Differential association of proinflammatory cytokines with left ventricular diastolic dysfunction in subjects with and without continuous ambulatory peritoneal dialysis

Abstract Background and aims The association between inflammation and left ventricular (LV) diastolic dysfunction in continuous ambulatory peritoneal dialysis (CAPD) and non-CAPD patients is not established. The objective of this study was to test the above association and whether inflammation inter...

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Veröffentlicht in:Nutrition, metabolism, and cardiovascular diseases metabolism, and cardiovascular diseases, 2012-11, Vol.22 (11), p.974-980
Hauptverfasser: Lee, J.-K, Lin, H.-H, Tsai, C.-T, Chen, J.-J, Kuo, C.-C, Lien, Y.-C, Lin, J.-W, Huang, J.-W, Hwang, S.-W, Hwang, J.-J, Tseng, C.-D, Chiang, F.-T, Wu, C.-K
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container_end_page 980
container_issue 11
container_start_page 974
container_title Nutrition, metabolism, and cardiovascular diseases
container_volume 22
creator Lee, J.-K
Lin, H.-H
Tsai, C.-T
Chen, J.-J
Kuo, C.-C
Lien, Y.-C
Lin, J.-W
Huang, J.-W
Hwang, S.-W
Hwang, J.-J
Tseng, C.-D
Chiang, F.-T
Wu, C.-K
description Abstract Background and aims The association between inflammation and left ventricular (LV) diastolic dysfunction in continuous ambulatory peritoneal dialysis (CAPD) and non-CAPD patients is not established. The objective of this study was to test the above association and whether inflammation interacts with CAPD to increase LV diastolic dysfunction risks. Methods and results 120 subjects with normal creatinine levels and 101 CAPD patients were recruited. Echocardiographic parameters were assessed in all patients. The participants were classified as having LV diastolic dysfunction by echocardiographic findings including mitral inflow E / A ratio  220 cm/s, or decreased peak annular early diastolic velocity in tissue Doppler imaging. Blood was sampled at the baseline for measurement of inflammation markers, including tissue necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6). Subjects with LV diastolic dysfunction had higher proinflammation cytokines levels in both groups. Inflamed markers correlated significantly with echocardiography parameters for LV diastolic dysfunction in patients receiving CAPD. In a multivariate regression analysis adjusting for all the factors associated with LV diastolic dysfunction, inflammation is still significantly associated with left ventricular diastolic dysfunction (TNF-alpha, OR: 2.6, 95% CI: 2.0–3.35, p  
doi_str_mv 10.1016/j.numecd.2011.01.001
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The objective of this study was to test the above association and whether inflammation interacts with CAPD to increase LV diastolic dysfunction risks. Methods and results 120 subjects with normal creatinine levels and 101 CAPD patients were recruited. Echocardiographic parameters were assessed in all patients. The participants were classified as having LV diastolic dysfunction by echocardiographic findings including mitral inflow E / A ratio &lt; 1, deceleration time &gt; 220 cm/s, or decreased peak annular early diastolic velocity in tissue Doppler imaging. Blood was sampled at the baseline for measurement of inflammation markers, including tissue necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6). Subjects with LV diastolic dysfunction had higher proinflammation cytokines levels in both groups. Inflamed markers correlated significantly with echocardiography parameters for LV diastolic dysfunction in patients receiving CAPD. In a multivariate regression analysis adjusting for all the factors associated with LV diastolic dysfunction, inflammation is still significantly associated with left ventricular diastolic dysfunction (TNF-alpha, OR: 2.6, 95% CI: 2.0–3.35, p  &lt; 0.001; IL-6, OR: 1.26, 95% CI: 1.25–1.26, p  = 0.01). In addition, the interaction of CAPD and inflammation significantly contributed to the development of LV diastolic dysfunction (CAPD∗ TNF-α: OR: 1.45, 95% CI: 1.13–1.79, P  = 0.004). Conclusion We found inflammation plays a vital role for LV diastolic dysfunction especially in CAPD patients. A synergistic effect between CAPD and inflammation, especially TNF-α, would further aggravate LV diastolic dysfunction.