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Contribution of cystatin C- and creatinine-based definitions of chronic kidney disease to cardiovascular risk assessment in 20 population-based and 3 disease cohorts: the BiomarCaRE project
by
Rehm, Martin
, Padró, Teresa
, Palosaari, Tarja
, Hultdin, Johan
, Kee, Frank
, Costanzo, Simona
, Jousilahti, Pekka
, Iacoviello, Licia
, Koenig, Wolfgang
, Rothenbacher, Dietrich
, Thorand, Barbara
, Tunstall-Pedoe, Hugh
, Waldeyer, Christoph
, Linneberg, Allan
, Meisinger, Christa
, Zeller, Tanja
, Belch, Jill J. F.
, McKnight, Amy Jayne
, Blankenberg, Stefan
, Kuulasmaa, Kari
, Sans, Susana
, Söderberg, Stefan
, Salomaa, Veikko
in
Adverse outcome
/ Age
/ Angina pectoris
/ Architects
/ Biomedicine
/ Blood pressure
/ Cardiovascular disease
/ Cardiovascular diseases
/ Cardiovascular Diseases - mortality
/ Cholesterol
/ Chronic kidney disease
/ Chronic kidney failure
/ Cohort analysis
/ Cohort study
/ Collaboration
/ Complications and side effects
/ Consortia
/ Coronary artery disease
/ Coronary Disease - etiology
/ Coronary Disease - pathology
/ Creatinine
/ Creatinine - metabolism
/ Cystatin C
/ Cystatin C - metabolism
/ Diabetes
/ Epidemiology
/ Epidermal growth factor receptors
/ Estimated glomerular filtration rate
/ Female
/ Females
/ Glomerular filtration rate
/ Hazard assessment
/ Health aspects
/ Health hazards
/ Health risks
/ Heart attacks
/ Heart Disease Risk Factors
/ Heart diseases
/ Humans
/ Hypertension
/ Immunoassay
/ Kidney diseases
/ Kidneys
/ Laboratories
/ Male
/ Markers
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Mortality
/ Older people
/ Peptides
/ Physiological aspects
/ Population
/ Population-based studies
/ Prognosis
/ Reclassification
/ Renal function
/ Research Article
/ Risk analysis
/ Risk Assessment
/ Risk factors
/ Statistical analysis
/ Statistical models
2020
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Contribution of cystatin C- and creatinine-based definitions of chronic kidney disease to cardiovascular risk assessment in 20 population-based and 3 disease cohorts: the BiomarCaRE project
by
Rehm, Martin
, Padró, Teresa
, Palosaari, Tarja
, Hultdin, Johan
, Kee, Frank
, Costanzo, Simona
, Jousilahti, Pekka
, Iacoviello, Licia
, Koenig, Wolfgang
, Rothenbacher, Dietrich
, Thorand, Barbara
, Tunstall-Pedoe, Hugh
, Waldeyer, Christoph
, Linneberg, Allan
, Meisinger, Christa
, Zeller, Tanja
, Belch, Jill J. F.
, McKnight, Amy Jayne
, Blankenberg, Stefan
, Kuulasmaa, Kari
, Sans, Susana
, Söderberg, Stefan
, Salomaa, Veikko
in
Adverse outcome
/ Age
/ Angina pectoris
/ Architects
/ Biomedicine
/ Blood pressure
/ Cardiovascular disease
/ Cardiovascular diseases
/ Cardiovascular Diseases - mortality
/ Cholesterol
/ Chronic kidney disease
/ Chronic kidney failure
/ Cohort analysis
/ Cohort study
/ Collaboration
/ Complications and side effects
/ Consortia
/ Coronary artery disease
/ Coronary Disease - etiology
/ Coronary Disease - pathology
/ Creatinine
/ Creatinine - metabolism
/ Cystatin C
/ Cystatin C - metabolism
/ Diabetes
/ Epidemiology
/ Epidermal growth factor receptors
/ Estimated glomerular filtration rate
/ Female
/ Females
/ Glomerular filtration rate
/ Hazard assessment
/ Health aspects
/ Health hazards
/ Health risks
/ Heart attacks
/ Heart Disease Risk Factors
/ Heart diseases
/ Humans
/ Hypertension
/ Immunoassay
/ Kidney diseases
/ Kidneys
/ Laboratories
/ Male
/ Markers
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Mortality
/ Older people
/ Peptides
/ Physiological aspects
/ Population
/ Population-based studies
/ Prognosis
/ Reclassification
/ Renal function
/ Research Article
/ Risk analysis
/ Risk Assessment
/ Risk factors
/ Statistical analysis
/ Statistical models
2020
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Contribution of cystatin C- and creatinine-based definitions of chronic kidney disease to cardiovascular risk assessment in 20 population-based and 3 disease cohorts: the BiomarCaRE project
by
Rehm, Martin
, Padró, Teresa
, Palosaari, Tarja
, Hultdin, Johan
, Kee, Frank
, Costanzo, Simona
, Jousilahti, Pekka
, Iacoviello, Licia
, Koenig, Wolfgang
, Rothenbacher, Dietrich
, Thorand, Barbara
, Tunstall-Pedoe, Hugh
, Waldeyer, Christoph
, Linneberg, Allan
, Meisinger, Christa
, Zeller, Tanja
, Belch, Jill J. F.
