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HGG advances · 2022

Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study.

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Elliott Alison M, Adam Shelin, du Souich Christèle, Lehman Anna, Nelson Tanya N, van Karnebeek Clara, Alderman Emily, Armstrong Linlea, Aubertin Gudrun, Blood Katherine, Boelman Cyrus, Boerkoel Cornelius, Bretherick Karla, Brown Lindsay, Chijiwa Chieko, Clarke Lorne, Couse Madeline, Creighton Susan, Watts-Dickens Abby, Gibson William T, Gill Harinder, Tarailo-Graovac Maja, Hamilton Sara, Heran Harindar, Horvath Gabriella, Huang Lijia, Hulait Gurdip K, Koehn David, Lee Hyun Kyung, Lewis Suzanne, Lopez Elena, Louie Kristal, Niederhoffer Karen, Matthews Allison, Meagher Kirsten, Peng Junran J, Patel Millan S, Race Simone, Richmond Phillip, Rupps Rosemarie, Salvarinova Ramona, Seath Kimberly, Selby Kathryn, Steinraths Michelle, Stockler Sylvia, Tang Kaoru, Tyson Christine, van Allen Margot, Wasserman Wyeth, Mwenifumbo Jill, Friedman Jan M

Аннотация

Genome-wide sequencing (GWS) is a standard of care for diagnosis of suspected genetic disorders, but the proportion of patients found to have pathogenic or likely pathogenic variants ranges from less than 30% to more than 60% in reported studies. It has been suggested that the diagnostic rate can be improved by interpreting genomic variants in the context of each affected individual's full clinical picture and by regular follow-up and reinterpretation of GWS laboratory results. Trio exome sequencing was performed in 415 families and trio genome sequencing in 85 families in the CAUSES study. The variants observed were interpreted by a multidisciplinary team including laboratory geneticists, bioinformaticians, clinical geneticists, genetic counselors, pediatric subspecialists, and the referring physician, and independently by a clinical laboratory using standard American College of Medical Genetics and Genomics (ACMG) criteria. Individuals were followed for an average of 5.1 years after testing, with clinical reassessment and reinterpretation of the GWS results as necessary. The multidisciplinary team established a diagnosis of genetic disease in 43.0% of the families at the time of initial GWS interpretation, and longitudinal follow-up and reinterpretation of GWS results produced new diagnoses in 17.2% of families whose initial GWS interpretation was uninformative or uncertain. Reinterpretation also resulted in rescinding a diagnosis in four families (1.9%). Of the families studied, 33.6% had ACMG pathogenic or likely pathogenic variants related to the clinical indication. Close collaboration among clinical geneticists, genetic counselors, laboratory geneticists, bioinformaticians, and individuals' primary physicians, with ongoing follow-up, reanalysis, and reinterpretation over time, can improve the clinical value of GWS.

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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