Assessment of Midbrain Structure Visualization with Modified 3 Tesla MRI Protocols for Enhanced Parkinson's Disease Diagnosis
- Авторлар: Matkevich E.I.1,2, Ladik Е.А.1, Bril E.V.1, Zimnyakova O.S.1, Bryukhov V.V.3
-
Мекемелер:
- A.I. Burnazyan Federal Medical Biophysical Center
- RUDN University
- Research Center of Neurology
- Шығарылым: Том 69, № 4 (2024)
- Беттер: 71-76
- Бөлім: Radiation Diagnostics
- URL: https://journals.rcsi.science/1024-6177/article/view/363934
- DOI: https://doi.org/10.33266/1024-6177-2024-69-4-71-76
- ID: 363934
Дәйексөз келтіру
Толық мәтін
Аннотация
Purpose: To assess the outcomes and implications of modifying SWAN protocol parameters on a 3 Tesla MRI for midbrain structure imaging in patients to detect signs of Parkinson’s disease.
Material and methods: The study was conducted on 22 patients of both genders, ranging in age from 30 to 77 years. Protocols for the standard MRI brain examination and its two variations in the SWAN program, which involved reducing the slice thickness, were analyzed. Key parameters for the visualization of midbrain structures were identified, and subsequently evaluated by expert radiologists.
Results: Parameters within the SWAN protocol for MRI scanning were identified, the modification of which enhances the clarity of nigrosome-1 visualization. It was established that thin-slice modifications of the brain scanning protocols (slice thicknesses of 1.2 and 2 mm) reveal early, diagnostically significant features of nigrosome-1 for Parkinson’s disease 3.4 to 4.1 times more frequently than the standard survey protocol with a slice thickness of 4 mm.
Conclusion: The significance of selecting appropriate MRI protocol parameters for studying midbrain structures to enhance the visualization effectiveness of nigrosome-1 has been confirmed. Employing the SWAN sequence on a 3 Tesla MRI scanner with a slice thickness of 2 mm or less in a neurological department setting during routine Parkinson’s disease examinations achieves superior imaging results compared to conventional survey MRI protocols with a 4 mm slice thickness. This approach demonstrates high inter-rater reliability and aligns with European recommendations for neuroimaging.
Негізгі сөздер
Авторлар туралы
E. Matkevich
A.I. Burnazyan Federal Medical Biophysical Center; RUDN University
Email: ei.matkevich@gmail.com
Moscow, Russia
Е. Ladik
A.I. Burnazyan Federal Medical Biophysical Center
Email: ei.matkevich@gmail.com
Moscow, Russia
E. Bril
A.I. Burnazyan Federal Medical Biophysical Center
Email: ei.matkevich@gmail.com
Moscow, Russia
O. Zimnyakova
A.I. Burnazyan Federal Medical Biophysical Center
Email: ei.matkevich@gmail.com
Moscow, Russia
V. Bryukhov
Research Center of Neurology
Email: ei.matkevich@gmail.com
Moscow, Russia
Әдебиет тізімі
- GBD 2016 Neurology Collaborators. Global, Regional, and National Burden of Neurological Disorders, 1990-2016: a Systematic Analysis for the Global Burden of Disease Study 2016 // Lancet Neurol. 2019. V.18, No. 5. P. 459-480. doi: 10.1016/S1474-4422(18)30499-X.
- Khan A.Z., Lavu D., Neal R.D. Parkinson’s Disease: a Scoping Review of the Quantitative and Qualitative Evidence of Its Diagnostic Accuracy in Primary Care // Br J Gen Pract. 2024. V.27, No. 74. P. e227-e232. doi: 10.3399/BJGP.2023.0409.
- Li T., Le W. Biomarkers for Parkinson’s Disease: How Good Are They? // Neurosci Bull. 2020. V.36, No. 2. P. 183-194. doi: 10.1007/s12264-019-00433-1.
- Aludin S., Schmill L.A. MRI Signs of Parkinson’s Disease and Atypical Parkinsonism // Fortschr Röntgenstr. 2021. No. 193. P. 1403 – 1410.
- Diagnostic Imaging: Brain. Ed. Anne G., Osborn, Karen L., Salzman Miral D. Jhaveri. Elsevier Editor, 2016. ISBN: 978-0-323-37754-6.
- Gramsch C., Reuter I., Kraff O., Nigrosome 1 Visibility at Susceptibility Weighted 7T MRI – a Dependable Diagnostic Marker for Parkinson’s Disease or Merely an Inconsistent Age-Dependent Imaging Finding? // Plos One. 2017. No. 12. P. e0185489. doi: 10.1371/journal.pone.0185489.
- Литвиненко И.В., Красаков И.В., Труфанов А.Г. Церебральные нарушения обмена железа как основа развития и прогрессирования нейродегенеративных заболеваний // Вестник Российской Военно-медицинской академии. 2018. № 3. С. 68-78.
- Андропова П.Л., Гаврилов П.В., Казанцева И.П., Кочанова Н.И., Наркевич А.Н., Трофимова Т.Н. Оценка межэкспертной согласованности при использовании ASPECTS врачами ургентной нейрорадиологии с различным стажем // Радиология – практика. 2022. № 5. С. 10-25. https://doi.org/10.52560/2713-0118-2022-5-10-25.
- Москаленко, А. Н., Филатов, А. С., Федотова, Е. Ю., Коновалов, Р. Н., Иллариошкин, С. Н. Визуальный анализ нигросомы-1 в дифференциальной диагностике болезни Паркинсона и эссенциального тремора // Вестник РГМУ. 2022. № 1. С. 50-55. doi: 10.24075/vrgmu.2022.002.
- Barkhof F., Jäger H.R., Thurnher M.M., Rovira Àlex // Clinical Neuroradiology (The ESNR Textbook). 2019. doi: 10.1007/978-3-319-68536-6.
- Haller S., Haacke E.M., Thurnher M.M., Barkhof F. Susceptibility-Weighted Imaging: Technical Essentials and Clinical Neurologic Applications // Radiology. 2021. V.299, No. 1: P. 3-26. doi: 10.1148/radiol.2021203071.
- Arnaldi D., Morbelli S., Picco A., Ferrara M., Buschiazzo A., Famà F., De Carli F., Nobili F. Functional Imaging in Pre-Motor Parkinson’s Disease. Q J Nucl Med Mol Imaging // 2014. V.58, No. 4. P. 366-375. PMID: 25366709.
- Kim E.Y., Sung Y.H., Lee J. Nigrosome 1 Imaging: Technical Considerations and Clinical Applications // Br J Radiol. 2019. V. 92, No. 1101. P. 20180842. doi: 10.1259/bjr.20180842.
- Cheng Z., He N., Huang P., Li Y., Tang R., Sethi S.K., Ghassaban K., Yerramsetty K.K., Palutla V.K., Chen S., Yan F., Haacke E.M. Imaging the Nigrosome 1 in the Substantia Nigra Using Susceptibility Weighted Imaging and Quantitative Susceptibility Mapping: An Application to Parkinson’s Disease // Neuroimage Clin. 2020. No. 25. P. 102103. doi: 10.1016/j.nicl.2019.102103.
Қосымша файлдар
