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Quantitative brain MRI morphology in severe and attenuated forms of mucopolysaccharidosis type I.
Kovac, Victor; Shapiro, Elsa G; Rudser, Kyle D; Mueller, Bryon A; Eisengart, Julie B; Delaney, Kathleen A; Ahmed, Alia; King, Kelly E; Yund, Brianna D; Cowan, Morton J; Raiman, Julian; Mamak, Eva G; Harmatz, Paul R; Shankar, Suma P; Ali, Nadia; Cagle, Stephanie R; Wozniak, Jeffrey R; Lim, Kelvin O; Orchard, Paul J; Whitley, Chester B; Nestrasil, Igor.
Afiliação
  • Kovac V; Division of Clinical Behavioral Neuroscience, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA. Electronic address: vjwkovac@gmail.com.
  • Shapiro EG; Division of Clinical Behavioral Neuroscience, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA. Electronic address: shapi004@umn.edu.
  • Rudser KD; Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN, USA. Electronic address: rudser@umn.edu.
  • Mueller BA; Department of Psychiatry & Behavioral Sciences, University of Minnesota, Minneapolis, MN, USA. Electronic address: muell093@umn.edu.
  • Eisengart JB; Division of Clinical Behavioral Neuroscience, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA. Electronic address: eisen139@umn.edu.
  • Delaney KA; Division of Clinical Behavioral Neuroscience, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA. Electronic address: delan011@umn.edu.
  • Ahmed A; Division of Clinical Behavioral Neuroscience, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA. Electronic address: ahmed306@umn.edu.
  • King KE; Division of Clinical Behavioral Neuroscience, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA. Electronic address: kingx780@umn.edu.
  • Yund BD; Division of Clinical Behavioral Neuroscience, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA. Electronic address: bdy@umn.edu.
  • Cowan MJ; UCSF Benioff Children's Hospital, University of California, San Francisco, CA, USA. Electronic address: mort.cowan@ucsf.edu.
  • Raiman J; Division of Clinical and Metabolic Genetics, Department of Paediatrics, University of Toronto, The Hospital for Sick Children, Toronto, ON, Canada. Electronic address: julian.raiman@nhs.net.
  • Mamak EG; Department of Psychology, The Hospital for Sick Children, Toronto, ON, Canada. Electronic address: eva.mamak@sickkids.ca.
  • Harmatz PR; UCSF Benioff Children's Hospital Oakland, Oakland, CA, USA. Electronic address: pharmatz@mail.cho.org.
  • Shankar SP; Department of Ophthalmology and Human Genetics, Emory University, Atlanta, GA, USA. Electronic address: spshankar@ucdavis.edu.
  • Ali N; Department of Human Genetics, Emory University, Atlanta, GA, USA. Electronic address: nadia.ali@emory.edu.
  • Cagle SR; Department of Human Genetics, Emory University, Atlanta, GA, USA.
  • Wozniak JR; Department of Psychiatry & Behavioral Sciences, University of Minnesota, Minneapolis, MN, USA. Electronic address: jwozniak@umn.edu.
  • Lim KO; Department of Psychiatry & Behavioral Sciences, University of Minnesota, Minneapolis, MN, USA. Electronic address: kolim@umn.edu.
  • Orchard PJ; Division of Pediatric Blood & Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA. Electronic address: orcha001@umn.edu.
  • Whitley CB; Gene Therapy Center, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA. Electronic address: whitley@umn.edu.
  • Nestrasil I; Division of Clinical Behavioral Neuroscience, Department of Pediatrics, University of Minnesota, Center for Magnetic Resonance Research (CMRR), Department of Radiology, Minneapolis, MN, USA. Electronic address: nestr007@umn.edu.
Mol Genet Metab ; 135(2): 122-132, 2022 02.
Article em En | MEDLINE | ID: mdl-35012890
OBJECTIVE: To assess our hypothesis that brain macrostructure is different in individuals with mucopolysaccharidosis type I (MPS I) and healthy controls (HC), we conducted a comprehensive multicenter study using a uniform quantitative magnetic resonance imaging (qMRI) protocol, with analyses that account for the effects of disease phenotype, age, and cognition. METHODS: Brain MRIs in 23 individuals with attenuated (MPS IA) and 38 with severe MPS I (MPS IH), aged 4-25 years, enrolled under the study protocol NCT01870375, were compared to 98 healthy controls. RESULTS: Cortical and subcortical gray matter, white matter, corpus callosum, ventricular and choroid plexus volumes in MPS I significantly differed from HC. Thicker cortex, lower white matter and corpus callosum volumes were already present at the youngest MPS I participants aged 4-5 years. Age-related differences were observed in both MPS I groups, but most markedly in MPS IH, particularly in cortical gray matter metrics. IQ scores were inversely associated with ventricular volume in both MPS I groups and were positively associated with cortical thickness only in MPS IA. CONCLUSIONS: Quantitatively-derived MRI measures distinguished MPS I participants from HC as well as severe from attenuated forms. Age-related neurodevelopmental trajectories in both MPS I forms differed from HC. The extent to which brain structure is altered by disease, potentially spared by treatment, and how it relates to neurocognitive dysfunction needs further exploration.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mucopolissacaridose I / Substância Branca Tipo de estudo: Clinical_trials / Guideline Limite: Humans Idioma: En Revista: Mol Genet Metab Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mucopolissacaridose I / Substância Branca Tipo de estudo: Clinical_trials / Guideline Limite: Humans Idioma: En Revista: Mol Genet Metab Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Ano de publicação: 2022 Tipo de documento: Article