Literature DB >> 32024675

MR biomarkers predict clinical function in Duchenne muscular dystrophy.

Alison M Barnard1, Rebecca J Willcocks1, William T Triplett1, Sean C Forbes1, Michael J Daniels1, Saptarshi Chakraborty1, Donovan J Lott1, Claudia R Senesac1, Erika L Finanger1, Ann T Harrington1, Gihan Tennekoon1, Harneet Arora1, Dah-Jyuu Wang1, H Lee Sweeney1, William D Rooney1, Glenn A Walter1, Krista Vandenborne2.   

Abstract

OBJECTIVE: To investigate the potential of lower extremity magnetic resonance (MR) biomarkers to serve as endpoints in clinical trials of therapeutics for Duchenne muscular dystrophy (DMD) by characterizing the longitudinal progression of MR biomarkers over 48 months and assessing their relationship to changes in ambulatory clinical function.
METHODS: One hundred sixty participants with DMD were enrolled in this longitudinal, natural history study and underwent MR data acquisition of the lower extremity muscles to determine muscle fat fraction (FF) and MRI T2 biomarkers of disease progression. In addition, 4 tests of ambulatory function were performed. Participants returned for follow-up data collection at 12, 24, 36, and 48 months.
RESULTS: Longitudinal analysis of the MR biomarkers revealed that vastus lateralis FF, vastus lateralis MRI T2, and biceps femoris long head MRI T2 biomarkers were the fastest progressing biomarkers over time in this primarily ambulatory cohort. Biomarker values tended to demonstrate a nonlinear, sigmoidal trajectory over time. The lower extremity biomarkers predicted functional performance 12 and 24 months later, and the magnitude of change in an MR biomarker over time was related to the magnitude of change in function. Vastus lateralis FF, soleus FF, vastus lateralis MRI T2, and biceps femoris long head MRI T2 were the strongest predictors of future loss of function, including loss of ambulation.
CONCLUSIONS: This study supports the strong relationship between lower extremity MR biomarkers and measures of clinical function, as well as the ability of MR biomarkers, particularly those from proximal muscles, to predict future ambulatory function and important clinical milestones. CLINICALTRIALSGOV IDENTIFIER: NCT01484678.
© 2020 American Academy of Neurology.

Entities:  

Mesh:

Substances:

Year:  2020        PMID: 32024675      PMCID: PMC7238941          DOI: 10.1212/WNL.0000000000009012

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  31 in total

1.  T2 mapping in Duchenne muscular dystrophy: distribution of disease activity and correlation with clinical assessments.

Authors:  Hee Kyung Kim; Tal Laor; Paul S Horn; Judy M Racadio; Brenda Wong; Bernard J Dardzinski
Journal:  Radiology       Date:  2010-06       Impact factor: 11.105

2.  Muscle fat-fraction and mapping in Duchenne muscular dystrophy: evaluation of disease distribution and correlation with clinical assessments. Preliminary experience.

Authors:  Michele Gaeta; Sonia Messina; Achille Mileto; Gian Luca Vita; Giorgio Ascenti; Sergio Vinci; Antonio Bottari; Giuseppe Vita; Nicola Settineri; Daniele Bruschetta; Sergio Racchiusa; Fabio Minutoli
Journal:  Skeletal Radiol       Date:  2011-11-10       Impact factor: 2.199

3.  Changes in muscle T2 and tissue damage after downhill running in mdx mice.

Authors:  Sunita Mathur; Ravneet S Vohra; Sean A Germain; Sean Forbes; Nathan D Bryant; Krista Vandenborne; Glenn A Walter
Journal:  Muscle Nerve       Date:  2011-04-12       Impact factor: 3.217

