Fatal insomnia

Short description: Prion disease of the human brain

Fatal insomnia

Longitudinal comparison of 18F-FDG PET/MRI in brain in a patient with fatal insomnia, demonstrating normal brain parenchyma on MRI, but prominent hypometabolism of the thalamus.
Specialty| Neurology, psychiatry, sleep medicine, neuropathology
Symptoms| Progressive insomnia, ataxia, double vision, weight loss, high blood pressure, excessive sweating
Complications| Permanent state of hypnagogia later in the illness
Usual onset| 45–50 years old[1]
Types| Fatal familial insomnia, sporadic fatal insomnia[2]
Causes| Genetic mutation, sporadic form (very rare)
Risk factors| Family history
Diagnostic method| Suspected based on symptoms, supported by sleep study, PET scan and genetic testing (if familial form is suspected)[3]
Differential diagnosis| Alzheimer's disease, frontotemporal dementia, other transmissible spongiform encephalopathies[4]
Prevention| None
Treatment| Supportive care[2]
Medication| None
Prognosis| Invariably fatal
Frequency| 70 families worldwide are known to carry the gene associated with the disease, 37 sporadic cases diagnosed (as of 20 September 2022)
Deaths| <1 per year

Fatal insomnia is a neurodegenerative prion disease that results in trouble sleeping as its hallmark symptom.[2] The majority of cases are familial (fatal familial insomnia [FFI]), stemming from a mutation in the PRNP gene, with the remainder of cases occurring sporadically (sporadic fatal insomnia [sFI]). The problems with sleeping typically start out gradually and worsen over time.[4] Eventually, the patient will succumb to total insomnia (agrypnia excitata), most often leading to other symptoms such as speech problems, coordination problems, and dementia.[5] It results in death within a few months to a few years, and there is no known disease-modifying treatment.[2]

## Contents

* 1 Signs and symptoms
* 2 Cause
* 3 Pathophysiology
* 4 Diagnosis
* 4.1 Differential diagnosis
* 5 Treatments
* 6 Prognosis
* 7 Epidemiology and history
* 7.1 Silvano, 1983, Bologna, Italy
* 7.2 Unnamed American patient, 2001
* 7.3 Egyptian man, 2011, Netherlands
* 8 Research
* 9 References
* 10 External links

## Signs and symptoms

The disease has four stages:[6]

1. Characterized by worsening insomnia, resulting in panic attacks, paranoia, and phobias. This stage lasts for about four months.
2. Hallucinations and panic attacks become noticeable, continuing for about five months.
3. Complete inability to sleep is followed by rapid loss of weight. This lasts for about three months.
4. Dementia, during which the person becomes unresponsive or mute over the course of six months, is the final stage of the disease, after which death follows.

Clinically, Fatal Insomnia manifests with a disordered sleep-wake cycle, dysautonomia, motor disturbances, and neuropsychiatric disorders.

Other symptoms include profuse sweating, miosis (pinpoint pupils), sudden entrance into menopause or impotence, neck stiffness, and elevation of blood pressure and heart rate. The sporadic form of the disease often presents with double vision. Prolonged constipation is common as well. As the disease progresses, the person becomes stuck in a state of pre-sleep limbo, or hypnagogia, which is the state just before sleep in healthy individuals. During these stages, people commonly and repeatedly move their limbs as if they were dreaming.[7]

The age of onset is variable, ranging from 13 to 60 years, with an average of 50.[8] The disease can be detected prior to onset by genetic testing.[9] Death usually occurs between 6–36 months from onset. The presentation of the disease varies considerably from person to person, even among people within the same family; in the sporadic form, for example, sleep problems are not commonly reported, and early symptoms are ataxia, cognitive impairment, and double vision.[10]

## Cause

This section may be too technical for most readers to understand. Please help improve it to make it understandable to non-experts, without removing the technical details. (September 2023) (Learn how and when to remove this template message)

|

Idiogram of chromosome 20 showing gene PRP location

Fatal familial insomnia is a rare hereditary prion disease that is associated with a mutation in PRNP. The gene, which provides instructions for making the prion protein PrPC, is located on the short arm of chromosome 20 at position p13.[11] Individuals with FFI or familial Creutzfeldt–Jakob disease (fCJD) both carry a mutation at codon 178 of the prion protein gene. FFI is also invariably linked to the presence of the methionine codon at position 129 of the mutant allele, whereas fCJD is linked to the presence of the valine codon at that position. The disease occurs when there is a change of amino acid at position 178 in which asparagine is found instead of the normal aspartic acid. This has to be accompanied with a methionine at position 129.[12]

