مجله علمی  رایانش نرم و فناوری اطلاعات

مجله علمی رایانش نرم و فناوری اطلاعات

الگوهای ضایعاتی اختصاصی جمعیت در مولتیپل اسکلروزیس: تحلیل خودکار یادگیری عمیق پایگاه داده بزرگ ایرانی

نوع مقاله : مقاله پژوهشی فارسی

نویسندگان
1 دانشکده مهندسی پزشکی، دانشگاه صنعتی تبریز، تبریز، ایران.
2 دانشکده رادیولوژی، دانشگاه علوم پزشکی تبریز، تبریز، ایران.
چکیده
مولتیپل اسکلروزیس تقریباً 2.8 میلیون نفر را در سراسر جهان تحت تأثیر قرار می‌دهد، بااین‌حال جمعیت‌های خاورمیانه علی‌رغم شیوع بالاتر بیماری، در مطالعات تصویربرداری عصبی کمتر بررسی‌شده‌اند که درک ویژگی‌های پاتولوژیک خاص جمعیت را محدود و توسعه استراتژی‌های درمانی متناسب را با مانع مواجه می‌سازد. بررسی‌های مقایسه‌ای بین بیماران ام‌اس و افراد سالم برای شناسایی تغییرات مغزی و تعریف محدوده‌های هنجار نشانگرهای زیستی حیاتی است. این مطالعه گذشته‌نگر 1,381 شرکت‌کننده (1,000 سالم، 381 ام‌اس) از شمال غرب ایران را با معماری‎های یادگیری عمیق برای تحلیل خودکار توالی‌های FLAIR بررسی کرد. طبقه‌بندی نوروآناتومیک ضایعات پری‌بطنی، پارابطنی و جاکستاکورتیکال را متمایز نمود و ارزیابی‌های آماری شامل طبقه‌بندی سن-جنسیت و تحلیل‌های همبستگی بود. معماری attention U-Net عملکرد بالینی قابل‌قبولی نشان داد (0.756IoU=، 0.858Dice=). شرکت‌کنندگان ام‎اس، با نسبت‌های نرمال‌شده از ۰.۱۳٪ به 0.71٪ (0.82=r=، 0.001>p)، بار ضایعاتی 5.5 برابری بالاتری نسبت به کنترل نشان دادند. ضایعات پری‌بطنی، با تفاوت‌های محسوس توزیع آناتومیک جنسیت‌محور، اکثریت بار کل را تشکیل دادند (٪58.02±28.35). ارتباطات سن‌محور در ام‌اس برجسته‌تر بود (نسبت بطنی: 0.319r=، بار ضایعاتی: 0.230r=). این مطالعه مقادیر مرجع معتبر برای نشانگرهای زیستی تصویربرداری ام‌اس در جمعیت‌های خاورمیانه تعیین می‌کند و ویژگی‌های تجمع ضایعات با غالبیت پری‌بطنی را نشان می‌دهد. روش خودکار بخش‌بندی و تحلیل آماری، شکاف‌های موجود در تحقیقات بین‌المللی ام‌اس را مرتفع می‌سازد.
کلیدواژه‌ها

  [1]     G. Khan and M. J. Hashim, “Epidemiology of Multiple Sclerosis: Global, Regional, National and Sub-National-Level Estimates and Future Projections,” Journal of Epidemiology and Global Health, vol. 15, no. 1, Feb. 2025, doi: https://doi.org/10.1007/s44197-025-00353-6.
  [2]     T. J. Simkins, G. J. Duncan, and D. Bourdette, “Chronic Demyelination and Axonal Degeneration in Multiple Sclerosis: Pathogenesis and Therapeutic Implications,” Current Neurology and Neuroscience Reports, vol. 21, no. 6, Apr. 2021, doi: https://doi.org/10.1007/s11910-021-01110-5.
  [3]     C. E. Sabel, J. F. Pearson, D. F. Mason, E. Willoughby, D. A. Abernethy, and B. V. Taylor, “The latitude gradient for multiple sclerosis prevalence is established in the early life course,” Brain, vol. 144, no. 7, pp. 2038–2046, Mar. 2021, doi: https://doi.org/10.1093/brain/awab104.
  [4]     G. Criste, B. Trapp, and R. Dutta, “Axonal loss in multiple sclerosis,” Handbook of Clinical Neurology, vol. 112, pp. 101–113, 2014, doi: https://doi.org/10.1016/b978-0-444-52001-2.00005-4.
