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The fibrinolytic system components are increased in systemic sclerosis and modulated by Alprostadil (alpha1 ciclodestryn)

To evaluate urokinase plasminogen activator (u-PA), urokinase plasminogen activator soluble receptor (su-PAR), plasminogen activator inhibitor 1 (PAI-1) and tissue plasminogen activator (t-PA) plasma levels in SSc patients (pts) versus healthy controls and their modulation by intravenous alphacyclod...

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Published in:Clinical and experimental rheumatology 2005-09, Vol.23 (5), p.671-677
Main Authors: BANDINELLI, F, BARTOLI, F, GIACOMELLI, R, BONGI, S. Maddali, ABBATE, R, DEL ROSSO, M, CERINIC, M. Matucci, PERFETTO, F, DEL ROSSO, A, MOGGI-PIGNONE, A, GUIDUCCI, S, CINELLI, M, FATINI, C, GENERINI, S, GABRIELLI, A
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container_issue 5
container_start_page 671
container_title Clinical and experimental rheumatology
container_volume 23
creator BANDINELLI, F
BARTOLI, F
GIACOMELLI, R
BONGI, S. Maddali
ABBATE, R
DEL ROSSO, M
CERINIC, M. Matucci
PERFETTO, F
DEL ROSSO, A
MOGGI-PIGNONE, A
GUIDUCCI, S
CINELLI, M
FATINI, C
GENERINI, S
GABRIELLI, A
description To evaluate urokinase plasminogen activator (u-PA), urokinase plasminogen activator soluble receptor (su-PAR), plasminogen activator inhibitor 1 (PAI-1) and tissue plasminogen activator (t-PA) plasma levels in SSc patients (pts) versus healthy controls and their modulation by intravenous alphacyclodestrine (Alprostadil). Plasma levels of u-PA, su-PAR, PAI-1 and t-PA were measured in 40 SSc (34 lSSc and 6 dSSc) pts and in 30 healthy controls. In SSc, blood was drawn before and after 3 consecutive daily of Alprostadil infusion (60 mg in 250 cc NaCl 0.9%). In SSc su-PAR basal levels were higher than controls (7.48 +/- 2.5 vs 4.69 +/- 0.4 ng/ml; p = 0.001) and were significantly reduced by Alprostadil (5.93 +/- 1.7; p = 0.002), but remain higher than controls (p = 0.03). u-PA basal levels were higher than controls (3.78 +/- 1.5 vs 1.29 +/- 0.3 ng/ml; p < 0.001) and were reduced by Alprostadil (2.39 +/- 1.7; p < 0.001) to control levels. SSc PAI-1 basal levels were lower than controls (31.60 +/- 7.7 vs 48.30 +/- 6.8 ng/ml; p < 0.001) and increased by Alprostadil (34.66 +/- 5.4; p = 0.04), but lower than controls (p < 0.001). SSc t-PA basal levels were higher in respect to controls (1645.81 +/- 792.7 vs 571.95 +/- 75.5 pg/ml; p < 0.0001) and reduced by Alprostadil (1318.06 +/- 603.5; p = 0.04), but still higher than controls (p = 0.001). Fibrinolysis were increased in SSc. Infusions of Alprostadil modulate u-PA, su-PAR, PAI-1 and t-PA, restoring near normal levels. In SSc, fibrinolysis system may become a potential target for new therapies.