FFI is an autosomal dominant disease caused by a missense GAC-to-AAC mutation at codon 178 of the PRNP prion protein gene located on chromosome 20, along with the presence of the methionine polymorphism at position 129 of the mutant allele. Pathologically, FFI is characterized predominantly by thalamic degeneration—especially in the medio-dorsal and anteroventral nuclei.[13] Phenotypic variability is a perplexing feature of FFI.[14]

Prion diseases are caused by the accumulation of misfolded prion proteins in the brain. Generally, prion disorders are characterized by long incubation periods and short clinical duration, which means the abnormal prions may accumulate for many years without causing symptoms (long incubation period), but once symptoms begin the disorder rapidly worsens.

## Pathophysiology

Given its striking clinical and neuropathologic similarities with fatal familial insomnia (FFI), a genetic prion disease linked to a point mutation at codon 178 (D178N) in the PRNP coupled with methionine at codon 129, the MM2T subtype is also known as sporadic FI (sFI). Transmission studies using susceptible transgenic mice have consistently demonstrated that the same prion strain is associated with both sFI and FFI. In contrast to what has been the rule for the most common neurodegenerative disorders, sFI is rarer than its genetic counterpart. Whereas the recognized patients with FFI are numerous and belong to >50 families worldwide, only about 30 cases of CJD MM2T and a few cases with mixed MM2T and MM2C features (MM2T+C) have been recorded to date.

In itself the presence of prions causes reduced glucose to be used by the thalamus and a mild hypo-metabolism of the cingulate cortex. The extent of this symptom varies between two variations of the disease: those presenting methionine homozygotes at codon 129 and methionine/valine heterozygotes, with some evidence that hypo-metabolism is more severe in the latter.[15] Given the relationship between the involvement of the thalamus in regulating sleep and alertness, a causal relationship can be drawn and is often mentioned as the cause of insomnia.[16][17]

## Diagnosis

This section may be too technical for most readers to understand. Please help improve it to make it understandable to non-experts, without removing the technical details. (June 2024) (Learn how and when to remove this template message)

|

Diagnosis is based on symptoms and can be supported by a sleep study, a PET scan and genetic testing if the patient's family has a history of the disease. As with other prion diseases, the diagnosis can be confirmed only by a brain autopsy.

The real-time quaking-induced conversion (RT-QuIC), a highly sensitive assay that detects minute amounts of PrPSc in the cerebrospinal fluid, has been reported to have a sensitivity of 50% in FFI and sFI.[18][19]Template:Missing long citation However, this low sensitivity may change since the examination was based on a low number of cases, and the RT-QuIC technology is continuously evolving.

A test that measures the cerebral metabolic rate of glucose by positron emission tomography (PET), referred to as [18F]-FDG-PET, has demonstrated severe hypometabolism of the thalamus bilaterally in FFI and sFI, also in the earliest stages of the disease. This hypometabolism then spreads, eventually impacting most cortical regions.[20]Template:Missing long citation The complexity and cost of this test currently impedes its use in routine diagnosis.

### Differential diagnosis

Other diseases involving the mammalian prion protein are known.[21] Some are transmissible (TSEs, including FFI) such as kuru, bovine spongiform encephalopathy (BSE, also known as mad cow disease) in cattle and chronic wasting disease in American deer and American elk in some areas of the United States and Canada, as well as Creutzfeldt–Jakob disease (CJD). Until recently, prion diseases were thought to be transmissible only by direct contact with infected tissue, such as from eating infected tissue, transfusion or transplantation; research suggests that prions can be transmitted by aerosols but that the general public is not at risk of airborne infection.[22]

## Treatments

Treatment involves palliative care.[2] There is conflicting evidence over the use of sleeping pills, including barbiturates, as a treatment for the disease.[23][24] Symptoms of fatal familial insomnia may be treated with medications.[contradictory]

Clonazepam may be prescribed to treat muscle spasms, and eszopiclone or zolpidem may be prescribed to help treat insomnia. However, these drugs do not work in the long term.[25]

## Prognosis

Timeline of a Fatal Familial Insomnia (FFI) patient

Like all prion diseases, FFI is invariably fatal.[26][2] Life expectancy ranges from seven months to six years,[2] with an average of 18 months.[26]

## Epidemiology and history

Hypnogram comparing the sleep pattern of a healthy control with five FFI patients, who display decreased sleep efficiency and disrupted sleep cycles. (W: wake; R: REM; N1-3: NREM sleep stages.)

