Inflammatory signals associated with hemodialysis

Inflammatory signals associated with hemodialysis. Inflammation is highly prevalent in chronic hemodialysis patients. Because hemodialysis involves the contact of blood with “foreign” surfaces, and the documented activation of several humoral and cellular pathways during the procedure, the hemodialy...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Kidney international 2002-10, Vol.62 (4), p.1408-1416
Hauptverfasser: Caglar, Kayser, Peng, Youming, Pupim, Lara B., Flakoll, Paul J., Levenhagen, Deanna, Hakim, Raymond M., Ikizler, T. Alp
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1416
container_issue 4
container_start_page 1408
container_title Kidney international
container_volume 62
creator Caglar, Kayser
Peng, Youming
Pupim, Lara B.
Flakoll, Paul J.
Levenhagen, Deanna
Hakim, Raymond M.
Ikizler, T. Alp
description Inflammatory signals associated with hemodialysis. Inflammation is highly prevalent in chronic hemodialysis patients. Because hemodialysis involves the contact of blood with “foreign” surfaces, and the documented activation of several humoral and cellular pathways during the procedure, the hemodialysis procedure has been suggested as a potential source of inflammation in this patient population. Earlier studies did not provide clear-cut evidence of the potential contribution of the hemodialysis procedure to inflammation, as assessed by markers of inflammation such as cytokine levels and acute-phase protein production. Nine patients were studied using primed-constant infusion of L-(l-13C) leucine 2 hours before, during, and 2 hours after a single hemodialysis session. We evaluated the effects of hemodialysis on induction of interleukin-6 (IL-6) production as well as the fractional synthetic rates (FSR) of albumin and fibrinogen, two well-known acute-phase proteins. During hemodialysis, albumin FSR and fibrinogen FSR increased significantly compared to the measurements obtained during baseline period. During this period, albumin and fibrinogen FSR increased 64% and 34%, respectively, compared to baseline (P < 0.05). While the increase in IL-6 concentration was modest during hemodialysis (14%), the levels further increased at the end of the 2-hour post-hemodialysis period (68% higher compared to baseline, P < 0.05). Fibrinogen FSR also demonstrated a further increase during the post-dialysis period (17% higher compared to the intradialytic period and 58% higher compared to baseline), while albumin FSR stabilized during this period. The results provide clear evidence of hemodialysis-induced inflammatory response. The process is most notable during the 2-hour post-hemodialysis period.
doi_str_mv 10.1111/j.1523-1755.2002.kid556.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72098855</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0085253815486855</els_id><sourcerecordid>72098855</sourcerecordid><originalsourceid>FETCH-LOGICAL-c413t-254c3460602b082d481486f467e81e9b01393b00909a3a8e90a7e2fd3946d803</originalsourceid><addsrcrecordid>eNqNkE1rGzEQhkVJaRy3f6E4gfbm7ehrVzoGkzYGQy--C1mareXshyOtE_vfV4tNAj1Vl0HomXk1DyG3FAqaz49dQSXjc1pJWTAAVjwFL2VZHD-QydvLFZkAKDlnkqtrcpPSDvJdc_hEriljXHDKJ4Quu7qxbWuHPp5mKfzpbJNmNqXeBTugn72GYTvbYtv7YJtTCukz-VhnBr9c6pSsfz6sF4_z1e9fy8X9au4E5UOOFY6LEkpgG1DMC0WFKmtRVqgo6g1QrvkGQIO23CrUYCtktedalF4Bn5Lv57H72D8fMA2mDclh09gO-0MyFQOtlJQZvPsH3PWHOK5hGIUcStkI6TPkYp9SxNrsY2htPBkKZnRqdmY0Z0ZzZnRqzk7NMfd-vQQcNi36986LxAx8uwA2OdvU0XYupHcuryQqqTK3OHOYtb0EjCa5gJ1DHyK6wfg-_Md3_gKmZZSS</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>210148125</pqid></control><display><type>article</type><title>Inflammatory signals associated with hemodialysis</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>ProQuest Central UK/Ireland</source><source>Alma/SFX Local Collection</source><creator>Caglar, Kayser ; Peng, Youming ; Pupim, Lara B. ; Flakoll, Paul J. ; Levenhagen, Deanna ; Hakim, Raymond M. ; Ikizler, T. Alp</creator><creatorcontrib>Caglar, Kayser ; Peng, Youming ; Pupim, Lara B. ; Flakoll, Paul J. ; Levenhagen, Deanna ; Hakim, Raymond M. ; Ikizler, T. Alp</creatorcontrib><description>Inflammatory signals associated with hemodialysis. Inflammation is highly prevalent in chronic hemodialysis patients. Because hemodialysis involves the contact of blood with “foreign” surfaces, and the