Pregled bibliografske jedinice broj: 1211797
Genetics of Pediatric Epilepsy: Next-Generation Sequencing in Clinical Practice
Genetics of Pediatric Epilepsy: Next-Generation Sequencing in Clinical Practice // Genes, 13 (2022), 8; 1466, 10 doi:10.3390/genes13081466 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1211797 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Genetics of Pediatric Epilepsy: Next-Generation
Sequencing in Clinical Practice
Autori
Blažeković, Antonela ; Gotovac Jerčić, Kristina ; Meglaj, Sarah ; Đuranović, Vlasta ; Prpić, Igor ; Lozić, Bernarda ; Malenica, Maša ; Markovic, Silvana ; Lujić, Lucija ; Petelin Gadže, Željka ; Gjergja- Juraski, Romana ; Barišic, Nina ; Barić, Ivo ; Borovečki, Fran
Izvornik
Genes (2073-4425) 13
(2022), 8;
1466, 10
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
epilepsy ; pediatric ; next-generation sequencing ; gene panel ; clinical decision making
Sažetak
Epilepsy is one of the most common neurological disorders with diverse phenotypic characteristics and high genetic heterogeneity. Epilepsy often occurs in childhood, so timely diagnosis and adequate therapy are crucial for preserving quality of life and unhindered development of a child. Next-generation- sequencing (NGS)-based tools have shown potential in increasing diagnostic yield. The primary objective of this study was to evaluate the impact of genetic testing and to investigate the diagnostic utility of targeted gene panel sequencing. This retrospective cohort study included 277 patients aged 6 months to 17 years undergoing NGS with an epilepsy panel covering 142 genes. Of 118 variants detected, 38 (32.2%) were not described in the literature. We identified 64 pathogenic or likely pathogenic variants with an overall diagnostic yield of 23.1%. We showed a significantly higher diagnostic yield in patients with developmental delay (28.9%). Furthermore, we showed that patients with variants reported as pathogenic presented with seizures at a younger age, which led to the conclusion that such children should be included in genomic diagnostic procedures as soon as possible to achieve a correct diagnosis in a timely manner, potentially leading to better treatment and avoidance of unnecessary procedures. Describing and discovering the genetic background of the disease not only leads to a better understanding of the mechanisms of the disorder but also opens the possibility of more precise and individualized treatment based on stratified medicine.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb,
KBC "Sestre Milosrdnice",
KBC Split,
Klinički bolnički centar Zagreb,
Medicinski fakultet, Split,
Klinički bolnički centar Rijeka,
Dječja bolnica Srebrnjak,
Klinika za dječje bolesti
Profili:
Antonela Blažeković
(autor)
Fran Borovečki
(autor)
Nina Barišić
(autor)
Željka Petelin Gadže
(autor)
Bernarda Lozić
(autor)
Ivo Barić
(autor)
Igor Prpić
(autor)
Romana Gjergja Juraški
(autor)
Kristina Gotovac Jerčić
(autor)
Lucija Lujić
(autor)
Sarah Meglaj
(autor)
Vlasta Đuranović
(autor)
Maša Malenica
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE