Cargando…

Clinical consequences of the presence of anti-RNA Pol III antibodies in systemic sclerosis

INTRODUCTION: Anti-RNA polymerase III (a-RNA Pol III) antibodies are marker antibodies in patients with systemic sclerosis (SSc). AIM: To assess the prevalence of a-RNA Pol III in patients with SSc and to identify the differences in the disease picture in SSc patients with and without a-RNA Pol III...

Descripción completa

Detalles Bibliográficos
Autores principales: Wielosz, Ewa, Dryglewska, Magdalena, Majdan, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874867/
https://www.ncbi.nlm.nih.gov/pubmed/33603608
http://dx.doi.org/10.5114/ada.2020.102107
_version_ 1783649675074600960
author Wielosz, Ewa
Dryglewska, Magdalena
Majdan, Maria
author_facet Wielosz, Ewa
Dryglewska, Magdalena
Majdan, Maria
author_sort Wielosz, Ewa
collection PubMed
description INTRODUCTION: Anti-RNA polymerase III (a-RNA Pol III) antibodies are marker antibodies in patients with systemic sclerosis (SSc). AIM: To assess the prevalence of a-RNA Pol III in patients with SSc and to identify the differences in the disease picture in SSc patients with and without a-RNA Pol III antibodies. MATERIAL AND METHODS: The study was performed in 126 SSc patients. The subtype of SSc, incidence of internal organ involvement, malignancy, death and serological profiles were determined in the entire group. The study groups were studied according to the presence of antibodies by applying the commercial test – EUROLINE SSc Profile. Due to the presence of a-RNA Pol III, patients were divided into two groups: the a-RNA Pol III (+) SSc group of 19 patients and the a-RNA Pol III (–) SSc group of 107 patients. RESULTS: A-RNA Pol III were present in 19/126 patients with SSc (15%), 13/19 (68.4%) patients had no other SSc marker antibodies. A-RNA Pol III were more common in patients with diffuse cutaneous SSc (p = 0.049). We showed a significant positive association between a-RNA Pol III and occurrence of malignancy (p = 0.007), scleroderma renal crisis (p = 0.001) and decreased DLCO (p = 0.007). CONCLUSIONS: Anti-a-RNA Pol III antibodies are common in patients with SSc, particularly with a diffuse subtype. In more than 50% of patients with a-RNA Pol III antibodies, they may be present as the sole marker of antibodies. In SSc, a-RNA Pol III antibodies are frequently associated with malignancy occurrence, kidney and lung involvement.
format Online
Article
Text
id pubmed-7874867
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Termedia Publishing House
record_format MEDLINE/PubMed
spelling pubmed-78748672021-02-17 Clinical consequences of the presence of anti-RNA Pol III antibodies in systemic sclerosis Wielosz, Ewa Dryglewska, Magdalena Majdan, Maria Postepy Dermatol Alergol Original Paper INTRODUCTION: Anti-RNA polymerase III (a-RNA Pol III) antibodies are marker antibodies in patients with systemic sclerosis (SSc). AIM: To assess the prevalence of a-RNA Pol III in patients with SSc and to identify the differences in the disease picture in SSc patients with and without a-RNA Pol III antibodies. MATERIAL AND METHODS: The study was performed in 126 SSc patients. The subtype of SSc, incidence of internal organ involvement, malignancy, death and serological profiles were determined in the entire group. The study groups were studied according to the presence of antibodies by applying the commercial test – EUROLINE SSc Profile. Due to the presence of a-RNA Pol III, patients were divided into two groups: the a-RNA Pol III (+) SSc group of 19 patients and the a-RNA Pol III (–) SSc group of 107 patients. RESULTS: A-RNA Pol III were present in 19/126 patients with SSc (15%), 13/19 (68.4%) patients had no other SSc marker antibodies. A-RNA Pol III were more common in patients with diffuse cutaneous SSc (p = 0.049). We showed a significant positive association between a-RNA Pol III and occurrence of malignancy (p = 0.007), scleroderma renal crisis (p = 0.001) and decreased DLCO (p = 0.007). CONCLUSIONS: Anti-a-RNA Pol III antibodies are common in patients with SSc, particularly with a diffuse subtype. In more than 50% of patients with a-RNA Pol III antibodies, they may be present as the sole marker of antibodies. In SSc, a-RNA Pol III antibodies are frequently associated with malignancy occurrence, kidney and lung involvement. Termedia Publishing House 2021-01-06 2020-12 /pmc/articles/PMC7874867/ /pubmed/33603608 http://dx.doi.org/10.5114/ada.2020.102107 Text en Copyright: © 2021 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Wielosz, Ewa
Dryglewska, Magdalena
Majdan, Maria
Clinical consequences of the presence of anti-RNA Pol III antibodies in systemic sclerosis
title Clinical consequences of the presence of anti-RNA Pol III antibodies in systemic sclerosis
title_full Clinical consequences of the presence of anti-RNA Pol III antibodies in systemic sclerosis
title_fullStr Clinical consequences of the presence of anti-RNA Pol III antibodies in systemic sclerosis
title_full_unstemmed Clinical consequences of the presence of anti-RNA Pol III antibodies in systemic sclerosis
title_short Clinical consequences of the presence of anti-RNA Pol III antibodies in systemic sclerosis
title_sort clinical consequences of the presence of anti-rna pol iii antibodies in systemic sclerosis
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874867/
https://www.ncbi.nlm.nih.gov/pubmed/33603608
http://dx.doi.org/10.5114/ada.2020.102107
work_keys_str_mv AT wieloszewa clinicalconsequencesofthepresenceofantirnapoliiiantibodiesinsystemicsclerosis
AT dryglewskamagdalena clinicalconsequencesofthepresenceofantirnapoliiiantibodiesinsystemicsclerosis
AT majdanmaria clinicalconsequencesofthepresenceofantirnapoliiiantibodiesinsystemicsclerosis