4.  Chemical shift-based MRI to measure fat fractions in dystrophic skeletal muscle.

Authors:  William T Triplett; Celine Baligand; Sean C Forbes; Rebecca J Willcocks; Donovan J Lott; Soren DeVos; Jim Pollaro; William D Rooney; H Lee Sweeney; Carsten G Bönnemann; Dah-Jyuu Wang; Krista Vandenborne; Glenn A Walter
Journal:  Magn Reson Med       Date:  2013-09-04       Impact factor: 4.668

5.  Dystrophin: the protein product of the Duchenne muscular dystrophy locus.

Authors:  E P Hoffman; R H Brown; L M Kunkel
Journal:  Cell       Date:  1987-12-24       Impact factor: 41.582

6.  Quantifying disease activity in fatty-infiltrated skeletal muscle by IDEAL-CPMG in Duchenne muscular dystrophy.

Authors:  Ami Mankodi; Courtney A Bishop; Sungyoung Auh; Rexford D Newbould; Kenneth H Fischbeck; Robert L Janiczek
Journal:  Neuromuscul Disord       Date:  2016-07-28       Impact factor: 4.296

7.  Skeletal muscles of ambulant children with Duchenne muscular dystrophy: validation of multicenter study of evaluation with MR imaging and MR spectroscopy.

Authors:  Sean C Forbes; Glenn A Walter; William D Rooney; Dah-Jyuu Wang; Soren DeVos; Jim Pollaro; William Triplett; Donovan J Lott; Rebecca J Willcocks; Claudia Senesac; Michael J Daniels; Barry J Byrne; Barry Russman; Richard S Finkel; James S Meyer; H Lee Sweeney; Krista Vandenborne
Journal:  Radiology       Date:  2013-05-21       Impact factor: 11.105

8.  Longitudinal functional and NMR assessment of upper limbs in Duchenne muscular dystrophy.

Authors:  Jean-Yves Hogrel; Claire Wary; Amélie Moraux; Noura Azzabou; Valérie Decostre; Gwenn Ollivier; Aurélie Canal; Charlotte Lilien; Isabelle Ledoux; Mélanie Annoussamy; Nacera Reguiba; Teresa Gidaro; Anne Gaelle Le Moing; Ruxandra Cardas; Thomas Voit; Pierre G Carlier; Laurent Servais
Journal:  Neurology       Date:  2016-02-17       Impact factor: 9.910

9.  Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophy.

Authors:  Jerry R Mendell; Nathalie Goemans; Linda P Lowes; Lindsay N Alfano; Katherine Berry; James Shao; Edward M Kaye; Eugenio Mercuri
Journal:  Ann Neurol       Date:  2016-01-08       Impact factor: 10.422

10.  Skeletal muscle magnetic resonance biomarkers correlate with function and sentinel events in Duchenne muscular dystrophy.

Authors:  Alison M Barnard; Rebecca J Willcocks; Erika L Finanger; Michael J Daniels; William T Triplett; William D Rooney; Donovan J Lott; Sean C Forbes; Dah-Jyuu Wang; Claudia R Senesac; Ann T Harrington; Richard S Finkel; Barry S Russman; Barry J Byrne; Gihan I Tennekoon; Glenn A Walter; H Lee Sweeney; Krista Vandenborne
Journal:  PLoS One       Date:  2018-03-19       Impact factor: 3.240

View more
  17 in total

1.  Clinical and Genetic Characteristics in Young, Glucocorticoid-Naive Boys With Duchenne Muscular Dystrophy.

Authors:  Marianela Schiava; Rachel Amos; Henriette VanRuiten; Michael P McDermott; Williams B Martens; Stephanie Gregory; Anna Mayhew; Elaine McColl; Rabi Tawil; Tracey Willis; Kate Bushby; Robert C Griggs; Michela Guglieri
Journal:  Neurology       Date:  2021-12-02       Impact factor: 9.910

2.  Leveraging cardiac magnetic resonance imaging to assess skeletal muscle progression in Duchenne muscular dystrophy.

Authors:  Jacob A Kaslow; Andrew G Sokolow; Thomas Donnelly; Maciej S Buchowski; Bruce M Damon; Larry W Markham; W Bryan Burnette; Jonathan H Soslow
Journal:  Neuromuscul Disord       Date:  2022-02-04       Impact factor: 3.538

