Literature DB >> 19487218

Digital ulcers: overt vascular disease in systemic sclerosis.

V Steen1, C P Denton, J E Pope, M Matucci-Cerinic.   

Abstract

RP is an almost universal manifestation of SSc, with 95% of all patients being affected, and resulting in digital ulcers (DUs) in approximately 30% of the patients each year. DUs are a major clinical problem, being associated with substantial morbidity (reduced quality of life, pain, disability and disfigurement) that can escalate to gangrene and amputation. Ideally, the treatment of DUs would improve tissue integrity and viability, promote ulcer healing and reduce the formation of new ulcers. Treatments that have shown potential include calcium channel blockers, prostacyclin analogues and endothelin receptor antagonists. However, until recently, management was based on empirical experience. The recent approval (in Europe) of the dual endothelin receptor antagonist, bosentan, to reduce the number of new DUs in patients with SSc and ongoing DU disease, means that there is now an approved therapy--and new hope--for the treatment of DUs in these severely afflicted patients.

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Year:  2009        PMID: 19487218     DOI: 10.1093/rheumatology/kep105

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  49 in total

1.  Management of digital vasculopathy in systemic sclerosis: benefits of multiple courses of endothelin-1 receptor antagonists.

Authors:  Tanaka Ngcozana; Voon Ong; Christopher Paul Denton
Journal:  BMJ Case Rep       Date:  2014-03-28

2.  [Critical limb ischemia in systemic sclerosis].

Authors:  M O Becker; G Riemekasten
Journal:  Z Rheumatol       Date:  2012-06       Impact factor: 1.372

3.  Serum Soluble CD163 and its association with various disease parameters in patients with systemic sclerosis.

Authors:  Waleed Ahmed Salah Eldeen Hassan; Eman Abd Elaleem Baraka; Basant Mohammed Elnady; Tahany Mahmoud Gouda; Nehad Fouad
Journal:  Eur J Rheumatol       Date:  2016-09-01

4.  An Update on the Treatment of the Cutaneous Manifestations of Systemic Sclerosis: The Dermatologist's Point of View.

Authors:  Magalys Vitiello; Adriana Abuchar; Néstor Santana; Luis Dehesa; Francisco A Kerdel
Journal:  J Clin Aesthet Dermatol       Date:  2012-07

5.  Severe vascular complications in patients affected by systemic sclerosis cyclically treated with iloprost.

Authors:  Paola Caramaschi; Alessandra Dalla Gassa; Daniele Prati; Giovanni Barausse; Ilaria Tinazzi; Viviana Ravagnani; Silvia Confente; Domenico Biasi
Journal:  Rheumatol Int       Date:  2011-03-30       Impact factor: 2.631

6.  Malnutrition, associated clinical factors, and depression in systemic sclerosis: a cross-sectional study.

Authors:  İpek Türk; Nihan Cüzdan; Volkan Çiftçi; Didem Arslan; Muharrem Cem Doğan; İlker Unal
Journal:  Clin Rheumatol       Date:  2019-05-26       Impact factor: 2.980

Review 7.  Raynaud phenomenon and digital ulcers in systemic sclerosis.

Authors:  Michael Hughes; Yannick Allanore; Lorinda Chung; John D Pauling; Christopher P Denton; Marco Matucci-Cerinic
Journal:  Nat Rev Rheumatol       Date:  2020-02-25       Impact factor: 20.543

8.  The critical need for accurately defining digital ulcers in scleroderma.

Authors:  Wendy Li; Tracy M Frech
Journal:  J Scleroderma Relat Disord       Date:  2017-05-19

9.  Registry evaluation of digital ulcers in systemic sclerosis.

Authors:  Felice Galluccio; Marco Matucci-Cerinic
Journal:  Int J Rheumatol       Date:  2010-08-25

10.  Interferon-γ promotes vascular remodeling in human microvascular endothelial cells by upregulating endothelin (ET)-1 and transforming growth factor (TGF) β2.

Authors:  Izabela Chrobak; Stefania Lenna; Lukasz Stawski; Maria Trojanowska
Journal:  J Cell Physiol       Date:  2013-08       Impact factor: 6.384

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