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Circulating miRNAs as footprints for liver fibrosis grading in schistosomiasis

BACKGROUND: Chronic infection with Schistosoma japonicum or S. mansoni results in hepatic fibrosis of the human host. Staging fibrosis is crucial for the prognosis and to determine the rapid need of treatment in patients with schistosomiasis. METHODS: To establish whether there is a correlation betw...

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Autores principales: Cai, Pengfei, Mu, Yi, Olveda, Remigio M., Ross, Allen G., Olveda, David U., McManus, Donald P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286190/
https://www.ncbi.nlm.nih.gov/pubmed/30482723
http://dx.doi.org/10.1016/j.ebiom.2018.10.048
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author Cai, Pengfei
Mu, Yi
Olveda, Remigio M.
Ross, Allen G.
Olveda, David U.
McManus, Donald P.
author_facet Cai, Pengfei
Mu, Yi
Olveda, Remigio M.
Ross, Allen G.
Olveda, David U.
McManus, Donald P.
author_sort Cai, Pengfei
collection PubMed
description BACKGROUND: Chronic infection with Schistosoma japonicum or S. mansoni results in hepatic fibrosis of the human host. Staging fibrosis is crucial for the prognosis and to determine the rapid need of treatment in patients with schistosomiasis. METHODS: To establish whether there is a correlation between circulating microRNA (miRNA) level and fibrosis progression in schistosomiasis, ten miRNAs were selected to assess their potential in grading schistosomiasis liver fibrosis. This was done firstly in two mouse strains (C57BL/6 and BALB/c) to determine the temporal expression profiles in serum over the course of S. japonicum infection, and then within a cohort of 163 schistosomiasis japonica patients with different grades of liver fibrosis. FINDING: Four miRNAs (miR-150-5p, let-7a-5p, let-7d-5p and miR-146a-5p) were able to distinguish patients with mild versus severe fibrosis. The level of serum miR-150-5p showed the most promising potential for grading hepatic fibrosis in schistosomiasis. The diagnostic performance of miR-150-5p in discriminating mild from severe fibrosis is comparable with that of the ELF test and serum HA level. In addition, the serum levels of the four miRNAs rebounded in infected C57BL/6 mice, after 6 months post treatment, following the regression of liver fibrosis, thereby providing further support for the utility of these miRNAs in grading schistosomal hepatic fibrosis. INTERPRETATION. Circulating miRNAs can be a supplementary tool for assessing hepatic fibrosis in human schistosomiasis. FUND: National Health and Medical Research Council (NHMRC) of Australia (APP1102926, APP1037304 and APP1098244).
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spelling pubmed-62861902018-12-13 Circulating miRNAs as footprints for liver fibrosis grading in schistosomiasis Cai, Pengfei Mu, Yi Olveda, Remigio M. Ross, Allen G. Olveda, David U. McManus, Donald P. EBioMedicine Research paper BACKGROUND: Chronic infection with Schistosoma japonicum or S. mansoni results in hepatic fibrosis of the human host. Staging fibrosis is crucial for the prognosis and to determine the rapid need of treatment in patients with schistosomiasis. METHODS: To establish whether there is a correlation between circulating microRNA (miRNA) level and fibrosis progression in schistosomiasis, ten miRNAs were selected to assess their potential in grading schistosomiasis liver fibrosis. This was done firstly in two mouse strains (C57BL/6 and BALB/c) to determine the temporal expression profiles in serum over the course of S. japonicum infection, and then within a cohort of 163 schistosomiasis japonica patients with different grades of liver fibrosis. FINDING: Four miRNAs (miR-150-5p, let-7a-5p, let-7d-5p and miR-146a-5p) were able to distinguish patients with mild versus severe fibrosis. The level of serum miR-150-5p showed the most promising potential for grading hepatic fibrosis in schistosomiasis. The diagnostic performance of miR-150-5p in discriminating mild from severe fibrosis is comparable with that of the ELF test and serum HA level. In addition, the serum levels of the four miRNAs rebounded in infected C57BL/6 mice, after 6 months post treatment, following the regression of liver fibrosis, thereby providing further support for the utility of these miRNAs in grading schistosomal hepatic fibrosis. INTERPRETATION. Circulating miRNAs can be a supplementary tool for assessing hepatic fibrosis in human schistosomiasis. FUND: National Health and Medical Research Council (NHMRC) of Australia (APP1102926, APP1037304 and APP1098244). Elsevier 2018-10-25 /pmc/articles/PMC6286190/ /pubmed/30482723 http://dx.doi.org/10.1016/j.ebiom.2018.10.048 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research paper
Cai, Pengfei
Mu, Yi
Olveda, Remigio M.
Ross, Allen G.
Olveda, David U.
McManus, Donald P.
Circulating miRNAs as footprints for liver fibrosis grading in schistosomiasis
title Circulating miRNAs as footprints for liver fibrosis grading in schistosomiasis
title_full Circulating miRNAs as footprints for liver fibrosis grading in schistosomiasis
title_fullStr Circulating miRNAs as footprints for liver fibrosis grading in schistosomiasis
title_full_unstemmed Circulating miRNAs as footprints for liver fibrosis grading in schistosomiasis
title_short Circulating miRNAs as footprints for liver fibrosis grading in schistosomiasis
title_sort circulating mirnas as footprints for liver fibrosis grading in schistosomiasis
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286190/
https://www.ncbi.nlm.nih.gov/pubmed/30482723
http://dx.doi.org/10.1016/j.ebiom.2018.10.048
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