학술논문

Urinary Biomarkers of Tubular Damage Are Associated with Mortality but Not Cardiovascular Risk among Systolic Blood Pressure Intervention Trial Participants with Chronic Kidney Disease.
Document Type
article
Source
American journal of nephrology. 49(5)
Subject
for the SPRINT Research Group
Kidney Tubules
Humans
Albuminuria
Cardiovascular Diseases
Hypertension
Disease Progression
Fibrosis
Antihypertensive Agents
Blood Pressure Determination
Glomerular Filtration Rate
Prognosis
Blood Pressure
Aged
Aged
80 and over
Female
Male
Renal Insufficiency
Chronic
Biomarkers
Chitinase-3-like protein-1
Interleukin-18
Kidney injury
Urinary biomarkers
Prevention
Kidney Disease
Cardiovascular
Clinical Trials and Supportive Activities
Clinical Research
Detection
screening and diagnosis
4.1 Discovery and preclinical testing of markers and technologies
Renal and urogenital
Good Health and Well Being
Clinical Sciences
Urology & Nephrology
Language
Abstract
BackgroundKidney tubulointerstitial fibrosis on biopsy is a strong predictor of chronic kidney disease (CKD) progression, and CKD is associated with elevated risk of cardiovascular disease (CVD). Tubular health is poorly quantified by traditional kidney function measures, including estimated glomerular filtration rate (eGFR) and albuminuria. We hypothesized that urinary biomarkers of tubular injury, inflammation, and repair would be associated with higher risk of CVD and mortality in persons with CKD.MethodsWe measured urinary concentrations of interleukin-18 (IL-18), kidney injury molecule-1, neutrophil gelatinase-associated lipocalin, monocyte chemoattractant protein-1, and chitinase-3-like protein-1 (YKL-40) at baseline among 2,377 participants of the Systolic Blood Pressure Intervention Trial who had an eGFR < 60 mL/min/1.73 m2. We used Cox proportional hazards models to evaluate biomarker associations with CVD events and all-cause mortality.ResultsAt baseline, the mean age of participants was 72 ± 9 years, and eGFR was 48 ± 11 mL/min/1.73 m2. Over a median follow-up of 3.8 years, 305 CVD events (3.6% per year) and 233 all-cause deaths (2.6% per year) occurred. After multivariable adjustment including eGFR, albuminuria, and urinary creatinine, none of the biomarkers showed statistically significant associations with CVD risk. Urinary IL-18 (hazard ratio [HR] per 2-fold higher value, 1.14; 95% CI 1.01-1.29) and YKL-40 (HR per 2-fold higher value, 1.08; 95% CI 1.02-1.14) concentrations were each incrementally associated with higher mortality risk. Associations were similar when stratified by randomized blood pressure arm.ConclusionsAmong hypertensive trial participants with CKD, higher urinary IL-18 and YKL-40 were associated with higher risk of mortality, but not CVD.