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Multicenter Study
. 2009 Oct;50(4):1072-8.
doi: 10.1002/hep.23050.

Cytokeratin-18 fragment levels as noninvasive biomarkers for nonalcoholic steatohepatitis: a multicenter validation study

Affiliations
Multicenter Study

Cytokeratin-18 fragment levels as noninvasive biomarkers for nonalcoholic steatohepatitis: a multicenter validation study

Ariel E Feldstein et al. Hepatology. 2009 Oct.

Abstract

Liver biopsy remains the gold standard for diagnosing nonalcoholic steatohepatitis (NASH). We have recently demonstrated that plasma cytokeratin 18 (CK-18) fragment levels correlate with the magnitude of hepatocyte apoptosis and independently predict the presence of NASH. The goal of this study was to validate the use of this biomarker for NASH diagnosis. The study was an ancillary study of the NASH Clinical Research Network (NASH CRN). Our cohort consisted of 139 patients with biopsy-proven nonalcoholic fatty liver disease (NAFLD) from eight CRN participant centers across the United States and 150 age-matched healthy controls. CK-18 fragments were measured using a specific enzyme-linked immunosorbent assay. Histology was assessed centrally by study pathologists. CK-18 fragments were markedly increased in patients with NASH versus those without NASH and borderline diagnosis (median [25th, 75th percentile], 335 [196, 511], 194 [151, 270], 200 [148, 284], respectively; P < 0.001). Moreover, the odds of having fibrosis on liver biopsy increased with increasing plasma CK-18 fragment levels (P < 0.001). On multivariate regression analysis, CK-18 fragments remained an independent predictor of NASH after adjusting for variables associated with CK-18 fragments or NASH on univariate analysis (fibrosis, alanine aminotransferase, aspartate aminotransferase, age, biopsy length). The area under the receiver operating characteristic curve for NASH diagnosis was estimated to be 0.83 (0.75, 0.91).

Conclusion: Determination of CK-18 fragments in the blood predicts histological NASH and severity of disease in a large, diverse population of patients with biopsy-proven NAFLD, supporting the potential usefulness of this test in clinical practice.

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Figures

Figure 1
Figure 1. CK-18 fragments are significantly increased in blood of patients with NAFLD compared to healthy volunteers.
Vertical axis represents plasma CK-18 levels in U/L and horizontal axis patient groups. The box represents the interquartile range (the 25th and 75th percentiles) from the median (the horizontal line), the bars the 95% confidence interval. Median and [interquartile ranges] are 244 U/L [161, 427], 145 U/L [126, 190], for NAFLD and healthy volunteers respectively (P<0.001).
Figure 2
Figure 2. CK-18 fragments are significantly increased in blood of patients with NASH compared to patients with simple steatosis and patients with borderline diagnosis.
Vertical axis is plasma CK-18 levels in U/L and horizontal axis patient groups. The box represents the interquartile range (the 25th and 75th percentiles) from the median (the horizontal line), the bars the 95% confidence interval. CK-18 levels were significantly higher in subjects with NASH as compared to those with not NASH or borderline diagnosis (median (Q25, Q75): 335 (196, 511), 194 (151, 270), 200 (148, 284), respectively; P < 0.001)
Figure 3
Figure 3. CK-18 fragment levels for diagnoses of NASH
CK-18 fragment levels accurately diagnose NASH in patients with NAFLD. The area under the ROC curve is shown for the performance of the CK-18 fragment levels for discriminating NASH from borderline and not NASH diagnosis.

Comment in

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