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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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&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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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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