AUTHOR=Li Hang , Li Qijun , Weng Qin , Cui Ruixue , Yen Tzu-Chen , Li Yanfeng TITLE=A novel MAPT variant (E342K) as a cause of familial progressive supranuclear palsy JOURNAL=Frontiers in Neurology VOLUME=15 YEAR=2024 URL=https://www.frontiersin.org/journals/neurology/articles/10.3389/fneur.2024.1372507 DOI=10.3389/fneur.2024.1372507 ISSN=1664-2295 ABSTRACT=Background

MAPT variants are a known cause of frontotemporal dementia and Parkinsonian syndrome, of which progressive supranuclear palsy syndrome (PSP) is a rare manifestation.

Objective

To report a novel MAPT variant in a PSP pedigree with autosomal dominant inheritance pattern, and to produce a literature review of PSP patients with MAPT variants.

Methods

A comprehensive clinical, genetic, and molecular neuroimaging investigation was conducted on a 61 years-old female proband diagnosed with PSP. We also collected the clinical presentation data and history of the patient’s pedigree, and performed further genetic analysis of 4 relatives, from two generations, with and without symptoms.

Results

The proband exhibited typical clinical manifestation of PSP. A cranial MRI revealed midbrain atrophy, and an FDG-PET scan suggested hypo-metabolic changes in caudate nucleus, left prefrontal lobe, both temporal poles, and midbrain. 18F-florzolo-tau-PET revealed tau-protein deposits in the thalamus and brainstem bilaterally. A gene test by whole-exome sequencing identified a novel MAPT variant [NM_005910.6, exon 11, c.1024G > A (p.E342K)], and the same variant was also identified in one affected relative and one asymptomatic relative, a probable pre-symptomatic carrier.

Conclusion

The PSP pedigree caused by the novel MAPT (E342K) variant, expanded the mutational spectrum of MAPT.