Impaired fibrinolysis and insulin resistance in patients with hypertension

Plasma plasminogen activator inhibitor type 1 (PAI-1) and tissue plasminogen activator (tPA) antigens and activities were measured in 28 patients with hypertension and 12 normal controls. Steady state plasma glucose (SSPG) concentrations were also determined after an infusion of somatostatin, insuli...

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Veröffentlicht in:American journal of hypertension 1996-05, Vol.9 (5), p.484-490
Hauptverfasser: Jeng, Jing-R., Sheu, Wayne H.-H., Jeng, Chii-Y., Huang, Shyuh-H., Shieh, Shyh-M.
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container_end_page 490
container_issue 5
container_start_page 484
container_title American journal of hypertension
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creator Jeng, Jing-R.
Sheu, Wayne H.-H.
Jeng, Chii-Y.
Huang, Shyuh-H.
Shieh, Shyh-M.
description Plasma plasminogen activator inhibitor type 1 (PAI-1) and tissue plasminogen activator (tPA) antigens and activities were measured in 28 patients with hypertension and 12 normal controls. Steady state plasma glucose (SSPG) concentrations were also determined after an infusion of somatostatin, insulin and glucose. Patients with hypertension were further subdivided into two groups: insulin resistance (SSPG > 190 mg/dL, n = 14) and no insulin resistance (SSPG < 190 mg/dL, n = 14). As compared to normal controls, hypertensive patients, either with or without insulin resistance, had significant ( P < .005) increases in PAI-1 activity (18.6 ± 1.3 ν 8.1 ± 0.8 IU/mL), PAI-1 antigen (31.1 ± 2.0 ν 12.7 ± 0.9 ng/mL) and tPA antigen (15.5 ± 0.9 ν 8.8 ± 0.9 ng/mL), and significant decrease in tPA activity (0.43 ± 0.05 ν 1.02 ± 0.16 IU/mL) than normotensive controls. Furthermore, hypertensive patients with insulin resistance had significantly higher PAI-1 activity (22.0 ± 2.2 ν 15.3 ± 0.8 IU/mL, P = .006) and tPA antigen (17.4 ± 1.2 ν 13.6 ± 1.3 ng/mL, P = .02) than did hypertensive patients without insulin resistance. However, PAI-1 antigen was insignificantly higher (34.1 ± 2.9 ν 28.1 ± 2.4 ng/mL, P = .06) and tPA activity insignificantly lower (0.42 ± 0.08 ν 0.43 ± 0.08 IU/mL, P = .45) in hypertensive patients with insulin resistance than in those without insulin resistance. In addition, PAI-1 activity and tPA antigen were significantly correlated with blood pressure, SSPG, triglyceride, HDL-cholesterol and integrated glucose response to an oral load of 75 g glucose. Thus, patients with hypertension have impaired fibrinolytic activity due to increased PAI-1 when compared to normotensive controls, and the magnitude of this fibrinolytic defect is greater in hypertensive patients who have insulin resistance. Insulin resistance with associated metabolic abnormalities may be one of the causes for impaired fibrinolysis in hypertension.
