Abstract
The objective of this work was to identify predictive factors of fibrosis regression after direct antiviral agents (DAAs) in HCV-monoinfected and HIV/HCV-coinfected patients. This was a prospective study of HCV-monoinfected (n = 20), HIV/HCV-co-infected (n = 66) patients and healthy controls (n = 15). Patients had started DAAs and achieved sustained virological response. Liver stiffness (LS) and serum concentrations of profibrotic transforming growth factor (TGF)-β1 and CXC chemokine ligand 4 (CXCL4) and antifibrotic HGF hepatocyte growth factor (HGF) were analyzed at baseline (M0) and 12 months after starting DAAs (M12). A M12 LS achievement of ≤ 9.5 kPa was considered the cutoff point to discharge from a liver clinic. The LS decrease from M0 to M12 was 34%. No significant differences were observed in LS decline between HCV- and HIV/HCV-infected individuals. Changes of serum CXCL4, TGF-β1 and HGF levels did not correlate with LS improvement. 16 out from 56 patients (28%) with a baseline LS > 9.5 achieved a M12 LS ≤ 9.5. HCV-monoinfected and HIV/HCV coinfected patients experienced a significant reduction of LS after sustained virological response. This improvement did not correlate with changes in serum profibrotic or antifibrotic markers. A 29% of those with a baseline LS > 9.5 achieved a LS under this cutoff point.
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Introduction
The achievement of a sustained virological response (SVR) after treating chronic hepatitis C virus (HCV) infection reduces all-cause mortality and liver complications, such as cirrhosis, liver decompensation, and hepatocellular carcinoma1. The impact is even more relevant in human immunodeficiency virus (HIV)-coinfected patients, in which HCV-induced disease progresses more rapidly than in monoinfected patients2.
It has been appreciated that inflammatory and coagulation pathways are both intrinsically involved in the pathophysiology of liver damage3. Blood platelets are activated in inflammatory and immune processes and in the hemostatic disorders in the liver, releasing active compounds [such as transforming growth factor (TGF)-β1 and CXC chemokine ligand 4 (CXCL4)]4. These proteins stimulate the fibrinogenesis and mitogenesis of Ito cells in the liver5. Both TGF-β1 and CXCL4 are circulating biomarkers of tissue fibrosis6,7.
Contradictory results have been published about serum concentrations of these markers. Some articles have demonstrated an increase of serum levels of TGF-β1 in HCV-monoinfected patients over time, mainly in patients with progressive liver fibrosis8,9. However, other authors have observed that liver stiffness values are inversely correlated with TGF-β110, mainly in HIV/HCV coinfected patients11,12. Anti-HCV therapy with interferon alpha and ribavirin affects the tissue expression of TGF-β1, and may thereby modulate hepatic fibrogenetic events13.
In the case of CXCL4, serum levels are significantly increased in HCV‐infected patients with moderate to severe liver fibrosis compared to individuals with no or only mild fibrosis or to healthy controls4,7. However, individuals with severe fibrosis and cirrhosis experience a decrease in CXCL4 serum levels owing to reduced numbers of platelets4.
In contrast with these profibrogenic molecules, hepatocyte growth factor (HGF) is a powerful inhibitor of hepatic stellate cells activation14. In addition to a potential antifibrogenic effect, several studies have shown that HGF is involved in hepatic cell regeneration15 and has a proangiogenic role in chronic viral liver disease16. Another process wherein HGF has been involved is the development of hepatocellular carcinoma (HCC)17. Our group has demonstrated that high serum HGF levels are associated with greater liver fibrosis in HCV-infected patients18. Serum HGF concentrations did not decrease after response to interferon plus ribavirin19.
Serum-based fibrosis markers, like AST to platelets ratio index (APRI)20 and Fibrosis-4 (FIB-4) score21, are readily available, but their diagnostic performance is suboptimal in both low- and high prevalence scenarios, with high false positive rates for detection of cirrhosis22. Transient elastometry (TE) is a noninvasive procedure that assesses liver fibrosis by measuring liver stiffness (LS). LS measurement has shown a high accuracy for detecting liver fibrosis in HCV-infected patients, either with21 or without HIV-coinfection22. TE has superior diagnostic performance in identifying cirrhosis, with lower rates of misclassification of patients20. Several studies, carried out mostly among monoinfected individuals, have reported a significant decrease in liver stiffness after treatment20,21. Nevertheless, there is scarce data regarding the impact of SVR on liver stiffness within HIV/HCV patients treated with DAAs23,24,25,26,27,28. Furthermore, data about the relationship between modifications of liver fibrosis, both in HCV-monoinfected and HIV/HCV coinfected patients, and the serum concentrations of serum markers of fibrosis (CXCL4 or TGF-β1) or regeneration/proliferation (HGF), are also scarce and controversial9,11,12, even though these parameters could be markers of fibrosis evolution.
