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The Potential Role of the Cardiac Mibg Scan in Differentiating the Drug-Induced Parkinsonism From Parkinson's Disease Publisher



Shafie M1, 2 ; Mayeli M1, 2 ; Saeidi S1 ; Mirsepassi Z3 ; Abbasi M4 ; Shafeghat M1, 2 ; Aghamollaii V5
Authors
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Authors Affiliations
  1. 1. School of Medicine, Tehran University of Medical Sciences
  2. 2. NeuroTRACT Association, Students’ Scientific Research Center, Tehran University of Medical Sciences
  3. 3. Assistant Professor of Psychiatry, Tehran University of Medical Sciences
  4. 4. Department of Nuclear Medicine, Valiasr Hospital, Tehran University of Medical Sciences
  5. 5. Associate Professor of Neurology, Cognitive Neurology and Neuropsychiatry Division, Tehran University of Medical Sciences

Source: Clinical Parkinsonism and Related Disorders Published:2022


Abstract

Introduction: Considering the difficulties of differentiating Parkinson's disease (PD) from drug-induced Parkinsonism (DIP) in patients receiving antipsychotics, developing robust diagnostic tools is essential. Herein, we used the metaiodobenzylguanidine (MIBG) scan to assess its diagnostic accuracy for this purpose. Methods: 44 DIP patients and 32 patients with PD as controls were enrolled. All the participants underwent a cardiac 131I-MIBG scan. Statistical analysis was conducted to determine the significance of the results, and accuracy analyses were conducted to calculate the related sensitivity and specificity of the MIBG scan. Results: The mean age of PD and DIP groups were 62.6 ± 5.9 and 51.5 ± 10.8 years, respectively. The mean duration of drug consumption in the DIP group was 52.2 ± 29.4 days (the mean interval between drug initiation and DIP onset was 28.5 ± 20.5). Symptoms relief occurred 40 ± 24.2 days after drug discontinuation. In the PD group, 15.6% showed negative and 84.4% positive results on the MIBG scan. In the DIP group, 86.4% were negative, and the remaining were positive. The difference in MIBG uptake between the two groups was statistically significant (P-value < 0.001). The sensitivity and specificity of the MIBG scan were 84.4% (CI: 84.0–84.8) and 86.36% (CI: 86.0–86.7) for the diagnosis of PD, respectively. Conclusion: Our results indicated more positive MIBG scans in the PD group than the DIP. Also, the MIBG scan's sensitivity and specificity in differentiating the PD are acceptable. Future works should assess these findings and the role of the MIBG scan in prognosis assessment of DIP and better allocation of the patients to related disciplines. © 2022 The Authors