Category: MSA, PSP, CBS (Other)
Objective: This prospective cohort study investigated the role of neuroimaging for the early and accurate identification of multiple system atrophy (MSA) in patients with indeterminate autonomic dysfunction.
Background: Multiple system atrophy (MSA) is a rapidly progressive neurodegenerative disorder for which early diagnosis is becoming increasingly important in the era of emerging disease-modifying therapies. However, current diagnostic and research criteria require autonomic dysfunction as an entry feature, which may exclude patients in the earliest disease stage because motor symptoms can precede autonomic failure.
Method: We recruited patients with suspected MSA based on clinical manifestation or neuroimaging findings from May 2024 to October 2025. The Movement Disorder Society criteria for MSA was used and exclusion rules were strictly applied. But patients without dysautonomia were also included if they exhibited the MRI markers and supportive clinical features of MDS criteria. Clinical symptoms were evaluated by unified MSA rating scale and autonomic function was assessed with head-up tilt test (HUT). Typical signs on brain magnetic resonance imaging (MRI), such as putaminal rim sign, hot-cross burn sign and middle cerebellar peduncle sign, were checked. We compared clinical and demographic data between MSA patients with and without OH.
Results: In total 45 enrolled subjects, OH was detected by tilt-table testing in 46.7% whereas only 47.6% of those with confirmed OH reported orthostatic dizziness. There was no difference in demographic and clinical data between subjects with and without OH. Characteristic MRI abnormalities were identified in 41(91.1%) patients at early symptomatic stages.
Conclusion: Our results demonstrated MRI abnormalities can precede objective autonomic dysfunction, suggesting that early imaging markers may aid timely MSA recognition and support future diagnostic frameworks.
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References: 1. Salunkhe J, Ugale R. Recent updates on immunotherapy in neurodegenerative diseases. Brain Res 2024;1845:149205.
2. Krismer F, Fanciulli A, Meissner WG, Coon EA, Wenning GK, et al. Multiple system atrophy: advances in pathophysiology, diagnosis, and treatment. Lancet Neurol 2024;23:1252-1266.
3. Wenning GK, Stankovic I, Vignatelli L, Fanciulli A, Calandra-Buonaura G, Seppi K, et al. The Movement Disorder Society criteria for the diagnosis of multiple system atrophy. Mov Disord 2022;37:1131-1148.
4. Lin DJ, Hermann KL, Schmahmann JD. The diagnosis and natural history of multiple system atrophy, cerebellar type. Cerebellum 2016;15:663-679.
5. Watanabe H, Riku Y, Hara K, Kawabata K, Nakamura T, Ito M, et al. Clinical and imaging features of multiple system atrophy: challenges for an early and clinically definitive diagnosis. J Mov Disord 2018;11:107-120.
6. Osaki Y, Morita Y, Miyamoto Y, Ohtsuru S, Shogase T, Furushima T, et al. Identification of a pre-possible multiple system atrophy phase. Acta Neurol Scand 2021;143:313-317.
7. Kim M, Ahn JH, Cho Y, Kim JS, Youn J, Cho JW. Differential value of brain magnetic resonance imaging in multiple system atrophy cerebellar phenotype and spinocerebellar ataxias. Sci Rep 2019;9:17329.
8. Batmani S, Jalali R, Mohammadi M, Bokaee S. Prevalence and factors related to urinary incontinence in older adult women worldwide: a comprehensive systematic review and meta-analysis of observational studies. BMC Geriatr 2021;21:212.
9. Ling H, Asi YT, Petrovic IN, Ahmed Z, Prashanth LK, Hazrati LN, et al. Minimal change multiple system atrophy: an aggressive variant? Mov Disord 2015;30:960-967.
10. Watanabe H, Saito Y, Terao S, Ando T, Kachi T, Mukai E, et al. Progression and prognosis in multiple system atrophy: an analysis of 230 Japanese patients. Brain 2002;125:1070-1083.
11. Way C, Pettersson D, Hiller A. The “hot cross bun” sign is not always multiple system atrophy: etiologies of 11 cases. J Mov Disord 2019;12:27-30.
12. Lee JY, Yun JY, Shin CW, Kim HJ, Jeon BS. Putaminal abnormality on 3-T magnetic resonance imaging in early parkinsonism-predominant multiple system atrophy. J Neurol 2010;257:2065-2070.
13. Jost WH, Rau A, Brumberg J, Urbach H, Meyer PT, Schroter N. Neuroimaging in multiple system atrophy: clinical implications and novel developments. J Neural Transm (Vienna) 2025.
To cite this abstract in AMA style:
J. Ahn, W. Kim, J. Youn, JH. Cho. Revisiting Prodromal Diagnostic Criteria in MSA: The Need for Early MRI-Based Diagnosis [abstract]. Mov Disord. 2026; 41 (suppl 1). https://www.mdsabstracts.org/abstract/revisiting-prodromal-diagnostic-criteria-in-msa-the-need-for-early-mri-based-diagnosis/. Accessed October 1, 2026.« Back to 2026 International Congress
MDS Abstracts - https://www.mdsabstracts.org/abstract/revisiting-prodromal-diagnostic-criteria-in-msa-the-need-for-early-mri-based-diagnosis/

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