Forced normalization

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Forced Normalization (FN) is a psychiatric phenomenon in which a long term episodic epilepsy or migraine disorder is treated, and, although the electroencephalogram (EEG) appears to have stabilized, acute behavioral, mood, and psychological disturbances begin to manifest. If, or when, treatment for the disorder is halted, the disturbances go away, but the episodic spikes on the EEG reappear. [1] H. Landolt coined the term 'Forced Normalization' in 1953 in response to a change he witnessed in epileptic EEGs, which monitor electrical activity in the brain. These changes were followed by abrupt behavioral changes in the patient. [2] Landolt concluded that forced normalization is "the phenomenon characterized by the fact that, with the occurrence of psychotic states, the electroencephalography becomes more normal or entirely normal, as compared with previous and subsequent EEG findings." Forced normalization, as described by Landolt, [3] was therefore an electrophysiological phenomenon with the electroencephalograph at its helm.

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Tellenbach's description of "alternative psychosis" or the reciprocal relationship between abnormal mental states and seizures differed from Landolt's in its clinical rather than EEG description. [4] Subsequently, this concept was refined by Wolf, [5] who suggested that the term "paradoxical normalization" was more appropriate and closer to what Landolt intended, wherein both inhibitory processes and epileptic processes (subcortical and restricted) are active at the same time.[ citation needed ]

Researchers have been rallying for the broadening of the FN diagnostic criteria to include more episodic disorders than just epilepsy. It was recently discovered that FN can and has occurred in instances of chronic migraine attacks. [6] This called into question not only the diagnostic criteria, but also which treatments will treat the most patients the most efficiently.

Forced Normalization in Epilepsy

Forced Normalization was first identified in 1953 and was believed to affect only epileptic patients. Though the converse nature of FN and epilepsy remains puzzling, the link between mental health conditions and epilepsy itself proved unsurprising to scientists. A systematic review compounded data from thousands of instances of FN and each patient's treatment. One of the patterns identified was that the comorbidity of psychiatric symptoms in epilepsy is significantly higher by calling upon the rate of schizophrenia in epilepsy patients, which is double that of the general population. [7] Furthermore, it found that the concomitance is highly dependent on the type of epilepsy a patient has: temporal lobe and cerebellum central epilepsy tend to be more susceptible to psychiatric behavioral disorders. [7]

FN in epilepsy patients has historically been treated using pharmacological stimulation, but electrical therapy has been utilized, though uncommon. In more severe cases, pharmacological stimuli improved the induced psychosis. [8] However, in the systematic review discussed previously, researchers found that pharmacological stimulation proved ineffective in a range of cases. In fact, they the most effective way to stop the psychosis was to completely halt epileptic treatment. [7] In one study, researchers combined pharmacological and electrical stimulation in an attempt to treat FN patients' psychosis without having to halt antiepileptic treatments. While this method did reduce the frequency and severity of seizures, the psychotic symptoms in the patients worsened. [9] This led researchers to the conclusion that the pathophysiological antagonism that electrical and pharmacological stimuli are capable of may be too different to combine the methods of treatment for FN.

Forced Normalization in Migraines

The occurrence of FN in migraine patients was discovered much more recently, and continues to be the topic of much scholarly debate. The most significant question is whether or not the FN diagnostic criteria should be broadened to include these psychiatric disturbances in any episodic disorder. Antonio Russo et al. were the first researchers to report on an instance of FN in migraine. In this instance, the pattern of episodic disorder remission and abrupt manifestation of psychiatric behaviors that are present in epileptic cases of FN mirrored that of their migraine patient. [10] These scholars were able to link the disturbance to FN, even though there had never been a case of FN in migraines. This is not only because of similarities in symptoms, but also because of the similarities in neuronal activity these episodic disorders share.

A point of reason to broaden the diagnostic criteria for FN is the similar locations of neuroelectrical activity during the psychosis, regardless of whether a patient suffers from epilepsy or migraines. Thus far, in both migraine and epileptic cases of FN, the psychosis that develops is hypothesized to be rooted largely in non limbic structures of the brain, like the amygdala, cerebrum, and olfactory bulb. [9] Both antiepileptic drugs (AEDs) and antimigraine medications do not affect these areas and, therefore, do not affect psychiatric activity. Yet, these medications still normalize the episodic activity on the EEG, creating the phenomenon of FN. [10] This points to the commonalities in the activity of non limbic areas of the brain, rather than the type of episodic disorder of the patient. Migraine researchers believe the primary focus of the diagnosis of FN should be placed on the activity in the cerebral cortex, as well as the psychiatric and behavioral changes that occur in a patient. [10]

