Lower estimated glomerular filtration rate and higher albuminuria are associated with all-cause and cardiovascular mortality. A collaborative meta-analysis of high-risk population cohorts
Screening for chronic kidney disease is recommended in people at high risk, but data on the independent and combined associations of estimated glomerular filtration rate (eGFR) and albuminuria with all-cause and cardiovascular mortality are limited. To clarify this, we performed a collaborative meta...
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creator | van der Velde, Marije Matsushita, Kunihiro Coresh, Josef Astor, Brad C. Woodward, Mark Levey, Andrew S. de Jong, Paul E. Gansevoort, Ron T. the Chronic Kidney Disease Prognosis Consortium |
description | Screening for chronic kidney disease is recommended in people at high risk, but data on the independent and combined associations of estimated glomerular filtration rate (eGFR) and albuminuria with all-cause and cardiovascular mortality are limited. To clarify this, we performed a collaborative meta-analysis of 10 cohorts with 266,975 patients selected because of increased risk for chronic kidney disease, defined as a history of hypertension, diabetes, or cardiovascular disease. Risk for all-cause mortality was not associated with eGFR between 60–105ml/min per 1.73m2, but increased at lower levels. Hazard ratios at eGFRs of 60, 45, and 15ml/min per 1.73m2 were 1.03, 1.38 and 3.11, respectively, compared to an eGFR of 95, after adjustment for albuminuria and cardiovascular risk factors. Log albuminuria was linearly associated with log risk for all-cause mortality without thresholds. Adjusted hazard ratios at albumin-to-creatinine ratios of 10, 30 and 300mg/g were 1.08, 1.38, and 2.16, respectively compared to a ratio of five. Albuminuria and eGFR were multiplicatively associated with all-cause mortality, without evidence for interaction. Similar associations were observed for cardiovascular mortality. Findings in cohorts with dipstick data were generally comparable to those in cohorts measuring albumin-to-creatinine ratios. Thus, lower eGFR and higher albuminuria are risk factors for all-cause and cardiovascular mortality in high-risk populations, independent of each other and of cardiovascular risk factors. |
doi_str_mv | 10.1038/ki.2010.536 |
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A collaborative meta-analysis of high-risk population cohorts</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>ProQuest Central UK/Ireland</source><source>Alma/SFX Local Collection</source><creator>van der Velde, Marije ; Matsushita, Kunihiro ; Coresh, Josef ; Astor, Brad C. ; Woodward, Mark ; Levey, Andrew S. ; de Jong, Paul E. ; Gansevoort, Ron T. ; the Chronic Kidney Disease Prognosis Consortium</creator><creatorcontrib>van der Velde, Marije ; Matsushita, Kunihiro ; Coresh, Josef ; Astor, Brad C. ; Woodward, Mark ; Levey, Andrew S. ; de Jong, Paul E. ; Gansevoort, Ron T. ; the Chronic Kidney Disease Prognosis Consortium ; Chronic Kidney Disease Prognosis Consortium ; the Chronic Kidney Disease Prognosis Consortium</creatorcontrib><description>Screening for chronic kidney disease is recommended in people at high risk, but data on the independent and combined associations of estimated glomerular filtration rate (eGFR) and albuminuria with all-cause and cardiovascular mortality are limited. To clarify this, we performed a collaborative meta-analysis of 10 cohorts with 266,975 patients selected because of increased risk for chronic kidney disease, defined as a history of hypertension, diabetes, or cardiovascular disease. Risk for all-cause mortality was not associated with eGFR between 60–105ml/min per 1.73m2, but increased at lower levels. Hazard ratios at eGFRs of 60, 45, and 15ml/min per 1.73m2 were 1.03, 1.38 and 3.11, respectively, compared to an eGFR of 95, after adjustment for albuminuria and cardiovascular risk factors. Log albuminuria was linearly associated with log risk for all-cause mortality without thresholds. Adjusted hazard ratios at albumin-to-creatinine ratios of 10, 30 and 300mg/g were 1.08, 1.38, and 2.16, respectively compared to a ratio of five. Albuminuria and eGFR were multiplicatively associated with all-cause mortality, without evidence for interaction. Similar associations were observed for cardiovascular mortality. Findings in cohorts with dipstick data were generally comparable to those in cohorts measuring albumin-to-creatinine ratios. Thus, lower eGFR and higher albuminuria are risk factors for all-cause and cardiovascular mortality in high-risk populations, independent of each other and of cardiovascular risk factors.