Transient elastography discloses identical distribution of liver fibrosis in chronic hepatitis C between HIV-negative and HIV-positive patients on HAART
- F Grünhage†1, 2,
- J-C Wasmuth†1,
- S Herkenrath1,
- N Vidovic3,
- G Goldmann3,
- J Rockstroh1,
- F Lammert2,
- J Oldenburg3,
- T Sauerbruch1 and
- U Spengler1Email author
© I. Holzapfel Publishers 2010
Received: 3 November 2009
Accepted: 7 December 2009
Published: 8 April 2010
Progressive immunodeficiency associated with HIV-infection leads to a progressive course of liver disease in HIV/HCV-co-infected patients. Highly active antiretroviral therapy (HAART) efficiently restores and preserves immune functions and has recently been demonstrated to also result in reduced liver-related mortality in HIV/HCV-co-infected patients.
To analyse differences in current liver fibrosis as a possible effect of HAART on fibrosis progression we assessed hepatic fibrosis by transient elastography in a cross-sectional comparison between HCV-mono-infected and HIV/HCV-co-infected patients presenting at our outpatient department in 2007.
Overall, we did not find any difference in the distribution of liver stiffness between mono- (n = 84) and double-infected (n = 57) patients (14.4 kPa (10.8 - 18.2) versus 12.4 kPa (9.1 - 16.1), mean (95%-CI)). However, in the 8 HIV+ patients with CD4 counts < 200/μl liver stiffness was markedly greater (18.4 kPa (0.8 - 36.0)) than in HIV+ patients with preserved immunity (11.5 kPa (8.4 - 15.0)).
These findings are in line with other data that show an improved prognosis of chronic hepatitis C in HIV+ patients under effective HAART, and may be a hint that fibrosis progression in well-treated HIV+ patients will no longer be different from that in HCV-mono-infected patients.
Chronic hepatitis C is a major cause of hepatocellular injury, activation of hepatic stellate cells, increased deposition of extracellular matrix proteins, and ultimately a profoundly disturbed hepatic micro-architecture. This process is modified by several co-factors such as increased alcohol intake (> 50 g/d), obesity, insulin resistance, and others [1–10]. Importantly, human immunodeficiency virus (HIV) co-infection has been identified to dramatically accelerate liver fibrosis in HIV/HCV-infected patients with advanced immune-deficiency [11–15].
Consequently death from end stage liver cirrhosis or liver cancer had been major factors contributing to death in HIV/HCV co-infected patients during the pre-HAART era. Effective HAART has reduced the burden of opportunistic diseases and overall mortality. Thus, deaths related to liver disease have now become one of the most important causes of death in HIV/HCV co-infected patients, although the absolute number of deaths due to liver disease has decreased possibly reflecting the beneficial impact of HAART on the speed of liver fibrosis progression [6, 16–18]. For this reason, it has meanwhile been recommended to initiate anti-HCV treatment in patients with HIV-co-infection as early as possible to avoid the increased risk of progressive liver disease. On the other hand, effective antiretroviral therapy can improve immune functions, and it has been proposed that preserved immunity may reduce fibrosis progression in HIV/HCV co-infected patients and result in reduced liver related mortality [6, 18].
The decision to initiate anti-HCV treatment pivotally depends on the assessment of hepatic fibrosis. However, liver histology is obtained by biopsy, i.e. an invasive procedure, which has poor acceptance among patients - in particular in those who require repeated assessment. In addition, liver biopsies are subjected to considerable sampling error, and a high degree of inter-observer variability . Thus, various non-invasive tests have been developed to assess liver fibrosis without the need for a biopsy. Transient elastography measures liver stiffness as an index of liver fibrosis. This procedure is easy to perform and entirely harmless. It enables to assess a greater fraction of the liver as a biopsy, and has been demonstrated to correctly reflect the degree of liver fibrosis in a great variety of different chronic liver diseases . Therefore, we applied this non-invasive technique in a cross-sectional analysis to compare liver fibrosis between HCV and HIV/HCV co-infected patients under HAART.
Patients and methods
Patients were prospectively recruited between January and December 2007 at the University Hospital of Bonn, Germany. Patients were eligible for the study if they had active HCV or HIV/HCV co-infection with detectable serum HCV-RNA. Patients with body mass index (BMI) > 28 or perihepatic ascites on abdominal ultrasound were excluded from the study. Informed consent was obtained prior to the study, and the protocol had been approved by our local ethics committee in accordance with the Declaration of Helsinki.