documented activation of several humoral and cellular pathways during the procedure, the hemodialysis procedure has been suggested as a potential source of inflammation in this patient population. Earlier studies did not provide clear-cut evidence of the potential contribution of the hemodialysis procedure to inflammation, as assessed by markers of inflammation such as cytokine levels and acute-phase protein production. Nine patients were studied using primed-constant infusion of L-(l-13C) leucine 2 hours before, during, and 2 hours after a single hemodialysis session. We evaluated the effects of hemodialysis on induction of interleukin-6 (IL-6) production as well as the fractional synthetic rates (FSR) of albumin and fibrinogen, two well-known acute-phase proteins. During hemodialysis, albumin FSR and fibrinogen FSR increased significantly compared to the measurements obtained during baseline period. During this period, albumin and fibrinogen FSR increased 64% and 34%, respectively, compared to baseline (P &lt; 0.05). While the increase in IL-6 concentration was modest during hemodialysis (14%), the levels further increased at the end of the 2-hour post-hemodialysis period (68% higher compared to baseline, P &lt; 0.05). Fibrinogen FSR also demonstrated a further increase during the post-dialysis period (17% higher compared to the intradialytic period and 58% higher compared to baseline), while albumin FSR stabilized during this period. The results provide clear evidence of hemodialysis-induced inflammatory response. The process is most notable during the 2-hour post-hemodialysis period.</description><identifier>ISSN: 0085-2538</identifier><identifier>EISSN: 1523-1755</identifier><identifier>DOI: 10.1111/j.1523-1755.2002.kid556.x</identifier><identifier>PMID: 12234313</identifier><identifier>CODEN: KDYIA5</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; albumin synthetic rate ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Biomarkers ; Carbon Isotopes ; catabolism ; Emergency and intensive care: renal failure. Dialysis management ; Female ; Fibrinogen - metabolism ; fibrinogen synthetic rate ; hemodialysis ; Humans ; inflammation ; Inflammation - diagnosis ; Intensive care medicine ; Interleukin-6 - blood ; Keto Acids - blood ; Kidney Failure, Chronic - immunology ; Kidney Failure, Chronic - therapy ; Male ; Medical sciences ; Middle Aged ; Nutrition Assessment ; Renal Dialysis ; Serum Albumin - metabolism</subject><ispartof>Kidney international, 2002-10, Vol.62 (4), p.1408-1416</ispartof><rights>2002 International Society of Nephrology</rights><rights>2002 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Oct 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c413t-254c3460602b082d481486f467e81e9b01393b00909a3a8e90a7e2fd3946d803</citedby><cites>FETCH-LOGICAL-c413t-254c3460602b082d481486f467e81e9b01393b00909a3a8e90a7e2fd3946d803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/210148125?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,64362,64364,64366,72216</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=13944758$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12234313$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Caglar, Kayser</creatorcontrib><creatorcontrib>Peng, Youming</creatorcontrib><creatorcontrib>Pupim, Lara B.</creatorcontrib><creatorcontrib>Flakoll, Paul J.</creatorcontrib><creatorcontrib>Levenhagen, Deanna</creatorcontrib><creatorcontrib>Hakim, Raymond M.</creatorcontrib><creatorcontrib>Ikizler, T. Alp</creatorcontrib><title>Inflammatory signals associated with hemodialysis</title><title>Kidney international</title><addtitle>Kidney Int</addtitle><description>Inflammatory signals associated with hemodialysis. Inflammation is highly prevalent in chronic hemodialysis patients. Because hemodialysis involves the contact of blood with “foreign” surfaces, and the documented activation of several humoral and cellular pathways during the procedure, the hemodialysis procedure has been suggested as a potential source of inflammation in this patient population. Earlier studies did not provide clear-cut evidence of the potential contribution of the hemodialysis procedure to inflammation, as assessed by markers of inflammation such as cytokine levels and acute-phase protein production. Nine patients were studied using