Classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology
8 March 2017
Ingrid E. Scheffer
E-mail address: email@example.com
Department of Medicine, The University of Melbourne, Austin Health, Melbourne, Victoria, Australia
The International League Against Epilepsy (ILAE) Classification of the Epilepsies has been updated to reflect our gain in understanding of the epilepsies and their underlying mechanisms following the major scientific advances that have taken place since the last ratified classification in 1989.
As a critical tool for the practicing clinician, epilepsy classification must be relevant and dynamic to changes in thinking, yet robust and translatable to all areas of the globe.
Its primary purpose is for diagnosis of patients, but it is also critical for epilepsy research, development of antiepileptic therapies, and communication around the world.
The new classification originates from a draft document submitted for public comments in 2013, which was revised to incorporate extensive feedback from the international epilepsy community over several rounds of consultation.
It presents three levels, starting with seizure type, where it assumes that the patient is having epileptic seizures as defined by the new 2017 ILAE Seizure Classification. After diagnosis of the seizure type, the next step is diagnosis of epilepsy type, including focal epilepsy, generalized epilepsy, combined generalized, and focal epilepsy, and also an unknown epilepsy group.
The third level is that of epilepsy syndrome, where a specific syndromic diagnosis can be made.
The new classification incorporates etiology along each stage, emphasizing the need to consider etiology at each step of diagnosis, as it often carries significant treatment implications.
Etiology is broken into six subgroups, selected because of their potential therapeutic consequences.
New terminology is introduced such as developmental and epileptic encephalopathy.
The term benign is replaced by the terms self-limited and pharmacoresponsive, to be used where appropriate.
It is hoped that this new framework will assist in improving epilepsy care and research in the 21st century.
•The ILAE presents a revised framework for the Classification of the Epilepsies, designed to work with the classification of seizure types
•Levels of diagnosis: seizure type, epilepsy type (focal, generalized, combined generalized and focal, unknown) and epilepsy syndrome
•An etiologic diagnosis should be considered from when the patient first presents, and at each step along the diagnostic pathway; a patient’s epilepsy may be classified into more than one etiological category
•The term “benign” is replaced by the terms self-limited and pharmacoresponsive to be used where appropriate
•The term “developmental and epileptic encephalopathy” can be applied in whole or in part where appropriate
Ongoing efforts to refine the classification of the epilepsies have been made by the International League Against Epilepsy (ILAE) almost since its inception in 1909 and gained special momentum in the early 1960s when new concepts of classification were proposed by Henri Gastaut.
Intense debate and acquisition of new knowledge in the next two decades led to the landmark 1985 ILAE “Classification of Epilepsies and Epileptic Syndromes,” which was soon followed by a revised version ratified by the ILAE General Assembly in 1989.
The 1989 Classification has been highly influential worldwide and has had a major impact on epilepsy care and research.
The work presented herein builds on the efforts of many over more than a century; we acknowledge their seminal contributions in the development of the classification of the epilepsies.
Although many concepts outlined in the 1989 ILAE classification remain valid to this day, it has become increasingly clear that a revision is needed to account for subsequent scientific discoveries that over the last few decades have fundamentally changed our understanding of the epilepsies as well as our approach to the diagnosis and management of individuals with epilepsy.
Epilepsy classification is the key clinical tool in evaluating an individual who is presenting with seizures.
It influences every clinical consultation yet its impact stretches far beyond the clinical domain to clinical and basic epilepsy research and to the development of novel therapies.
Classification serves many purposes: providing a framework for understanding the type of seizures that the patient has, the other seizure types that are more likely to occur in that individual, the potential triggers for their seizures, and often their prognosis.
Classification also informs the risks of comorbidities including learning difficulties, intellectual disability, psychiatric features such as autism spectrum disorder, and mortality risk such as sudden unexpected death in epilepsy (SUDEP).
It is notable that classification often guides the selection of antiepileptic therapies.
