Wernicke-Korsakoff syndrome

Last updated: February 11, 2023

Wernicke-Korsakoff syndrome

FOUNDATIONS

FOUNDATIONS

Carbohydrates and sugars
Fats and lipids
Proteins
Amino acids and protein folding
Ionic bonding
Covalent bonding
Definitions of acids and bases
DNA damage and repair
DNA structure
Enzyme function
DNA replication
Translation of mRNA
Transcription of DNA
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
Gel electrophoresis and genetic testing
Nuclear structure
Atomic units and moles
Atoms and the periodic table
Gene regulation
Cellular structure and function
Selective permeability of the cell membrane
Cell membrane
Free radicals and cellular injury
Cell-cell junctions
Extracellular matrix
Endocytosis and exocytosis
Cytoskeleton and intracellular motility
Osmosis
Glycolysis
Electron transport chain and oxidative phosphorylation
Physiological changes during exercise
Citric acid cycle
Fatty acid synthesis
Ketone body metabolism
Fatty acid oxidation
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Lactose intolerance
Pyruvate dehydrogenase deficiency
Galactosemia
Hereditary fructose intolerance
Body fluid compartments
Movement of water between body compartments
Gluconeogenesis
Pentose phosphate pathway
Glycogen metabolism
Amino acid metabolism
Nitrogen and urea cycle
Cholesterol metabolism
Wernicke-Korsakoff syndrome
Beriberi
Folate (Vitamin B9) deficiency
Niacin (Vitamin B3) deficiency
Development of the axial skeleton
Development of the muscular system
Development of the limbs
Bone remodeling and repair
Fibrous, cartilage, and synovial joints
Cartilage structure and growth
Neuromuscular junction and motor unit
Slow twitch and fast twitch muscle fibers
Sliding filament model of muscle contraction
Muscle contraction
Purine and pyrimidine synthesis and metabolism disorders: Pathology review
Disorders of fatty acid metabolism: Pathology review
Disorders of carbohydrate metabolism: Pathology review
Lesch-Nyhan syndrome
Cell signaling pathways
Nucleotide metabolism
Protein structure and synthesis
Lac operon
Cell cycle
Mitosis and meiosis
DNA mutations
Resting membrane potential
Nernst equation
Orotic aciduria
Adenosine deaminase deficiency
Xeroderma pigmentosum
Li-Fraumeni syndrome
Bloom syndrome
Fanconi anemia
McCune-Albright syndrome
Acute radiation syndrome
ELISA (Enzyme-linked immunosorbent assay)
Karyotyping
DNA cloning
Fluorescence in situ hybridization

Transcript

Watch video only

Wernicke Korsakoff syndrome is named after Carl Wernicke and Sergei Korsakoff, the physicians who discovered the condition in the late 1800s. Wernicke Korsakoff syndrome is caused by Vitamin B1 or thiamine deficiency and it refers to a spectrum of disease. Wernicke's encephalopathy is the acute, reversible stage of the syndrome, and if left untreated it can later lead to Korsakoff syndrome, which is chronic and irreversible.

Thiamine is typically stored in the liver and absorbed in the jejunum and ileum, and then moves throughout the body, where it’s involved in numerous cellular processes that require thiamine. The enzyme thiamine pyrophosphate synthetase transfers a pyrophosphate group from ATP to thiamine, turning it into the coenzyme thiamine pyrophosphate - which is the metabolically active form of thiamine. Now, as a coenzyme, thiamine pyrophosphate functions to assist other enzymes such as pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, and transketolase carry out reactions, particularly regarding glucose metabolism. Furthermore, within the brain, thiamine pyrophosphate helps metabolize lipids and carbohydrates as well as maintain normal amino acid and neurotransmitter levels. In some neurons, thiamine even helps with propagation of a neural impulses down the axon.

Given it’s multifaceted role, a deficiency of thiamine can have serious consequences. Specifically, thiamine deficiency impairs glucose metabolism and this leads to a decrease in cellular energy. One of the major causes of thiamine deficiency, and therefore Wernicke Korsakoff syndrome, is alcohol abuse. Alcohol leads to decreased thiamine levels in various ways. First, alcohol interferes with the conversion of thiamine to its active form, thiamine pyrophosphate by blocking the phosphorylation of thiamine. Second, thiamine is normally absorbed through the first portion of the small intestine called the duodenum. However, ethanol prevents this absorption process, and it is believed that alcohol does this by reducing the gene expression for thiamine transporter-1 within the intestinal brush border. Third, chronic alcohol abuse can lead to fatty liver or cirrhosis which interferes with the storage of thiamine within the liver. Other causes of thiamine deficiency are inadequate intake like in malnutrition and anorexia or due to malabsorption like in stomach cancer and inflammatory bowel disease.

The brain is particularly vulnerable to impaired glucose metabolism since it utilizes so much energy. Early on in thiamine deficiency, the cerebellum gets affected and that can affect movement and balance. In addition, the brainstem can be affected, and that’s the region that gives rise to the cranial nerves that provide motor and sensory innervation to the face and eyes. If the medulla region of the brainstem is affected, it can impair the heart rate and breathing. Later findings in thiamine deficiency are hemorrhage and necrosis of the mammillary bodies. The mammillary bodies are two small round structures located under the brain and are part of the limbic system which is responsible for memory, emotion, and behavior.

Now Wernicke Korsakoff syndrome can be thought of as a spectrum of disorders: Wernicke's encephalopathy symptoms occur first, and can eventually develop into the more severe symptoms found in Korsakoff syndrome. Wernicke's encephalopathy is characterized by ophthalmoplegia, meaning weakness or paralysis of the eye muscles, ataxia or unsteady gait, and changes in mental state like confusion, apathy, and difficulty concentrating. And untreated Wernicke's encephalopathy can lead to coma and death if not treated quickly.

Key Takeaways

Wernicke-Korsakoff syndrome (WKS) is a neurological disorder caused by a deficiency of thiamine (vitamin B1), often due to chronic alcohol abuse. It is a combination of Wernicke encephalopathy and Korsakoff syndrome, presenting with confusion, ophthalmoplegia, and ataxia. Wernicke encephalopathy can progress to Korsakoff syndrome, which causes severe memory loss, disorientation, and confabulation. Treatment includes thiamine supplements, rehabilitation, and cognitive therapy to manage symptoms.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
  4. "THE NATURAL HISTORY AND PATHOPHYSIOLOGY OF WERNICKE'S ENCEPHALOPATHY AND KORSAKOFF'S PSYCHOSIS" Alcohol and Alcoholism (2005)
  5. "Health problems and care needs in patients with Korsakoff’s syndrome: A systematic review" Journal of Psychiatric and Mental Health Nursing (2020)