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Use of the AST to platelet ratio index in HCV/HIV co‐infected patients
Author(s) -
Singal A. G.,
Thomassen L. V.,
Gretch D. R.,
Shuhart M. C.
Publication year - 2011
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/j.1365-2036.2010.04560.x
Subject(s) - medicine , gastroenterology , hepatitis c virus , receiver operating characteristic , liver biopsy , hepatitis c , platelet , human immunodeficiency virus (hiv) , population , liver disease , virus , biopsy , immunology , environmental health
Aliment Pharmacol Ther 2011; 33: 566–577 Summary Background  The AST to platelet ratio index (APRI), a non‐invasive marker of liver fibrosis, has not been well studied in HCV/HIV (hepatitis C virus/human immunodeficiency virus) co‐infected patients with advanced HIV. Aim  To compare the accuracy of APRI in HCV/HIV co‐infected patients to that in HCV mono‐infected patients and to determine the impact of CD4+ T‐cell counts on its performance. Methods  We identified 106 consecutive HCV/HIV co‐infected patients and 105 matched HCV mono‐infected patients who underwent liver biopsy at Harborview Medical Center over a 5‐year period. Performance characteristics were calculated and receiver operating characteristic (ROC) analysis conducted. Results  The area under the ROC curve (AUROC) of APRI for predicting significant fibrosis was similar when comparing those with and without HIV co‐infection (0.77 vs. 0.86, P  = 0.18), but was lower in HIV co‐infected patients with CD4 counts <250 cells/mm 3 (0.64 vs. 0.86, P  = 0.05). In HIV co‐infected patients with CD4 counts ≥250, APRI had higher negative predictive value (93% vs. 88%, P  = 0.57), positive predictive value (63% vs. 40%, P  = 0.43) and specificity (95% vs. 88%, P  = 0.05) than in those with lower CD4 counts. Conclusions  The AST to platelet ratio index (APRI) performance characteristics appear to be suboptimal in HCV/HIV co‐infected patients with CD4 counts <250 and they require further study in this population at increased risk for advanced liver disease.

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