Our objectives were: (1) analyze the liver stiffness improvement, measured by transient elastography, in patients with SVR after DAAs, and those factors related with it. (2) Compare the liver stiffnes evolution in HIV/HCV coinfected and HCV-monoinfected patients. (3) Correlate changes of serum markers of fibrosis (CXCL4 or TGF-β1) or proliferation (HGF), and modification of LS.
Results
Baseline results
A total of 86 patients naïve to DAA underwent HCV, achieving SVR, and had two TE and serum samples separated by 12 months. Baseline characteristics of the healthy controls, HCV-monoinfected and HIV/HCV coinfected patients are shown in Table 1.
Regarding HIV status, 100% had undetectable HIV viral load (< 50 copies/ml) and the median CD4 + count was 494/ml (312–791), with 9 subjects (14%) presenting severe immunosuppression (< 200 cells/ml).
CXCL4 and TGF-β1 were significantly decreased in HCV-monoinfected and HIV/HCV-coinfected patients in comparison with healthy controls. Serum levels of HGF were significantly increased in HIV/HCV coinfected patients compared with HCV-monoinfected or healthy individuals (Table 1).
Relationship between liver stiffness and other variables at baseline
LS was directly correlated with serum HGF (r = 0.600, p < 0.001) and inversely correlated with TGF-β1 levels (r = −0.374, p = 0.001), but not with CXCL4 concentration. TGF-β1 and CXCL4 levels were significantly correlated (r = 0.414, p < 0.001). Platelet counts were significantly correlated with serum CXCL4 (r = 0.400, p < 0.001) and TGF-β1 levels (r = 0.414, p < 0.001). In HIV/HCV coinfected patients, a significant correlation was detected between CD4 + T cell count and CXCL4 concentration (r = 0.309, p = 0.015), but not with TGF-β1 or HGF levels.
Modifications of liver stiffness and serum CXCL4, TGF-β1 and HGF concentrations during follow-up
Modifications from M0 to M12 in LS, APRI, FIB-4, CXCL4, TGF-β1 and HGF from M0 to M12 are shown in Table 2. A significant decrease of LS, APRI and FIB-4 values were detected from M0 to M12. Likewise, a significant diminution of HGF, but not of CXCL4 or TGF-β1, levels were observed. Changes of LS were not correlated with those of TGF-β1, CXCL4 or HGF levels (Fig. 1). Modifications of LS, APRI and FIB-4 score, CXCL4, TGF-β1 and HGF levels or CXCL4/platelets or TGF-β1/platelets ratios were similar in patients with and without cirrhosis (Fig. 2).
After the follow-up of 12 months, the median of LS decrease was 34% (IQR: − 59, 0). There was no significant difference in the percentage of LS, CXCL4, TGF-β1 and HGF levels decrease among HCV monoinfected and HIV/HCV coinfected patients (Fig. 3).
In HIV/HCV coinfected patients, there was no significant difference in LS change between individuals with a CD4 + T lymphocyte count higher or lower than 200/mm3 [− 37 (− 60, + 9) vs − 41 (− 78, + 3), respectively; p = 0.770]. Changes of serum TGF-β1, CXCL4 and HGF levels were similar in patients with more or less than 200/mm3 (data not shown).
Modifications of fibrosis stage after SVR
Overall, 26% were reclassified into a different fibrosis stage after follow-up. No change in fibrosis stage was observed in patients with baseline non-significant fibrosis. In those with significant fibrosis (n = 41), 15 of them (37%) were re-classified as non-significant fibrosis and one (2%) as cirrhosis. In those with cirrhosis (n = 32), 7 of them (22%) were re-classified as significant fibrosis.
