Integration of Genetic and Clinical Risk Factors for Risk Classification of Uveitis in Patients With Juvenile Idiopathic Arthritis

Author:

Tordoff Melissa1ORCID,Smith Samantha L.1,Lawson‐Tovey Saskia2ORCID,Dick Andrew D.3,Beresford Michael W.4,Ramanan Athimalaipet V.5,Hyrich Kimme L.2,Morris Andrew P.2,Eyre Stephen2,Wedderburn Lucy R.6ORCID,Bowes John2,

Affiliation:

1. The University of Manchester Manchester United Kingdom

2. NIHR Manchester Biomedical Research Centre, Manchester University NHS Foundation Trust Manchester UK

3. University of Bristol, Bristol, UCL Institute of Ophthalmology, London, and Moorfields Eye Hospital London United Kingdom

4. University of Liverpool and Alder Hey Children's NHS Foundation Trust Hospital Liverpool United Kingdom

5. Bristol Royal Hospital for Children and University of Bristol Bristol United Kingdom

6. UCL Great Ormond Street Institute of Child Health, UCL Hospital and Great Ormond Street Hospital, and NIHR Biomedical Research Centre at Great Ormond Street Hospital London United Kingdom

Abstract

ObjectiveJuvenile idiopathic arthritis (JIA)–associated uveitis (JIAU) is a serious JIA comorbidity that can result in vision impairment. This study aimed to identify genetic risk factors within the major histocompatibility complex for JIAU and evaluate their contribution for improving risk classification when combined with clinical risk factors.MethodsData on single nucleotide polymorphisms, amino acids, and classical HLA alleles were available for 2,497 patients with JIA without uveitis and 579 patients with JIAU (female 2,060, male 1,015). Analysis was restricted to patients with inferred European ancestry. Forward conditional logistic regression identified genetic markers exceeding a Bonferroni‐corrected significance (6 × 10−6). Multivariable logistic regression estimated the effects of clinical and genetic risk factors, and a likelihood ratio test calculated the improvement in model fit when adding genetic factors. Uveitis risk classification performance of a model integrating genetic and clinical risk factors was estimated using area under the receiver operator characteristic curve and compared with a model of clinical risk factors alone.ResultsThree genetic risk factors were identified, mapping to HLA‐DRB1, HLA‐DPB1, and HLA‐A. These markers were statistically independent from clinical risk factors and significantly improved the fit of a model when included with clinical risk factors (P = 3.3 × 10−23). The addition of genetic markers improved the classification of JIAU compared with a model of clinical risk factors alone (area under the curve 0.75 vs 0.71).ConclusionIntegration of a genetic and clinical risk prediction model outperforms a model based solely on clinical risk factors. Future JIAU risk prediction models should include genetic risk factors.

Funder

Great Ormond Street Hospital Charity

Centre for Epidemiology Versus Arthritis, University of Manchester

Medical Research Council

Arthritis Research UK

Versus Arthritis

Publisher

Wiley

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