Framingham score, renal dysfunction, and cardiovascular risk in liver transplant patients
Cardiovascular (CV) events represent major impediments to the long‐term survival of liver transplantation (LT) patients. The aim of this study was to assess whether the Framingham risk score (FRS) at transplantation can predict the development of post‐LT cardiovascular events (CVEs). Patients transp...
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Veröffentlicht in: | Liver transplantation 2015-06, Vol.21 (6), p.812-822 |
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creator | Di Maira, Tommaso Rubin, Angel Puchades, Lorena Aguilera, Victoria Vinaixa, Carmen Garcia, Maria De Maria, Nicola Villa, Erica Lopez‐Andujar, Rafael San Juan, Fernando Montalva, Eva Perez, Judith Prieto, Martin Berenguer, Marina |
description | Cardiovascular (CV) events represent major impediments to the long‐term survival of liver transplantation (LT) patients. The aim of this study was to assess whether the Framingham risk score (FRS) at transplantation can predict the development of post‐LT cardiovascular events (CVEs). Patients transplanted between 2006 and 2008 were included. Baseline features, CV risk factors, and CVEs occurring after LT (ischemic heart disease, stroke, heart failure, de novo arrhythmias, and peripheral arterial disease) were recorded. In total, 250 patients (69.6% men) with a median age of 56 years (range, 18‐68 years) were included. At transplantation, 34.4%, 34.4%, and 33.2% of patients, respectively, had a low, moderate, and high FRS with a median FRS of 14.9 (range, 0.09‐30); 14.4% of LT recipients developed at least 1 CVE at a median of 2.619 years (range, 0.006‐6.945 years). In the univariate analysis, factors associated with the development of CVEs were the continuous FRS at LT (P = 0.003), age (P = 0.007), creatinine clearance [estimated glomerular filtration rate (eGFR); P = 0.020], and mycophenolate mofetil use at discharge (P = 0.011). In the multivariate analysis, only the eGFR [hazard ratio (HR), 0.98; 95% confidence interval (CI), 0.97‐1.00; P = 0.009] and FRS (HR, 1.06; 95% CI, 1.02‐1.10; P = 0.002) remained in the model. Moreover, an association was also found between the FRS and overall survival (P = 0.004) with 5‐year survival rates of 82.5%, 77.8%, and 61.4% for the low‐, moderate‐, and high‐risk groups, respectively. Continuous FRS, eGFR, and hepatitis C virus infection were independent risk factors for overall mortality. In our series, the FRS and eGFR at LT were able to predict the development of post‐LT CVEs and poor outcomes. Liver Transpl 21:812‐822, 2015. © 2015 AASLD. |
doi_str_mv | 10.1002/lt.24128 |
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The aim of this study was to assess whether the Framingham risk score (FRS) at transplantation can predict the development of post‐LT cardiovascular events (CVEs). Patients transplanted between 2006 and 2008 were included. Baseline features, CV risk factors, and CVEs occurring after LT (ischemic heart disease, stroke, heart failure, de novo arrhythmias, and peripheral arterial disease) were recorded. In total, 250 patients (69.6% men) with a median age of 56 years (range, 18‐68 years) were included. At transplantation, 34.4%, 34.4%, and 33.2% of patients, respectively, had a low, moderate, and high FRS with a median FRS of 14.9 (range, 0.09‐30); 14.4% of LT recipients developed at least 1 CVE at a median of 2.619 years (range, 0.006‐6.945 years). In the univariate analysis, factors associated with the development of CVEs were the continuous FRS at LT (P = 0.003), age (P = 0.007), creatinine clearance [estimated glomerular filtration rate (eGFR); P = 0.020], and mycophenolate mofetil use at discharge (P = 0.011). In the multivariate analysis, only the eGFR [hazard ratio (HR), 0.98; 95% confidence interval (CI), 0.97‐1.00; P = 0.009] and FRS (HR, 1.06; 95% CI, 1.02‐1.10; P = 0.002) remained in the model. Moreover, an association was also found between the FRS and overall survival (P = 0.004) with 5‐year survival rates of 82.5%, 77.8%, and 61.4% for the low‐, moderate‐, and high‐risk groups, respectively. Continuous FRS, eGFR, and hepatitis C virus infection were independent risk factors for overall mortality. In our series, the FRS and eGFR at LT were able to predict the development of post‐LT CVEs and poor outcomes. Liver Transpl 21:812‐822, 2015. © 2015 AASLD.