Literature DB >> 24419752

Myopathy in scleroderma, its identification, prevalence, and treatment: lessons learned from cohort studies.

Julie J Paik1, Andrew L Mammen, Fredrick M Wigley, Allan C Gelber.   

Abstract

PURPOSE OF REVIEW: This review discusses the characterization of myopathy in scleroderma with a focus on new developments in imaging, biomarkers, and therapy, and details several current reports and several seminal reports prior to 2012. RECENT
FINDINGS: In the past year, studies have shown that MRI techniques highlight the importance of muscle edema in scleroderma, and that aldolase may be a useful biomarker to predict incident myopathy. When compared to studies preceding 2012, both the current and prior reports too often fail to account for the full spectrum of muscle disease in scleroderma. There remain no uniform classification criteria that are routinely integrated into clinical research reports. Thus, important questions remain to be answered, including risk factors for developing myopathy, optimal screening and diagnostic strategies, and efficacious therapies. But, just as important is the priority to systematically define what the true entity(ies) of myopathy is in scleroderma.
SUMMARY: Scleroderma myopathy is a heterogeneous group of muscle disorders among patients with underlying scleroderma which requires robust studies to clarify the full spectrum of disease.

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Year:  2014        PMID: 24419752     DOI: 10.1097/BOR.0000000000000024

Source DB:  PubMed          Journal:  Curr Opin Rheumatol        ISSN: 1040-8711            Impact factor:   5.006


  5 in total

1.  Histopathological findings in systemic sclerosis-related myopathy: fibrosis and microangiopathy with lack of cellular inflammation.

Authors:  Claudio Corallo; Maurizio Cutolo; Nila Volpi; Daniela Franci; Margherita Aglianò; Antonio Montella; Chiara Chirico; Stefano Gonnelli; Ranuccio Nuti; Nicola Giordano
Journal:  Ther Adv Musculoskelet Dis       Date:  2016-10-03       Impact factor: 5.346

2.  Dystrophic calcification in muscles of legs in calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome: Accurate evaluation of the extent with (99m)Tc-methylene diphosphonate single photon emission computed tomography/computed tomography.

Authors:  Partha Sarathi Chakraborty; Sellam Karunanithi; Varun Singh Dhull; Kunal Kumar; Madhavi Tripathi
Journal:  Indian J Nucl Med       Date:  2015 Oct-Dec

3.  Whole-body MRI for full assessment and characterization of diffuse inflammatory myopathy.

Authors:  Saleh Saleh Elessawy; Eman Muhammad Abdelsalam; Eman Abdel Razek; Samar Tharwat
Journal:  Acta Radiol Open       Date:  2016-09-21

Review 4.  The Involvement of Smooth Muscle, Striated Muscle, and the Myocardium in Scleroderma: A Review.

Authors:  Ioana Bratoiu; Alexandra Maria Burlui; Anca Cardoneanu; Luana Andreea Macovei; Patricia Richter; Gabriela Rusu-Zota; Ciprian Rezus; Minerva Codruta Badescu; Andreea Szalontay; Elena Rezus
Journal:  Int J Mol Sci       Date:  2022-10-09       Impact factor: 6.208

5.  Myopathy is a Risk Factor for Poor Prognosis of Patients with Systemic Sclerosis: A retrospective cohort study.

Authors:  Meiju Zhou; Lichun Jiang; Liuyan Nie; Ting Chen; Ting Zhang; Wenjia Sun; Joshua Sutikno; Yan Du; Jing Xue
Journal:  Medicine (Baltimore)       Date:  2020-08-14       Impact factor: 1.817

  5 in total

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