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Effect of Renin-Angiotensin-Aldosterone System Inhibition, Dietary Sodium Restriction, and/or Diuretics on Urinary Kidney Injury Molecule 1 Excretion in Nondiabetic Proteinuric Kidney Disease: A Post Hoc Analysis of a Randomized Controlled Trial
- Source :
- American Journal of Kidney Diseases, 53(1), 16-25. W B SAUNDERS CO-ELSEVIER INC, American journal of kidney diseases, 53(1), 16-25. W.B. Saunders Ltd
- Publication Year :
- 2009
- Publisher :
- Elsevier BV, 2009.
-
Abstract
- Background: Tubulointerstitial damage plays an important role in chronic kidney disease (CKD) with proteinuria. Urinary kidney injury molecule 1 (KIM-1) reflects tubular KIM-1 and is considered a sensitive biomarker for early tubular damage. We hypothesized that a decrease in proteinuria by using therapeutic interventions is associated with decreased urinary KIM-1 levels.Study Design: Post hoc analysis of a randomized, double-blind, placebo-controlled, crossover trial.Setting & Participants: 34 proteinuric patients without diabetes from our outpatient renal clinic.Intervention: Stepwise 6-week interventions of losartan, sodium restriction (low-sodium [LS] diet), their combination, losartan plus hydrochlorothiazide (HCT), and the latter plus an LS diet.Outcomes & Measurements: Urinary excretion of KIM-1, total protein, and N-acetyl-beta-D-glucosaminidase (NAG) as a positive control for tubular injury.Results: Mean baseline urine protein level was 3.8 +/- 0.4 (SE) g/d, and KIM-1 level was 1,706 498 ng/d (increased compared with healthy controls; 74 ng/d). KIM-1 level was decreased by using placebo/LS (1,201 388 ng/d; P = 0.04), losartan/high sodium (1,184 +/- 296 ng/d; P = 0.09), losartan/LS (921 +/- 176 ng/d; P = 0.008), losartan/high sodium plus HCT (862 +/- 151 ng/d; P = 0.008) and losartan/LS plus HCT (743 +/- 170 ng/d; P = 0.001). The decrease in urinary KIM-1 levels paralleled the decrease in proteinuria (R = 0.523; P Limitations: Post hoc analysis.Conclusions: Urinary KIM-1 level was increased in patients with nondiabetic CKD with proteinuria and decreased in parallel with proteinuria by using losartan, sodium restriction, their combination, losartan plus HCT, and the latter plus sodium restriction. These results are consistent with the hypothesis of amelioration of proteinuria-induced tubular damage. Long-term studies are warranted to evaluate whether targeting treatment on KIM-1 can improve outcomes in patients with CKD with proteinuria. Am J Kidney Dis 53:16-25. (C) 2008 by the National Kidney Foundation, Inc.
- Subjects :
- Male
medicine.medical_treatment
LONG-TERM PROGNOSIS
PROGRESSION
urologic and male genital diseases
angiotensin II type 1 receptor blockade
Renin-Angiotensin System
Hydrochlorothiazide
Hepatitis A Virus Cellular Receptor 1
Diuretics
tubular damage marker
II RECEPTOR BLOCKER
Cross-Over Studies
Membrane Glycoproteins
Proteinuria
Middle Aged
Combined Modality Therapy
Treatment Outcome
Losartan
Nephrology
biomarker
Receptors, Virus
Drug Therapy, Combination
Female
Kidney Diseases
medicine.symptom
medicine.drug
Adult
medicine.medical_specialty
kidney injury molecule 1
NEPHROPATHY
Diet therapy
Urology
KAPPA-B
Nephropathy
GLOMERULONEPHRITIS
Double-Blind Method
Internal medicine
Acetylglucosaminidase
medicine
Humans
N-acetyl-beta-D-glucosaminidase
Antihypertensive Agents
Aged
ACETYL-BETA-GLUCOSAMINIDASE
urogenital system
business.industry
interstitial renal damage
Sodium, Dietary
medicine.disease
Angiotensin II
RENAL-DISEASE
Endocrinology
Renin-angiotensin-aldosterone system
CELLS
Chronic Disease
Diuretic
business
CONVERTING-ENZYME-INHIBITOR
Biomarkers
Kidney disease
Subjects
Details
- ISSN :
- 02726386
- Volume :
- 53
- Database :
- OpenAIRE
- Journal :
- American Journal of Kidney Diseases
- Accession number :
- edsair.doi.dedup.....9b1fac23f1e32166c327ba1021e1294e