Treatment with Fluvastatin Rapidly Modulates, via Different Pathways, and in Dependence on the Baseline Level, Inflammation in Hemodialysis Patients

Background: Hemodialysis (HD) patients are frequently in an elevated inflammatory state which is correlated to the atherosclerosis-related and overall morbidity and mortality in this population. Statins, beyond their antilipidemic effects, are also considered to have anti-inflammatory, immunomodulat...

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Veröffentlicht in:Blood purification 2004-01, Vol.22 (6), p.518-524
Hauptverfasser: Tsirpanlis, George, Boufidou, Fotini, Manganas, Stamatios, Chantzis, Konstantinos, Bleta, Aliki, Stamatelou, Kyriaki, Psimenou, Erasmia, Nicolaou, Chrysoula
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container_end_page 524
container_issue 6
container_start_page 518
container_title Blood purification
container_volume 22
creator Tsirpanlis, George
Boufidou, Fotini
Manganas, Stamatios
Chantzis, Konstantinos
Bleta, Aliki
Stamatelou, Kyriaki
Psimenou, Erasmia
Nicolaou, Chrysoula
description Background: Hemodialysis (HD) patients are frequently in an elevated inflammatory state which is correlated to the atherosclerosis-related and overall morbidity and mortality in this population. Statins, beyond their antilipidemic effects, are also considered to have anti-inflammatory, immunomodulating and antioxidant properties. The individual response of HD patients to a short course of fluvastatin, the mechanisms involved in the immunomodulating and anti-inflammatory effects of this drug and the time interval to the appearance of these effects are investigated in this longitudinal study. Methods: In a group of 51 HD patients, fluvastatin 40 mg/day was administered for 4 weeks. Serial measurements of the lipid profile, C-reactive protein (CRP), interleukin-6 (IL-6), soluble IL-6 receptor (sIL-6R), interleukin-10 (IL-10), and serum oxidized LDL (ox-LDL), were performed before, during, and after the treatment period. Results: Total cholesterol was significantly reduced after 14 days of treatment with fluvastatin (from mean ± SD 216.7 ± 34.3 to 179.2 ± 42.3 mg/dl, p < 0.001). IL-6 and ox-LDL were reduced on day 28 (p < 0.001 and p < 0.01, respectively) and IL-10 was increased on day 14 (p = 0.05); CRP did not change significantly during the treatment period while sIL-6R was increased on day 28 of fluvastatin administration (p < 0.05). In a subgroup of patients with CRP, IL-6, sIL-6R, and ox-LDL baseline serum values ≧ the median and IL-10 ≤ the median, CRP was reduced on day 28 of fluvastatin treatment (p < 0.01), IL-6 and ox-LDL were reduced earlier, on day 14 (p = 0.05 and p < 0.05, respectively) while sIL-6R did not change significantly during the treatment period. Conclusions: Treatment with fluvastatin rapidly modulates inflammation in HD patients. Enhancement of anti-inflammatory mechanisms and attenuation of the inflammatory and oxidative state contribute to this modulation. Patients in an elevated baseline inflammatory state respond more rapidly and effectively to the treatment. This immediate and multi-potent action of the statins could be clinically useful in acute atherosclerosis complications or in the treatment of chronic inflammation in HD patients.
