Effects of Atorvastatin Alongside Conventional Medical Treatment on Liver Fibrosis and Dysfunction in Patients with Chronic Hepatitis B: A Double-Blinded Clinical Trial


Ahmad Hormati ORCID 1 , Maryam Jameshorani 2 , Seyed Saeed Sarkeshikian 1 , Mansureh Molaei 1 , Mahdi Jahangiri 1 , Mohammad Reza Ghadir ORCID 1 , *

1 Gastroenterology and Hepatology Disease Research Center, Qom University of Medical Sciences, Qom, Iran

2 Metabolic Disease Research Center, Zanjan University of Medical Sciences, Zanjan, Iran

How to Cite: Hormati A, Jameshorani M, Sarkeshikian S S, Molaei M, Jahangiri M , et al. Effects of Atorvastatin Alongside Conventional Medical Treatment on Liver Fibrosis and Dysfunction in Patients with Chronic Hepatitis B: A Double-Blinded Clinical Trial, Hepat Mon. 2019 ; 19(2):e84656. doi: 10.5812/hepatmon.84656.


Hepatitis Monthly: 19 (2); e84656
Published Online: February 12, 2019
Article Type: Research Article
Received: September 26, 2018
Revised: December 25, 2018
Accepted: February 1, 2019


Background: Liver fibrosis and related hepatic dysfunction are among major medical issues in patients with chronic hepatitis B (CHB). It finally may lead to cirrhosis, hepatocellular carcinoma (HCC), and liver-related death.

Objectives: This study aimed to investigate the effects of adding atorvastatin to the standard antiviral therapy on the hepatic fibrosis and progression of cirrhosis in CHB patients.

Methods: In this double-blinded clinical trial, 77 CHB patients referring to the gastroenterology and hepatology clinics in Qom, Iran, were selected by simple random sampling from 2016 to 2017. The participants were randomly divided into an intervention group that received tenofovir (300 mg) with atorvastatin (20 mg) daily and a control group that received tenofovir (300 mg) and placebo of atorvastatin daily.

Results: According to the findings, changes in the aspartate aminotransferase (AST) level were not significant in the control (P = 0.771) and intervention (P = 0.266) groups. Changes in the alanine aminotransferase (ALT) level were non-significant in the control group (P = 0.893) but significant in the intervention group (P = 0.018). Changes in the liver fibrosis were significant in the intervention group (P = 0.001) and between the two groups (P < 0.001).

Conclusions: According to the study results, adding atorvastatin to the standard antiviral regimen improves the liver function and reduces liver fibrosis in CHB patients. Therefore, it is suggested that atorvastatin be used as complementary therapy.

1. Background

Chronic hepatitis B (CHB) is an important public health threat. It is estimated that 350 - 400 million people are suffering from the disease worldwide. These patients are at a higher risk of liver cirrhosis and hepatocellular carcinoma compared to the general population and about 20% of them are afflicted with cirrhosis (1). In a long-term study on CHB patients, the estimated five-year survival rates were as follows: 97% for patients with chronic persistent hepatitis, 86% for patients with chronic active hepatitis (CAH), and 55% for CAH patients with cirrhosis (2).

Cirrhosis was considered irreversible for a long time, but recent studies proved that the elimination of the underlying cause of liver damage would reverse the fibrosis. The common symptoms of chronic liver disease include weakness, fatigue, and right upper quadrant abdominal pain. It may also present with abnormal laboratory test results (1). Hepatitis B virus (HBV) usually causes chronic infection and leads to cirrhosis, hepatocellular carcinoma, and other severe liver diseases. Diagnostic tests include hepatitis B serology that comprises hepatitis B surface antigen (HBs Ag), hepatitis B surface antibody (HBs Ab), hepatitis B envelope antigen (HBe Ag), hepatitis B envelope antibody (HBe Ab), and hepatitis B Core IgM antibody (HBc Ab IgM). HBV surface antigens are indispensable for HBV virion formation (3). The quantitative assessment of HBV DNA is also necessary. Many studies have demonstrated the benefits of antiviral therapy in patients with CHB. An efficient treatment will suppress the HBV-DNA and reduce aminotransferases level (4). The histological response to treatment is indicated by a decrease in liver inflammation and fibrosis. Various clinical trials have shown that patients with decompensated liver disease can return to the compensated stage using antiviral therapy for hepatitis B (1).

