Tag Archives: sleep

Should we end Daylight Saving Time?

Who hasn’t looked at their clock early in the morning and wished for an extra hour in bed? Well, as of last week, daylight saving time has finally come to an end, which means an extra hour of sweet sleep. Many clocks around the world have officially been pushed back an hour, and some researchers want to keep it that way permanently.

Daylight saving time was first introduced during World War I to save energy, and since then it has been continued to be practised in many countries. Yet, the health effects linked with daylight saving have been unclear, until now. Recently, Beth Marlow and her team have reported that daylight saving may be doing us more harm than simply making us lose an hour of sleep.

The team analyzed multiple studies that looked at brain activity and the effects of daylight saving. They concluded that a person’s circadian rhythms are thrown off by the simple time change. The circadian rhythms are responsible for behavioural, physical, and mental changes in a person, which can be affected by both light and darkness. The disruption to the circadian rhythms can cause serious and deadly health effects. For instance, Marlow found that there was an increased number of strokes and heart attacks reported during the start of daylight saving time. In addition, the lack of sleep caused by daylight saving time has led to increase in fatal car crashes.

So, why do many nations still practise daylight saving time? Well, as mentioned before, daylight saving does save energy. As the US Department of Energy found, the energy saved is equivalent to more than 100,000 households energy use in a year. Therefore, the economics behind daylight saving is a major factor for keeping it.

As Marlow and her team have reported, daylight saving time has major impacts on the health of many individuals, and like many other researchers, they advocate the end of daylight saving time altogether. However, the energy saved during this time has outweighed decisions of ending it.

-Anum Khan

Fatal Familial Insomnia: Dying without sleep

Sleeping. Source: Flickr

What if one day you woke up and didn’t have the ability to fall back to sleep again? Unfortunately, this is the devastating reality for almost 50 families around the world today.

Fatal Familial insomnia (FFI) is a rare neurodegenerative disease caused by prions, which are abnormal forms of normally harmless proteins found in the brain. Since this mutation is dominant, in that one copy of this mutated gene can automatically lead to its expression, this disease affects both males and females equally. Furthermore, individuals with FFI normally present symptoms of this disease between the ages of 20 to 61 years old. These symptoms include an onset of dementia, speech problems, and coordination problems.

Dementia. Source: Flickr

 

The tragic family curse

Generation. Source: Flickr

FFI is a genetic disease, thus it is able to be passed on through generations. Fortunately, however, if one parent has this genetic mutation, there is only a 50% chance that it would be passed on to their offspring. Nonetheless, the following generations that receive this mutation eventually succumb to this disease without escape.

This inevitable disease causes death of neurons in the brain and the first symptoms are apparent at around the age of 50 and are followed by four symptomatic stages.

There are four stages that individuals with FFI encounter. The first stage is insomnia, which is followed by the second stage of hallucinations and severe panic attacks. The third stage is defined by weight loss and the total loss of the ability to sleep and lastly, the fourth stage is marked by dementia. Each of these stages are short as the rapid progression of FFI causes death within 12 to 18 months.

The main cause of death from this disease is due to progressive physical and mental deterioration, which is the consequence of one of the fatal symptoms of FFI, the inability to sleep.

 

Searching for a cure

FFI is a subtype of prion diseases which itself has no cure. Additionally, since FFI is a rare disease, it is still incurable as there has been limited research done on this disease. However, there are some potential treatments that are being examined today.

Currently, there is an ongoing 10-year trial being conducted on individuals that carry this genetic mutation. In this study they observe the effects of the antibiotic doxyclycline on pre-symptomatic patients, as researchers believe the use of this antibiotic may be an effective way to prevent FFI in individuals who carry this disease.

Sadly, effective long-term treatments for FFI are non-existent. Therefore, presently, short-term treatments are being used. One of these treatments include the used of sedatives, such as sleeping pills, which can temporarily help manage the symptoms of insomnia. However, its effectiveness varies from person to person.

Although FFI is a rare disease, it still affects families around the world today. Therefore, without a cure, this leaves families hopeless for their future ahead. However, with research currently being conducted, hopefully this can provide individuals with FFI a fighting chance to overcome this disease.

– Karina To