Classification of the epilepsies has evolved dramatically since its inception in the 1960s.
The many iterations in classification reflect advances in understanding phenotypic patterns and underlying mechanisms, based on major contributions from clinical and basic research from around the world.
These insights are incorporated into the many facets of clinical care for patients and lead to progress in the development of innovative treatments, be they pharmacologic or dietary therapies, surgical approaches or device development.
Classification will always be a dynamic process, iterative to the new insights gained through research and improved understanding of this heterogeneous group of diseases. Its continued evolution into the future promises to lead to further advances in patient care.
Classification engenders passionate debate.
This is partly because it is built on the complex clinical constructs underpinning epilepsy diagnosis and partly because it is so critical to our daily practice.
Classification has been based on expert opinion drawing together epileptologists and related experts from around the world. Although there is no doubt that the desired endpoint is a scientifically based classification, our understanding is not sufficiently advanced to construct a classification on a scientifically rigorous basis.
Thus current proposals are based on a combination of the latest scientific understanding coupled with high-level expert opinion, including an extensive consultation with epilepsy professionals and the wider epilepsy community worldwide.
When a patient presents with seizures, the clinician works through several critical steps in making a diagnosis.
Before attempting to classify a seizure, the physician must determine whether the paroxysmal event is indeed an epileptic seizure with a myriad of differential diagnoses being possible.
These include convulsive syncope, parasomnias, movement disorders, and other nonepileptic events (https://www.epilepsydiagnosis.org/epilepsy-imitators.html).
This diagnostic step is taken as already established at the point of beginning to classify the patient’s epilepsy.
In terms of epilepsy classification, the clinician starts by classifying the type of seizure. This is the subject of the companion paper on the new classification of seizure types.
Then, the patient’s type of epilepsy needs to be classified and, in many cases, a specific epilepsy syndrome diagnosis can be made.
Just as importantly, strenuous attempts to identify the etiology of the patient’s epilepsy should be made at each step in the diagnostic pathway.
Classification of seizure type and epilepsy type both take into account the results of investigations such as electroencephalography (EEG) and neuroimaging studies together with other studies exploring the underlying etiology of the epilepsy. Herein, we present the first major Classification of the Epilepsies since the last ratified ILAE Classification in 1989.
In the past, ILAE position papers on fundamental matters such terminology, definition, and classification of seizures and epilepsy required ratification by the General Assembly through a vote by the representatives of the ILAE Chapters from around the world. This approach is no longer optimal, since it does not permit adequate engagement of the greatly expanded constituency of epilepsy experts around the world and fails to exploit opportunities offered by impressive advances in communication tools.
Consequently, in 2013, the League set in place a new process for the finalization and approval of position documents, that is, documents that reflect the ILAE position on topics that involve adoption of a common language or set of definitions (e.g., defining epilepsy, classification).
This process is highly iterative and involves initial production of the document by a group of experts selected by the League, posting the document on the ILAE website, soliciting comments and criticism by all stakeholders, and appointing a separate expert panel to review and incorporate the public comments.
This process takes place in parallel with the peer review conducted by the journal to which the document is submitted for publication (http://www.ilae.org/Visitors/Documents/Guideline-PublPolicy-2013Aug.pdf).
In the case of the revised Classification, a first proposal that preceded implementation of the procedure outlined above was published by the ILAE Commission on Classification and Terminology in 2010.
The emphasis was on employing transparent terminology, where words mean what they say.
The 2010 publication triggered extensive discussion and commentaries.
A new Commission on Classification and Terminology was subsequently appointed by the ILAE Executive and tasked to produce a revised Classification through the procedure outlined for ILAE position documents.
The Commission submitted the initial document in 2013, and the document was posted online inviting discussion (Supporting Information for Scheffer et al.). Avid community engagement and debate occurred, with 128 comments received from 43 countries.
The response was so extensive and the feedback on important concepts so conflicting that the panel in charge of reviewing the public comments determined that further pubic engagement was necessary to ensure the highest possible level of agreement.