New Treatments

Due to the neuroelectrical similarities of FN in migraines and epilepsy, researchers have begun to theorize about new treatment methods. These new treatments could encompass more instances of FN, rather than cases solely in epilepsy patients. While commonly utilized to treat independent instances of mood disorders and psychosis, electroconvulsive therapy has yet to be used alone to treat FN. Due to pathophysiological similarities in the psychosis caused by FN and nonconcurrent psychosis, researchers have begun to theorize about the success of electrical stimulation alone in treating FN. [11] In a case study, two patients with debilitating psychosis were followed. Both of the patients had no history of epilepsy or migraines. Yet, the patients each experienced one or more naturally occurring seizures, and their psychosis was largely alleviated after the occurrence of such. [11] Researchers gathered from this occurrence that the episodic activity in the brain caused by epilepsy may be exactly what wards off psychosis: when patients' seizures go into remission, the psychosis emerges. These researchers hypothesize about the efficiency of electroconvulsive therapy, or some form of clinically induced seizures, to treat the psychosis without having to stop AED or antimigraine therapy. [11] Furthermore, based on the pathophysiological similarities in both epilepsy and migraines and the regions of the brain the concurrent psychoses effect, a theoretical electrical treatment could be the jumping off point for an all encompassing treatment plan of FN.

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<span class="mw-page-title-main">Epilepsy</span> Group of neurological disorders causing seizures

Epilepsy is a group of non-communicable neurological disorders characterized by recurrent epileptic seizures. An epileptic seizure is the clinical manifestation of an abnormal, excessive, and synchronized electrical discharge in the brain cells called neurons. The occurrence of two or more unprovoked seizures defines epilepsy. The occurrence of just one seizure may warrant the definition in a more clinical usage where recurrence may be able to be prejudged. Epileptic seizures can vary from brief and nearly undetectable periods to long periods of vigorous shaking due to abnormal electrical activity in the brain. These episodes can result in physical injuries, either directly such as broken bones or through causing accidents. In epilepsy, seizures tend to recur and may have no immediate underlying cause. Isolated seizures that are provoked by a specific cause such as poisoning are not deemed to represent epilepsy. People with epilepsy may be treated differently in various areas of the world and experience varying degrees of social stigma due to the alarming nature of their symptoms.

<span class="mw-page-title-main">Seizure</span> Period of symptoms due to excessive or synchronous neuronal brain activity

An epileptic seizure, informally known as a seizure, is a period of symptoms due to abnormally excessive or synchronous neuronal activity in the brain. Outward effects vary from uncontrolled shaking movements involving much of the body with loss of consciousness, to shaking movements involving only part of the body with variable levels of consciousness, to a subtle momentary loss of awareness. Most of the time, these episodes last less than two minutes and it takes some time to return to normal. Loss of bladder control may occur.

A convulsion is a medical condition where the body muscles contract and relax rapidly and repeatedly, resulting in uncontrolled shaking. Because epileptic seizures typically include convulsions, the term convulsion is often used as a synonym for seizure. However, not all epileptic seizures result in convulsions, and not all convulsions are caused by epileptic seizures. Non-epileptic convulsions have no relation with epilepsy, and are caused by non-epileptic seizures.

Absence seizures are one of several kinds of generalized seizures. In the past, absence epilepsy was referred to as "pyknolepsy," a term derived from the Greek word "pyknos," signifying "extremely frequent" or "grouped". These seizures are sometimes referred to as petit mal seizures ; however, usage of this terminology is no longer recommended. Absence seizures are characterized by a brief loss and return of consciousness, generally not followed by a period of lethargy. Absence seizures are most common in children. They affect both sides of the brain.

A headache is often present in patients with epilepsy. If the headache occurs in the vicinity of a seizure, it is defined as peri-ictal headache, which can occur either before (pre-ictal) or after (post-ictal) the seizure, to which the term ictal refers. An ictal headache itself may or may not be an epileptic manifestation. In the first case it is defined as ictal epileptic headache or simply epileptic headache. It is a real painful seizure, that can remain isolated or be followed by other manifestations of the seizure. On the other hand, the ictal non-epileptic headache is a headache that occurs during a seizure but it is not due to an epileptic mechanism. When the headache does not occur in the vicinity of a seizure it is defined as inter-ictal headache. In this case it is a disorder autonomous from epilepsy, that is a comorbidity.

