Vitamin B6 

No Results

No Results

processing….

Vitamin B6 is a complex of 6 vitamers: pyridoxal, pyridoxol, pyridoxamine, and their 5′-phosphate esters. Vitamin B6 deficiency causes blood, skin, and nerve changes.

The reference range for pyridoxal phosphate (PLP), the biologically active form of vitamin B6, is 5-50 µg/L. [1, 2, 3]

Conditions associated with vitamin B6 deficiency include the following:

Atherosclerosis

Early myocardial infarction

Early stroke

Recurrent thromboembolism

Peripheral neuropathy

Depression

Generalized seizures

Anemia

Progressive nerve compression disorders (carpal tunnel syndrome, tarsal tunnel syndrome)

Factors that may increase the risk of vitamin B6 deficiency include the following:

Malabsorption

Malnutrition

Sickle cell disease

Inflammatory conditions

Rheumatoid arthritis

Hospitalization

Celiac disease

Hepatitis and extrahepatic biliary obstruction

Hepatocellular carcinoma

Chronic renal failure

Kidney transplant

Hyperoxaluria types I and II

Excessive alcohol ingestion

High serum alkaline phosphatase (eg, in cirrhosis, tissue injury)

Catabolic state

Hemodialysis

Peritoneal dialysis

Phototherapy for hyperbilirubinemia

Certain medications (cycloserine, hydralazine, isoniazid, D-penicillamine, pyrazinamide)

Marked increases in serum pyridoxal phosphate (PLP) levels are seen in hypophosphatasia.

Specifics for collection and panels are as follows:

Specimen type: Blood plasma

Container: Vacutainer, green top (heparin)

Collection method: Venipuncture

Specimen volume: 1 mL

Other instructions include the following:

Overnight fasting specimen

No vitamin supplements in preceding 24 hours

Transport in light-protective container

Centrifuge at 4°C; refrigerate immediately

Transfer plasma to dark-brown polypropylene or polyethylene transport tubes to protect from light

Panels include vitamin B complex.

Related tests include alkaline phosphatase and pyridoxic acid.

Vitamin B6 is a complex of 6 vitamers: pyridoxal, pyridoxol, pyridoxamine, and their 5′-phosphate esters. Pyridoxine 5′-phosphate (PLP) is an essential cofactor in various transamination, decarboxylation, and synthesis pathways involving carbohydrates, sphingolipids, sulfur-containing amino acids, heme, and neurotransmitters. Vitamin B6 deficiency causes blood, skin, and nerve changes. This vitamin is unique in that either deficiency or excess can cause peripheral neuropathy.

Dietary sources of vitamin B6 include cereals, beans, vegetables, liver, meat, and eggs. After absorption, pyridoxine, pyridoxamine, and pyridoxal are transported into hepatic cells by facilitated diffusion. Pyridoxal kinase phosphorylates pyridoxine and pyridoxamine, after which they are converted to PLP, a coenzyme in tryptophan and methionine metabolism. PLP is the primary active pyridoxal form, and serum PLP is used as the primary index of whole-body pyridoxal levels.

In methionine deficiency, S -adenosylmethionine accumulates, resulting in the inhibition of sphingolipid and myelin synthesis. Tryptophan is a precursor to several neurotransmitters and is required for niacin production. Thus, pyridoxine deficiency can cause a syndrome indistinguishable from pellagra. The neurotransmitters dopamine, serotonin, epinephrine, norepinephrine, glycine, glutamate, and gamma aminobutyric acid (GABA) also require PLP for their production. Homocystine metabolism is dependent on pyridoxine, and high homocystine levels can result from pyridoxine deficiency.

Hypophosphatasia is a rare inborn error of metabolism caused by low activity of the tissue-nonspecific isoenzyme of alkaline phosphatase (TNSALP). Alterations in the TNSALP gene lead to rickets, osteomalacia, or both. Serum PLP levels are typically elevated and are used in determining the diagnosis.

Laboratory methods to detect deficiency are as follows:

Pyridoxine level in blood

Xanthurenic-acid level in urine

Erythrocyte glutamic oxalo-acetic transaminase

Lymphocytic growth response

Methods to make a quantitative assessment are as follows:

High-performance liquid chromatography (HPLC) method, using cyanide derivatization: Method to determine the plasma pyridoxal-5-phosphate (PLP) concentrations as an indicator of vitamin B6 adequacy

Tandem mass spectrometry

Serum PLP analysis is indicated for the following:

Evaluation of suspected vitamin B6 deficiency

Diagnosis of hypophosphatasia

Other manifestations of vitamin B6 deficiency may include the following:

Scaling of the skin

Severe gingivitis

Cheilosis

Stomatitis

Irritability

Weakness

Dizziness

Diarrhea

Manifestations of vitamin B6 toxicity may include tachypnea and/or the following neurologic effects:

Sensory neuropathy (eg, burning pains, paresthesias, perioral numbness)

Progressive sensory ataxia

Impaired proprioception

Impaired vibration sense

Diminished tendon reflexes

Burris CA, Ashwood ER, Burns DE. Tietz Textbook of Clinical Chemistry and Molecular Diagnostics. 4th ed. St. Louis: Elsevier Saunders; 2006.

McPherson RA, Pincus MR. Henry’s Clinical Diagnosis and Management by Laboratory Methods. 22nd ed. Philadelphia: Elsevier Saunders; 2011.

Wallach J. Interpretation of Diagnostic Tests. 6th ed. New York: Little, Brown; 1996.

Ashwin Pai, MBBS, MS (GenSurg), MRCS Honorary Assistant Medical Officer, Department of Surgery, Kasturba Medical College, India

Disclosure: Nothing to disclose.

Eric B Staros, MD Associate Professor of Pathology, St Louis University School of Medicine; Director of Clinical Laboratories, Director of Cytopathology, Department of Pathology, St Louis University Hospital

Eric B Staros, MD is a member of the following medical societies: American Medical Association, American Society for Clinical Pathology, College of American Pathologists, Association for Molecular Pathology

Disclosure: Nothing to disclose.

Judy Lin, MD

Disclosure: Nothing to disclose.

Vitamin B6 

Research & References of Vitamin B6 |A&C Accounting And Tax Services
Source

error: Content is protected !!