Literature DB >> 7738956

von Willebrand factor in juvenile dermatomyositis.

B J Bloom1, L B Tucker, L C Miller, J G Schaller.   

Abstract

OBJECTIVE: To evaluate whether plasma von Willebrand factor (vWF) levels are a useful indicator of disease activity in juvenile dermatomyositis (DM).
METHODS: Serum vWF levels were prospectively measured in 15 patients with juvenile DM and were compared to serum muscle enzyme levels, muscle strength, and presence of extramuscular manifestations.
RESULTS: 6/15 active disease periods were accompanied by an increase in vWF; 9 were not. Elevated vWF levels did not relate to the presence of active skin disease or calcinosis. vWF was not consistently related to muscle strength, CPK, or aldolase in the study group. Two patients had elevations of vWF in association with viral infections while their DM was quiescent.
CONCLUSION: An elevated vWF level is often indicative of a disease exacerbation in DM, and thus may be helpful in managing difficult cases. However, it is not consistently elevated in, nor specific for active disease in DM. It therefore cannot be recommended as a routine test in patients with DM. When used, results should be interpreted with caution.

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Year:  1995        PMID: 7738956

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   4.666


  6 in total

1.  Clinical significance of von Willebrand factor in patients with adult dermatomyositis.

Authors:  Toshiyuki Komiya; Nobuo Negoro; Kyoko Kondo; Katsuyuki Miura; Yoshio Hirota; Junichi Yoshikawa
Journal:  Clin Rheumatol       Date:  2004-11-23       Impact factor: 2.980

2.  Changes in novel biomarkers of disease activity in juvenile and adult dermatomyositis are sensitive biomarkers of disease course.

Authors:  Ann M Reed; Erik Peterson; Hatice Bilgic; Steven R Ytterberg; Shreyasee Amin; Molly S Hein; Cynthia S Crowson; Floranne Ernste; Emily Baechler Gillespie
Journal:  Arthritis Rheum       Date:  2012-12

Review 3.  The assessment and importance of disease activity versus disease damage in patients with inflammatory myopathy.

Authors:  Shabina M Sultan
Journal:  Curr Rheumatol Rep       Date:  2003-12       Impact factor: 4.592

4.  Suppression of soluble T cell-associated proteins by an anti-interferon-α monoclonal antibody in adult patients with dermatomyositis or polymyositis.

Authors:  Xiang Guo; Brandon W Higgs; Marlon Rebelatto; Wei Zhu; Warren Greth; Yihong Yao; Lorin K Roskos; Wendy I White
Journal:  Rheumatology (Oxford)       Date:  2013-12-19       Impact factor: 7.580

Review 5.  Systemic and Tissue Inflammation in Juvenile Dermatomyositis: From Pathogenesis to the Quest for Monitoring Tools.

Authors:  Judith Wienke; Claire T Deakin; Lucy R Wedderburn; Femke van Wijk; Annet van Royen-Kerkhof
Journal:  Front Immunol       Date:  2018-12-18       Impact factor: 7.561

Review 6.  Consensus-based recommendations for the management of juvenile dermatomyositis.

Authors:  Felicitas Bellutti Enders; Brigitte Bader-Meunier; Eileen Baildam; Tamas Constantin; Pavla Dolezalova; Brian M Feldman; Pekka Lahdenne; Bo Magnusson; Kiran Nistala; Seza Ozen; Clarissa Pilkington; Angelo Ravelli; Ricardo Russo; Yosef Uziel; Marco van Brussel; Janjaap van der Net; Sebastiaan Vastert; Lucy R Wedderburn; Nicolaas Wulffraat; Liza J McCann; Annet van Royen-Kerkhof
Journal:  Ann Rheum Dis       Date:  2016-08-11       Impact factor: 19.103

  6 in total

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