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Research ArticleNeurodegenerative Disorder Imaging
Open Access

The Inferior Cerebellar Peduncle Sign: A Novel Imaging Marker for Differentiating Multiple System Atrophy Cerebellar Type from Spinocerebellar Ataxia

Chae Y. Lim, Yujin Seo, Beomseok Sohn, Minjung Seong, Sung T. Kim, Sungjun Hong, Jinyoung Youn and Eung Y. Kim
American Journal of Neuroradiology June 2025, 46 (6) 1223-1230; DOI: https://doi.org/10.3174/ajnr.A8623
Chae Y. Lim
aFrom the Department of Radiology and Center for Imaging Science (C.Y.L., Y.S., B.S., M.S., S.T.K., E.Y.K.), Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea
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  • ORCID record for Chae Y. Lim
Yujin Seo
aFrom the Department of Radiology and Center for Imaging Science (C.Y.L., Y.S., B.S., M.S., S.T.K., E.Y.K.), Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea
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Beomseok Sohn
aFrom the Department of Radiology and Center for Imaging Science (C.Y.L., Y.S., B.S., M.S., S.T.K., E.Y.K.), Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea
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Minjung Seong
aFrom the Department of Radiology and Center for Imaging Science (C.Y.L., Y.S., B.S., M.S., S.T.K., E.Y.K.), Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea
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Sung T. Kim
aFrom the Department of Radiology and Center for Imaging Science (C.Y.L., Y.S., B.S., M.S., S.T.K., E.Y.K.), Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea
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Sungjun Hong
bDepartment of Digital Health (S.H.), Samsung Advanced Institute of Health Sciences and Technology, Sungkyunkwan University, Seoul, Republic of Korea
cMedical AI Research Center (S.H.) Research Institute for Future Medicine, Samsung Medical Center, Seoul, Republic of Korea
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Jinyoung Youn
dDepartment of Neurology (J.Y.), Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea
eNeuroscience Center (J.Y.), Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea
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Eung Y. Kim
aFrom the Department of Radiology and Center for Imaging Science (C.Y.L., Y.S., B.S., M.S., S.T.K., E.Y.K.), Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea
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  • FIG 1.
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    FIG 1.

    Study flow chart.

  • FIG 2.
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    FIG 2.

    Representative cases of positive/negative ICP signs. A, A 45-year-old woman presented with cerebellar ataxia. A FLAIR image reveals increased signal intensity in the bilateral inferior cerebellar peduncles (arrows; arrowheads in an inset) compared with the medulla. The patient was diagnosed with MSA-C. B, In the T2 FLAIR image of a 48-year-old man diagnosed with spinocerebellar ataxia, no ICP sign is seen.

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    FIG 3.

    FLAIR imaging in a 53-year-old man who presented with cerebellar ataxia. The initial imaging (left) showed high signal intensity in both inferior cerebellar peduncles (arrows), defined as the ICP sign. However, the MCP sign was not evident. On 15-month follow-up MRI (right), the ICP sign was again noted (arrowheads), and both the HCB and MCP signs appeared. The patient was diagnosed as having MSA-C.

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    FIG 4.

    Receiver operating curves of ICP, MCP, combined ICP and MCP signs and the integrated clinicoradiologic model for predicting MSA-C. The AUCs of the ICP sign, MCP sign, and combined ICP and MCP signs are 0.82, 0.67, and 0.86, respectively. The integrated model shows the highest diagnostic performance (AUC = 0.98, 95% CI, 0.96–1.00).

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    FIG 5.

    Calibration plots with ICIs of the ICP, MCP, combined ICP and MCP hyperintensity signs, and the integrated clinicoradiologic model for predicting MSA-C. Calibration plots comparing the ICP sign (intercept = 0.12, slope = 1.25, ICI = 0.03), MCP sign (intercept = –0.13, slope = 0.71, ICI = 0.61), combined signs (intercept = 0.30, slope = 1.17, ICI = 0.62), and integrated model (intercept= 0.02, slope = 1.74, ICI = 0.03). The ICP sign demonstrates reliable calibration overall. Bars in the calibration plot denote observed outcome frequencies within each bin, reflecting the calibration level of the prediction model. The diagonal line indicates perfect calibration. Brier indicates the Brier score (average squared difference in predicted and actual probabilities); Emax/E90/ICI, the maximum/90th quantile/weighted average of absolute difference in predicted and actual calibrated probabilities.

