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Genetic Landscape of Common Epilepsies: Advancing towards Precision in Treatment

Epilepsy, a neurological disease characterized by recurrent seizures, is highly heterogeneous in nature. Based on the prevalence, epilepsy is classified into two types: common and rare epilepsies. Common epilepsies affecting nearly 95% people with epilepsy, comprise generalized epilepsy which encomp...

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Autores principales: Thakran, Sarita, Guin, Debleena, Singh, Pooja, Singh, Priyanka, Kukal, Samiksha, Rawat, Chitra, Yadav, Saroj, Kushwaha, Suman S., Srivastava, Achal K., Hasija, Yasha, Saso, Luciano, Ramachandran, Srinivasan, Kukreti, Ritushree
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589654/
https://www.ncbi.nlm.nih.gov/pubmed/33096746
http://dx.doi.org/10.3390/ijms21207784
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author Thakran, Sarita
Guin, Debleena
Singh, Pooja
Singh, Priyanka
Kukal, Samiksha
Rawat, Chitra
Yadav, Saroj
Kushwaha, Suman S.
Srivastava, Achal K.
Hasija, Yasha
Saso, Luciano
Ramachandran, Srinivasan
Kukreti, Ritushree
author_facet Thakran, Sarita
Guin, Debleena
Singh, Pooja
Singh, Priyanka
Kukal, Samiksha
Rawat, Chitra
Yadav, Saroj
Kushwaha, Suman S.
Srivastava, Achal K.
Hasija, Yasha
Saso, Luciano
Ramachandran, Srinivasan
Kukreti, Ritushree
author_sort Thakran, Sarita
collection PubMed
description Epilepsy, a neurological disease characterized by recurrent seizures, is highly heterogeneous in nature. Based on the prevalence, epilepsy is classified into two types: common and rare epilepsies. Common epilepsies affecting nearly 95% people with epilepsy, comprise generalized epilepsy which encompass idiopathic generalized epilepsy like childhood absence epilepsy, juvenile myoclonic epilepsy, juvenile absence epilepsy and epilepsy with generalized tonic-clonic seizure on awakening and focal epilepsy like temporal lobe epilepsy and cryptogenic focal epilepsy. In 70% of the epilepsy cases, genetic factors are responsible either as single genetic variant in rare epilepsies or multiple genetic variants acting along with different environmental factors as in common epilepsies. Genetic testing and precision treatment have been developed for a few rare epilepsies and is lacking for common epilepsies due to their complex nature of inheritance. Precision medicine for common epilepsies require a panoramic approach that incorporates polygenic background and other non-genetic factors like microbiome, diet, age at disease onset, optimal time for treatment and other lifestyle factors which influence seizure threshold. This review aims to comprehensively present a state-of-art review of all the genes and their genetic variants that are associated with all common epilepsy subtypes. It also encompasses the basis of these genes in the epileptogenesis. Here, we discussed the current status of the common epilepsy genetics and address the clinical application so far on evidence-based markers in prognosis, diagnosis, and treatment management. In addition, we assessed the diagnostic predictability of a few genetic markers used for disease risk prediction in individuals. A combination of deeper endo-phenotyping including pharmaco-response data, electro-clinical imaging, and other clinical measurements along with genetics may be used to diagnose common epilepsies and this marks a step ahead in precision medicine in common epilepsies management.
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spelling pubmed-75896542020-10-29 Genetic Landscape of Common Epilepsies: Advancing towards Precision in Treatment Thakran, Sarita Guin, Debleena Singh, Pooja Singh, Priyanka Kukal, Samiksha Rawat, Chitra Yadav, Saroj Kushwaha, Suman S. Srivastava, Achal K. Hasija, Yasha Saso, Luciano Ramachandran, Srinivasan Kukreti, Ritushree Int J Mol Sci Review Epilepsy, a neurological disease characterized by recurrent seizures, is highly heterogeneous in nature. Based on the prevalence, epilepsy is classified into two types: common and rare epilepsies. Common epilepsies affecting nearly 95% people with epilepsy, comprise generalized epilepsy which encompass idiopathic generalized epilepsy like childhood absence epilepsy, juvenile myoclonic epilepsy, juvenile absence epilepsy and epilepsy with generalized tonic-clonic seizure on awakening and focal epilepsy like temporal lobe epilepsy and cryptogenic focal epilepsy. In 70% of the epilepsy cases, genetic factors are responsible either as single genetic variant in rare epilepsies or multiple genetic variants acting along with different environmental factors as in common epilepsies. Genetic testing and precision treatment have been developed for a few rare epilepsies and is lacking for common epilepsies due to their complex nature of inheritance. Precision medicine for common epilepsies require a panoramic approach that incorporates polygenic background and other non-genetic factors like microbiome, diet, age at disease onset, optimal time for treatment and other lifestyle factors which influence seizure threshold. This review aims to comprehensively present a state-of-art review of all the genes and their genetic variants that are associated with all common epilepsy subtypes. It also encompasses the basis of these genes in the epileptogenesis. Here, we discussed the current status of the common epilepsy genetics and address the clinical application so far on evidence-based markers in prognosis, diagnosis, and treatment management. In addition, we assessed the diagnostic predictability of a few genetic markers used for disease risk prediction in individuals. A combination of deeper endo-phenotyping including pharmaco-response data, electro-clinical imaging, and other clinical measurements along with genetics may be used to diagnose common epilepsies and this marks a step ahead in precision medicine in common epilepsies management. MDPI 2020-10-21 /pmc/articles/PMC7589654/ /pubmed/33096746 http://dx.doi.org/10.3390/ijms21207784 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Thakran, Sarita
Guin, Debleena
Singh, Pooja
Singh, Priyanka
Kukal, Samiksha
Rawat, Chitra
Yadav, Saroj
Kushwaha, Suman S.
Srivastava, Achal K.
Hasija, Yasha
Saso, Luciano
Ramachandran, Srinivasan
Kukreti, Ritushree
Genetic Landscape of Common Epilepsies: Advancing towards Precision in Treatment
title Genetic Landscape of Common Epilepsies: Advancing towards Precision in Treatment
title_full Genetic Landscape of Common Epilepsies: Advancing towards Precision in Treatment
title_fullStr Genetic Landscape of Common Epilepsies: Advancing towards Precision in Treatment
title_full_unstemmed Genetic Landscape of Common Epilepsies: Advancing towards Precision in Treatment
title_short Genetic Landscape of Common Epilepsies: Advancing towards Precision in Treatment
title_sort genetic landscape of common epilepsies: advancing towards precision in treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589654/
https://www.ncbi.nlm.nih.gov/pubmed/33096746
http://dx.doi.org/10.3390/ijms21207784
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