</description><identifier>ISSN: 0939-4753</identifier><identifier>EISSN: 1590-3729</identifier><identifier>DOI: 10.1016/j.numecd.2011.01.001</identifier><identifier>PMID: 21592755</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Aged ; Aged, 80 and over ; Biomarkers - blood ; blood ; Cardiovascular ; Case-Control Studies ; Continuous ambulatory peritoneal dialysis ; creatinine ; Creatinine - blood ; dialysis ; echocardiography ; Echocardiography, Doppler - methods ; Female ; Humans ; image analysis ; Inflammation ; Inflammation - complications ; Inflammation - physiopathology ; interleukin-6 ; Interleukin-6 - blood ; Left ventricular diastolic dysfunction ; Logistic Models ; Male ; Middle Aged ; Multivariate Analysis ; patients ; Peritoneal Dialysis, Continuous Ambulatory ; regression analysis ; risk ; Risk Factors ; synergism ; tumor necrosis factor-alpha ; Tumor Necrosis Factor-alpha - blood ; Ventricular Dysfunction, Left - complications ; Ventricular Dysfunction, Left - physiopathology</subject><ispartof>Nutrition, metabolism, and cardiovascular diseases, 2012-11, Vol.22 (11), p.974-980</ispartof><rights>Elsevier B.V.</rights><rights>2011 Elsevier B.V.</rights><rights>Copyright © 2011 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c487t-65ba9dd3a250c14c569bee870c834fa5bf5fc39834d39030723fba3a595233c33</citedby><cites>FETCH-LOGICAL-c487t-65ba9dd3a250c14c569bee870c834fa5bf5fc39834d39030723fba3a595233c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0939475311000056$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21592755$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, J.-K</creatorcontrib><creatorcontrib>Lin, H.-H</creatorcontrib><creatorcontrib>Tsai, C.-T</creatorcontrib><creatorcontrib>Chen, J.-J</creatorcontrib><creatorcontrib>Kuo, C.-C</creatorcontrib><creatorcontrib>Lien, Y.-C</creatorcontrib><creatorcontrib>Lin, J.-W</creatorcontrib><creatorcontrib>Huang, J.-W</creatorcontrib><creatorcontrib>Hwang, S.-W</creatorcontrib><creatorcontrib>Hwang, J.-J</creatorcontrib><creatorcontrib>Tseng, C.-D</creatorcontrib><creatorcontrib>Chiang, F.-T</creatorcontrib><creatorcontrib>Wu, C.-K</creatorcontrib><title>Differential association of proinflammatory cytokines with left ventricular diastolic dysfunction in subjects with and without continuous ambulatory peritoneal dialysis</title><title>Nutrition, metabolism, and cardiovascular diseases</title><addtitle>Nutr Metab Cardiovasc Dis</addtitle><description>Abstract Background and aims The association between inflammation and left ventricular (LV) diastolic dysfunction in continuous ambulatory peritoneal dialysis (CAPD) and non-CAPD patients is not established. The objective of this study was to test the above association and whether inflammation interacts with CAPD to increase LV diastolic dysfunction risks. Methods and results 120 subjects with normal creatinine levels and 101 CAPD patients were recruited. Echocardiographic parameters were assessed in all patients. The participants were classified as having LV diastolic dysfunction by echocardiographic findings including mitral inflow E / A ratio &lt; 1, deceleration time &gt; 220 cm/s, or decreased peak annular early diastolic velocity in tissue Doppler imaging. Blood was sampled at the baseline for measurement of inflammation markers, including tissue necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6). Subjects with LV diastolic dysfunction had higher proinflammation cytokines levels in both groups. Inflamed markers correlated significantly with echocardiography parameters for LV diastolic dysfunction in patients receiving CAPD. In a multivariate regression analysis adjusting for all the factors associated with LV diastolic dysfunction, inflammation is still significantly associated with left ventricular diastolic dysfunction (TNF-alpha, OR: 2.6, 95% CI: 2.0–3.35, p  &lt; 0.001; IL-6, OR: 1.26, 95% CI: 1.25–1.26, p  = 0.01). In addition, the interaction of CAPD and inflammation significantly contributed to the development of LV diastolic dysfunction (CAPD∗ TNF-α: OR: 1.45, 95% CI: 1.13–1.79, P  = 0.004). Conclusion We found inflammation plays a vital role for LV diastolic dysfunction especially in CAPD patients. A synergistic effect between CAPD and inflammation, especially TNF-α, would further aggravate LV diastolic dysfunction.