Computer modelling of epilepsy

Key Points Computer modelling of epilepsy is a branch of systems biology, a science that aims to combine the discoveries made by reductionist approaches into systems in order to understand how primary pathologies and secondary reactions interact to produce disease. Epilepsy, a dynamical disease of t...

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Veröffentlicht in:Nature reviews. Neuroscience 2008-08, Vol.9 (8), p.626-637
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description Key Points Computer modelling of epilepsy is a branch of systems biology, a science that aims to combine the discoveries made by reductionist approaches into systems in order to understand how primary pathologies and secondary reactions interact to produce disease. Epilepsy, a dynamical disease of the brain, is well suited to study from the perspective of dynamical systems. Epilepsy is a complex set of syndromes with the commonality of recurrent seizures. Not only do the many individual epilepsy syndromes have different causes, but most epilepsies develop owing to the interaction of many causes at molecular, cellular, network and developmental levels, defying efforts to define simple cause-and-effect relations and suggesting the need for computer modelling. Knowledge discovery and data mining provides the substrate and support for dynamical modelling and allows the findings to be applied back to the research and clinical settings. The various dynamical modelling techniques that are used include stochastic models, low-dimensional (lumped) deterministic models and detailed neuronal network models. Computer models are applied across the range of epilepsy phenomenology, from the molecular to the clinical. At the patient level, Markov models have been used to assess patterns of remission and relapse in pediatric epilepsy. At the molecular level, deterministic models can predict alterations in cellular activity with ion-channel mutations. Many seizure models simulate activity at the network level. Some of these are lumped models, which use mean-field approximations to reduce the activity of many neurons to simple oscillators that are then coupled to produce complex activity patterns. Other models incorporate the details of neural activity and synaptic interactions, in order to reach down to the molecular level at which drug effects take place. Uncommonly among areas of neuroscience research, computer modelling is immediately accessible through downloads of established models. An intrinsically collaborative activity, the future of the endeavour lies in the cooperative efforts of clinicians, experimentalists and modellers. As a dynamical disorder, epilepsy is an attractive target for computer modelling. Here, Lytton provides an overview of the different types of computer model that have been used to describe epilepsy and shows how they can provide new insights into the disorder. Epilepsy is a complex set of disorders that can involve many areas of the cortex, as w
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Epilepsy, a dynamical disease of the brain, is well suited to study from the perspective of dynamical systems. Epilepsy is a complex set of syndromes with the commonality of recurrent seizures. Not only do the many individual epilepsy syndromes have different causes, but most epilepsies develop owing to the interaction of many causes at molecular, cellular, network and developmental levels, defying efforts to define simple cause-and-effect relations and suggesting the need for computer modelling. Knowledge discovery and data mining provides the substrate and support for dynamical modelling and allows the findings to be applied back to the research and clinical settings. The various dynamical modelling techniques that are used include stochastic models, low-dimensional (lumped) deterministic models and detailed neuronal network models. Computer models are applied across the range of epilepsy phenomenology, from the molecular to the clinical. At the patient level, Markov models have been used to assess patterns of remission and relapse in pediatric epilepsy. At the molecular level, deterministic models can predict alterations in cellular activity with ion-channel mutations. Many seizure models simulate activity at the network level. Some of these are lumped models, which use mean-field approximations to reduce the activity of many neurons to simple oscillators that are then coupled to produce complex activity patterns. Other models incorporate the details of neural activity and synaptic interactions, in order to reach down to the molecular level at which drug effects take place. Uncommonly among areas of neuroscience research, computer modelling is immediately accessible through downloads of established models. An intrinsically collaborative activity, the future of the endeavour lies in the cooperative efforts of clinicians, experimentalists and modellers. As a dynamical disorder, epilepsy is an attractive target for computer modelling. Here, Lytton provides an overview of the different types of computer