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...

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Veröffentlicht in:European journal of clinical investigation 2021-11, Vol.51 (11), p.e13594-n/a
Hauptverfasser: Anderson, Josephine L. C., Giet, Markus, Gomes Neto, Antonio W., Bakker, Stephan J. L., Tietge, Uwe J. F.
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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
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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 &amp; numerical data ; cardiovascular disease ; Cardiovascular diseases ; Cardiovascular Diseases - mortality ; Cause of Death ; Cohort Studies ; Coronary Artery Bypass - statistics &amp; 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 &amp; 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 &amp; Sons Ltd on behalf of Stichting European Society for Clinical Investigation Journal Foundation.</rights><rights>2021 The Authors. 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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 &amp; 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 &amp; 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 &amp; 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. 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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>
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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
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