal cord and superior cerebellar peduncles during childhood in Friedreich ataxia and open the way for the use of neuroimaging biomarkers in clinical trials. ANN NEUROL 2025;98:386–397.
AB - Objective: We aimed to quantify differences in the brain and spinal cord between Friedreich ataxia and controls, stratified by age and disease stage, including for the first time in young children. Methods: TRACK-FA is the largest prospective, longitudinal, multi-modal neuroimaging study in Friedreich ataxia to date. We assessed individuals with Friedreich ataxia and controls, 5 to 42 years, at 7 sites across 4 continents. The 17 imaging primary outcome measures (POMs) were selected from metrics that showed a significant longitudinal change in previous small-scale studies. These included brain and spinal cord morphometry (structural magnetic resonance imaging [MRI]) and microstructure (diffusion MRI); brain iron levels (quantitative susceptibility mapping); and spinal cord biochemistry (magnetic resonance spectroscopy). This study is registered with ClinicalTrials.gov (NCT04349514). Results: Between February 2021 and August 2023, we assessed 169 individuals with Friedreich ataxia and 95 controls. Compared to controls, individuals with Friedreich ataxia had lower volume of dentate nucleus and superior cerebellar peduncles; smaller cross-sectional area of spinal cord; lower fractional anisotropy and higher diffusivity in spinal cord and superior cerebellar peduncles; and lower total N-acetyl-aspartate/myo-inositol ratio in spinal cord. Morphometric differences in spinal cord and superior cerebellar peduncles increased dramatically with age during childhood, with rapid development in controls, but not in Friedreich ataxia. Many imaging POMs showed significant associations with clinical severity. Interpretation: Our findings provide strong imaging evidence of impaired development of spinal cord and superior cerebellar peduncles during childhood in Friedreich ataxia and open the way for the use of neuroimaging biomarkers in clinical trials. ANN NEUROL 2025;98:386–397.
UR - https://www.scopus.com/pages/publications/105000609304
UR - https://www.scopus.com/pages/publications/105000609304#tab=citedBy
U2 - 10.1002/ana.27237
DO - 10.1002/ana.27237
M3 - Article
C2 - 40119735
AN - SCOPUS:105000609304
SN - 0364-5134
VL - 98
SP - 386
EP - 397
JO - Annals of Neurology
JF - Annals of Neurology
IS - 2
ER -