doi_str_mv 10.1016/0895-7061(95)00442-4
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Steady state plasma glucose (SSPG) concentrations were also determined after an infusion of somatostatin, insulin and glucose. Patients with hypertension were further subdivided into two groups: insulin resistance (SSPG &gt; 190 mg/dL, n = 14) and no insulin resistance (SSPG &lt; 190 mg/dL, n = 14). As compared to normal controls, hypertensive patients, either with or without insulin resistance, had significant ( P &lt; .005) increases in PAI-1 activity (18.6 ± 1.3 ν 8.1 ± 0.8 IU/mL), PAI-1 antigen (31.1 ± 2.0 ν 12.7 ± 0.9 ng/mL) and tPA antigen (15.5 ± 0.9 ν 8.8 ± 0.9 ng/mL), and significant decrease in tPA activity (0.43 ± 0.05 ν 1.02 ± 0.16 IU/mL) than normotensive controls. Furthermore, hypertensive patients with insulin resistance had significantly higher PAI-1 activity (22.0 ± 2.2 ν 15.3 ± 0.8 IU/mL, P = .006) and tPA antigen (17.4 ± 1.2 ν 13.6 ± 1.3 ng/mL, P = .02) than did hypertensive patients without insulin resistance. However, PAI-1 antigen was insignificantly higher (34.1 ± 2.9 ν 28.1 ± 2.4 ng/mL, P = .06) and tPA activity insignificantly lower (0.42 ± 0.08 ν 0.43 ± 0.08 IU/mL, P = .45) in hypertensive patients with insulin resistance than in those without insulin resistance. In addition, PAI-1 activity and tPA antigen were significantly correlated with blood pressure, SSPG, triglyceride, HDL-cholesterol and integrated glucose response to an oral load of 75 g glucose. Thus, patients with hypertension have impaired fibrinolytic activity due to increased PAI-1 when compared to normotensive controls, and the magnitude of this fibrinolytic defect is greater in hypertensive patients who have insulin resistance. 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Steady state plasma glucose (SSPG) concentrations were also determined after an infusion of somatostatin, insulin and glucose. Patients with hypertension were further subdivided into two groups: insulin resistance (SSPG &gt; 190 mg/dL, n = 14) and no insulin resistance (SSPG &lt; 190 mg/dL, n = 14). As compared to normal controls, hypertensive patients, either with or without insulin resistance, had significant ( P &lt; .005) increases in PAI-1 activity (18.6 ± 1.3 ν 8.1 ± 0.8 IU/mL), PAI-1 antigen (31.1 ± 2.0 ν 12.7 ± 0.9 ng/mL) and tPA antigen (15.5 ± 0.9 ν 8.8 ± 0.9 ng/mL), and significant decrease in tPA activity (0.43 ± 0.05 ν 1.02 ± 0.16 IU/mL) than normotensive controls. Furthermore, hypertensive patients with insulin resistance had significantly higher PAI-1 activity (22.0 ± 2.2 ν 15.3 ± 0.8 IU/mL, P = .006) and tPA antigen (17.4 ± 1.2 ν 13.6 ± 1.3 ng/mL, P = .02) than did hypertensive patients without insulin resistance. However, PAI-1 antigen was insignificantly higher (34.1 ± 2.9 ν 28.1 ± 2.4 ng/mL, P = .06) and tPA activity insignificantly lower (0.42 ± 0.08 ν 0.43 ± 0.08 IU/mL, P = .45) in hypertensive patients with insulin resistance than in those without insulin resistance. In addition, PAI-1 activity and tPA antigen were significantly correlated with blood pressure, SSPG, triglyceride, HDL-cholesterol and integrated glucose response to an oral load of 75 g glucose. Thus, patients with hypertension have impaired fibrinolytic activity due to increased PAI-1 when compared to normotensive controls, and the magnitude of this fibrinolytic defect is greater in hypertensive patients who have insulin resistance. Insulin resistance with associated metabolic abnormalities may be one of the causes for impaired fibrinolysis in hypertension.</description><subject>Adult</subject><subject>Aged</subject><subject>Arterial hypertension. 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Etiology</subject><subject>Female</subject><subject>Fibrinolysis - physiology</subject><subject>glucose intolerance</subject><subject>Glucose Tolerance Test</subject><subject>Humans</subject><subject>hypertension</subject><subject>Hypertension - blood</subject><subject>Hypertension - physiopathology</subject><subject>Insulin - blood</subject><subject>insulin resistance</subject><subject>Insulin Resistance - physiology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Plasminogen activator inhibitor</subject><subject>Plasminogen Activator Inhibitor 1 - metabolism</subject><subject>tissue plasminogen