, McKnight, Amy Jayne
, Blankenberg, Stefan
, Kuulasmaa, Kari
, Sans, Susana
, Söderberg, Stefan
, Salomaa, Veikko
in
Adverse outcome
/ Age
/ Angina pectoris
/ Architects
/ Biomedicine
/ Blood pressure
/ Cardiovascular disease
/ Cardiovascular diseases
/ Cardiovascular Diseases - mortality
/ Cholesterol
/ Chronic kidney disease
/ Chronic kidney failure
/ Cohort analysis
/ Cohort study
/ Collaboration
/ Complications and side effects
/ Consortia
/ Coronary artery disease
/ Coronary Disease - etiology
/ Coronary Disease - pathology
/ Creatinine
/ Creatinine - metabolism
/ Cystatin C
/ Cystatin C - metabolism
/ Diabetes
/ Epidemiology
/ Epidermal growth factor receptors
/ Estimated glomerular filtration rate
/ Female
/ Females
/ Glomerular filtration rate
/ Hazard assessment
/ Health aspects
/ Health hazards
/ Health risks
/ Heart attacks
/ Heart Disease Risk Factors
/ Heart diseases
/ Humans
/ Hypertension
/ Immunoassay
/ Kidney diseases
/ Kidneys
/ Laboratories
/ Male
/ Markers
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Mortality
/ Older people
/ Peptides
/ Physiological aspects
/ Population
/ Population-based studies
/ Prognosis
/ Reclassification
/ Renal function
/ Research Article
/ Risk analysis
/ Risk Assessment
/ Risk factors
/ Statistical analysis
/ Statistical models
2020
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Contribution of cystatin C- and creatinine-based definitions of chronic kidney disease to cardiovascular risk assessment in 20 population-based and 3 disease cohorts: the BiomarCaRE project
Journal Article
Contribution of cystatin C- and creatinine-based definitions of chronic kidney disease to cardiovascular risk assessment in 20 population-based and 3 disease cohorts: the BiomarCaRE project
2020
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Overview
Background
Chronic kidney disease has emerged as a strong cardiovascular risk factor, and in many current guidelines, it is already considered as a coronary heart disease (CHD) equivalent. Routinely, creatinine has been used as the main marker of renal function, but recently, cystatin C emerged as a more promising marker. The aim of this study was to assess the comparative cardiovascular and mortality risk of chronic kidney disease (CKD) using cystatin C-based and creatinine-based equations of the estimated glomerular filtration rate (eGFR) in participants of population-based and disease cohorts.
Methods
The present study has been conducted within the BiomarCaRE project, with harmonized data from 20 population-based cohorts (
n
= 76,954) from 6 European countries and 3 cardiovascular disease (CVD) cohorts (
n
= 4982) from Germany. Cox proportional hazards models were used to assess hazard ratios (HRs) for the various CKD definitions with adverse outcomes and mortality after adjustment for the Systematic COronary Risk Evaluation (SCORE) variables and study center. Main outcome measures were cardiovascular diseases, cardiovascular death, and all-cause mortality.
Results
The overall prevalence of CKD stage 3–5 by creatinine- and cystatin C-based eGFR, respectively, was 3.3% and 7.4% in the population-based cohorts and 13.9% and 14.4% in the disease cohorts. CKD was an important independent risk factor for subsequent CVD events and mortality. For example, in the population-based cohorts, the HR for CVD mortality was 1.72 (95% CI 1.53 to 1.92) with creatinine-based CKD and it was 2.14 (95% CI 1.90 to 2.40) based on cystatin-based CKD compared to participants without CKD. In general, the HRs were higher for cystatin C-based CKD compared to creatinine-based CKD, for all three outcomes and risk increased clearly below the conventional threshold for CKD, also in older adults. Net reclassification indices were larger for a cystatin-C based CKD definition. Differences in HRs (between the two CKD measures) in the disease cohorts were less pronounced than in the population-based cohorts.
Conclusion
CKD is an important risk factor for subsequent CVD events and total mortality. However, point estimates of creatinine- and cystatin C-based CKD differed considerably between low- and high-risk populations. Especially in low-risk settings, the use of cystatin C-based CKD may result in more accurate risk estimates and have better prognostic value.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
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