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Curation and expansion of the Human Phenotype Ontology for systemic autoinflammatory diseases improves phenotype-driven disease-matching.
Maassen, Willem; Legger, Geertje; Kul Cinar, Ovgu; van Daele, Paul; Gattorno, Marco; Bader-Meunier, Brigitte; Wouters, Carine; Briggs, Tracy; Johansson, Lennart; van der Velde, Joeri; Swertz, Morris; Omoyinmi, Ebun; Hoppenreijs, Esther; Belot, Alexandre; Eleftheriou, Despina; Caorsi, Roberta; Aeschlimann, Florence; Boursier, Guilaine; Brogan, Paul; Haimel, Matthias; van Gijn, Marielle.
Afiliação
  • Maassen W; Genomics Coordination Centre, Department of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
  • Legger G; Department of Rheumatology and Clinical Immunology, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
  • Kul Cinar O; Department of Paediatric Rheumatology, Great Ormond Street Hospital for Children National Health Service Trust, London, United Kingdom.
  • van Daele P; Department of Internal Medicine, Erasmus Medical Centre, Rotterdam, Netherlands.
  • Gattorno M; Department of Immunology, Erasmus Medical Centre, Rotterdam, Netherlands.
  • Bader-Meunier B; UOC Reumatologia e Malattie Autoinfiammatorie, IRCCS Istituto Giannini Gaslini, Genoa, Italy.
  • Wouters C; Department of Paediatric Immunology-Hematology and Rheumatology, Necker University Hospital - APHP, Paris, France.
  • Briggs T; Laboratory of Immunogenetics of Paediatric Autoimmune Diseases, UMR 1163, Imagine Institute, INSERM, Paris, France.
  • Johansson L; Department of Pediatric Rheumatology, University Hospital Leuven, Leuven, Belgium.
  • van der Velde J; Division of Evolution and Genomic Sciences, School of Biological Sciences, University of Manchester, Manchester, United Kingdom.
  • Swertz M; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University Hospitals National Health Service Foundation Trust, Manchester, United Kingdom.
  • Omoyinmi E; Genomics Coordination Centre, Department of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
  • Hoppenreijs E; Genomics Coordination Centre, Department of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
  • Belot A; Genomics Coordination Centre, Department of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.
  • Eleftheriou D; Department of Paediatric Rheumatology, Great Ormond Street Hospital for Children National Health Service Trust, London, United Kingdom.
  • Caorsi R; Department of Pediatric Rheumatology, Pediatrics, Radboud University Medical Center, Nijmegen, Netherlands.
  • Aeschlimann F; National Referee Centre for Rheumatic and AutoImmune and Systemic Diseases in Children (RAISE), Pediatric Nephrology, Rheumatology, Dermatology Unit, INSERM, Hospital of Mother and Child, Hospices Civils of Lyon, Lyon, France.
  • Boursier G; International Center of Infectiology Research (CIRI), University of Lyon, INSERM, Claude Bernard University, Lyon, France.
  • Brogan P; Department of Paediatric Rheumatology, Great Ormond Street Hospital for Children National Health Service Trust, London, United Kingdom.
  • Haimel M; UOC Reumatologia e Malattie Autoinfiammatorie, IRCCS Istituto Giannini Gaslini, Genoa, Italy.
  • van Gijn M; Department of Paediatric Immunology-Hematology and Rheumatology, Necker University Hospital - APHP, Paris, France.
Front Immunol ; 14: 1215869, 2023.
Article em En | MEDLINE | ID: mdl-37781402
Introduction: Accurate and standardized phenotypic descriptions are essential in diagnosing rare diseases and discovering new diseases, and the Human Phenotype Ontology (HPO) system was developed to provide a rich collection of hierarchical phenotypic descriptions. However, although the HPO terms for inborn errors of immunity have been improved and curated, it has not been investigated whether this curation improves the diagnosis of systemic autoinflammatory disease (SAID) patients. Here, we aimed to study if improved HPO annotation for SAIDs enhanced SAID identification and to demonstrate the potential of phenotype-driven genome diagnostics using curated HPO terms for SAIDs. Methods: We collected HPO terms from 98 genetically confirmed SAID patients across eight different European SAID expertise centers and used the LIRICAL (Likelihood Ratio Interpretation of Clinical Abnormalities) computational algorithm to estimate the effect of HPO curation on the prioritization of the correct SAID for each patient. Results: Our results show that the percentage of correct diagnoses increased from 66% to 86% and that the number of diagnoses with the highest ranking increased from 38 to 45. In a further pilot study, curation also improved HPO-based whole-exome sequencing (WES) analysis, diagnosing 10/12 patients before and 12/12 after curation. In addition, the average number of candidate diseases that needed to be interpreted decreased from 35 to 2. Discussion: This study demonstrates that curation of HPO terms can increase identification of the correct diagnosis, emphasizing the high potential of HPO-based genome diagnostics for SAIDs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Imunodeficiência Adquirida dos Símios / Doenças Hereditárias Autoinflamatórias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Imunodeficiência Adquirida dos Símios / Doenças Hereditárias Autoinflamatórias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article