activator</subject><subject>Tissue Plasminogen Activator - metabolism</subject><subject>Triglycerides - blood</subject><issn>0895-7061</issn><issn>1879-1905</issn><issn>1941-7225</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2LFDEQhoMo67j6DxT7IKKH1qTzfRFk2HVXRlRQWLyEdLqaydqTbpO0Ov_ejD2MN08FVc9bUE8h9JjgVwQT8RorzWuJBXmh-UuMGWtqdgetiJK6Jhrzu2h1Qu6jBynd4kIJQc7QmZKUE4VX6P31brI-Qlf1vo0-jMM--VTZ0FU-pHnwoYpQOtkGB6VVTTZ7CDlVv3zeVtv9BDFDSH4MD9G93g4JHh3rOfp6efFlfVVvPr67Xr_d1I5plmvLWm21bqQgtlFCtpTZ1qqeM8J6B5brrtcEJNOgO9dAq4SjHLctbVlPQdFz9HzZO8Xxxwwpm51PDobBBhjnZKRqiKaMF5AtoItjShF6M0W_s3FvCDYHhebgxxz8mFL_KjSsxJ4c98_tDrpT6OiszJ8d5zY5O_SxqPHphFFcjhKyYE8XLNg8RzjN7e2WaC24LkS9EEUv_P4HxO-m5CU3VzffzPqGfv70gW_MpvBvFh6K3Z8eokmu_MJBVx7osulG___L_gBg06gc</recordid><startdate>19960501</startdate><enddate>19960501</enddate><creator>Jeng, Jing-R.</creator><creator>Sheu, Wayne H.-H.</creator><creator>Jeng, Chii-Y.</creator><creator>Huang, Shyuh-H.</creator><creator>Shieh, Shyh-M.</creator><general>Elsevier Inc</general><general>Oxford University Press</general><general>Elsevier Science</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19960501</creationdate><title>Impaired fibrinolysis and insulin resistance in patients with hypertension</title><author>Jeng, Jing-R. ; Sheu, Wayne H.-H. ; Jeng, Chii-Y. ; Huang, Shyuh-H. ; Shieh, Shyh-M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c494t-a4b9a992761a2867b34aba8f5414fcea59df91e749e9dc2eb86c350bb3b4f3e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Arterial hypertension. 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Steady state plasma glucose (SSPG) concentrations were also determined after an infusion of somatostatin, insulin and glucose. Patients with hypertension were further subdivided into two groups: insulin resistance (SSPG &gt; 190 mg/dL, n = 14) and no insulin resistance (SSPG &lt; 190 mg/dL, n = 14). As compared to normal controls, hypertensive patients, either with or without insulin resistance, had significant ( P &lt; .005) increases in PAI-1 activity (18.6 ± 1.3 ν 8.1 ± 0.8 IU/mL), PAI-1 antigen (31.1 ± 2.0 ν 12.7 ± 0.9 ng/mL) and tPA antigen (15.5 ± 0.9 ν 8.8 ± 0.9 ng/mL), and significant decrease in tPA activity (0.43 ± 0.05 ν 1.02 ± 0.16 IU/mL) than normotensive controls. Furthermore, hypertensive patients with insulin resistance had significantly higher PAI-1 activity (22.0 ± 2.2 ν 15.3 ± 0.8 IU/mL, P = .006) and tPA antigen (17.4 ± 1.2 ν 13.6 ± 1.3 ng/mL, P = .02) than did hypertensive patients without insulin resistance. However, PAI-1 antigen was insignificantly higher (34.1 ± 2.9 ν 28.1 ± 2.4 ng/mL, P = .06) and tPA activity insignificantly lower (0.42 ± 0.08 ν 0.43 ± 0.08 IU/mL, P = .45) in hypertensive patients with insulin resistance than in those without insulin resistance. In addition, PAI-1 activity and tPA antigen were significantly correlated with blood pressure, SSPG, triglyceride, HDL-cholesterol and integrated glucose response to an oral load of 75 g glucose. Thus, patients with hypertension have impaired fibrinolytic activity due to increased PAI-1 when compared to normotensive controls, and the magnitude of this fibrinolytic defect is greater in hypertensive patients who have insulin resistance. Insulin resistance with associated metabolic abnormalities may be one of the causes for impaired fibrinolysis in hypertension.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>8735180</pmid><doi>10.1016/0895-7061(95)00442-4</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Arterial hypertension. Arterial hypotension
Biological and medical sciences
Blood and lymphatic vessels
Blood Glucose - metabolism
Blood Pressure - physiology
Cardiology. Vascular system
Cholesterol - blood
Clinical manifestations. Epidemiology. Investigative techniques. Etiology
Female
Fibrinolysis - physiology
glucose intolerance
Glucose Tolerance Test
Humans
hypertension
Hypertension - blood
Hypertension - physiopathology
Insulin - blood
insulin resistance
Insulin Resistance - physiology
Male
Medical sciences
Middle Aged
Plasminogen activator inhibitor
Plasminogen Activator Inhibitor 1 - metabolism
tissue plasminogen activator
Tissue Plasminogen Activator - metabolism
Triglycerides - blood
title Impaired fibrinolysis and insulin resistance in patients with hypertension
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