TY - JOUR
T1 - Imaging biomarkers for early prediction of the transition from idiopathic late-onset cerebellar ataxia to multiple system atrophy
AU - Lee, Jun Seok
AU - Kwon, Junmo
AU - Ha, Jongmok
AU - Won, Ji Hye
AU - Youn, Jinyoung
AU - Watanabe, Hirohisa
AU - Kim, Hee Tae
AU - Park, Hyunjin
AU - Cho, Jin Whan
N1 - Publisher Copyright:
© 2026
PY - 2026/3
Y1 - 2026/3
N2 - Introduction: Idiopathic late-onset cerebellar ataxia (ILOCA) is a degenerative, non-hereditary form of adult-onset cerebellar ataxia. A subset of patients with ILOCA eventually develop multiple system atrophy of the cerebellar type (MSA-C), but imaging biomarkers that predict this transition remain unidentified. This study aimed to identify imaging biomarkers that may predict phenoconversion from ILOCA to MSA-C. Methods: A retrospective cohort of patients diagnosed with ILOCA who underwent baseline T1-weighted and diffusion-weighted magnetic resonance imaging (MRI) was analyzed. Patients were followed longitudinally and reclassified as ‘phenoconverters’ if they met diagnostic criteria for MSA-C, or as ‘non-phenoconverters’ otherwise. Clinical characteristics were compared between groups, and infratentorial volumetric and microstructural changes were assessed using diffusion tensor imaging (DTI). Results: Over a mean follow-up of 5.7 years, 13 of 45 patients (28.9 %) transitioned to a diagnosis of MSA-C. Phenoconverters exhibited more severe baseline ataxia compared to non-phenoconverters. While cerebellar volumes were similar between groups, phenoconverters had significantly reduced volumes in the pons and superior and middle cerebellar peduncles. Additionally, they demonstrated lower mean fractional anisotropy in the middle and inferior cerebellar peduncles. Conclusions: Patients with ILOCA who later develop MSA-C show early microstructural changes and volume loss in the pons and cerebellar peduncles. Combining infratentorial volumetry with DTI may offer complementary imaging biomarkers for predicting phenoconversion to MSA-C.
AB - Introduction: Idiopathic late-onset cerebellar ataxia (ILOCA) is a degenerative, non-hereditary form of adult-onset cerebellar ataxia. A subset of patients with ILOCA eventually develop multiple system atrophy of the cerebellar type (MSA-C), but imaging biomarkers that predict this transition remain unidentified. This study aimed to identify imaging biomarkers that may predict phenoconversion from ILOCA to MSA-C. Methods: A retrospective cohort of patients diagnosed with ILOCA who underwent baseline T1-weighted and diffusion-weighted magnetic resonance imaging (MRI) was analyzed. Patients were followed longitudinally and reclassified as ‘phenoconverters’ if they met diagnostic criteria for MSA-C, or as ‘non-phenoconverters’ otherwise. Clinical characteristics were compared between groups, and infratentorial volumetric and microstructural changes were assessed using diffusion tensor imaging (DTI). Results: Over a mean follow-up of 5.7 years, 13 of 45 patients (28.9 %) transitioned to a diagnosis of MSA-C. Phenoconverters exhibited more severe baseline ataxia compared to non-phenoconverters. While cerebellar volumes were similar between groups, phenoconverters had significantly reduced volumes in the pons and superior and middle cerebellar peduncles. Additionally, they demonstrated lower mean fractional anisotropy in the middle and inferior cerebellar peduncles. Conclusions: Patients with ILOCA who later develop MSA-C show early microstructural changes and volume loss in the pons and cerebellar peduncles. Combining infratentorial volumetry with DTI may offer complementary imaging biomarkers for predicting phenoconversion to MSA-C.
KW - Diffusion tensor imaging
KW - Idiopathic late-onset cerebellar ataxia
KW - Imaging biomarker
KW - Magnetic resonance imaging
KW - Multiple system atrophy with cerebellar type
UR - https://www.scopus.com/pages/publications/105027106209
UR - https://www.scopus.com/pages/publications/105027106209#tab=citedBy
U2 - 10.1016/j.parkreldis.2026.108176
DO - 10.1016/j.parkreldis.2026.108176
M3 - Article
C2 - 41520408
AN - SCOPUS:105027106209
SN - 1353-8020
VL - 144
JO - Parkinsonism and Related Disorders
JF - Parkinsonism and Related Disorders
M1 - 108176
ER -