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Dopamine transporter SPECT imaging in corticobasal syndrome: A peak into the underlying pathology?
Constantinides, Vasilios C; Souvatzoglou, Michail; Paraskevas, George P; Chalioti, Maria; Boufidou, Fotini; Stefanis, Leonidas; Kapaki, Elisabeth.
Afiliação
  • Constantinides VC; 1st Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, Eginition Hospital, Athens, Greece.
  • Souvatzoglou M; Nuclear Medicine Division, 1st Radiology Department, National and Kapodistrian University of Athens, Aretaieion Hospital, Athens, Greece.
  • Paraskevas GP; 1st Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, Eginition Hospital, Athens, Greece.
  • Chalioti M; 2nd Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, Attikon Hospital, Athens, Greece.
  • Boufidou F; Nuclear Medicine Division, 1st Radiology Department, National and Kapodistrian University of Athens, Aretaieion Hospital, Athens, Greece.
  • Stefanis L; 1st Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, Eginition Hospital, Athens, Greece.
  • Kapaki E; 1st Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, Eginition Hospital, Athens, Greece.
Acta Neurol Scand ; 145(6): 762-769, 2022 Jun.
Article em En | MEDLINE | ID: mdl-35307816
ABSTRACT

BACKGROUND:

Multiple pathologies may underlie corticobasal syndrome (CBS), including Alzheimer's disease (AD). Dopamine transporter density imaging with Ioflupane 123 I SPECT (DaTscan) may be normal in CBS. No studies to date have examined the relationship between DaTscan status and underlying pathology in CBS.

OBJECTIVES:

The main objective of the study was to test whether a normal DaTscan in CBS patients is indicative of an underlying AD pathology, as determined by cerebrospinal fluid (CSF) biomarkers.

METHODS:

Eighteen CBS patients were included. They were divided into patients with an AD and a non-AD disease pathology, based on their cerebrospinal fluid biochemical profile. A typical AD CSF profile was defined as an increase in total and phosphorylated at threonine 181 tau protein in addition to a decrease in amyloid-beta with 42 amino acids. DaTscan data were compared in these two groups.

RESULTS:

Eight of the 18 CBS patients (44%) had a normal DaTscan. Seven of the 18 CBS patients (39%) had an AD cerebrospinal fluid biochemical profile. Two of seven CBS patients with AD biomarker profile had abnormal DaTscans. Three of 11 CBS patients with a non-AD biomarker profile had normal DaTscans. A normal DaTscan was indicative of AD pathology with suboptimal (~70%) sensitivity and specificity. Semi-quantitative DaTscan analysis did not differentiate between AD from non-AD CSF biomarker profile in CBS.

CONCLUSION:

A normal DaTscan is indicative of AD in CBS, but the sensitivity and specificity of DaTscan as an in vivo marker of AD pathology is suboptimal.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Degeneração Corticobasal Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Degeneração Corticobasal Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article