Literature DB >> 30149461

Bone Health and Endocrine Care of Boys with Duchenne Muscular Dystrophy: Data from the MD STARnet.

David R Weber1, Shiny Thomas2, Stephen W Erickson3, Deborah Fox2, Joyce Oleszek4, Shree Pandya1, Yedatore Venkatesh5, Christina Westfield2, Emma Ciafaloni1.   

Abstract

BACKGROUND: Patients with Duchenne muscular dystrophy (DMD) are at high risk of endocrine and bone health complications resulting from the high glucocorticoid (GC) doses used to treat this condition. There are limited data characterizing the clinical management of these complications.
OBJECTIVE: To determine the frequency of bone health screening, endocrinologist evaluation, and use of endocrine and bone health pharmacotherapy in the clinical care of males with DMD.
METHODS: A population based cohort study using data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet) was conducted. Clinical data was abstracted from the medical records of 683 males with DMD at five surveillance sites across the US.
RESULTS: A DXA scan had been documented in 24% of cases; the percentage of cases with DXA varied across surveillance sites from 13% to 43%, p < 0.001. History of fracture and greater disease duration were associated with greater odds of having a DXA. Only 4.7% of cases had documentation of an endocrinologist evaluation. The frequency of documented endocrine and bone health pharmacotherapy use included calcium (42.8%), vitamin D (36.6%), bisphosphonates (13.3%), growth hormone (1.9%), testosterone (1.7%), insulin (1.2%), and metformin (0.3%)Conclusions:A low percentage of DMD males had record of DXA scan, endocrinologist evaluation, or treatment with endocrine or bone health pharmacotherapy. Endocrine and bone health care may represent an unmet need in the DMD population.

Entities:  

Keywords:  Muscular dystrophy; bisphosphonates; duchenne; glucocorticoids; hypogonadism; osteoporosis

Mesh:

Substances:

Year:  2018        PMID: 30149461      PMCID: PMC6277257          DOI: 10.3233/JND-180317

Source DB:  PubMed          Journal:  J Neuromuscul Dis


  45 in total

Review 1.  Short stature and pubertal delay in Duchenne muscular dystrophy.

Authors:  Claire L Wood; Volker Straub; Michela Guglieri; Kate Bushby; Tim Cheetham
Journal:  Arch Dis Child       Date:  2015-07-03       Impact factor: 3.791

2.  The muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): surveillance methodology.

Authors:  Lisa A Miller; Paul A Romitti; Christopher Cunniff; Charlotte Druschel; Katherine D Mathews; F John Meaney; Dennis Matthews; Jiji Kantamneni; Zhen-Fang Feng; Nancy Zemblidge; Timothy M Miller; Jennifer Andrews; Deborah Fox; Emma Ciafaloni; Shree Pandya; April Montgomery; Aileen Kenneson
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2006-11

Review 3.  Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management.

Authors:  Katharine Bushby; Richard Finkel; David J Birnkrant; Laura E Case; Paula R Clemens; Linda Cripe; Ajay Kaul; Kathi Kinnett; Craig McDonald; Shree Pandya; James Poysky; Frederic Shapiro; Jean Tomezsko; Carolyn Constantin
Journal:  Lancet Neurol       Date:  2009-11-27       Impact factor: 44.182

Review 4.  Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care.

Authors:  Katharine Bushby; Richard Finkel; David J Birnkrant; Laura E Case; Paula R Clemens; Linda Cripe; Ajay Kaul; Kathi Kinnett; Craig McDonald; Shree Pandya; James Poysky; Frederic Shapiro; Jean Tomezsko; Carolyn Constantin
Journal:  Lancet Neurol       Date:  2009-11-27       Impact factor: 44.182

5.  Orthopedic outcomes of long-term daily corticosteroid treatment in Duchenne muscular dystrophy.

Authors:  W M King; R Ruttencutter; H N Nagaraja; V Matkovic; J Landoll; C Hoyle; J R Mendell; J T Kissel
Journal:  Neurology       Date:  2007-05-08       Impact factor: 9.910

Review 6.  Duchenne and Becker muscular dystrophies.

Authors:  Kevin M Flanigan
Journal:  Neurol Clin       Date:  2014-08       Impact factor: 3.806

7.  Why short stature is beneficial in Duchenne muscular dystrophy.

Authors:  Marko Bodor; Craig M McDonald
Journal:  Muscle Nerve       Date:  2013-07-27       Impact factor: 3.217

8.  Patterns of growth in ambulatory males with Duchenne muscular dystrophy.

Authors:  Nancy A West; Michele L Yang; David A Weitzenkamp; Jennifer Andrews; F John Meaney; Joyce Oleszek; Lisa A Miller; Dennis Matthews; Carolyn DiGuiseppi
Journal:  J Pediatr       Date:  2013-10-06       Impact factor: 4.406

Review 9.  Optimizing Bone Health in Duchenne Muscular Dystrophy.

Authors:  Jason L Buckner; Sasigarn A Bowden; John D Mahan
Journal:  Int J Endocrinol       Date:  2015-06-01       Impact factor: 3.257

10.  Long-Term Pulmonary Function in Duchenne Muscular Dystrophy: Comparison of Eteplirsen-Treated Patients to Natural History.

Authors:  T Bernard Kinane; Oscar H Mayer; Petra W Duda; Linda P Lowes; Stephanie L Moody; Jerry R Mendell
Journal:  J Neuromuscul Dis       Date:  2018
View more
  3 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.  Direct costs of adhering to selected Duchenne muscular dystrophy Care Considerations: Estimates from a midwestern state.

Authors:  Kristin M Conway; Scott D Grosse; Lijing Ouyang; Natalie Street; Paul A Romitti
Journal:  Muscle Nerve       Date:  2022-02-09       Impact factor: 3.852

3.  The role of delayed bone age in the evaluation of stature and bone health in glucocorticoid treated patients with Duchenne muscular dystrophy.

Authors:  E J Annexstad; J Bollerslev; J Westvik; A G Myhre; K Godang; I Holm; M Rasmussen
Journal:  Int J Pediatr Endocrinol       Date:  2019-12-23
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.