doi_str_mv 10.1159/000082166
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Statins, beyond their antilipidemic effects, are also considered to have anti-inflammatory, immunomodulating and antioxidant properties. The individual response of HD patients to a short course of fluvastatin, the mechanisms involved in the immunomodulating and anti-inflammatory effects of this drug and the time interval to the appearance of these effects are investigated in this longitudinal study. Methods: In a group of 51 HD patients, fluvastatin 40 mg/day was administered for 4 weeks. Serial measurements of the lipid profile, C-reactive protein (CRP), interleukin-6 (IL-6), soluble IL-6 receptor (sIL-6R), interleukin-10 (IL-10), and serum oxidized LDL (ox-LDL), were performed before, during, and after the treatment period. Results: Total cholesterol was significantly reduced after 14 days of treatment with fluvastatin (from mean ± SD 216.7 ± 34.3 to 179.2 ± 42.3 mg/dl, p < 0.001). IL-6 and ox-LDL were reduced on day 28 (p < 0.001 and p < 0.01, respectively) and IL-10 was increased on day 14 (p = 0.05); CRP did not change significantly during the treatment period while sIL-6R was increased on day 28 of fluvastatin administration (p < 0.05). In a subgroup of patients with CRP, IL-6, sIL-6R, and ox-LDL baseline serum values ≧ the median and IL-10 ≤ the median, CRP was reduced on day 28 of fluvastatin treatment (p < 0.01), IL-6 and ox-LDL were reduced earlier, on day 14 (p = 0.05 and p < 0.05, respectively) while sIL-6R did not change significantly during the treatment period. Conclusions: Treatment with fluvastatin rapidly modulates inflammation in HD patients. Enhancement of anti-inflammatory mechanisms and attenuation of the inflammatory and oxidative state contribute to this modulation. Patients in an elevated baseline inflammatory state respond more rapidly and effectively to the treatment. This immediate and multi-potent action of the statins could be clinically useful in acute atherosclerosis complications or in the treatment of chronic inflammation in HD patients.]]></description><identifier>ISSN: 0253-5068</identifier><identifier>EISSN: 1421-9735</identifier><identifier>DOI: 10.1159/000082166</identifier><identifier>PMID: 15557765</identifier><identifier>CODEN: BLPUDO</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Aged ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Antioxidants - therapeutic use ; Biological and medical sciences ; C-Reactive Protein - analysis ; Emergency and intensive care: renal failure. Dialysis management ; Fatty Acids, Monounsaturated - therapeutic use ; Female ; Glomerulonephritis ; Humans ; Indoles - therapeutic use ; Inflammation - drug therapy ; Intensive care medicine ; Interleukin-10 - blood ; Interleukin-6 - blood ; Kidney Failure, Chronic - diet therapy ; Lipids - blood ; Lipoproteins, LDL - blood ; Longitudinal Studies ; Male ; Medical sciences ; Middle Aged ; Nephrology. Urinary tract diseases ; Nephropathies. Renovascular diseases. Renal failure ; Original Paper ; Oxidation-Reduction ; Receptors, Interleukin-6 - blood ; Renal Dialysis ; Time Factors</subject><ispartof>Blood purification, 2004-01, Vol.22 (6), p.518-524</ispartof><rights>2004 S. Karger AG, Basel</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c358t-de7dc10796e4fd56a36d5443ddf53c059ebd87f85259decad3621cd6abaa3cc63</citedby><cites>FETCH-LOGICAL-c358t-de7dc10796e4fd56a36d5443ddf53c059ebd87f85259decad3621cd6abaa3cc63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2429,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16379082$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15557765$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tsirpanlis, George</creatorcontrib><creatorcontrib>Boufidou, Fotini</creatorcontrib><creatorcontrib>Manganas, Stamatios</creatorcontrib><creatorcontrib>Chantzis, Konstantinos</creatorcontrib><creatorcontrib>Bleta, Aliki</creatorcontrib><creatorcontrib>Stamatelou, Kyriaki</creatorcontrib><creatorcontrib>Psimenou, Erasmia</creatorcontrib><creatorcontrib>Nicolaou, Chrysoula</creatorcontrib><title>Treatment with Fluvastatin Rapidly Modulates, via Different Pathways, and in Dependence on the Baseline Level, Inflammation in Hemodialysis Patients</title><title>Blood purification</title><addtitle>Blood Purif</addtitle><description><![CDATA[Background: Hemodialysis (HD) patients are frequently in an elevated inflammatory state which is correlated to the atherosclerosis-related and overall morbidity and mortality in this population. Statins, beyond their antilipidemic effects, are also considered to have anti-inflammatory, immunomodulating and antioxidant properties. The individual response of HD patients to a short course of fluvastatin, the mechanisms involved in the immunomodulating and anti-inflammatory effects of this drug and the time interval to the appearance of these effects are investigated in this longitudinal