Talk:Fatal insomnia

Sorry if this sounds stupid, but couldn’t a person help to cure fatal familial insomnia by getting nightly injections of a sedative?- EKN

I understand that these drugs have no effect as the mechanism in the brain that they act on is what is malfunctioning. I'll see if I can find some more and add it to the article... Dan100 (Talk) 20:43, 16 March 2006 (UTC)Reply

I couldn't, but I gave the article a tidy up anyway. Dan100 (Talk) 07:31, 17 March 2006 (UTC)Reply

Thanks Dan. This is very peculiar. So there is no way of "putting them to sleep"?- EKN 19 March 2006

What about inducing a coma? - moon octopus

I'm wondering about that too. EKN 14:26, 5 April 2006 (UTC)EKNReply

As far as I've been able to tell, inducing a coma wouldn't have any effect at all on the health of the patient, because the disease would continue to advance regardless of their state of consciousness. Sedatives wouldn't work, either, because the patient is not in a state of full consciousness once the disease sets in, anyway, and the action of the prions on the brain matter produces much, much more action on the vital parts of the brain than any sedative could hope to do by shifting dopamine or serotonin or melatonin around. The thing is, the sufferers of this disease aren't simply casual insomniacs; they can't sleep at all, so they slowly degenerate into a semi-conscious, disabled stupor, until they die after the prions destroy enough of their brains. The MSNBC piece on this really explains it well. The link is in the article. Avalyn 08:43, 26 April 2006 (UTC)Reply

The way I read it, the protein anomaly is what causes the health deterioration and eventual death. You could probably put them in a coma with barbs or something, and that might improve quality of life until the plaque buildup starts to cause noticeable health deterioration, but it wouldn't affect the progression. Successful treatment would require gene therapy, a way to remove the plaques or a way to replace the anomalous protein with functional protein. Zuiram 18:44, 23 April 2007 (UTC)Reply

The phrase "death is inevitable" seems highly unencyclopedic to me--this is a tautology! Death is inevitable with or without this condition. Perhaps this should be rephrase to reflect the intended meaning. 128.237.245.71 12:05, 13 May 2006 (UTC)Reply

Would "the disease invariably leads to death within 7-36 months" be better? Zuiram 18:44, 23 April 2007 (UTC)Reply

Wouldn't putting them in a coma every night at least relieve the tiredness even if it doesn't stop the disease? —Preceding unsigned comment added by 69.180.75.74 (talk) 07:21, 7 October 2007 (UTC)Reply

You are confusing sleep with coma/unconsiousness. Sleep is a biologically planned event, in which the brain and body carry out certain functions. Neither coma nor unonsiousness are equvivalent. 129.118.38.198 (talk) 20:18, 26 March 2009 (UTC)Reply

Systemic enzymes could be a possible answer.TwoHotMinutes (talk) 18:15, 21 September 2008 (UTC)Reply

The first time I heard of this disease was on a news show (either 20/20 or 60 minutes). On the show, they said that when doctors tried to sedate the patients or give them sleeping pills, it only made matter worse, and the disease progressed more rapidly. I don't know the exact source of this information, but it's worth looking into, I guess Shu ster (talk) 22:12, 16 January 2009 (UTC)Reply

The main article said "The gene responsible is carried in just 28 families worldwide". I moved this statement here so we could talk about it. At first glance, it sounds like an impossible claim to support, as no one has analyzed the genes for all families worldwide, nor is there any statement about how the families are counted. I suspect the statement is a misinterpretation of something much more nuanced from the medical literature, but I was unable to find the original. I would like to hear what other peopel think. --Zippy 05:58, 5 June 2006 (UTC)Reply

Agreed. Perhaps: "The gene responisble has been identified in only 28 families worldwide."

I just heard on NPR today that it has been documented in 40 families worldwide, and estimates based on genetics put the total number somewhere about 200. However, I am hesitant to put this in because I am not sure that 40 was an exact number ('though I believe it was). --Azsymkamen 19:40, 18 November 2006

An unfounded speculative remedy might be meditation which I'm told reduces ther meditator's need for sleep.