</description><identifier>ISSN: 0085-2538</identifier><identifier>EISSN: 1523-1755</identifier><identifier>DOI: 10.1038/ki.2010.536</identifier><identifier>PMID: 21307840</identifier><identifier>CODEN: KDYIA5</identifier><language>eng</language><publisher>Basingstoke: Elsevier Inc</publisher><subject>Adult ; Aged ; albumin-to-creatinine ratio (albuminuria) ; Albuminuria - diagnosis ; Albuminuria - etiology ; Albuminuria - mortality ; Albuminuria - physiopathology ; all-cause mortality ; Biological and medical sciences ; Biomarkers - blood ; Biomarkers - urine ; Cardiovascular Diseases - diagnosis ; Cardiovascular Diseases - etiology ; Cardiovascular Diseases - mortality ; cardiovascular mortality ; Cause of Death ; Chi-Square Distribution ; Cohort Studies ; Creatine - blood ; Disease Progression ; eGFR (kidney function) ; Female ; Glomerular Filtration Rate ; high-risk cohorts ; Humans ; Kidney - physiopathology ; Kidney Diseases - complications ; Kidney Diseases - diagnosis ; Kidney Diseases - mortality ; Kidney Diseases - physiopathology ; Male ; Medical sciences ; meta-analysis ; Middle Aged ; Nephrology. Urinary tract diseases ; Nephropathies. Renovascular diseases. Renal failure ; Predictive Value of Tests ; Prognosis ; Proportional Hazards Models ; Regression Analysis ; Renal failure ; Risk Assessment ; Risk Factors</subject><ispartof>Kidney international, 2011-06, Vol.79 (12), p.1341-1352</ispartof><rights>2011 International Society of Nephrology</rights><rights>2015 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Jun 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-1e5e70b3cd1250e6d1105b6aad521f1d5d26bc2323419c24b10fe3ff1d30fd5c3</citedby><cites>FETCH-LOGICAL-c428t-1e5e70b3cd1250e6d1105b6aad521f1d5d26bc2323419c24b10fe3ff1d30fd5c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/869113560?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,64364,64366,64368,72218</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24249899$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21307840$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van der Velde, Marije</creatorcontrib><creatorcontrib>Matsushita, Kunihiro</creatorcontrib><creatorcontrib>Coresh, Josef</creatorcontrib><creatorcontrib>Astor, Brad C.</creatorcontrib><creatorcontrib>Woodward, Mark</creatorcontrib><creatorcontrib>Levey, Andrew S.</creatorcontrib><creatorcontrib>de Jong, Paul E.</creatorcontrib><creatorcontrib>Gansevoort, Ron T.</creatorcontrib><creatorcontrib>the Chronic Kidney Disease Prognosis Consortium</creatorcontrib><creatorcontrib>Chronic Kidney Disease Prognosis Consortium</creatorcontrib><creatorcontrib>the Chronic Kidney Disease Prognosis Consortium</creatorcontrib><title>Lower estimated glomerular filtration rate and higher albuminuria are associated with all-cause and cardiovascular mortality. A collaborative meta-analysis of high-risk population cohorts</title><title>Kidney international</title><addtitle>Kidney Int</addtitle><description>Screening for chronic kidney disease is recommended in people at high risk, but data on the independent and combined associations of estimated glomerular filtration rate (eGFR) and albuminuria with all-cause and cardiovascular mortality are limited. To clarify this, we performed a collaborative meta-analysis of 10 cohorts with 266,975 patients selected because of increased risk for chronic kidney disease, defined as a history of hypertension, diabetes, or cardiovascular disease. Risk for all-cause mortality was not associated with eGFR between 60–105ml/min per 1.73m2, but increased at lower levels. Hazard ratios at eGFRs of 60, 45, and 15ml/min per 1.73m2 were 1.03, 1.38 and 3.11, respectively, compared to an eGFR of 95, after adjustment for albuminuria and cardiovascular risk factors. Log albuminuria was linearly associated with log risk for all-cause mortality without thresholds. Adjusted hazard ratios at albumin-to-creatinine ratios of 10, 30 and 300mg/g were 1.08, 1.38, and 2.16, respectively compared to a ratio of five. Albuminuria and eGFR were multiplicatively associated with all-cause mortality, without evidence for interaction. Similar associations were observed for cardiovascular mortality. Findings in cohorts with dipstick data were generally comparable to those in cohorts measuring albumin-to-creatinine ratios. Thus, lower eGFR and higher albuminuria are risk factors for all-cause and cardiovascular mortality in high-risk populations, independent of each other and of cardiovascular risk factors.