Metabolic Syndrome Is Associated with Impaired Long‐term Renal Allograft Function; Not All Component criteria Contribute Equally
Chronic renal transplant dysfunction (CRTD) remains a leading cause of renal allograft loss. Evidence suggests that immunological and ischemic insults are mainly associated with CRTD occurring within the first year after transplantation, whereas nonimmunological insults are predominantly associated...
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Veröffentlicht in: | American journal of transplantation 2004-10, Vol.4 (10), p.1675-1683 |
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creator | De Vries, Aiko P. J. Bakker, Stephan J. L. Van Son, Willem J. Van Der Heide, Jaap J. Homan Ploeg, Rutger J. The, Hauw T. De Jong, Paul E. Gans, Reinold O. B. |
description | Chronic renal transplant dysfunction (CRTD) remains a leading cause of renal allograft loss. Evidence suggests that immunological and ischemic insults are mainly associated with CRTD occurring within the first year after transplantation, whereas nonimmunological insults are predominantly associated with CRTD beyond the first year. Several cardiovascular risk factors, such as obesity, dyslipidemia, hypertension, and diabetes mellitus have been identified as important nonimmunological risk factors for CRTD. These risk factors constitute the metabolic syndrome (MS). As renal allograft function is a surrogate marker of renal allograft loss, we investigated the association of MS with impairment of renal allograft function beyond the first year after transplantation in a cross‐sectional study of 606 renal transplant outpatients. Metabolic syndrome was defined using the definition of the National Cholesterol Education Program. Renal allograft function was assessed as the 24‐h urinary creatinine clearance. A total of 383 out of 606 patients (63%) suffered from MS at a median time of 6 years (2.6–11.4) post‐transplant. Presence of MS was associated with impaired renal allograft function beyond 1 year post‐transplant [−4.1 mL/min, 95%CI (−7.1, −1.1)]. The impact of MS did not change appreciably after adjustment for established risk factors for CRTD [−3.1 mL/min, 95%CI (−6.0, −0.2)]. However, not all component criteria of MS contributed equally. Only systolic blood pressure and hypertriglyceridemia were independently associated with impaired renal allograft function beyond 1 year post‐transplant in multivariate analyses. |
doi_str_mv | 10.1111/j.1600-6143.2004.00558.x |
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J. ; Bakker, Stephan J. L. ; Van Son, Willem J. ; Van Der Heide, Jaap J. Homan ; Ploeg, Rutger J. ; The, Hauw T. ; De Jong, Paul E. ; Gans, Reinold O. B.</creator><creatorcontrib>De Vries, Aiko P. J. ; Bakker, Stephan J. L. ; Van Son, Willem J. ; Van Der Heide, Jaap J. Homan ; Ploeg, Rutger J. ; The, Hauw T. ; De Jong, Paul E. ; Gans, Reinold O. B.</creatorcontrib><description>Chronic renal transplant dysfunction (CRTD) remains a leading cause of renal allograft loss. Evidence suggests that immunological and ischemic insults are mainly associated with CRTD occurring within the first year after transplantation, whereas nonimmunological insults are predominantly associated with CRTD beyond the first year. Several cardiovascular risk factors, such as obesity, dyslipidemia, hypertension, and diabetes mellitus have been identified as important nonimmunological risk factors for CRTD. These risk factors constitute the metabolic syndrome (MS). As renal allograft function is a surrogate marker of renal allograft loss, we investigated the association of MS with impairment of renal allograft function beyond the first year after transplantation in a cross‐sectional study of 606 renal transplant outpatients. Metabolic syndrome was defined using the definition of the National Cholesterol Education Program. Renal allograft function was assessed as the 24‐h urinary creatinine clearance. A total of 383 out of 606 patients (63%) suffered from MS at a median time of 6 years (2.6–11.4) post‐transplant. Presence of MS was associated with impaired renal allograft function beyond 1 year post‐transplant [−4.1 mL/min, 95%CI (−7.1, −1.1)]. The impact of MS did not change appreciably after adjustment for established risk factors for CRTD [−3.1 mL/min, 95%CI (−6.0, −0.2)]. However, not all component criteria of MS contributed equally. Only systolic blood pressure and hypertriglyceridemia were independently associated with impaired renal allograft function beyond 1 year post‐transplant in multivariate analyses.