Cargando…

Potential impact of autoimmune diseases family history in IgG4-related disease: a retrospective cohort study

OBJECTIVE: Autoimmune comorbidities may be associated with IgG4-related disease (IgG4-RD), here we aimed to determine the correlation of autoimmune diseases (AID) family history and IgG4-RD in a Chinese cohort. METHODS: This retrospective cohort study identified 628 cases of IgG4-RD in Peking Union...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Ruijie, Liu, Zheng, Lu, Hui, Peng, Yu, Li, Jieqiong, Nie, Yuxue, Li, Jingna, Peng, Linyi, Zhou, Jiaxin, Fei, Yunyun, Zeng, Xiaofeng, Zhang, Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923356/
https://www.ncbi.nlm.nih.gov/pubmed/36759004
http://dx.doi.org/10.1136/rmdopen-2022-002865
_version_ 1784887720890335232
author Sun, Ruijie
Liu, Zheng
Lu, Hui
Peng, Yu
Li, Jieqiong
Nie, Yuxue
Li, Jingna
Peng, Linyi
Zhou, Jiaxin
Fei, Yunyun
Zeng, Xiaofeng
Zhang, Wen
author_facet Sun, Ruijie
Liu, Zheng
Lu, Hui
Peng, Yu
Li, Jieqiong
Nie, Yuxue
Li, Jingna
Peng, Linyi
Zhou, Jiaxin
Fei, Yunyun
Zeng, Xiaofeng
Zhang, Wen
author_sort Sun, Ruijie
collection PubMed
description OBJECTIVE: Autoimmune comorbidities may be associated with IgG4-related disease (IgG4-RD), here we aimed to determine the correlation of autoimmune diseases (AID) family history and IgG4-RD in a Chinese cohort. METHODS: This retrospective cohort study identified 628 cases of IgG4-RD in Peking Union Medical College Hospital. Patients were classified into two groups, with AID family history group (AID-positive) and without AID family history group (AID-negative). We viewed the potential value of AID family history on IgG4-RD by comparing the differences between the two groups. In addition, Cox regression analysis estimated CIs and HR for IgG4-RD risk. RESULTS: 93 (14.8%) IgG4-RD patients had AID family history. Compared with AID-negative group, baseline data analysis revealed that AID-positive group patients had an earlier age of IgG4-RD onset (50.4±14.8 vs 54.2±12.6, p=0.014*), a higher percentage of antinuclear antibody (ANA) positivity (38.9% vs 22.7%, p=0.0277*) and Riedel thyroiditis (10.9% vs 2.4%, p=0.001*), were prone to comorbid with other AID (16.1% vs 6.2%, p=0.0238*). Cox analysis found that younger age (HR 0.97 (95% CI 0.94 to 0.99), p=0.0384*) and higher proportions of baseline peripheral eosinophils (HR 1.1 (95% CI 1.02 to 1.2), p=0.0199*) increased the risk of unfavourable prognosis for AID-positive IgG4-RD patients. CONCLUSIONS: 14.8% of IgG4-RD patients had AID family history, with younger age of disease onset age and higher frequency of ANA positivity in AID-positive group, indicating that IgG4-RD may share genetic background with other AID.
