Evaluation of the effect of ambrisentan on digital microvascular flow in patients with systemic sclerosis using laser Doppler perfusion imaging: a 12-week randomized double-blind placebo controlled trial
Autor: | Nilanjana Bose, James Bena, Soumya Chatterjee |
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Rok vydání: | 2014 |
Předmět: |
Male
Time Factors Placebo-controlled study Perfusion scanning Pilot Projects law.invention 0302 clinical medicine Randomized controlled trial law Laser-Doppler Flowmetry Immunology and Allergy 030212 general & internal medicine Prospective Studies skin and connective tissue diseases integumentary system Phenylpropionates Laser Doppler velocimetry Middle Aged 3. Good health Pyridazines Cardiology Female Endothelin receptor medicine.drug Research Article Adult medicine.medical_specialty Ambrisentan Perfusion Imaging Immunology Ischemia Fingers 03 medical and health sciences Young Adult Rheumatology Double-Blind Method Internal medicine medicine Humans Aged 030203 arthritis & rheumatology Scleroderma Systemic Dose-Response Relationship Drug business.industry Microcirculation Blood flow medicine.disease Surgery Regional Blood Flow business Follow-Up Studies |
Zdroj: | Arthritis Research & Therapy |
ISSN: | 1478-6362 |
Popis: | Introduction In patients with systemic sclerosis (SSc), digital ischemia results from an occlusive microvasculopathy that may not respond adequately to conventional vasodilators. Endothelin receptor antagonists can potentially modify the fibroproliferative vascular remodeling in SSc, and hence their use may be justified in the management of digital ischemia. The objective of this clinical trial was to evaluate the effect of ambrisentan, a selective endothelin type A receptor antagonist, on microvascular blood flow in patients with limited systemic sclerosis (SSc) using laser Doppler perfusion imaging (LDPI). Methods In this randomized, double-blind, placebo controlled study we enrolled 20 patients with limited SSc. Fifteen patients received ambrisentan 5 mg daily for one month and then 10 mg daily for two months, and five received a placebo. There were three visits: weeks 0 (baseline), one and 12. Three patient-oriented questionnaires were completed at each visit: Scleroderma-Health Assessment Questionnaire (S-HAQ), Raynaud Condition Score (RCS), and Pain-Visual Analog Scale (P-VAS). At each visit, LDPI was used to obtain three blood flow readings involving regions of interest in second to fifth fingers of the non-dominant hand at room temperature (25°C) and after cooling (10°C) for two minutes. Results There were 16 females (80%); mean age was 50 years. None of the differences in blood flow (as measured by LDPI) were significant both at baseline and after cooling. However, patients in the ambrisentan group showed significant improvement in the patient-oriented outcomes: RCS (P = 0.001) and S-HAQ score (P = 0.005). Conclusions This pilot study did not show evidence of significant increase in digital blood flow over time; however, there was an improvement in RCS and S-HAQ score. We conclude that continuous use of ambrisentan for three months does not seem to significantly improve digital blood flow in SSc patients. Trial registration Clinicaltrials.gov NCT01072669. Registered 19 February 2010. Electronic supplementary material The online version of this article (doi:10.1186/s13075-015-0558-9) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
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