From diagnosis to treatment in genetic epilepsies: Implementation of precision medicine in real-world clinical practice

被引:2
|
作者
De Wachter, Matthias [1 ]
Schoonjans, An-Sofie [1 ]
Weckhuysen, Sarah [2 ,4 ,5 ]
Van Schil, Kristof [3 ]
Lofgren, Ann [3 ]
Meuwissen, Marije [3 ]
Jansen, Anna [1 ,5 ]
Ceulemans, Berten [1 ]
机构
[1] Univ Antwerp, Antwerp Univ Hosp, Dept Pediat Neurol, Drie eikenstr 655, B-2650 Edegem, Belgium
[2] Univ Antwerp, Antwerp Univ Hosp, Dept Neurol, Drie eikenstr 655, B-2650 Edegem, Belgium
[3] Univ Antwerp, Antwerp Univ Hosp, Dept Med Genet, Drie eikenstr 655, B-2650 Edegem, Belgium
[4] Univ Antwerpen VIB, Appl &Translat Neurogenom Grp, VIB CMN, Univ Pl 1, B-2610 Antwerp, Belgium
[5] Univ Antwerp, Translat Neurosci, Univ Pl 1, B-2610 Antwerp, Belgium
关键词
(mono)genetic epilepsy; Whole exome sequencing; Diagnostic yield; Precision medicine; HOC TASK-FORCE; ILAE COMMISSION; MUTATIONS; GUIDELINES; VARIANTS; THERAPY;
D O I
10.1016/j.ejpn.2023.11.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The implementation of whole exome sequencing (WES) has had a major impact on the diagnostic yield of genetic testing in individuals with epilepsy. The identification of a genetic etiology paves the way to precision medicine: an individualized treatment approach, based on the disease pathophysiology. The aim of this retrospective cohort study was to: (1) determine the diagnostic yield of WES in a heterogeneous cohort of individuals with epilepsy referred for genetic testing in a real-world clinical setting, (2) investigate the influence of epilepsy characteristics on the diagnostic yield, (3) determine the theoretical yield of treatment changes based on genetic diagnosis and (4) explore the barriers to implementation of precision medicine. WES was performed in 247 individuals with epilepsy, aged between 7 months and 68 years. In 34/247 (14 %) a (likely) pathogenic variant was identified. In 7/34 (21 %) of these individuals the variant was found using a HPO-based filtering. Diagnostic yield was highest for individuals with an early onset of epilepsy (39 %) or in those with a developmental and epileptic encephalopathy (34 %). Precision medicine was a theoretical possibility in 20/34 (59 %) of the individuals with a (likely) pathogenic variant but implemented in only 11/34 (32 %). The major barrier to implementation of precision treatment was the limited availability or reimbursement of a given drug. These results confirm the potential impact of genetic analysis on treatment choices, but also highlight the hurdles to the implementation of precision medicine. To optimize precision medicine in real-world practice, additional endeavors are needed: unifying definitions of precision medicine, establishment of publicly accessible databases that include data on the functional effect of gene variants, increasing availability and reimbursement of precision therapeutics, and broadening access to innovative clinical trials.
引用
收藏
页码:46 / 60
页数:15
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