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Definition
Vitamin A
Function: Antioxidant; constituent of visual pigments (retinal). Found in liver and leagy vegetables.
Deficiency: Night blindness, dry skin
Excess: Arthralgias, fatigue, headaches, skin changes, sore throat, alopecia. Teratogenic (cleft palate, cardiac abnormalities |
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Thiamine Vitamin B1
Function: thiamine pyrophosphate (TPP) cofactor for several enzymes
-Pyruvate Dehydrogenase (glycolysis)
-alpha-ketoglutarate dehydrogenase (TCA)
-Branched-chain AA dehydrogenase
-transketolase (HMP shunt) |
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Wernicke-Korsakoff syndrome and beriberi both cause neurologic and cardiac manifestations. Seen in malnutrition and alcoholism.
Wernicke-korsakoff- confusion, ophthalmoplegia, ataxia plus memory loss, confabulation, personality change
Dry Beriberi- polyneuritis, symmetrical muscle wasting
Web Beriberi- high output cardiac failure (dilated cardiomyopathy), edema |
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Definition
Deficiency in Vitamin B1 or Thiamine
Dry Beriberi- polyneuritis, symmetrical muscle wasting
Wet Beriberi- high output cardiac failure (dilated cardiomyopathy), edema
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Term
Wernicke-Korsakoff syndrome |
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Definition
-Deficiency in Vitamin B1 or Thiamine
Wernicke-Korsakoff syndrome and beriberi both cause neurologic and cardiac manifestations. Seen in malnutrition and alcoholism.
Wernicke-korsakoff- confusion, ophthalmoplegia, ataxia plus memory loss, confabulation, personality change
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Riboflavin Vitamin B2
Function: cofactor in oxidation and reduction (FADH2)
Deficiency: Cheilosis (inflammation of lips, scaling and fissures at the corners of the mouth), Corneal vascularization. |
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Naicin Vitamin B3
Function: Constituent of NAD+ (used in redox reactions). Derived from tryptophan. Synthesis requires Vitamin B6 (pyridoxine).
Deficiency: Glossitis. Severe deficiency leads to pellagra, which can be caused by Hartnup disease
Excess: facial flushing (due to pharmacologic doses for treatment of hyperlipidemia) |
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Naicin Vitamin B3
-Glossitis. Severe deficiency leads to Pellagra, which can be caused by
-Hartnup disease (decrease tryptophan absorption)
-malignant carcinoid syndrome (increased tryptophan metabolism)
-INH (decrease vitamin B6 (pyridoxine))
Pellagra: Diarrhea, Dermatitis, Dementia |
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Naicin Vitamin B3
Excess: Facial flushing due to pharmacologic doses for treatment of hyperlipidemia |
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Pyridoxine Vitamin B6
Function: Converted to pyridoxal phosphate, a cofactor used in transamination (ALT and AST), decarboxylation reactions, glycogen phosphorylase, and heme synthesis. Required for synthesis of niacin (Vitamin B3) from tryptophan. |
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Pyridoxine Vitamin B6
Deficiency: convulsions, hyperirritability, peripheral neuropathy (deficiency inducible by INH and oral contraceptives) |
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Cobalamin Vitamin B12 Found in animal products
Function: Cofactor for homocysteine methyltransferase (transfer CH3 group as methylcobalamin) and methylmalonyl-CoA mutase
Deficiency: Macrocytic, megaloblastic anemia; neurologic symptoms |
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Vitamin B12 Cobalamin
Deficiency: Macrocytic, megaloblastic anemia; neurologic symptoms (paresthesias, subacute combined degeneration) due to abnormal myelin. Prolonged deficiency leads to irreversible nervous system damage
-Deficiency usually caused by malabsorption, lack of intrinsic factor (pernicous anemia, gastric bypass), or absence of terminal ileum (Crohn's)
-Schilling test to detect etiology of deficiency |
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Definition
-Found in green leaves
Function: converted to tetrahydrofolate, a coenzyme for 1-carbon transfer/methylation reactions. Important for the synthesis of nitrogenous bases in DNA and RNA.
