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Anti-rods and rings autoantibodies can occur in the hepatitis c-naïve population
INTRODUCTION. The anti-Rods and Rings autoantibody recently described in clinical populations is thought to occur in the setting of hepatitis C treatment, specifically in the context of cytidine triphosphate (CTP) and guanosine triphosphate (GTP) synthetic pathway inhibitors, and is important in its...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pacini Editore SpA
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718377/ https://www.ncbi.nlm.nih.gov/pubmed/24783898 |
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author | SHAIKH, Y. KRANTZ, A. EL-FARRA, Y. |
author_facet | SHAIKH, Y. KRANTZ, A. EL-FARRA, Y. |
author_sort | SHAIKH, Y. |
collection | PubMed |
description | INTRODUCTION. The anti-Rods and Rings autoantibody recently described in clinical populations is thought to occur in the setting of hepatitis C treatment, specifically in the context of cytidine triphosphate (CTP) and guanosine triphosphate (GTP) synthetic pathway inhibitors, and is important in its potential impact on response to therapy. This study asks the question: what is the epidemiology of anti-RR autoantibody in the general, non-clinical population? MATERIALS AND METHODS. This is a cross-sectional study using the National Health and Nutrition Examination Survey (NHANES). Immunofluorescence assay for anti-Rods and Rings autoantibody were performed by NHANES labs and the results made publically available. Sample weights were used to calculate the prevalence and distribution of the autoantibody across demographics. A medication profile of the autoantibody positive population was also constructed. RESULTS. The study sample consisted of 4738 persons over the age of 12 years. Anti-Rods and Rings autoantibodies were found in 39 persons representing 1.3 million persons in the United States population. 38 of 39 persons with anti-Rods and Rings autoantibody had no prior history of hepatitis C virus infection. A majority of these persons were found to have poly-pharmacy. DISCUSSION. This is the first study to show that anti-RR can occur in the general population without evidence of hepatits C virus infection, and that the majority of persons with anti-RR in the population have no evidence of prior hepatitis C infection. This indicates that there may be another undetermined etiology for anti-rods and rings autoantibodies besides the currently accepted exposure etiology of hepatitis C virus infection and treatment found in clinical studies. |
format | Online Article Text |
id | pubmed-4718377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Pacini Editore SpA |
record_format | MEDLINE/PubMed |
spelling | pubmed-47183772016-02-02 Anti-rods and rings autoantibodies can occur in the hepatitis c-naïve population SHAIKH, Y. KRANTZ, A. EL-FARRA, Y. J Prev Med Hyg Original Article INTRODUCTION. The anti-Rods and Rings autoantibody recently described in clinical populations is thought to occur in the setting of hepatitis C treatment, specifically in the context of cytidine triphosphate (CTP) and guanosine triphosphate (GTP) synthetic pathway inhibitors, and is important in its potential impact on response to therapy. This study asks the question: what is the epidemiology of anti-RR autoantibody in the general, non-clinical population? MATERIALS AND METHODS. This is a cross-sectional study using the National Health and Nutrition Examination Survey (NHANES). Immunofluorescence assay for anti-Rods and Rings autoantibody were performed by NHANES labs and the results made publically available. Sample weights were used to calculate the prevalence and distribution of the autoantibody across demographics. A medication profile of the autoantibody positive population was also constructed. RESULTS. The study sample consisted of 4738 persons over the age of 12 years. Anti-Rods and Rings autoantibodies were found in 39 persons representing 1.3 million persons in the United States population. 38 of 39 persons with anti-Rods and Rings autoantibody had no prior history of hepatitis C virus infection. A majority of these persons were found to have poly-pharmacy. DISCUSSION. This is the first study to show that anti-RR can occur in the general population without evidence of hepatits C virus infection, and that the majority of persons with anti-RR in the population have no evidence of prior hepatitis C infection. This indicates that there may be another undetermined etiology for anti-rods and rings autoantibodies besides the currently accepted exposure etiology of hepatitis C virus infection and treatment found in clinical studies. Pacini Editore SpA 2013-09 /pmc/articles/PMC4718377/ /pubmed/24783898 Text en © Copyright by Pacini Editore SpA, Pisa, Italy http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives License, which permits for noncommercial use, distribution, and reproduction in any digital medium, provided the original work is properly cited and is not altered in any way. For details, please refer to http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article SHAIKH, Y. KRANTZ, A. EL-FARRA, Y. Anti-rods and rings autoantibodies can occur in the hepatitis c-naïve population |
title | Anti-rods and rings autoantibodies can occur in the hepatitis c-naïve population |
title_full | Anti-rods and rings autoantibodies can occur in the hepatitis c-naïve population |
title_fullStr | Anti-rods and rings autoantibodies can occur in the hepatitis c-naïve population |
title_full_unstemmed | Anti-rods and rings autoantibodies can occur in the hepatitis c-naïve population |
title_short | Anti-rods and rings autoantibodies can occur in the hepatitis c-naïve population |
title_sort | anti-rods and rings autoantibodies can occur in the hepatitis c-naïve population |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718377/ https://www.ncbi.nlm.nih.gov/pubmed/24783898 |
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