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Maddali ; ABBATE, R ; DEL ROSSO, M ; CERINIC, M. Matucci ; PERFETTO, F ; DEL ROSSO, A ; MOGGI-PIGNONE, A ; GUIDUCCI, S ; CINELLI, M ; FATINI, C ; GENERINI, S ; GABRIELLI, A</creator><creatorcontrib>BANDINELLI, F ; BARTOLI, F ; GIACOMELLI, R ; BONGI, S. Maddali ; ABBATE, R ; DEL ROSSO, M ; CERINIC, M. Matucci ; PERFETTO, F ; DEL ROSSO, A ; MOGGI-PIGNONE, A ; GUIDUCCI, S ; CINELLI, M ; FATINI, C ; GENERINI, S ; GABRIELLI, A</creatorcontrib><description>To evaluate urokinase plasminogen activator (u-PA), urokinase plasminogen activator soluble receptor (su-PAR), plasminogen activator inhibitor 1 (PAI-1) and tissue plasminogen activator (t-PA) plasma levels in SSc patients (pts) versus healthy controls and their modulation by intravenous alphacyclodestrine (Alprostadil). Plasma levels of u-PA, su-PAR, PAI-1 and t-PA were measured in 40 SSc (34 lSSc and 6 dSSc) pts and in 30 healthy controls. In SSc, blood was drawn before and after 3 consecutive daily of Alprostadil infusion (60 mg in 250 cc NaCl 0.9%). In SSc su-PAR basal levels were higher than controls (7.48 +/- 2.5 vs 4.69 +/- 0.4 ng/ml; p = 0.001) and were significantly reduced by Alprostadil (5.93 +/- 1.7; p = 0.002), but remain higher than controls (p = 0.03). u-PA basal levels were higher than controls (3.78 +/- 1.5 vs 1.29 +/- 0.3 ng/ml; p &lt; 0.001) and were reduced by Alprostadil (2.39 +/- 1.7; p &lt; 0.001) to control levels. SSc PAI-1 basal levels were lower than controls (31.60 +/- 7.7 vs 48.30 +/- 6.8 ng/ml; p &lt; 0.001) and increased by Alprostadil (34.66 +/- 5.4; p = 0.04), but lower than controls (p &lt; 0.001). SSc t-PA basal levels were higher in respect to controls (1645.81 +/- 792.7 vs 571.95 +/- 75.5 pg/ml; p &lt; 0.0001) and reduced by Alprostadil (1318.06 +/- 603.5; p = 0.04), but still higher than controls (p = 0.001). Fibrinolysis were increased in SSc. 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Maddali</creatorcontrib><creatorcontrib>ABBATE, R</creatorcontrib><creatorcontrib>DEL ROSSO, M</creatorcontrib><creatorcontrib>CERINIC, M. Matucci</creatorcontrib><creatorcontrib>PERFETTO, F</creatorcontrib><creatorcontrib>DEL ROSSO, A</creatorcontrib><creatorcontrib>MOGGI-PIGNONE, A</creatorcontrib><creatorcontrib>GUIDUCCI, S</creatorcontrib><creatorcontrib>CINELLI, M</creatorcontrib><creatorcontrib>FATINI, C</creatorcontrib><creatorcontrib>GENERINI, S</creatorcontrib><creatorcontrib>GABRIELLI, A</creatorcontrib><title>The fibrinolytic system components are increased in systemic sclerosis and modulated by Alprostadil (alpha1 ciclodestryn)</title><title>Clinical and experimental rheumatology</title><addtitle>Clin Exp Rheumatol</addtitle><description>To evaluate urokinase plasminogen activator (u-PA), urokinase plasminogen activator soluble receptor (su-PAR), plasminogen activator inhibitor 1 (PAI-1) and tissue plasminogen activator (t-PA) plasma levels in SSc patients (pts) versus healthy controls and their modulation by intravenous alphacyclodestrine (Alprostadil). Plasma levels of u-PA, su-PAR, PAI-1 and t-PA were measured in 40 SSc (34 lSSc and 6 dSSc) pts and in 30 healthy controls. In SSc, blood was drawn before and after 3 consecutive daily of Alprostadil infusion (60 mg in 250 cc NaCl 0.9%). In SSc su-PAR basal levels were higher than controls (7.48 +/- 2.5 vs 4.69 +/- 0.4 ng/ml; p = 0.001) and were significantly reduced by Alprostadil (5.93 +/- 1.7; p = 0.002), but remain higher than controls (p = 0.03). u-PA basal levels were higher than controls (3.78 +/- 1.5 vs 1.29 +/- 0.3 ng/ml; p &lt; 0.001) and were reduced by Alprostadil (2.39 +/- 1.7; p &lt; 0.001) to control levels. SSc PAI-1 basal levels were lower than controls (31.60 +/- 7.7 vs 48.30 +/- 6.8 ng/ml; p &lt; 0.001) and increased by Alprostadil (34.66 +/- 5.4; p = 0.04), but lower than controls (p &lt; 0.001). SSc t-PA basal levels were higher in respect to controls (1645.81 +/- 792.7 vs 571.95 +/- 75.5 pg/ml; p &lt; 0.0001) and reduced by Alprostadil (1318.06 +/- 603.5; p = 0.04), but still higher than controls (p = 0.001). Fibrinolysis were increased in SSc. Infusions of Alprostadil modulate u-PA, su-PAR, PAI-1 and t-PA, restoring near normal levels. 