Because a LS ≤ 9.5 after DAAs is a cutoff indicative for discharge from specialized liver clinic24, those patients with a baseline LS > 9.5 (n = 56) were evaluated 12 months after starting DAAs, grouped in function of the LS at M12 (Table 3). 16 of these patients achieved a LS ≤ 9.5 12 months after starting DAAs. After univariate analysis of variables from patients with a baseline LS > 9.5, parameters associated with a LS at M12 ≤ 9.5 were baseline LS, change in the LS after therapy, baseline platelets count and serum HGF levels; baseline TGF-β1 and APRI and risk factor for transmission “people who inject drugs” approached statistical significance. After binary logistic regression, only baseline LS was significantly associated with a M12 LS ≤ 9.5. Range of baseline LS of those with a M12 LS ≤ 9.5 after DAAs was 9.6–21.6, whereas that of patients with a M12 LS > 9.5 was 9.6–53.2.
Discussion
The prospective study presented here showed a significant decline on LS after 12 months with DAA therapy and achieving SVR. The LS improvement was not related with the existence of HIV/HCV coinfection or changes in serum levels of CXCL4, TGF-β1 or HGF.
Besides LS and APRI or FIB-4 score, serum levels of CXCL4, TGF-β1 and HGF were analyzed. It was remarkable that a significant lower concentration of CXCL4 and TGF-β1 was observed in HCV-infected patients compared with healthy controls. On the other hand, LS values were inversely correlated with TGF-β1 in our series, corroborating other authors observations10,11,12. Lower concentrations of fibrosis markers could be explained by one or several of the following: (a) Serum concentrations could be a mirror image of liver levels, justifying the inverse correlation between TGF-β1 and LS. (b) Individuals with severe fibrosis and cirrhosis show decreased serum CXCL4 and TGF-β1 levels owing to reduced numbers of platelets5. In fact, platelet counts were significantly correlated with serum CXCL4 and TGF-β1 levels. (c) It could be also possible that the lower concentrations of TGF-β1 and CXCL4 were related with a lower leukocyte or lymphocyte count. Effectively, in HIV/HCV coinfected patients, a significant correlation was detected between CD4 + T cell count (this was not a variable measured in HCV-monoinfected patients) and CXCL4 concentration.
HGF is a mitogenic cytokine implicated in regeneration of hepatic tissue15. Because liver cirrhosis is characterized by hepatocyte necrosis, fibrosis and liver regeneration3, the direct correlation among serum concentrations of HGF and LS, detected in this and in previous articles18,29 was expected: circulating HGF level may reflect hepatic injury during feedback mechanism for repairing the hepatic tissue.
True fibrosis regression (biopsy-proven) is developed when SVR is achieved30. Likewise, previous studies have indicated that LS measures may improve following anti-HCV antiviral therapy31,32. This was also the case in our series: the median LS decrease after 12 months of follow-up was a 34%. Considering patients with significant fibrosis, a 37% of them achieved posttreatment LS lower than 7.81 kPa (non-significant fibrosis), and a 22% of those with baseline cirrhosis achieved posttreatment LS lower than 15.56 kPa (significant fibrosis, but not cirrhosis).
Some studies have found that TE improvements could be overstated when compared with histologic staging27,33, and that this decline might be correlated with inflammation or necrosis improvement26,34,35,36,37. Our data support this hypothesis: if changes in LS were attributed only to fibrosis modifications, a direct correlation could have been detected with fibrosis marker changes; however, this correlation between changes in serum levels of CXCL4 or TGF-β1 and LS decline was not observed. Furthermore, changes in serum CXCL4 or TGF-β1 concentrations from M0 to M12 were not significant. Attending to these results and measuring liver fibrosis by TE, we can conclude that CXCL4 or TGF-β1 measurements are not convenient for monitoring fibrosis changes.
The technical review on TE by the American Gastroenterological Association suggested that patients without metabolic comorbidities, history of alcohol excess, or HBV–HIV coinfection, and with a liver stiffness of ≤ 9.5 kPa after sustained HCV viral response may be considered for discharge from a specialized liver clinic24. A M12 LS ≤ 9.5 kPa was achieved by a 29% (16 out of 56) of those with baseline LS higher than this cutoff point. Baseline LS, change in the LS after therapy, baseline platelets count and serum HGF levels (but not CXCL4 or TGF-β1 concentration) were associated with the achievement of a M12 LS ≤ 9.5 kPa in the univariate analysis.