study. Methods: In a group of 51 HD patients, fluvastatin 40 mg/day was administered for 4 weeks. Serial measurements of the lipid profile, C-reactive protein (CRP), interleukin-6 (IL-6), soluble IL-6 receptor (sIL-6R), interleukin-10 (IL-10), and serum oxidized LDL (ox-LDL), were performed before, during, and after the treatment period. Results: Total cholesterol was significantly reduced after 14 days of treatment with fluvastatin (from mean ± SD 216.7 ± 34.3 to 179.2 ± 42.3 mg/dl, p < 0.001). IL-6 and ox-LDL were reduced on day 28 (p < 0.001 and p < 0.01, respectively) and IL-10 was increased on day 14 (p = 0.05); CRP did not change significantly during the treatment period while sIL-6R was increased on day 28 of fluvastatin administration (p < 0.05). In a subgroup of patients with CRP, IL-6, sIL-6R, and ox-LDL baseline serum values ≧ the median and IL-10 ≤ the median, CRP was reduced on day 28 of fluvastatin treatment (p < 0.01), IL-6 and ox-LDL were reduced earlier, on day 14 (p = 0.05 and p < 0.05, respectively) while sIL-6R did not change significantly during the treatment period. Conclusions: Treatment with fluvastatin rapidly modulates inflammation in HD patients. Enhancement of anti-inflammatory mechanisms and attenuation of the inflammatory and oxidative state contribute to this modulation. Patients in an elevated baseline inflammatory state respond more rapidly and effectively to the treatment. This immediate and multi-potent action of the statins could be clinically useful in acute atherosclerosis complications or in the treatment of chronic inflammation in HD patients.]]></description><subject>Aged</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Antioxidants - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>C-Reactive Protein - analysis</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Fatty Acids, Monounsaturated - therapeutic use</subject><subject>Female</subject><subject>Glomerulonephritis</subject><subject>Humans</subject><subject>Indoles - therapeutic use</subject><subject>Inflammation - drug therapy</subject><subject>Intensive care medicine</subject><subject>Interleukin-10 - blood</subject><subject>Interleukin-6 - blood</subject><subject>Kidney Failure, Chronic - diet therapy</subject><subject>Lipids - blood</subject><subject>Lipoproteins, LDL - blood</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nephropathies. Renovascular diseases. Renal failure</subject><subject>Original Paper</subject><subject>Oxidation-Reduction</subject><subject>Receptors, Interleukin-6 - blood</subject><subject>Renal Dialysis</subject><subject>Time Factors</subject><issn>0253-5068</issn><issn>1421-9735</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0V1rFDEUBuAgil2rF14LkhuFQkeTySQzc6n9sIUVRer1cDY5caOZzJpktuz_8AebZZc2N4HwvG_gHEJec_aBc9l_ZOV0NVfqCVnwpuZV3wr5lCxYLUUlmepOyIuUfjPGGyX75-SESynbVskF-XcXEfKIIdN7l9f02s9bSBmyC_QHbJzxO_p1MrOHjOmcbh3QS2ctxn3iO-T1PezKOwRDS-ISNxgMBo10CjSvkX6GhN4FpEvcoj-nt8F6GMfSX0BJ3OA4GQd-l1za97nSm16SZxZ8wlfH-5T8vL66u7iplt--3F58WlZayC5XBlujOWt7hY01UoFQRjaNMMZKoZnscWW61naylr1BDUaommujYAUgtFbilLw_9G7i9HfGlIfRJY3eQ8BpToNqa9ZKyQs8O0Adp5Qi2mET3QhxN3A27FcwPKyg2LfH0nk1onmUx5kX8O4IIGnwNkLQLj06Jdq-dBX35uD-QPyF8QEcvvkPEiKZkA</recordid><startdate>20040101</startdate><enddate>20040101</enddate><creator>Tsirpanlis, George</creator><creator>Boufidou, Fotini</creator><creator>Manganas, Stamatios</creator><creator>Chantzis, Konstantinos</creator><creator>Bleta, Aliki</creator><creator>Stamatelou, Kyriaki</creator><creator>Psimenou, Erasmia</creator><creator>Nicolaou, Chrysoula</creator><general>Karger</general><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>20040101</creationdate><title>Treatment with Fluvastatin Rapidly Modulates, via Different Pathways, and in Dependence on the Baseline Level, Inflammation in Hemodialysis Patients</title><author>Tsirpanlis, George ; Boufidou, Fotini ; Manganas, Stamatios ; Chantzis, Konstantinos ; Bleta, Aliki ; Stamatelou, Kyriaki ; Psimenou, Erasmia ; Nicolaou, Chrysoula</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-de7dc10796e4fd56a36d5443ddf53c059ebd87f85259decad3621cd6abaa3cc63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Aged</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</topic><topic>Antioxidants - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>C-Reactive Protein - analysis</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>Fatty Acids, Monounsaturated - therapeutic use</topic><topic>Female</topic><topic>Glomerulonephritis</topic><topic>Humans</topic><topic>Indoles - therapeutic use</topic><topic>Inflammation - drug therapy</topic><topic>Intensive care medicine</topic><topic>Interleukin-10 - blood</topic><topic>Interleukin-6 - blood</topic><topic>Kidney Failure, Chronic - diet therapy</topic><topic>Lipids - blood</topic><topic>Lipoproteins, LDL - blood</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Nephropathies. Renovascular