Statin use and incident cardiovascular events in renal transplant recipients
Background Statins achieve potent LDL lowering in the general population leading to a significant cardiovascular (CV) risk reduction. In renal transplant recipients (RTR) statins are included in treatment guidelines, however, conclusive evidence of improved cardiovascular outcomes has not been unifo...
Gespeichert in:
Veröffentlicht in: | European journal of clinical investigation 2021-11, Vol.51 (11), p.e13594-n/a |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | n/a |
---|---|
container_issue | 11 |
container_start_page | e13594 |
container_title | European journal of clinical investigation |
container_volume | 51 |
creator | Anderson, Josephine L. C. Giet, Markus Gomes Neto, Antonio W. Bakker, Stephan J. L. Tietge, Uwe J. F. |
description | Background
Statins achieve potent LDL lowering in the general population leading to a significant cardiovascular (CV) risk reduction. In renal transplant recipients (RTR) statins are included in treatment guidelines, however, conclusive evidence of improved cardiovascular outcomes has not been uniformly provided and concerns have been raised about simultaneous use of statins and the immunosuppressant cyclosporine. This study aimed to elucidate the effect of statins on a compound CV endpoint, comprised of ischaemic CV events and CV mortality in RTR, with subgroup analysis focussing on cyclosporine users.
Method
622 included RTR (follow‐up 5.4 years) were matched based on propensity scores and dichotomized by statin use. Survival analysis was conducted.
Results
Cox regression showed that statin use was not significantly associated with the compound CV endpoint in a fully adjusted model (HR = 0.81, 95% CI = 0.53‐1.24, P = .33). Subgroup analyses in RTR using cyclosporine revealed a strong positive association of statin use with the CV compound outcome in a fully adjusted model (HR = 6.60, 95% CI 1.75‐24.9, P = .005). Furthermore, statin use was positively correlated with cyclosporine trough levels (correlation coefficient 0.11, P = .04).
Conclusion
In conclusion, statin use does not significantly decrease incident CV events in an overall RTR cohort, but is independently associated with CV‐specific mortality and events in cyclosporine using RTR, possibly due to a bilateral pharmacological interaction. |
doi_str_mv | 10.1111/eci.13594 |
format | Article |
fullrecord | <record><control><sourceid>proquest_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_swepub_ki_se_461721</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2533315329</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4814-cdb4b394c768a928ac99c7f9a9a57b8d93e7c3db0e71a315c4e621075ee56523</originalsourceid><addsrcrecordid>eNp1kU9v1DAQxS0EotuWA18AReICh7T-G8cXpGpVSqWVOLR3a-LMgks2Wexkq357ZslStZXwxda8n5-fZxh7L_iZoHWOIZ4JZZx-xRZCVaaUqpKv2YJzoUvprDxixznfcc5roeRbdqQ011JYvWCrmxHG2BdTxgL6toh9iC32YxEgtXHYQQ5TB6nAHRUzyUXCHrpiTNDnbQdEJnp-G_fyKXuzhi7ju8N-wm6_Xt4uv5Wr71fXy4tVGXRNiULb6EY5HWxVg5M1BOeCXTtwYGxTt06hDaptOFoBSpigsZKCW4NoKiPVCStn23yP26nx2xQ3kB78ANEfSr_ohF5XwkpB_JeZJ2WDbaCoCbpn154rffzpfww7XxtXaanJ4NPBIA2_J8yj38QcsKPv4zBlL41SlFNJR-jHF-jdMCXq2J6qpXSaK0PU55kKacg54foxjOB-P1JPPfV_R0rsh6fpH8l_MyTgfAbuY4cP_3fyl8vr2fIP4k-sKg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2582294035</pqid></control><display><type>article</type><title>Statin use and incident cardiovascular events in renal transplant recipients</title><source>Wiley Online Library - AutoHoldings Journals</source><source>MEDLINE</source><source>SWEPUB Freely available online</source><creator>Anderson, Josephine L. C. ; Giet, Markus ; Gomes Neto, Antonio W. ; Bakker, Stephan J. L. ; Tietge, Uwe J. F.</creator><creatorcontrib>Anderson, Josephine L. C. ; Giet, Markus ; Gomes Neto, Antonio W. ; Bakker, Stephan J. L. ; Tietge, Uwe J. F.</creatorcontrib><description>Background
Statins achieve potent LDL lowering in the general population leading to a significant cardiovascular (CV) risk reduction. In renal transplant recipients (RTR) statins are included in treatment guidelines, however, conclusive evidence of improved cardiovascular outcomes has not been uniformly provided and concerns have been raised about simultaneous use of statins and the immunosuppressant cyclosporine. This study aimed to elucidate the effect of statins on a compound CV endpoint, comprised of ischaemic CV events and CV mortality in RTR, with subgroup analysis focussing on cyclosporine users.
