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Unsupervised Pattern Analysis to Differentiate Multiple Sclerosis Phenotypes Using Principal Component Analysis on Various MRI Sequences.
van der Weijden, Chris W J; Pitombeira, Milena S; Peretti, Débora E; Campanholo, Kenia R; Kolinger, Guilherme D; Rimkus, Carolina M; Buchpiguel, Carlos Alberto; Dierckx, Rudi A J O; Renken, Remco J; Meilof, Jan F; de Vries, Erik F J; de Paula Faria, Daniele.
  • van der Weijden CWJ; Department of Nuclear Medicine and Molecular Imaging, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9700 RB Groningen, The Netherlands.
  • Pitombeira MS; Department of Radiology, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9700 RB Groningen, The Netherlands.
  • Peretti DE; Laboratory of Nuclear Medicine, Department of Radiology and Oncology, University of Sao Paulo, São Paulo 05508-220, Brazil.
  • Campanholo KR; Department of Nuclear Medicine and Molecular Imaging, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9700 RB Groningen, The Netherlands.
  • Kolinger GD; Laboratory of Nuclear Medicine, Department of Radiology and Oncology, University of Sao Paulo, São Paulo 05508-220, Brazil.
  • Rimkus CM; Department of Nuclear Medicine and Molecular Imaging, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9700 RB Groningen, The Netherlands.
  • Buchpiguel CA; Laboratory of Nuclear Medicine, Department of Radiology and Oncology, University of Sao Paulo, São Paulo 05508-220, Brazil.
  • Dierckx RAJO; Laboratory of Nuclear Medicine, Department of Radiology and Oncology, University of Sao Paulo, São Paulo 05508-220, Brazil.
  • Renken RJ; Department of Nuclear Medicine and Molecular Imaging, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9700 RB Groningen, The Netherlands.
  • Meilof JF; Department of Neuroscience, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9700 RB Groningen, The Netherlands.
  • de Vries EFJ; Department of Biomedical Sciences of Cells and Systems, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9700 RB Groningen, The Netherlands.
  • de Paula Faria D; Department of Neurology, Martini Ziekenhuis, 9728 NT Groningen, The Netherlands.
J Clin Med ; 13(17)2024 Sep 04.
Article en En | MEDLINE | ID: mdl-39274448
ABSTRACT

Background:

Multiple sclerosis (MS) has two main phenotypes relapse-remitting MS (RRMS) and progressive MS (PMS), distinguished by disability profiles and treatment response. Differentiating them using conventional MRI is challenging.

Objective:

This study explores the use of scaled subprofile modelling using principal component analysis (SSM/PCA) on MRI data to distinguish between MS phenotypes.

Methods:

MRI scans were performed on patients with RRMS (n = 30) and patients with PMS (n = 20), using the standard sequences T1w, T2w, T2w-FLAIR, and the myelin-sensitive sequences magnetisation transfer (MT) ratio (MTR), quantitative MT (qMT), inhomogeneous MT ratio (ihMTR), and quantitative inhomogeneous MT (qihMT).

Results:

SSM/PCA analysis of qihMT images best differentiated PMS from RRMS, with the highest specificity (87%) and positive predictive value (PPV) (83%), but a lower sensitivity (67%) and negative predictive value (NPV) (72%). Conversely, T1w data analysis showed the highest sensitivity (93%) and NPV (89%), with a lower PPV (67%) and specificity (53%). Phenotype classification agreement between T1w and qihMT was observed in 57% of patients. In the subset with concordant classifications, the sensitivity, specificity, PPV, and NPV were 100%, 88%, 90%, and 100%, respectively.

Conclusions:

SSM/PCA on MRI data revealed distinctive patterns for MS phenotypes. Optimal discrimination occurred with qihMT and T1w sequences, with qihMT identifying PMS and T1w identifying RRMS. When qihMT and T1w analyses align, MS phenotype prediction improves.
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