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Wernicke-Korsakoff syndrome

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Aditya Govindavarjhulla, M.B.B.S. [3]

Synonyms and keywords: Alcohol induced encephalopathy; transketolase defect; Korsakoff psychosis; alcoholic encephalopathy

Overview

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Aditya Govindavarjhulla, M.B.B.S. [3]

Overview

Wernicke-Korsakoff syndrome is a is a degenerative brain disorder cause by thiamine deficiency. This is usually secondary to alcohol abuse. Although Wernicke’s and Korsakoff’s may appear to be two different disorders, they are generally considered to be different stages of the same disorder, which is called Wernicke-Korsakoff syndrome(WKS). Wernicke’s encephalopathy represents the acute phase of the disorder, and Korsakoff’s amnesic syndrome represents the chronic phase.

Historical Perspective

The syndrome is a combined manifestation of two eponymous disorders, Korsakoff’s Psychosis and Wernicke’s encephalopathy, named for Drs. Sergei Korsakoff and Carl Wernicke.

Daignosis

MRI

MRI may show changes in the brain tissue – atrophy of mammilary body.

Treatment

Medical Therapy

Treatment consists of reversing the thiamine deficiency by giving supplemental thiamine, usually by starting with an initial intravenous or intramuscular dose followed by supplemental oral doses. It is important to start the thiamine treatment before giving any glucose as the encephalopathy will be worsened by the glucose. (Glucose administration promotes dehydrogenation of pyruvate, a biochemical reaction which consumes thiamine.) By the time amnesia and psychosis have occurred, complete recovery is unlikely.

Primary Prevention

Not drinking alcohol or drinking in moderation and getting enough nutrition reduce the risk of developing Wernicke-Korsakoff syndrome. Thiamine supplements and a good diet may reduce the chance of getting this condition, but do not eliminate the risk.

References

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Historical Perspective

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Aditya Govindavarjhulla, M.B.B.S. [3]

Overview

The syndrome is a combined manifestation of two eponymous disorders, Korsakoff’s Psychosis and Wernicke’s encephalopathy, named for Drs. Sergei Korsakoff and Carl Wernicke.

References

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Pathophysiology

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Aditya Govindavarjhulla, M.B.B.S. [3]

Pathophysiology

Wernicke-Korsakoff syndrome results from thiamin deficiency. It is generally agreed that Wernicke’s encephalpathy results from severe acute deficiency of thiamine (Vitamin B1), whilst Korsakoff’s psychosis results from chronic deficiency of thiamin. The metabolically active form of thiamine is thiamine diphosphate which plays a major role as a cofactor in glucose metabolism. The enzymes which are dependent on thiamin diphosphate are associated with the TCA Cycle and catalyse the oxidation of pyruvate,alphaketoglutarate and branched chain amino acids. Thus, anything that encourages glucose metabolism will exacerbate an existing clinical or sub-clinical thiamine deficiency. 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, though a recognised episode of Wernicke’s is not always obvious.

There is an unreplicated study that has associated susceptiblity to this syndrome with a hereditary deficiency of transketolase, an enzyme involved in thiamine metabolism.[1]

Gross Pathology

Wernicke-Korsakoff syndrome in alcoholics especially is associated with atrophy[2] of specific regions of the brain, especially the mamillary bodies. Other regions include the anterior region of the thalamus (accounting for amnesic symptoms), the medial dorsal thalamus, the basal forebrain, and median and dorsal raphe nuclei.[3]

Microscopic Pathology

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 in mammillary bodies. Damage to the dorsomedial nucleus of the thalamus is also associated with this disorder. Frequently, for unknown reasons, patients with Korsakoff’s psychosis will exhibit marked degeneration of the mamillary bodies. The mechanism of this degeneration is unknown, but it supports current neurological theory that the mamillary bodies play a role in various memory circuit within the brain. An example of a memory circuit is the Papez circuit.

References

  1. Nixon P, Kaczmarek M, Tate J, Kerr R, Price J (1984). “An erythrocyte transketolase isoenzyme pattern associated with the Wernicke-Korsakoff syndrome”. Eur J Clin Invest. 14 (4): 278–81. PMID 6434322.
  2. Kolb & Whishaw: Fundamentals of Human Neuropsychology, 2003, pages 473-473
  3. Mann K, Agartz I, Harper C, Shoaf S; et al. (2001). “Neuroimaging in alcoholism: ethanol and brain damage”. Alcohol Clin Exp Res. 25 (5 Suppl ISBRA): 104S–109S. PMID 11391058.

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Causes

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Aditya Govindavarjhulla, M.B.B.S. [3]

Causes

Common Causes

References

  1. Zimitat C, Nixon P, (2000). “Glucose loading precipitates encephalopathy in thiamine-deficient rats”. Metabolic Brain Disease. 14 (1): 1–10.

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Differentiating Wernicke-Korsakoff Syndrome from other Diseases
Epidemiology and Demographics

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Aditya Govindavarjhulla, M.B.B.S. [3]

Epidemiology and Demography

Prevalence

  • In France, a country with one of the highest per capita consumptions of alcohol, the prevalence of the WKS was found to be only 0.4% in a small retrospective autopsy study.[1]
  • Prevalence rates in Australia are highest 2.8%.[2]
  • Per capita consumption of alcohol is not corelating with the prevalence of the syndrome in many countries.[3]

Age

  • It is more common in middle aged persons.

Gender

  • It is more common in men.

References

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Risk Factors

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References

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Natural History, Complications and Prognosis

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Aditya Govindavarjhulla, M.B.B.S. [3]

Complications

Prognosis

  • Without treatment, Wernicke-Korsakoff syndrome gets steadily worse and can be life threatening.
  • With treatment, symptoms can be controlled (such as uncoordinated movement and vision difficulties) from getting worse.
  • Some symptoms, especially the loss of memory and thinking skills, may be permanent. Other disorders related to alcohol abuse may also occur.

References

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Diagnosis

Diagnosis

History and Symptoms | Physical Examination | Laboratory Findings | MRI | Other Imaging Findings | Other Diagnostic Studies

Treatment

Treatment

Medical Therapy | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies

Case Studies

Case Studies

Caes #1

de:Wernicke-Korsakow-Syndrom is:Wernicke-Korsakoff heilkenni nl:Syndroom van Wernicke sq:Sindroma Wernicke-Korsakoff


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