Coeliac disease and C virus-related chronic hepatitis: a non association
- Antonietta Gerarda Gravina†1Email author,
- Alessandro Federico†1,
- Mario Masarone2,
- Antonio Cuomo3,
- Concetta Tuccillo1,
- Carmelina Loguercio1,
- Marcello Persico2 and
- Marco Romano1
© Gravina et al.; licensee BioMed Central Ltd. 2012
Received: 18 April 2012
Accepted: 22 September 2012
Published: 26 September 2012
A higher prevalence of coeliac disease has recently been reported among patients with HCV-related chronic hepatitis. Moreover, development of clinically overt coeliac disease has been described in a number of HCV-related chronic hepatitis patients during α-interferon therapy. This prospective study was designed to evaluate 1) the prevalence of coeliac disease in patients with HCV-related chronic hepatitis; 2) the prevalence of HCV infection in patients with coeliac disease; 3) whether PEG interferon-α treatment might favour the development of coeliac disease in patients with chronic hepatitis C.
Materials and methods
Two hundred-ten consecutive patients (M/F = 140/70, range of age 35–58 years, median age 46.5 years) with biopsy proven chronic hepatitis C underwent serological screening for antiendomysial and tissue transglutaminase IgA antibodies. One hundred ninety-four coeliac patients (M/F = 52/142, range of age 18–74 years, median age 34 years) were screened for HCV antibodies. Positivity for HCV antibodies in coeliac disease patients was confirmed by detection of serum HCV-RNA by RT-PCR. This work was carried out in accordance to ethical guidelines of Declaration of Helsinki and was approved by Institutional Ethics Committee of the Second University of Naples. All patients gave informed written consent.
1) none of the 210 HCV-related chronic hepatitis patients were positive for coeliac disease serologic screening; 2) prevalence of HCV infection among coeliac patients was 1.54% (3/194) which is comparable to that reported in the Southern Italy population; 3) PEG interferon-α treatment was not associated with development of coeliac disease either clinical or serological.
1) coeliac disease is not associated with HCV infection; 2) PEG interferon-α does not trigger celiac disease.
Coeliac disease (CD) is a condition characterized by damage to the mucosa of the small bowel in sensitive individuals and subsequent malabsorption, with a prevalence in the Western Countries of about 1/100[1–3]. The clinical spectrum ranges from overt malabsorption to no clinical signs when the damage of the small intestine mucosa is mild (i.e. latent CD). CD is the only human autoimmune disease in which an environmental factor (i.e., gluten) has been identified that triggers an immune-mediated injury to the intestine in genetically predisposed individuals[4, 5].
Hepatitis C virus (HCV) infection is the major cause of chronic liver disease worldwide. Moreover, HCV infection is associated with a number of autoimmune disorders such as cryoglobulinemia, Sjogren syndrome, and lichen planus[7, 8].
Even though the association between CD and liver diseases has been extensively investigated, a definite correlation between these pathological conditions has not been unequivocally established. An increased prevalence of CD has been described by Fine et al. in patients with HCV-related chronic hepatitis, thus leading to speculate that CD is epidemiologically associated with HCV-related chronic hepatitis. In this study, four patients tested positive for specific markers of CD among 259 patients infected with HCV. In another study, one patient with CD was found to have HCV infection when investigators looked for causes of increased alanine aminotransferases (ALT) levels in this setting. Also, liver involvement is a frequent finding in CD patients. On the other hand, Germenis et al. found a 0.54% prevalence of positive CD serology among 738 patients with liver disease, which was not different than what found in the general population. Therefore, whether CD is part of the spectrum of HCV infection-related autoimmune disorders is still controversial.
A number of cases of clinically overt CD have been described in patients with HCV-related chronic hepatitis during treatment with interferon alpha (IFN-α)[14–17]. Also, Hernandez et al. suggested that IFN-α may precipitate the development of CD in susceptible individuals. On the other hand Ruggeri et al. failed to demonstrate development of positive CD serology in 42 HCV-infected patients treated with IFN-α. Therefore, whether IFN-α is able to trigger CD is still unclear.
In order to specifically address these issues we designed a prospective study aimed at evaluating the prevalence of CD in patients with HCV-related chronic hepatitis and the prevalence of HCV infection in a population of patients with CD. Moreover, we studied whether pegylated (PEG) IFN-α treatment might be associated with the development of CD.
