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EVALUATION OF THE ABSENCE OF NIGROSOME 1 BY MAGNETIC RESONANCE 3 TESLA IN PARKINSON’S DISEASE ACCORDING TO TIME OF EVOLUTION TO DIAGNOSIS VS MESENCEPHALIC ECOGRAPHY.

J. Bestoso, L. Ciancaglini, C. Stefani, F. Silveira, M. Pérez Akly, J. Norscini, J. Funes, C. Besada, D. Bauso (Buenos Aires, Argentina)

Meeting: MDS Virtual Congress 2021

Abstract Number: 811

Keywords: Magnetic resonance imaging(MRI), Parkinson’s

Category: Parkinson's Disease: Neuroimaging

Objective:
The primary objective was to evaluate the absence of nigrosome 1 in 3TMRI in a group of patients with PD according to their evolutionary time to diagnosis. And the secondary one to assess its diagnostic performance in relation to that of the midbrain ultrasound.

Background: The SWI sequence by magnetic resonance 3 tesla (MRI3T) allows to identify the area of ​​Nigrosome 1, which is absent in patients with idiopathic Parkinson’s disease (PD). In our center, this method demonstrated a sensitivity for the diagnosis of PD of 93.75% and a specificity of 87.5% when comparing patients with advanced PD vs essential tremor.

Method: All the MRI3T performed on patients diagnosed with PD in the 2018-2020 period were considered. For the diagnosis of PD, the criteria of the International Parkinson and Movement Disorders Society were followed.
The presence or absence of nigrosome 1 in the midbrain region was diagnosed. The images were evaluated by two independent neuroradiology specialists blind to diagnosis.
All patients underwent a midbrain ultrasound to assess the echogenicity of the substantia nigra.
The patients were divided into 3 subgroups according to their evolution time.
The results of MRI3T and midbrain ultrasound were compared in the three subgroups.

Results: N 68 patients.
Group 1 (up to 12 months): N: 17; mean age: 70 years; women: 8; Hoehn and Yahr: 1.47; UPDRS-MDS III: 10.5; Nigrosome 1: absent: 13 (76.4%). Mesencephalic hyperechogenicity: 9 (52.9%). Bad window: 0.
Group 2 (13 to 35 months): N: 29; mean age: 73 years; women: 14; Hoehn and Yahr: 1.6; UPDRS-MDS III: 17; Nigrosome1 absent: 26 (89.6%). Mesencephalic hyperechogenicity: 18 (66.6%). Bad window: 2 (6.89%).
Group 3 (≥36 months): N: 22; mean age: 72.5 years; women: 8; Hoehn and Yahr: 1.8; UPDRS-MDS III: 22; Nigrosome absent: 21 (95.5%). Mesencephalic hyperechogenicity: 13 (76.5%). Bad window: 5 (31.25%).

Conclusion: The percentage of positivity of the SWI sequence by MRI3T to detect the absence of Nigrosome 1 was higher as the evolutionary time increased.
After 36 months, its accuracy was close to 100%.
The performance of the midbrain ultrasound was also progressive but with a lower performance than the MRI3T in all the stages evaluated.

 this work was presented in the   57th Argentine Neurological Society VIRTUAL  Congress November 2020

References: 2. Schwarz ST, Afzal M, Morgan PS, Bajaj N, Gowland PA, Auer DP. The ‘swallow tail’ appearance of the healthy nigrosome – a new accurate test of Parkinson’s disease: a case-control and retrospective cross-sectional MRI study at 3T. PloS one 2014 3. Cosottini M, Frosini D, Pesaresi I, et al. Comparison of 3T and 7T Susceptibility-Weighted Angiography of the Substantia Nigra in Diagnosing Parkinson Disease. AJNR American journal of neuroradiology 2015;36:461-6. 4. Mahlknecht P, Krismer F, Poewe W, Seppi K .Meta-analysis of dorsolateral nigral hyperintensity on magnetic resonance imaging as a marker for Parkinson’s disease. Mov Disord. 2017 Apr;32(4):619-623 5. Noh Y, Sung YH, Lee J, Kim EY .Nigrosome 1 Detection at 3T MRI for the Diagnosis of Early-Stage Idiopathic Parkinson Disease: Assessment of Diagnostic Accuracy and Agreement on Imaging Asymmetry and Clinical Laterality..AJNR Am J Neuroradiol. 2015 Nov;36(11):2010 6. Berg D, Merz B, Reiners K, Naumann M, Becker G. Five-year follow-up study of hyperechogenicity of the substantia nigra in Parkinson’s disease. Mov Disord. 2005;20(3):383–385. 7. Perez Akly MS, Stefani CV, Ciancaglini L, Bestoso JS, Funes JA, Bauso DJ, Besada CH. Accuracy of nigrosome-1 detection to discriminate patients with Parkinson’s disease and essential tremor. Neuroradiol J. 2019 Dec;32(6):395-4005. 8. Weise D, Lorenz R, Schliesser M et al. Substantia nigra echogenicity: A structural correlate of functional impairment of the dopaminergic striatal projection in Parkinson’s disease. Mov Disord. 2009 Aug 15;24(11):1669-75. 9. Lobsein E, Schreiner s, Plotkin M. No correlation of substancia nigra echogenicity and nigroestriatal degradation in Parkinson´s disease. Mov Disord 2012 mar;27(3).450-3. 10. Bestoso JS, Pérez Akly M, Ciancaglini L, Stefani, C Rojas J, Funes J, Besada C, Bauso D. Evaluación de la ausencia de nigrosoma 1 en pacientes con enfermedad de Parkinson de Novo (EP de Novo) vs enfermedad de Parkinson avanzada (EP avanzada). Congreso Argentino de neurología. 2018

To cite this abstract in AMA style:

J. Bestoso, L. Ciancaglini, C. Stefani, F. Silveira, M. Pérez Akly, J. Norscini, J. Funes, C. Besada, D. Bauso. EVALUATION OF THE ABSENCE OF NIGROSOME 1 BY MAGNETIC RESONANCE 3 TESLA IN PARKINSON’S DISEASE ACCORDING TO TIME OF EVOLUTION TO DIAGNOSIS VS MESENCEPHALIC ECOGRAPHY. [abstract]. Mov Disord. 2021; 36 (suppl 1). https://www.mdsabstracts.org/abstract/evaluation-of-the-absence-of-nigrosome-1-by-magnetic-resonance-3-tesla-in-parkinsons-disease-according-to-time-of-evolution-to-diagnosis-vs-mesencephalic-ecography/. Accessed June 15, 2025.
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