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biomarkers - blood</subject><subject>blood</subject><subject>Cardiovascular</subject><subject>Case-Control Studies</subject><subject>Continuous ambulatory peritoneal dialysis</subject><subject>creatinine</subject><subject>Creatinine - blood</subject><subject>dialysis</subject><subject>echocardiography</subject><subject>Echocardiography, Doppler - methods</subject><subject>Female</subject><subject>Humans</subject><subject>image analysis</subject><subject>Inflammation</subject><subject>Inflammation - complications</subject><subject>Inflammation - physiopathology</subject><subject>interleukin-6</subject><subject>Interleukin-6 - blood</subject><subject>Left ventricular diastolic dysfunction</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>patients</subject><subject>Peritoneal Dialysis, Continuous Ambulatory</subject><subject>regression analysis</subject><subject>risk</subject><subject>Risk Factors</subject><subject>synergism</subject><subject>tumor necrosis factor-alpha</subject><subject>Tumor Necrosis Factor-alpha - blood</subject><subject>Ventricular Dysfunction, Left - complications</subject><subject>Ventricular Dysfunction, Left - physiopathology</subject><issn>0939-4753</issn><issn>1590-3729</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUsuO1DAQjBCIHRb-AIGPXDK043gyuSCh5SmtxGHZs-U4behZxx5sZ1H-iM_E84ADF6SWbEtV1eWurqrnHNYc-Ob1bu3nCc24boDzNZQC_qBacdlDLbqmf1itoBd93XZSXFRPUtoBiA5E-7i6aAqq6aRcVb_ekbUY0WfSjumUgiGdKXgWLNvHQN46PU06h7gws-RwRx4T-0n5O3NoM7sv1EhmdjqykXTKwZFh45Ls7M1RiDxL87BDk8887cfjJcyZmVA6-znMielpKCrHRnuMlIPHYqlouiVRelo9stolfHY-L6vbD--_Xn2qr798_Hz19ro27bbL9UYOuh9HoRsJhrdGbvoBcduB2YrWajlYaY3oy2MUPQjoGmEHLbTsZSOEEeKyenXSLZ__MWPKaqJk0DntsbhUnIt-0zRd3xVoe4KaGFKKaNU-0qTjojioQ0Zqp04ZqUNGCkoBL7QX5w7zMOH4l_QnlAJ4eQJYHZT-Fimp25uiIAFgy0ucBfHmhMAyiXvCqJIh9AZHimXOagz0Pw__ChhHnox2d7hg2oU5-jJlxVVqFKibwyYdFonz4gHkRvwGI23IoQ</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>Lee, J.-K</creator><creator>Lin, H.-H</creator><creator>Tsai, C.-T</creator><creator>Chen, J.-J</creator><creator>Kuo, C.-C</creator><creator>Lien, Y.-C</creator><creator>Lin, J.-W</creator><creator>Huang, J.-W</creator><creator>Hwang, S.-W</creator><creator>Hwang, J.-J</creator><creator>Tseng, C.-D</creator><creator>Chiang, F.-T</creator><creator>Wu, C.-K</creator><general>Elsevier B.V</general><scope>FBQ</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>20121101</creationdate><title>Differential association of proinflammatory cytokines with left ventricular diastolic dysfunction in subjects with and without continuous ambulatory peritoneal dialysis</title><author>Lee, J.-K ; Lin, H.-H ; Tsai, C.-T ; Chen, J.-J ; Kuo, C.-C ; Lien, Y.-C ; Lin, J.-W ; Huang, J.-W ; Hwang, S.-W ; Hwang, J.-J ; Tseng, C.-D ; Chiang, F.-T ; Wu, C.-K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-65ba9dd3a250c14c569bee870c834fa5bf5fc39834d39030723fba3a595233c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biomarkers - blood</topic><topic>blood</topic><topic>Cardiovascular</topic><topic>Case-Control Studies</topic><topic>Continuous ambulatory peritoneal dialysis</topic><topic>creatinine</topic><topic>Creatinine - blood</topic><topic>dialysis</topic><topic>echocardiography</topic><topic>Echocardiography, Doppler - methods</topic><topic>Female</topic><topic>Humans</topic><topic>image analysis</topic><topic>Inflammation</topic><topic>Inflammation - complications</topic><topic>Inflammation - physiopathology</topic><topic>interleukin-6</topic><topic>Interleukin-6 - blood</topic><topic>Left ventricular diastolic dysfunction</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>patients</topic><topic>Peritoneal Dialysis, Continuous Ambulatory</topic><topic>regression analysis</topic><topic>risk</topic><topic>Risk Factors</topic><topic>synergism</topic><topic>tumor necrosis factor-alpha</topic><topic>Tumor Necrosis Factor-alpha - blood</topic><topic>Ventricular Dysfunction, Left - complications</topic><topic>Ventricular Dysfunction, Left - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, J.-K</creatorcontrib><creatorcontrib>Lin, H.-H</creatorcontrib><creatorcontrib>Tsai, C.-T</creatorcontrib><creatorcontrib>Chen, J.-J</creatorcontrib><creatorcontrib>Kuo, C.-C</creatorcontrib><creatorcontrib>Lien, Y.-C</creatorcontrib><creatorcontrib>Lin, J.-W</creatorcontrib><creatorcontrib>Huang, J.-W</creatorcontrib><creatorcontrib>Hwang, S.