Infect Chemother.  2018 Jun;50(2):128-137. 10.3947/ic.2018.50.2.128.

Neutrophil Gelatinase-associated Lipocalin as a Predictor of Acute Kidney Injury in Patients during Treatment with Colistimethate Sodium

Affiliations
  • 1Division of Infectious Diseases, Kangdong Sacred Heart Hospital, Hallym University School of Medicine, Seoul, Korea.
  • 2Division of Infectious Diseases, Gachon University Gil Medical Center, Gachon University of School of Medicine, Inchon, Korea. helppl@gilhospital.com
  • 3Department of Occupational and Environmental Medicine, Hallym University Sacred Heart Hospital, Anyang, Korea.
  • 4Department of Laboratory Medicine, Kangdong Sacred Heart Hospital, Seoul, Korea.

Abstract

BACKGROUND
The emergence of multidrug-resistant, Gram-negative bacteria has resulted in reconsideration of colistimethate sodium (CMS) as a last resort for treatment of such infections. However, acute kidney injury (AKI) may represent a major limiting adverse effect of use of CMS. Early AKI detection in CMS-treated patients can help prevent progression to acute failure and reduce the need of renal replacement therapy. We hypothesized that plasma neutrophil gelatinase-associated lipocalin (NGAL) may be an early biomarker of AKI in CMS-treated patients.
MATERIALS AND METHODS
This prospective cohort study included patients aged ≥20 years who received intravenous CMS between March 2014 and November 2015. AKI was defined according to Kidney Disease: Improving Global Outcomes criteria. The primary endpoint was the difference between the average time to AKI onset based on serum creatinine and empirically derived plasma NGAL levels.
RESULTS
Among 109 CMS-treated patients, 23 patients (mean age, 61.3 ± 16.1 years; men, 65.2%) were evaluated. Thirteen (56.5%) patients fulfilled the AKI criteria. The mean time to AKI onset based on serum creatinine after CMS initiation was 78.15 ± 30.49 hours. AKI was detected approximately 22 hours earlier using plasma NGAL than when using serum creatinine as an indicator of AKI (P = 0.035). The baseline plasma NGAL level was 264.0 ± 167.3 ng/mL and 192.7 ± 65.3 ng/mL in patients with and without AKI, respectively (P = 0.218). The area under the curve for plasma NGAL level at 56 hours was 0.796 (95% confidence interval, 0.609-0.983; P = 0.017), with a sensitivity and specificity of 69.2% and 90.0%, respectively (cutoff value, 285 ng/mL).
CONCLUSION
NGAL level was found to be a strong predictor of AKI. This study provides additional evidence of the utility of NGAL for AKI in patients with treated CMS. Plasma NGAL represent sensitive and specific predictive early biomarkers for AKI in patient treated CMS.

Keyword

Acute kidney injury; Biomarker; Colistimethate sodium; Neutrophil gelatinase-associated lipocalin; Predictor

MeSH Terms

Acute Kidney Injury*
Biomarkers
Cohort Studies
Creatinine
Gram-Negative Bacteria
Health Resorts
Humans
Kidney Diseases
Lipocalins*
Male
Neutrophils*
Plasma
Prospective Studies
Renal Replacement Therapy
Sensitivity and Specificity
Sodium*
Biomarkers
Creatinine
Lipocalins
Sodium

Figure

  • Figure 1 Mean plasma NGAL level during 7 days of treatment with intravenous CMS. All values are expressed as the mean ± two times standard error. CMS, colistimethate sodium; Cr, creatinine; NGAL, neutrophil gelatinase-associated lipocalin.

  • Figure 2 Analysis of plasma NGAL. Graph shows a scatterplot of all plasma NGAL measurements at 56 hours after beginning CMS therapy. The solid thick line represents the plasma NGAL level of 285 ng/mL. CMS, colistimethate sodium; NGAL, neutrophil gelatinase-associated lipocalin.


Cited by  1 articles

Exploring New Predictors of Colistin-Associated Nephrotoxicity
Eun Jung Kim, Eu Suk Kim
Infect Chemother. 2018;50(3):283-285.    doi: 10.3947/ic.2018.50.3.283.


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