The lack of sleep is not what causes death. Zuiram 18:45, 23 April 2007 (UTC)Reply

Think of a prion as a tightly coiled spring. What happens is the disease causes the "coil" to unravel. There is no way to reverse the uncoiling/straightening out of the protein. Once the protein is "uncoiled" there is no way to fix it. As the condition progresses, more and more unraveling occurs, and eventually causes death. Since this is not a virus or a bacteria, is difficult next to impossible to destroy. In the prion disease that causes mad cow, the brain matter of an infected animal, even if incinerated, can still cause infection if circulated back into the food source. I hope this helps explain why this disease is not treatable. —Preceding unsigned comment added by 68.104.188.59 (talk) 22:53, 28 May 2010 (UTC)Reply

There are families in Canada with this illness. Canada is not mentioned above. — Preceding unsigned comment added by 207.61.86.5 (talk) 19:29, 13 April 2017 (UTC)Reply

The msnbc report (http://www.msnbc.msn.com/id/6822468/) says that-"The Roiters’ extended family has formed an association to help find a cure, and raise the money for research."-is there any other information about this association as i can't find anything, anywhere.

--Frills 04:51, 15 August 2006 (UTC)Reply

The official website is http://www.afiff.net It is also the only website involving the FATAL FAMILIAL INSOMNIA FAMILIES ASSOCIATION - PRION DISEASES, that I can find. I'll get back to you if I find anymore.

"There are other diseases hello involving the mammalian prion."

- This sentence is nonsensical -- there is no such thing as "the mammalian prion." -- 201.51.236.252 11:59, 7 November 2006 (UTC)Reply

It would seem to be the group of proteins synthesized to eventually become Silver-staining amyloid plaques, whatever the cause. This protein is probably different in different mammals and organs, and it often localizes copper. Perhaps that shouldn't be a wonder, because Copper and Silver are in the same group. Brewhaha@edmc.net 08:41, 8 May 2007 (UTC)Reply

"Some are transmissible (TSEs) such as kuru, bovine spongiform encephalopathy (BSE, also known as "mad cow disease") in cows, and chronic wasting disease in American deer and American elk (in some areas of the Rocky Mountains). Some forms of congestive heart failure are also believed to be caused by variant prion, as well as Creutzfeldt-Jakob disease (CJD). These are generally not considered to be transmissible, except by direct contact with infected tissue, such as cannibalism, transfusion or transplantation."

- This is irrelevant to sleep deprivation and should be deleted. -- 201.51.236.252 11:59, 7 November 2006 (UTC)Reply

If amyloidosis is a symptom common to several diseases, one of them jenetic, and we can prevent the symptom, then maybe that will lead to finding and preventing the cause. That should lead to sleep. Hmmm. I want to hear "Flypaper" by Kaos, again. I think I might've conversed with Kaos. Brewhaha@edmc.net 08:41, 8 May 2007 (UTC)Reply

If this is a dominent trait couldn't the possibility be there for 100% inheritance. Look at this. Say someone had parents each with one of the dominant genes (Pp and Pp) and their child had two of the genes (PP). All of their gammetes would contain the dominant gene thus making it impossible for the offspring not to inherit the gene.

The chances of both parents having the defective alleles are astronomical and even then there would only be a 25% chance of having offspring with a PP genotype. If this person went on to breed then yes there would be 100% inheritance but I presume that the onset would be far earlier and more rapid than in the heterozygous individual reducing their chances of having children. Those are my thoughts anyway. --Meridius 23:25, 5 February 2007 (UTC)Reply

That makes sense to me, but I didn't formally take Jenetiks. Brewhaha@edmc.net 08:48, 8 May 2007 (UTC)Reply

This one - http://www.afiff.net

I went there just now, and it has a "Hacked by / y@kışıkLı® / CAPRAZ ATES TEAM" message. If this is not reversed, then the external link to it will be useless, and should be removed. 81.153.110.46 (talk) 16:02, 20 January 2008 (UTC)Reply

Well, it still appears to be, so I deleted the link. dcd139 (talk) 01:47, 29 January 2008 (UTC)Reply

What a shame, I really wanted to do some research on the disease. Whomever is maintaining that website should wake up. —Preceding unsigned comment added by 71.59.140.95 (talk) 04:20, 25 February 2008 (UTC)Reply

Better news now: the site has recovered and seems to be operating normally again, so I've re-added it to the external links. Loganberry (Talk) 04:36, 6 March 2008 (UTC)Reply

CJD is a TCE, so this should be edited to reflect that. Snellios (talk) 19:23, 13 April 2008 (UTC)Reply

I put 'prion' with an internal link in the beginning Snellios (talk) 18:29, 4 May 2008 (UTC)Reply

"Some forms of congestive heart failure are also believed to be caused by variant prion" - really? I don't think I've ever come across this in any of the literature. If it doesn't get a citation I'm going to remove it. Snellios (talk) 18:28, 4 May 2008 (UTC)Reply

I think this comes from the history of one of the families with this disease. A lot of them died of what was thought to be congestive heart failure, but was probably/could have been FFI instead. That would have to be confirmed... i heard it somewhere a while ago... 58.108.18.123 (talk) 13:51, 7 May 2008 (UTC)Reply

"These are generally not considered to be transmissible, except by direct contact with infected tissue, such as from eating infected tissue, transfusion or transplantation."

All prion diseases are experimentally transmissable, what this sentence should say is that they are not considered an infectious biological agent. Snellios (talk) 16:56, 9 May 2008 (UTC)Reply

By the same "Turkish hackers" at yakisikli@caprazAtes.org

Take off the link and it won't be targeted.

Lunakeet 14:32, 19 May 2008 (UTC)Reply

in the presentation section the following appear,separated by 2 sentences: 'death usually occurs between 7 and 36 months of onset.' and 'the disease has 4 stages, taking from 7 to 18 months to run its course.'seems to me it's gotta be one or the other or something else, but not both.Toyokuni3 (talk) 02:48, 4 June 2008 (UTC)Reply

Complete inability to sleep is followed by rapid loss of weight. This lasts for about three months.

I am not familiar with this condition, and I suppose the number of people who truly are could be counted on three hands. I am, however, familiar with how much sleep deprivation a person can undergo before they die, and it's far less than three months. So I'm guessing that when this says "complete inability to sleep" it means complete inability to fall asleep normally, but with periods of passing out for short time intervals all throughout the day. The current world record for sleep deprivation is on the order of 280 hours, and much more than that is potentially fatal. --68.252.213.218 (talk) 05:50, 24 July 2008 (UTC)Reply

Can you cite evidence that anyone who did not suffer from FFI has ever died from sleep deprivation? bbi5291 (talk) 00:51, 25 July 2012 (UTC)Reply

Under the symptoms it said people with this syndrome crave Taco Bell. This is obviously a joke, so I removed it.

--68.44.13.238 (talk) 12:05, 4 February 2010 (UTC)Quba OsmanReply

How rare is this disease? Because I am scared of it. —Preceding unsigned comment added by 203.96.2.2 (talk) 12:06, 21 December 2010 (UTC)Reply

It is very rare. There is a gene-test to find out if someone is a carrier. But even if someone has the mutation, it does not mean person will get it 100% sure. Count yourself: 100 persons might have it of all the people of the world. It is more probable someone kills you with a car than you getting FFI. Sleep well.--RicHard-59 (talk) 04:40, 28 December 2010 (UTC)Reply

I was trying to find something about FFI & sleeping pills or sedatives but no luck.--RicHard-59 (talk) 04:44, 28 December 2010 (UTC)Reply

Sleeping pills only put you into a coma and accelerate (Spelling)your path towards death. :/ —Preceding unsigned comment added by 203.96.12.235 (talk) 08:55, 4 January 2011 (UTC)Reply

Seems that they can work to get sleep, more or less. You might take a look here: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1781306/#__sec16title --#Reaper (talk) 01:19, 2 December 2016 (UTC)Reply

The existence of this disease must have been disporven because the doctor in Fight Club said you couldnt die from insomnia. — Preceding unsigned comment added by 86.148.50.141 (talk) 01:44, 21 September 2011 (UTC)Reply

Heh. Looie496 (talk) 03:12, 21 September 2011 (UTC)Reply

Well, if the doctor in fight club said it, it must be right, right? Perhaps the film was...WRONG, because this disease certainly exists;)92.41.4.193 (talk) 16:38, 24 July 2012 (UTC)Reply

The article states multiple times that prolonged lack of sleep is eventually followed by death, but as a layman I feel like it's unclear on what specifically causes the afflicted to die. "Lack of sleep" is very vague as a description of the cause - precisely what physiological process occurs (or fails to occur) in the body or brain or a person who does not sleep that results in death? — Preceding unsigned comment added by 58.84.237.200 (talk) 13:57, 19 January 2012 (UTC)Reply

Usually due to a secondary infection, or respiratory failure. It's not true that you're dying of lack of sleep, you're dying of brain/CNS degeneration of which a secondary side effect is that you cannot sleep. This isn't a great analogy, but someone that has Alzheimers doesn't die because they can't remember things

they die because their brain is calcifying, which also causes them not to remember things. 96.18.20.181 (talk) 08:11, 14 May 2012 (UTC)Reply

This is not true at all. NREM is the most important for health, and avoiding REM sleep has been linked to improvement of health. You treat depression by avoiding REM sleep. Polyphasic sleep is based on avoiding REM sleep. Melatonin supplementation promotes NREM sleep and reduces REM sleep. During REM phase, stress hormones are released, they are more of a shock for the body. That's why by practicing polyphasic sleep, people can avoid REM phase, nightmares (vivid dreams) and stay healthier.