Baseline LS, but not baseline APRI or FIB-4, was able to discriminate between patients with an initial LS > 9.5 who achieved a final LS lower than the mentioned cut-off point. In fact, only the baseline LS was independently associated with a M12 LS ≤ 9.5. However, patients with a wide range of baseline LS (9.6–21.6 kPa) could achieve that cutoff point, limiting the usefulness of baseline LS as predictive marker.
It has been stated that the achievement of SVR plays a determinant role in preventing additional liver damage32. This is even more remarkable in HIV/HCV coinfected patients33. Thus, a particular analysis of these patients was performed. They were characterized by a relatively preserved immune status, as proved by a median CD4 + count of 494/mm3, and undetectable HIV viral load. The LS and the proportion of them with liver cirrhosis was significantly higher than those of HCV-monoinfected patients. After 12 months of follow-up and having achieved SVR, HIV/HCV coinfected patients showed similar change of LS to HCV-monoinfected individuals. This decrease was similar in patients with more or less than 200 CD4 + lymphocytes/mm3, although the number of patients with less than 200/mm3 (n = 9) limits the extrapolation of results. Serum levels of profibrotic (TGF-β1 and CXCL4) markers and changes of these serum concentrations were similar in HCV-monoinfected and HIV/HCV coinfected individuals, suggesting that liver fibrosis regulatory mechanisms function in a similar mode in both groups of patients. Attending to direct correlation among serum concentrations of HGF and LS, serum HGF were significantly increased in HIV/HCV coinfected patients, in which the proportion of cirrhotic patients was higher. However, modification of serum HGF from M0 to M12 was similar in HCV-monoinfected and HIV/HCV coinfected individuals.
Our study might have some limitations. First, the sample size limited our ability to control for confounding factors that might interfere with SVR; the power of the study was insufficient to identify differences in several covariates, such as genotype, immune status or HCV viral load. Second, histologic assessment was not available, so correlations between TE results and biopsies could not be performed. Third, as it has been previously detected in articles that have compared HIV/HCV coinfected and HCV-monoinfected patients38,39, HIV/HCV coinfected individuals are younger, with a predominance of drug use as risk factor. HCV genotype 1b predominantly affects to HCV-monoinfected individuals. However, these factors were not significantly correlated with serum levels of CXCL4, TGF-β1 and HGF or with LS measures or associated with an achievement of a LS < 9.5 kPa in the bivariate or multivariate analyses.
In summary, a third of HCV-infected patients that achieved HCV eradication experienced a significant reduction of LS, assessed by TE. LS decline was similar in HCV-monoinfected and HIV/HCV coinfected patients. The significance of this reduction is unclear, because there was no correlation with change in serum levels of fibrosis markers CXCL4 and TGF-β1 or in the proliferative HGF.
Methods
Patients and study design
This is a prospective cohort study of HCV-infected patients conducted at the Hospital Universitario Puerta del Mar (Cádiz, Spain). Two groups of patients were analyzed: HCV monoinfected patients (n = 20) and HIV/HCV coinfected patients (n = 66). A group of healthy individuals (n = 15) served as controls.
Subjects were eligible for analysis if they were treated with DAAs; started the therapy between 1 January 2016 and 31 December 2018, and achieved sustained virological response. They underwent a baseline transient elastography (TE) and were taken a serum sample at inclusion and at least another TE and serum sample 12 months after starting anti-HCV treatment.
All patients with detectable serum HCV RNA naïve to DAAs were consecutively enrolled. Anti-HCV therapy was performed under routine clinical care conditions, according to the best medical judgment and the prevailing HCV treatment guidelines at the time [www.seimc.org], based on HCV genotype, history of HCV treatment, drug interactions with antiretroviral treatment (ART) against HIV, and liver fibrosis assessed through TE. Anti-HCV therapy was administered for 12 weeks in all cases. In HIV/HCV coinfected patients, there were no modifications in the ART during the study period.
The exclusion criteria were hepatitis B virus coinfection, other concomitant causes of liver disease, including active alcohol abuse, active infections, and past or present treatment with steroids or immunosuppressive drugs prior to starting anti-HCV therapy.
The follow-up period covered from the date of the treatment onset (M0) until 12 months (M12) after starting anti-HCV treatment. Information on blood cells counts, kidney and liver function parameters, and virological markers was collected at M0, at week 12 posttreatment visits and at M12. Data about LS and fibrosis (CXCL4 and TGF-β1)- or proliferation (HGF)-related variables was collected at M0 and M12.