The roadmap followed by the panel to solicit further engagement and to respond to feedback from stakeholders is described in an article published in Epilepsia Open in 2016, which again invited feedback from the global community.
Further comments and opinions were then deliberated and considered in finalizing the present position document which defines the Classification of the Epilepsies in 2017.
Classification of the Epilepsies
The new Classification of the Epilepsies is a multilevel classification, designed to cater to classifying epilepsy in different clinical environments (Fig. 1).
The starting point of the Epilepsy classification framework is the Seizure Type;
it assumes that the clinician has already made a definite diagnosis of an epileptic seizure and is not meant to be a diagnostic algorithm to distinguish epileptic from nonepileptic events.
Seizures are classified into
generalized onset, and
In some settings, classification according to Seizure Type may be the maximum level possible for diagnosis as there may be no access to EEG, video. and imaging studies.
In other cases, there may simply be too little information available to be able to make a higher level diagnosis, such as when a patient has only had a single seizure.
The second level is that of Epilepsy Type and assumes that the patient has a diagnosis of epilepsy based on the 2014 definition.
The Epilepsy Type level includes a new category of “Combined Generalized and Focal Epilepsy”
in addition to the well-established Generalized Epilepsy and Focal Epilepsies.
It also includes an Unknown category.
Many epilepsies will include multiple types of seizures.
For a diagnosis of Generalized Epilepsy, the patient would typically show generalized spike-wave activity on EEG. Individuals with generalized epilepsies may have a range of seizure types including absence, myoclonic, atonic, tonic, and tonic–clonic seizures.
The diagnosis of generalized epilepsy is made on clinical grounds, supported by the finding of typical interictal EEG discharges.
Caution needs to be exercised for a patient with generalized tonic–clonic seizures and a normal EEG. In this case, supportive evidence would need to be present to make a diagnosis of generalized epilepsy, such as myoclonic jerks or a relevant family history.
Focal Epilepsies include unifocal and multifocal disorders as well as seizures involving one hemisphere. A range of seizure types can be seen including focal aware seizures, focal impaired awareness seizures, focal motor seizures, focal non-motor seizures, and focal to bilateral tonic–clonic seizures.
The interictal EEG typically shows focal epileptiform discharges, but the diagnosis is made on clinical grounds, supported by EEG findings.
The new group of Combined Generalized and Focal Epilepsies exists, as there are patients who have both generalized and focal seizures.
The diagnosis is made on clinical grounds, supported by EEG findings.
Ictal recordings are helpful but not essential.
The interictal EEG may show both generalized spike-wave and focal epileptiform discharges, but epileptiform activity is not required for the diagnosis.
Common examples in which both types of seizures occur are Dravet syndrome and Lennox-Gastaut syndrome.
The Epilepsy type may also be the final level of diagnosis achievable where the clinician is unable to make an Epilepsy Syndrome diagnosis.
Examples include the following: the common situation of a child or adult with nonlesional temporal lobe epilepsy who has Focal Epilepsy with no known etiology; a 5-year-old child presenting with generalized tonic–clonic seizures and generalized spike-wave activity on EEG who cannot be classified into a known epilepsy syndrome but has a clear-cut diagnosis of Generalized Epilepsy;
or the less common scenario of a 20-year-old woman with both focal impaired awareness seizures and absence seizures with both focal discharges and generalized spike wave on EEG recordings and normal MRI, who would therefore have a diagnosis of Combined Generalized and Focal Epilepsy.
The term “Unknown” is used to denote where it is understood that the patient has Epilepsy but the clinician is unable to determine if the Epilepsy Type is focal or generalized because there is insufficient information available. This may be for a variety of reasons.
There may be no access to EEG, or the EEG studies may have been uninformative, for example, normal. If the Seizure Type(s) are unknown, then the Epilepsy Type may be unknown for similar reasons, although the two may not always be concordant.
