Online self-report data for duchenne muscular dystrophy confirms natural history and can be used to assess for therapeutic benefits

Richard T Wang, Cheri A Silverstein Fadlon, J Wes Ulm, Ivana Jankovic, Ascia Eskin, Ake Lu, Vanessa Rangel Miller, Rita M Cantor, Ning Li, Robert Elashoff, Anne S Martin, Holly L Peay, Nancy Halnon, Stanley F Nelson, Richard T Wang, Cheri A Silverstein Fadlon, J Wes Ulm, Ivana Jankovic, Ascia Eskin, Ake Lu, Vanessa Rangel Miller, Rita M Cantor, Ning Li, Robert Elashoff, Anne S Martin, Holly L Peay, Nancy Halnon, Stanley F Nelson

Abstract

To assess the utility of online patient self-report outcomes in a rare disease, we attempted to observe the effects of corticosteroids in delaying age at fulltime wheelchair use in Duchenne muscular dystrophy (DMD) using data from 1,057 males from DuchenneConnect, an online registry. Data collected were compared to prior natural history data in regard to age at diagnosis, mutation spectrum, and age at loss of ambulation. Because registrants reported differences in steroid and other medication usage, as well as age and ambulation status, we could explore these data for correlations with age at loss of ambulation. Using multivariate analysis, current steroid usage was the most significant and largest independent predictor of improved wheelchair-free survival. Thus, these online self-report data were sufficient to retrospectively observe that current steroid use by patients with DMD is associated with a delay in loss of ambulation. Comparing commonly used steroid drugs, deflazacort prolonged ambulation longer than prednisone (median 14 years and 13 years, respectively). Further, use of Vitamin D and Coenzyme Q10, insurance status, and age at diagnosis after 4 years were also significant, but smaller, independent predictors of longer wheelchair-free survival. Nine other common supplements were also individually tested but had lower study power. This study demonstrates the utility of DuchenneConnect data to observe therapeutic differences, and highlights needs for improvement in quality and quantity of patient-report data, which may allow exploration of drug/therapeutic practice combinations impractical to study in clinical trial settings. Further, with the low barrier to participation, we anticipate substantial growth in the dataset in the coming years.

Figures

Study sample selection from Duchenne Connect Registry.
Study sample selection from Duchenne Connect Registry.
Selection criteria included: an indicated diagnosis of DMD, male gender, and residence in one of the 34 Organization for Economic Co-operation and Development (OECD) countries. Of the 1,164 who met the criteria above, 107 were excluded due to concerns about data quality. 71 were excluded due to inconclusive data for the outcome variable: age at loss of ambulation. 29 subjects were excluded who first required a wheelchair more than 20 years ago, and 6 extreme outlier subjects were excluded, who reported ambulation at age 39 or above, as they are unlikely to have DMD. The final sample size was 1,057, of which 384 had reached the primary endpoint of loss of ambulation.
Age at loss of ambulation among those…
Age at loss of ambulation among those using a wheelchair fulltime.
Histogram of age at loss of ambulation for the 384 males who reached that endpoint.
Effect of steroid treatments on wheelchair-free survival.
Effect of steroid treatments on wheelchair-free survival.
Kaplan-Meier curves of wheelchair-free survival stratified by (A) steroid use category (p