Liver fibrosis staging
LS was examined through TE by the FibroScan system (Echosens, Paris, France) at M0 and M12. A minimum of 10 LS measurements were required. The median value was assumed to be representative of LS. A set of measurements was considered to be reliable if the success rate was ≥ 60% and the interquartile range was less than one-third of the median LS value. Unreliable measurements of LS were excluded. All measurements were obtained by two trained operators (MRP and JAGG) using a single device. Results, expressed in kilopascals (kPa), were categorized in three stages as follows: non-significant fibrosis (F0–F1), under 7.81 kPa; significant fibrosis (F2–F3), equal or more than 7.81 kPa; cirrhosis (F4), ≥ 15.56 kPa, according to Stebbing’s meta-analysis40. Besides fibrosis, other factors may also result in increased liver stiffness, such as the presence of severe hepatic inflammation, extrahepatic arteriovenous or biliary obstruction, and congestive heart failure24. They were excluded by clinical and complementary explorations.
AST to platelets ratio index (APRI)20 and Fibrosis-4 (FIB-4) score21 were also calculated.
Variables
Change in LS was the dependent variable and was defined by the difference between the values obtained at M12 and the M0 by TE, measured in kPa, divided by the M0 value [(M12 liver stiffness − M0 liver stiffness)/M0 liver stiffness].
Independent variables included: demographic factors [sex, age, HIV/HCV transmission mechanism, alcohol consumption (> 50 g/day, for more than 5 years)]; HIV-coinfection and HIV-related factors (viral load, CD4 + count and percentage); HCV-related factors (viral load, genotype, previous treatment experience); (d) other laboratory data (serum transaminases); (e) treatment-related factors (DAA regimen); (f) serum levels of fibrosis (CXCL4 and TGF-β1) and proliferation (HGF)-related markers; (g) APRI and FIB-4 score.
Changes from M0 to M12 of LS, APRI, FIB-4, or serum fibrosis and proliferation markers were calculated as the values at M12 minus the values at M0, divided by the values at M0 [(M12 value − M0 value)/M0 value].
SVR at week 12 (SVR12) was defined as HCV RNA undetectable at week 12 after the treatment had ended.
Statistical analysis
For comparisons of patient’s characteristics, we used the Fisher and Chi-square tests (categorical variables) or the Student’s t test and Mann–Whitney test (continuous variables), depending on the normality of distributions.
The primary outcome was the assessment of evolution of LS after 12 months of follow-up. Likewise, a LS equal or lower of 9.5 was selected, because a post-SVR LS of ≤ 9.5 kPa may be considered as a cutoff point for discharge from a dedicated liver clinic24. To establish nonadjusted associations between LS decline and patient’s clinical or analytical findings, we used univariant models. Multivariable linear regression models were implemented to analyze the impact on LS of statistical significant independent variables. The study length was calculated from the date of the DAA regimen prescription to the 12 months after starting anti-HCV therapy. Statistical analyses were performed with SPSS for Windows version 22.0 (SPSS, Inc), considering a value of p < 0.05 significant.
Ethical aspects
The study was designed and conducted following the Helsinki declaration. The Ethics Committee of the Hospital Universitario Puerta del Mar (Cádiz) approved the study, and all the patients gave their written informed consent.
References
Carrat, F. et al. French ANRS CO22 Hepather cohort. Clinical outcomes in patients with chronic hepatitis C after direct-acting antiviral treatment: a prospective cohort study. Lancet 393, 1453–1464 (2019).
Martinez-Sierra, C. et al. Progression to liver fibrosis and cirrhosis of chronic hepatitis C in HIV co-infected patients. Clin. Infect. Dis. 36, 491–498 (2003).
Calvaruso, V. et al. Coagulation and fibrosis in chronic liver disease. Gut 57, 1722–1727 (2008).
Ponomarev, E. D. Fresh evidence for platelets as neuronal and innate immune cells: their role in the activation, differentiation, and deactivation of Th1, Th17, and Tregs during tissue inflammation. Front. Immunol. 9, 406 (2018).
Panasiuk, A., Zak, J., Kasprzycka, E., Janicka, K. & Prokopowicz, D. Blood platelet and monocyte activations and relation to stages of liver cirrhosis. World J. Gastroenterol. 11, 2754–2758 (2005).
Border, W. A. & Noble, N. A. Transforming growth factor beta in tissue fibrosis. N. Engl. J. Med. 331, 1286–1292 (1994).
