Literature DB >> 30706490

Twice-weekly glucocorticosteroids in infants and young boys with Duchenne muscular dystrophy.

Anne M Connolly1,2, Craig M Zaidman1,2, Paul T Golumbek1,2, Mary M Cradock2, Kevin M Flanigan3, Nancy L Kuntz4, Richard S Finkel5, Craig M McDonald6, Susan T Iannaccone7, Pallavi Anand1, Catherine A Siener1, Julaine M Florence1, Linda P Lowes3, Lindsay N Alfano3, Linda B Johnson6, Alina Nicorici6, Leslie L Nelson7, Jerry R Mendell3.   

Abstract

INTRODUCTION: Glucocorticosteroids (GC) are effective in slowing weakness in boys with Duchenne muscular dystrophy (DMD).
METHODS: This is a multisite, 1-year, open-label trial of twice-weekly prednisolone (5 mg/kg/dose) in infants/young boys (0.4-2.4 years) with DMD. We compared changes in Bayley III Scales of Infant Development (Bayley-III) with untreated boys followed for 1 year (historical control cohort [HCC]). Twenty-three of 25 participants completed the study.
RESULTS: Treated boys gained an average of 0.5 points on the Bayley-III gross motor scaled score (GMSS) compared with the HCC who, on average, declined 1.3 points (P = 0.03). All boys maintained linear growth, and none developed Cushingoid features. Excessive weight gain occurred in 13 of 23 (56%) boys. DISCUSSION: This study provides evidence that twice-weekly GC is well tolerated in infants and young boys with DMD and improves GMSS. Excessive weight gain is a potential risk. Longer follow-up is required to determine whether early GC initiation is feasible in most infants/boys with DMD. Muscle Nerve 59:650-657, 2019.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  Bayley-III Scales of Infant and Toddler Development; DMD; Duchenne muscular dystrophy; GC; infants; twice-weekly glucocorticosteroid

Mesh:

Substances:

Year:  2019        PMID: 30706490     DOI: 10.1002/mus.26441

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  5 in total

1.  Pulsed glucocorticoids enhance dystrophic muscle performance through epigenetic-metabolic reprogramming.

Authors:  Mattia Quattrocelli; Aaron S Zelikovich; Zhen Jiang; Clara Bien Peek; Alexis R Demonbreun; Nancy L Kuntz; Grant D Barish; Saptarsi M Haldar; Joseph Bass; Elizabeth M McNally
Journal:  JCI Insight       Date:  2019-12-19

2.  Efficacy and Safety of Vamorolone in Duchenne Muscular Dystrophy: A 30-Month Nonrandomized Controlled Open-Label Extension Trial.

Authors:  Jean K Mah; Paula R Clemens; Michela Guglieri; Edward C Smith; Richard S Finkel; Mar Tulinius; Yoram Nevo; Monique M Ryan; Richard Webster; Diana Castro; Nancy L Kuntz; Craig M McDonald; Jesse M Damsker; Benjamin D Schwartz; Laurel J Mengle-Gaw; Stefan Jackowski; Georgia Stimpson; Deborah A Ridout; Vandana Ayyar-Gupta; Giovanni Baranello; Adnan Y Manzur; Francesco Muntoni; Heather Gordish-Dressman; Mika Leinonen; Leanne M Ward; Eric P Hoffman; Utkarsh J Dang
Journal:  JAMA Netw Open       Date:  2022-01-04

3.  An Open Label Exploratory Clinical Trial Evaluating Safety and Tolerability of Once-Weekly Prednisone in Becker and Limb-Girdle Muscular Dystrophy.

Authors:  Aaron S Zelikovich; Benjamin C Joslin; Patricia Casey; Elizabeth M McNally; Senda Ajroud-Driss
Journal:  J Neuromuscul Dis       Date:  2022

4.  Cost of Illness in Patients with Duchenne Muscular Dystrophy in Portugal: The COIDUCH Study.

Authors:  Pedro Labisa; Valeska Andreozzi; Melina Mota; Susana Monteiro; Rita Alves; João Almeida; Björn Vandewalle; Jorge Felix; Katharina Buesch; Hugo Canhão; Igor Beitia Ortiz de Zarate
Journal:  Pharmacoecon Open       Date:  2021-10-03

Review 5.  Mechanisms and Clinical Applications of Glucocorticoid Steroids in Muscular Dystrophy.

Authors:  Mattia Quattrocelli; Aaron S Zelikovich; Isabella M Salamone; Julie A Fischer; Elizabeth M McNally
Journal:  J Neuromuscul Dis       Date:  2021
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.