Fatal insomnia was first described by Elio Lugaresi et al. in 1986.

In 1998, 40 families were known to carry the gene for FFI globally: eight German, five Italian, four American, two French, two Australian, two British, one Japanese and one Austrian.[27] In the Basque Country of Spain, 16 family cases of the 178N mutation were seen between 1993 and 2005 related to two families with a common ancestor in the 18th century.[28] In 2011, another family was added to the list when researchers found the first man in the Netherlands to be diagnosed with FFI. Whilst he had lived in the Netherlands for 19 years, he was of Egyptian descent.[29] Other prion diseases are similar to FFI and may be related but are missing the D178N gene mutation.[7]

As of 20 September 2022[update], 37 cases of sporadic fatal insomnia have been diagnosed.[3] Unlike in FFI, those with sFI do not have the D178N mutation in the PRNP gene; they all have a different mutation in the same gene causing methionine homozygosity at codon 129.[30][31] Nonetheless, the methionine presence in lieu of the valine (Val129) is what causes the sporadic form of disease. The targeting of this mutation has been suggested as a strategy for treatment, or possibly as a cure for the disease.[32]

### Silvano, 1983, Bologna, Italy

In late 1983, Italian neurologist/sleep expert Dr. Ignazio Roiter received a patient at the University of Bologna hospital's sleep institute. The man, known only as Silvano, decided in a rare moment of consciousness to be recorded for future studies and to donate his brain for research in hopes of finding a cure for future victims.[33]

In 1986, Lugaresi and colleagues first named and described in detail the clinical and histopathological features of fatal familial insomnia.[34] This report was primarily based on the aforementioned Silvano. Dr. Roiter referred the case to Prof. Elio Lugaresi, a well-known sleep expert, who, along with his colleagues, carried out advanced sleep analyses. As Silvano's condition quickly deteriorated, Lugaresi arranged for a postmortem neuropathological examination of the brain to be carried out by Dr. Gambetti, Lugaresi's former trainee. The collaboration of these two groups led to the 1986 publication.[29] At the time, a prion disease was not suspected due to a lack of prion-related histopathology and frozen brain tissue for advanced analysis. However, due to the devotion of Dr. Roiter and Silvano's family, more cases were obtained, resulting in the classification of FFI as a familial prion disease tied to the 178Asn genetic mutation.[35]

### Unnamed American patient, 2001

In an article published in 2006, Schenkein and Montagna wrote of a 52-year-old American man who was able to exceed the average survival time by nearly one year with various strategies that included vitamin therapy and meditation, different stimulants and hypnotics and even complete sensory deprivation in an attempt to induce sleep at night and increase alertness during the day. He managed to write a book and drive hundreds of miles in this time, but nonetheless, over the course of his trials, the man succumbed to the classic four-stage progression of the illness.[33]

### Egyptian man, 2011, Netherlands

In 2011, the first reported case in the Netherlands was of a 57-year-old man of Egyptian descent. The man came in with symptoms of double vision and progressive memory loss, and his family also noted he had recently become disoriented, paranoid and confused. Whilst he tended to fall asleep at random during daily activities, he experienced vivid dreams and random muscular jerks during normal slow-wave sleep. After four months of these symptoms, he began to have convulsions in his hands, trunk and lower limbs while awake. The person died at age 58, seven months after the onset of symptoms. An autopsy revealed mild atrophy of the frontal cortex and moderate atrophy of the thalamus. The latter is one of the most common signs of FFI.[29]

## Research

Still with unclear benefit in humans, a number of treatments have had tentative success in slowing disease progression in animal models, including pentosan polysulfate, mepacrine, and amphotericin B.[3] As of 2016[update], a study investigating doxycycline is being carried out.[3][36]

In 2009, a mouse model was made for FFI. These mice expressed a humanized version of the PrP protein that also contains the D178N FFI mutation.[37] These mice appear to have progressively fewer and shorter periods of uninterrupted sleep, damage in the thalamus, and early deaths, similar to humans with FFI. The Prion Alliance was established by husband and wife duo Eric Minikel and Sonia Vallabh after Vallabh's mother was diagnosed with the fatal disease.[38] They conduct research at the Broad Institute to develop therapeutics for human prion diseases. Their hypothesis is that lowering PrP-levels may prevent the onset of FFI.[39] Other research interests involve identifying biomarkers to track the progression of prion disease in living people.[40][41]

