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DOI 10.1002/ana.27237

Медицинская библиотека · Annals of neurology · 2025

Neuroimaging Biomarkers for Friedreich Ataxia: A Cross-Sectional Analysis of the TRACK-FA Study.

Georgiou-Karistianis Nellie, Corben Louise A, Lock Eric F, Bujalka Helena, Adanyeguh Isaac, Corti Manuela, Deelchand Dinesh K, Delatycki Martin B, Dogan Imis, Farmer Jennifer, França Marcondes C, Gabay Anthony S, Gaetz William, Harding Ian H, Joers James, Lax Michelle A, Li Jiakun, Lynch David R, Mareci Thomas H, Martinez Alberto R M, Pandolfo Massimo, Papoutsi Marina, Parker Richard G, Reetz Kathrin, Rezende Thiago J R, Roberts Timothy P, Romanzetti Sandro, Rudko David A, Saha Susmita, Schulz Jörg B, Subramony Sub H, Supramaniam Veena G, Lenglet Christophe, Henry Pierre-Gilles

СтатьяМногоцентровое исследованиеНаблюдательное исследованиеПеревод в очереди

Аннотация

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.

Для цитирования: Georgiou-Karistianis Nellie, Corben Louise A, Lock Eric F, Bujalka Helena, Adanyeguh Isaac, Corti Manuela, Deelchand Dinesh K, Delatycki Martin B, Dogan Imis, Farmer Jennifer, França Marcondes C, Gabay Anthony S, Gaetz William, Harding Ian H, Joers James, Lax Michelle A, Li Jiakun, Lynch David R, Mareci Thomas H, Martinez Alberto R M, Pandolfo Massimo, Papoutsi Marina, Parker Richard G, Reetz Kathrin, Rezende Thiago J R, Roberts Timothy P, Romanzetti Sandro, Rudko David A, Saha Susmita, Schulz Jörg B, Subramony Sub H, Supramaniam Veena G, Lenglet Christophe, Henry Pierre-Gilles. Neuroimaging Biomarkers for Friedreich Ataxia: A Cross-Sectional Analysis of the TRACK-FA Study.. Annals of neurology. 2025. DOI: 10.1002/ana.27237.

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