Clinical and Genetic Risk Factors Associated with Psoriatic Arthritis among Patients with Psoriasis

Dermatology and Therapy

卷:8

Stephen Leslie¹  Di Yan²  Wilson Liao²  Richard Ahn³ 

[1] Centre for Systems Genomics, Schools of Mathematics and Statistics, and BioSciences, The University of Melbourne;

[2] Department of Dermatology, University of California San Francisco;

[3] Department of Microbiology, Immunology and Molecular Genetics, Institute for Quantitative and Computational Biosciences, University of California;

关键词: Association;    Demographics;    Genetics;    Prediction;    Psoriasis;    Psoriatic arthritis;   

DOI  :  10.1007/s13555-018-0266-x

来源: DOAJ

【 摘 要 】

Abstract Introduction Psoriatic arthritis (PsA) is a chronic, inflammatory arthritis that affects an estimated 30% of patients with psoriasis. PsA is underdiagnosed in primary care and dermatology clinics due to a variety of reasons, including failure of healthcare providers to ask about symptoms, overlap of symptoms and signs with other rheumatologic conditions, and lack of a specific diagnostic test. A delay in PsA diagnosis and treatment, even as short as 6 months, can lead to decreased quality of life, increased joint damage, and worse long-term physical function. In this study, we sought to identify the clinical and genetic factors that help discriminate patients with PsA from those with cutaneous psoriasis only. Methods We analyzed a cohort of 974 psoriasis patients at an academic medical center, of whom 175 had confirmed PsA, and performed univariate, multivariate, and predictive modeling to determine factors associated with PsA. Results The univariate analysis revealed significant positive associations of PsA with age, nail involvement, scalp involvement, skin fold involvement, elbow/knee involvement, psoriasis severity, plaque subtype, erythrodermic subtype, hypertension, type 2 diabetes, and coronary artery disease, and a significant negative association of PsA with the human leukocyte antigen (HLA)-C*06:02 allele. In the multivariate analysis, nail involvement, type 2 diabetes, and pustular psoriasis remained significantly associated with PsA, while HLA-C*06:02 positivity remained protective. There was a trend towards an association of PsA with older age, younger age of psoriasis onset, and skin fold involvement, while there was protective trend for smoking. A predictive model including both clinical and genetic factors showed reasonable discriminative ability between psoriasis and PsA, with an area under the curve of 0.87 for a receiver operating characteristic curve. Conclusion This study identified a number of clinical and genetic features that could help stratify patients who are at higher risk for having PsA and for whom rheumatology referral may be beneficial.

【 授权许可】

Unknown