Reduced estimated GFR and cancer mortality.
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BORIS DOI
Publisher DOI
PubMed ID
23993153
Description
BACKGROUND
Chronic kidney disease is associated with an increased risk of cancer, but whether reduced kidney function also leads to increased cancer mortality is uncertain. The aim of our study was to assess the independent effects of reduced kidney function on the risk of cancer deaths.
STUDY DESIGN
Prospective population-based cohort study.
SETTING & PARTICIPANTS
Participants of the Blue Mountains Eye Study (n=4,077; aged 49-97 years).
PREDICTOR
Estimated glomerular filtration rate (eGFR).
OUTCOMES
Overall and site-specific cancer mortality.
RESULTS
During a median follow-up of 12.8 (IQR, 8.6-15.8) years, 370 cancer deaths were observed in our study cohort. For every 10-mL/min/1.73 m(2) reduction in eGFR, there was an increase in cancer-specific mortality of 18% in the fully adjusted model (P<0.001). Compared with participants with eGFR ≥ 60 mL/min/1.73 m(2), the adjusted HR for cancer-specific mortality for those with eGFR<60 mL/min/1.73 m(2) was 1.27 (95% CI, 1.00-1.60; P=0.05). This excess cancer mortality varied with site, with the greatest risk for breast and urinary tract cancer deaths (adjusted HRs of 1.99 [95% CI, 1.05-3.85; P=0.01] and 2.54 [95% CI, 1.02-6.44; P=0.04], respectively).
LIMITATIONS
Residual confounding, such as from unmeasured socioeconomic factors and the potential effects of erythropoiesis-stimulating agents on cancer deaths, may have occurred.
CONCLUSIONS
eGFR<60 mL/min/1.73m(2) appears to be a significant risk factor for death from cancer. These effects appear to be site specific, with breast and urinary tract cancers incurring the greatest risk of death among those with reduced kidney function.
Chronic kidney disease is associated with an increased risk of cancer, but whether reduced kidney function also leads to increased cancer mortality is uncertain. The aim of our study was to assess the independent effects of reduced kidney function on the risk of cancer deaths.
STUDY DESIGN
Prospective population-based cohort study.
SETTING & PARTICIPANTS
Participants of the Blue Mountains Eye Study (n=4,077; aged 49-97 years).
PREDICTOR
Estimated glomerular filtration rate (eGFR).
OUTCOMES
Overall and site-specific cancer mortality.
RESULTS
During a median follow-up of 12.8 (IQR, 8.6-15.8) years, 370 cancer deaths were observed in our study cohort. For every 10-mL/min/1.73 m(2) reduction in eGFR, there was an increase in cancer-specific mortality of 18% in the fully adjusted model (P<0.001). Compared with participants with eGFR ≥ 60 mL/min/1.73 m(2), the adjusted HR for cancer-specific mortality for those with eGFR<60 mL/min/1.73 m(2) was 1.27 (95% CI, 1.00-1.60; P=0.05). This excess cancer mortality varied with site, with the greatest risk for breast and urinary tract cancer deaths (adjusted HRs of 1.99 [95% CI, 1.05-3.85; P=0.01] and 2.54 [95% CI, 1.02-6.44; P=0.04], respectively).
LIMITATIONS
Residual confounding, such as from unmeasured socioeconomic factors and the potential effects of erythropoiesis-stimulating agents on cancer deaths, may have occurred.
CONCLUSIONS
eGFR<60 mL/min/1.73m(2) appears to be a significant risk factor for death from cancer. These effects appear to be site specific, with breast and urinary tract cancers incurring the greatest risk of death among those with reduced kidney function.
Date of Publication
2014-01
Publication Type
Article
Keyword(s)
Cancer chronic kidney disease estimated glomerular filtration rate mortality survival analyses
Language(s)
en
Contributor(s)
Craig, Jonathan C | |
Turner, Robin | |
Chapman, Jeremy R | |
Wang, Jie J | |
Mitchell, Paul | |
Wong, Germaine |
Additional Credits
Series
American Journal of Kidney Diseases
Publisher
W.B. Saunders
ISSN
0272-6386
Access(Rights)
restricted