Grammar And Sentence Structure

Some of the sentences in this article are slightly lengthy, and could be broken down making the article easier to understand for the reader. Specifically the opening statement. Wilson0624 (talk) 18:48, 4 March 2014 (UTC)Reply

Is there any more information available on SFI?

"Gene therapy has been unsuccessful thus far"

An overall lack of sleep is the cause of death? Or the exact reasons are... We need to find more information on this interesting topic!! Doing this for a class has been difficult, but I want to find more information!

76.84.119.31 (talk) 04:46, 5 March 2014 (UTC)Reply

sFI

An article in Livescience: Teen Boy Is Youngest to Have Rare Fatal Brain Disorder dated feb 2014, is he tenth known case of sFI?--RicHard-59 (talk) 15:05, 10 May 2014 (UTC)Reply

As someone reading this article without special knowledge of biological functions, I found it quite difficult to follow along with some of the terminology. After reading the page I understand that simplifying information about prions and chromosomes and their role in FFI is not easy, but it would make the page much more interesting and beneficial to an average reader!

Csmith2017 (talk) 07:56, 2 May 2014 (UTC)Reply

I want to applaud the edits that have been made to this article since I read it last. As a student studying sleeping and dreaming, I understand a lot of these terms, but somebody who may not know the terms could become confused, especially by the scientific sections such as the prion and the sleep stage sections. I am not by any means saying that it needs to be dumbed down, but maybe we could go back through and explain some of that in a more simplistic way, that could really make this article more accessible and understandable to the public.

Also, I think it would be helpful for more to be added into the Epidemiology section. The sentence structures look fantastic, but as mentioned before, more simplified detail could be helpful.

Sam.kazda04 (talk) 16:37, 9 May 2014 (UTC)Reply

The initial summary of the article dated the first documented case in 1765, found in an Italian man. The source seems iffy.

Later, under the Onset section, there's this line:

>The first case was reported in the Netherlands of a 57 year old man of Egyptian descent.

The source for that only says "scientific correspondence".

It may well be that the first definite case was the case in the Netherlands and the former is simply a suspicion, but either way, clarification needed!

I came to post the same question. The citation for the Netherlands case is simply given as 'scientific correspondence'. I would suggest that these correspondences be presented or the attribution of this as the 'first case' be removed. The Italian case also rests on shaky grounds: the citation links to a website that contains an excerpt from the book labeled in the citation discussing the 1765 case without mention of its primacy, and a YouTube video describing the Italian case as 'patient zero'.

I think better sources and citations would be helpful for both of these claims; if they cannot be provided a rewording might be in order. Bearnfæder (talk) 15:26, 12 October 2014 (UTC)Reply

This article appears to include two claims regarding first presentation:

• Lede: The first recorded case was an Italian man, who died in Venice in the year 1765.<ref name="The Family">[http://www.world-of-lucid-dreaming.com/fatal-familial-insomnia.html The Family That Couldn't Sleep].</ref>
• Presentation: The first case was reported in the Netherlands of a 57-year-old man of Egyptian descent.<ref name="Scientific Correspondence">Scientific Correspondence</ref> [...] The atrophy of the thalamus is one of the most common signs of fatal familial insomnia.<ref name="Scientific Correspondence"/><ref>Jansen, C. C., Parchi, P. P., Jelles, B. B., Gouw, A. A., Beunders, G. G., van Spaendonk, R. L., & ... Rozemuller, A. M. (2011). The first case of fatal familial insomnia (FFI) in the Netherlands: a patient of Egyptian descent with concurrent four repeat tau deposits. Neuropathology & Applied Neurobiology, 37(5), 549–553. doi:10.1111/j.1365-2990.2010.01126.x</ref>

Several problems exist here. The key one is that the "Scientific Correspondence" references go nowhere, and therefore are uselessly unverifiable unless someone can expand them. Another is that the two claims appear to contradict each other on first reading; however, the second one might be implying, not that the Netherlands case was the first recorded case of FFI, but that this subject was the first case to be recorded in the Netherlands. If someone can confirm the latter to be true (I don't have access to the cited journal), then this can be clarified by changing the opening of the sentence in the Presentation section to something like, "The first case of FFI to be reported in the Netherlands was a 57-year-old man of Egyptian descent." —KGF0 ( T | C ) 22:07, 22 June 2015 (UTC)Reply

This is also the first thing I've noticed..if as Kgf0 says the Egyptian man was just the first case in the Netherlands, then I don't even know that it would be worth even mentioning in the article. If there are two competing claims about the first case, then this is something which needs to be resolved. — Preceding unsigned comment added by Chilltherevolutionist (talk • contribs) 07:44, 28 June 2015 (UTC)Reply

While I don't have any sources, I do recall some information from a documentary I watched years ago. From my recollection, an Italian man with the disease came forward (possible "Silvano" mentioned in the wiki article). Using church records, they were able to trace the disorder several generations back in his family. This may be why the first "reported" case was in Netherlands in the 20th century, while the first "recorded" case was much earlier (recorded in church records, but not reported to the world / medical community).

