Dyschronometria

Cerebellum
A human brain, with the cerebellum colored in purple
Drawing of the human brain, showing cerebellum and pons
Details
Part ofMetencephalon
ArterySCA, AICA, PICA
Veinsuperior, inferior
Identifiers
NeuroLex IDbirnlex_1489
Anatomical terms of neuroanatomy

Dyschronometria is a condition of cerebellar dysfunction in which an individual cannot accurately estimate the amount of time that has passed (i.e., distorted time perception). It is associated with cerebellar ataxia,[1][2] when the cerebellum has been damaged and does not function to its fullest ability. Lesions to the cerebellum can cause dyssynergia, dysmetria, dysdiadochokinesia, dysarthria, and ataxia of stance and gait.[3] Dyschronometria can result from autosomal dominant cerebellar ataxia (ADCA).[4]

Andreas Vesalius Fabrica, published in 1543, showing the base of the human brain, including optic chiasma, cerebellum, olfactory bulbs, etc.

Signs and symptoms

Common signs of dyschronometria are often generic to cerebellar ataxia, including a lack of spatial awareness, poor short term memory, and inability to keep track of time. The defining symptoms, while not completely understood, involve time perception. For example, when asked to wait for thirty seconds, or tap every second that has gone by, those affected will be able to perform the task for a short time and then become derailed. This can result from a loss of focus, however, more often than not the individual affected can no longer tell what they are doing and they become disoriented.[5] This often takes form in forgetting basic time keeping unless a timer is set, such as when cooking for example. Dyschronometria does not affect the 24-hour circadian rhythm, which is sustained by a different biological process.

Cross-section of human cerebellum, showing the dentate nucleus, as well as the pons and inferior olivary nucleus

Causes

The most common cause of cerebellar ataxia, and by extension dyschronometria, is cerebellar damage. This can be by form of a trauma, or by disease and genetics. Examples of trauma include a car accident, stroke, epilepsy, and head trauma.[6] These traumas are especially detrimental to children and the elderly due to decreased brain matter, increasing the risk that trauma may damage the cerebellum. This also explains why dyschronometria is seen more commonly in the elderly due to the deterioration of physical brain matter with age. Other probable causes for the deterioration of brain matter in the elderly include increased supranational activation, decreased cerebellar activation (which is consistent with fronto-cerebellar dissociation).[7]

Dyslexia

An interesting case of dyschronometria has to do with dyslexia. When dyslexia was studied within children, it was found that dyslexic children were often stressed as well as mentally exhausted. These children would place little to no importance on their present state, a behavior that would continue into adulthood.[8] It remains unclear as to whether dyslexia is a symptom of dyschronometria, a cause, or both.

Dementia

Dementia has a huge effect on dyschronometria and was one of the main sources of how dyschronometria was discovered. Through studies, dementia is both a cause and an effect of dyschronometria. This has to do completely with the fact that with dementia the brain is constantly rewiring itself and thus information becomes lost causing the person who has dementia to become confused as well as disoriented, and in most cases completely unaware of the passage of time. As a cause, dyschronometria causes the person to become disoriented and completely unaware of time, thus making bits and pieces of their brain involving a memory to become lost, ultimately leading to dementia in the long term. [9]

Errors and Inaccuracies

Diagnosing

Despite dyschronometria's easily recognizable symptoms, the fact that they may also be present in other cerebellar ataxias can make diagnosis difficult. Other ataxias may also have symptoms that affect gait, speech, thought process, spatial awareness, and time orientation used in their diagnoses, covering up the fact that most of these patients also have dyschronometria. The most common ataxias dyschronometria has been seen to be evident in are dyssynergia, dysmetria, dysdiadochokinesia, dysarthria as well as ataxias effecting stance and gait. Dyslexia can be another problem in those individuals affected by dyschronometria, however it is uncertain whether dyslexia is developed or worsened by having it, or if it is the opposite in that having dyslexia increases the chance of developing dyschronometria. Another problem that dyschronometria faces in detection is that it is a relatively new term for this side effect and precursor to dementia, compared with other cerebellar ataxias such as those mentioned above. Even when dyschronometria is detected, it has usually progressed to the point where it cannot be reversed, and there is no benefit in taking the testing medication to either slow down the dyschronometria or the process of dementia setting in, which is what dyschronometria is a signal for.

However the greatest error in diagnosing dyschronometria is that this cerebellar ataxia hides itself in its symptoms and signs. The signs seen in those diagnosed with dyschronometria are not obvious, and are often mistaken for other cerebellar ataxias or dementia by medical professionals. In addition, medical professionals usually expect to see circadian rhythm being disrupted by noting sleeping cycles and patterns that have no logical sense to them, which has nothing to do with dyschronometria. Other errors in diagnosing dyschronometria include the idea that those who have dyschronometria have a speech impediment, suffer from delusions bordering psychosis, impairment of long term memory, or the complete loss of conscious understanding of time. These misconceptions mostly stem from the fact that this cerebellar ataxia is rarely diagnosed without being seen in dementia or with another ataxia.[1]

Clinical testing

Testing and diagnosing for dyschronometria have also been shown to be ineffective. Dementia is caught so late despite the signals seeming obvious because psychological tests that try to catch signs of dementia, such as dyschronometria, are not very helpful. With these tests, the bell curves formed after statistical analysis and a wide range among normal test takers ensure that only patients that have extremely abnormal tests are given a positive diagnosis, and these cases are often already obvious to diagnose.[10] Diagnosis of dyschronometria is also difficult due to the lack of research and professional concentrating on this cerebellar ataxia. Neuroscientists are only just beginning to conduct more research into this lack of awareness and keeping of time. When the science and the tests are more specialized and dyschronometria has been researched at greater depth, the sensitivity of future tests conducted will likely yield more insights into the phenomenon.