Previous studies in animal models showed that statins are effective in the prevention of liver fibrosis progression, but data from human studies are limited. According to a few available studies, statins may slow down the progression of liver fibrosis in patients with chronic hepatitis C (CHC) (2, 5). In addition, research on a large statistical population reported that adding statins to the antiviral therapy of CHB patients decreases the incidence of cirrhosis and hepatic decompensation significantly (6).

Statins have anti-inflammatory effects. Observations confirm that these drugs reduce the C-reactive protein (CRP) levels in serum (7) and pro-inflammatory cytokines; moreover, they downregulate the activation of T-cells and infiltration of macrophages and neutrophils (8, 9).

Determining the level of parenchymal damage in chronic liver disease is crucial to make the best decision for patient management. For example, a study showed that the level of hepatic and portal veins damage is correlated with the severity of fatty liver disease, but the stage of hepatic parenchymal fibrosis is an independent factor that can be evaluated by FibroScan. They also concluded that the elevation of liver enzymes and serum CRP level correlates with the stage of liver fibrosis (10).

2. Objectives

Given the anti-inflammatory and anti-fibrotic effects of statins and respecting the fact that they are affordable and accessible drugs for patients, the present study aimed to determine the effect of adding atorvastatin to antiviral therapy on hepatic fibrosis or inhibiting the progression of cirrhosis in CHB patients.

3. Methods

This double-blinded clinical trial was approved by the Research Ethics Committee of Qom University of Medical Sciences on January 14, 2017, with the reference code of IR.MUQ.REC.133.1395. It was also registered in the Iranian Registry of Clinical Trials on March 2, 2017, with the reference code of IRCT2017010631252N3.

The statistical population included CHB patients who were eligible for antiviral therapy and attended the gastroenterology and hepatology clinics in Qom, Iran, between 2016 and 2017. According to a study by Trebicka et al. (11) and using the sample size formula and comparing the means of the two groups, 32 patients were assigned to each group. CHB patients with an indication for treatment who had an age of 18 to 75 years, with a serum LDL level of greater than 90 mg/dL, were included consecutively until the calculated sample size reached. The exclusion criteria were: Hepatitis B infection for less than six months; hepatitis B inactive carriers; no signs of liver fibrosis and cirrhosis; decompensated cirrhosis; the presence of other chronic liver diseases such as hemochromatosis and Wilson’s disease or autoimmune hepatitis (12-14) concomitant with hepatocellular carcinoma or any type of malignancy (including digestive and blood), severe and debilitating diseases such as heart, lung, and kidney failure and progressive neurological disorders; coinfection or superinfection with hepatitis A virus (HAV), hepatitis D virus (HDV), hepatitis C virus (HCV), and HIV; any previous use of atorvastatin therapy and lipid-lowering medications; pregnant or lactating females; serum LDL levels of < 90 mg/dL; and elevation of liver enzymes level as twice the normal upper limits within one month of treatment. All patients signed informed consent forms.

Patients’ demographic and laboratory data were collected by a checklist. The Child-Pugh Score was measured using the data from the checklist (Tables 1 and 2). Liver stiffness in all the patients was assessed by FibroScan device (FibroScan® 402, Echosens, Paris, France). Patients were grouped as intervention and control by simple random sampling. The intervention group received tenofovir (300 mg) and atorvastatin (20 mg) and the control group received tenofovir (300 mg) and placebo on a daily basis. The medications and placebo were purchased from the Abidi Pharmaceutical Company, Tehran, Iran. Placebo was made of starch material in the shape and size of Atrovastatin pills.

Table 1. Child-Pugh Scorea
Clinical and Lab CriteriaPoints*
EncephalopathyNoneMild to moderate (grade 1 or 2)Severe (grade 3 or 4)
AscitesMild to moderate (diuretic responsive)Severe (diuretic responsive)
Bilirubin, mg/dL< 22 - 3> 3
Albumin, g/dL> 3.52.8 - 3.5< 2.8
Prothrombin time
Second prolonged< 44 - 6> 6
International normalized ratio< 1.71.7 - 2.3> 2.3

aChild-Turcotte-Pugh class obtained by adding score for each parameter (total points): Class A = 5 to 6 points (least severe liver disease), class B = 7 to 9 points (moderately severe liver disease), class C = 10 to 15 points (most severe liver disease).