For example, the patient may have had several symmetrical tonic–clonic seizures without focal features and normal EEG recordings.
Thus the onset of the seizures is unknown and the person has an unknown epilepsy type.
The third level is an Epilepsy Syndrome diagnosis.
An epilepsy syndrome refers to a cluster of features incorporating seizure types, EEG, and imaging features that tend to occur together. It often has age-dependent features such as age at onset and remission (where applicable), seizure triggers, diurnal variation, and sometimes prognosis.
It may also have distinctive comorbidities such as intellectual and psychiatric dysfunction, together with specific findings on EEG and imaging studies.
It may have associated etiologic, prognostic, and treatment implications.
It is important to note that an epilepsy syndrome does not have a one-to-one correlation with an etiologic diagnosis and serves a different purpose such as guiding management.
There are many well-recognized syndromes, such as childhood absence epilepsy, West syndrome, and Dravet syndrome, although it should be noted that there has never been a formal classification of syndromes by the ILAE.
The recently developed educational ILAE website,epilepsydiagnosis.org,
provides an excellent resource to understand the parameters for diagnosis, review videos of seizure types and the EEG features of many established syndromes, and has been devised as a teaching tool.
Idiopathic Generalized Epilepsies
Within the Generalized Epilepsies is the well-recognized and common subgroup of the Idiopathic Generalized Epilepsies (IGEs).
The IGEs encompass four well-established epilepsy syndromes:
Childhood Absence Epilepsy, Juvenile Absence Epilepsy,
Juvenile Myoclonic Epilepsy and Generalized Tonic–Clonic Seizures Alone (formerly known as Generalized Tonic–Clonic Seizures on Awakening but modified in recognition that seizures can occur at any time of day).
The intention to remove the term “idiopathic” from the nomenclature of Epilepsy Classification was suggested, as its definition was “no known or suspected etiology other than possible hereditary predisposition.”
The Greek term “idios” refers to self, own, and personal, and is thus meant to reflect the genetic etiology without explicitly saying so.
Idiopathic may therefore be regarded as an imprecise term given our increasing recognition and discovery of the genes involved in many epilepsies, including those with monogenic (with inherited or de novo pathogenic variants) or complex (polygenic with or without environmental factors) inheritance. In addition, the word “genetic” may sometimes be wrongly interpreted as synonymous with “inherited.”
It is therefore more meaningful to refer to this group of syndromes as Genetic Generalized Epilepsies (GGEs), where the clinician feels there is sufficient evidence for this classification.
Such evidence is drawn from meticulous clinical research of the inheritance of these syndromes in twin and family studies and does not mean that specific genetic mutations have been identified. Indeed, it is currently rarely the case that the genetic mutation(s) causing a patient’s epilepsy has been determined, perhaps with the exception of the infantile onset developmental and epileptic encephalopathies, where many patients have been shown to have a de novo pathogenic variant.
There has been, however, considerable desire to retain the term IGE.
The Task Force has therefore decided that the term IGE will be acceptable specifically for the group of four epilepsy syndromes: Childhood Absence Epilepsy, Juvenile Absence Epilepsy, Juvenile Myoclonic Epilepsy, and Generalized Tonic–Clonic Seizures Alone. In individual cases, the term Genetic Generalized Epilepsy may be used where the clinician is comfortable with invoking a genetic etiology.
Self-limited focal epilepsies
There are several self-limited focal epilepsies, typically beginning in childhood.
The most common is self-limited epilepsy with centrotemporal spikes, formerly called “benign epilepsy with centrotemporal spikes.”
Others included in this broad group are the self-limited occipital epilepsies of childhood, with the early-onset form described by Panayiotopoulos and the late-onset form by Gastaut.
Other self-limited frontal lobe, temporal, and parietal lobe epilepsies have been described with some beginning in adolescence and even adult life.
From the moment that the patient presents with a first epileptic seizure, the clinician should be aiming to determine the etiology of the patient’s epilepsy.
