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Substantia nigra nigrosome-1 imaging correlates with the severity of motor symptoms in Parkinson's disease.
Chu, Yung-Tsai; Yu, Chin-Feng; Fan, Sung-Pin; Chen, Ta-Fu; Chiu, Ming-Jang; Jang, Jyh-Shing Roger; Chiu, Shu-I; Lin, Chin-Hsien.
Afiliación
  • Chu YT; Department of Neurology, National Taiwan University Hospital, Taiwan.
  • Yu CF; Department of Computer Science, National Chengchi University, Taiwan.
  • Fan SP; Department of Neurology, National Taiwan University Hospital, Taiwan.
  • Chen TF; Department of Neurology, National Taiwan University Hospital, Taiwan.
  • Chiu MJ; Department of Neurology, National Taiwan University Hospital, Taiwan.
  • Jang JR; Department of Computer Science and Information Engineering, National Taiwan University, Taiwan.
  • Chiu SI; Department of Computer Science, National Chengchi University, Taiwan. Electronic address: sichiu@nccu.edu.tw.
  • Lin CH; Department of Neurology, National Taiwan University Hospital, Taiwan. Electronic address: chlin@ntu.edu.tw.
J Neurol Sci ; 451: 120731, 2023 08 15.
Article en En | MEDLINE | ID: mdl-37454574
BACKGROUND: Nigrosome-1 imaging has been used for assisting the diagnosis of Parkinson's disease (PD). We aimed to examine the diagnostic performance of loss of nigrosome-1 in PD and the correlation between the size of the nigrosome-1 and motor severity of PD. METHODS: We included 237 patients with PD and 165 controls. The motor severity of PD was assessed with the Unified Parkinson's Disease Rating Scale (UPDRS) part III score and Hoehn-Yahr staging. The 3 or 1.5 Tesla susceptibility-weighted imaging combined with a deep-learning algorithm was applied for detecting the loss and the size of nigrosome-1. Clinical correlations and diagnostic performance of size of nigrosome-1 were also investigated. RESULTS: The mean nigrosome-1 size was significantly smaller in PD patients than in controls (0.06 ± 0.07 cm2 vs. 0.20 ± 0.05 cm2, P < 0.001). The area under the receiver operating characteristic curve (AUC) of the established model showed 0.94 accuracy (95% confidence interval [CI]: 0.87, 1.01, P < 0.01) in differentiating between the PD and control groups. Moreover, the partial loss of nigrosome-1 detected with SWI had an AUC of 0.96 in discriminating early-stage PD from controls (95% CI: 0.88, 1.02, P < 0.001). After adjusting for age, sex, disease duration, and levodopa equivalent daily dose, the estimated size of nigrosome-1 was negatively associated with the UPDRS part III motor score (ρ = -0.433, P < 0.001), but not with Mini-Mental State Examination scores (ρ = 0.006, P = 0.894). CONCLUSIONS: The extent of loss and the size of nigrosome-1 may potentially assist in the diagnosis of PD. Nigrosome-1 size reflects the motor severity of PD.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Parkinson Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: J Neurol Sci Año: 2023 Tipo del documento: Article País de afiliación: Taiwán

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Parkinson Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: J Neurol Sci Año: 2023 Tipo del documento: Article País de afiliación: Taiwán