</description><identifier>ISSN: 1600-6135</identifier><identifier>EISSN: 1600-6143</identifier><identifier>DOI: 10.1111/j.1600-6143.2004.00558.x</identifier><identifier>PMID: 15367224</identifier><language>eng</language><publisher>9600 Garsington Road , Oxford , OX4 2DQ , UK: Munksgaard International Publishers</publisher><subject>Adult ; Chronic allograft nephropathy ; Creatinine - metabolism ; Female ; Humans ; insulin‐resistance syndrome ; kidney ; Kidney - metabolism ; Kidney Failure, Chronic - metabolism ; Kidney Transplantation ; Male ; Metabolic Syndrome - metabolism ; Middle Aged ; renal function ; Time Factors ; transplantation ; Transplants</subject><ispartof>American journal of transplantation, 2004-10, Vol.4 (10), p.1675-1683</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3648-52f8b2dfbc31b67fc5337ee6ed7b29a7b5b1e1361d7eeec569e9806cce5625e53</citedby><cites>FETCH-LOGICAL-c3648-52f8b2dfbc31b67fc5337ee6ed7b29a7b5b1e1361d7eeec569e9806cce5625e53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1600-6143.2004.00558.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1600-6143.2004.00558.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15367224$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>De Vries, Aiko P. J.</creatorcontrib><creatorcontrib>Bakker, Stephan J. L.</creatorcontrib><creatorcontrib>Van Son, Willem J.</creatorcontrib><creatorcontrib>Van Der Heide, Jaap J. Homan</creatorcontrib><creatorcontrib>Ploeg, Rutger J.</creatorcontrib><creatorcontrib>The, Hauw T.</creatorcontrib><creatorcontrib>De Jong, Paul E.</creatorcontrib><creatorcontrib>Gans, Reinold O. B.</creatorcontrib><title>Metabolic Syndrome Is Associated with Impaired Long‐term Renal Allograft Function; Not All Component criteria Contribute Equally</title><title>American journal of transplantation</title><addtitle>Am J Transplant</addtitle><description>Chronic renal transplant dysfunction (CRTD) remains a leading cause of renal allograft loss. Evidence suggests that immunological and ischemic insults are mainly associated with CRTD occurring within the first year after transplantation, whereas nonimmunological insults are predominantly associated with CRTD beyond the first year. Several cardiovascular risk factors, such as obesity, dyslipidemia, hypertension, and diabetes mellitus have been identified as important nonimmunological risk factors for CRTD. These risk factors constitute the metabolic syndrome (MS). As renal allograft function is a surrogate marker of renal allograft loss, we investigated the association of MS with impairment of renal allograft function beyond the first year after transplantation in a cross‐sectional study of 606 renal transplant outpatients. Metabolic syndrome was defined using the definition of the National Cholesterol Education Program. Renal allograft function was assessed as the 24‐h urinary creatinine clearance. A total of 383 out of 606 patients (63%) suffered from MS at a median time of 6 years (2.6–11.4) post‐transplant. Presence of MS was associated with impaired renal allograft function beyond 1 year post‐transplant [−4.1 mL/min, 95%CI (−7.1, −1.1)]. The impact of MS did not change appreciably after adjustment for established risk factors for CRTD [−3.1 mL/min, 95%CI (−6.0, −0.2)]. However, not all component criteria of MS contributed equally. Only systolic blood pressure and hypertriglyceridemia were independently associated with impaired renal allograft function beyond 1 year post‐transplant in multivariate analyses.</description><subject>Adult</subject><subject>Chronic allograft nephropathy</subject><subject>Creatinine - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>insulin‐resistance syndrome</subject><subject>kidney</subject><subject>Kidney - metabolism</subject><subject>Kidney Failure, Chronic - metabolism</subject><subject>Kidney Transplantation</subject><subject>Male</subject><subject>Metabolic Syndrome - metabolism</subject><subject>Middle Aged</subject><subject>renal function</subject><subject>Time Factors</subject><subject>transplantation</subject><subject>Transplants</subject><issn>1600-6135</issn><issn>1600-6143</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkM9uEzEQxi0EoqXwCsgnbln8J_ZuBJcoamlQoBKUs2V7Z4sjr53aXrW5oT4Bz8iTsEuicq0vM_P5-2akH0KYkoqO7_22opKQmaRzXjFC5hUhQjTV_TN0-vjx_LHn4gS9ynlLCK1Zw16iEyq4rBmbn6KHL1C0id5Z_H0f2hR7wOuMlzlH63SBFt-58hOv-512aZw2Mdz8-fW7QOrxNwja46X38SbpruCLIdjiYviAv8Yy6XgV-10MEAq2yY0Zp0cplOTMUACf3w7a-_1r9KLTPsObYz1DPy7Or1eXs83Vp_VquZlZLufNTLCuMaztjOXUyLqzgvMaQEJbG7bQtRGGAuWStqMKVsgFLBoirQUhmQDBz9C7w95dircD5KJ6ly14rwPEISspm7qpOR-NzcFoU8w5Qad2yfU67RUlauKvtmpCqybMauKv_vFX92P07fHGYHpo_wePwEfDx4PhznnYP3mxWn6-Hhv-F8mgluE</recordid><startdate>200410</startdate><enddate>200410</enddate><creator>De Vries, Aiko P. J.