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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:American journal of transplantation 2004-10, Vol.4 (10), p.1675-1683
Hauptverfasser: 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.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1683
container_issue 10
container_start_page 1675
container_title American journal of transplantation
container_volume 4
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_66878733</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>66878733</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3648-52f8b2dfbc31b67fc5337ee6ed7b29a7b5b1e1361d7eeec569e9806cce5625e53</originalsourceid><addsrcrecordid>eNqNkM9uEzEQxi0EoqXwCsgnbln8J_ZuBJcoamlQoBKUs2V7Z4sjr53aXrW5oT4Bz8iTsEuicq0vM_P5-2akH0KYkoqO7_22opKQmaRzXjFC5hUhQjTV_TN0-vjx_LHn4gS9ynlLCK1Zw16iEyq4rBmbn6KHL1C0id5Z_H0f2hR7wOuMlzlH63SBFt-58hOv-512aZw2Mdz8-fW7QOrxNwja46X38SbpruCLIdjiYviAv8Yy6XgV-10MEAq2yY0Zp0cplOTMUACf3w7a-_1r9KLTPsObYz1DPy7Or1eXs83Vp_VquZlZLufNTLCuMaztjOXUyLqzgvMaQEJbG7bQtRGGAuWStqMKVsgFLBoirQUhmQDBz9C7w95dircD5KJ6ly14rwPEISspm7qpOR-NzcFoU8w5Qad2yfU67RUlauKvtmpCqybMauKv_vFX92P07fHGYHpo_wePwEfDx4PhznnYP3mxWn6-Hhv-F8mgluE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>66878733</pqid></control><display><type>article</type><title>Metabolic Syndrome Is Associated with Impaired Long‐term Renal Allograft Function; Not All Component criteria Contribute Equally</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><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.</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. B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3648-52f8b2dfbc31b67fc5337ee6ed7b29a7b5b1e1361d7eeec569e9806cce5625e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Chronic allograft nephropathy</topic><topic>Creatinine - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>insulin‐resistance syndrome</topic><topic>kidney</topic><topic>Kidney - metabolism</topic><topic>Kidney Failure, Chronic - metabolism</topic><topic>Kidney Transplantation</topic><topic>Male</topic><topic>Metabolic Syndrome - metabolism</topic><topic>Middle Aged</topic><topic>renal function</topic><topic>Time Factors</topic><topic>transplantation</topic><topic>Transplants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><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>
fulltext fulltext
identifier ISSN: 1600-6135
ispartof American journal of transplantation, 2004-10, Vol.4 (10), p.1675-1683
issn 1600-6135
1600-6143
language eng
recordid cdi_proquest_miscellaneous_66878733
source MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T05%3A04%3A48IST&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=Metabolic%20Syndrome%20Is%20Associated%20with%20Impaired%20Long%E2%80%90term%20Renal%20Allograft%20Function;%20Not%20All%20Component%20criteria%20Contribute%20Equally&rft.jtitle=American%20journal%20of%20transplantation&rft.au=De%20Vries,%20Aiko%20P.%20J.&rft.date=2004-10&rft.volume=4&rft.issue=10&rft.spage=1675&rft.epage=1683&rft.pages=1675-1683&rft.issn=1600-6135&rft.eissn=1600-6143&rft_id=info:doi/10.1111/j.1600-6143.2004.00558.x&rft_dat=%3Cproquest_cross%3E66878733%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=66878733&rft_id=info:pmid/15367224&rfr_iscdi=true