Evidence map›Paper›PMID 40954333›Full record

ReviewNature reviews. Rheumatology2025

Global epidemiology of spondyloarthritis.

John D Reveille, Lihi Eder, Nelly Ziade, Percival D Sampaio-Barros, Tae-Hwan Kim, Nurullah Akkoç, Matthew A Brown

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

John D ReveilleDivision of Rheumatology, Department of Medicine, University of Texas McGovern Medical School, Houston, TX, USA. john.d.reveille@uth.tmc.edu.ORCID http://orcid.org/0000-0001-5950-0913
Lihi EderDivision of Rheumatology, Women's College Hospital, University of Toronto, Toronto, Ontario, Canada.ORCID http://orcid.org/0000-0002-1473-1715
Nelly ZiadeRheumatology Department, Saint Joseph University and Hotel-Dieu de France Hospital, Beirut, Lebanon.ORCID http://orcid.org/0000-0002-4479-7678
Percival D Sampaio-BarrosDivision of Rheumatology, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-9843-6686
Tae-Hwan KimDepartment of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, South Korea.ORCID http://orcid.org/0000-0002-3542-2276
Nurullah AkkoçDivision of Rheumatology, Department of Internal Medicine, School of Medicine, Manisa Celal Bayar University, Manisa, Turkey.ORCID http://orcid.org/0000-0002-3718-171X
Matthew A BrownDepartment of Medical and Molecular Genetics, Faculty of Life Sciences and Medicine, King's College London, London, UK.ORCID http://orcid.org/0000-0003-0538-8211

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The worldwide epidemiology of axial spondyloarthritis (axSpA), psoriatic arthritis (PsA) and peripheral spondyloarthritis, as well as of HLA-B27 and other MHC and non-MHC genes in these diseases, is reviewed herein. The frequency of axSpA is highest in circumpolar groups (such as Sami people and certain Indigenous American groups) and lowest in those of Japanese and African ancestry. The same pattern holds for PsA, although the overall prevalence of PsA seems much lower in East Asia, where it is less frequent than axSpA. The prevalence of PsA in people with psoriasis is increased where rheumatological assessment was carried out and seems to be increasing over time. HLA-B27 remains the most important genetic factor in axSpA susceptibility, although its frequency is lower in African American, South American and Middle Eastern populations than in others. The presence of HLA-B27 and other HLA alleles seems to be important in discerning clinical subsets of SpA and PsA, particularly those characterized by acute anterior uveitis or by axSpA with psoriasis, although these HLA-B27 and other MHC and non-MHC associations are derived from genome-wide association studies and other chip-based studies in large populations. These studies have been carried out mainly in populations of European and East Asian ancestry, and similar data from Latin America, sub-Saharan Africa and South Asia are lacking. This under-representation is an unmet need in applying genetic factors to understand the pathogenesis, diagnosis and classification of SpA and PsA.

Indexed as

Axial SpondyloarthritisSpondylarthritisArthritis, PsoriaticGenetic Predisposition to DiseaseGenome-Wide Association StudyGlobal HealthHLA-B27 AntigenHumansPrevalenceHLA-B27 Antigen

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.