Clinical and demographic data such as age, gender, BMI and medication were recorded in all patients. Detection of anti-HCV, anti-HIV, HCV-RNA, and HIV-RNA, as well as determination of HCV genotypes, HCV and HIV viral loads, CD4 counts, liver function tests and platelet counts were done with standard routine tests as described previously . The AST to platelet ratio index (APRI) was calculated from platelet counts and AST values as a serum surrogate marker of fibrosis .
Transient elastography (TE)
All patients were examined by TE following previously published guidelines [23–25]. In brief, the tip of the probe transducer was placed on the skin between the rib bones over the right lobe of the liver. Measurement depth was between 25 and 65 mm below the skin surface. Ten measurements were performed with a minimum success rate of at least 60%. IQR for TE were lower than 20% of the median for all measurements included in this analysis. The results are expressed as median stiffness of all measurements in kilopascals.
Categorical and quantitative variables were compared by Fischer's exact test and the nonparametric MannWhitney-U test, respectively. Mean values in each group were compared by one-way analysis of variance (ANOVA) and Bonferroni correction. Correlations of liver stiffness to biochemical markers or surrogate fibrosis scores and to age were analyzed by non-parametric Spearman rank correlation, and associations of infection status to severe fibrosis or cirrhosis were checked by Fisher's exact test.
A total number of 147 patients had been screened for the study, but 3 patients in each group had to be excluded because obesity made transient elastography impossible (BMI > 28 kg/m2). Thus, 141 patients - 84 patients with HCV mono-infection and 57 patients with HIV/HCV co-infection - were included into the study.
Clinical Characteristics of the study groups
N = 84
N = 57
Age, median (range)
1, n (%)
non-1, n (%)
Risk factor for HCV or HIV/HCV infection
i.v. drug abuse, n (%)
Blood products, n (%)
unknown, n (%)
No, n (%)
Yes, n (%)
PI-based HAART, n (%)
CD4 count, median (range)
CD4 < 200/μl, n (%)
AST (U/l), mean ± SD
59.7 ± 42.4
66.6 ± 60.1
ALT (U/l), mean ± SD
76.3 ± 48.8
94.4 ± 84.3
GGT (U/l), mean ± SD
104.0 ± 128.0
128.0 ± 129.0
Bilirubin (mg/dl), mean ± SD
0.7 ± 0.5
1.0 ± 1.0*
Platelets (T/l), mean ± SD
198.3 ± 81.0
155.9 ± 68.4*
APRI-score†, mean ± SD
1.5 ± 2.3
2.7 ± 5.3
Metavir-Score according to transient elastography (% of patients)°
52 of the 57 HIV-infected patients had been exposed to a median duration of 3661 days of HAART (range 115 - 6209). 31 patients had received stavudine as part of prior regimens (median exposure time 1185 days, range 121 - 3516), and 24 had received didanosine (406 days, 15 - 2685). There was no difference in liver stiffness with regard to prior exposure to stavudine (exposed 8.8, 3.3 - 66.4 vs. not-exposed 6.1, 3.6 - 30.7; p = 0.369) or didanosine (exposed 9.2, 4.6 - 66.4 vs. not-exposed 6.1, 3.3 - 60.4; p = 0.208).
HIV/HCV co-infected patients had significantly higher bilirubin (1.0 ± 1.0 mg/dl vs. 0.7 ± 0.5; p = 0.007) and lower platelet counts (155.9 ± 68.4 G/l vs. 198.3 ± 81.0; p = 0.001) than HCV mono-infected patients but the difference in APRI score did not reach statistical significance (1.5 ± 2.3 vs. 2.7 ± 5.3). Moreover, we did not detect significant differences in AST, ALT and γ-GT between the groups. Furthermore, clinical and biochemical markers did also not differ between HIV+ patients on PI versus NNRTI-based antiretroviral regimens (data not shown).
Liver stiffness results correlated significantly with bilirubin (r = 0.35; p < 0.001), and γ-GT levels (r = 0.55; p < 0.001). In addition, liver stiffness results were also highly significantly correlated with the APRI-score which has been established as a non-invasive laboratory surrogate marker of liver fibrosis and cirrhosis in patients with HCV-mono-infection and HIV/HCV-co-infection (r = 0.66, p < 0.001).
Studies from the pre-HAART era suggested that liver fibrosis progressed more rapidly in HIV/HCV co-infected patients than in patients with chronic hepatitis C alone. When highly active antiretroviral therapy became available it was demonstrated to markedly reduce opportunistic infections but not viral hepatitis. Thus, it was predicted that accelerated progression of fibrosis might become a leading problem in HIV/HCV co-infected patients in the HAART era.
