An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Almeida Ligia S, Pereira Catarina, Aanicai Ruxandra, Schröder Sabine, Bochinski Tomasz, Kaune Anett, Urzi Alice, Spohr Tania C L S, Viceconte Nikenza, Oppermann Sebastian, Alasel Mohammed, Ebadat Saeedeh, Iftikhar Sana, Jasinge Eresha, Elsayed Solaf M, Tomoum Hoda, Marzouk Iman, Jalan Anil B, Cerkauskaite Agne, Cerkauskiene Rimante, Tkemaladze Tinatin, Nadeem Anjum Muhammad, El Din Mahmoud Iman Gamal, Mossad Fawzia Amer, Kamel Mona, Selim Laila Abdel, Cheema Huma Arshad, Paknia Omid, Cozma Claudia, Juaristi-Manrique Carlos, Guatibonza-Moreno Pilar, Böttcher Tobias, Vogel Florian, Pinto-Basto Jorge, Bertoli-Avella Aida, Bauer Peter
Аннотация
To present our experience using a multiomic approach, which integrates genetic and biochemical testing as a first-line diagnostic tool for patients with inherited metabolic disorders (IMDs). A cohort of 3720 patients from 62 countries was tested using a panel including 206 genes with single nucleotide and copy number variant (SNV/CNV) detection, followed by semi-automatic variant filtering and reflex biochemical testing (25 assays). In 1389 patients (37%), a genetic diagnosis was achieved. Within this cohort, the highest diagnostic yield was obtained for patients from Asia (57.5%, mainly from Pakistan). Overall, 701 pathogenic/likely pathogenic unique SNVs and 40 CNVs were identified. In 620 patients, the result of the biochemical tests guided variant classification and reporting. Top five diagnosed diseases were: Gaucher disease, Niemann-Pick disease type A/B, phenylketonuria, mucopolysaccharidosis type I, and Wilson disease. We show that integrated genetic and biochemical testing facilitated the decision on clinical relevance of the variants and led to a high diagnostic yield (37%), which is comparable to exome/genome sequencing. More importantly, up to 43% of these patients (n = 610) could benefit from medical treatments (e.g., enzyme replacement therapy). This multiomic approach constitutes a unique and highly effective tool for the genetic diagnosis of IMDs.