-W</creatorcontrib><creatorcontrib>Hwang, J.-J</creatorcontrib><creatorcontrib>Tseng, C.-D</creatorcontrib><creatorcontrib>Chiang, F.-T</creatorcontrib><creatorcontrib>Wu, C.-K</creatorcontrib><collection>AGRIS</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>Nutrition, metabolism, and cardiovascular diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, J.-K</au><au>Lin, H.-H</au><au>Tsai, C.-T</au><au>Chen, J.-J</au><au>Kuo, C.-C</au><au>Lien, Y.-C</au><au>Lin, J.-W</au><au>Huang, J.-W</au><au>Hwang, S.-W</au><au>Hwang, J.-J</au><au>Tseng, C.-D</au><au>Chiang, F.-T</au><au>Wu, C.-K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential association of proinflammatory cytokines with left ventricular diastolic dysfunction in subjects with and without continuous ambulatory peritoneal dialysis</atitle><jtitle>Nutrition, metabolism, and cardiovascular diseases</jtitle><addtitle>Nutr Metab Cardiovasc Dis</addtitle><date>2012-11-01</date><risdate>2012</risdate><volume>22</volume><issue>11</issue><spage>974</spage><epage>980</epage><pages>974-980</pages><issn>0939-4753</issn><eissn>1590-3729</eissn><abstract>Abstract Background and aims The association between inflammation and left ventricular (LV) diastolic dysfunction in continuous ambulatory peritoneal dialysis (CAPD) and non-CAPD patients is not established. The objective of this study was to test the above association and whether inflammation interacts with CAPD to increase LV diastolic dysfunction risks. Methods and results 120 subjects with normal creatinine levels and 101 CAPD patients were recruited. Echocardiographic parameters were assessed in all patients. The participants were classified as having LV diastolic dysfunction by echocardiographic findings including mitral inflow E / A ratio &lt; 1, deceleration time &gt; 220 cm/s, or decreased peak annular early diastolic velocity in tissue Doppler imaging. Blood was sampled at the baseline for measurement of inflammation markers, including tissue necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6). Subjects with LV diastolic dysfunction had higher proinflammation cytokines levels in both groups. Inflamed markers correlated significantly with echocardiography parameters for LV diastolic dysfunction in patients receiving CAPD. In a multivariate regression analysis adjusting for all the factors associated with LV diastolic dysfunction, inflammation is still significantly associated with left ventricular diastolic dysfunction (TNF-alpha, OR: 2.6, 95% CI: 2.0–3.35, p  &lt; 0.001; IL-6, OR: 1.26, 95% CI: 1.25–1.26, p  = 0.01). In addition, the interaction of CAPD and inflammation significantly contributed to the development of LV diastolic dysfunction (CAPD∗ TNF-α: OR: 1.45, 95% CI: 1.13–1.79, P  = 0.004). Conclusion We found inflammation plays a vital role for LV diastolic dysfunction especially in CAPD patients. A synergistic effect between CAPD and inflammation, especially TNF-α, would further aggravate LV diastolic dysfunction.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>21592755</pmid><doi>10.1016/j.numecd.2011.01.001</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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ispartof Nutrition, metabolism, and cardiovascular diseases, 2012-11, Vol.22 (11), p.974-980
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1590-3729
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Aged
Aged, 80 and over
Biomarkers - blood
blood
Cardiovascular
Case-Control Studies
Continuous ambulatory peritoneal dialysis
creatinine
Creatinine - blood
dialysis
echocardiography
Echocardiography, Doppler - methods
Female
Humans
image analysis
Inflammation
Inflammation - complications
Inflammation - physiopathology
interleukin-6
Interleukin-6 - blood
Left ventricular diastolic dysfunction
Logistic Models
Male
Middle Aged
Multivariate Analysis
patients
Peritoneal Dialysis, Continuous Ambulatory
regression analysis
risk
Risk Factors
synergism
tumor necrosis factor-alpha
Tumor Necrosis Factor-alpha - blood
Ventricular Dysfunction, Left - complications
Ventricular Dysfunction, Left - physiopathology
title Differential association of proinflammatory cytokines with left ventricular diastolic dysfunction in subjects with and without continuous ambulatory peritoneal dialysis
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