Literature DB >> 28341975

Longitudinal volumetric and 2D assessment of cerebellar atrophy in a large cohort of children with phosphomannomutase deficiency (PMM2-CDG).

Víctor de Diego1,2, Antonio F Martínez-Monseny3, Jordi Muchart1,2, Daniel Cuadras4, Raquel Montero1,2, Rafael Artuch1,2, Celia Pérez-Cerdá5, Belén Pérez5, Belén Pérez-Dueñas1,2, Andrea Poretti6, Mercedes Serrano7,8,9,10.   

Abstract

OBJECTIVE: We aim to delineate the progression of cerebellar atrophy (the primary neuroimaging finding) in children with phosphomannomutase-deficiency (PMM2-CDG) by analyzing longitudinal MRI studies and performing cerebellar volumetric analysis and a 2D cerebellar measurement.
METHODS: Statistical analysis was used to compare MRI measurements [midsagittal vermis relative diameter (MVRD) and volume] of children with PMM2-CDG and sex- and age-matched controls, and to determine the rate of progression of cerebellar atrophy at different ages.
RESULTS: Fifty MRI studies of 33 PMM2-CDG patients were used for 2D evaluation, and 19 MRI studies were available for volumetric analysis. Results from a linear regression model showed that patients have a significantly lower MVRD and cerebellar volume compared to controls (p < 0.001 and p < 0.001 respectively). There was a significant negative correlation between age and MVRD for patients (p = 0.014). The rate of cerebellar atrophy measured by the loss of MVRD and cerebellar volume per year was higher at early ages (r = -0.578, p = 0.012 and r = -0.323, p = 0.48 respectively), particularly in patients under 11 years (p = 0.004). There was a significant positive correlation between MVRD and cerebellar volume in PMM2-CDG patients (r = 0.669, p = 0.001).
CONCLUSIONS: Our study quantifies a progression of cerebellar atrophy in PMM2-CDG patients, particularly during the first decade of life, and suggests a simple and reliable measure, the MVRD, to monitor cerebellar atrophy. Quantitative measurement of MVRD and cerebellar volume are essential for correlation with phenotype and outcome, natural follow-up, and monitoring in view of potential therapies in children with PMM2-CDG.

Entities:  

Keywords:  Cerebellar Atrophy; Cerebellar Volume; Focal Epilepsy; Spinocerebellar Ataxia; Volumetric Analysis

Mesh:

Substances:

Year:  2017        PMID: 28341975     DOI: 10.1007/s10545-017-0028-4

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  11 in total

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2.  The shrunken, bright cerebellum: a characteristic MRI finding in congenital disorders of glycosylation type 1a.

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4.  Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology.

Authors:  E Aronica; A A M W van Kempen; M van der Heide; B T Poll-The; H J van Slooten; D Troost; J M Rozemuller-Kwakkel
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10.  Phosphomannomutase deficiency (PMM2-CDG): ataxia and cerebellar assessment.

Authors:  Mercedes Serrano; Víctor de Diego; Jordi Muchart; Daniel Cuadras; Ana Felipe; Alfons Macaya; Ramón Velázquez; M Pilar Poo; Carmen Fons; M Mar O'Callaghan; Angels García-Cazorla; Cristina Boix; Bernabé Robles; Francisco Carratalá; Marisa Girós; Paz Briones; Laura Gort; Rafael Artuch; Celia Pérez-Cerdá; Jaak Jaeken; Belén Pérez; Belén Pérez-Dueñas
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6.  Clinical and radiological correlates of activities of daily living in cerebellar atrophy caused by PMM2 mutations (PMM2-CDG).

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