primed-constant infusion of L-(l-13C) leucine 2 hours before, during, and 2 hours after a single hemodialysis session. We evaluated the effects of hemodialysis on induction of interleukin-6 (IL-6) production as well as the fractional synthetic rates (FSR) of albumin and fibrinogen, two well-known acute-phase proteins. During hemodialysis, albumin FSR and fibrinogen FSR increased significantly compared to the measurements obtained during baseline period. During this period, albumin and fibrinogen FSR increased 64% and 34%, respectively, compared to baseline (P &lt; 0.05). While the increase in IL-6 concentration was modest during hemodialysis (14%), the levels further increased at the end of the 2-hour post-hemodialysis period (68% higher compared to baseline, P &lt; 0.05). Fibrinogen FSR also demonstrated a further increase during the post-dialysis period (17% higher compared to the intradialytic period and 58% higher compared to baseline), while albumin FSR stabilized during this period. The results provide clear evidence of hemodialysis-induced inflammatory response. The process is most notable during the 2-hour post-hemodialysis period.</description><subject>Adult</subject><subject>albumin synthetic rate</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Carbon Isotopes</subject><subject>catabolism</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Female</subject><subject>Fibrinogen - metabolism</subject><subject>fibrinogen synthetic rate</subject><subject>hemodialysis</subject><subject>Humans</subject><subject>inflammation</subject><subject>Inflammation - diagnosis</subject><subject>Intensive care medicine</subject><subject>Interleukin-6 - blood</subject><subject>Keto Acids - blood</subject><subject>Kidney Failure, Chronic - immunology</subject><subject>Kidney Failure, Chronic - therapy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nutrition Assessment</subject><subject>Renal Dialysis</subject><subject>Serum Albumin - metabolism</subject><issn>0085-2538</issn><issn>1523-1755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqNkE1rGzEQhkVJaRy3f6E4gfbm7ehrVzoGkzYGQy--C1mareXshyOtE_vfV4tNAj1Vl0HomXk1DyG3FAqaz49dQSXjc1pJWTAAVjwFL2VZHD-QydvLFZkAKDlnkqtrcpPSDvJdc_hEriljXHDKJ4Quu7qxbWuHPp5mKfzpbJNmNqXeBTugn72GYTvbYtv7YJtTCukz-VhnBr9c6pSsfz6sF4_z1e9fy8X9au4E5UOOFY6LEkpgG1DMC0WFKmtRVqgo6g1QrvkGQIO23CrUYCtktedalF4Bn5Lv57H72D8fMA2mDclh09gO-0MyFQOtlJQZvPsH3PWHOK5hGIUcStkI6TPkYp9SxNrsY2htPBkKZnRqdmY0Z0ZzZnRqzk7NMfd-vQQcNi36986LxAx8uwA2OdvU0XYupHcuryQqqTK3OHOYtb0EjCa5gJ1DHyK6wfg-_Md3_gKmZZSS</recordid><startdate>20021001</startdate><enddate>20021001</enddate><creator>Caglar, Kayser</creator><creator>Peng, Youming</creator><creator>Pupim, Lara B.</creator><creator>Flakoll, Paul J.</creator><creator>Levenhagen, Deanna</creator><creator>Hakim, Raymond M.</creator><creator>Ikizler, T. Alp</creator><general>Elsevier Inc</general><general>Nature Publishing</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</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>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20021001</creationdate><title>Inflammatory signals associated with hemodialysis</title><author>Caglar, Kayser ; Peng, Youming ; Pupim, Lara B. ; Flakoll, Paul J. ; Levenhagen, Deanna ; Hakim, Raymond M. ; Ikizler, T. Alp</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-254c3460602b082d481486f467e81e9b01393b00909a3a8e90a7e2fd3946d803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>albumin synthetic rate</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Biomarkers</topic><topic>Carbon Isotopes</topic><topic>catabolism</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>Female</topic><topic>Fibrinogen - metabolism</topic><topic>fibrinogen synthetic rate</topic><topic>hemodialysis</topic><topic>Humans</topic><topic>inflammation</topic><topic>Inflammation - diagnosis</topic><topic>Intensive care medicine</topic><topic>Interleukin-6 - blood</topic><topic>Keto Acids - blood</topic><topic>Kidney Failure, Chronic - immunology</topic><topic>Kidney Failure, Chronic - therapy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nutrition Assessment</topic><topic>Renal Dialysis</topic><topic>Serum Albumin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Caglar, Kayser</creatorcontrib><creatorcontrib>Peng, Youming</creatorcontrib><creatorcontrib>Pupim, Lara B.