Zaldivar, M. M. et al. CXC chemokine ligand 4 (CXCL4) is a platelet-derived mediator of experimental liver fibrosis. Hepatology 51, 1345–1353 (2010).
Kanzler, S. et al. Prediction of progressive liver fibrosis in hepatitis C infection by serum and tissue levels of transforming growth factor-beta. J. Viral Hepat. 8, 430–437 (2001).
Neuman, M. G. et al. Kinetics of serum cytokines reflect changes in the severity of chronic hepatitis C presenting minimal fibrosis. J. Viral Hepat. 9, 134–140 (2002).
Valva, P. et al. The role of serum biomarkers in predicting fibrosis progression in pediatric and adult hepatitis C virus chronic infection. PLoS ONE 6, e23218 (2011).
Rallon, N. et al. Elevated TGF-b1 levels might protect HCV/HIV-co-infected patients from liver fibrosis. Eur. J. Clin. Invest. 41, 70–76 (2011).
Sacchi, P. et al. Liver fibrosis, microbial translocation and immune activation markers in HIV and HCV infections and in HIV/HCV co-infection. Dig. Liver Dis. 47, 218–225 (2015).
Guido, M. et al. Effects of interferon plus ribavirin treatment on NF-kappaB, TGF-beta1, and metalloproteinase activity in chronic hepatitis C. Mod. Pathol. 19, 1047–1054 (2006).
Michalopoulos, G. K. & Khan, Z. Liver regeneration, growth factors, and amphiregulin. Gastroenterology 128, 503–506 (2005).
Huh, C. G. et al. Hepatocyte growth factor/c-met signaling pathway is required for efficient liver regeneration and repair. Proc. Natl. Acad. Sci. U.S.A. 101, 4477–4482 (2004).
Medina, J. et al. Hepatocyte growth factor activates endothelial proangiogenic mechanisms relevant in chronic hepatitis C-associated neoangiogenesis. J. Hepatol. 38, 660–667 (2003).
Chau, G. Y. et al. Significance of serum hepatocyte growth factor levels in patients with hepatocellular carcinoma undergoing hepatic resection. Eur. J. Surg. Oncol. 34, 333–338 (2008).
Marín-Serrano, E. et al. Hepatocyte growth factor and chronic hepatitis C. Rev. Esp. Enferm. Dig. 102, 365–371 (2010).
Anatol, P., Robert, F. & Danuta, P. Effect of interferon alpha2b plus ribavirin treatment on selected growth factors in respect to inflammation and fibrosis in chronic hepatitis C. World J. Gastroenterol. 11, 1854–1858 (2005).
Lin, Z. H. et al. Performance of the aspartate aminotransferase-to-platelet ratio index for the staging of hepatitis C-related fibrosis: an updated meta-analysis. Hepatology 53, 726–736 (2011).
Sterling, R. K. et al. Development of a simple noninvasive index to predict significant fibrosis patients with HIV/HCV co-infection. Hepatology 43, 1317–1325 (2006).
Vergara, S. et al. The use of transient elastometry for assessing liver fibrosis in patients with HIV and hepatitis C virus coinfection. Clin. Infect. Dis. 45, 969–974 (2007).
Castéra, L. et al. Prospective comparison of transient elastography, fibrostest, APRI, and liver biopsy for the assessment of fibrosis in chronic hepatitis C. Gastroenterology 128, 343–350 (2005).
Singh, S., Muir, A. J., Dieterich, D. T. & Falck-Ytter, Y. T. American Gastroenterological Association Institute technical review on the role of elastography in chronic liver diseases. Gastroenterology 152, 1544–1577 (2017).
Lledo, G. M. et al. Regression of liver fibrosis after curing chronic hepatitis C with oral antivirals in patients with and without HIV coinfection. AIDS 32, 2347–2352 (2018).
Pons, M. et al. Rapid liver and spleen stiffness improvement in compensated advanced chronic liver disease patients treated with oral antivirals. Therap. Adv. Gastroenterol. 10, 619–629 (2017).
Rial-Crestelo, D. et al. Does fibrosis really regress in HIV/hepatitis C virus co-infected patients after treatment with direct antiviral agents?. AIDS 34, 427–432 (2020).
Corma-Gómez, A. et al. Liver stiffness at the time of sustained virological response predicts the clinical outcome in HIV/HCV-coinfected patients with advanced fibrosis treated with direct-acting antivirals. Clin. Infect. Dis. 71, 2354–2362 (2020).