## References

1. ↑ "Fatal Familial Insomnia" (in en-US). https://rarediseases.org/rare-diseases/fatal-familial-insomnia/.
2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 "Fatal Insomnia – Neurologic Disorders" (in en-CA). https://www.merckmanuals.com/en-ca/professional/neurologic-disorders/prion-diseases/fatal-insomnia.
3. ↑ 3.0 3.1 3.2 3.3 "Fatal familial insomnia". https://rarediseases.info.nih.gov/diseases/6429/fatal-familial-insomnia.
4. ↑ 4.0 4.1 "Fatal Familial Insomnia". https://rarediseases.org/rare-diseases/fatal-familial-insomnia/.
5. ↑ Merck Manual. https://www.merckmanuals.com/home/brain,-spinal-cord,-and-nerve-disorders/prion-diseases/fatal-insomnia. Retrieved 4 May 2018.
6. ↑ "Dying To Sleep: Fatal Familial Insomnia (FFI)". http://www.world-of-lucid-dreaming.com/fatal-familial-insomnia.html.
7. ↑ 7.0 7.1 "Fatal familial insomnia: clinical features and molecular genetics". Journal of Sleep Research 8 (Suppl 1): 23–29. June 1999. doi:10.1046/j.1365-2869.1999.00005.x. PMID 10389103.
8. ↑ "Episode 25: Fatal Insomnia". https://www.obscuracrimepodcast.com/podcast/2018/10/10/episode-25-fatal-insomnia.
9. ↑ "The Secrets of Sleep". National Geographic 217 (5): 74. May 2010. https://www.nationalgeographic.com/magazine/article/sleep.
10. ↑ "Fatal Insomnia - Neurologic Disorders". https://www.merckmanuals.com/en-ca/professional/neurologic-disorders/prion-diseases/fatal-insomnia.
11. ↑ "PRNP gene". https://medlineplus.gov/genetics/gene/prnp/.
12. ↑ "Fatal Familial Insomnia". StatPearls. StatPearls Publishing. 2024. https://www.ncbi.nlm.nih.gov/books/NBK482208/.
13. ↑ "Specific structuro-metabolic pattern of thalamic subnuclei in fatal familial insomnia: A PET/MRI imaging study". NeuroImage. Clinical 34. 2022. doi:10.1016/j.nicl.2022.103026. PMID 35504222.
14. ↑ "Clinical profile of fatal familial insomnia: phenotypic variation in 129 polymorphisms and geographical regions". Journal of Neurology, Neurosurgery, and Psychiatry 93 (3): 291–297. March 2022. doi:10.1136/jnnp-2021-327247. PMID 34667102.
15. ↑ "Cerebral metabolism in fatal familial insomnia: relation to duration, neuropathology, and distribution of protease-resistant prion protein". Neurology 49 (1): 126–133. July 1997. doi:10.1212/wnl.49.1.126. PMID 9222180.
16. ↑ "Sleep homeostasis". Encyclopedia of Sleep and Circadian Rhythms. 2023. pp. 39–47. doi:10.1016/B978-0-12-822963-7.00243-7. ISBN 978-0-323-91094-1.
17. ↑ "Circadian and sleep disorder in Huntington's disease". Experimental Neurology 243: 34–44. May 2013. doi:10.1016/j.expneurol.2012.10.014. PMID 23099415.
18. ↑ Cracco et al. Handbook of Clinical Neurology 2018
19. ↑ Mock et al. Scientific Reports 2021
20. ↑ Cortelli et al. Brain 2006
21. ↑ "Prion diseases: immunotargets and therapy". ImmunoTargets and Therapy 5: 57–68. 2016. doi:10.2147/ITT.S64795. PMID 27529062.
22. ↑ "Airborne prions make for 100 percent lethal whiff". Wired. 13 January 2011. https://www.wired.com/wiredscience/2011/01/airborne-prions-disease/. Retrieved 20 May 2011.
23. ↑ "The man who never slept: Michael Corke". World of Lucid Dreaming. http://www.world-of-lucid-dreaming.com/the-man-who-never-slept.html.
24. ↑ "Self management of fatal familial insomnia. Part 1: what is FFI?". MedGenMed 8 (3): 65. September 2006. PMID 17406188.
25. ↑ "Fatal familial insomnia: Everything you need to know" (in en). 14 April 2020. https://www.medicalnewstoday.com/articles/fatal-familial-insomnia.