  [5]     E. Portaccio et al., “Multiple sclerosis: emerging epidemiological trends and redefining the clinical course,” The Lancet Regional Health - Europe, vol. 44, p. 100977, Sep. 2024, doi: https://doi.org/10.1016/j.lanepe.2024.100977.
  [6]     T. L. Vollmer, K. V. Nair, I. M. Williams, and E. Alvarez, “Multiple Sclerosis Phenotypes as a Continuum: The Role of Neurologic Reserve,” Neurology: Clinical Practice, vol. 11, no. 4, pp. 342–351, Aug. 2021, doi: https://doi.org/10.1212/CPJ.0000000000001045.
  [7]     F. D. Lublin et al., “Defining the clinical course of multiple s clerosis: The 2013 revisions,” Neurology, vol. 83, no. 3, pp. 278–286, May 2014, doi: https://doi.org/10.1212/wnl.0000000000000560.
  [8]     A. J. Thompson et al., “Diagnosis of Multiple sclerosis: 2017 Revisions of the McDonald Criteria,” The Lancet Neurology, vol. 17, no. 2, pp. 162–173, Feb. 2018, doi: https://doi.org/10.1016/s1474-4422(17)30470-2.
  [9]     M. A. Rocca et al., “Current and future role of MRI in the diagnosis and prognosis of multiple sclerosis,” The Lancet Regional Health - Europe, vol. 44, no. 100978, pp. 100978–100978, Aug. 2024, doi: https://doi.org/10.1016/j.lanepe.2024.100978.
[10]     F. Dehghani, H. Arabi, and A. Karimian, “Automated brain tumor segmentation on multi-mr sequences to determine the most efficient sequence using a deep learning method,” Computational Intelligence in Electrical Engineering, vol. 14, Art. no. 1, 2023, doi: https://doi.org/10.22108/isee.2021.126101.1427.
[11]     M. Filippi et al., “MRI criteria for the diagnosis of multiple sclerosis: MAGNIMS consensus guidelines,” The Lancet. Neurology, vol. 15, no. 3, pp. 292–303, 2016, doi: https://doi.org/10.1016/S1474-4422(15)00393-2.
[12]     A. Jankowska, Kamil Chwojnicki, and Edyta Szurowska, “The diagnosis of multiple sclerosis: what has changed in diagnostic criteria?,” Polish Journal of Radiology, vol. 88, no. 1, pp. 574–581, Jan. 2023, doi: https://doi.org/10.5114/pjr.2023.133677.
[13]     P. Schwenkenbecher et al., “Impact of the McDonald Criteria 2017 on Early Diagnosis of Relapsing-Remitting Multiple Sclerosis,” Frontiers in Neurology, vol. 10, Mar. 2019, doi: https://doi.org/10.3389/fneur.2019.00188.
[14]     C. H. Polman et al., “Diagnostic criteria for multiple sclerosis: 2010 Revisions to the McDonald criteria,” Annals of Neurology, vol. 69, no. 2, pp. 292–302, Feb. 2011, doi: https://doi.org/10.1002/ana.22366.
[15]     O. I. Alomair, “Conventional and Advanced Magnetic Resonance Imaging Biomarkers of Multiple Sclerosis in the Brain,” Cureus, vol. 17, no. 3, Mar. 2025, doi: https://doi.org/10.7759/cureus.79914.
[16]     M. Filippi et al., “Assessment of lesions on magnetic resonance imaging in multiple sclerosis: practical guidelines,” Brain, vol. 142, no. 7, pp. 1858–1875, Jun. 2019, doi: https://doi.org/10.1093/brain/awz144.
[17]     M. A. Sahraian and A. Eshaghi, “Role of MRI in diagnosis and treatment of multiple sclerosis,” Clinical Neurology and Neurosurgery, vol. 112, no. 7, pp. 609–615, Sep. 2010, doi: https://doi.org/10.1016/j.clineuro.2010.03.022.
[18]     A. Fahmi Jafargholkhanloo, M. Shamsi, and M. Bashiri Bawil, “A novel fuzzy-based clustering algorithm for segmentation of brain tissues with bias correction based on MRI images,” Journal of Machine Vision and Image Processing, vol. 12, Art. no. 2, 2025, Available: https://jmvip.sinaweb.net/article_229851.html.