format Online
Article
Text
id pubmed-9923356
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-99233562023-02-14 Potential impact of autoimmune diseases family history in IgG4-related disease: a retrospective cohort study Sun, Ruijie Liu, Zheng Lu, Hui Peng, Yu Li, Jieqiong Nie, Yuxue Li, Jingna Peng, Linyi Zhou, Jiaxin Fei, Yunyun Zeng, Xiaofeng Zhang, Wen RMD Open Autoinflammatory Disorders OBJECTIVE: Autoimmune comorbidities may be associated with IgG4-related disease (IgG4-RD), here we aimed to determine the correlation of autoimmune diseases (AID) family history and IgG4-RD in a Chinese cohort. METHODS: This retrospective cohort study identified 628 cases of IgG4-RD in Peking Union Medical College Hospital. Patients were classified into two groups, with AID family history group (AID-positive) and without AID family history group (AID-negative). We viewed the potential value of AID family history on IgG4-RD by comparing the differences between the two groups. In addition, Cox regression analysis estimated CIs and HR for IgG4-RD risk. RESULTS: 93 (14.8%) IgG4-RD patients had AID family history. Compared with AID-negative group, baseline data analysis revealed that AID-positive group patients had an earlier age of IgG4-RD onset (50.4±14.8 vs 54.2±12.6, p=0.014*), a higher percentage of antinuclear antibody (ANA) positivity (38.9% vs 22.7%, p=0.0277*) and Riedel thyroiditis (10.9% vs 2.4%, p=0.001*), were prone to comorbid with other AID (16.1% vs 6.2%, p=0.0238*). Cox analysis found that younger age (HR 0.97 (95% CI 0.94 to 0.99), p=0.0384*) and higher proportions of baseline peripheral eosinophils (HR 1.1 (95% CI 1.02 to 1.2), p=0.0199*) increased the risk of unfavourable prognosis for AID-positive IgG4-RD patients. CONCLUSIONS: 14.8% of IgG4-RD patients had AID family history, with younger age of disease onset age and higher frequency of ANA positivity in AID-positive group, indicating that IgG4-RD may share genetic background with other AID. BMJ Publishing Group 2023-02-09 /pmc/articles/PMC9923356/ /pubmed/36759004 http://dx.doi.org/10.1136/rmdopen-2022-002865 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Autoinflammatory Disorders
Sun, Ruijie
Liu, Zheng
Lu, Hui
Peng, Yu
Li, Jieqiong
Nie, Yuxue
Li, Jingna
Peng, Linyi
Zhou, Jiaxin
Fei, Yunyun
Zeng, Xiaofeng
Zhang, Wen
Potential impact of autoimmune diseases family history in IgG4-related disease: a retrospective cohort study
title Potential impact of autoimmune diseases family history in IgG4-related disease: a retrospective cohort study
title_full Potential impact of autoimmune diseases family history in IgG4-related disease: a retrospective cohort study
title_fullStr Potential impact of autoimmune diseases family history in IgG4-related disease: a retrospective cohort study
title_full_unstemmed Potential impact of autoimmune diseases family history in IgG4-related disease: a retrospective cohort study
title_short Potential impact of autoimmune diseases family history in IgG4-related disease: a retrospective cohort study
title_sort potential impact of autoimmune diseases family history in igg4-related disease: a retrospective cohort study
topic Autoinflammatory Disorders
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923356/
https://www.ncbi.nlm.nih.gov/pubmed/36759004
http://dx.doi.org/10.1136/rmdopen-2022-002865
work_keys_str_mv AT sunruijie potentialimpactofautoimmunediseasesfamilyhistoryinigg4relateddiseasearetrospectivecohortstudy
AT liuzheng potentialimpactofautoimmunediseasesfamilyhistoryinigg4relateddiseasearetrospectivecohortstudy
AT luhui potentialimpactofautoimmunediseasesfamilyhistoryinigg4relateddiseasearetrospectivecohortstudy
AT pengyu potentialimpactofautoimmunediseasesfamilyhistoryinigg4relateddiseasearetrospectivecohortstudy
AT lijieqiong potentialimpactofautoimmunediseasesfamilyhistoryinigg4relateddiseasearetrospectivecohortstudy
AT nieyuxue potentialimpactofautoimmunediseasesfamilyhistoryinigg4relateddiseasearetrospectivecohortstudy
AT lijingna potentialimpactofautoimmunediseasesfamilyhistoryinigg4relateddiseasearetrospectivecohortstudy
AT penglinyi potentialimpactofautoimmunediseasesfamilyhistoryinigg4relateddiseasearetrospectivecohortstudy
AT zhoujiaxin potentialimpactofautoimmunediseasesfamilyhistoryinigg4relateddiseasearetrospectivecohortstudy
AT feiyunyun potentialimpactofautoimmunediseasesfamilyhistoryinigg4relateddiseasearetrospectivecohortstudy
AT zengxiaofeng potentialimpactofautoimmunediseasesfamilyhistoryinigg4relateddiseasearetrospectivecohortstudy
AT zhangwen potentialimpactofautoimmunediseasesfamilyhistoryinigg4relateddiseasearetrospectivecohortstudy