The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy

Abstract Objective We performed a prospective, cross‐sectional cognitive assessment in subjects with Duchenne Muscular Dystrophy (DMD) and their biological mothers. Methods Thirty subjects with out‐of‐frame mutations in the dystrophin (DMD) gene, and 25 biological mothers were evaluated using the Na...

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Main Authors: Mathula Thangarajh, Aaron J. Kaat, Genila Bibat, Jennifer Mansour, Katherine Summerton, Anthony Gioia, Carly Berger, Kristina K. Hardy, Kathryn R. Wagner
Format: Article
Language:English
Published: Wiley 2019-09-01
Series:Annals of Clinical and Translational Neurology
Online Access:https://doi.org/10.1002/acn3.50867
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spelling doaj-59905b583bb54600ac7fd367b5bea18f2021-05-02T14:20:14ZengWileyAnnals of Clinical and Translational Neurology2328-95032019-09-01691696170610.1002/acn3.50867The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophyMathula Thangarajh0Aaron J. Kaat1Genila Bibat2Jennifer Mansour3Katherine Summerton4Anthony Gioia5Carly Berger6Kristina K. Hardy7Kathryn R. Wagner8Department of Neurology Children’s National Health SystemDistrict of ColumbiaWashingtonDepartment of Medical Social Sciences Northwestern University Chicago IllinoisCenter for Genetic Muscle Disorders Kennedy Krieger Institute, Johns Hopkins School of Medicine Baltimore MarylandCenter for Genetic Muscle Disorders Kennedy Krieger Institute, Johns Hopkins School of Medicine Baltimore MarylandCenter for Genetic Muscle Disorders Kennedy Krieger Institute, Johns Hopkins School of Medicine Baltimore MarylandDepartments of Psychiatry & Behavioral Science and Pediatrics George Washington University School of MedicineDistrict of ColumbiaWashingtonDepartments of Psychiatry & Behavioral Science and Pediatrics George Washington University School of MedicineDistrict of ColumbiaWashingtonDepartments of Psychiatry & Behavioral Science and Pediatrics George Washington University School of MedicineDistrict of ColumbiaWashingtonCenter for Genetic Muscle Disorders Kennedy Krieger Institute, Johns Hopkins School of Medicine Baltimore MarylandAbstract Objective We performed a prospective, cross‐sectional cognitive assessment in subjects with Duchenne Muscular Dystrophy (DMD) and their biological mothers. Methods Thirty subjects with out‐of‐frame mutations in the dystrophin (DMD) gene, and 25 biological mothers were evaluated using the National Institutes of Health Toolbox Cognition Battery (NIHTB‐CB). A parent completed the Behavior Rating Inventory of Executive Functioning (BRIEF), a standardized rating scale of executive functioning, for their child. Mothers completed self‐reports of BRIEF and Neuro Quality‐of‐Life (NeuroQoL) Cognitive Function. Results Overall, the subjects with DMD scored approximately one standard deviation (SD) below age‐corrected norms on the NIHTB‐CB Total Cognition score. They scored 1.5 SD below age‐corrected norms in Fluid Cognition, which evaluates the cognitive domains of executive function, working memory, episodic memory, attention, and processing speed. Their performance was consistent with age expectations (i.e., within 1 SD below age‐corrected norms) in Crystalized Cognition, which evaluates vocabulary and reading. Subjects with DMD had higher T‐scores in several domains of BRIEF, demonstrating greater difficulty in executive functioning. The biological mothers had overall average or above average T‐scores on NIHTB‐CB. Mothers who were carriers of DMD mutation performed lower overall compared to mothers who were not carriers of DMD mutation (Cohen’s d = −1.1). Carrier mothers performed lower than average (1.5 SD) in Executive Function, measured by Flanker Inhibitory Control and Attention. Biological mothers scored within expected score ranges for adults in BRIEF and NeuroQoL. Interpretation The NIHTB‐CB, combined with standardized self‐reported measures, can be a sensitive screening tool for cognitive surveillance in DMD.https://doi.org/10.1002/acn3.50867
collection DOAJ
language English
format Article
sources DOAJ
author Mathula Thangarajh
Aaron J. Kaat
Genila Bibat
Jennifer Mansour
Katherine Summerton
Anthony Gioia
Carly Berger
Kristina K. Hardy
Kathryn R. Wagner
spellingShingle Mathula Thangarajh
Aaron J. Kaat
Genila Bibat
Jennifer Mansour
Katherine Summerton
Anthony Gioia
Carly Berger
Kristina K. Hardy
Kathryn R. Wagner
The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy
Annals of Clinical and Translational Neurology
author_facet Mathula Thangarajh
Aaron J. Kaat
Genila Bibat
Jennifer Mansour
Katherine Summerton
Anthony Gioia
Carly Berger
Kristina K. Hardy
Kathryn R. Wagner
author_sort Mathula Thangarajh
title The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy
title_short The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy
title_full The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy
title_fullStr The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy
title_full_unstemmed The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy
title_sort nih toolbox for cognitive surveillance in duchenne muscular dystrophy
publisher Wiley
series Annals of Clinical and Translational Neurology
issn 2328-9503
publishDate 2019-09-01
description Abstract Objective We performed a prospective, cross‐sectional cognitive assessment in subjects with Duchenne Muscular Dystrophy (DMD) and their biological mothers. Methods Thirty subjects with out‐of‐frame mutations in the dystrophin (DMD) gene, and 25 biological mothers were evaluated using the National Institutes of Health Toolbox Cognition Battery (NIHTB‐CB). A parent completed the Behavior Rating Inventory of Executive Functioning (BRIEF), a standardized rating scale of executive functioning, for their child. Mothers completed self‐reports of BRIEF and Neuro Quality‐of‐Life (NeuroQoL) Cognitive Function. Results Overall, the subjects with DMD scored approximately one standard deviation (SD) below age‐corrected norms on the NIHTB‐CB Total Cognition score. They scored 1.5 SD below age‐corrected norms in Fluid Cognition, which evaluates the cognitive domains of executive function, working memory, episodic memory, attention, and processing speed. Their performance was consistent with age expectations (i.e., within 1 SD below age‐corrected norms) in Crystalized Cognition, which evaluates vocabulary and reading. Subjects with DMD had higher T‐scores in several domains of BRIEF, demonstrating greater difficulty in executive functioning. The biological mothers had overall average or above average T‐scores on NIHTB‐CB. Mothers who were carriers of DMD mutation performed lower overall compared to mothers who were not carriers of DMD mutation (Cohen’s d = −1.1). Carrier mothers performed lower than average (1.5 SD) in Executive Function, measured by Flanker Inhibitory Control and Attention. Biological mothers scored within expected score ranges for adults in BRIEF and NeuroQoL. Interpretation The NIHTB‐CB, combined with standardized self‐reported measures, can be a sensitive screening tool for cognitive surveillance in DMD.
url https://doi.org/10.1002/acn3.50867
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