HCV-related chronic hepatitis patients
The study population consisted of 210 consecutive patients (M/F = 140/70, range of age 35–58 years, median age 46.5) with a biopsy proven HCV-related chronic hepatitis enrolled from September 2008 to July 2010. All these patients were tested for routine liver function tests (i.e., aminotranferases, γ-glutamyltranspeptidase, alkaline phosphatase, bilirubin, prothrombin activity, cholinesterase), immunoglobulins (Ig)A, IgG, and IgM, platelet count, blood cell count, haemoglobin, albumin, HBsAg, HBsAb, HBcAb (IgM-IgG), HBeAg, HBeAb, HCVAb, ANA, AMA, SMA, anti-LKM, plasma iron and copper levels, ceruloplasmin and ferritin and for antibodies against endomysium (EMA) tested on thin sections of human cord using an indirect immunofluorescent method and for tissue transglutaminase (tTG) by using ELISA assays. All underwent ultrasonography.
One hundred and sixty eight patients with HCV-related chronic hepatitis naïve to treatment (M/F = 125/43, range of age 35–52 years, median age 44) were eligible for interferon therapy and were treated with standard of care (PEG interferon-α plus ribavirin). These patients underwent screening for coeliac disease before the treatment and at 24 and 48 week of treatment.
This work was carried out in accordance to ethical guidelines of Declaration of Helsinki and was approved by Institutional Ethics Committee of the Second University of Naples. All patients gave informed written consent.
RNA preparation and HCV-RNA determination
All steps were carried out under RNase-free conditions. The polymerase chain reaction (PCR) procedure was used to determine HCV RNA. Sera were rapidly (within 30 min of blood drawing) frozen at −20°C. RNA was extracted according to Chomczynsky and Sacchi, and c-DNA was derived. To identify HCV-RNA, a nested PCR was performed using primers that expanded the highly conserved 5’ non-coding genomic region. Carryover PCR contamination was avoided by applying the measures suggested by Kwok and Higuchi. Limit of the house virus detection test applied was of 10 copies/ml.
The genotype analysis of HCV was performed using a commercial hybridization assay (Inno Lipa HCV II; Innogenetics, Gent, Belgium); utilizing HCV-positive amplification products from the PCR assay (Amplicor HCV Amplification 2.0; Roche Diagnostics, Indianapolis, IN, USA). Serum PCR products were hybridized to type- and subtype-specific probes 1a, 1b, 2a, 2b and 3a, in order to classify the HCV genotypes. The probes used were to fulfill two main criteria: no more than two mismatches to three corresponding published sequences of the same subtype and they were to differ by three or more mismatches compared to published sequences of other types and subtypes. The only exception is probe 2b showing only two mismatches to the corresponding sequence of type 3a.
Liver biopsy and histology
Main clinical, biochemical and histological features of the 210 patients with HCV-related chronic hepatitis
N = 210
Age (years; mean ± SD)
46.5 ± 11.56
Body Mass Index (mean ± SD)
26.7 ± 4.01
HCV-RNA levels (I.U./mL; mean ± SD)
4.318.618 ± 28.174
ALT (I.U./L) (mean ± SD) (n.v. < 40 U/I)
125 ± 101
Liver fibrosis (Ishak score)
Prevalence of autoimmune disorders in our series of 194 coeliac subjects
Primary biliary cirrhosis
Recurrent oral aphtosys
IgA mesangial nephropathy
Difference between groups was assessed by Fisher’s exact test. A value of p < 0.05 was considered statistically significant.
Prevalence of coeliac disease in HCV-related chronic hepatitis patients and prevalence of HCV-related chronic hepatitis in coeliac disease patients
HCV-related chronic hepatitis
(n = 210)
(n = 194)
HCV-related Chronic Hepatitis
Main characteristics of the three HCV positive coeliac patients
Liver fibrosis score
Risk factors for HCV infection
History of i.v. heroin use
Married to subject with HCV infection
Duodenal histology degree
Marsh III a
Marsh III a
Marsh III b
Celiac disease symptoms at presentation
Syderopenic anaemia, weakness, bloating
Chronic diarrhoea, weight loss, syderopenic anaemia
In order to assess whether IFN-α treatment might trigger CD we determined serum EMA and tTG in HCV-related chronic hepatitis patients before the treatment and at 24 and 48 week of treatment. One hundred and thirty patients completed the therapy, while thirty-eight discontinued for serious adverse events (54% anemia, 34% leukopenia, 12% thrombocytopenia). A virological (i.e. disappearance of serum HVCV-RNA) and biochemical (normal AST and ALT serum levels) was observed at the end of treatment in 91/130 (70%) of patients. None of the 130 patients who completed therapy turned positive for EMA or tTG nor did any of them develop clinical signs or symptoms suggestive for CD at any time point during the follow-up period.