Method
622 included RTR (follow‐up 5.4 years) were matched based on propensity scores and dichotomized by statin use. Survival analysis was conducted.
Results
Cox regression showed that statin use was not significantly associated with the compound CV endpoint in a fully adjusted model (HR = 0.81, 95% CI = 0.53‐1.24, P = .33). Subgroup analyses in RTR using cyclosporine revealed a strong positive association of statin use with the CV compound outcome in a fully adjusted model (HR = 6.60, 95% CI 1.75‐24.9, P = .005). Furthermore, statin use was positively correlated with cyclosporine trough levels (correlation coefficient 0.11, P = .04).
Conclusion
In conclusion, statin use does not significantly decrease incident CV events in an overall RTR cohort, but is independently associated with CV‐specific mortality and events in cyclosporine using RTR, possibly due to a bilateral pharmacological interaction.</description><identifier>ISSN: 0014-2972</identifier><identifier>EISSN: 1365-2362</identifier><identifier>DOI: 10.1111/eci.13594</identifier><identifier>PMID: 34042174</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Angina Pectoris - epidemiology ; Angioplasty, Balloon, Coronary - statistics & numerical data ; cardiovascular disease ; Cardiovascular diseases ; Cardiovascular Diseases - mortality ; Cause of Death ; Cohort Studies ; Coronary Artery Bypass - statistics & numerical data ; Correlation coefficient ; Correlation coefficients ; cyclosporine ; Cyclosporins ; Female ; Health risks ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use ; Immunosuppression Therapy ; Incidence ; Ischemia ; Ischemic Stroke - epidemiology ; Kidney Failure, Chronic - surgery ; Kidney Transplantation ; Kidney transplants ; Low density lipoprotein ; Male ; Middle Aged ; Mortality ; Myocardial Infarction - epidemiology ; Myocardial Revascularization - statistics & numerical data ; Original ; pharmacological interaction ; renal transplantation ; Risk management ; Risk reduction ; Statins ; Subgroups ; Survival analysis</subject><ispartof>European journal of clinical investigation, 2021-11, Vol.51 (11), p.e13594-n/a</ispartof><rights>2021 The Authors. published by John Wiley & Sons Ltd on behalf of Stichting European Society for Clinical Investigation Journal Foundation.</rights><rights>2021 The Authors. European Journal of Clinical Investigation published by John Wiley & Sons Ltd on behalf of Stichting European Society for Clinical Investigation Journal Foundation.</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4814-cdb4b394c768a928ac99c7f9a9a57b8d93e7c3db0e71a315c4e621075ee56523</citedby><cites>FETCH-LOGICAL-c4814-cdb4b394c768a928ac99c7f9a9a57b8d93e7c3db0e71a315c4e621075ee56523</cites><orcidid>0000-0002-2802-6769</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Feci.13594$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Feci.13594$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,550,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34042174$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:146717514$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Anderson, Josephine L. C.</creatorcontrib><creatorcontrib>Giet, Markus</creatorcontrib><creatorcontrib>Gomes Neto, Antonio W.</creatorcontrib><creatorcontrib>Bakker, Stephan J. L.</creatorcontrib><creatorcontrib>Tietge, Uwe J. F.</creatorcontrib><title>Statin use and incident cardiovascular events in renal transplant recipients</title><title>European journal of clinical investigation</title><addtitle>Eur J Clin Invest</addtitle><description>Background
Statins achieve potent LDL lowering in the general population leading to a significant cardiovascular (CV) risk reduction. In renal transplant recipients (RTR) statins are included in treatment guidelines, however, conclusive evidence of improved cardiovascular outcomes has not been uniformly provided and concerns have been raised about simultaneous use of statins and the immunosuppressant cyclosporine. This study aimed to elucidate the effect of statins on a compound CV endpoint, comprised of ischaemic CV events and CV mortality in RTR, with subgroup analysis focussing on cyclosporine users.
Method
622 included RTR (follow‐up 5.4 years) were matched based on propensity scores and dichotomized by statin use. Survival analysis was conducted.
Results
Cox regression showed that statin use was not significantly associated with the compound CV endpoint in a fully adjusted model (HR = 0.81, 95% CI = 0.53‐1.24, P = .33). Subgroup analyses in RTR using cyclosporine revealed a strong positive association of statin use with the CV compound outcome in a fully adjusted model (HR = 6.60, 95% CI 1.75‐24.9, P = .005). Furthermore, statin use was positively correlated with cyclosporine trough levels (correlation coefficient 0.11, P = .04).
