Genotype-phenotype correlations in focal malformations of cortical development: a pathway to integrated pathological diagnosis in epilepsy surgery
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, systematický přehled
Grantová podpora
Cancer Research UK - United Kingdom
PubMed
30485578
PubMed Central
PMC8028510
DOI
10.1111/bpa.12686
Knihovny.cz E-zdroje
- Klíčová slova
- mTOR, epilepsy surgery, malformations of cortical development, neuropathology, somatic variant,
- MeSH
- epilepsie genetika patologie MeSH
- fosfatidylinositol-3-kinasy MeSH
- genetické asociační studie MeSH
- lidé MeSH
- malformace mozkové kůry genetika patologie MeSH
- mozek abnormality patologie MeSH
- mozková kůra patologie MeSH
- nemoci mozku patologie MeSH
- refrakterní epilepsie genetika patologie MeSH
- signální transdukce MeSH
- TOR serin-threoninkinasy MeSH
- záchvaty patologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- systematický přehled MeSH
- Názvy látek
- fosfatidylinositol-3-kinasy MeSH
- TOR serin-threoninkinasy MeSH
Malformations of cortical development (MCD) comprise a broad spectrum of developmental brain abnormalities. Patients presenting with MCDs often suffer from drug-resistant focal epilepsy, and some become candidates for epilepsy surgery. Their likelihood of achieving freedom from seizures, however, remains uncertain, and depends in a major part on the underlying pathology. Tissue samples obtained in epilepsy surgery form the basis of definite histopathological diagnosis; however, new molecular genetic methods have not yet been implemented in diagnostic processes for MCD cases. Furthermore, it has not been completely understood how the underlying pathology affects patients' outcomes after epilepsy surgery. We performed a systematic literature review of studies describing both histopathological and molecular genetic findings in MCD, along with studies on epilepsy surgery outcomes. We aimed to correlate the genetic causes with the underlying morphological abnormalities in focal cortical malformations and to stress the importance of the underlying biology for patient management and counseling. From the summarized findings of multiple authors, it is obvious that MCD may have a diverse genetic background despite a similar or even identical histopathological picture. Even though most of their molecular genetic findings converge on various levels of the PI3K/AKT/mTOR pathway, the exact mechanisms underlying MCD formation have not yet been completely described or indeed how this pathway generates a diverse range of histological abnormalities. Based on our findings, we therefore propose that all patients diagnosed and operated for drug-resistant epilepsy should have an integrated molecular and pathological diagnosis similar to the current practice in brain tumor diagnostic processes that might lead to more accurate diagnosis and effective stratification of patients undergoing epilepsy surgery.
2nd Faculty of Medicine Charles University Prague Czech Republic
Developmental Biology and Cancer Programme UCL GOS Institute of Child Health London UK
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