Viral infections have been thought to act as a potential trigger for the development of CD in genetically susceptible individuals[26, 27]. In particular, because of its association with a number of autoimmune disorders, the role of HCV infection in the pathogenesis of CD has been the object of several investigations, but the results are controversial[9–13].
In order to specifically address this issue we prospectively evaluated the prevalence of CD in 210 HCV-related chronic hepatitis patients. None of these patients had clinical signs or symptoms suggestive for CD nor did any of them show positivity for serological markers of CD (EMA and/or tTG). Moreover, in a population of 194 CD patients, we found a prevalence of HCV infection as low as 1.54%, which is not higher than the prevalence of HCV infection in Southern Italy. Also, all of the CD patients who resulted HCV positive were at risk for HCV infection. This suggests that HCV-related chronic hepatitis and CD are not associated disorders. In partial support of our finding, Teml and Vogelsang in a retrospective study found that 3/488 (0.6%) CD patients were positive for HCV infection. However, all of them were at risk for HCV infection, one patient having a history of i.v. drug abuse and two having received blood transfusion because of severe anaemia. Also, more recently, Thevenot et al. found 0% prevalence of CD in 624 consecutive patients with HCV infection. Finally, our results are in agreement with the findings of Hernandez et al. who found no association between CD and HCV both in a retrospective and prospective analysis. However, a report by Ruggeri et al. investigated CD-related antibodies in a large series of HCV-infected subjects that were also tested for non-organ-specific autoantibodies as surrogate marker of autoimmune disorders. The authors found that EMA occurred in 5/244 (2%) of HCV patients, which was significantly higher than the prevalence of EMA positivity found in healthy controls. However, only in three of these patients CD was confirmed histologically and, in one of them, non-organ-specific autoantibodies were positive.
IFN-α treatment has been shown to potentially trigger autoimmune disorders. Also, development of clinically overt CD has been described in patients with HCV-related chronic hepatitis during IFN-α treatment[14–17]. However, in these reports, half of the patients were EMA and tTG positive with no clinical or biochemical signs of malabsorption before starting IFN-α therapy whereas the EMA and tTG status was not available in the remaining patients. This suggests that IFN-α may trigger overt CD in asymptomatic EMA and tTG positive subjects (i.e. latent CD patients). However, the question as to whether IFN treatment may induce EMA and tTG positivity with/without malabsorption remains unanswered. We therefore prospectively studied whether EMA and tTG negative, chronic hepatitis C patients might develop clinically overt or latent CD during IFN-α plus ribavirin combined therapy. None of these patients showed clinical signs or symptoms suggestive for CD or positivity for EMA and tTG before or after treatment, thus making it unlikely that IFN-α may serve as a trigger for CD. This is also in agreement with Ruggeri et al. who found no CD-related antibody in 42 HCV-infected patients treated with IFN-α. More recently, Hernandez et al. found that 6/878 CD patients had concomitant HCV infection and that in four of these 6 patients, symptoms that prompted CD diagnosis occurred during or after IFN-α therapy. This may suggest that IFN-α therapy may precipitate the development of CD in susceptible individuals. However, none of these subjects had been screened for CD prior to start IFN-α therapy.
A limit of this study is represented by the small number of patients studied. Also, this study lacked a control group of patients with chronic hepatitis other than HCV-related. However, we evaluated the prevalence of coeliac disease in a group of 131 patients with non alcoholic fatty liver disease (NAFLD) who were admitted to our GI Unit over the same period of time and found that none of these patients had a serology positive for coeliac disease (Romano M and Persico M unpublished observation). Similarly, the prevalence of HCV infection found in our coeliac patients (i.e. 1.5%) is comparable to that found in 315 non coeliac patients who underwent screening for HCV prior to esophagogastroduodenoscopy (i.e. 1.7%, p, ns) (Romano M unpublished observation).
In summary, 1) none of HCV infected patients showed positivity for CD serology; 2) prevalence of HCV infection among CD patients was comparable to that of general population; 3) none of IFN-α-treated HCV patients developed CD. Based on this study, we conclude that HCV infection and CD do not seem to be epidemiologically associated. Moreover, IFN-α treatment seems unlikely to cause CD.
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