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Matucci</au><au>PERFETTO, F</au><au>DEL ROSSO, A</au><au>MOGGI-PIGNONE, A</au><au>GUIDUCCI, S</au><au>CINELLI, M</au><au>FATINI, C</au><au>GENERINI, S</au><au>GABRIELLI, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The fibrinolytic system components are increased in systemic sclerosis and modulated by Alprostadil (alpha1 ciclodestryn)</atitle><jtitle>Clinical and experimental rheumatology</jtitle><addtitle>Clin Exp Rheumatol</addtitle><date>2005-09-01</date><risdate>2005</risdate><volume>23</volume><issue>5</issue><spage>671</spage><epage>677</epage><pages>671-677</pages><issn>0392-856X</issn><eissn>1593-098X</eissn><abstract>To evaluate urokinase plasminogen activator (u-PA), urokinase plasminogen activator soluble receptor (su-PAR), plasminogen activator inhibitor 1 (PAI-1) and tissue plasminogen activator (t-PA) plasma levels in SSc patients (pts) versus healthy controls and their modulation by intravenous alphacyclodestrine (Alprostadil). Plasma levels of u-PA, su-PAR, PAI-1 and t-PA were measured in 40 SSc (34 lSSc and 6 dSSc) pts and in 30 healthy controls. In SSc, blood was drawn before and after 3 consecutive daily of Alprostadil infusion (60 mg in 250 cc NaCl 0.9%). In SSc su-PAR basal levels were higher than controls (7.48 +/- 2.5 vs 4.69 +/- 0.4 ng/ml; p = 0.001) and were significantly reduced by Alprostadil (5.93 +/- 1.7; p = 0.002), but remain higher than controls (p = 0.03). u-PA basal levels were higher than controls (3.78 +/- 1.5 vs 1.29 +/- 0.3 ng/ml; p &lt; 0.001) and were reduced by Alprostadil (2.39 +/- 1.7; p &lt; 0.001) to control levels. SSc PAI-1 basal levels were lower than controls (31.60 +/- 7.7 vs 48.30 +/- 6.8 ng/ml; p &lt; 0.001) and increased by Alprostadil (34.66 +/- 5.4; p = 0.04), but lower than controls (p &lt; 0.001). SSc t-PA basal levels were higher in respect to controls (1645.81 +/- 792.7 vs 571.95 +/- 75.5 pg/ml; p &lt; 0.0001) and reduced by Alprostadil (1318.06 +/- 603.5; p = 0.04), but still higher than controls (p = 0.001). Fibrinolysis were increased in SSc. Infusions of Alprostadil modulate u-PA, su-PAR, PAI-1 and t-PA, restoring near normal levels. In SSc, fibrinolysis system may become a potential target for new therapies.</abstract><cop>Pisa</cop><pub>Clinical and Experimental Rheumatology</pub><pmid>16173244</pmid><tpages>7</tpages></addata></record>
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identifier ISSN: 0392-856X
ispartof Clinical and experimental rheumatology, 2005-09, Vol.23 (5), p.671-677
issn 0392-856X
1593-098X
language eng
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source World Web Science Journals
subjects Aged
Alprostadil - pharmacology
Alprostadil - therapeutic use
Biological and medical sciences
Diseases of the osteoarticular system
Female
Fibrinolysis - drug effects
Fibrinolytic Agents - pharmacology
Fibrinolytic Agents - therapeutic use
Humans
Male
Medical sciences
Middle Aged
Plasminogen Activator Inhibitor 1 - blood
Receptors, Cell Surface - blood
Receptors, Urokinase Plasminogen Activator
Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
Scleroderma, Systemic - blood
Scleroderma, Systemic - drug therapy
Tissue Plasminogen Activator - blood
Urokinase-Type Plasminogen Activator - blood
title The fibrinolytic system components are increased in systemic sclerosis and modulated by Alprostadil (alpha1 ciclodestryn)
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