TY - JOUR
T1 - 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
AU - Van Der Velde, Marije
AU - Matsushita, Kunihiro
AU - Coresh, Josef
AU - Astor, Brad C.
AU - Woodward, Mark
AU - Levey, Andrew
AU - De Jong, Paul
AU - Gansevoort, Ron T.
AU - El-Nahas, Meguid
AU - Eckardt, Kai Uwe
AU - Kasiske, Bertram L.
AU - Ninomiya, Toshiharu
AU - Chalmers, John
AU - MacMahon, Stephen
AU - Tonelli, Marcello
AU - Hemmelgarn, Brenda
AU - Sacks, Frank
AU - Curhan, Gary
AU - Collins, Allan J.
AU - Li, Suying
AU - Chen, Shu Cheng
AU - Hawaii Cohort, K. P.
AU - Lee, Brian J.
AU - Ishani, Areef
AU - Neaton, James
AU - Svendsen, Ken
AU - Mann, Johannes F.E.
AU - Yusuf, Salim
AU - Teo, Koon K.
AU - Gao, Peggy
AU - Nelson, Robert G.
AU - Knowler, William C.
AU - Bilo, Henk J.
AU - Joosten, Hanneke
AU - Kleefstra, Nanno
AU - Groenier, K. H.
AU - Auguste, Priscilla
AU - Veldhuis, Kasper
AU - Wang, Yaping
AU - Camarata, Laura
AU - Thomas, Beverly
AU - Manley, Tom
N1 - Funding Information:
The CKD Prognosis Consortium is supported by KDIGO and the US National Kidney Foundation. The meta-analyses work conducted jointly at Johns Hopkins Bloomberg School of Public Health, Baltimore, USA and University Medical Center Groningen, Groningen, the Netherlands were supported by the US National Kidney Foundation and the Dutch Kidney Foundation, respectively. The Consensus Conference that led to these studies was funded by KDIGO. A variety of institutions have supported the cohorts contributing to the CKD Prognosis Consortium, and are described in publications on these cohorts.
PY - 2011/6
Y1 - 2011/6
N2 - 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 60-105 ml/min per 1.73 m 2, but increased at lower levels. Hazard ratios at eGFRs of 60, 45, and 15 ml/min per 1.73 m 2 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 300 mg/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.
AB - 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 60-105 ml/min per 1.73 m 2, but increased at lower levels. Hazard ratios at eGFRs of 60, 45, and 15 ml/min per 1.73 m 2 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 300 mg/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.
KW - albumin-to-creatinine ratio (albuminuria)
KW - all-cause mortality
KW - cardiovascular mortality
KW - eGFR (kidney function)
KW - high-risk cohorts
KW - meta-analysis
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UR - http://www.scopus.com/inward/citedby.url?scp=79957858617&partnerID=8YFLogxK
U2 - 10.1038/ki.2010.536
DO - 10.1038/ki.2010.536
M3 - Article
C2 - 21307840
AN - SCOPUS:79957858617
SN - 0085-2538
VL - 79
SP - 1341
EP - 1352
JO - Kidney international
JF - Kidney international
IS - 12
ER -