A range of etiologic groups has been recognized, with emphasis on those that have implications for treatment.
Often the first investigation carried out involves neuroimaging, ideally MRI where available.
This enables the clinician to decide if there is a structural etiology for the patient’s epilepsy.
The five additional etiologic groups are
as well as an unknown group (Fig. 1).
A patient’s epilepsy may be classified into more than one etiologic category; the etiologies are not hierarchical, and the importance given to the patient’s etiological group may depend on the circumstance.
For instance, a patient with tuberous sclerosis has both a structural and a genetic etiology; the structural etiology is critical for epilepsy surgery, whereas the genetic etiology is key for genetic counseling and consideration of novel therapies such as mammalian target of rapamycin (mTOR) inhibitors.
The concept behind a structural etiology is that a structural abnormality has a substantially increased risk of being associated with epilepsy based on appropriately designed studies.
A structural etiology refers to abnormalities visible on structural neuroimaging where the electroclinical assessment together with the imaging findings lead to a reasonable inference that the imaging abnormality is the likely cause of the patient’s seizures. Structural etiologies may be acquired such as stroke, trauma, and infection, or genetic such as many malformations of cortical development.
Despite there being a genetic basis with such malformations, the structural correlate underpins the person’s epilepsy. Identification of a subtle structural lesion requires appropriate MRI studies using specific epilepsy protocols.
There are well-recognized associations within the epilepsies with a structural etiology. These include the relatively frequent finding of mesial temporal lobe seizures with hippocampal sclerosis.
Other key associations include gelastic seizures with hypothalamic hamartoma, Rasmussen syndrome, and hemiconvulsion-hemiplegia-epilepsy.
Recognition of these associations is important to ensure that the patient’s imaging is carefully examined for a specific structural abnormality.
This in turn highlights the need for consideration for epilepsy surgery should the patient fail medical therapy.
The underlying basis for a structural abnormality may be genetic or acquired, or both. For example, polymicrogyria may be secondary to mutations in genes such as GPR56, or acquired, secondary to intrauterine cytomegalovirus infection.
Acquired structural causes include hypoxic-ischemic encephalopathy, trauma, infection, and stroke.
Where a structural etiology has a well-defined genetic basis such as tuberous sclerosis complex, which is caused by mutations in the genes TSC1 and TSC2 encoding hamartin and tuberin, respectively, both etiologic terms, structural and genetic can be used.
The concept of a genetic epilepsy is that it results directly from a known or presumed genetic mutation in which seizures are a core symptom of the disorder.
The epilepsies in which a genetic etiology has been implicated are quite diverse and, in most cases, the underlying genes are not yet known.
First, the inference of a genetic etiology may be based solely on a family history of an autosomal dominant disorder.
For example, in the syndrome of Benign Familial Neonatal Epilepsy, most families have mutations of one of the potassium channel genes, KCNQ2 or KCNQ3.
Conversely, in the syndrome of Autosomal Dominant Nocturnal Frontal Lobe epilepsy, the underlying mutation is known in only a small proportion of individuals at this time.
Second, a genetic etiology may be suggested by clinical research in populations with the same syndrome such as Childhood Absence Epilepsy or Juvenile Myoclonic Epilepsy. Evidence for a genetic basis comes from elegant studies such as Lennox’s twin studies in the 1950s and familial aggregation studies.
Third, a molecular basis may have been identified and may implicate a single gene or copy number variant of major effect.
There is an increasing number of patients with known genetic abnormalities causing both severe and mild epilepsies.
Molecular genetics has led to identification of the causative mutation in a large number of epilepsy genes, most frequently arising de novo, in 30–50% of infants with severe developmental and epileptic encephalopathies.
The best known example is Dravet syndrome in which >80% of patients have a pathogenic variant of SCN1A.
