Hybrid 18F-florbetapir PET/MRI for assessing myelin recovery in GFAP-A patients

Glial fibrillary acidic protein astrocytopathy (GFAP-A) is a rare autoimmune disease of the central nervous system that was newly reported in 2016. Previous studies have speculated that the pathological mechanism and clinical outcome of GFAP-A lie in the demyelination of the central nervous system,...

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Published inTranslational neuroscience Vol. 13; no. 1; pp. 120 - 124
Main Authors Meng, Huanyu, Zheng, Shuyu, Yuan, Shaicun, Zhou, Qinming, Gao, Yining, Ni, You, He, Lu, Yin, Dou, Zhang, Min, Chen, Sheng
Format Journal Article
LanguageEnglish
Published Warsaw De Gruyter 09.06.2022
De Gruyter Poland
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Summary:Glial fibrillary acidic protein astrocytopathy (GFAP-A) is a rare autoimmune disease of the central nervous system that was newly reported in 2016. Previous studies have speculated that the pathological mechanism and clinical outcome of GFAP-A lie in the demyelination of the central nervous system, but due to the limitations of MR, this conclusion has not been further confirmed from the perspective of neuroimaging. A non-invasive, quantitative measurement of demyelination would be clinically valuable, given its critical role in mediating GFAP-A. Here, we report a case in which we use F-florbetapir positron emission tomography-magnetic resonance imaging (PET/MRI) to evaluate myelin recovery with follow-up in the patient with GFAP-A. Our patient displayed a decreased uptake of PET tracer F-florbetapir in the brain lesions and lower distribution volume ratio in the damaged white matter lesions compared to the normal-appearing white matter, indicating significant intracranial demyelination. After treatment, the F-florbetapir PET/MRI examination showed a significant increase in the uptake of F-florbetapir in the brain lesions, along with a reduced Expanded Disability Status Scale score. Although only a small number of patients have been validated, this case first reported F-florbetapir PET/MRI could quantitatively and non-invasively assess the myelin recovery in GFAP-A patients, which may lead to improvements in the early diagnosis and long-term prognosis.
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These authors contribute equally to this work.
ISSN:2081-3856
2081-6936
DOI:10.1515/tnsci-2022-0223