Literature DB >> 30055340

Growth, bone health & ambulatory status of boys with DMD treated with daily vs. intermittent oral glucocorticoid regimen.

N J Crabtree1, J E Adams2, R Padidela3, N J Shaw4, W Högler4, H Roper5, I Hughes6, A Daniel3, M Z Mughal3.   

Abstract

Oral glucocorticoids (GC) preserve muscle strength and prolong walking in boys with Duchenne muscular dystrophy (DMD). Although vertebral fractures have been reported in boys taking GC, fracture rates for different GC regimes have not been investigated. The aim of this pragmatic longitudinal study was to compare growth, body mass, bone mineral density (BMD), vertebral fractures (VF) and ambulatory status in boys with DMD on daily (DAILY) or intermittent (INTERMITTENT), oral GC regimens. A convenience sample of 50 DMD boys from two centres was included in the study; 25 boys each were on the DAILY or INTERMITTENT regimen. Size adjusted lumbar spine BMD (LS BMAD), total body less head BMD (TBLH), by DXA and distal forearm bone densities by pQCT, GC exposure, VF assessment and ambulatory status were analysed at three time points; baseline, 1 and 2 years. At baseline, there were no differences in age, GC duration or any bone parameters. However, DAILY boys were shorter (height SDS DAILY = -1.4(0.9); INTERMITTENT = -0.8(1.0), p = 0.04) with higher BMI (BMI SDS DAILY = 1.5(0.9); INTERMITTENT = 0.8(1.0), p = 0.01). Over 2 years, DAILY boys got progressively shorter (delta height SDS DAILY = -0.9(1.1); INTERMITTENT = +0.1(0.6), p < 0.001). At their 2 year assessment, 5 DAILY and 10 INTERMITTENT boys were non-ambulant. DAILY boys had more VFs than INTERMITTENT boys (10 versus 2; χ2 p = 0.008). BMAD SDS remained unchanged between groups. TBLH and radius BMD declined significantly but the rate of loss was not different. In conclusion, there was a trend for more boys on daily GCs to remain ambulant but at the cost of more VFs, greater adiposity and markedly diminished growth. In contrast, boys on intermittent GCs had fewer vertebral fractures but there was a trend for more boys to loose independent ambulation.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Ambulation; Bone density; Glucocorticoids; Growth; Muscular dystrophy; Vertebral fracture

Mesh:

Substances:

Year:  2018        PMID: 30055340     DOI: 10.1016/j.bone.2018.07.019

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  8 in total

Review 1.  Growth, pubertal development, and skeletal health in boys with Duchenne Muscular Dystrophy.

Authors:  Leanne M Ward; David R Weber
Journal:  Curr Opin Endocrinol Diabetes Obes       Date:  2019-02       Impact factor: 3.243

2.  Fractures and Linear Growth in a Nationwide Cohort of Boys With Duchenne Muscular Dystrophy With and Without Glucocorticoid Treatment: Results From the UK NorthStar Database.

Authors:  Shuko Joseph; Cunyi Wang; Kate Bushby; Michaela Guglieri; Iain Horrocks; Volker Straub; S Faisal Ahmed; Sze Choong Wong
Journal:  JAMA Neurol       Date:  2019-06-01       Impact factor: 18.302

Review 3.  Glucocorticoid-Induced Osteoporosis: Why Kids Are Different.

Authors:  Leanne M Ward
Journal:  Front Endocrinol (Lausanne)       Date:  2020-12-16       Impact factor: 5.555

4.  Bone Mineral Density Assessment by Quantitative Computed Tomography in Glucocorticoid-Treated Boys With Duchenne Muscular Dystrophy: A Linear Mixed-Effects Modeling Approach.

Authors:  Chuan Liu; Dan-Dan Yang; Lu Zhang; Xian-Gao Lei; Feng-Lin Jia; Yi Liao; Xi-Jian Chen; Gang Ning; Wen Luo; Hai-Bo Qu
Journal:  Front Endocrinol (Lausanne)       Date:  2022-03-23       Impact factor: 5.555

Review 5.  Osteoporosis in children and adolescents: when to suspect and how to diagnose it.

Authors:  Silvia Ciancia; Rick R van Rijn; Wolfgang Högler; Natasha M Appelman-Dijkstra; Annemieke M Boot; Theo C J Sas; Judith S Renes
Journal:  Eur J Pediatr       Date:  2022-04-06       Impact factor: 3.860

6.  Reduced bone mineral density in adolescents with Duchenne Muscular Dystrophy (DMD) and scoliosis.

Authors:  K Tsaknakis; K Jäckle; K A Lüders; H M Lorenz; L Braunschweig; A K Hell
Journal:  Osteoporos Int       Date:  2022-05-18       Impact factor: 5.071

7.  C-X-C motif chemokine ligand 12: a potential therapeutic target in Duchenne muscular dystrophy.

Authors:  Xinsheng Lai; Jie Chen
Journal:  Bioengineered       Date:  2021-12       Impact factor: 3.269

Review 8.  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
  8 in total

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