Table 2. Metavir Scoring System
Activity score (A)
A0No activity
A1Mild activity
A2Moderate activity
A3Severe activity
Fibrosis score (F)
F0No fibrosis
F1Portal fibrosis without septa
F2Portal fibrosis with few septa
F3Numerous septa without cirrhosis

In order to maintain the study blind, the drugs were coded and administered to the patients by a person, other than the attending physician, who was unaware of the drugs. One month after the treatment, liver enzymes were checked and in case of the elevation of enzymes’ level more than twice the normal upper limits, the patients were excluded from the study. Liver enzymes were checked monthly. In the sixth month, the liver function, liver enzyme level, and liver stiffness were re-measured.

Among 40 patients in each group, one from the control group and two from the intervention group were excluded because they failed to take part in the follow-up examination. Finally, 39 patients in the control group and 38 patients in the intervention group completed the study (Figure 1).

Data were analyzed with statistical package for social sciences (SPSS) version 24 using descriptive statistics including frequency, mean, and standard deviation to interpret the findings. Statistical tests applied in the study included the chi-square test, the independent t-test, and the paired t-test. P values of < 0.05 were considered statistically significant.

4. Results

Among 39 patients in the control group, 27 were male and 12 were female. From among 38 patients in the intervention group, 21 were male and 17 were female. The distribution of gender (P = 0.72), age (P = 0.59), and BMI (P = 0.72) did not show any statistically significant difference between the two groups. The mean levels of aspartate aminotransferase (AST) (P = 0.41), alanine aminotransferase (ALT) (P = 0.17), and liver fibrosis according to the FibroScan findings (P = 0.72) before the treatment were statistically similar between the two groups, which indicates the appropriate randomization of the patients. Table 3 summarizes patients’ demographics, laboratory findings, and transient elastography results of the two groups. Changes in the ALT level were not significant in both groups (P = 0.266). AST level changes were non-significant in the control group (P = 0.893), but significant in the intervention group (P = 0.018). Changes in the transient elastography results were significant only in the intervention group (P = 0.001). This finding indicates the efficacy of statins in improving liver fibrosis. Table 4 compares the means of the live enzyme levels and the transient elastography results before and after the treatment in both groups. Table 5 shows the frequency and percentage of the patients according to the METAVIR scoring system after the intervention in both groups. Table 6 shows changes in the stage of liver fibrosis following the treatment in both groups. There was no statistically significant difference between the two groups after the intervention respecting the frequency percentage of transient elastography (P = 0.064). Pre-intervention and post-intervention transient elastography were significantly associated with tenofovir and placebo in the control group (P = 0.001). This reveals the relative effect of tenofovir on improving the liver histology in CHB patients. Moreover, in the intervention group, this association was significant before and after the intervention (P = 0.001). There were no significant changes in the Child-Pugh score in the control group after the treatment (P = 0.66); however, the changes were significant in the intervention group (P < 0.001).

Table 3. The Frequency Distribution of the Demographics and Variables in the Two Groups Before and After the Intervention
VariablesControl Group (N = 39)aIntervention Group (N = 38)aMean DifferenceTDegree of FreedomP Value
Age53.47 ± 68.1324.49 ± 69.14-711.1-0.525740.601
BMI13.24 ± 94.486.24 ± 56.5-723.0-0.541740.590
First AST44.33 ± 13.2386.29 ± 57.13581.30.826750.412
First ALT51.39 ± 94.3071.31 ± 39.17802.71.359750.178
Second AST54.32 ± 42.1595.31 ± 73.10591.00.195750.846
Second ALT90.38 ± 23.1845.37 ± 03.18450.10.351750.727
First Transient Elastography test63.10 ± 63.1252.11 ± 52.8-887.0-0.359740.721
Second Transient Elastography test64.10 ± 05.1309.9 ± 15.6552.10.663740.040

Abbreviations: ALT, alanine aminotransferase; AST, aspartate aminotransferase, BMI, body mass index.

aValues are expressed as mean ± SD.

