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ISSAID/EMQN Best Practice Guidelines for the Genetic Diagnosis of Monogenic Autoinflammatory Diseases in the Next-Generation Sequencing Era

Authors :
Osamu Ohara
Guilaine Boursier
Dorota Rowczenio
Christian Oberkanins
Hiroaki Ida
Marco Gattorno
Nicola Wolstenholme
Laura Obici
Ivona Aksentijevich
Yael Shinar
Anna Mensa-Vilaro
Ryuta Nishikomori
Isabella Ceccherini
Hasmik Hayrapetyan
Nobuo Kanazawa
Helen J. Lachmann
Seza Ozen
Marielle E. van Gijn
Tamara Sarkisian
Evelien Zonneveld-Huijssoon
Isabelle Touitou
Katie Sheils
Juan I. Aróstegui
Eldad Ben-Chetrit
Chaim Sheba Medical Center
IRCCS Istituto Giannina Gaslini [Genoa, Italy]
UCL Medical School
National Human Genome Research Institute (NHGRI)
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)
Universitat de Barcelona (UB)
Hadassah Hebrew University Medical Center [Jerusalem]
Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)
Kurume University School of Medicine
Kurume University
Wakayama Medical University
Hospital Clinic [Barcelona, Spain]
ViennaLab Diagnostics GmbH
Fondazione IRCCS Policlinico San Matteo [Pavia]
Università di Pavia
Kazusa DNA Research Institute (KDRI)
Hacettepe University = Hacettepe Üniversitesi
St Mary's Hospital [London]
University of Groningen [Groningen]
Cellules Souches, Plasticité Cellulaire, Médecine Régénératrice et Immunothérapies (IRMB)
Université de Montpellier (UM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)
Source :
Clinical Chemistry, 66(4), 525-536. AMER ASSOC CLINICAL CHEMISTRY, Clinical Chemistry, Clinical Chemistry, American Association for Clinical Chemistry, 2020, 66 (4), pp.525-536. ⟨10.1093/clinchem/hvaa024⟩
Publication Year :
2020

Abstract

Background Monogenic autoinflammatory diseases are caused by pathogenic variants in genes that regulate innate immune responses, and are characterized by sterile systemic inflammatory episodes. Since symptoms can overlap within this rapidly expanding disease category, accurate genetic diagnosis is of the utmost importance to initiate early inflammation-targeted treatment and prevent clinically significant or life-threatening complications. Initial recommendations for the genetic diagnosis of autoinflammatory diseases were limited to a gene-by-gene diagnosis strategy based on the Sanger method, and restricted to the 4 prototypic recurrent fevers (MEFV, MVK, TNFRSF1A, and NLRP3 genes). The development of best practices guidelines integrating critical recent discoveries has become essential. Methods The preparatory steps included 2 online surveys and pathogenicity annotation of newly recommended genes. The current guidelines were drafted by European Molecular Genetics Quality Network members, then discussed by a panel of experts of the International Society for Systemic Autoinflammatory Diseases during a consensus meeting. Results In these guidelines, we combine the diagnostic strength of next-generation sequencing and recommendations to 4 more recently identified genes (ADA2, NOD2, PSTPIP1, and TNFAIP3), nonclassical pathogenic genetic alterations, and atypical phenotypes. We present a referral-based decision tree for test scope and method (Sanger versus next-generation sequencing) and recommend on complementary explorations for mosaicism, copy-number variants, and gene dose. A genotype table based on the 5-category variant pathogenicity classification provides the clinical significance of prototypic genotypes per gene and disease. Conclusions These guidelines will orient and assist geneticists and health practitioners in providing up-to-date and appropriate diagnosis to their patients.

Details

Language :
English
ISSN :
00099147 and 15308561
Database :
OpenAIRE
Journal :
Clinical Chemistry, 66(4), 525-536. AMER ASSOC CLINICAL CHEMISTRY, Clinical Chemistry, Clinical Chemistry, American Association for Clinical Chemistry, 2020, 66 (4), pp.525-536. ⟨10.1093/clinchem/hvaa024⟩
Accession number :
edsair.doi.dedup.....399ebacfc3cf95004485836dc3ab9c35
Full Text :
https://doi.org/10.1093/clinchem/hvaa024⟩