model that have been used to describe epilepsy and shows how they can provide new insights into the disorder. Epilepsy is a complex set of disorders that can involve many areas of the cortex, as well as underlying deep-brain systems. The myriad manifestations of seizures, which can be as varied as déjà vu and olfactory hallucination, can therefore give researchers insights into regional functions and relations. Epilepsy is also complex genetically and pathophysiologically: it involves microscopic (on the scale of ion channels and synaptic proteins), macroscopic (on the scale of brain trauma and rewiring) and intermediate changes in a complex interplay of causality. It has long been recognized that computer modelling will be required to disentangle causality, to better understand seizure spread and to understand and eventually predict treatment efficacy. Over the past few years, substantial progress has been made in modelling epilepsy at levels ranging from the molecular to the socioeconomic. We review these efforts and connect them to the medical goals of understanding and treating the disorder.</description><identifier>ISSN: 1471-003X</identifier><identifier>EISSN: 1471-0048</identifier><identifier>EISSN: 1469-3178</identifier><identifier>DOI: 10.1038/nrn2416</identifier><identifier>PMID: 18594562</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Animal Genetics and Genomics ; Animals ; Anticonvulsants. Antiepileptics. Antiparkinson agents ; Behavioral Sciences ; Biological and medical sciences ; Biological Techniques ; Biomedical and Life Sciences ; Biomedicine ; Brain - metabolism ; Brain - pathology ; Brain - physiopathology ; Care and treatment ; Cerebral Cortex - metabolism ; Cerebral Cortex - pathology ; Cerebral Cortex - physiopathology ; Computer Simulation ; Computer-generated environments ; Diagnosis ; Epilepsy ; Epilepsy - diagnosis ; Epilepsy - pathology ; Epilepsy - physiopathology ; Epilepsy, Temporal Lobe - pathology ; Epilepsy, Temporal Lobe - physiopathology ; Genetic aspects ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Humans ; Markov Chains ; Medical sciences ; Methods ; Models, Neurological ; Nervous system (semeiology, syndromes) ; Neurobiology ; Neurology ; Neuropharmacology ; Neurosciences ; Pharmacology. Drug treatments ; Predictive Value of Tests ; review-article ; Seizures - diagnosis ; Seizures - pathology ; Seizures - physiopathology</subject><ispartof>Nature reviews. 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Neuroscience</title><addtitle>Nat Rev Neurosci</addtitle><addtitle>Nat Rev Neurosci</addtitle><description>Key Points Computer modelling of epilepsy is a branch of systems biology, a science that aims to combine the discoveries made by reductionist approaches into systems in order to understand how primary pathologies and secondary reactions interact to produce disease. Epilepsy, a dynamical disease of the brain, is well suited to study from the perspective of dynamical systems. Epilepsy is a complex set of syndromes with the commonality of recurrent seizures. Not only do the many individual epilepsy syndromes have different causes, but most epilepsies develop owing to the interaction of many causes at molecular, cellular, network and developmental levels, defying efforts to define simple cause-and-effect relations and suggesting the need for computer modelling. Knowledge discovery and data mining provides the substrate and support for dynamical modelling and allows the findings to be applied back to the research and clinical settings. The various dynamical modelling techniques that are used include stochastic models, low-dimensional (lumped) deterministic models and detailed neuronal network models. Computer models are applied across the range of epilepsy phenomenology, from the molecular to the clinical. At the patient level, Markov models have been used to assess patterns of remission and relapse in pediatric epilepsy. At the molecular level, deterministic models can predict alterations in cellular activity with ion-channel mutations. Many seizure models simulate activity at the network level. Some of these are lumped models, which use mean-field approximations to reduce the activity of many neurons to simple oscillators that are then coupled to produce complex activity patterns. Other models incorporate the details of neural activity and synaptic interactions, in order to reach down to the molecular level at which drug effects take place. Uncommonly among areas of neuroscience research, computer modelling is immediately accessible through downloads of established models. An intrinsically collaborative activity, the future of the endeavour lies in the cooperative efforts of clinicians, experimentalists and modellers. As a dynamical disorder, epilepsy is an attractive target for computer modelling. Here, Lytton provides an overview of the different types of computer model that have been used to describe epilepsy and shows how they can provide new insights into the disorder. Epilepsy is a complex set of disorders that can involve many areas of the cortex, as well as underlying