Literature DB >> 29733899

Cataract development associated with long-term glucocorticoid therapy in Duchenne muscular dystrophy patients.

Melissa L Rice1, Brenda Wong2, Paul S Horn2, Michael B Yang3.   

Abstract

PURPOSE: To evaluate the development of cataracts or elevated intraocular pressure (IOP) in patients with Duchenne muscular dystrophy (DMD) on long-term glucocorticoid (GC) treatment.
METHODS: The medical records of DMD patients evaluated from 2010 to 2015 at a single center were reviewed retrospectively. The main outcome measures were prevalence of cataracts and elevated IOP, age of first detection of cataract, time from initial steroid use to first detection of cataract, and relative risk of cataract development for deflazacort versus prednisone treatment.
RESULTS: Of 596 DMD patients, 514 underwent GC therapy; all but one was male. The racial distribution was 82.1% white, 1.0% African American, 5.0% Hispanic, 2.9% Asian, and 8.0% more than one race or "other." The prevalence of cataracts was 22.4% in patients on GC therapy. The mean age at which cataract formation was first documented was 12.9 ± 4.1 years (IQR, 9.6-14.6). The mean time from initial steroid use to the first detection of cataract was 6.5 ± 3.6 years (IQR, 4.0-8.6). The odds of cataract development were 2.4-fold higher for patients on deflazacort compared with prednisone (95% CI, 1.3-4.5; P = 0.004). Only 7 patients (1.4%) underwent cataract surgery, at a mean age of 16.9 years (range, 10.7-24.6 years); all were on deflazacort. Among patients with available intraocular pressure measurements, elevated IOP occurred in only 1 patient (1.1%), who was on deflazacort.
CONCLUSIONS: In patients undergoing GC therapy for DMD, the rate of cataract formation was slow and well tolerated, with a higher risk among deflazacort patients. The percentage of patients requiring cataract extraction or with elevated IOP was very small. These findings suggest that a schedule of annual eye examinations is appropriate.
Copyright © 2018 American Association for Pediatric Ophthalmology and Strabismus. Published by Elsevier Inc. All rights reserved.

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Year:  2018        PMID: 29733899     DOI: 10.1016/j.jaapos.2018.01.017

Source DB:  PubMed          Journal:  J AAPOS        ISSN: 1091-8531            Impact factor:   1.220


  6 in total

1.  Cataract development associated with long-term glucocorticoid therapy in Duchenne muscular dystrophy patients.

Authors:  Tuy Nga Brignol; Patrice E Fort; Dora Fix Ventura; Ramin Tadayoni; Alvaro Rendon
Journal:  J AAPOS       Date:  2018-09-26       Impact factor: 1.220

2.  Single-transcript multiplex in situ hybridisation reveals unique patterns of dystrophin isoform expression in the developing mammalian embryo.

Authors:  John C W Hildyard; Abbe H Crawford; Faye Rawson; Dominique O Riddell; Rachel C M Harron; Richard J Piercy
Journal:  Wellcome Open Res       Date:  2020-07-20

Review 3.  Evidence of Polyphenols Efficacy against Dry Eye Disease.

Authors:  Gaia Favero; Enrico Moretti; Kristína Krajčíková; Vladimíra Tomečková; Rita Rezzani
Journal:  Antioxidants (Basel)       Date:  2021-01-28

Review 4.  Comparing Deflazacort and Prednisone in Duchenne Muscular Dystrophy.

Authors:  W Douglas Biggar; Andrew Skalsky; Craig M McDonald
Journal:  J Neuromuscul Dis       Date:  2022

5.  Olive Pomace Phenolic Compounds: From an Agro-Industrial By-Product to a Promising Ocular Surface Protection for Dry Eye Disease.

Authors:  Nikolaos Katsinas; Uta Gehlsen; Laura García-Posadas; Soraya Rodríguez-Rojo; Philipp Steven; María J González-García; Amalia Enríquez-de-Salamanca
Journal:  J Clin Med       Date:  2022-08-11       Impact factor: 4.964

6.  Panel-based targeted exome sequencing reveals novel candidate susceptibility loci for age-related cataracts in Chinese Cohort.

Authors:  Jian-Kang Li; Li-Li Li; Wei Li; Zi-Wei Wang; Feng-Juan Gao; Fang-Yuan Hu; Sheng-Hai Zhang; Shou-Fang Qu; Jie Huang; Lu-Sheng Wang; Ji-Hong Wu; Fang Chen
Journal:  Mol Genet Genomic Med       Date:  2020-04-26       Impact factor: 2.183

  6 in total

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