</description><subject>Adult</subject><subject>Aged</subject><subject>albumin-to-creatinine ratio (albuminuria)</subject><subject>Albuminuria - diagnosis</subject><subject>Albuminuria - etiology</subject><subject>Albuminuria - mortality</subject><subject>Albuminuria - physiopathology</subject><subject>all-cause mortality</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Biomarkers - urine</subject><subject>Cardiovascular Diseases - diagnosis</subject><subject>Cardiovascular Diseases - etiology</subject><subject>Cardiovascular Diseases - mortality</subject><subject>cardiovascular mortality</subject><subject>Cause of Death</subject><subject>Chi-Square Distribution</subject><subject>Cohort Studies</subject><subject>Creatine - blood</subject><subject>Disease Progression</subject><subject>eGFR (kidney function)</subject><subject>Female</subject><subject>Glomerular Filtration Rate</subject><subject>high-risk cohorts</subject><subject>Humans</subject><subject>Kidney - physiopathology</subject><subject>Kidney Diseases - complications</subject><subject>Kidney Diseases - diagnosis</subject><subject>Kidney Diseases - mortality</subject><subject>Kidney Diseases - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>meta-analysis</subject><subject>Middle Aged</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nephropathies. Renovascular diseases. Renal failure</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Regression Analysis</subject><subject>Renal failure</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><issn>0085-2538</issn><issn>1523-1755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNptkU2LFDEQhoMo7jh68i5BEA_SYz46Pd3HZfELFrzoOaST6p3spDtjkp5lfpt_zpoPFcRTUdRTbyrvS8hLzlacyfb91q8Ew0bJ5hFZcCVkxddKPSYLxlpVCSXbK_Is53uGfSfZU3IluGTrtmYL8vM2PkCikIsfTQFH70IcIc3BJDr4UJIpPk4UC1AzObrxdxvkTejn0U9z8oaahKOco_UngQdfNjgPlTVzPi9Zk5yPe5PtSXeMqZjgy2FFr6mNIZg-Ht_ZAx2hmMpMJhyyzzQOp_eq5POW7uIOt0_X2LhBifycPBlMyPDiUpfk-8cP324-V7dfP325ub6tbC3aUnFQsGa9tI4LxaBxnDPVN8Y4JfjAnXKi6a2QQta8s6LuORtADjiRbHDKyiV5e9bdpfhjRqv06LMFvHuCOGfdrlvViQ5NXZLX_5D3cU74HYSajnOpGobQuzNkU8w5waB3Cc1PB82ZPiaqt14fE9WYKNKvLpJzP4L7w_6OEIE3FwD9NWFIZrI-_-VqUXdt1yGnzhygVXsPSWfrYbLgfAJbtIv-vwf8AtLav4M</recordid><startdate>20110601</startdate><enddate>20110601</enddate><creator>van der Velde, Marije</creator><creator>Matsushita, Kunihiro</creator><creator>Coresh, Josef</creator><creator>Astor, Brad C.</creator><creator>Woodward, Mark</creator><creator>Levey, Andrew S.</creator><creator>de Jong, Paul E.</creator><creator>Gansevoort, Ron T.</creator><creator>the Chronic Kidney Disease Prognosis Consortium</creator><general>Elsevier Inc</general><general>Nature Publishing Group</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</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>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20110601</creationdate><title>Lower estimated glomerular filtration rate and higher albuminuria are associated with all-cause and cardiovascular mortality. A collaborative meta-analysis of high-risk population cohorts</title><author>van der Velde, Marije ; Matsushita, Kunihiro ; Coresh, Josef ; Astor, Brad C. ; Woodward, Mark ; Levey, Andrew S. ; de Jong, Paul E. ; Gansevoort, Ron T. ; the Chronic Kidney Disease Prognosis Consortium</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-1e5e70b3cd1250e6d1105b6aad521f1d5d26bc2323419c24b10fe3ff1d30fd5c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Aged</topic><topic>albumin-to-creatinine ratio (albuminuria)</topic><topic>Albuminuria - diagnosis</topic><topic>Albuminuria - etiology</topic><topic>Albuminuria - mortality</topic><topic>Albuminuria - physiopathology</topic><topic>all-cause mortality</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Biomarkers - urine</topic><topic>Cardiovascular Diseases - diagnosis</topic><topic>Cardiovascular Diseases - etiology</topic><topic>Cardiovascular Diseases - mortality</topic><topic>cardiovascular mortality</topic><topic>Cause of Death</topic><topic>Chi-Square Distribution</topic><topic>Cohort Studies</topic><topic>Creatine - blood</topic><topic>Disease Progression</topic><topic>eGFR (kidney function)</topic><topic>Female</topic><topic>Glomerular Filtration Rate</topic><topic>high-risk cohorts</topic><topic>Humans</topic><topic>Kidney - physiopathology</topic><topic>Kidney Diseases - complications</topic><topic>Kidney Diseases - diagnosis</topic><topic>Kidney Diseases - mortality</topic><topic>Kidney Diseases - physiopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>meta-analysis</topic><topic>Middle Aged</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Nephropathies. Renovascular diseases. Renal failure</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Regression Analysis</topic><topic>Renal failure</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van der Velde, Marije</creatorcontrib><creatorcontrib>Matsushita, Kunihiro</creatorcontrib><creatorcontrib>Coresh, Josef</creatorcontrib><creatorcontrib>Astor, Brad C.