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Determinants of cerebral radiological progression in Fabry disease.
Körver, Simon; Longo, Maria G F; Lima, Marjana R; Hollak, Carla E M; El Sayed, Mohamed; van Schaik, Ivo N; Vedolin, Leonardo; Dijkgraaf, Marcel G W; Langeveld, Mirjam.
Afiliación
  • Körver S; Endocrinology and Metabolism, Amsterdam UMC-Locatie AMC, Amsterdam, The Netherlands.
  • Longo MGF; Department of Radiology, Massachusetts General Hospital Institute for Patient Care, Boston, Massachusetts, USA.
  • Lima MR; Department of Radiology, Hospital Moinhos de Vento, Porto Alegre, RS, Brazil.
  • Hollak CEM; Endocrinology and Metabolism, Amsterdam UMC-Locatie AMC, Amsterdam, The Netherlands.
  • El Sayed M; Endocrinology and Metabolism, Amsterdam UMC-Locatie AMC, Amsterdam, The Netherlands.
  • van Schaik IN; Department of Neurology, Amsterdam UMC-Locatie AMC, Amsterdam, North Holland, The Netherlands.
  • Vedolin L; Spaarne Gasthuis, Haarlem, Noord-Holland, The Netherlands.
  • Dijkgraaf MGW; Imaging Director, Diagnosticos da America SA, Barueri, São Paulo, Brazil.
  • Langeveld M; Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Amsterdam UMC-Locatie AMC, Amsterdam, North Holland, The Netherlands.
J Neurol Neurosurg Psychiatry ; 91(7): 756-763, 2020 07.
Article en En | MEDLINE | ID: mdl-32317398
ABSTRACT
BACKGROUND AND

AIM:

It is unclear which patients with Fabry disease (FD) are at risk for progression of white matter lesions (WMLs) and brain infarctions and whether enzyme replacement therapy (ERT) changes this risk. The aim of this study was to determine the effect of ERT and clinical characteristics on progression of WMLs and infarctions on MRI in patients with FD.

METHODS:

MRIs were assessed for WMLs (Fazekas scale), infarctions and basilar artery diameter (BAD). The effect of clinical characteristics (renal and cardiac involvement, cardiovascular risk factors, cardiac complications, BAD) and ERT on WML and infarction progression was evaluated using mixed models.

RESULTS:

One hundred forty-nine patients were included (median age 39 years, 38% men, 79% classical phenotype). Median follow-up time was 7 years (range 0-13 years) with a median number of MRIs per patient of 5 (range 1-14), resulting in a total of 852 scans. Variables independently associated with WML and infarction progression were age, male sex and a classical phenotype. Progression of WMLs and infarctions was not affected by adding ERT to the model, neither for the whole group, nor for early treated patients. Progression was highly variable among patients which could not be explained by other known variables such as hypertension, cholesterol, atrial fibrillation and changes in kidney function, left ventricular mass or BAD.

CONCLUSION:

Progression of WMLs and cerebral infarctions in FD is mainly related to age, sex and phenotype. Additional effects of established cardiovascular risk factors, organ involvement and treatment with ERT are probably small to negligible.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Encéfalo / Enfermedad de Fabry / Sustancia Blanca Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurol Neurosurg Psychiatry Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Encéfalo / Enfermedad de Fabry / Sustancia Blanca Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurol Neurosurg Psychiatry Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos