||It has been suggested that this article be merged into Wernicke–Korsakoff syndrome. (Discuss) Proposed since August 2013.|
|Classification and external resources|
|Patient UK||Korsakoff's syndrome|
Korsakoff's syndrome (also called Korsakoff's dementia, Korsakoff's psychosis, or amnesic-confabulatory syndrome) is a manifestation of Wernicke's encephalopathy, also called Wernicke´s disease. It happens in Wernicke's disease in almost all alcohol abusers. Is rare among the other patients, for example, some cases after bariatric surgeries were observed when not prevented by nutritional supplements. This neurological disorder is caused by a lack of thiamine (vitamin B1) in the brain, and is also added by neurotoxic effects of alcohol. When Wernicke's encephalopathy accompanies Korsakoff's syndrome, the combination is called the Wernicke-Korsakoff syndrome. Korsakoff's is a continuum of Wernicke's encephalopathy or disease, though a recognized episode of Wernicke's is not always obvious. The syndrome is named after Sergei Korsakoff, a Russian neuropsychiatrist who discovered the syndrome during the late 19th century.
Signs and symptoms
There are six major symptoms of Korsakoff's syndrome:
- anterograde amnesia
- retrograde amnesia, severe memory loss
- confabulation, that is, invented memories which are then taken as true due to gaps in memory sometimes associated with blackouts
- minimal content in conversation
- lack of insight
- apathy - the patients lose interest in things quickly and generally appear indifferent to change.
Thiamine is essential for the carboxylation of pyruvate and deficiency during this metabolic process is thought to cause damage to the medial thalamus and mammillary bodies of the posterior hypothalamus as well as generalized cerebral atrophy. These brain regions are all parts of the limbic system, which is heavily involved in emotion and memory.
Korsakoff's involves neuronal loss, that is, damage to neurons; gliosis which is a result of damage to supporting cells of the central nervous system, and hemorrhage or bleeding also in mammillary bodies. Damage to the dorsomedial nucleus or anterior group of the thalamus (limbic-specific nuclei) is also associated with this disorder. Cortical dysfunction may have arisen from thiamine deficiency, alcohol neurotoxicity, and/ or structural damage in the diencephalon.
Originally it was thought that a lack of initiative and a flat affect were important characteristics of emotion. Studies have questioned this, proposing that it is not necessarily a symptom of Korsakoff’s. Research suggesting that Korsakoff patients are emotionally unimpaired has made this a controversial topic. It can be argued that apathy, which usually characterizes Korsakoff patients, reflects a deficit of emotional expressions, without affecting the experience or perception of emotion.
Korsakoff's Syndrome causes deficits in declarative memory in most patients, but keeps implicit spatial, verbal, and procedural memory functioning intact. People who have Korsakoff’s syndrome have deficits in the processing of contextual information. Context memories refers to the where and when of experiences and is an essential part of recollection. The ability to store and retrieve this information, such as spatial location or temporal order information is impaired. Research has also suggested that Korsakoff patients have impaired executive functions, which can lead to behavioral problems and interfere with daily activities. It is unclear however, which executive functions are affected most. However, IQ is usually not affected by the brain damage associated with Korsakoff's syndrome.
At first it was thought that Korsakoff patients used confabulation to fill in memory gaps. However, it has been found that confabulation and amnesia do not necessarily co-occur. Studies have shown that there is dissociation between provoked confabulation, spontaneous confabulation (which is unprovoked) and false memories. That is, patients could be led to believe certain things that haven’t happened, just like people without Korsakoff’s syndrome.
Conditions resulting in the vitamin deficiency and its effects include chronic alcoholism and severe malnutrition. Alcoholism may be an indicator of poor nutrition, which in addition to inflammation of the stomach lining, causes thiamine deficiency. Other causes include dietary deficiencies, prolonged vomiting, eating disorders, or the effects of chemotherapy. It can also occur in pregnant women who have a form of extreme morning sickness known as hyperemesis gravidarum. Mercury poisoning can also lead to Korsakoff's syndrome. It has also been caused by centipede (mukade) bites in Japan. Though not always, this disorder frequently can emerge as a consequential result of Wernicke’s encephalopathy.
PET scans show that there is a decrease of glucose metabolism in the frontal, parietal and cingulated regions of the brain in Korsakoff patients. This may contribute to memory loss / amnesia. Structural neuroimaging has also shown the presence of midline diencephalic lesions and cortical atrophy.
Structural lesions of the central nervous system, though rare, can also contribute to symptoms of Korsakoff’s syndrome. Severe damage to the medial dorsal nucleus inevitably results in memory deficit. Additionally, autopsies of patients with Korsakoff have showed lesions in both the midline and anterior thalamus and thalamic infarctions. Bilateral infarctions to the thalamus can result in Korsakoff-induced amnesia as well. These findings imply damage to anterior thalamic nuclei can result in disruptive memory.
A number of factors may increase a person's risk to develop Korsakoff's syndrome. These factors are often related to patients' general health and their food intake habits.
- Extreme dieting
- Genetic factors
The prevalence varies from country to country, but is estimated to be around 12,5% of the heavy drinkers.
It was once assumed that anyone suffering from Korsakoff's syndrome would eventually need full-time care. This is still often the case, but rehabilitation can help regain some, often limited, level of independence. Treatment involves the replacement or supplementation of thiamine by intravenous (IV) or intramuscular (IM) injection, together with proper nutrition and hydration. However, the amnesia and brain damage caused by the disease does not always respond to thiamine replacement therapy. In some cases, drug therapy is recommended. Treatment of the patient requires taking thiamine orally for 3 to 12 months, though only about 20 percent of the cases are reversible. If treatment is successful, improvement will become apparent within two years although recovery is slow and often incomplete.
As an immediate form of treatment, a pairing of IV or IM with a high concentration of B-complex vitamins can be administered three times daily for period of 2–3 days. In most cases, an effective response from patients will be observed. A dose of 1 gram of thiamine can also be administered to achieve a clinical response. In patients who are seriously malnourished, the sudden availability of glucose without proper bodily levels of thiamine to metabolize is thought to cause damage to cells. Thus the administration of thiamine along with an intravenous form of glucose is often good practice.
Treatment for the memory aspect of Korsakoff’s syndrome can also include domain-specific learning, which when used for rehabilitation is called the method of vanishing cues. Such treatments aim to use patients’ intact memory processes as the basis for rehabilitation. Patients who used the method of vanishing cues in therapy were found to learn and retain information more easily.
People diagnosed with Korsakoff’s are reported to have a normal life expectancy presuming that they abstain from alcohol. Empirical research has suggested that good health practices have beneficial effects.
The most effective method of preventing Korsakoff's syndrome is to avoid B vitamin/thiamine deficiency. In Western nations, the most common causes of such a deficiency are alcoholism and weight disorders. Because these are behavioral-induced causes, Korsakoff syndrome is essentially considered a preventable disease. Thus, fortifying foods with thiamine, or requiring companies that sell alcoholic beverages to supplement them with B vitamin/thiamine would avert many cases of Korsakoff's Syndrome. 
In a case of a non-alcoholic 63-year old man with severe right hippocampal hemorrhaging, neuropsychological assessments showed that he displayed severe anterograde amnesia, loss of recall, impaired recognition, and overall disorientation. He knew his birthday and could recall genuine memories of his childhood, but consistently asked about his parents who had died 25 years ago. Thalamic damage is thought to have been the trigger for the amnestic syndrome.
- Alcoholic dementia
- Wernicke–Korsakoff syndrome
- Wernicke's encephalopathy
- Kolb, Bryan; Whishaw, Ian Q. (2003). Fundamentals of human neuropsychology. New York: Worth Publishers. p. 473. ISBN 978-0-7167-5300-1. OCLC 55617319.
- Paller, K. A.; Acharya, A.; Richardson, Brian C.; Plaisant, Odile; Shimamura, Arthur P.; Reed, Bruce R.; Jagust, William J. (1997). "Functional neuroimaging of cortical dysfunction in alcoholic Korsakoff's syndrome". Journal of Cognitive Neuroscience 9 (2): 277–293. doi:10.1162/jocn.19220.127.116.117.
- Doulas, J.; Wilkinson, D. A. (1993). "Evidence of normal emotional responsiveness in alcoholic Korsakoff's syndrome in the presence of profound memory impairment". Addiction 88 (12): 1637–1645. doi:10.1111/j.1360-0443.1993.tb02038.x. PMID 8130702.
- Kessels, Roy P. C.; Kortrijk, Hans E.; Wester, Arie J.; Nys, Gudrun M. S. (1 April 2008). "Confabulation behavior and false memories in Korsakoff's syndrome: Role of source memory and executive functioning". Psychiatry and Clinical Neurosciences 62 (2): 220–225. doi:10.1111/j.1440-1819.2008.01758.x. PMID 18412846.
- Oudman, Erik; Van Der Stigchel, Stefan; Wester, Arie J.; Kessels, Roy P.C.; Postma, Albert (2011). "Intact memory for implicit contextual information in Korsakoff's amnesia". Neuropsychologia 49 (10): 2848–2855. doi:10.1016/j.neuropsychologia.2011.06.010. PMID 21704050.