Table 4. A Comparison Between the Two Groups Respecting the Pre-Intervention and Post-Intervention Means of the Variables
VariablesControl Group (N = 39)Intervention Group (N = 38)
Pre-InterventionPost-InterventionMean DifferenceTP ValuePre-InterventionPost-InterventionMean DifferenceTP Value
AST44.33 (13.23)54.32 (42.15)89.0293.0771.086.29 (57.13)95.31 (73.10)-092.2-131.10.266
ALT51.39 (94.30)90.38 (23.18)615.0136.0893.071.31 (39.17)45.37 (03.18)-737.5-476.20.018
Transient Elastography test63.10 (63.12)64.10 (05.13)-053.0442.0-661.052.11 (52.8)09.9 (15.6)500.0346.40.001

Abbreviations: ALT, alanine aminotransferase; AST, aspartate aminotransferase.

Table 5. The Frequency Percentage of Post-Intervention Transient Elastography in the Two Groupsa
GroupLast Transient Elastography TestChi-SquareDegree of FreedomP Value
Control17 (7.44)15 (5.39)4 (5.10)2 (3.5)668.130.644
Intervention20 (6.52)11 (9.28)3 (9.7)4 (5.10)

aValues are expressed as No. (%).

Table 6. The Relationship Between the Pre-Intervention and Post-Intervention Transient Elastography Tests in the Two Groupsa
First Transient Elastography testLast Transient Elastography TestChi-SquareDegree of FreedomP Value
115 (8.93)1 (3.6)--
22 (5.12)12 (75)2 (5.12)-
3-1 (3.33)2 (7.66)-
4-1 (3.33)-2 (7.66)
116 (1.94)1 (9.5)--
24 (50)4 (50)--
3-4 (80)1 (20)-
4-2 (25)1 (25)4 (50)

aValues are expressed as No. (%).

5. Discussion

According to the results of the present study, there were no significant changes in the AST level in the two groups. The changes in the ALT level before and after treatment were significant in the intervention group, but compared to the control group, no significant changes were detected. According to the findings of the present study and some previous studies, patients consuming these drugs are not at a higher risk of liver enzyme disturbance (13, 14).

Assessing the liver fibrosis after treatment represented a significant reduction in the stage of fibrosis, which indicates the efficacy of antiviral treatment for improving liver histology. These findings are consistent with the results of studies by Hou et al. (15) and Li et al. (16).

Statins have anti-inflammatory effects and can reduce the serum levels of CRP and pro-inflammatory cytokines (7). Since the inflammatory cascade, which starts with the signals of liver stellate cells following hepatocytes damage, may lead to hepatitis and hepatic fibrosis, the anti-inflammatory and anti-fibrotic effects of statins may control the liver damage (8, 17). Some studies have shown that statins might offer clinical benefits in viral hepatitis, progression of cirrhosis, and hepatocellular carcinoma; moreover, statins were shown to ameliorate liver histological (in both imaging and biopsy studies) and functional alterations in patients with non-alcoholic fatty liver disease or non-alcoholic steatohepatitis (18), although the present study did not indicate histological amelioration.

Simon et al. in 2015 evaluated the effectiveness of statins in reducing the hepatic fibrosis progression in patients with CHC. In this study, subjects with CHC and advanced fibrosis underwent serial liver biopsies over 3.5 years. The study results demonstrated that fibrosis progression occurred in 10% of statin users and 29% of non-users. It could be concluded that using statins is associated with a reduced risk of hepatic fibrosis progression in advanced CHC (19). This finding is in line with the results of the present study.

Chen et al. explored the effects of statin and metformin on the incidence of liver or non-liver cancers in patients suffering from chronic infection with HBV during 2000 - 2008. The study revealed that either statin or metformin reduced the incidence of cancer. It also demonstrated that consuming both statin and metformin had a synergistic effect and reduced the incidence of many cancers (20). In the current study, complementary therapy was found to be more effective than antiviral therapy alone in improving liver fibrosis; however, the present study did not aim to determine the risk of liver cancer.

Kamal et al. in 2017 conducted a systematic review in the United States of America. It indicated that statins could retard the progression of fibrosis, prevent hepatic decompensation in cirrhosis, and decrease mortality in patients with chronic liver disease (21). Likewise, the findings of the present study showed that atorvastatin therapy reduced liver fibrosis significantly.