[19]     M. Filippi et al., “Present and future of the diagnostic work-up of multiple sclerosis: the imaging perspective,” Journal of Neurology, vol. 270, no. 3, Nov. 2022, doi: https://doi.org/10.1007/s00415-022-11488-y.
[20]     Fahmi Jafargholkhanloo, M. Shamsi, and M. Bashiri Bawil, “Segmentation of brain tissues in MRI images using improved gustafson-kessel clustering algorithm,” Journal of Soft Computing and Information Technology, vol. 13, Art. no. 4, 2025, Available: https://jscit.nit.ac.ir/article_217009.html.
[21]     O. Ronneberger, P. Fischer, and T. Brox, “U-Net: Convolutional networks for biomedical image segmentation,” arXiv (Cornell University), May 2015, doi: https://doi.org/10.48550/arxiv.1505.04597.
[22]     O. Oktay et al., “Attention u-net: Learning where to look for the pancreas,” 2018. https://arxiv.org/abs/1804.03999.
[23]     T. Brosch, L. Y. W. Tang, Y. Yoo, D. K. B. Li, A. Traboulsee, and R. Tam, “Deep 3D Convolutional Encoder Networks With Shortcuts for Multiscale Feature Integration Applied to Multiple Sclerosis Lesion Segmentation,” IEEE Transactions on Medical Imaging, vol. 35, no. 5, pp. 1229–1239, May 2016, doi: https://doi.org/10.1109/tmi.2016.2528821.
[24]     Z. Chen, X. Wang, J. Huang, J. Lu, and J. Zheng, “Deep Attention and Graphical Neural Network for Multiple Sclerosis Lesion Segmentation From MR Imaging Sequences,” IEEE Journal of Biomedical and Health Informatics, vol. 26, no. 3, pp. 1196–1207, Mar. 2022, doi: https://doi.org/10.1109/jbhi.2021.3109119.
[25]     M. Sadeghibakhi, H. Pourreza, and H. Mahyar, “Multiple Sclerosis Lesions Segmentation Using Attention-Based CNNs in FLAIR Images,” IEEE Journal of Translational Engineering in Health and Medicine, vol. 10, pp. 1–11, 2022, doi: https://doi.org/10.1109/jtehm.2022.3172025.
[26]     M. Bashiri Bawil, M. Shamsi, A. Shakeri Bavil, and S. Danishvar, “Specialized gray matter segmentation via a generative adversarial network: application on brain white matter hyperintensities classification,” Frontiers in Neuroscience, vol. Volume 18 - 2024, 2024, doi: https://doi.org/10.3389/fnins.2024.1416174.
[27]     S. Umirzakova, Muksimova Shakhnoza, Mardieva Sevara, and Taeg Keun Whangbo, “Deep learning for multiple sclerosis lesion classification and stratification using MRI,” Computers in Biology and Medicine, vol. 192, pp. 110078–110078, Apr. 2025, doi: https://doi.org/10.1016/j.compbiomed.2025.110078.
[28]     F. Isensee, P. F. Jaeger, S. A. A. Kohl, J. Petersen, and K. H. Maier-Hein, “nnU-Net: a self-configuring method for deep learning-based biomedical image segmentation,” Nature Methods, vol. 18, no. 2, pp. 203–211, Dec. 2020, doi: https://doi.org/10.1038/s41592-020-01008-z.
[29]     P. De et al., “Consensus of algorithms for lesion segmentation in brain MRI studies of multiple sclerosis,” Scientific Reports, vol. 14, no. 1, Sep. 2024, doi: https://doi.org/10.1038/s41598-024-72649-9.
[30]     O. Mirmosayyeb, V. Shaygannejad, S. Bagherieh, A. M. Hosseinabadi, and M. Ghajarzadeh, “Prevalence of multiple sclerosis (MS) in Iran: a systematic review and meta-analysis,” Neurological Sciences, vol. 43, no. 1, pp. 233–241, Nov. 2021, doi: https://doi.org/10.1007/s10072-021-05750-w.
[31]     C. Walton et al., “Rising Prevalence of Multiple Sclerosis worldwide: Insights from the Atlas of MS, Third Edition,” Multiple Sclerosis Journal, vol. 26, no. 14, pp. 1816–1821, Nov. 2020, doi: https://doi.org/10.1177/1352458520970841.