3.  Development of Contractures in DMD in Relation to MRI-Determined Muscle Quality and Ambulatory Function.

Authors:  Rebecca J Willcocks; Alison M Barnard; Ryan J Wortman; Claudia R Senesac; Donovan J Lott; Ann T Harrington; Kirsten L Zilke; Sean C Forbes; William D Rooney; Dah-Jyuu Wang; Erika L Finanger; Gihan I Tennekoon; Michael J Daniels; William T Triplett; Glenn A Walter; Krista Vandenborne
Journal:  J Neuromuscul Dis       Date:  2022

4.  Step Activity Monitoring in Boys with Duchenne Muscular Dystrophy and its Correlation with Magnetic Resonance Measures and Functional Performance.

Authors:  Kavya S Nair; Donovan J Lott; Sean C Forbes; Alison M Barnard; Rebecca J Willcocks; Claudia R Senesac; Michael J Daniels; Ann T Harrington; Gihan I Tennekoon; Kirsten Zilke; Erika L Finanger; Richard S Finkel; William D Rooney; Glenn A Walter; Krista Vandenborne
Journal:  J Neuromuscul Dis       Date:  2022

5.  Baseline fat fraction is a strong predictor of disease progression in Becker muscular dystrophy.

Authors:  Thom T J Veeger; Nienke M van de Velde; Kevin R Keene; Erik H Niks; Melissa T Hooijmans; Andrew G Webb; Jurriaan H de Groot; Hermien E Kan
Journal:  NMR Biomed       Date:  2022-02-05       Impact factor: 4.478

6.  Quantitative magnetic resonance imaging measures as biomarkers of disease progression in boys with Duchenne muscular dystrophy: a phase 2 trial of domagrozumab.

Authors:  Sarah P Sherlock; Jeffrey Palmer; Kathryn R Wagner; Hoda Z Abdel-Hamid; Enrico Bertini; Cuixia Tian; Jean K Mah; Anna Kostera-Pruszczyk; Francesco Muntoni; Michela Guglieri; John F Brandsema; Eugenio Mercuri; Russell J Butterfield; Craig M McDonald; Lawrence Charnas; Shannon Marraffino
Journal:  J Neurol       Date:  2022-04-08       Impact factor: 6.682

7.  Assessment of rAAVrh.74.MHCK7.micro-dystrophin Gene Therapy Using Magnetic Resonance Imaging in Children With Duchenne Muscular Dystrophy.

Authors:  Rebecca J Willcocks; Sean C Forbes; Glenn A Walter; Lee Sweeney; Louise R Rodino-Klapac; Jerry R Mendell; Krista Vandenborne
Journal:  JAMA Netw Open       Date:  2021-01-04

8.  Skeletal Muscle Magnetic Resonance Biomarkers in GNE Myopathy.

Authors:  Chia-Ying Liu; Jianhua Yao; William C Kovacs; Joseph A Shrader; Galen Joe; Ronald Ouwerkerk; Ami K Mankodi; William A Gahl; Ronald M Summers; Nuria Carrillo
Journal:  Neurology       Date:  2020-11-20       Impact factor: 9.910

9.  Quantitative muscle MRI biomarkers in Duchenne muscular dystrophy: cross-sectional correlations with age and functional tests.

Authors:  Sarah P Sherlock; Yao Zhang; Michael Binks; Shannon Marraffino
Journal:  Biomark Med       Date:  2021-06-22       Impact factor: 2.851

10.  Plasma lipidomic analysis shows a disease progression signature in mdx mice.

Authors:  Roula Tsonaka; Alexandre Seyer; Annemieke Aartsma-Rus; Pietro Spitali
Journal:  Sci Rep       Date:  2021-06-21       Impact factor: 4.379

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.