</creatorcontrib><creatorcontrib>Flakoll, Paul J.</creatorcontrib><creatorcontrib>Levenhagen, Deanna</creatorcontrib><creatorcontrib>Hakim, Raymond M.</creatorcontrib><creatorcontrib>Ikizler, T. Alp</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Kidney international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Caglar, Kayser</au><au>Peng, Youming</au><au>Pupim, Lara B.</au><au>Flakoll, Paul J.</au><au>Levenhagen, Deanna</au><au>Hakim, Raymond M.</au><au>Ikizler, T. Alp</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inflammatory signals associated with hemodialysis</atitle><jtitle>Kidney international</jtitle><addtitle>Kidney Int</addtitle><date>2002-10-01</date><risdate>2002</risdate><volume>62</volume><issue>4</issue><spage>1408</spage><epage>1416</epage><pages>1408-1416</pages><issn>0085-2538</issn><eissn>1523-1755</eissn><coden>KDYIA5</coden><abstract>Inflammatory signals associated with hemodialysis. Inflammation is highly prevalent in chronic hemodialysis patients. Because hemodialysis involves the contact of blood with “foreign” surfaces, and the documented activation of several humoral and cellular pathways during the procedure, the hemodialysis procedure has been suggested as a potential source of inflammation in this patient population. Earlier studies did not provide clear-cut evidence of the potential contribution of the hemodialysis procedure to inflammation, as assessed by markers of inflammation such as cytokine levels and acute-phase protein production. Nine patients were studied using primed-constant infusion of L-(l-13C) leucine 2 hours before, during, and 2 hours after a single hemodialysis session. We evaluated the effects of hemodialysis on induction of interleukin-6 (IL-6) production as well as the fractional synthetic rates (FSR) of albumin and fibrinogen, two well-known acute-phase proteins. During hemodialysis, albumin FSR and fibrinogen FSR increased significantly compared to the measurements obtained during baseline period. During this period, albumin and fibrinogen FSR increased 64% and 34%, respectively, compared to baseline (P &lt; 0.05). While the increase in IL-6 concentration was modest during hemodialysis (14%), the levels further increased at the end of the 2-hour post-hemodialysis period (68% higher compared to baseline, P &lt; 0.05). Fibrinogen FSR also demonstrated a further increase during the post-dialysis period (17% higher compared to the intradialytic period and 58% higher compared to baseline), while albumin FSR stabilized during this period. The results provide clear evidence of hemodialysis-induced inflammatory response. The process is most notable during the 2-hour post-hemodialysis period.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>12234313</pmid><doi>10.1111/j.1523-1755.2002.kid556.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0085-2538
ispartof Kidney international, 2002-10, Vol.62 (4), p.1408-1416
issn 0085-2538
1523-1755
language eng
recordid cdi_proquest_miscellaneous_72098855
source MEDLINE; EZB-FREE-00999 freely available EZB journals; ProQuest Central UK/Ireland; Alma/SFX Local Collection
subjects Adult
albumin synthetic rate
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
Biomarkers
Carbon Isotopes
catabolism
Emergency and intensive care: renal failure. Dialysis management
Female
Fibrinogen - metabolism
fibrinogen synthetic rate
hemodialysis
Humans
inflammation
Inflammation - diagnosis
Intensive care medicine
Interleukin-6 - blood
Keto Acids - blood
Kidney Failure, Chronic - immunology
Kidney Failure, Chronic - therapy
Male
Medical sciences
Middle Aged
Nutrition Assessment
Renal Dialysis
Serum Albumin - metabolism
title Inflammatory signals associated with hemodialysis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T09%3A08%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Inflammatory%20signals%20associated%20with%20hemodialysis&rft.jtitle=Kidney%20international&rft.au=Caglar,%20Kayser&rft.date=2002-10-01&rft.volume=62&rft.issue=4&rft.spage=1408&rft.epage=1416&rft.pages=1408-1416&rft.issn=0085-2538&rft.eissn=1523-1755&rft.coden=KDYIA5&rft_id=info:doi/10.1111/j.1523-1755.2002.kid556.x&rft_dat=%3Cproquest_cross%3E72098855%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=210148125&rft_id=info:pmid/12234313&rft_els_id=S0085253815486855&rfr_iscdi=true