Skip Navigation

Rheumatology 2009 48(6):696-703; doi:10.1093/rheumatology/kep066
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Mugii, N.
Right arrow Articles by Takehara, K.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mugii, N.
Right arrow Articles by Takehara, K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2009. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Reduced red blood cell velocity in nail-fold capillaries as a sensitive and specific indicator of microcirculation injury in systemic sclerosis

Naoki Mugii1, Minoru Hasegawa2, Yasuhito Hamaguchi2, Chihiro Tanaka2, Kenzo Kaji2, Kazuhiro Komura2, Ikuko Ueda-Hayakawa2, Sho Horie1, Munehiro Ikuta3, Katsuhiko Tachino3, Fumihide Ogawa4, Shinichi Sato4, Manabu Fujimoto2 and Kazuhiko Takehara2

1Department of Rehabilitation, Kanazawa University Hospital, 2Department of Dermatology, 3Division of Rehabilitation Science, Kanazawa University Graduate School of Medical Science, Kanazawa and 4Department of Dermatology, Nagasaki University Graduate School of Biomedical Science, Nagasaki, Japan.

Correspondence to: Minoru Hasegawa, Department of Dermatology, Kanazawa University Graduate School of Medical Science, 13-1 Takaramachi, Kanazawa, Ishikawa 920-8641, Japan. E-mail: minoruha{at}derma.m.kanazawa-u.ac.jp


   Abstract

Objective. To assess red blood cell velocity in finger nail-fold capillaries using video capillaroscopy in patients with SSc and other collagen diseases.

Methods. This study included 127 patients with SSc as well as patients with SLE (n = 33), DM/PM (n = 21), RA (n = 13) and APS (n = 12), and 20 healthy subjects. Red blood cell velocity was evaluated using frame-to-frame determination of the position of capillary plasma gaps.

Results. The mean red blood cell velocity was significantly decreased in patients with SSc compared to healthy controls (63.0% reduction) and patients with other conditions. Mean blood velocity was similar between patients with dcSSc and lcSSc. Importantly, even SSc patients with normal or non-specific nail-fold video capillaroscopic (NVC) patterns or a scleroderma early NVC pattern exhibited a significantly lower red blood cell velocity compared to healthy controls (51.7 and 61.4% reduction, respectively) or patients with other conditions, despite normal or mild capillary changes. Patients with the scleroderma active and late NVC pattern showed a more decreased blood velocity (65.5 and 66.2% reduction, respectively). This reduced blood velocity was significantly associated with NVC findings, including capillary ramification and capillary loss. Although remarkably reduced velocity was observed in SSc patients with intractable digital ulcers (72.1% reduction), it was significantly improved by lipo-prostaglandin E1 (lipo-PGE1) infusion.

Conclusion. Our results suggest that reduced blood velocity is a hallmark of SSc. Furthermore, measurement of red blood cell velocity may be useful in evaluating therapeutic effects on microcirculation.

KEY WORDS: Systemic sclerosis, Capillaroscopy, Red blood cell velocity, Digital ulcer, Lipo-prostaglandin E1

Submitted 14 December 2008; revised version accepted 4 March 2009.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.