<span class="mw-page-title-main">Clonazepam</span> Benzodiazepine medication

Clonazepam, sold under the brand names Klonopin and Rivotril, is a medication used to prevent and treat anxiety disorders, seizures, bipolar mania, agitation associated with psychosis, OCD and akathisia. It is a tranquilizer of the benzodiazepine class. It possesses anxiolytic, anticonvulsant, sedative, hypnotic, and skeletal muscle relaxant properties. It is typically taken by mouth but is also used intravenously. Effects begin within one hour and last between six and twelve hours.

<span class="mw-page-title-main">Lennox–Gastaut syndrome</span> Medical condition

Lennox–Gastaut syndrome (LGS) is a complex, rare, and severe childhood-onset epilepsy syndrome. It is characterized by multiple and concurrent seizure types including tonic seizure, cognitive dysfunction, and slow spike waves on electroencephalogram (EEG), which are very abnormal. Typically, it presents in children aged 3–5 years and most of the time persists into adulthood with slight changes in the electroclinical phenotype. It has been associated with perinatal injuries, congenital infections, brain malformations, brain tumors, genetic disorders such as tuberous sclerosis and numerous gene mutations. Sometimes LGS is observed after infantile epileptic spasm syndrome. The prognosis for LGS is marked by a 5% mortality in childhood and persistent seizures into adulthood.

Landau–Kleffner syndrome (LKS)—also called infantile acquired aphasia, acquired epileptic aphasia or aphasia with convulsive disorder—is a rare childhood neurological syndrome.

<span class="mw-page-title-main">Vagus nerve stimulation</span> Medical treatment that involves delivering electrical impulses to the vagus nerve.

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<span class="mw-page-title-main">Aura (symptom)</span> Symptom of epilepsy and migraine

An aura is a perceptual disturbance experienced by some with epilepsy or migraine. An epileptic aura is a seizure.

Psychogenic non-epileptic seizures (PNES), which have been more recently classified as functional seizures, are events resembling an epileptic seizure, but without the characteristic electrical discharges associated with epilepsy. PNES fall under the category of disorders known as functional neurological disorders (FND), also known as conversion disorders. These are typically treated by psychologists or psychiatrists. PNES has previously been called pseudoseizures, psychogenic seizures, and hysterical seizures, but these terms have fallen out of favor.

<span class="mw-page-title-main">Temporal lobe epilepsy</span> Chronic focal seizure disorder

In the field of neurology, temporal lobe epilepsy is an enduring brain disorder that causes unprovoked seizures from the temporal lobe. Temporal lobe epilepsy is the most common type of focal onset epilepsy among adults. Seizure symptoms and behavior distinguish seizures arising from the medial temporal lobe from seizures arising from the lateral (neocortical) temporal lobe. Memory and psychiatric comorbidities may occur. Diagnosis relies on electroencephalographic (EEG) and neuroimaging studies. Anticonvulsant medications, epilepsy surgery and dietary treatments may improve seizure control.

Frontal lobe epilepsy (FLE) is a neurological disorder that is characterized by brief, recurring seizures arising in the frontal lobes of the brain, that often occur during sleep. It is the second most common type of epilepsy after temporal lobe epilepsy (TLE), and is related to the temporal form in that both forms are characterized by partial (focal) seizures.

The postictal state is the altered state of consciousness after an epileptic seizure. It usually lasts between 5 and 30 minutes, but sometimes longer in the case of larger or more severe seizures, and is characterized by drowsiness, confusion, nausea, hypertension, headache or migraine, and other disorienting symptoms.

Panayiotopoulos syndrome is a common idiopathic childhood-related seizure disorder that occurs exclusively in otherwise normal children and manifests mainly with autonomic epileptic seizures and autonomic status epilepticus. An expert consensus has defined Panayiotopoulos syndrome as "a benign age-related focal seizure disorder occurring in early and mid-childhood. It is characterized by seizures, often prolonged, with predominantly autonomic symptoms, and by an EEG [electroencephalogram] that shows shifting and/or multiple foci, often with occipital predominance."

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<span class="mw-page-title-main">Epilepsy in children</span>

Epilepsy is a neurological condition of recurrent episodes of unprovoked epileptic seizures. A seizure is an abnormal neuronal brain activity that can cause intellectual, emotional, and social consequences. Epilepsy affects children and adults of all ages and races, it is one of the most common neurological disorders of the nervous system. As well as, this condition is more common among children than adults affecting about 6 out of 1000 US children that are between the age of 0 to 5 years old. The epileptic seizures can be of different types depending on the part of the brain that was affected, seizures are classified in 2 main types partial seizure or genralized seizure.

