Changes in Biomarkers of Liver Disease during Successful Combination Antiretroviral Therapy in HIV–HCV-Coinfected Individuals. Issue 2 (February 2014)
- Record Type:
- Journal Article
- Title:
- Changes in Biomarkers of Liver Disease during Successful Combination Antiretroviral Therapy in HIV–HCV-Coinfected Individuals. Issue 2 (February 2014)
- Main Title:
- Changes in Biomarkers of Liver Disease during Successful Combination Antiretroviral Therapy in HIV–HCV-Coinfected Individuals
- Authors:
- Rohrbach, Janine
Stickel, Felix
Schmid, Patrick
Thormann, Wolfgang
Kovari, Helen
Scherrer, Alexandra
Günthard, Huldrych F
Vuichard, Danielle
Cavassini, Matthias
Ambrosioni, Juan
Bernasconi, Enos
Furrer, Hansjakob
Rauch, Andri - Abstract:
- Background: We investigated changes in biomarkers of liver disease in HIV–HCV-coinfected individuals during successful combination antiretroviral therapy (cART) compared to changes in biomarker levels during untreated HIV infection and to HIV-monoinfected individuals. Methods: Non-invasive biomarkers of liver disease (hyaluronic acid [HYA], aspartate aminotransferase-to-platelet ratio index [APRI], Fibrosis-4 [FIB-4] index and cytokeratin-18 [CK-18]) were correlated with liver histology in 49 HIV–HCV-coinfected patients. Changes in biomarkers over time were then assessed longitudinally in HIV–HCV-coinfected patients during successful cART ( n =58), during untreated HIV-infection ( n =59), and in HIV-monoinfected individuals ( n =17). The median follow-up time was 3.4 years on cART. All analyses were conducted before starting HCV treatment. Results: Non-invasive biomarkers of liver disease correlated significantly with the histological METAVIR stage ( P <0.002 for all comparisons). The mean ±sd area under the receiver operating characteristic (AUROC) curve values for advanced fibrosis (≥F3 METAVIR) for HYA, APRI, FIB-4 and CK-18 were 0.86 ±0.05, 0.84 ±0.08, 0.80 ±0.09 and 0.81 ±0.07, respectively. HYA, APRI and CK-18 levels were higher in HIV-HCV-coinfected compared to HIV-monoinfected patients ( P <0.01). In the first year on cART, APRI and FIB-4 scores decreased (-35% and -33%, respectively; P =0.1), mainly due to the reversion of HIV-induced thrombocytopaenia, whereas HYABackground: We investigated changes in biomarkers of liver disease in HIV–HCV-coinfected individuals during successful combination antiretroviral therapy (cART) compared to changes in biomarker levels during untreated HIV infection and to HIV-monoinfected individuals. Methods: Non-invasive biomarkers of liver disease (hyaluronic acid [HYA], aspartate aminotransferase-to-platelet ratio index [APRI], Fibrosis-4 [FIB-4] index and cytokeratin-18 [CK-18]) were correlated with liver histology in 49 HIV–HCV-coinfected patients. Changes in biomarkers over time were then assessed longitudinally in HIV–HCV-coinfected patients during successful cART ( n =58), during untreated HIV-infection ( n =59), and in HIV-monoinfected individuals ( n =17). The median follow-up time was 3.4 years on cART. All analyses were conducted before starting HCV treatment. Results: Non-invasive biomarkers of liver disease correlated significantly with the histological METAVIR stage ( P <0.002 for all comparisons). The mean ±sd area under the receiver operating characteristic (AUROC) curve values for advanced fibrosis (≥F3 METAVIR) for HYA, APRI, FIB-4 and CK-18 were 0.86 ±0.05, 0.84 ±0.08, 0.80 ±0.09 and 0.81 ±0.07, respectively. HYA, APRI and CK-18 levels were higher in HIV-HCV-coinfected compared to HIV-monoinfected patients ( P <0.01). In the first year on cART, APRI and FIB-4 scores decreased (-35% and -33%, respectively; P =0.1), mainly due to the reversion of HIV-induced thrombocytopaenia, whereas HYA and CK-18 levels remained unchanged. During long-term cART, there were only small changes (<5%) in median biomarker levels. Median biomarker levels changed <3% during untreated HIV-infection. Overall, 3 patients died from end-stage liver disease, and 10 from other causes. Conclusions: Biomarkers of liver disease highly correlated with fibrosis in HIV-HCV-coinfected individuals and did not change significantly during successful cART. These findings suggest a slower than expected liver disease progression in many HIV-HCV-coinfected individuals, at least during successful cART. … (more)
- Is Part Of:
- Antiviral therapy. Volume 19:Issue 2(2014)
- Journal:
- Antiviral therapy
- Issue:
- Volume 19:Issue 2(2014)
- Issue Display:
- Volume 19, Issue 2 (2014)
- Year:
- 2014
- Volume:
- 19
- Issue:
- 2
- Issue Sort Value:
- 2014-0019-0002-0000
- Page Start:
- 149
- Page End:
- 159
- Publication Date:
- 2014-02
- Subjects:
- Antiviral agents -- Periodicals
Antiviral Agents -- therapeutic use
Virus Diseases -- therapy
Viruses -- drug effects
Antiviral agents
Periodical
Electronic journals
Periodicals
616.9106 - Journal URLs:
- http://www.intmedpress.com/General/showSectionSub.cfm?SectionID=2&SectionSubID=1&SectionSubSubID=1 ↗
http://www.uk.sagepub.com/home.nav ↗ - DOI:
- 10.3851/IMP2686 ↗
- Languages:
- English
- ISSNs:
- 1359-6535
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24112.xml