[32]     M. Saadatnia, Masoud Etemadifar, and Amir-Hadi Maghzi, “Multiple Sclerosis in Isfahan, Iran,” Elsevier eBooks, pp. 357–375, Jan. 2007, doi: https://doi.org/10.1016/s0074-7742(07)79016-5.
[33]     S. Eskandarieh, P. Heydarpour, S.-R. Elhami, and M. A. Sahraian, “Prevalence and Incidence of Multiple Sclerosis in Tehran, Iran,” Iranian journal of public health, vol. 46, no. 5, pp. 699–704, May 2017, Available: https://pubmed.ncbi.nlm.nih.gov/28560202/
[34]     M. Azami, M. H. YektaKooshali, M. Shohani, A. Khorshidi, and L. Mahmudi, “Epidemiology of multiple sclerosis in Iran: A systematic review and meta-analysis,” PLOS ONE, vol. 14, no. 4, p. e0214738, Apr. 2019, doi: https://doi.org/10.1371/journal.pone.0214738.
[35]     N. Fattahi et al., “Burden of multiple sclerosis in Iran from 1990 to 2017,” BMC Neurology, vol. 21, no. 1, Oct. 2021, doi: https://doi.org/10.1186/s12883-021-02431-1.
[36]     F. Spagnolo et al., “How far MS lesion detection and segmentation are integrated into the clinical workflow? A systematic review,” NeuroImage: Clinical, vol. 39, pp. 103491–103491, Jan. 2023, doi: https://doi.org/10.1016/j.nicl.2023.103491.
[37]     A. J. Solomon, R. Pettigrew, R. T. Naismith, S. Chahin, S. Krieger, and B. Weinshenker, “Challenges in multiple sclerosis diagnosis: Misunderstanding and misapplication of the McDonald criteria,” Multiple Sclerosis Journal, p. 135245852091049, Mar. 2020, doi: https://doi.org/10.1177/1352458520910496.
[38]     O. Ronneberger et al., "U-Net: Convolutional Networks for Biomedical Image Segmentation," in Medical Image Computing and Computer-Assisted Intervention, pp. 234-241, 2015.doi: https://doi.org/10.48550/arXiv.1505.04597.
[39]     L.-C. Chen et al., "Encoder-Decoder with Atrous Separable Convolution for Semantic Image Segmentation," in European Conference on Computer Vision, pp. 833-851, 2018. doi: https://doi.org/10.48550/arXiv.1802.02611.
[40]     J. Chen et al., "TransUNet: Transformers Make Strong Encoders for Medical Image Segmentation," arXiv preprint arXiv:2102.04306, 2021. doi: https://doi.org/10.48550/arXiv.2102.04306.
[41]     G. Arrambide et al., “Lesion topographies in multiple sclerosis diagnosis,” Neurology, vol. 89, no. 23, pp. 2351–2356, Nov. 2017, doi: https://doi.org/10.1212/wnl.0000000000004715.
[42]     A. Traboulsee et al., “Revised Recommendations of the Consortium of MS Centers Task Force for a Standardized MRI Protocol and Clinical Guidelines for the Diagnosis and Follow-Up of Multiple Sclerosis,” American Journal of Neuroradiology, vol. 37, no. 3, pp. 394–401, Nov. 2015, doi: https://doi.org/10.3174/ajnr.a4539.
[43]     K. W. Kim, J. R. MacFall, and M. E. Payne, “Classification of white matter lesions on magnetic resonance imaging in elderly persons,” Biological Psychiatry, vol. 64, no. 4, pp. 273–280, Aug. 2008, doi: https://doi.org/10.1016/j.biopsych.2008.03.024.
[44]     C. DeCarli, E. Fletcher, V. Ramey, D. Harvey, and W. J. Jagust, “Anatomical Mapping of White Matter Hyperintensities (WMH),” Stroke, vol. 36, no. 1, pp. 50–55, Jan. 2005, doi: https://doi.org/10.1161/01.str.0000150668.58689.f2.
[45]     W. I. McDonald et al., “Recommended diagnostic criteria for multiple sclerosis: Guidelines from the international panel on the diagnosis of multiple sclerosis,” Annals of Neurology, vol. 50, no. 1, pp. 121–127, 2001, doi: https://doi.org/10.1002/ana.1032.
[46]     Y. Shan et al., “Risk Factors and Clinical Manifestations of Juxtacortical Small Lesions: A Neuroimaging Study,” Frontiers in Neurology, vol. 8, Sep. 2017, doi: https://doi.org/10.3389/fneur.2017.00497.