</description><identifier>ISSN: 1527-6465</identifier><identifier>EISSN: 1527-6473</identifier><identifier>DOI: 10.1002/lt.24128</identifier><identifier>PMID: 27396823</identifier><identifier>CODEN: LITRFO</identifier><language>eng</language><publisher>United States: Wolters Kluwer Health, Inc</publisher><subject>Adolescent ; Adult ; Aged ; Cardiovascular Diseases - diagnosis ; Cardiovascular Diseases - epidemiology ; Cardiovascular Diseases - mortality ; Female ; Glomerular Filtration Rate ; Hepatitis C - epidemiology ; Humans ; Kaplan-Meier Estimate ; Kidney - physiopathology ; Kidney Diseases - diagnosis ; Kidney Diseases - epidemiology ; Kidney Diseases - mortality ; Kidney Diseases - physiopathology ; Liver Transplantation - adverse effects ; Liver Transplantation - mortality ; Logistic Models ; Male ; Middle Aged ; Multivariate Analysis ; Proportional Hazards Models ; Retrospective Studies ; Risk Assessment ; Risk Factors ; Spain - epidemiology ; Time Factors ; Transplant Recipients ; Treatment Outcome ; Young Adult</subject><ispartof>Liver transplantation, 2015-06, Vol.21 (6), p.812-822</ispartof><rights>2015 American Association for the Study of Liver Diseases</rights><rights>2015 American Association for the Study of Liver Diseases.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3498-7843c9539ceadd4a4fa93361c42820fb7a48cd501059a4efae47aacd943d64eb3</citedby><cites>FETCH-LOGICAL-c3498-7843c9539ceadd4a4fa93361c42820fb7a48cd501059a4efae47aacd943d64eb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Flt.24128$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Flt.24128$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27396823$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Di Maira, Tommaso</creatorcontrib><creatorcontrib>Rubin, Angel</creatorcontrib><creatorcontrib>Puchades, Lorena</creatorcontrib><creatorcontrib>Aguilera, Victoria</creatorcontrib><creatorcontrib>Vinaixa, Carmen</creatorcontrib><creatorcontrib>Garcia, Maria</creatorcontrib><creatorcontrib>De Maria, Nicola</creatorcontrib><creatorcontrib>Villa, Erica</creatorcontrib><creatorcontrib>Lopez‐Andujar, Rafael</creatorcontrib><creatorcontrib>San Juan, Fernando</creatorcontrib><creatorcontrib>Montalva, Eva</creatorcontrib><creatorcontrib>Perez, Judith</creatorcontrib><creatorcontrib>Prieto, Martin</creatorcontrib><creatorcontrib>Berenguer, Marina</creatorcontrib><title>Framingham score, renal dysfunction, and cardiovascular risk in liver transplant patients</title><title>Liver transplantation</title><addtitle>Liver Transpl</addtitle><description>Cardiovascular (CV) events represent major impediments to the long‐term survival of liver transplantation (LT) patients. The aim of this study was to assess whether the Framingham risk score (FRS) at transplantation can predict the development of post‐LT cardiovascular events (CVEs). Patients transplanted between 2006 and 2008 were included. Baseline features, CV risk factors, and CVEs occurring after LT (ischemic heart disease, stroke, heart failure, de novo arrhythmias, and peripheral arterial disease) were recorded. In total, 250 patients (69.6% men) with a median age of 56 years (range, 18‐68 years) were included. At transplantation, 34.4%, 34.4%, and 33.2% of patients, respectively, had a low, moderate, and high FRS with a median FRS of 14.9 (range, 0.09‐30); 14.4% of LT recipients developed at least 1 CVE at a median of 2.619 years (range, 0.006‐6.945 years). In the univariate analysis, factors associated with the development of CVEs were the continuous FRS at LT (P = 0.003), age (P = 0.007), creatinine clearance [estimated glomerular filtration rate (eGFR); P = 0.020], and mycophenolate mofetil use at discharge (P = 0.011). In the multivariate analysis, only the eGFR [hazard ratio (HR), 0.98; 95% confidence interval (CI), 0.97‐1.00; P = 0.009] and FRS (HR, 1.06; 95% CI, 1.02‐1.10; P = 0.002) remained in the model. Moreover, an association was also found between the FRS and overall survival (P = 0.004) with 5‐year survival rates of 82.5%, 77.8%, and 61.4% for the low‐, moderate‐, and high‐risk groups, respectively. Continuous FRS, eGFR, and hepatitis C virus infection were independent risk factors for overall mortality. In our series, the FRS and eGFR at LT were able to predict the development of post‐LT CVEs and poor outcomes. Liver Transpl 21:812‐822, 2015. © 2015 AASLD.