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    Table 1:

    Demographic characteristics and frequency analysis of MRI findingsa

    VariablesTotal (n = 225)MSA-C (n = 153)SCA (n = 72)P Values
    Clinical features
     Agea59 (53–65)60 (56–67)53 (44–61)<.001
     Disease duration (yr)a3 (1–5)2 (1–3.3)5 (2–11)<.001
     Sex
      Male124 (55)b79 (52)45 (63).204
      Female101 (45)74 (48)27 (38)
    Imaging features
     Scanner.053
      A182 (81)119 (78)63 (88)
      B6 (2.7)4 (2.6)2 (2.8)
      C36 (16)30 (20)6 (8.3)
      D1 (0.4)0 (0.0)1 (1.4)
     ICP sign105 (47)100 (65)5 (6.9)<.001
     HCB sign129 (57)110 (72)19 (26)<.001
     MCP sign164 (73)134 (88)30 (42)<.001
     Cerebellar atrophy191 (85)135 (88)56 (78).065
     Vertical line180 (80)132 (86)48 (67).011
    • ↵a Data are presented as median (1st quartile, 3rd quartile).

    • ↵b Percentages in parenthesis.

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    Table 2:

    Univariable and multivariable logistic regression analyses for predicting the MSA with predominant cerebellar ataxia group

    VariablesUnivariable AnalysisMultivariable Analysis
    OR95% CIP ValueOR95% CIP Value
    Age1.101.07–1.14<.0011.161.09–1.28<.001
    Disease duration (yr)0.770.70–0.85<.0010.630.53–0.75<.001
    Sex (male)1.580.89–2.81.117
    Scanner (A)a2.020.91–4.47.084
    ICP sign (absence)25.79.78–67.9<.00132.75.74–186<.001
    HCB sign (absence)7.313.88–13.8<.001
    MCP sign (absence)10.45.28–20.6<.00116.85.08–55.8<.001
    Cerebellar atrophy (absence)2.271.07–4.81.032
    Vertical line (absence)3.301.67–6.54.001
    • ↵a Scanner A (the most frequently used scanner type) is the reference, with the OR calculated for other scanner types combined. The reference category for each variable is presented in parentheses.

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    Table 3:

    Diagnostic performance of imaging and clinical features for predicting the MSA with the predominant cerebellar ataxia group

    ParametersSensitivityaSpecificityaF1 ScoreAUCbP Valuec
    ICP0.69 [31/45]0.95 [20/21]0.730.82 (0.74–0.90)–
    MCP0.87 [39/45]0.48 [10/21]0.690.67 (0.55–0.79).029
    HCB0.69 [31/45]0.71 [15/21]0.640.70 (0.58,0.82).052
    ICP + MCP0.62 [28/45]0.95 [20/21]0.700.86 (0.78–0.98).114
    Integrated modeld0.87 [39/45]1.00 [21/21]0.880.98 (0.96–1.00)<.001
    • Note:—The en dash indicates not applicable.

    • ↵a Data in brackets indicate the number of corresponding patients for each of the metric.

    • ↵b Data in parentheses are 95% CIs with the DeLong test.

    • ↵c P values of AUCs compared with ICP as a reference.

    • ↵d Integrated model includes the ICP, MCP sign, age, and disease duration as variables.

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American Journal of Neuroradiology: 46 (6)
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Chae Y. Lim, Yujin Seo, Beomseok Sohn, Minjung Seong, Sung T. Kim, Sungjun Hong, Jinyoung Youn, Eung Y. Kim
The Inferior Cerebellar Peduncle Sign: A Novel Imaging Marker for Differentiating Multiple System Atrophy Cerebellar Type from Spinocerebellar Ataxia
American Journal of Neuroradiology Jun 2025, 46 (6) 1223-1230; DOI: 10.3174/ajnr.A8623

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ICP Sign: New Imaging Marker for MSA-C vs SCA
Chae Y. Lim, Yujin Seo, Beomseok Sohn, Minjung Seong, Sung T. Kim, Sungjun Hong, Jinyoung Youn, Eung Y. Kim
American Journal of Neuroradiology Jun 2025, 46 (6) 1223-1230; DOI: 10.3174/ajnr.A8623
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