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White matter involvement and cortical thickness in PFBC (Primary Familial Brain Calcifications)

G. Bonato, G. Librizzi, A. Adraman, M. Corazza, A. Fabris, F. Pistonesi, C. Bertolin, L. Salviati, A. Antonini, R. Manara, M. Carecchio (Padua, Italy)

Meeting: 2025 International Congress

Keywords: Calcium

Category: Parkinsonism (Other)

Objective: describing MRI findings in PFBC

Background: PFBC is a rare genetic neurodegenerative disorder characterized by bilateral calcium deposition in basal ganglia, featuring movement disorders, psychiatric or cognitive symptoms; prognostic factors are scarse. CT scan is the gold standard technique, whereas the role of MRI is still unexplored

Method: 48 PFBC subjects and 67 matched healthy controls (HC) from the ERN-RND Center of Padua University underwent 3T brain MRI (T1, FLAIR, SWI sequences, FreeSurfer cortical thickness analysis), genetic testing (NGS Illumina NextSeq), clinical and neuropsychological evaluations

Results: 33 subjects had neurological symptoms (parkinsonism 46%, tremor 42%, brisk reflexes 44%, cerebellar symptoms or dysarthria 23%, mild cognitive impairment 36%); 29 had anxiety or depression. A genetic cause was found in 29 PFBCs.

White matter changes were best rated by FLAIR. Centra semiovalia were involved in 23 patients, with band-like supratentorial leukopathy pattern in 17 and scattered centra semiovalia lesions in 6; 15 patients had concurrent deep and periventricular alterations with intermediate sparing.

PDGFB/PDGFRB and MYORG mutations were associated with more severe white matter involvement with band-like pattern (p<0.001) and deep and periventricular alterations with intermediate sparing (p<0.01), compared to HC and other genetic or non-genetic PFBC subgroups.

Cerebellar white matter alterations were found in 13 PFBC subjects, more severe in MYORG mutation carriers (8/9, p<0.001).

White matter involvement in both cerebrum and cerebellum were significantly associated with cognitive impairment (OR 5.7, p=0.02; mean MoCA 21 vs 26, p=0.004). The presence of dentate nuclei calcifications was a significant predictor of a genetic diagnosis (OR 7.3, p=0.03) and of behavioral-psychiatric symptoms (91% vs 56%, p=0.04).

Cortical thickness reduction was observed in the left premotor cortex in PFBC (p<0.05), compared to HC, but not in asymptomatic PFBC. Cerebellar atrophy was more pronounced in MYORG subjects (p<0.05)

Conclusion: beside CT scan, brain MRI may be a useful tool in PFBC with potentially relevant prognostic correlates.

Data partially submitted as abstract at 2025 EAN Congress

To cite this abstract in AMA style:

G. Bonato, G. Librizzi, A. Adraman, M. Corazza, A. Fabris, F. Pistonesi, C. Bertolin, L. Salviati, A. Antonini, R. Manara, M. Carecchio. White matter involvement and cortical thickness in PFBC (Primary Familial Brain Calcifications) [abstract]. Mov Disord. 2025; 40 (suppl 1). https://www.mdsabstracts.org/abstract/white-matter-involvement-and-cortical-thickness-in-pfbc-primary-familial-brain-calcifications/. Accessed October 15, 2026.
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