Deficiency: Macrocytic, megaloblastic anemia, no neurologic symptoms (unlike Vitamin B12 deficiency). Most common vitamin deficiency in United states. |
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Definition
Deficiency: Macrocytic, megaloblastic anemia, no neurologic symptoms (unlike Vitamin B12 deficiency). Most common vitamin deficiency in United states.
-Ovalocytosis and neutrophils with hypersegmented nuclei.
-deficiency can be caused by several drugs (phenytoin, sulfonamides, MTX)
-supplemental folic acid in early pregnancy reduces neural tube defects
-small reserve pool stored primarily in the liver. |
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Term
S-adenosyl-methionine (SAM) |
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Definition
-ATP + methionine --> S-adenosyl-methionine (SAM)
-SAM transfers methyl units
-Regeneration of methionine and thus SAM is dependent on Vitamin B12 and folate
Methioine --> via SAM--> Homocysteine + CH3 (given up)
Methionine + THF <-- B12 <-- CH3 + THF |
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Biotin
Cofactor for carboxylation enzymes
-Pyruvate carboxylase: Pyruvate to oxaloacetate
-Acetyl-CoA carboxylase: acetyl-CoA to malonyl-CoA
-Propionyl-CoA carboxylase: Propionyl-CoA to Methylmalonyl-Coa |
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Deficiency- relatively rare. Dermatitis, alopecia, enteritis. Caused by antibiotic use or excessive ingestion of raw eggs. |
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Vitamin C Asorbic Acid In fruits and vegetables
Function: Antioxidant
1. Facilitates iron absorption by keeping iron in Fe2+ reduced state (more absorbable)
2. Necessary for hydroxylation of proline and lysine in collagen synthesis
3. Necessary for dopamine B-hydroxylase which converts dopamine to NE
Deficiency: Scurvy: swollen gums, bruising, anemia, poor wound healing |
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Vitamin C Ascorbic acid found in fruits and vegetables
Deficiency: Scurvy: swollen gums, bruising, anemia, poor wound healing |
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Vitamin D
Function: Increase intestinal absorption of calcium and phosphate, increase bone resorption
Deficiency: Rickets in children (bending bones), osteomalacia in adults (soft bones), hypocalcemic tetany
Excess: Hypercalcemia, hypercalciuria, loss of appetitie, stupor, seen in sarcoidosis (increase activation of vitamin D by epithelioid macrophages) |
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Deficiency: Rickets in children (bending bones), osteomalacia in adults (soft bones), hypocalcemic tetany |
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Excess: Hypercalcemia, hypercalciuria, loss of appetitie, stupor, seen in sarcoidosis (increase activation of vitamin D by epithelioid macrophages) |
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4 forms of Vitamin D found in the body |
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Definition
1. D2 = ergocalciferol- ingested from plants, used as pharmacologic agent
2. D3 = cholecalciferol- consumed in milk, formed in sun-exposed skin.
3. 25-OH-D3 = storage form
4. 1,25-(OH)2D3 (calcitriol) = active form |
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Vitamin E
Function: Antioxidant (protects erythrocytes and membranes from free radical damage)
Deficiency: Increase fragility of erythrocytes (hemolytic anemia), muscle weakness, neurodysfunction. |
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Vitamin K
Function: catalyzes gama-carboxylation of glutamic acid residues on various proteins concerned with blood clotting. Made by intestinal flora. Necessary for synthesis of clotting factors 2,7, 9, 10, and protein C and S. Warfarin is vitamin K antagonist.
Deficiency: Neonatal hemorrhage with increase PT and increase in aPTT but normal bleeding time and after prolonged use of broad-spectrum antibiotics. |
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Definition
Deficiency:
-Neonatal hemorrhage with increase PT and increase in aPTT but normal bleeding time (neonates have sterile intestines and are unable to make vitamin K). Neonates are given vitamin K injection at birth to prevent hemorrhage.
-Can occur after prolonged use of broad-spectrum antibiotics. |
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Function: Essential for the activity of 100+ enzymes. Important in the formation of zinc fingers (transcription factor motif).
Deficiency: Delayed wound healing, hypogonadism, decrease adult hair (axillary, facial, pubic). May predispose to alcoholic cirrhosis. |
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