A study carried out by Huang et al. in Taiwan between 2007 and 2009 demonstrated that CHB patients who received statin therapy in combination with antiviral therapy had a significantly lower cumulative incidence of cirrhosis and decompensated cirrhosis compared to patients who did not take statins (6). These are consistent with the results of the present study that indicated adding statins to antiviral therapy would improve liver fibrosis. A study showed that statins might reduce liver-related adverse outcomes in chronic liver disease. Kamal et al. in a recent meta-analysis found that statin use was associated with a reduced risk of fibrosis progression, decompensated cirrhosis, and mortality (22). Similarly, our study showed that there are beneficial liver effects for statins. More-robust studies including randomized trials and research on its safety in patients with advanced liver disease are needed before statins can be routinely recommended for the prevention of liver-related morbidity and mortality.

5.1. Conclusions

By setting the results of the present study against the findings of other studies, it is concluded that using atorvastatin therapy in combination with standard antiviral treatment has a positive impact on liver fibrosis and dysfunction in CHB patients. Furthermore, through its anti-inflammatory and anti-fibrotic effects, atorvastatin leads to the regression of fibrosis in the early stages of liver fibrosis, thereby improving liver function. In addition, these drugs are affordable and accessible to patients and all health plans cover them. Hence, it is suggested that atorvastatin be used as complementary therapy.




  • 1.

    Ghadir MR, Belbasi M, Heidari A, Jandagh M, Ahmadi I, Habibinejad H, et al. Distribution and risk factors of hepatitis B virus infection in the general population of Central Iran. Hepat Mon. 2012;12(2):112-7. doi: 10.5812/hepatmon.822. [PubMed: 22509188]. [PubMed Central: PMC3321318].

  • 2.

    Honda K, Seike M, Murakami K. Benefits of nucleos(t)ide analog treatments for hepatitis B virus-related cirrhosis. World J Hepatol. 2015;7(22):2404-10. doi: 10.4254/wjh.v7.i22.2404. [PubMed: 26464756]. [PubMed Central: PMC4598611].

  • 3.

    Wu CC, Chen YS, Cao L, Chen XW, Lu MJ. Hepatitis B virus infection: Defective surface antigen expression and pathogenesis. World J Gastroenterol. 2018;24(31):3488-99. doi: 10.3748/wjg.v24.i31.3488. [PubMed: 30131655]. [PubMed Central: PMC6102499].

  • 4.

    Shamsdin SA, Sepehrimanesh M, Pezeshki B, Nejabat M. Seroprevalence of hepatitis B and C in patients with hemophilia: a single-centre descriptive study. Shiraz E-Med J. 2015;16(7). e24573. doi: 10.17795/semj24573.

  • 5.

    Koohi-Hosseinabadi O, Moini M, Safarpoor A, Derakhshanfar A, Sepehrimanesh M. Effects of dietary Thymus vulgaris extract alone or with atorvastatin on the liver, kidney, heart, and brain histopathological features in diabetic and hyperlipidemic male rats. Comp Clin Path. 2015;24(6):1311-5. doi: 10.1007/s00580-015-2070-7.

  • 6.

    Huang YW, Lee CL, Yang SS, Fu SC, Chen YY, Wang TC, et al. Statins reduce the risk of cirrhosis and its decompensation in chronic hepatitis B Patients: A nationwide cohort study. Am J Gastroenterol. 2016;111(7):976-85. doi: 10.1038/ajg.2016.179. [PubMed: 27166128].

  • 7.

    Albert MA, Danielson E, Rifai N, Ridker PM, Prince Investigators . Effect of statin therapy on C-reactive protein levels: The pravastatin inflammation/CRP evaluation (PRINCE): A randomized trial and cohort study. JAMA. 2001;286(1):64-70. doi: 10.1001/jama.286.1.64. [PubMed: 11434828].

  • 8.

    Blake GJ, Ridker PM. Are statins anti-inflammatory? Curr Control Trials Cardiovasc Med. 2000;1(3):161-5. doi: 10.1186/cvm-1-3-161. [PubMed: 11714433]. [PubMed Central: PMC59622].

  • 9.

    Antonopoulos AS, Margaritis M, Lee R, Channon K, Antoniades C. Statins as anti-inflammatory agents in atherogenesis: Molecular mechanisms and lessons from the recent clinical trials. Curr Pharm Des. 2012;18(11):1519-30. doi: 10.2174/138161212799504803. [PubMed: 22364136]. [PubMed Central: PMC3394171].

  • 10.