Abdelgawad, M. E., El-Zakzok, H., Salah, M. & El-Mezayen, H. A. Diagnostic accuracy of hepatocyte growth factor, Fas/CD95 and Endostatin for non-invasive assessment of hepatic fibrosis in biopsy-proven hepatitis C virus patients. Infect. Genet. Evol. 85, 104526 (2020).
Akhtar, E., Manne, V. & Saab, S. Cirrhosis regression in hepatitis C patients with sustained virological response after antiviral therapy: a meta-analysis. Liver Int. 35, 30–36 (2015).
Vergniol, J. et al. Changes of non-invasive markers and FibroScan values during HCV treatment. J. Viral Hepat. 16, 132–140 (2009).
Hezode, C. et al. Liver stiffness diminishes with antiviral response in chronic hepatitis C. Aliment. Pharmacol. Ther. 34, 656–663 (2011).
Pan, J. J. et al. Morphometry confirms fibrosis regression from sustained virologic response to direct-acting antivirals for hepatitis C. Hepatol. Commun. 2, 1320–1330 (2018).
Vispo, E. et al. Overestimation of liver fibrosis staging using transient elastography in patients with chronic hepatitis C and significant liver inflammation. Antivir. Ther. 14, 187–193 (2009).
Castera, L. et al. Direct antiviral agent treatment of chronic hepatitis C results in rapid regression of transient elastography and fibrosis markers fibrosis-4 score and aspartate aminotransferase-platelet ratio index. Liver Int. 37, 369–376 (2017).
Dolmazashvili, E. et al. Regression of liver fibrosis over a 24-week period after completing direct-acting antiviral therapy in patients with chronic hepatitis C receiving care within the national hepatitis C elimination program in Georgia: results of hepatology clinic HEPA experience. Eur. J. Gastroenterol. Hepatol. 29, 1223–1230 (2017).
Macías, J. et al. Fast fibrosis progression between repeated liver biopsies in patients coinfected with human immunodeficiency virus/hepatitis C virus. Hepatology 50, 1056–1063 (2009).
Fernandez-Fuertes, M. et al. Similar prevalence of hepatic steatosis among patients with chronic hepatitis C with and without HIV coinfection. Sci. Rep. 10, 6736 (2020).
Merchante, N. et al. Sustained virological response to direct-acting antiviral regimens reduces the risk of hepatocellular carcinoma in HIV/HCV-coinfected patients with cirrhosis. J. Antimicrob. Chemother. 73, 2435–2443 (2018).
Stebbing, J. et al. A meta-analysis of transient elastography for the detection of hepatic fibrosis. J. Clin. Gastroenterol. 44, 214–219 (2010).
Acknowledgements
We acknowledge to Adrianne E. Jones for technical assitance with English language. This work was supported by Grants of the Secretaría General de Investigación, Desarrollo e Innovación en Salud, Junta de Andalucía, Iniciativa Territorial Integrada 2014–2020 para la provincia de Cádiz (No. PI-0076-2017), Spain; and Consejería de Salud, Proyectos de Investigación en Salud, Junta de Andalucía, Convocatoria 2018 (No. PI 0128/2018). Co-financed by FEDER (Fondo Europeo de Desarrollo Regional).
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Conception: M.M.-C., S.C.-S., J.-A.G.-G. Acquisition of data: M.M.-C., A.A., M.R.-P., F.I.-Á., D.M., S.C.-S., J.-A.G.-G.. Analysis and interpretation of data: M.M.-C., S.C.-Sa., J.-A.G.-G. Article drafting: S.C.-S., J.-A.G.-G. Critical revision: M.M.-C., A.A., M.R.-P., F.I.-Á., D.M., S.C.-S., J.-A.G.-G. Final approval of the versión submitted: M.M.-C., A.A., M.R.-P., F.I.-Á., D.M., S.C.-S., J.-A.G.-G. All authors reviewed the manuscript.
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Márquez-Coello, M., Arizcorreta, A., Rodríguez-Pardo, M. et al. Modifications of liver stiffness and CXCL4, TGF-β1 and HGF are similar in HCV- and HIV/HCV-infected patients after DAAs. Sci Rep 11, 9824 (2021). https://doi.org/10.1038/s41598-021-89370-6
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DOI: https://doi.org/10.1038/s41598-021-89370-6
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