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Prediction of autoimmune connective tissue disease in an at-risk cohort: prognostic value of a novel two-score system for interferon status

OBJECTIVE: To evaluate clinical, interferon and imaging predictors of progression from ‘At Risk’ to autoimmune connective tissue diseases (AI-CTDs). METHODS: A prospective observational study was conducted in At-Risk of AI-CTD (defined as antinuclear antibody (ANA) positive; ≤1 clinical systemic lup...

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Autores principales: Md Yusof, Md Yuzaiful, Psarras, Antonios, El-Sherbiny, Yasser M, Hensor, Elizabeth M A, Dutton, Katherine, Ul-Hassan, Sabih, Zayat, Ahmed S, Shalbaf, Mohammad, Alase, Adewonuola, Wittmann, Miriam, Emery, Paul, Vital, Edward M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161671/
https://www.ncbi.nlm.nih.gov/pubmed/29929956
http://dx.doi.org/10.1136/annrheumdis-2018-213386
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author Md Yusof, Md Yuzaiful
Psarras, Antonios
El-Sherbiny, Yasser M
Hensor, Elizabeth M A
Dutton, Katherine
Ul-Hassan, Sabih
Zayat, Ahmed S
Shalbaf, Mohammad
Alase, Adewonuola
Wittmann, Miriam
Emery, Paul
Vital, Edward M
author_facet Md Yusof, Md Yuzaiful
Psarras, Antonios
El-Sherbiny, Yasser M
Hensor, Elizabeth M A
Dutton, Katherine
Ul-Hassan, Sabih
Zayat, Ahmed S
Shalbaf, Mohammad
Alase, Adewonuola
Wittmann, Miriam
Emery, Paul
Vital, Edward M
author_sort Md Yusof, Md Yuzaiful
collection PubMed
description OBJECTIVE: To evaluate clinical, interferon and imaging predictors of progression from ‘At Risk’ to autoimmune connective tissue diseases (AI-CTDs). METHODS: A prospective observational study was conducted in At-Risk of AI-CTD (defined as antinuclear antibody (ANA) positive; ≤1 clinical systemic lupus erythematosus (SLE) criterion; symptom duration <12 months and treatment-naïve). Bloods and skin biopsy (non-lesional) were analysed for two interferon-stimulated gene expression scores previously described (IFN-Score-A and IFN-Score-B). Forty-nine healthy controls (HCs) and 114 SLE were used as negative and positive controls. Musculoskeletal ultrasound was performed. Progression was defined by meeting classification criteria for AI-CTDs at 12 months. RESULTS: 118 individuals with 12-month follow-up were included. Of these, 19/118 (16%) progressed to AI-CTD (SLE=14, primary Sjogren’s=5). At baseline, both IFN scores differed among At-Risk, HCs and SLE groups (p<0.001) and both were elevated in At-Risk who progressed to AI-CTD at 12 months versus non-progressors, to a greater extent for IFN-Score-B (fold difference (95% CI) 3.22 (1.74 to 5.95), p<0.001) than IFN-Score-A (2.94 (1.14 to 7.54); p=0.018). Progressors did not have significantly greater baseline clinical characteristics or ultrasound findings. Fold difference between At-Risk and HCs for IFN-Score-A was markedly greater in skin than blood. In multivariable logistic regression, only family history of autoimmune rheumatic disease, OR 8.2 (95% CI 1.58 to 42.53) and IFN-Score-B, 3.79 (1.50–9.58) increased the odds of progression. CONCLUSION: A two-factor interferon score and family history predict progression from ANA positivity to AI-CTD. These interferon scores may allow stratification of individuals At-Risk of AI-CTD permitting early intervention for disease prevention and avoid irreversible organ damage.