deep-brain systems. The myriad manifestations of seizures, which can be as varied as déjà vu and olfactory hallucination, can therefore give researchers insights into regional functions and relations. Epilepsy is also complex genetically and pathophysiologically: it involves microscopic (on the scale of ion channels and synaptic proteins), macroscopic (on the scale of brain trauma and rewiring) and intermediate changes in a complex interplay of causality. It has long been recognized that computer modelling will be required to disentangle causality, to better understand seizure spread and to understand and eventually predict treatment efficacy. Over the past few years, substantial progress has been made in modelling epilepsy at levels ranging from the molecular to the socioeconomic. We review these efforts and connect them to the medical goals of understanding and treating the disorder.</description><subject>Animal Genetics and Genomics</subject><subject>Animals</subject><subject>Anticonvulsants. Antiepileptics. Antiparkinson agents</subject><subject>Behavioral Sciences</subject><subject>Biological and medical sciences</subject><subject>Biological Techniques</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain - metabolism</subject><subject>Brain - pathology</subject><subject>Brain - physiopathology</subject><subject>Care and treatment</subject><subject>Cerebral Cortex - metabolism</subject><subject>Cerebral Cortex - pathology</subject><subject>Cerebral Cortex - physiopathology</subject><subject>Computer Simulation</subject><subject>Computer-generated environments</subject><subject>Diagnosis</subject><subject>Epilepsy</subject><subject>Epilepsy - diagnosis</subject><subject>Epilepsy - pathology</subject><subject>Epilepsy - physiopathology</subject><subject>Epilepsy, Temporal Lobe - pathology</subject><subject>Epilepsy, Temporal Lobe - physiopathology</subject><subject>Genetic aspects</subject><subject>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</subject><subject>Humans</subject><subject>Markov Chains</subject><subject>Medical sciences</subject><subject>Methods</subject><subject>Models, Neurological</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neurobiology</subject><subject>Neurology</subject><subject>Neuropharmacology</subject><subject>Neurosciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Predictive Value of Tests</subject><subject>review-article</subject><subject>Seizures - diagnosis</subject><subject>Seizures - pathology</subject><subject>Seizures - physiopathology</subject><issn>1471-003X</issn><issn>1471-0048</issn><issn>1469-3178</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkduKFDEQhoMo7kHxCVwGFw83s-bUOdwIy-AJFrxR8C5k0pUxS3fSJt3Cvr0Zup11VZBcJKS--qvqL4SeEHxBMFOvY46UE3EPHRMuyRpjru4f3uzrETop5RpjIogUD9ERUY3mjaDH6GyT-mEaIa_61ELXhbhbJb-CIXQwlJtH6IG3XYHHy32Kvrx7-3nzYX316f3HzeXV2jVSjmvlhG9aBltvlVUUGOYW25b6Vvmt57LRaktY_RZUCs21sFgo7JhqbW1PYXaK3sy6w7TtoXUQx2w7M-TQ23xjkg3mbiSGb2aXfhgqmdZSVIEXi0BO3ycoo-lDcXUgGyFNxQjNKK-u_BekWCncEFnBZ3-A12nKsbpgKOVaV7V92fMZ2tkOTIg-1e7cXtFcEs04l3Utlbr4B1VPC31wKYKvbt9NeDknuJxKyeAPThBs9gs3y8Irefa7cbfcsuEKPF8AW5ztfLbRhXLgKG5oI8Re6NXMlRqKO8i34_5d8-mMRjtOGQ5av-I_Acd5x68</recordid><startdate>20080801</startdate><enddate>20080801</enddate><creator>Lytton, William W</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20080801</creationdate><title>Computer modelling of epilepsy</title><author>Lytton, William W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c577t-8c6f5d3ebfa8a82e304a0ad2fd8fbf47598b13e3062769496a0680c38da003803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animal Genetics and Genomics</topic><topic>Animals</topic><topic>Anticonvulsants. Antiepileptics. Antiparkinson agents</topic><topic>Behavioral Sciences</topic><topic>Biological and medical sciences</topic><topic>Biological Techniques</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain - metabolism</topic><topic>Brain - pathology</topic><topic>Brain - physiopathology</topic><topic>Care and treatment</topic><topic>Cerebral Cortex - metabolism</topic><topic>Cerebral Cortex - pathology</topic><topic>Cerebral Cortex - physiopathology</topic><topic>Computer Simulation</topic><topic>Computer-generated environments</topic><topic>Diagnosis</topic><topic>Epilepsy</topic><topic>Epilepsy - diagnosis</topic><topic>Epilepsy - pathology</topic><topic>Epilepsy - physiopathology</topic><topic>Epilepsy, Temporal Lobe - pathology</topic><topic>Epilepsy, Temporal Lobe - physiopathology</topic><topic>Genetic aspects</topic><topic>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</topic><topic>Humans</topic><topic>Markov Chains</topic><topic>Medical sciences</topic><topic>Methods</topic><topic>Models, Neurological</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neurobiology</topic><topic>Neurology</topic><topic>Neuropharmacology</topic><topic>Neurosciences</topic><topic>Pharmacology. 