2005
DOI: 10.1111/j.1468-1293.2005.00330.x
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Validation of a simple model for predicting liver fibrosis in HIV/hepatitis C virus‐coinfected patients

Abstract: ObjectivesRecently, several models incorporating laboratory measurements have been validated for use as surrogate markers for liver fibrosis in hepatitis C virus (HCV) mono-infection, the simplest of these being the aspartate aminotransferase (AST) to platelet ratio index (APRI). We evaluated how well the APRI predicts significant hepatic fibrosis in patients with HIV/HCV coinfection. MethodsForty-six HIV/HCV-coinfected patients who underwent liver biopsy and had concomitant laboratory measurements (AE3 months… Show more

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Cited by 78 publications
(67 citation statements)
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“…Cox proportional hazards regression models were conducted to assess possible associations of the following factors with either grade ‡ III or IV hyperbilirubinemia: gender, age, risk factor for HIV acquisition, clinical class C {i.e., occurrence of major opportunistic infections according to the Centers of Disease Control (CDC'93) classification [7]), HCV-Ab and hepatitis B surface antigen (HBsAg) serostatus, CD4+ T-cell count and HIV-RNA at baseline (i.e., at initiation of ATV-containing regimens), baseline ALT, baseline bilirubinemia, aspartate aminotransferase (AST)/platelet ratio index (APRI)-score as a surrogate of the stage of liver disease [8], use of low-dose ritonavir, inclusion of other protease inhibitors (PIs) at active dosages in the regimens, and non-nucleoside reverse transcriptase inhibitors (NNRTI) or tenofovir (TDF) co-medications. The variables found to be significant (p < 0.2) by the univariate analysis were entered into multivariable models.…”
Section: Discussionmentioning
confidence: 99%
“…Cox proportional hazards regression models were conducted to assess possible associations of the following factors with either grade ‡ III or IV hyperbilirubinemia: gender, age, risk factor for HIV acquisition, clinical class C {i.e., occurrence of major opportunistic infections according to the Centers of Disease Control (CDC'93) classification [7]), HCV-Ab and hepatitis B surface antigen (HBsAg) serostatus, CD4+ T-cell count and HIV-RNA at baseline (i.e., at initiation of ATV-containing regimens), baseline ALT, baseline bilirubinemia, aspartate aminotransferase (AST)/platelet ratio index (APRI)-score as a surrogate of the stage of liver disease [8], use of low-dose ritonavir, inclusion of other protease inhibitors (PIs) at active dosages in the regimens, and non-nucleoside reverse transcriptase inhibitors (NNRTI) or tenofovir (TDF) co-medications. The variables found to be significant (p < 0.2) by the univariate analysis were entered into multivariable models.…”
Section: Discussionmentioning
confidence: 99%
“…Nineteen studies included HCVmonoinfected patients (n ϭ 3,822), 17,20,[22][23][24][25][26][27][28][29][30][31][32][33][34][35][36][37][38] and 4 included HIV/HCV-co-infected patients (n ϭ 444). [48][49][50][51] Biopsy quality was considered acceptable in only 4 of the 22 studies. 51,53,57,63 According to the Quality Assessment of Diagnostic Accuracy Studies scale, the methodological quality of the included studies was very good.…”
Section: Characteristics Of the Included Studiesmentioning
confidence: 99%
“…Subsequently, numerous studies have attempted to externally validate these findings, but results have been controversial. 11,17,48 Differences in patient populations, including the prevalence of significant fibrosis, and reference ranges for AST, may explain these discrepancies.…”
mentioning
confidence: 99%
“…not by CD4 cell criteria alone) [12]. The aspartate aminotransferase (AST) to platelet ratio index (APRI) was used as a noninvasive surrogate for liver fibrosis and defined as: 100 ¥ (AST/upper limit of normal)/platelet count (10 9 /L) [13,14]. An APRI score > 1.5 was considered to indicate significant fibrosis (corresponding to a biopsy score > F2) [14].…”
Section: Outcome Measuresmentioning
confidence: 99%