Subacute sclerosing panencephalitis

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Medical condition

Subacute sclerosing panencephalitis
Other names	Dawson disease
Subacute sclerosing panencephalitis.
Specialty	Neurology, Infectious Disease
Symptoms	Behavior changes, seizures, spasticity, poor coordination, coma
Usual onset	6–15 years after infection with measles
Causes	Measles virus
Risk factors	Measles infection
Diagnostic method	EEG, Serologic testing, brain biopsy
Prevention	Measles vaccine
Treatment	Supportive treatment
Medication	Intrathecal interferon alpha, intravenous ribavirin, isoprinosine
Prognosis	Usually fatal
Frequency	2 in 10,000 for all age groups;[1] as high as 1 in 609 for unvaccinated infants under 15 months[2]

Subacute sclerosing panencephalitis (SSPE), also known as Dawson disease, is a rare form of progressive brain inflammation caused by a persistent infection with the measles virus. The condition primarily affects children, teens, and young adults. It has been estimated that about 2 in 10,000 people who get measles will eventually develop SSPE.^[1] However, a 2016 study estimated that the rate for unvaccinated infants under 15 months was as high as 1 in 609.^[2][3] No cure for SSPE exists, and the condition is almost always fatal. SSPE is sometimes confused with acute disseminated encephalomyelitis, which can also be caused by the measles virus, but has a very different timing and course.^[4]

SSPE is caused by some strains of the wild-type (naturally occurring) measles virus, such as the B3 strain,^[5] but not by the strains used in measles vaccines.^[6][5]

SSPE is characterized by a history of primary measles infection, followed by a normal, unremarkable recovery.^[5] Symptoms of SSPE appear later.^[5] On average, the first symptoms appear about 10 years after the initial infection, though this varies significantly, as some people have developed SSPE symptoms as soon as 1 month after infection, and others as long as 27 years later.^[5]

After the asymptomatic period, progressive neurological deterioration occurs, characterized by behavior change, intellectual problems, myoclonic seizures, blindness, ataxia, and eventually death.^[7][8]

The very earliest symptoms are small, subtle changes in behavior, such as not paying attention or struggling with schoolwork.^[9] By the time family members have become concerned, the disease is at Stage 1, and shows nonspecific symptoms of neurological problems, such as being more irritable than usual, more affectionate than usual, lethargic, or having speech difficulties.^[9] Because the symptoms are nonspecific, in this stage it may be obvious to people who know the child well that something is wrong, but unclear what the problem is.

Later symptoms include myoclonic seizures, epileptic seizures, loss of vision, loss of coordination, and difficulty moving.^[9]

There are multiple staging systems. Symptoms progress through four stages, such as these:^[10][11]

• Stage 1: There may be personality changes, mood swings, or depression. Fever, headache, and memory loss may also be present. This stage may last up to 6 months.
• Stage 2: This stage may involve jerking, muscle spasms, seizures, loss of vision, and dementia.
• Stage 3: Jerking movements are replaced by writhing (twisting) movements and rigidity. At this stage, complications may result in blindness or death.
• Stage 4: Progressive loss of consciousness into a persistent vegetative state, which may be preceded by or concomitant with paralysis, occurs in the final stage, during which breathing, heart rate, and blood pressure are affected. Death usually occurs as a result of fever, heart failure, or the brain’s inability to control the autonomic nervous system.

SSPE is caused by a latent infection by mutated copies of wild type (naturally occurring) measles virus.^[5] A large number of nucleocapsids are produced in the neurons and the glial cells. In these cells the viral genes that encode envelope proteins have restricted expression.^[12] As a result, infectious particles like the M protein are not produced, and the virus is able to survive persistently without evoking an immune response. Eventually the infection will lead to SSPE.^[13]

When SSPE begins, it demyelinates nerves, causing them to signal unreliably.^[9] Later, the brain cortex atrophies, and the ventricular system becomes dilated.^[9] Nerve cells are destroyed through phagocytosis.^[9] Tauopathies and neurofibrillary tangles develop.^[9]

SSPE may be suspected in any child with symptoms of a progressive (keeps getting worse) neurological disease and who has never been vaccinated against measles.^[9]

Typical diagnostic tests include electroencephalography (EEG) to look for evidence of epilepsy or other disturbances to brain waves and a test of the cerebrospinal fluid to look for elevated levels of antibodies against measles and to rule out multiple sclerosis.^[9] Magnetic resonance imaging (MRI) of the brain usually looks normal early in the disease.^[9]

There is no cure.^[14] Most treatments are supportive measures, such as anticonvulsants to reduce seizures.^[8]

If the diagnosis is made early, oral isoprinosine (Inosiplex) is standard,^[9] but it is expensive and only stabilizes or improves symptoms for about 30% of people with SSPE.^[5] Less effective medications include intraventricular interferon alfa, amantadine, ribavirin, and others.^[5] Immunoglobulin therapy (IVIG) is also used.^[9] Isoprinosine is sometimes combined with interferon alfa.^[5][9]

Following onset of stage 2, the disease is invariably fatal.

SSPE is a disease for which prevention is the best medicine.^[5][9] SSPE can be prevented by vaccinating children against measles before they become infected.^[5] The strain of measles virus in the measles vaccines do not cause SSPE.^[5]

Almost everyone who develops SSPE dies as a result of SSPE or secondary complications.^[5] Commonly, the person dies within a few months to a few years.^[5] Faster deterioration in cases of acute fulminant SSPE can lead to death within 3 months of diagnosis.^[15][16] This faster progression may be called measles inclusion body encephalitis.^[9]

Although the prognosis is bleak for SSPE past stage 1, there is a 5% spontaneous remission rate. This may take the form of either a full remission of symptoms that may last many years, or an improvement in condition, giving a longer progression period, or else at least a longer period with the less severe symptoms.^[16][17]

If a remission is achieved, the subsequent relapse is untreatable.^[18]

The number of people who develop SSPE depends on the number of people who get sick with measles.^[5] For every 100,000 children or adults who get measles, between 4 and 11 of them will develop SSPE.^[5] An outbreak of measles within any community is "inevitably" followed by an uptick in SSPE among the people (usually children) who had been infected with measles.^[9]

The chance of developing SSPE is higher for babies (about 1 in 600 infected babies will later develop SSPE) than for those who had measles when they were older.^[5] Boys develop SSPE about three times as often as girls.^[9]

SSPE is a rare condition, although there is still relatively high incidence in Asia and the Middle East. However, the number of reported cases is declining since the introduction of the measles vaccine. Eradication of the measles virus prevents the SSPE mutation and therefore the progression of the disease, or even the initial infection itself.^[19]

SSPE was first described by James R. Dawson, Jr. of the Vanderbilt University School of Medicine in 1933.^[9]

• Bonthius D, Stanek N, Grose C (2000). "Subacute sclerosing panencephalitis, a measles complication, in an internationally adopted child". Emerg Infect Dis. 6 (4): 377–81. doi:10.3201/eid0604.000409. PMC 2640885. PMID 10905971.

• 23-273l. at Merck Manual of Diagnosis and Therapy Home Edition
• Subacute Sclerosing Panencephalitis at NINDS
• PubMed Health: Subacute sclerosing panencephalitis Archived 2014-08-08 at the Wayback Machine
• synd/1889 at Whonamedit?