Conclusion
In conclusion, statin use does not significantly decrease incident CV events in an overall RTR cohort, but is independently associated with CV‐specific mortality and events in cyclosporine using RTR, possibly due to a bilateral pharmacological interaction.</description><subject>Adult</subject><subject>Aged</subject><subject>Angina Pectoris - epidemiology</subject><subject>Angioplasty, Balloon, Coronary - statistics & numerical data</subject><subject>cardiovascular disease</subject><subject>Cardiovascular diseases</subject><subject>Cardiovascular Diseases - mortality</subject><subject>Cause of Death</subject><subject>Cohort Studies</subject><subject>Coronary Artery Bypass - statistics & numerical data</subject><subject>Correlation coefficient</subject><subject>Correlation coefficients</subject><subject>cyclosporine</subject><subject>Cyclosporins</subject><subject>Female</subject><subject>Health risks</subject><subject>Humans</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</subject><subject>Immunosuppression Therapy</subject><subject>Incidence</subject><subject>Ischemia</subject><subject>Ischemic Stroke - epidemiology</subject><subject>Kidney Failure, Chronic - surgery</subject><subject>Kidney Transplantation</subject><subject>Kidney transplants</subject><subject>Low density lipoprotein</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Myocardial Infarction - epidemiology</subject><subject>Myocardial Revascularization - statistics & numerical data</subject><subject>Original</subject><subject>pharmacological interaction</subject><subject>renal transplantation</subject><subject>Risk management</subject><subject>Risk reduction</subject><subject>Statins</subject><subject>Subgroups</subject><subject>Survival analysis</subject><issn>0014-2972</issn><issn>1365-2362</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNp1kU9v1DAQxS0EotuWA18AReICh7T-G8cXpGpVSqWVOLR3a-LMgks2Wexkq357ZslStZXwxda8n5-fZxh7L_iZoHWOIZ4JZZx-xRZCVaaUqpKv2YJzoUvprDxixznfcc5roeRbdqQ011JYvWCrmxHG2BdTxgL6toh9iC32YxEgtXHYQQ5TB6nAHRUzyUXCHrpiTNDnbQdEJnp-G_fyKXuzhi7ju8N-wm6_Xt4uv5Wr71fXy4tVGXRNiULb6EY5HWxVg5M1BOeCXTtwYGxTt06hDaptOFoBSpigsZKCW4NoKiPVCStn23yP26nx2xQ3kB78ANEfSr_ohF5XwkpB_JeZJ2WDbaCoCbpn154rffzpfww7XxtXaanJ4NPBIA2_J8yj38QcsKPv4zBlL41SlFNJR-jHF-jdMCXq2J6qpXSaK0PU55kKacg54foxjOB-P1JPPfV_R0rsh6fpH8l_MyTgfAbuY4cP_3fyl8vr2fIP4k-sKg</recordid><startdate>202111</startdate><enddate>202111</enddate><creator>Anderson, Josephine L. C.</creator><creator>Giet, Markus</creator><creator>Gomes Neto, Antonio W.</creator><creator>Bakker, Stephan J. L.</creator><creator>Tietge, Uwe J. F.</creator><general>Blackwell Publishing Ltd</general><general>John Wiley and Sons Inc</general><scope>24P</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>7QO</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0002-2802-6769</orcidid></search><sort><creationdate>202111</creationdate><title>Statin use and incident cardiovascular events in renal transplant recipients</title><author>Anderson, Josephine L. C. ; Giet, Markus ; Gomes Neto, Antonio W. ; Bakker, Stephan J. L. ; Tietge, Uwe J. F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4814-cdb4b394c768a928ac99c7f9a9a57b8d93e7c3db0e71a315c4e621075ee56523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Angina Pectoris - epidemiology</topic><topic>Angioplasty, Balloon, Coronary - statistics & numerical data</topic><topic>cardiovascular disease</topic><topic>Cardiovascular diseases</topic><topic>Cardiovascular Diseases - mortality</topic><topic>Cause of Death</topic><topic>Cohort Studies</topic><topic>Coronary Artery Bypass - statistics & numerical data</topic><topic>Correlation coefficient</topic><topic>Correlation coefficients</topic><topic>cyclosporine</topic><topic>Cyclosporins</topic><topic>Female</topic><topic>Health risks</topic><topic>Humans</topic><topic>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</topic><topic>Immunosuppression Therapy</topic><topic>Incidence</topic><topic>Ischemia</topic><topic>Ischemic Stroke - epidemiology</topic><topic>Kidney Failure, Chronic - surgery</topic><topic>Kidney Transplantation</topic><topic>Kidney transplants</topic><topic>Low density lipoprotein</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Myocardial Infarction - epidemiology</topic><topic>Myocardial Revascularization - statistics & numerical data</topic><topic>Original</topic><topic>pharmacological interaction</topic><topic>renal transplantation</topic><topic>Risk management</topic><topic>Risk reduction</topic><topic>Statins</topic><topic>Subgroups</topic><topic>Survival analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anderson, Josephine L. C.