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18 F-Florzolotau Tau Positron Emission Tomography Imaging in Patients with Multiple System Atrophy-Parkinsonian Subtype.
Liu, Feng-Tao; Li, Xin-Yi; Lu, Jia-Ying; Wu, Ping; Li, Ling; Liang, Xiao-Niu; Ju, Zi-Zhao; Jiao, Fang-Yang; Chen, Ming-Jia; Ge, Jing-Jie; Sun, Yi-Min; Wu, Jian-Jun; Yen, Tzu-Chen; Luo, Jian-Feng; Zuo, Chuantao; Wang, Jian.
Afiliação
  • Liu FT; Department of Neurology, National Research Center for Aging and Medicine, National Center for Neurological Disorders, and State Key Laboratory of Medical Neurobiology, Huashan Hospital, Fudan University, Shanghai, China.
  • Li XY; Department of Neurology, National Research Center for Aging and Medicine, National Center for Neurological Disorders, and State Key Laboratory of Medical Neurobiology, Huashan Hospital, Fudan University, Shanghai, China.
  • Lu JY; PET Center, National Center for Neurological Disorders, and National Clinical Research Center for Aging and Medicine, Huashan Hospital, Huashan Hospital, Fudan University, Shanghai, China.
  • Wu P; PET Center, National Center for Neurological Disorders, and National Clinical Research Center for Aging and Medicine, Huashan Hospital, Huashan Hospital, Fudan University, Shanghai, China.
  • Li L; PET Center, National Center for Neurological Disorders, and National Clinical Research Center for Aging and Medicine, Huashan Hospital, Huashan Hospital, Fudan University, Shanghai, China.
  • Liang XN; Department of Neurology, National Research Center for Aging and Medicine, National Center for Neurological Disorders, and State Key Laboratory of Medical Neurobiology, Huashan Hospital, Fudan University, Shanghai, China.
  • Ju ZZ; Institute of Neurology, Fudan University, Shanghai, China.
  • Jiao FY; PET Center, National Center for Neurological Disorders, and National Clinical Research Center for Aging and Medicine, Huashan Hospital, Huashan Hospital, Fudan University, Shanghai, China.
  • Chen MJ; PET Center, National Center for Neurological Disorders, and National Clinical Research Center for Aging and Medicine, Huashan Hospital, Huashan Hospital, Fudan University, Shanghai, China.
  • Ge JJ; Department of Neurology, National Research Center for Aging and Medicine, National Center for Neurological Disorders, and State Key Laboratory of Medical Neurobiology, Huashan Hospital, Fudan University, Shanghai, China.
  • Sun YM; PET Center, National Center for Neurological Disorders, and National Clinical Research Center for Aging and Medicine, Huashan Hospital, Huashan Hospital, Fudan University, Shanghai, China.
  • Wu JJ; Department of Neurology, National Research Center for Aging and Medicine, National Center for Neurological Disorders, and State Key Laboratory of Medical Neurobiology, Huashan Hospital, Fudan University, Shanghai, China.
  • Yen TC; Department of Neurology, National Research Center for Aging and Medicine, National Center for Neurological Disorders, and State Key Laboratory of Medical Neurobiology, Huashan Hospital, Fudan University, Shanghai, China.
  • Luo JF; APRINOIA Therapeutics Co., Ltd, Suzhou, China.
  • Zuo C; Department of Biostatistics, School of Public Health, Fudan University, Shanghai, China.
  • Wang J; PET Center, National Center for Neurological Disorders, and National Clinical Research Center for Aging and Medicine, Huashan Hospital, Huashan Hospital, Fudan University, Shanghai, China.
Mov Disord ; 37(9): 1915-1923, 2022 09.
Article em En | MEDLINE | ID: mdl-35861378
ABSTRACT

BACKGROUND:

Anecdotal evidence suggests that patients diagnosed with the parkinsonian subtype of multiple system atrophy (MSA-P) may show uptake of the second-generation tau positron emission tomography (PET) tracer 18 F-Florzolotau (previously known as 18 F-APN-1607) in the putamen.

OBJECTIVES:

This study systematically investigated the localization and magnitude of 18 F-Florzolotau uptake in a relatively large cohort of patients with MSA-P.

METHODS:

18 F-Florzolotau PET imaging was performed in 31 patients with MSA-P, 24 patients with Parkinson's disease (PD), and 20 age-matched healthy controls. 18 F-Florzolotau signal in the striatum was analyzed by visual inspection and classified as either positive or negative. Regional 18 F-Florzolotau binding was also expressed as standardized uptake value ratio (SUVR) to assess whether it was associated with core symptoms of MSA-P after adjustment for potential confounders.

RESULTS:

By visual inspection and semiquantitative SUVR comparisons, patients with MSA-P showed elevated 18 F-Florzolotau uptake in the putamen, globus pallidus, and dentate-a finding that was not observed in PD. This increased signal was significantly associated with the core symptoms of MSA-P. In addition, patients with MSA-P with cerebellar ataxia showed an elevated 18 F-Florzolotau uptake in the cerebellar dentate.

CONCLUSIONS:

18 F-Florzolotau tau PET imaging findings may reflect the clinical severity of MSA-P and can potentially discriminate between this condition and PD. © 2022 International Parkinson and Movement Disorder Society.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Atrofia de Múltiplos Sistemas Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Atrofia de Múltiplos Sistemas Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China