A google search (silvano fatal insomnia) gives me this article/transcript from Dateline NBC. This seems to match what I describe, but it doesn't list year of first death. This article, about the same family, lists the first recorded death (in this particular family) as "a man named Giacomo, who died ... near Venice ... in 1836". Here is an article by NY Times confirming the same name/location/year. This NPR story about this family states that they could "trace the disease back to the 1760s" in this family. This Telegraph article confirms this. This ABC article goes further, stating: "Researchers believe a wealthy Italian doctor unknowingly carried the original genetic mutation for FFI, 250 years ago. We don't know his name, but experts simply refer to him as Patient Zero — the first known case of the disease. By the time he died in 1765, he had passed the disease on to his children, and the curse had begun."

I don't really know much about this, except small recollections of a documentary I watched a decade ago. But a quick google search gives plenty of news articles, which aren't as good as medical journals, but better than blogs. Cheers, 15zulu (talk) —Preceding undated comment added 02:14, 24 September 2015 (UTC)Reply

Can someone expand/explain what source 5 is? Using page version 678814086. Thanks, 15zulu (talk) 00:54, 8 October 2015 (UTC)Reply

Good question. It was added by Wilson0624 in April 2014. That editor hasn't made any edits since then, so it's unlikely they will be back to explain. Since this fails Wikipedia's requirement for verifiability, and medical sources, the reference and any contentious content only supported by it should be removed. Grayfell (talk) 01:54, 8 October 2015 (UTC)Reply

@Grayfell: actually the diff you found is the answer. Apparently Wilson0624 was incorrectly using WP:CITESHORT. In short, <ref>Scientific Correspondence</ref> refers to <ref>Jansen, C. C., Parchi ...</ref>. Doing a google search, got me the article, which happens to be in a section titled "Scientific Correspondence". Wilson0624 does two more unique short cites: <ref>Journal of Sleep Research</ref> and <ref>Gambetti and Lugaresi 1998</ref>. I assume the "Journal of Sleep Research" refers to <ref>Cortelli, Gambetti, Montagna, ...</ref> but that doesn't make sense for "Gambetti and Lugaresi 1998" since that's only the second & fourth author and a different year. Joyful mess. Cheers, 15zulu (talk) 08:59, 10 October 2015 (UTC)Reply

Oh! I see. Good catch. I guess that explains why "Scientific Correspondence" is capitalized. I've removed the refs and replaced them with "Jansen et al." as that appears to have been the intention. Right? Grayfell (talk) 09:23, 10 October 2015 (UTC)Reply

Yeah, that's what I think s/he wanted. I've expanded & wikified the ref. Thanks for the help. 15zulu (talk) 05:45, 18 October 2015 (UTC)Reply

The 'cause' section only says that the disease is caused by a certain mutation. It doesn't say how that mutation causes the symptoms. I think that information should be added. — Preceding unsigned comment added by ChengduTeacher (talk • contribs) 11:43, 23 September 2018 (UTC)Reply

I added the explanation that seems to be the most cited, but there might be more to the disease. No study seems to mention an exact neurological explanation.

--James Az. H (talk) 00:21, 2 November 2019 (UTC)Reply

“Fatal familial insomnia (FFI) is a prion disease of the brain.[1] It is usually caused by a mutation to the gene encoding protein PrPC.[2] It has two forms: fatal familial insomnia (FFI), which is autosomal dominant and sporadic fatal insomnia (sFI) which is due to a noninherited mutation.”

These sentences are confused. Per the Merck citation in [2], FFI is genetic, whereas sFI is a non-genetic prion disease. But these sentences seem to be saying that FFI and sFI are two forms of…FFI? And that FFI is always a prion disease, whereas sFI is apparently the prion-caused syndrome and FFI is genetic but not prion. Foijsdf (talk) 13:15, 8 March 2022 (UTC)Reply

  This article was the subject of a Wiki Education Foundation-supported course assignment, between 16 August 2022 and 9 December 2022. Further details are available on the course page. Student editor(s): MeadorBriannaM (article contribs).

— Assignment last updated by MeadorBriannaM (talk) 18:52, 6 October 2022 (UTC)Reply