The uni-directional association of atopic dermatitis and rheumatoid arthritis: a systematic review and meta-analysis

• Published in: Archives of dermatological research Vol. 315; no. 8; pp. 2261 - 2269
• Main Authors: Williams, Ryan C., Brako, Maame Yaa O., Guo, William, Usmani, Hunya, Na, Sean, Clark, Richard A. F.
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.10.2023; Springer Nature B.V
• Subjects: Atopic dermatitis; Autoimmune diseases; Comorbidity; Dermatitis; Dermatology; Eczema; Joint diseases; Medicine; Medicine & Public Health; Meta-analysis; Osteoarthritis; Psoriatic arthritis; Quantitative analysis; Review; Rheumatoid arthritis; Skin diseases; Synovitis; Systematic review; Systematic review; Atopic dermatitis; Epidemiology; Rheumatoid arthritis; Meta-analysis
• ISSN: 1432-069X; 0340-3696; 1432-069X
• DOI: 10.1007/s00403-023-02619-0

Atopic dermatitis (AD) is a highly pruritic, inflammatory skin disease with a strong immune component. Rheumatoid arthritis (RA) is a systemic autoimmune disease that causes synovitis and destruction of small joints. Researchers have attempted to quantify an association between both diseases with mixed conclusions. This systematic review and meta-analysis will study the association between AD and RA. Additionally, we conducted a systematic review between AD and other arthritic conditions including osteoarthritis (OA), psoriatic arthritis (PsA), and juvenile idiopathic arthritis (JIA). Medline, Web of Science, Cochrane, and EMBASE databases were searched for relevant studies from inception to March 2021. Observational studies examining relationships between AD and arthritic conditions were selected. 2539 studies were screened; nine were found suitable for quantitative analysis, all of which examined AD and RA. All studies had low risk of bias as determined by the Newcastle–Ottawa Scale. Patients with RA did not have significantly increased odds of comorbid AD. These findings were consistent across multiple study designs. However, patients with AD had significantly increased odds of comorbid RA. There were not enough studies identified to perform quantitative analysis between AD and other arthritic conditions. Two studies, one on JIA and one PsA, found no association with AD. Two studies on AD and OA had conflicting results. The present study provides definitive evidence of increased odds of comorbid RA in AD patients. There were no such increased odds of comorbid AD in RA patients. No such association was found between AD and PsA, OA or JIA.