Epilepsy is a neurological disorder characterized by recurrent seizures. It affects people of all ages and can significantly impact daily life. Understanding epilepsy is crucial for proper management and support.
When a person has had two or more seizures more than twenty-four hours apart that have not been provoked by specific events such as a stroke, brain injury, infection, fever, or fluctuations in blood sugar, they are considered to have epilepsy. A person can also be diagnosed with epilepsy if they have one or more unprovoked seizures and a probability of future seizures.
A seizure is an electrical disturbance in the brain that interferes with its normal function. Many scientists and clinicians compare it to an “electrical storm in the brain” in which your brain cells hyper-synchronize in an abnormal pattern, disrupting that delicate brain signal balance.
Seizures vary from person-to-person, depending upon their seizure type. That’s because epilepsy is a spectrum disorder, meaning the causes, type, and severity can differ greatly amongst those affected by it. Some people have visible symptoms, such as a tonic-clonic seizure (previously called grand-mal), and others may have no visible symptoms, such as absence seizures (previously called petit mal).
While the exact causes of epilepsy are varied and not entirely known, in general epilepsy and seizures result from abnormal signals from neurons (a type of brain cell) in the brain. It can be genetic, meaning it is the result of mutations in a person’s genes, or it can be acquired through events such as physical injury or infection[1]. In up to 50% of epilepsy cases worldwide, the cause is idiopathic, which means unknown.
Some underlying causes of acquired epilepsy include:
Epilepsy is more common than many people realize. It’s estimated that approximately 1 in 26 people will develop epilepsy at some point in their lives. This means that millions of individuals worldwide are affected by epilepsy, regardless of age, gender, or background. While the frequency of epilepsy varies depending on factors such as age group and geographic region, it is considered one of the most prevalent neurological disorders globally. Despite its prevalence, there is still a need for greater awareness, understanding, and support for individuals living with epilepsy and their families.
While epilepsy and seizures can develop in any person at any age, new cases are most common in children, especially in their early years of life. The incidence of epilepsy lessens after childhood but then increases again in older adults (>60 years of age).
Infants in their first year of life are vulnerable to seizures (and epilepsy) because their brains are rapidly developing, with neurons growing and making new connections all the time. For many infants, their brains will develop without disruption; for others, however, they may experience disturbances that can cause epilepsy. This may include head trauma, genetic mutation, or viral infection in the birthing parent during pregnancy.
Neonatal seizures (seizures during the first four weeks of a baby’s life) may be difficult to diagnose because they are subtle and resemble normal movements of a baby, or because some doctors do not have specialized training in epilepsy. A pediatric neurologist can help diagnose neonatal seizures and identify their cause.
Though incidence begins to decrease as an infant’s brain continues to develop, toddlers and young children also develop epilepsy. Most commonly, this age group is susceptible to febrile seizures (seizures associated with fever), but epilepsy can develop from genetic disorders, central nervous system (CNS) infections, developmental disorders, and head trauma.
The incidence of epilepsy decreases during the teenage, early adult, and middle-aged years but then rises again in adults 60 years of age and older. In this age range, epilepsy can be associated with strokes, Alzheimer’s disease, head trauma, and brain tumors, among other things.
There is limited research available on the incidence of epilepsy across race and ethnicity. There is no direct evidence that a person’s race or ethnicity alone puts them at a higher risk for developing epilepsy; however, there is research to suggest that there are commonalities between people with similar socioeconomic, racial, or ethnic backgrounds.
The prevalence of active epilepsy was found to be higher in non-Hispanic White Americans and non-Hispanic Black Americans, as compared to Hispanic Americans.[7] The prevalence of active epilepsy was higher in Black Americans as compared to White Americans.[8]
The proportion of people with “unclassifiable” epilepsy was found to be higher in people with African ancestry as compared to whites. The latter finding may be due to the lack of access to diagnostic testing, such as prolonged EEG monitoring, making diagnosis difficult and uncertain.[9]
It is estimated that 1.5% of Asian Americans are living with epilepsy, though more research is needed.[10]
It’s important to note that there are disparities in epilepsy care, both in the United States and abroad, which can result in certain ethnicities and races being over or underreported in epilepsy research. This is known as the treatment gap or the mismatch between those who need treatment and those who have access to treatment.
When treating epilepsy, patients are prescribed treatment based on the type or types of seizures they are experiencing. A variety of treatments are available, including medication, dietary changes, devices, and surgery. While the goal of epilepsy treatments is straightforward—no seizures, no side effects—finding the right treatment plan may require trial and error.
Usually, newly diagnosed people with epilepsy will start an oral medication that is appropriate for their diagnosis. If the first drug treatment does not stop their seizures, their neurologist will work with the patient to try other medications, or a combination thereof, as well as evaluate if they are a potential candidate for surgery.
While there are many medications, medical devices, and surgical options to treat epilepsy, right now, there are no known cures for epilepsy. However, incredible advancements in research have helped us understand the mechanisms that cause seizures better than at any other point in history. That’s why we must invest in research – to understand the underlying causes of epilepsies – so we can cure them.
Living with epilepsy requires careful management of triggers, adherence to medication regimens, and awareness of safety precautions. Building a strong support network and staying informed about the condition can help individuals lead fulfilling lives despite the challenges posed by epilepsy.
When diagnosing epilepsy, medical professionals conduct tests to detect abnormalities in a patient’s brainwaves. Tests can also detect seizure activity, including where in the brain a seizure starts. The most common diagnostic test for epilepsy is the EEG, but other brain scans, like MRI or PET, can also be used depending on the patient’s seizure or epilepsy type (or both). To determine if a patient does (or does not) have epilepsy, their healthcare provider compares their test results to the guidelines and criteria established by the International League Against Epilepsy (ILAE).
Common signs of epilepsy include seizures, which can manifest as convulsions, staring spells, or temporary confusion.
Epilepsy can often be managed with medications, lifestyle modifications, and other therapies. However, there is currently no cure. That’s why we must invest in research – to understand the underlying causes of epilepsy – so we can advance science towards a cure.
While genetics can play a role in some cases of epilepsy, not all forms of the condition are hereditary. Environmental factors and other variables also contribute to the risk of developing epilepsy.
Epilepsy can impact daily life in various ways, including limitations on activities, driving restrictions, and the need for medication management. However, many individuals with epilepsy lead productive and fulfilling lives with proper management.
If someone is having a seizure, stay calm and ensure their safety by removing any nearby hazards. Do not restrain them or put anything in their mouth. Once the seizure has ended, offer reassurance and support as needed and seek medical attention if necessary.