</creatorcontrib><creatorcontrib>Woodward, Mark</creatorcontrib><creatorcontrib>Levey, Andrew S.</creatorcontrib><creatorcontrib>de Jong, Paul E.</creatorcontrib><creatorcontrib>Gansevoort, Ron T.</creatorcontrib><creatorcontrib>the Chronic Kidney Disease Prognosis Consortium</creatorcontrib><creatorcontrib>Chronic Kidney Disease Prognosis Consortium</creatorcontrib><creatorcontrib>the Chronic Kidney Disease Prognosis Consortium</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Kidney international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van der Velde, Marije</au><au>Matsushita, Kunihiro</au><au>Coresh, Josef</au><au>Astor, Brad C.</au><au>Woodward, Mark</au><au>Levey, Andrew S.</au><au>de Jong, Paul E.</au><au>Gansevoort, Ron T.</au><au>the Chronic Kidney Disease Prognosis Consortium</au><aucorp>Chronic Kidney Disease Prognosis Consortium</aucorp><aucorp>the Chronic Kidney Disease Prognosis Consortium</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lower estimated glomerular filtration rate and higher albuminuria are associated with all-cause and cardiovascular mortality. A collaborative meta-analysis of high-risk population cohorts</atitle><jtitle>Kidney international</jtitle><addtitle>Kidney Int</addtitle><date>2011-06-01</date><risdate>2011</risdate><volume>79</volume><issue>12</issue><spage>1341</spage><epage>1352</epage><pages>1341-1352</pages><issn>0085-2538</issn><eissn>1523-1755</eissn><coden>KDYIA5</coden><abstract>Screening for chronic kidney disease is recommended in people at high risk, but data on the independent and combined associations of estimated glomerular filtration rate (eGFR) and albuminuria with all-cause and cardiovascular mortality are limited. To clarify this, we performed a collaborative meta-analysis of 10 cohorts with 266,975 patients selected because of increased risk for chronic kidney disease, defined as a history of hypertension, diabetes, or cardiovascular disease. Risk for all-cause mortality was not associated with eGFR between 60–105ml/min per 1.73m2, but increased at lower levels. Hazard ratios at eGFRs of 60, 45, and 15ml/min per 1.73m2 were 1.03, 1.38 and 3.11, respectively, compared to an eGFR of 95, after adjustment for albuminuria and cardiovascular risk factors. Log albuminuria was linearly associated with log risk for all-cause mortality without thresholds. Adjusted hazard ratios at albumin-to-creatinine ratios of 10, 30 and 300mg/g were 1.08, 1.38, and 2.16, respectively compared to a ratio of five. Albuminuria and eGFR were multiplicatively associated with all-cause mortality, without evidence for interaction. Similar associations were observed for cardiovascular mortality. Findings in cohorts with dipstick data were generally comparable to those in cohorts measuring albumin-to-creatinine ratios. Thus, lower eGFR and higher albuminuria are risk factors for all-cause and cardiovascular mortality in high-risk populations, independent of each other and of cardiovascular risk factors.</abstract><cop>Basingstoke</cop><pub>Elsevier Inc</pub><pmid>21307840</pmid><doi>10.1038/ki.2010.536</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged albumin-to-creatinine ratio (albuminuria) Albuminuria - diagnosis Albuminuria - etiology Albuminuria - mortality Albuminuria - physiopathology all-cause mortality Biological and medical sciences Biomarkers - blood Biomarkers - urine Cardiovascular Diseases - diagnosis Cardiovascular Diseases - etiology Cardiovascular Diseases - mortality cardiovascular mortality Cause of Death Chi-Square Distribution Cohort Studies Creatine - blood Disease Progression eGFR (kidney function) Female Glomerular Filtration Rate high-risk cohorts Humans Kidney - physiopathology Kidney Diseases - complications Kidney Diseases - diagnosis Kidney Diseases - mortality Kidney Diseases - physiopathology Male Medical sciences meta-analysis Middle Aged Nephrology. Urinary tract diseases Nephropathies. Renovascular diseases. Renal failure Predictive Value of Tests Prognosis Proportional Hazards Models Regression Analysis Renal failure Risk Assessment Risk Factors |
title | Lower estimated glomerular filtration rate and higher albuminuria are associated with all-cause and cardiovascular mortality. A collaborative meta-analysis of high-risk population cohorts |
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