It is notable that a monogenic etiology may cause a spectrum of mild to severe epilepsies, such as SCN1A mutations, which are associated with Dravet syndrome and Genetic Epilepsy with Febrile Seizures Plus (GEFS+), and may have implications for treatment.
Understanding the phenotypic spectrum associated with mutations of a specific gene is critical information, as the finding of a mutation in a specific gene may not, on its own, enable prediction of the outcome.
Interpretation of its significance needs to be considered in the context of the electroclinical presentation.
Thus, to date, the majority of genes show phenotypic heterogeneity and the majority of syndromes reveal genetic heterogeneity.
Where epilepsy follows complex inheritance, which implies multiple genes with/without an environmental contribution, susceptibility variants may be identified that contribute to causation but are insufficient alone to cause epilepsy.
In this setting, there may be no family history of seizures because other family members do not have enough epilepsy genetic variants to be affected.
It is important to note that genetic does not equate with inherited.
An increasing number of de novo mutations are being identified in both severe and mild epilepsies.
This means that the patient has a new mutation that has arisen in him or her, and therefore is unlikely to have a family history of seizures and has not inherited the genetic mutation.
Nevertheless, this patient may now have a heritable form of epilepsy. For example if the individual has a de novo dominant mutation, their offspring will have a 50% risk of inheriting the mutation.
This does not necessarily mean that their children will have epilepsy, as its expression will depend on the penetrance of the mutation.
Drilling down further, patients may be mosaic for a mutation.
This means they have two populations of cells, with one population having the mutation and the other having the wild-type (normal) allele.
Mosaicism may affect the severity of their epilepsy, with lower mosaicism rates resulting in a milder severity of epilepsy, as shown in SCN1A studies.
A genetic etiology does not exclude an environmental contribution. It is well accepted that environmental factors contribute to seizure disorders; for example, many individuals with epilepsy are more likely to have seizures with sleep deprivation, stress, and illness.
A genetic etiology refers to a pathogenic variant (mutation) of significant effect in causing the individual’s epilepsy.
The most common etiology worldwide is where epilepsy occurs as a result of an infection.
The concept of an infectious etiology is that it directly results from a known infection in which seizures are a core symptom of the disorder.
An infectious etiology refers to a patient with epilepsy, rather than with seizures occurring in the setting of acute infection such as meningitis or encephalitis.
Common examples in specific regions of the world include neurocysticercosis, tuberculosis, HIV, cerebral malaria, subacute sclerosing panencephalitis, cerebral toxoplasmosis, and congenital infections such as Zika virus and cytomegalovirus.
These infections sometimes have a structural correlate.
An infectious etiology carries specific treatment implications.
An infectious etiology may also refer to the postinfectious development of epilepsy, such as viral encephalitis leading to seizures in the aftermath of the acute infection.
A range of metabolic disorders is associated with epilepsy.
This area is expanding and a greater understanding of the phenotypic spectrum emerging.
The concept of a metabolic epilepsy is that it results directly from a known or presumed metabolic disorder in which seizures are a core symptom of the disorder. Metabolic causes refer to a well-delineated metabolic defect with manifestations or biochemical changes throughout the body such as porphyria, uremia, aminoacidopathies, or pyridoxine-dependent seizures.
In many cases, metabolic disorders will have a genetic defect.
It is likely that most metabolic epilepsies will have a genetic basis, but some may be acquired such as cerebral folate deficiency.
The identification of specific metabolic causes of epilepsy is extremely important due to implications for specific therapies and potential prevention of intellectual impairment.
The concept of an immune epilepsy is that it results directly from an immune disorder in which seizures are a core symptom of the disorder.
A range of immune epilepsies has been recently recognized with characteristic presentations in both adults and children.
An immune etiology can be conceptualized as where there is evidence of autoimmune-mediated central nervous system inflammation.
Diagnosis of these autoimmune encephalitides is rapidly increasing, particularly with greater access to antibody testing.