</creator><creator>Bakker, Stephan J. L.</creator><creator>Van Son, Willem J.</creator><creator>Van Der Heide, Jaap J. Homan</creator><creator>Ploeg, Rutger J.</creator><creator>The, Hauw T.</creator><creator>De Jong, Paul E.</creator><creator>Gans, Reinold O. B.</creator><general>Munksgaard International Publishers</general><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>200410</creationdate><title>Metabolic Syndrome Is Associated with Impaired Long‐term Renal Allograft Function; Not All Component criteria Contribute Equally</title><author>De Vries, Aiko P. J. ; Bakker, Stephan J. L. ; Van Son, Willem J. ; Van Der Heide, Jaap J. Homan ; Ploeg, Rutger J. ; The, Hauw T. ; De Jong, Paul E. ; Gans, Reinold O. 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L.</creatorcontrib><creatorcontrib>Van Son, Willem J.</creatorcontrib><creatorcontrib>Van Der Heide, Jaap J. Homan</creatorcontrib><creatorcontrib>Ploeg, Rutger J.</creatorcontrib><creatorcontrib>The, Hauw T.</creatorcontrib><creatorcontrib>De Jong, Paul E.</creatorcontrib><creatorcontrib>Gans, Reinold O. B.</creatorcontrib><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>American journal of transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>De Vries, Aiko P. J.</au><au>Bakker, Stephan J. L.</au><au>Van Son, Willem J.</au><au>Van Der Heide, Jaap J. Homan</au><au>Ploeg, Rutger J.</au><au>The, Hauw T.</au><au>De Jong, Paul E.</au><au>Gans, Reinold O. B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic Syndrome Is Associated with Impaired Long‐term Renal Allograft Function; Not All Component criteria Contribute Equally</atitle><jtitle>American journal of transplantation</jtitle><addtitle>Am J Transplant</addtitle><date>2004-10</date><risdate>2004</risdate><volume>4</volume><issue>10</issue><spage>1675</spage><epage>1683</epage><pages>1675-1683</pages><issn>1600-6135</issn><eissn>1600-6143</eissn><abstract>Chronic renal transplant dysfunction (CRTD) remains a leading cause of renal allograft loss. Evidence suggests that immunological and ischemic insults are mainly associated with CRTD occurring within the first year after transplantation, whereas nonimmunological insults are predominantly associated with CRTD beyond the first year. Several cardiovascular risk factors, such as obesity, dyslipidemia, hypertension, and diabetes mellitus have been identified as important nonimmunological risk factors for CRTD. These risk factors constitute the metabolic syndrome (MS). As renal allograft function is a surrogate marker of renal allograft loss, we investigated the association of MS with impairment of renal allograft function beyond the first year after transplantation in a cross‐sectional study of 606 renal transplant outpatients. Metabolic syndrome was defined using the definition of the National Cholesterol Education Program. Renal allograft function was assessed as the 24‐h urinary creatinine clearance. A total of 383 out of 606 patients (63%) suffered from MS at a median time of 6 years (2.6–11.4) post‐transplant. Presence of MS was associated with impaired renal allograft function beyond 1 year post‐transplant [−4.1 mL/min, 95%CI (−7.1, −1.1)]. The impact of MS did not change appreciably after adjustment for established risk factors for CRTD [−3.1 mL/min, 95%CI (−6.0, −0.2)]. However, not all component criteria of MS contributed equally. Only systolic blood pressure and hypertriglyceridemia were independently associated with impaired renal allograft function beyond 1 year post‐transplant in multivariate analyses.</abstract><cop>9600 Garsington Road , Oxford , OX4 2DQ , UK</cop><pub>Munksgaard International Publishers</pub><pmid>15367224</pmid><doi>10.1111/j.1600-6143.2004.00558.x</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Chronic allograft nephropathy Creatinine - metabolism Female Humans insulin‐resistance syndrome kidney Kidney - metabolism Kidney Failure, Chronic - metabolism Kidney Transplantation Male Metabolic Syndrome - metabolism Middle Aged renal function Time Factors transplantation Transplants |
title | Metabolic Syndrome Is Associated with Impaired Long‐term Renal Allograft Function; Not All Component criteria Contribute Equally |
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