Cargando…
Heterogeneity of axial spondyloarthritis: genetics, sex and structural damage matter
OBJECTIVE: Axial spondyloarthritis (axSpA) comprises both radiographic and non-radiographic disease. However, the paucity of specific objective measures for the disease and current classification criteria showing suboptimal specificity contribute to disease heterogeneity observed in clinical practic...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9083385/ https://www.ncbi.nlm.nih.gov/pubmed/35523521 http://dx.doi.org/10.1136/rmdopen-2022-002302 |
_version_ | 1784703409645944832 |
---|---|
author | Li, Zhixiu van der Linden, Sjef M Khan, Muhammad Asim Baumberger, Heinz van Zandwijk, Hermine Khan, Mohammad Kazim Villiger, Peter M Brown, Matthew A |
author_facet | Li, Zhixiu van der Linden, Sjef M Khan, Muhammad Asim Baumberger, Heinz van Zandwijk, Hermine Khan, Mohammad Kazim Villiger, Peter M Brown, Matthew A |
author_sort | Li, Zhixiu |
collection | PubMed |
description | OBJECTIVE: Axial spondyloarthritis (axSpA) comprises both radiographic and non-radiographic disease. However, the paucity of specific objective measures for the disease and current classification criteria showing suboptimal specificity contribute to disease heterogeneity observed in clinical practice and research. We used a historical cohort of patients with axSpA to assess sources of heterogeneity. METHODS: The study involved 363 axSpA probands recruited from membership of the Swiss Ankylosing Spondylitis Patient Society. Participants underwent examination by a rheumatologist, completed questionnaires and provided blood samples for HLA typing. Patients underwent radiography of sacroiliac joints and were categorised according to the New York (NY) criteria (ankylosing spondylitis (AS) or non-radiographic axSpA (nr-axSpA)) and HLA-B27 status. Genetic characterisation by single nucleotide polymorphism microarray was performed and AS polygenic risk scores (PRS) were calculated. RESULTS: Considerable heterogeneity was observed. The male to female ratio for AS (NY+) was 3:1, but 1:1 for nr-axSpA. For HLA-27(+) AS, the ratio was 2.5:1, but nearly 1:1 for HLA-B27(−) disease. Women with nr-axSpA had strikingly lower mean PRS and lower HLA-B27 prevalence than men with nr-axSpA or NY(+) male and female patients with AS. PRS was able to distinguish male but not female patients with nr-axSpA from related healthy first-degree relatives. Radiographic sacroiliitis was strongly associated with HLA-B27, especially in men. CONCLUSION: Women clinically diagnosed with axSpA but without radiographic sacroiliitis as a group have a disease that is distinct from AS by the modified New York criteria overall and from nr-axSpA in men. Given the high degree of heterogeneity, stratified or adjusted analysis of effectiveness studies is indicated, taking genetics, sex and radiographic damage (sacroiliitis) into account. |
format | Online Article Text |
id | pubmed-9083385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-90833852022-05-20 Heterogeneity of axial spondyloarthritis: genetics, sex and structural damage matter Li, Zhixiu van der Linden, Sjef M Khan, Muhammad Asim Baumberger, Heinz van Zandwijk, Hermine Khan, Mohammad Kazim Villiger, Peter M Brown, Matthew A RMD Open Spondyloarthritis OBJECTIVE: Axial spondyloarthritis (axSpA) comprises both radiographic and non-radiographic disease. However, the paucity of specific objective measures for the disease and current classification criteria showing suboptimal specificity contribute to disease heterogeneity observed in clinical practice and research. We used a historical cohort of patients with axSpA to assess sources of heterogeneity. METHODS: The study involved 363 axSpA probands recruited from membership of the Swiss Ankylosing Spondylitis Patient Society. Participants underwent examination by a rheumatologist, completed questionnaires and provided blood samples for HLA typing. Patients underwent radiography of sacroiliac joints and were categorised according to the New York (NY) criteria (ankylosing spondylitis (AS) or non-radiographic axSpA (nr-axSpA)) and HLA-B27 status. Genetic characterisation by single nucleotide polymorphism microarray was performed and AS polygenic risk scores (PRS) were calculated. RESULTS: Considerable heterogeneity was observed. The male to female ratio for AS (NY+) was 3:1, but 1:1 for nr-axSpA. For HLA-27(+) AS, the ratio was 2.5:1, but nearly 1:1 for HLA-B27(−) disease. Women with nr-axSpA had strikingly lower mean PRS and lower HLA-B27 prevalence than men with nr-axSpA or NY(+) male and female patients with AS. PRS was able to distinguish male but not female patients with nr-axSpA from related healthy first-degree relatives. Radiographic sacroiliitis was strongly associated with HLA-B27, especially in men. CONCLUSION: Women clinically diagnosed with axSpA but without radiographic sacroiliitis as a group have a disease that is distinct from AS by the modified New York criteria overall and from nr-axSpA in men. Given the high degree of heterogeneity, stratified or adjusted analysis of effectiveness studies is indicated, taking genetics, sex and radiographic damage (sacroiliitis) into account. BMJ Publishing Group 2022-05-06 /pmc/articles/PMC9083385/ /pubmed/35523521 http://dx.doi.org/10.1136/rmdopen-2022-002302 Text en © Author(s) (or their employer(s)) 2022. 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 | Spondyloarthritis Li, Zhixiu van der Linden, Sjef M Khan, Muhammad Asim Baumberger, Heinz van Zandwijk, Hermine Khan, Mohammad Kazim Villiger, Peter M Brown, Matthew A Heterogeneity of axial spondyloarthritis: genetics, sex and structural damage matter |
title | Heterogeneity of axial spondyloarthritis: genetics, sex and structural damage matter |
title_full | Heterogeneity of axial spondyloarthritis: genetics, sex and structural damage matter |
title_fullStr | Heterogeneity of axial spondyloarthritis: genetics, sex and structural damage matter |
title_full_unstemmed | Heterogeneity of axial spondyloarthritis: genetics, sex and structural damage matter |
title_short | Heterogeneity of axial spondyloarthritis: genetics, sex and structural damage matter |
title_sort | heterogeneity of axial spondyloarthritis: genetics, sex and structural damage matter |
topic | Spondyloarthritis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9083385/ https://www.ncbi.nlm.nih.gov/pubmed/35523521 http://dx.doi.org/10.1136/rmdopen-2022-002302 |
work_keys_str_mv | AT lizhixiu heterogeneityofaxialspondyloarthritisgeneticssexandstructuraldamagematter AT vanderlindensjefm heterogeneityofaxialspondyloarthritisgeneticssexandstructuraldamagematter AT khanmuhammadasim heterogeneityofaxialspondyloarthritisgeneticssexandstructuraldamagematter AT baumbergerheinz heterogeneityofaxialspondyloarthritisgeneticssexandstructuraldamagematter AT vanzandwijkhermine heterogeneityofaxialspondyloarthritisgeneticssexandstructuraldamagematter AT khanmohammadkazim heterogeneityofaxialspondyloarthritisgeneticssexandstructuraldamagematter AT villigerpeterm heterogeneityofaxialspondyloarthritisgeneticssexandstructuraldamagematter AT brownmatthewa heterogeneityofaxialspondyloarthritisgeneticssexandstructuraldamagematter |