Examples include anti-NMDA (N-methyl-d-aspartate) receptor encephalitis and anti-LGI1 encephalitis.l
With the emergence of these entities, this etiologic subgroup deserves a specific category, particularly given the treatment implications with targeted immunotherapies.
Unknown means that the cause of the epilepsy is not yet known. There remain many patients with epilepsy for whom the cause is not known.
In this category it is not possible to make a specific diagnosis apart from the basic electroclinical semiology such as frontal lobe epilepsy.
The extent to which a cause can be found depends on the extent of the evaluation available to the patient.
This differs across different health care settings and countries and hopefully will improve over time in resource-poor countries.
There is increasing awareness that many of the epilepsies are associated with comorbidities such as learning, psychological, and behavioral problems (Fig. 1, left hand vertical oval).
These range in type and severity, from subtle learning difficulties to intellectual disability, to psychiatric features such as autism spectrum disorders and depression, to psychosocial concerns.
In the more severe epilepsies, a complex range of comorbidities may be seen, including motor deficits such as cerebral palsy or deterioration in gait, movement disorders, scoliosis, sleep, and gastrointestinal disorders.
Like etiology, it is important that the presence of comorbidities be considered for every patient with epilepsy at each stage of classification, enabling early identification, diagnosis, and appropriate management.
New Terminology and Definitions
Developmental and epileptic encephalopathies
The term “epileptic encephalopathy” was redefined in the Berg et al. report as where the epileptic activity itself contributes to severe cognitive and behavioral impairments above and beyond what might be expected from the underlying pathology alone (e.g., cortical malformation).
Global or selective impairments can worsen over time.
These impairments can be seen along a spectrum of severity and across all epilepsies, and can occur at any age.
The concept of the epileptic encephalopathy may be applicable to epilepsies at all ages and should be utilized more widely than just for the severe epilepsies with onset in infancy and childhood.
Many epilepsy syndromes associated with encephalopathy have a genetic etiology, such as West syndrome, where there is marked genetic heterogeneity, and Epileptic encephalopathy with continuous spike-and-wave during sleep (CSWS), where the first genes have begun to emerge.
Equally, such syndromes may have an acquired cause such as hypoxic-ischemic encephalopathy or stroke, or may be associated with a malformation of cortical development that may also have a genetic or acquired etiology.
The concept of an epileptic encephalopathy can also be applied to single gene disorders, such as CDKL5 encephalopathy and CHD2 encephalopathy.
However, a single gene may cause an epileptic encephalopathy in some individuals and a self-limited epilepsy in others; examples include SCN1A, SCN2A, SLC2A1, KCNQ2, KCNA2, and CHD2. In an epileptic encephalopathy, the abundant epileptiform activity interferes with development resulting in cognitive slowing and often regression, and sometimes is associated with psychiatric and behavioral consequences.
The epileptiform activity can cause regression in an individual with normal development or preexisting developmental delay, who then shows developmental plateauing or regression.
A key component of the concept is that amelioration of the epileptiform activity may have the potential to improve the developmental consequences of the disorder.
This is a critical issue from a clinical perspective and one often mirrored in the observations of families and clinicians.
Many of these severe genetic disorders also have developmental consequences arising directly from the effect of the genetic mutation, in addition to the effect of the frequent epileptic activity on development. There are several ways in which this may manifest.
There may be preexisting developmental delay, complicated by plateauing or regression with seizure onset or with prolonged seizures.
In other disorders, developmental slowing may occur on a background of normal development, with the slowing emerging prior to the presence of frequent epileptic activity on EEG.
A well-known example is the relatively common encephalopathy of Dravet syndrome, in which developmental slowing or regression occurs between 1 and 2 years of age, at a time when epileptiform activity on EEG is typically not yet frequent.
This suggests a developmental component in addition to an epileptic component, with both occurring secondary to the underlying sodium channel subunit gene (SCN1A) mutation found in >80% of cases.
In a third group, the epilepsy may settle down relatively early in the child’s history, but the developmental consequences may remain profound as seen in some patients with KCNQ2 encephalopathy or STXBP1 encephalopathy.
