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Genetic signature to provide robust risk assessment of psoriatic arthritis development in psoriasis patients.

Matthew T PatrickPhilip E StuartKalpana RajaJohann E GudjonssonTrilokraj TejasviJingjing YangVinod ChandranSayantan DasKristina Callis-DuffinEva EllinghausCharlotta EnerbäckTõnu EskoAndre FrankeHyun M KangGerald G KruegerHenry W LimProton RahmanCheryl F RosenStephan WeidingerMichael WeichenthalXiaoquan WenJohn J VoorheesGonçalo R AbecasisDafna D GladmanRajan P NairJames T ElderLam C Tsoi
Published in: Nature communications (2018)
Psoriatic arthritis (PsA) is a complex chronic musculoskeletal condition that occurs in ~30% of psoriasis patients. Currently, no systematic strategy is available that utilizes the differences in genetic architecture between PsA and cutaneous-only psoriasis (PsC) to assess PsA risk before symptoms appear. Here, we introduce a computational pipeline for predicting PsA among psoriasis patients using data from six cohorts with >7000 genotyped PsA and PsC patients. We identify 9 new loci for psoriasis or its subtypes and achieve 0.82 area under the receiver operator curve in distinguishing PsA vs. PsC when using 200 genetic markers. Among the top 5% of our PsA prediction we achieve >90% precision with 100% specificity and 16% recall for predicting PsA among psoriatic patients, using conditional inference forest or shrinkage discriminant analysis. Combining statistical and machine-learning techniques, we show that the underlying genetic differences between psoriasis subtypes can be used for individualized subtype risk assessment.
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