AI Article Synopsis

  • Psoriatic arthritis (PsA) affects about 30% of psoriasis patients, and there's currently no systematic way to predict its onset based on genetic differences from psoriasis without arthritis (PsC).
  • A new computational pipeline was developed using genetic data from over 7,000 patients, identifying 9 new genetic locations associated with psoriasis subtypes.
  • The model shows a strong ability to distinguish between PsA and PsC, achieving over 90% precision in predictions for high-risk patients through advanced statistical and machine-learning methods.

Article Abstract

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177414PMC
http://dx.doi.org/10.1038/s41467-018-06672-6DOI Listing

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