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Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lytton, William W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Computer modelling of epilepsy</atitle><jtitle>Nature reviews. Neuroscience</jtitle><stitle>Nat Rev Neurosci</stitle><addtitle>Nat Rev Neurosci</addtitle><date>2008-08-01</date><risdate>2008</risdate><volume>9</volume><issue>8</issue><spage>626</spage><epage>637</epage><pages>626-637</pages><issn>1471-003X</issn><eissn>1471-0048</eissn><eissn>1469-3178</eissn><abstract>Key Points Computer modelling of epilepsy is a branch of systems biology, a science that aims to combine the discoveries made by reductionist approaches into systems in order to understand how primary pathologies and secondary reactions interact to produce disease. Epilepsy, a dynamical disease of the brain, is well suited to study from the perspective of dynamical systems. Epilepsy is a complex set of syndromes with the commonality of recurrent seizures. Not only do the many individual epilepsy syndromes have different causes, but most epilepsies develop owing to the interaction of many causes at molecular, cellular, network and developmental levels, defying efforts to define simple cause-and-effect relations and suggesting the need for computer modelling. Knowledge discovery and data mining provides the substrate and support for dynamical modelling and allows the findings to be applied back to the research and clinical settings. The various dynamical modelling techniques that are used include stochastic models, low-dimensional (lumped) deterministic models and detailed neuronal network models. Computer models are applied across the range of epilepsy phenomenology, from the molecular to the clinical. At the patient level, Markov models have been used to assess patterns of remission and relapse in pediatric epilepsy. At the molecular level, deterministic models can predict alterations in cellular activity with ion-channel mutations. Many seizure models simulate activity at the network level. Some of these are lumped models, which use mean-field approximations to reduce the activity of many neurons to simple oscillators that are then coupled to produce complex activity patterns. Other models incorporate the details of neural activity and synaptic interactions, in order to reach down to the molecular level at which drug effects take place. Uncommonly among areas of neuroscience research, computer modelling is immediately accessible through downloads of established models. An intrinsically collaborative activity, the future of the endeavour lies in the cooperative efforts of clinicians, experimentalists and modellers. As a dynamical disorder, epilepsy is an attractive target for computer modelling. Here, Lytton provides an overview of the different types of computer model that have been used to describe epilepsy and shows how they can provide new insights into the disorder. Epilepsy is a complex set of disorders that can involve many areas of the cortex, as well as underlying deep-brain systems. The myriad manifestations of seizures, which can be as varied as déjà vu and olfactory hallucination, can therefore give researchers insights into regional functions and relations. Epilepsy is also complex genetically and pathophysiologically: it involves microscopic (on the scale of ion channels and synaptic proteins), macroscopic (on the scale of brain trauma and rewiring) and intermediate changes in a complex interplay of causality. It has long been recognized that computer modelling will be required to disentangle causality, to better understand seizure spread and to understand and eventually predict treatment efficacy. Over the past few years, substantial progress has been made in modelling epilepsy at levels ranging from the molecular to the socioeconomic. We review these efforts and connect them to the medical goals of understanding and treating the disorder.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>18594562</pmid><doi>10.1038/nrn2416</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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language eng
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source MEDLINE; Nature; SpringerNature Journals
subjects Animal Genetics and Genomics
Animals
Anticonvulsants. Antiepileptics. Antiparkinson agents
Behavioral Sciences
Biological and medical sciences
Biological Techniques
Biomedical and Life Sciences
Biomedicine
Brain - metabolism
Brain - pathology
Brain - physiopathology
Care and treatment
Cerebral Cortex - metabolism
Cerebral Cortex - pathology
Cerebral Cortex - physiopathology
Computer Simulation
Computer-generated environments
Diagnosis
Epilepsy
Epilepsy - diagnosis
Epilepsy - pathology
Epilepsy - physiopathology
Epilepsy, Temporal Lobe - pathology
Epilepsy, Temporal Lobe - physiopathology
Genetic aspects
Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy
Humans
Markov Chains
Medical sciences
Methods
Models, Neurological
Nervous system (semeiology, syndromes)
Neurobiology
Neurology
Neuropharmacology
Neurosciences
Pharmacology. Drug treatments
Predictive Value of Tests
review-article
Seizures - diagnosis
Seizures - pathology
Seizures - physiopathology
title Computer modelling of epilepsy
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