References

    1. Kaplan-Meier estimates of time to loss of ambulation. P values represent the log-rank test of current steroid use plus each supplemental therapy compared to current steroids alone. Values for probability of walking through age 12 are derived from Kaplan-Meier lifetable probability estimates.
    1. Center for Disease Control and Prevention (CDC). Prevalence of Duchenne/Becker muscular dystrophy among males aged 5-24 years: four states, 2007. MMWR Morb Mortal Wkly Rep 2009;58:1119-1122.
    1. Drachman DB, Toyka KV, Myer E. Prednisone in Duchenne muscular dystrophy. Lancet 1974;2:1409-12.
    1. Drachman DB, Toyka KV, Myer E. Prednisone in Duchenne muscular dystrophy. Lancet 1974;2:1409-12.
    1. Fenichel GM, Mendell JR, Moxley III RT, et al. A comparison of daily and alternate-day prednisone therapy in the treatment of Duchenne muscular dystrophy. Archives of neurology 1991;48:575.
    1. Griggs RC, Moxley III RT, Mendell JR, et al. Prednisone in Duchenne dystrophy: a randomized, controlled trial defining the time course and dose response. Archives of neurology 1991;48:383.
    1. Griggs RC, Moxley RT, Mendell JR, et al. Duchenne dystrophy: Randomized, controlled trial of prednisone (18 months) and azathioprine (12 months). Neurology 1993;43:520.
    1. Manzur AY, Kuntzer T, Pike M, Swan A. Glucocorticoid corticosteroids for Duchenne muscular dystrophy. Cochrane database of systematic reviews 2008:CD003725.
    1. Manzur AY, Kuntzer T, Pike M, Swan AV. Glucocorticoid corticosteroids for Duchenne muscular dystrophy. The Cochrane Library 2004;2.
    1. Mendell J, Moxley R, Griggs R, et al. Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy. The New England journal of medicine 1989;320:1592.
    1. Bushby K, Muntoni F, Urtizberea A, Hughes R, Griggs R. Report on the 124th ENMC International Workshop. Treatment of Duchenne muscular dystrophy; defining the gold standards of management in the use of corticosteroids 2–4 April 2004, Naarden, The Netherlands. Neuromuscular Disorders 2004;14:526-534.
    1. Moxley RT, Ashwal S, Pandya S, et al. Practice Parameter: Corticosteroid treatment of Duchenne dystrophy: Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology 2005;64:13-20.
    1. University of Rochester, Duchenne Muscular Dystrophy: Double-blind Randomized Trial to Find Optimum Steroid Regimen, in identifier: NCT01603407. 2013: [Internet]. Bethesda (MD): National Library of Medicine (US).
    1. Griggs RC, Herr BE, Reha A, et al. Corticosteroids in duchenne muscular dystrophy: Major variations in practice. Muscle & Nerve 2013.
    1. Malik V, Rodino-Klapac LR, Mendell JR. Emerging drugs for Duchenne muscular dystrophy. Expert opinion on emerging drugs 2012;17:261-77.
    1. Rangel V, Martin AS, Peay HL. DuchenneConnect Registry Report. PLoS currents 2012;4:RRN1309.
    1. Cox DR. Regression Models and Life-Tables. J Roy Stat Soc B 1972;34:187
    1. Kaplan EL, Meier P. Nonparametric-Estimation from Incomplete Observations. J Am Stat Assoc 1958;53:457-481.
    1. Mantel N. Evaluation of survival data and two new rank order statistics arising in its consideration. Cancer chemotherapy reports. Part 1 1966;50:163-70.
    1. Mathews KD, Cunniff C, Kantamneni JR, et al. Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): case definition in surveillance for childhood-onset Duchenne/Becker muscular dystrophy. Journal of child neurology 2010;25:1098-102.
    1. Tuffery-Giraud S, Beroud C, Leturcq F, et al. Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase. Human mutation 2009;30:934-45.
    1. Aartsma-Rus A, Van Deutekom JC, Fokkema IF, Van Ommen GJ, Den Dunnen JT. Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule. Muscle Nerve 2006;34:135-44.
    1. Angelini C, Peterle E. Old and new therapeutic developments in steroid treatment in Duchenne muscular dystrophy. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2012;31:9-15.
    1. Richesson R, Sutphen R, Shereff D, Krischer J. The Rare Diseases Clinical Research Network Contact Registry update: Features and functionality. Contemporary Clinical Trials 2012.
    1. Magri F, Govoni A, D'Angelo MG, et al. Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up. Journal of neurology 2011;258:1610-23.
    1. Bach JR, Martinez D, Saulat B. Duchenne muscular dystrophy: the effect of glucocorticoids on ventilator use and ambulation. American journal of physical medicine & rehabilitation / Association of Academic Physiatrists 2010;89:620-4.
    1. Shaw RF, Dreifuss FE. Mild and severe forms of X-linked muscular dystrophy. Arch Neurol 1969;20:451-60.
    1. McDonald CM, Abresch RT, Carter GT, et al. Profiles of neuromuscular diseases. Duchenne muscular dystrophy. American journal of physical medicine & rehabilitation / Association of Academic Physiatrists 1995;74:S70-92.
    1. Matthews DJ, James KA, Miller LA, et al. Use of corticosteroids in a population-based cohort of boys with duchenne and becker muscular dystrophy. Journal of child neurology 2010;25:1319-1324.
    1. Mesa LE, Dubrovsky AL, Corderi J, Marco P, Flores D. Steroids in Duchenne muscular dystrophy--deflazacort trial. Neuromuscular disorders : NMD 1991;1:261-6.
    1. Biggar WD, Harris VA, Eliasoph L, Alman B. Long-term benefits of deflazacort treatment for boys with Duchenne muscular dystrophy in their second decade. Neuromuscular disorders : NMD 2006;16:249-55.
    1. Ricotti V, Ridout DA, Scott E, et al. Long-term benefits and adverse effects of intermittent versus daily glucocorticoids in boys with Duchenne muscular dystrophy. Journal of neurology, neurosurgery, and psychiatry 2012.
    1. Spurney CF, Rocha CT, Henricson E, et al. CINRG pilot trial of coenzyme Q10 in steroid-treated Duchenne muscular dystrophy. Muscle Nerve 2011;44:174-8.
    1. Munot P, Krishnaumar, D., Robb, S., Davies, T., Muntoni, F., Manzur, A. Prevalence of vitamin D deficiency in 157 boys with duchenne muscular dystrophy Archives of Disease in Childhood 2010;95:A10.
    1. Schoenfeld DA. Sample-size formula for the proportional-hazards regression model. Biometrics. 1983 Jun;39(2):499-503. PubMed PMID:6354290.

Source: PubMed

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