The Circulating miRNA Profile of Chronic Hepatitis D and B Patients Is Comparable but Differs from That of Individuals with HBeAg-Negative HBV Infection

Author:

Cavallone Daniela12,Ornos Eric134ORCID,Ricco Gabriele1ORCID,Oliveri Filippo1ORCID,Coco Barbara1ORCID,Colombatto Piero1,De Rosa Laura56ORCID,Dalmacio Leslie7,Bonino Ferruccio12ORCID,Brunetto Maurizia128ORCID

Affiliation:

1. Hepatology Unit and Laboratory of Molecular Genetics and Pathology of Hepatitis Viruses, Reference Centre of the Tuscany Region for Chronic Liver Disease and Cancer, University Hospital of Pisa, Via Paradisa 2, 56124 Pisa, Italy

2. Institute of Biostructure and Bioimaging, National Research Council, Via De Amicis 95, 80145 Naples, Italy

3. Department of Medical Microbiology, College of Medicine, University of the Philippines Manila, Pedro Gil Street, Ermita, Manila 1000, Philippines

4. Fondazione Italiana Fegato (FIF), 34149 Trieste, Italy

5. Institute of Clinical Physiology, National Research Council, 56124 Pisa, Italy

6. Department of Information Engineering and Computer Science, University of Trento, 38123 Trento, Italy

7. Department of Biochemistry and Molecular Biology, College of Medicine, University of the Philippines Manila, Pedro Gil Street, Ermita, Manila 1000, Philippines

8. Department of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy

Abstract

miRNAs circulating in whole serum and HBsAg-particles are differentially expressed in chronic hepatitis B (CHB) and HBeAg-negative-HBV infection (ENI); their profiles are unknown in chronic hepatitis D (CHD). Serum- and HBsAg-associated miRNAs were analyzed in 75 subjects of 3 well-characterized groups (CHB 25, CHD 25, ENI 25) using next-generation sequencing (NGS). Overall miRNA profiles were consonant in serum and HBsAg-particles but significantly different according to the presence of hepatitis independently of Hepatitis D Virus (HDV)-co-infection. Stringent (Bonferroni Correction < 0.001) differential expression analysis showed 39 miRNAs upregulated in CHB vs. ENI and 31 of them also in CHD vs. ENI. miRNA profiles were coincident in CHB and CHD with only miR-200a-3p upregulated in CHB. Three miRNAs (miR-625-3p, miR-142-5p, and miR-223-3p) involved in immune response were upregulated in ENI. All 3 hepatocellular miRNAs of MiR-B-Index (miR-122-5p, miR-99a-5p, miR-192-5p) were overexpressed in both CHB and CHD patients. In conclusion, CHD and CHB patients showed highly similar serum miRNA profiling that was significantly different from that of individuals with HBeAg-negative infection and without liver disease.

Funder

Hepatology Unit Research Fund

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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