Treatments

It has not been determined what role drugs may play in the treatment of cerebellar ataxia. In research done by Trouillas in Lyon, France, the pharmacology of cerebellar ataxia was examined by manipulating key components found at the nerve level within the cerebellum or the inferior Olive. This was done mostly through the modification of the GABA, dopamine, and serotonin receptors which did seem to show positive results in the primary stages of the experimentation. The clinical benefits presented in this study justifying the prescription of d-l-5-HTP or better with the l-5-HTP with benserazide to patients with certain cerebellar ataxias including that of dyschronometria. At the present as stated, this is the best indication for treatment of the cerebellar cortical atrophies. Even still, it is important to stress that the response to this treatment may be slow and irregular.[11]

Neuroplastic rehabilitation

Previously, neuroplasticity used as a rehabilitation method was considered as a potential treatment for dyschronometria. However these studies were not further developed since the 1980s. With current techniques and research from the neuroscience community, this is still a viable option not to eliminate cerebellar ataxia, but to slow its progress of development.[12]

References

  1. 1 2 Lagarde, J.; Hajjioui, A.; Yelnik, A. (2009). "Neuropsychological disorders induced by cerebellar damage". Annals of Physical and Rehabilitation Medicine. 52 (4): 360–370. doi:10.1016/j.rehab.2009.02.002. PMID 19874739.
  2. ↑ Ferrarin, M; Gironi, M; Mendozzi, L; Nemni, R; Mazzoleni, P; Rabuffetti, M (2005). "Procedure for the quantitative evaluation of motor disturbances in cerebellar ataxic patients". Med. Biol. Eng. Comput. 43 (3): 349–356. doi:10.1007/BF02345812. PMID 16035223. S2CID 1307431.
  3. ↑ Diener, HC; Dichgans, J (1992). "Pathophysiology of Cerebellar Ataxia". Movement Disorders. 7 (2): 95–109. doi:10.1002/mds.870070202. PMID 1584245. S2CID 19100385.
  4. ↑ Whaley, N.R.; Fujioka, S.; Wszolek, Z.K. (2011). "Autosomal dominant cerebellar ataxia type I: A review of the phenotypic and genotypic characteristics". Orphanet Journal of Rare Diseases. 6: 33. doi:10.1186/1750-1172-6-33. PMC 3123548. PMID 21619691.
  5. ↑ "Cerebellar ataxia". BBC News. 2004-11-30. Retrieved 2007-07-29.
  6. ↑ Tobe, E.H. (2012). "Behavioral Effects of Incomplete Temporal Lobe Necrosis and Cerebellar Damage". Biological Psychiatry. 71 (9): e41–2. doi:10.1016/j.biopsych.2012.01.005. PMID 22305977. S2CID 876527.
  7. ↑ Lapresle, J.; Metreau, R.; Annabi, A. (1977-05-13). "Transient achromatopsia in vertebrobasilar insufficiency". Journal of Neurology. 215 (2): 155–158. ISSN 0340-5354. PMID 68108.
  8. ↑ Bruno, J.E.; Maguire, S.R. (1993). "Perception and Allocation of time by dyslexic children". Perceptual and Motor Skills. 77 (2): 419–32. doi:10.2466/pms.1993.77.2.419. PMID 8247661. S2CID 21301291.
  9. ↑ Mochizuki, Hitoshi; Ugawa, Yoshikazu (November 2010). "[Cerebellar ataxic gait]". Brain and Nerve = Shinkei Kenkyu No Shinpo. 62 (11): 1203–1210. ISSN 1881-6096. PMID 21068457.
  10. ↑ Shibusawa, Nobuyuki; Hashimoto, Koshi; Yamada, Masanobu (2008). "Thyrotropin-releasing hormone (TRH) in the cerebellum". Cerebellum (London, England). 7 (1): 84–95. doi:10.1007/s12311-008-0033-0. ISSN 1473-4230. PMID 18418668.
  11. ↑ Trouillas, P. (September 1984). "Regression of cerebellar syndrome with long-term administration of 5-HTP or the combination 5-HTP-benserazide". Italian Journal of Neurological Sciences. 5 (3): 253–266. doi:10.1007/BF02043955. ISSN 0392-0461. PMID 6334064.
  12. ↑ Morgan, M. H. (1980). "Ataxia — its causes, measurement, and management". Disability and Rehabilitation. 2 (3): 126–132. doi:10.3109/09638288009163972. PMID 6110638.
This article is issued from Offline. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.