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Diagnostic Effectiveness of [I]Ioflupane Single Photon Emission Computed Tomography (SPECT) in Multiple System Atrophy. | LitMetric

AI Article Synopsis

  • Multiple system atrophy (MSA) is a serious neurodegenerative disorder with no cure, and its diagnosis follows specific criteria.
  • A study involving 139 patients at the initial suspicion of MSA found that [I]Ioflupane SPECT is effective, revealing positive results in 78.45% of cases, especially strong in MSA-P subtypes.
  • The findings suggest that [I]Ioflupane SPECT is a reliable diagnostic tool that significantly differentiates between healthy individuals and those with MSA, as well as between the different subtypes of the disease.

Article Abstract

Background: Multiple system atrophy (MSA) is a rapidly progressive neurodegenerative disorder that has no curative treatment. Diagnosis is based on a set of criteria established by Gilman (1998 and 2008) and recently updated by Wenning (2022). We aim to determine the effectiveness of [I]Ioflupane SPECT in MSA, especially at the initial clinical suspicion.

Methods: A cross-sectional study of patients at the initial clinical suspicion of MSA, referred for [I]Ioflupane SPECT.

Results: Overall, 139 patients (68 men, 71 women) were included, 104 being MSA-probable and 35 MSA-possible. MRI was normal in 89.2%, while SPECT was positive in 78.45%. SPECT showed high sensitivity (82.46%) and positive predictive value (86.24), reaching maximum sensitivity in MSA-P (97.26%). Significant differences were found when relating both SPECT assessments in the healthy-sick and inconclusive-sick groups. We also found an association when relating SPECT to the subtype (MSA-C or MSA-P), as well as to the presence of parkinsonian symptoms. Lateralization of striatal involvement was detected (left side).

Conclusions: [I]Ioflupane SPECT is a useful and reliable tool for diagnosing MSA, with good effectiveness and accuracy. Qualitative assessment shows a clear superiority when distinguishing between the healthy-sick categories, as well as between the parkinsonian (MSA-P) and cerebellar (MSA-C) subtypes at initial clinical suspicion.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219509PMC
http://dx.doi.org/10.3390/jcm12103478DOI Listing

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