4.7 Article

Acute kidney injury is a risk factor for subsequent proteinuria

Journal

KIDNEY INTERNATIONAL
Volume 93, Issue 2, Pages 460-469

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.kint.2017.07.007

Keywords

acute kidney injury; albuminuria; proteinuria

Funding

  1. Department of Veterans Affairs, Office of Academic Affiliations, Advanced Fellowship Program in Medical Informatics
  2. National Institutes of Health National Institute of Diabetes, Digestive, and Kidney Disease [T32-DK07569-25, K23-DK090304, K24-DK062849]
  3. Vanderbilt Center for Kidney Disease
  4. Veterans Health Administration Health Services Research and Development Career Development Award [CDA 08-020]
  5. Investigator Initiated Research [IIR 11-292]
  6. National Institutes of Health Office of the Director [U2C-OD023196]
  7. Veterans Health Administration Clinical Science Research and Development Merit Award [1I01CX000982-01A1, 1I01CX000414]
  8. Veterans Health Administration Health Services Research and Development Investigator Initiated Research [IIR 13-073]

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Acute kidney injury (AKI) is associated with subsequent chronic kidney disease (CKD), but the mechanism is unclear. To clarify this, we examined the association of AKI and new-onset or worsening proteinuria during the 12 months following hospitalization in a national retrospective cohort of United States Veterans hospitalized between 2004-2012. Patients with and without AKI were matched using baseline demographics, comorbidities, proteinuria, estimated glomerular filtration rate, blood pressure, angiotensin-converting enzyme inhibitor or angiotensin II receptor blocker (ACEI/ARB) use, and inpatient exposures linked to AKI. The distribution of proteinuria over one year post-discharge in the matched cohort was compared using inverse probability sampling weights. Subgroup analyses were based on diabetes, pre-admission ACEI/ARB use, and AKI severity. Among the 90,614 matched AKI and non-AKI pairs, the median estimated glomerular filtration rate was 62 mL/min/1.73m(2). The prevalence of diabetes and hypertension were 48% and 78%, respectively. The odds of having one plus or greater dipstick proteinuria was significantly higher during each month of follow-up in patients with AKI than in patients without AKI (odds ratio range 1.20-1.39). Odds were higher in patients with Stage II or III AKI (odds ratios 1.32-1.81) than in Stage I AKI (odds ratios 1.18-1.32), using non-AKI as the reference group. Results were consistent regardless of diabetes status or baseline ACEI/ARB use. Thus, AKI is a risk factor for incident or worsening proteinuria, suggesting a possible mechanism linking AKI and future CKD. The type of proteinuria, physiology, and clinical significance warrant further study as a potentially modifiable risk factor in the pathway from AKI to CKD.

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