diseases. Renal failure</topic><topic>Original Paper</topic><topic>Oxidation-Reduction</topic><topic>Receptors, Interleukin-6 - blood</topic><topic>Renal Dialysis</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tsirpanlis, George</creatorcontrib><creatorcontrib>Boufidou, Fotini</creatorcontrib><creatorcontrib>Manganas, Stamatios</creatorcontrib><creatorcontrib>Chantzis, Konstantinos</creatorcontrib><creatorcontrib>Bleta, Aliki</creatorcontrib><creatorcontrib>Stamatelou, Kyriaki</creatorcontrib><creatorcontrib>Psimenou, Erasmia</creatorcontrib><creatorcontrib>Nicolaou, Chrysoula</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Blood purification</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsirpanlis, George</au><au>Boufidou, Fotini</au><au>Manganas, Stamatios</au><au>Chantzis, Konstantinos</au><au>Bleta, Aliki</au><au>Stamatelou, Kyriaki</au><au>Psimenou, Erasmia</au><au>Nicolaou, Chrysoula</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment with Fluvastatin Rapidly Modulates, via Different Pathways, and in Dependence on the Baseline Level, Inflammation in Hemodialysis Patients</atitle><jtitle>Blood purification</jtitle><addtitle>Blood Purif</addtitle><date>2004-01-01</date><risdate>2004</risdate><volume>22</volume><issue>6</issue><spage>518</spage><epage>524</epage><pages>518-524</pages><issn>0253-5068</issn><eissn>1421-9735</eissn><coden>BLPUDO</coden><abstract><![CDATA[Background: Hemodialysis (HD) patients are frequently in an elevated inflammatory state which is correlated to the atherosclerosis-related and overall morbidity and mortality in this population. Statins, beyond their antilipidemic effects, are also considered to have anti-inflammatory, immunomodulating and antioxidant properties. The individual response of HD patients to a short course of fluvastatin, the mechanisms involved in the immunomodulating and anti-inflammatory effects of this drug and the time interval to the appearance of these effects are investigated in this longitudinal study. Methods: In a group of 51 HD patients, fluvastatin 40 mg/day was administered for 4 weeks. Serial measurements of the lipid profile, C-reactive protein (CRP), interleukin-6 (IL-6), soluble IL-6 receptor (sIL-6R), interleukin-10 (IL-10), and serum oxidized LDL (ox-LDL), were performed before, during, and after the treatment period. Results: Total cholesterol was significantly reduced after 14 days of treatment with fluvastatin (from mean ± SD 216.7 ± 34.3 to 179.2 ± 42.3 mg/dl, p < 0.001). IL-6 and ox-LDL were reduced on day 28 (p < 0.001 and p < 0.01, respectively) and IL-10 was increased on day 14 (p = 0.05); CRP did not change significantly during the treatment period while sIL-6R was increased on day 28 of fluvastatin administration (p < 0.05). In a subgroup of patients with CRP, IL-6, sIL-6R, and ox-LDL baseline serum values ≧ the median and IL-10 ≤ the median, CRP was reduced on day 28 of fluvastatin treatment (p < 0.01), IL-6 and ox-LDL were reduced earlier, on day 14 (p = 0.05 and p < 0.05, respectively) while sIL-6R did not change significantly during the treatment period. Conclusions: Treatment with fluvastatin rapidly modulates inflammation in HD patients. Enhancement of anti-inflammatory mechanisms and attenuation of the inflammatory and oxidative state contribute to this modulation. Patients in an elevated baseline inflammatory state respond more rapidly and effectively to the treatment. This immediate and multi-potent action of the statins could be clinically useful in acute atherosclerosis complications or in the treatment of chronic inflammation in HD patients.]]></abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>15557765</pmid><doi>10.1159/000082166</doi><tpages>7</tpages></addata></record>
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ispartof Blood purification, 2004-01, Vol.22 (6), p.518-524
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subjects Aged
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Anti-Inflammatory Agents, Non-Steroidal - therapeutic use
Antioxidants - therapeutic use
Biological and medical sciences
C-Reactive Protein - analysis
Emergency and intensive care: renal failure. Dialysis management
Fatty Acids, Monounsaturated - therapeutic use
Female
Glomerulonephritis
Humans
Indoles - therapeutic use
Inflammation - drug therapy
Intensive care medicine
Interleukin-10 - blood
Interleukin-6 - blood
Kidney Failure, Chronic - diet therapy
Lipids - blood
Lipoproteins, LDL - blood
Longitudinal Studies
Male
Medical sciences
Middle Aged
Nephrology. Urinary tract diseases
Nephropathies. Renovascular diseases. Renal failure
Original Paper
Oxidation-Reduction
Receptors, Interleukin-6 - blood
Renal Dialysis
Time Factors
title Treatment with Fluvastatin Rapidly Modulates, via Different Pathways, and in Dependence on the Baseline Level, Inflammation in Hemodialysis Patients
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