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spelling pubmed-61616712018-10-01 Prediction of autoimmune connective tissue disease in an at-risk cohort: prognostic value of a novel two-score system for interferon status Md Yusof, Md Yuzaiful Psarras, Antonios El-Sherbiny, Yasser M Hensor, Elizabeth M A Dutton, Katherine Ul-Hassan, Sabih Zayat, Ahmed S Shalbaf, Mohammad Alase, Adewonuola Wittmann, Miriam Emery, Paul Vital, Edward M Ann Rheum Dis Clinical and Epidemiological Research OBJECTIVE: To evaluate clinical, interferon and imaging predictors of progression from ‘At Risk’ to autoimmune connective tissue diseases (AI-CTDs). METHODS: A prospective observational study was conducted in At-Risk of AI-CTD (defined as antinuclear antibody (ANA) positive; ≤1 clinical systemic lupus erythematosus (SLE) criterion; symptom duration <12 months and treatment-naïve). Bloods and skin biopsy (non-lesional) were analysed for two interferon-stimulated gene expression scores previously described (IFN-Score-A and IFN-Score-B). Forty-nine healthy controls (HCs) and 114 SLE were used as negative and positive controls. Musculoskeletal ultrasound was performed. Progression was defined by meeting classification criteria for AI-CTDs at 12 months. RESULTS: 118 individuals with 12-month follow-up were included. Of these, 19/118 (16%) progressed to AI-CTD (SLE=14, primary Sjogren’s=5). At baseline, both IFN scores differed among At-Risk, HCs and SLE groups (p<0.001) and both were elevated in At-Risk who progressed to AI-CTD at 12 months versus non-progressors, to a greater extent for IFN-Score-B (fold difference (95% CI) 3.22 (1.74 to 5.95), p<0.001) than IFN-Score-A (2.94 (1.14 to 7.54); p=0.018). Progressors did not have significantly greater baseline clinical characteristics or ultrasound findings. Fold difference between At-Risk and HCs for IFN-Score-A was markedly greater in skin than blood. In multivariable logistic regression, only family history of autoimmune rheumatic disease, OR 8.2 (95% CI 1.58 to 42.53) and IFN-Score-B, 3.79 (1.50–9.58) increased the odds of progression. CONCLUSION: A two-factor interferon score and family history predict progression from ANA positivity to AI-CTD. These interferon scores may allow stratification of individuals At-Risk of AI-CTD permitting early intervention for disease prevention and avoid irreversible organ damage. BMJ Publishing Group 2018-10 2018-06-21 /pmc/articles/PMC6161671/ /pubmed/29929956 http://dx.doi.org/10.1136/annrheumdis-2018-213386 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
spellingShingle Clinical and Epidemiological Research
Md Yusof, Md Yuzaiful
Psarras, Antonios
El-Sherbiny, Yasser M
Hensor, Elizabeth M A
Dutton, Katherine
Ul-Hassan, Sabih
Zayat, Ahmed S
Shalbaf, Mohammad
Alase, Adewonuola
Wittmann, Miriam
Emery, Paul
Vital, Edward M
Prediction of autoimmune connective tissue disease in an at-risk cohort: prognostic value of a novel two-score system for interferon status
title Prediction of autoimmune connective tissue disease in an at-risk cohort: prognostic value of a novel two-score system for interferon status
title_full Prediction of autoimmune connective tissue disease in an at-risk cohort: prognostic value of a novel two-score system for interferon status
title_fullStr Prediction of autoimmune connective tissue disease in an at-risk cohort: prognostic value of a novel two-score system for interferon status
title_full_unstemmed Prediction of autoimmune connective tissue disease in an at-risk cohort: prognostic value of a novel two-score system for interferon status
title_short Prediction of autoimmune connective tissue disease in an at-risk cohort: prognostic value of a novel two-score system for interferon status
title_sort prediction of autoimmune connective tissue disease in an at-risk cohort: prognostic value of a novel two-score system for interferon status
topic Clinical and Epidemiological Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161671/
https://www.ncbi.nlm.nih.gov/pubmed/29929956
http://dx.doi.org/10.1136/annrheumdis-2018-213386
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