</creatorcontrib><creatorcontrib>Giet, Markus</creatorcontrib><creatorcontrib>Gomes Neto, Antonio W.</creatorcontrib><creatorcontrib>Bakker, Stephan J. L.</creatorcontrib><creatorcontrib>Tietge, Uwe J. F.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>European journal of clinical investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anderson, Josephine L. C.</au><au>Giet, Markus</au><au>Gomes Neto, Antonio W.</au><au>Bakker, Stephan J. L.</au><au>Tietge, Uwe J. F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Statin use and incident cardiovascular events in renal transplant recipients</atitle><jtitle>European journal of clinical investigation</jtitle><addtitle>Eur J Clin Invest</addtitle><date>2021-11</date><risdate>2021</risdate><volume>51</volume><issue>11</issue><spage>e13594</spage><epage>n/a</epage><pages>e13594-n/a</pages><issn>0014-2972</issn><eissn>1365-2362</eissn><abstract>Background
Statins achieve potent LDL lowering in the general population leading to a significant cardiovascular (CV) risk reduction. In renal transplant recipients (RTR) statins are included in treatment guidelines, however, conclusive evidence of improved cardiovascular outcomes has not been uniformly provided and concerns have been raised about simultaneous use of statins and the immunosuppressant cyclosporine. This study aimed to elucidate the effect of statins on a compound CV endpoint, comprised of ischaemic CV events and CV mortality in RTR, with subgroup analysis focussing on cyclosporine users.
Method
622 included RTR (follow‐up 5.4 years) were matched based on propensity scores and dichotomized by statin use. Survival analysis was conducted.
Results
Cox regression showed that statin use was not significantly associated with the compound CV endpoint in a fully adjusted model (HR = 0.81, 95% CI = 0.53‐1.24, P = .33). Subgroup analyses in RTR using cyclosporine revealed a strong positive association of statin use with the CV compound outcome in a fully adjusted model (HR = 6.60, 95% CI 1.75‐24.9, P = .005). Furthermore, statin use was positively correlated with cyclosporine trough levels (correlation coefficient 0.11, P = .04).
Conclusion
In conclusion, statin use does not significantly decrease incident CV events in an overall RTR cohort, but is independently associated with CV‐specific mortality and events in cyclosporine using RTR, possibly due to a bilateral pharmacological interaction.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>34042174</pmid><doi>10.1111/eci.13594</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-2802-6769</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0014-2972 |
ispartof | European journal of clinical investigation, 2021-11, Vol.51 (11), p.e13594-n/a |
issn | 0014-2972 1365-2362 |
language | eng |
recordid | cdi_swepub_primary_oai_swepub_ki_se_461721 |
source | Wiley Online Library - AutoHoldings Journals; MEDLINE; SWEPUB Freely available online |
subjects | Adult Aged Angina Pectoris - epidemiology Angioplasty, Balloon, Coronary - statistics & numerical data cardiovascular disease Cardiovascular diseases Cardiovascular Diseases - mortality Cause of Death Cohort Studies Coronary Artery Bypass - statistics & numerical data Correlation coefficient Correlation coefficients cyclosporine Cyclosporins Female Health risks Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use Immunosuppression Therapy Incidence Ischemia Ischemic Stroke - epidemiology Kidney Failure, Chronic - surgery Kidney Transplantation Kidney transplants Low density lipoprotein Male Middle Aged Mortality Myocardial Infarction - epidemiology Myocardial Revascularization - statistics & numerical data Original pharmacological interaction renal transplantation Risk management Risk reduction Statins Subgroups Survival analysis |
title | Statin use and incident cardiovascular events in renal transplant recipients |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-21T18%3A33%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Statin%20use%20and%20incident%20cardiovascular%20events%20in%20renal%20transplant%20recipients&rft.jtitle=European%20journal%20of%20clinical%20investigation&rft.au=Anderson,%20Josephine%20L.%20C.&rft.date=2021-11&rft.volume=51&rft.issue=11&rft.spage=e13594&rft.epage=n/a&rft.pages=e13594-n/a&rft.issn=0014-2972&rft.eissn=1365-2362&rft_id=info:doi/10.1111/eci.13594&rft_dat=%3Cproquest_swepu%3E2533315329%3C/proquest_swepu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2582294035&rft_id=info:pmid/34042174&rfr_iscdi=true |