Using transient elastography, a highly reliable surrogate test to assess liver fibrosis, our study demonstrated that the distribution of liver fibrosis was identical in HCV mono-infected patients and HIV/HCV-co-infected patients under HAART. Since our study groups reflected all patients (95.5%) who had been studied by transient elastography for hepatitis C and HIV/HCV co-infection in 2007, selection bias can largely be excluded and the study groups are representative for HCV- and HIV/HCV-infected patients in our region. Thus, our results suggest, that increased liver fibrosis is no longer encountered in HIV/HCV-co-infected patients under HAART as compared to HCV mono-infection. Of note, our results are in line with the previous observation that accelerated liver disease in HIV/HCV co-infection was linked with advanced immunodeficiency , and our co-infected patients with CD4 counts <200/μl still revealed markedly increased fibrosis. However, this subgroup was rather small and thus did not contribute significantly to the overall distribution of liver fibrosis.
HAART restores CD4 counts and preserves immune functions, which may prevent accelerated progression of fibrosis associated with hepatitis C. For instance, in serial liver biopsies Benhamou and co-workers have directly demonstrated that PI-based antiretroviral therapy can decrease the rate of fibrosis progression in HIV/HCV co-infected patients . Improved fibrosis progression under HAART is further supported by a small number of other studies which reported reduced rates of fibrosis, when HIV co-infection was effectively controlled by HAART [26, 27]. Finally, a decreased rate of fibrosis under HAART may explain, why liver-related mortality is markedly improved under HAART, although antiretroviral drugs do not act directly on HCV replication [11, 18].
Liver stiffness was well correlated to platelet counts and the APRI score, surrogate markers, which have also been used to predict fibrosis in HCV and HIV/HCV co-infection. Of note, differences in APRI scores were not significant in line with our TE results, while cohort platelet counts were significantly lower in the co-infected group. This difference, however, is more likely to reflect suppressive effects of HIV infection on bone marrow function rather than advanced liver fibrosis .
Longer duration of HCV might be associated with advanced stages of fibrosis, as fibrosis is a dynamic process leading to increased fibrosis after long term HCV infection. In most studies information on exact duration of HCV is not precise. However, we can exclude differences in hepatitis C duration as a confounding factor for two reasons: First, HIV-positive patients were hemophiliacs to a large extent. This group has been infected in a relatively short time interval during the late 70ies. Second, we found an identical relationship between patient age as a surrogate marker of disease duration and liver stiffness scores in the two patient groups suggesting identical rates of fibrosis progression.
Contrary to our results, several recent studies still continued to report excess morbidity and mortality in HIV/HCV co-infected patients [29–31]. For instance, also using TE de Ledinghen et al. reported increased fibrosis in their co-infected patients despite antiretroviral therapy . However, discrepancies to our study are probably explained by the very low number of patients with advanced immunodeficiency in our cohort. Moreover, an increased prevalence of other co-factors such as drug and alcohol abuse may have contributed to the more unfavourable results in the other studies, whereas our HIV/HCV patients mainly comprised haemophiliac men who have a considerably better prognosis than drug addicts. Although we did not directly assess life-style related parameters as co-factors (especially alcohol use), we are confident from previous studies, that potential bias due to such cofactors is negligible . Finally, the vast majority of our co-infected patients received a PI-based HAART (83%), which is known to exert greater antifibrotic activity than other HAART regimens [6, 16, 17].
It is noteworthy that the proportion of patients with significant fibrosis and cirrhosis in both groups is large, indicating that many patients have already progressed to fibrosis. Therefore the difference in fibrosis between both groups may be too small as to enable detection of differences in progression rates by a retrospective study.
In summary, our cross-sectional study suggests that the distribution of fibrosis between HCV mono-infected patients and HIV/HCV co-infected patients does not differ when immune functions are well preserved under HAART. This observation may be a first hint that in principle effective HAART can reduce fibrosis progression in HIV/HCV co-infected patients to the same rate as in HCV mono-infection. Prospective longitudinal studies on large patient cohorts with repeated long-term monitoring of fibrosis progression in HCV-mono-infected as well as HIV/HCV co-infected patients are needed to ascertain this attractive hypothesis.
Conflicts of interests
JO has received reimbursement for attending a symposium/congress, funds for research and fees for consulting from CLS Behring. None of the other authors has personal, financial or any other relations with ZLB Behring.
Purchase of the Fibroscan system was supported financially by ZLB Behring GmbH, Marburg. There was no influence of design, realisation, analysis of the study or writing of the paper by ZLB Behring.
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