- Parkin, A. J., Montaldi, D., Leng, N. R., & Hunkin, N. M. (1999). Contextual cueing effects in the remote memory of alcoholic Korsakoff patients and normal subjects. The Quarterly Journal of Experimental Psychology, 42A, 585–596.
- Kessels, R. P. C.; Van Oort, R. (2009). "Executive dysfunction in Korsakoff's syndrome: time to revise the DSM criteria for alcohol-induced persisting amnestic disorder?". International Journal of Psychiatry in Clinical Practice 13 (1): 78–81. doi:10.1080/13651500802308290.
- Oscar-Berman, M. (Jun 2012). "Function and dysfunction of prefrontal brain circuitry in alcoholic Korsakoff's syndrome.". Neuropsychol Rev 22 (2): 154–69. doi:10.1007/s11065-012-9198-x. PMID 22538385.
- "What is Korsakoff’s syndrome?". Alzheimer's Society. October 2008.
- Jasmin, Luc (13 February 2008). "Wernicke-Korsakoff syndrome". MedlinePlus Medical Encyclopedia. United States National Library of Medicine. Retrieved 16 July 2009.
- ATSDR. 1999. Toxicological Profile for Mercury. Atlanta, GA:Agency for Toxic Substances and Disease Registry. http://www.atsdr.cdc.gov/toxprofiles/tp46.pdf
- Mohri S, Sugiyama A, Saito K, Nakajima H (March 1991). "Centipede bites in Japan". Cutis; Cutaneous Medicine for the Practitioner 47 (3): 189–90. PMID 2022129.
- Pitel, A. L., Zahr, N. M., Jackson, K., Sassoon, S. A., Rosenbloom, M. J., Pfefferbaum, A., & Sullivan, E. V. (2011). Signs of preclinical Wernicke’s encephalopathy and thiamine levels as predictors of neuropsychological deficits in alcoholism without Korsakoff’s syndrome. Neuropsychopharmacology, 36, 580–538
- Rahme, R; Moussa, R; Awada, A; Ibrahim, I; Ali, Y; Maarrawi, J; Rizk, T; Nohra, G; Okais, N; Samaha, E (April 2007). "Acute Korsakoff-like amnestic syndrome resulting from left thalamic infarction following a right hippocampal hemorrhage". AJNR. American journal of neuroradiology 28 (4): 759–60. PMID 17416834.
- Kopelman, MD; Thomson, AD; Guerrini, I; Marshall, EJ (Mar–Apr 2009). "The Korsakoff syndrome: clinical aspects, psychology and treatment". Alcohol and alcoholism (Oxford, Oxfordshire) 44 (2): 148–54. doi:10.1093/alcalc/agn118. PMID 19151162.
- Rosenblum, Laurie B. (Last reviewed March 2011). "Korsakoff's Syndrome". NYU Langone Medical Center. Retrieved February 12, 2012. Check date values in:
- Harper, C; Gold, J; Rodriguez, M; Perdices, M (1 February 1989). "The prevalence of the Wernicke-Korsakoff syndrome in Sydney, Australia: a prospective necropsy study". Journal of Neurology, Neurosurgery & Psychiatry 52 (2): 282–285. doi:10.1136/jnnp.52.2.282.
- Carlson, N. R. (2013). Physiology of behavior. Boston: Pearson. 547.
- Cook, CC (May–Jun 2000). "Prevention and treatment of Wernicke-Korsakoff syndrome". Alcohol and alcoholism (Oxford, Oxfordshire). Supplement 35 (1): 19–20. PMID 11304070.
- Komatsu, Shin-Ichi; Mimura, Masaru; Kato, Motoichiro; Wakamatsu, Naoki; Kashima, Haruo (1 March 2000). "Errorless and Effortful Processes Involved in the Learning of Face-name Associations by Patients with Alcoholic Korsakoff's Syndrome". Neuropsychological Rehabilitation 10 (2): 113–132. doi:10.1080/096020100389200.
- Harper, CG; Sheedy, DL; Lara, AI; Garrick, TM; Hilton, JM; Raisanen, J (Jun 1, 1998). "Prevalence of Wernicke-Korsakoff syndrome in Australia: has thiamine fortification made a difference?". The Medical journal of Australia 168 (11): 542–5. PMC 3391549. PMID 9640303.
- Centerwall, BS; Criqui, MH (1978). "Prevention of the Wernicke-Korsakoff syndrome: a cost-benefit analysis". New England Journal of Medicine 299: 285–9. PMID 96343.
- The Merck Manual: Function And Dysfunction Of The Cerebral Lobes - Amnesias - Korsakoff's syndrome
- An Amnesic Patient With An Extraordinary Distorted Memory
- Monitoring an acute case for twelve years.