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Cardiovascular Diseases - diagnosis</subject><subject>Cardiovascular Diseases - epidemiology</subject><subject>Cardiovascular Diseases - mortality</subject><subject>Female</subject><subject>Glomerular Filtration Rate</subject><subject>Hepatitis C - epidemiology</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Kidney - physiopathology</subject><subject>Kidney Diseases - diagnosis</subject><subject>Kidney Diseases - epidemiology</subject><subject>Kidney Diseases - mortality</subject><subject>Kidney Diseases - physiopathology</subject><subject>Liver Transplantation - adverse effects</subject><subject>Liver Transplantation - mortality</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Proportional Hazards Models</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Spain - epidemiology</subject><subject>Time Factors</subject><subject>Transplant Recipients</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>1527-6465</issn><issn>1527-6473</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtKxDAUQIMoOj7AL5CAGxd2zKttspTBFwy4GReuyp0k1Wiajkk7Mn9vdUYFwdW9i8Ph3oPQMSVjSgi78N2YCcrkFhrRnJVZIUq-_bMX-R7aT-mFEEpzRXbRHiu5KiTjI_R4HaFx4ekZGpx0G-05jjaAx2aV6j7ozrXhHEMwWEM0rl1C0r2HiKNLr9gF7N3SRtxFCGnhIXR4AZ2zoUuHaKcGn-zRZh6gh-ur2eQ2m97f3E0up5nmQsmslIJrlXOlLRgjQNSgOC-oFkwyUs9LEFKbnFCSKxC2BitKAG2U4KYQds4P0Nnau4jtW29TVzUuaeuHY2zbp4pKwkXOaE4G9PQP-tL2cfh2oArJiSKFlL9CHduUoq2rRXQNxFVFSfWZu_Jd9ZV7QE82wn7eWPMDfvcdgGwNvDtvV_-KqulsLfwADuyIsQ</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>Di Maira, Tommaso</creator><creator>Rubin, Angel</creator><creator>Puchades, Lorena</creator><creator>Aguilera, Victoria</creator><creator>Vinaixa, Carmen</creator><creator>Garcia, Maria</creator><creator>De Maria, Nicola</creator><creator>Villa, Erica</creator><creator>Lopez‐Andujar, Rafael</creator><creator>San Juan, Fernando</creator><creator>Montalva, Eva</creator><creator>Perez, Judith</creator><creator>Prieto, Martin</creator><creator>Berenguer, Marina</creator><general>Wolters Kluwer Health, Inc</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>K9.</scope><scope>7X8</scope></search><sort><creationdate>201506</creationdate><title>Framingham score, renal dysfunction, and cardiovascular risk in liver transplant patients</title><author>Di Maira, Tommaso ; 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The aim of this study was to assess whether the Framingham risk score (FRS) at transplantation can predict the development of post‐LT cardiovascular events (CVEs). Patients transplanted between 2006 and 2008 were included. Baseline features, CV risk factors, and CVEs occurring after LT (ischemic heart disease, stroke, heart failure, de novo arrhythmias, and peripheral arterial disease) were recorded. In total, 250 patients (69.6% men) with a median age of 56 years (range, 18‐68 years) were included. At transplantation, 34.4%, 34.4%, and 33.2% of patients, respectively, had a low, moderate, and high FRS with a median FRS of 14.9 (range, 0.09‐30); 14.4% of LT recipients developed at least 1 CVE at a median of 2.619 years (range, 0.006‐6.945 years). In the univariate analysis, factors associated with the development of CVEs were the continuous FRS at LT (P = 0.003), age (P = 0.007), creatinine clearance [estimated glomerular filtration rate (eGFR); P = 0.020], and mycophenolate mofetil use at discharge (P = 0.011). In the multivariate analysis, only the eGFR [hazard ratio (HR), 0.98; 95% confidence interval (CI), 0.97‐1.00; P = 0.009] and FRS (HR, 1.06; 95% CI, 1.02‐1.10; P = 0.002) remained in the model. Moreover, an association was also found between the FRS and overall survival (P = 0.004) with 5‐year survival rates of 82.5%, 77.8%, and 61.4% for the low‐, moderate‐, and high‐risk groups, respectively. Continuous FRS, eGFR, and hepatitis C virus infection were independent risk factors for overall mortality. In our series, the FRS and eGFR at LT were able to predict the development of post‐LT CVEs and poor outcomes. Liver Transpl 21:812‐822, 2015. © 2015 AASLD.</abstract><cop>United States</cop><pub>Wolters Kluwer Health, Inc</pub><pmid>27396823</pmid><doi>10.1002/lt.24128</doi><tpages>11</tpages></addata></record> |
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subjects | Adolescent Adult Aged Cardiovascular Diseases - diagnosis Cardiovascular Diseases - epidemiology Cardiovascular Diseases - mortality Female Glomerular Filtration Rate Hepatitis C - epidemiology Humans Kaplan-Meier Estimate Kidney - physiopathology Kidney Diseases - diagnosis Kidney Diseases - epidemiology Kidney Diseases - mortality Kidney Diseases - physiopathology Liver Transplantation - adverse effects Liver Transplantation - mortality Logistic Models Male Middle Aged Multivariate Analysis Proportional Hazards Models Retrospective Studies Risk Assessment Risk Factors Spain - epidemiology Time Factors Transplant Recipients Treatment Outcome Young Adult |
title | Framingham score, renal dysfunction, and cardiovascular risk in liver transplant patients |
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