These observations, pertinent to many of the genetic encephalopathies, suggest that a broadening of the terminology, where appropriate, to include the word “developmental,” acknowledges that both aspects may be playing a role in the clinical presentation.
These concepts are crucial to understanding the disease process for both families and clinicians.
It is therefore suggested that the term “developmental and epileptic encephalopathy” be used where appropriate and can be applied to individuals of any age.
This allows for the use of either or both descriptors: developmental encephalopathy where there is just developmental impairment without frequent epileptic activity associated with regression or further slowing of development; epileptic encephalopathy where there is no preexisting developmental delay and the genetic mutation is not thought to cause slowing in its own right; and developmental and epileptic encephalopathy where both factors play a role.
Often it may not be possible to disentangle whether the epileptic or developmental component is more important in contributing to a patient’s presentation.
Many patients with these disorders have been classified previously as having “symptomatic generalized epilepsies”; however, this term will no longer be used as it was applied to a highly heterogeneous group of patients.
This term has been applied to patients with developmental encephalopathies and epilepsy (e.g., static intellectual disability and mild epilepsy), those with epileptic encephalopathies, those with developmental and epileptic encephalopathies, as well as some patients with generalized epilepsy or combined generalized and focal epilepsy.
The new classification will allow more precise classification of these individuals’ epilepsy.
In many instances where a genetic mutation of major effect is identified, the terms “developmental and epileptic encephalopathy” may be subsumed by using the name of the underlying condition.
For example, many of the well-recognized developmental and epileptic encephalopathies can now be called by their gene name together with the word encephalopathy, such as “STXBP1 encephalopathy” or “KCNQ2 encephalopathy.” This is particularly important when referring to a genetic disease where genes are associated with both severe and self-limited, pharmacoresponsive epilepsies, such as KCNQ2 or SCN2A.
Then the term “encephalopathy” can be used to denote the severe form of the disease associated with developmental impairment.
Self-limited and pharmacoresponsive
With increasing recognition of the impact of these comorbidities on an individual’s life, there has been considerable concern that the term “benign” underestimates this burden, particularly in the milder epilepsy syndromes such as benign epilepsy with centrotemporal spikes (BECTS) and childhood absence epilepsy (CAE).
Despite the gestalt of a benign syndrome, BECTS may be associated with transient or long-lasting cognitive effects and CAE with significant psychosocial consequences such as increased risk of early pregnancy.
The Berg et al. report suggested new terms to distill the elements implied in the term “benign.”
Thus “benign,” as a descriptor for epilepsy, is replaced by both “self-limited” and “pharmacoresponsive,” each replacing different components of the meaning of benign.
“Self-limited” refers to the likely spontaneous resolution of a syndrome.
“Pharmacoresponsive” means that the epilepsy syndrome will be likely to be controlled with appropriate antiepileptic therapy.
It is important to acknowledge, however, that there will be individuals with these syndromes who are not pharmacoresponsive.
As noted previously, there is no formal ILAE classification of syndromes; however, we expect the word benign in time will be replaced in the names of specific syndromes.
The terms “malignant” and “catastrophic” will no longer be used; they will be removed from the epilepsy lexicon because of their serious and devastating connotations.
It is hoped that this new Classification of the Epilepsies will serve the epilepsy community well, leading to improved diagnosis, understanding of etiology, and targeted therapies to the patient’s disease.
It is notable that even where the etiology is clearly defined, the underlying mechanism producing recurrent seizures still requires elucidation.
With significant advances in understanding the neurobiology of seizures and epileptic diseases, there have been major paradigm shifts in the concepts underpinning classification.
This Classification is designed to mirror current understanding, so that it is relevant to clinical practice as the preeminent tool for communication in both clinical and research domains.
Dr. Ingrid E. Scheffer chairs the ILAE Task Force on the Classification of the Epilepsies.