26. ↑ 26.0 26.1 "Self management of fatal familial insomnia. Part 1: what is FFI?". MedGenMed 8 (3): 65. September 2006. PMID 17406188.
27. ↑ "Familial and sporadic fatal insomnia". The Lancet. Neurology 2 (3): 167–176. March 2003. doi:10.1016/S1474-4422(03)00323-5. PMID 12849238.
28. ↑ "A subtype of sporadic prion disease mimicking fatal familial insomnia". Neurology 52 (9): 1757–1763. June 1999. doi:10.1016/S0304-4858(07)74572-9. PMID 10371520.
29. ↑ 29.0 29.1 29.2 "The first case of fatal familial insomnia (FFI) in the Netherlands: a patient from Egyptian descent with concurrent four repeat tau deposits". Neuropathology and Applied Neurobiology 37 (5): 549–553. August 2011. doi:10.1111/j.1365-2990.2010.01126.x. PMID 20874730.
30. ↑ "Sporadic fatal insomnia masquerading as a paraneoplastic cerebellar syndrome". Archives of Neurology 65 (7): 971–973. July 2008. doi:10.1001/archneur.65.7.971. PMID 18625868.
31. ↑ "Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report". BMC Neurology 11. October 2011. doi:10.1186/1471-2377-11-136. PMID 22040318.
32. ↑ "A review of drug therapy for sporadic fatal insomnia". Prion 11 (5): 293–299. September 2017. doi:10.1080/19336896.2017.1368937. PMID 28976233.
33. ↑ 33.0 33.1 "Self-management of fatal familial insomnia. Part 2: case report". MedGenMed 8 (3): 66. September 2006. PMID 17406189.
34. ↑ Lugaresi, E.; Medori, R.; Montagna, P.; Baruzzi, A.; Cortelli, P.; Lugaresi, A.; Tinuper, P.; Zucconi, M. et al. (1986-10-16). "Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei". The New England Journal of Medicine 315 (16): 997–1003. doi:10.1056/NEJM198610163151605. ISSN 0028-4793. PMID 3762620.
35. ↑ Medori, R.; Tritschler, H. J.; LeBlanc, A.; Villare, F.; Manetto, V.; Chen, H. Y.; Xue, R.; Leal, S. et al. (1992-02-13). "Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene". The New England Journal of Medicine 326 (7): 444–449. doi:10.1056/NEJM199202133260704. ISSN 0028-4793. PMID 1346338.
36. ↑ "Preventive study in subjects at risk of fatal familial insomnia: Innovative approach to rare diseases". Prion 9 (2): 75–79. 21 May 2015. doi:10.1080/19336896.2015.1027857. PMID 25996399.
37. ↑ "Spontaneous generation of prion infectivity in fatal familial insomnia knockin mice". Neuron 63 (4): 438–450. August 2009. doi:10.1016/j.neuron.2009.07.026. PMID 19709627.
38. ↑ "One Couple's Tireless Crusade to Stop a Genetic Killer". Wired. 15 January 2019. https://www.wired.com/story/sleep-no-more-crusade-genetic-killer/.
39. ↑ "Driving at Night in the Fog: Sonia Vallabh and Eric Minikel's Unique Path to a Cure for Prion Disease" (in en). https://www.massgeneral.org/neurology/news/vallabh-minikel-path-to-cure-for-prion-disease.
40. ↑ "Sonia Vallabh" (in en). 2015-08-20. https://www.broadinstitute.org/bios/sonia-vallabh. [self-published source?]
41. ↑ "Prion Alliance". http://www.prionalliance.org/. [self-published source?]

## External links

Classification|

* ICD-11: 8E02.2
* ICD-10-CM: A81.83
* ICD-9-CM: 046.72
* OMIM: 600072
* MeSH: D034062
* DiseasesDB: 32177

|

* "AFIFF Fatal Familial Insomnia Families Association". http://www.afiff.net/.

Template:Prion diseases

0.00

(0 votes)

Original source: https://en.wikipedia.org/wiki/Fatal insomnia. Read more

|

Retrieved from "https://handwiki.org/wiki/index.php?title=Medicine:Fatal_insomnia&oldid=4017826"