    Alizadeh A, Mansour-Ghanaei F, Roozdar A, Joukar F, Sepehrimanesh M, Hojati SA, et al. Laboratory tests, liver vessels color doppler sonography, and fibroscan findings in patients with nonalcoholic fatty liver disease: An observation study. J Clin Imaging Sci. 2018;8:12. doi: 10.4103/jcis.JCIS_93_17. [PubMed: 29692949]. [PubMed Central: PMC5894278].

  • 11.

    Trebicka J, Hennenberg M, Odenthal M, Shir K, Klein S, Granzow M, et al. Atorvastatin attenuates hepatic fibrosis in rats after bile duct ligation via decreased turnover of hepatic stellate cells. J Hepatol. 2010;53(4):702-12. doi: 10.1016/j.jhep.2010.04.025. [PubMed: 20633948].

  • 12.

    Hormati A, Hajiani E, Alavinejad P, Shayesteh AA, Masjedizadeh AR, Hashemi SJ. Evaluation of breast cancer radiotherapy induced liver fibrosis by elastography. J Gastroenterol Hepatol Res. 2014;3(8):1026-209.

  • 13.

    Hormati A, Shakeri M, Iranikhah A, Afifian M, Sarkeshikian SS. [Non-alcoholic fatty liver disease]. Govaresh. 2019;23(4):203-12. Persian.

  • 14.

    Iranikhah A, Hormati A, Shakeri M, Aghaali M. [Non-alcoholic fatty liver disease in children]. J Mazandaran Univ Med Sci. 2018;28(165):230-42. Persian.

  • 15.

    Hou JL, Xu D, Shi G, Wan M, Goodman Z, Tan D, et al. Long-term telbivudine treatment results in resolution of liver inflammation and fibrosis in patients with chronic hepatitis B. Adv Ther. 2015;32(8):727-41. doi: 10.1007/s12325-015-0232-2. [PubMed: 26329749]. [PubMed Central: PMC4572721].

  • 16.

    Li N, Xu JH, Yu M, Wang S, Si CW, Yu YY. Relationship between virological response and FIB-4 index in chronic hepatitis B patients with entecavir therapy. World J Gastroenterol. 2015;21(43):12421-9. doi: 10.3748/wjg.v21.i43.12421. [PubMed: 26604649]. [PubMed Central: PMC4649125].

  • 17.

    Vukobrat-Bijedic Z, Husic-Selimovic A, Mehinovic L, Mehmedovic A, Junuzovic D, Bjelogrlic I, et al. Analysis of effect of antiviral therapy on regression of liver fibrosis in patient with HCV infection. Mater Sociomed. 2014;26(3):172-6. doi: 10.5455/msm.2014.26.172-176. [PubMed: 25126010]. [PubMed Central: PMC4130668].

  • 18.

    Imprialos KP, Stavropoulos K, Doumas M, Skalkou A, Zografou I, Athyros VG. The potential role of statins in treating liver disease. Expert Rev Gastroenterol Hepatol. 2018;12(4):331-9. doi: 10.1080/17474124.2018.1439379. [PubMed: 29431526].

  • 19.

    Simon TG, King LY, Zheng H, Chung RT. Statin use is associated with a reduced risk of fibrosis progression in chronic hepatitis C. J Hepatol. 2015;62(1):18-23. doi: 10.1016/j.jhep.2014.08.013. [PubMed: 25135867]. [PubMed Central: PMC4272642].

  • 20.

    Chen CI, Kuan CF, Fang YA, Liu SH, Liu JC, Wu LL, et al. Cancer risk in HBV patients with statin and metformin use: A population-based cohort study. Medicine (Baltimore). 2015;94(6). e462. doi: 10.1097/MD.0000000000000462. [PubMed: 25674734]. [PubMed Central: PMC4602747].

  • 21.

    Kamal S, Khan MA, Seth A, Cholankeril G, Gupta D, Singh U, et al. Beneficial effects of statins on the rates of hepatic fibrosis, hepatic decompensation, and mortality in chronic liver disease: A systematic review and meta-analysis. Am J Gastroenterol. 2017;112(10):1495-505. doi: 10.1038/ajg.2017.170. [PubMed: 28585556].

  • 22.

    Price JC, Tien PC. Editorial: Statins and liver disease: Is it time to recommend statins to prevent liver disease progression? Am J Gastroenterol. 2017;112(10):1506-7. doi: 10.1038/ajg.2017.250. [PubMed: 28978973].

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