Assessment of liver fibrosis and associated risk factors in HIV-infected individuals using transient elastography and serum biomarkers
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- 作者：Johannes Vermehren (1)
Annika Vermehren (1)
Axel Mueller (2)
Amina Carlebach (2)
Thomas Lutz (2)
Peter Gute (2)
Gaby Knecht (2)
Christoph Sarrazin (1)
Mireen Friedrich-Rust (1)
Nicole Forestier (1)
Thierry Poynard (3)
Stefan Zeuzem (1)
Eva Herrmann (4)
Wolf Peter Hofmann (1) (5) - 关键词：HIV ; HCV ; co ; infection ; cART ; Hepatotoxicity ; Transient elastography ; Fibrotest ; Liver enzymes
- 刊名：BMC Gastroenterology
- 出版年：2012
- 出版时间：December 2012
- 年：2012
- 卷：12
- 期：1
- 全文大小：189KB
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34. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-230X/12/27/prepub - 作者单位：Johannes Vermehren (1)
Annika Vermehren (1)
Axel Mueller (2)
Amina Carlebach (2)
Thomas Lutz (2)
Peter Gute (2)
Gaby Knecht (2)
Christoph Sarrazin (1)
Mireen Friedrich-Rust (1)
Nicole Forestier (1)
Thierry Poynard (3)
Stefan Zeuzem (1)
Eva Herrmann (4)
Wolf Peter Hofmann (1) (5)
1. Medizinische Klinik 1, Klinikum der J. W. Goethe-Universit?t, Frankfurt am Main, Germany
2. Infektiologikum, Frankfurt am Main, Germany
3. H?pital Pitié Salpétrière, Paris, France
4. Institut für Biostatistik und mathematische Modellierung, Fachbereich Medizin der J. W. Goethe-Universit?t, Frankfurt am Main, Germany
5. POLIKUM Gesundheitszentren, Berlin, Germany
文摘
Background Liver fibrosis in human immunodeficiency virus (HIV)-infected individuals is mostly attributable to co-infection with hepatitis B or C. The impact of other risk factors, including prolonged exposure to combined antiretroviral therapy (cART) is poorly understood. Our aim was to determine the prevalence of liver fibrosis and associated risk factors in HIV-infected individuals based on non-invasive fibrosis assessment using transient elastography (TE) and serum biomarkers (Fibrotest [FT]). Methods In 202 consecutive HIV-infected individuals (159 men; mean age 47 ± 9 years; 35 with hepatitis-C-virus [HCV] co-infection), TE and FT were performed. Repeat TE examinations were conducted 1 and 2 years after study inclusion. Results Significant liver fibrosis was present in 16% and 29% of patients, respectively, when assessed by TE (?7.1 kPa) and FT (> 0.48). A combination of TE and FT predicted significant fibrosis in 8% of all patients (31% in HIV/HCV co-infected and 3% in HIV mono-infected individuals). Chronic ALT, AST and γ-GT elevation was present in 29%, 20% and 51% of all cART-exposed patients and in 19%, 8% and 45.5% of HIV mono-infected individuals. Overall, factors independently associated with significant fibrosis as assessed by TE (OR, 95% CI) were co-infection with HCV (7.29, 1.95-27.34), chronic AST (6.58, 1.30-33.25) and γ-GT (5.17, 1.56-17.08) elevation and time on dideoxynucleoside therapy (1.01, 1.00-1.02). In 68 HIV mono-infected individuals who had repeat TE examinations, TE values did not differ significantly during a median follow-up time of 24 months (median intra-patient changes at last TE examination relative to baseline: -0.2 kPa, p = 0.20). Conclusions Chronic elevation of liver enzymes was observed in up to 45.5% of HIV mono-infected patients on cART. However, only a small subset had significant fibrosis as predicted by TE and FT. There was no evidence for fibrosis progression during follow-up TE examinations.