People with epilepsy may be classified into different syndromes based on specific clinical features. These features include the age at which seizures begin, the seizure types, and EEG findings, among others. Identifying an epilepsy syndrome is useful as it helps determine the underlying causes as well as deciding what anti-seizure medication should be tried. Epilepsy syndromes are more commonly diagnosed in infants and children. Some examples of epilepsy syndromes include benign rolandic epilepsy, childhood absence epilepsy and juvenile myoclonic epilepsy. Severe syndromes with diffuse brain dysfunction caused, at least partly, by some aspect of epilepsy, are also referred to as epileptic encephalopathies. These are associated with frequent seizures that are resistant to treatment and severe cognitive dysfunction, for instance Lennox-Gastaut syndrome and West syndrome.

Musicogenic seizure, also known as music-induced seizure, is a rare type of seizure, with an estimated prevalence of 1 in 10,000,000 individuals, that arises from disorganized or abnormal brain electrical activity when a person hears or is exposed to a specific type of sound or musical stimuli. There are challenges when diagnosing a music-induced seizure due to the broad scope of triggers, and time delay between a stimulus and seizure. In addition, the causes of musicogenic seizures are not well-established as solely limited cases and research have been discovered and conducted respectively. Nevertheless, the current understanding of the mechanism behind musicogenic seizure is that music triggers the part of the brain that is responsible for evoking an emotion associated with that music. Dysfunction in this system leads to an abnormal release of dopamine, eventually inducing seizure.

References

  1. Calle-Lopez, Yamille; et al. (2019). "Forced normalization: A systematic review" (PDF). Epilepsia. 60 (8): 1610–1618. doi:10.1111/epi.16276. PMID   31260102. S2CID   195756980.
  2. Augusto Bragatti, José (2021). "Forced Normalization Revisited: New Concepts About a Paradoxical Phenomenon". Frontiers in Integrative Neuroscience (Review). 15: 736248. doi: 10.3389/fnint.2021.736248 . PMC   8429494 . PMID   34512281.
  3. Landolt, H (1958). Serial EEG investigations during psychotic episodes in epileptic patients and during schizophrenic attacks. In: Lectures on Epilepsy, LorentzDe Haas A. M. (Ed). Amsterdam: Elsevier. pp. 91–133.
  4. Tellenbach, H (1965). "Epilepsy as a convulsive disorder and as a psychosis. On alternative psychoses of paranoid nature in "forced normalisation" (Landolt) of the electroencephalogram of epileptics". Nervenarzt. 36: 190–202. PMID   14308489.
  5. Wolf, P (1991). Acute behavioral symptomatology at disappearance of epileptiform EEG abnormality: paradoxical or forced normalisation. In: Neurobehavioral Problems in Epilepsy, SmithD., TreimanD. and Trimble M. R. (Eds.). New York: Raven Press. pp. 127–42.
  6. Russo, Antonio; et al. (2017). ""Forced Normalization": Could It Occur Also in Migraine Patients?". Headache: The Journal of Head and Face Pain. 57 (5): 803–805. doi:10.1111/head.13079. PMID   28390100. S2CID   29729196.
  7. 1 2 3 Calle-Lopez, Yamille; et al. (2019). "Forced normalization: A systematic review". Epilepsia. 60 (8): 1610–1618. doi:10.1111/epi.16276. PMID   31260102. S2CID   195756980.
  8. Carazo Barrios, Lina; et al. (2020). "Forced normalization: case series from a Spanish epilepsy unit". Seizure. 81: 132–137. doi: 10.1016/j.seizure.2020.07.020 . PMID   32795944.
  9. 1 2 Augusto Bragatti, José (2021). "Forced Normalization Revisited: New Concepts About a Paradoxical Phenomenon". Frontiers in Integrative Neuroscience. 15: 736248. doi: 10.3389/fnint.2021.736248 . PMC   8429494 . PMID   34512281.
  10. 1 2 3 Russo, Antonio; et al. (2017). ""Forced Normalization": Could It Occur Also in Migraine Patients?". Headache: The Journal of Head and Face Pain. 57 (5): 803–805. doi:10.1111/head.13079. PMID   28390100. S2CID   29729196 via American Headache Society.
  11. 1 2 3 Green, Andrea L.; et al. (2016). "Forced normalization's converse as nature's model for use of ECT in the management of psychosis: An observational case series". Epilepsy & Behavior Case Reports. 6: 36–38. doi: 10.1016/j.ebcr.2016.05.004 . PMC   4959916 . PMID   27489775.

Further reading