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ISSAID/EMQN Best Practice Guidelines for the Genetic Diagnosis of Monogenic Autoinflammatory Diseases in the Next-Generation Sequencing Era
- 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.
- Subjects :
- 0301 basic medicine
Adenosine Deaminase
[SDV]Life Sciences [q-bio]
Clinical Biochemistry
Next-Generation Sequencing (NGS)
VARIANT
Nod2 Signaling Adaptor Protein
Familial Mediterranean fever
Disease
Bioinformatics
0302 clinical medicine
Prenatal Diagnosis
Genotype
guidelines
Sanger sequencing
medicine.diagnostic_test
High-Throughput Nucleotide Sequencing
MEFV
3. Good health
AMYLOIDOSIS
Practice Guidelines as Topic
symbols
Intercellular Signaling Peptides and Proteins
FAMILIAL MEDITERRANEAN FEVER
medicine.medical_specialty
SOMATIC MOSAICISM
Prenatal diagnosis
HAPLOINSUFFICIENCY
CARD15 MUTATIONS
PATIENT
03 medical and health sciences
symbols.namesake
genetic diagnosis
Molecular genetics
medicine
Humans
Genetic Testing
Tumor Necrosis Factor alpha-Induced Protein 3
Genetic testing
Adaptor Proteins, Signal Transducing
030203 arthritis & rheumatology
business.industry
DELETION
Biochemistry (medical)
Hereditary Autoinflammatory Diseases
medicine.disease
autoinflammatory diseases
variant analysis
Cytoskeletal Proteins
030104 developmental biology
business
Subjects
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⟩