AI Article Synopsis

  • α-synuclein seed amplification assays (α-syn SAA) show promise but may have reduced sensitivity due to variations among patients with Lewy body disease (LBD).
  • In a study of 34 Parkinson's disease (PD) patients and 7 with dementia with Lewy bodies (DLB), 85.2% of those with abnormal cardiac MIBG scans tested positive for α-syn SAA, while only 14.3% of those with normal scans did.
  • MIBG cardiac scintigraphy was identified as a significant factor influencing α-syn SAA positivity, indicating that while α-syn SAA can be sensitive for LBD in specific cases, its effectiveness may be diminished in patients with normal M

Article Abstract

Although α-synuclein seed amplification assays (α-syn SAA) are promising, its sensitivity may be affected by heterogeneity among patients with Lewy body disease (LBD). We evaluated whether α-syn SAA sensitivity is affected by patient heterogeneity, using I-meta-iodobenzylguanidine (MIBG) cardiac scintigraphy in early drug-naïve patients. Thirty-four patients with clinically established or probable Parkinson's disease (PD) and seven with dementia with Lewy bodies (DLB) or prodromal DLB were included. While 85.2% of patients with abnormal cardiac MIBG were α-syn SAA positive, only 14.3% were positive among those with normal scans. Logistic regression analysis showed that MIBG positivity was the only significant variable associated with α-syn SAA positivity (odds ratio 74.2 [95% confidence interval 6.1-909]). Although α-syn SAA is sensitive for LBD in patients with abnormal MIBG, the sensitivity may be lower in those with normal MIBG. Further studies are necessary to evaluate the association between patient heterogeneity and α-syn SAA sensitivity.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11494045PMC
http://dx.doi.org/10.1038/s41531-024-00806-yDOI Listing

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