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Test Code LAB2699 Vitamin K1, Serum

Additional Codes

Test Name in EPIC EPIC Test Code Mnemonic Mayo Test ID
Vitamin K1 LAB2699 VITK1 VITK1

 

Useful For

Assessment of circulating vitamin K1 concentration.

Method Name

Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)

Reporting Name

Vitamin K1, S

Specimen Type

Serum


Specimen Required


Patient Preparation: Patient should fast overnight (12-14 hours); infants should have specimen collected before next feeding.

Supplies: Amber Frosted Tube, 5 mL (T915)

Collection Container/Tube:

Preferred: Red top

Acceptable: Serum gel

Submission Container/Tube: Amber vial

Specimen Volume: 2 mL

Collection Instructions:

1. Within 2 hours of collection, centrifuge the specimen.

2. For red top tubes, immediately aliquot serum into an amber vial (preferred). Serum may sit on whole blood cells up to a maximum of two hours before aliquoting.

3. For serum gel tubes, immediately aliquot serum into an amber vial (preferred). Serum may sit on gel at ambient temperature for a maximum of 24 hours or refrigerated for a maximum of 7 days before aliquoting.


Specimen Minimum Volume

0.75 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred) 30 days
  Ambient  30 days
  Frozen  30 days

Reject Due To

Gross hemolysis OK
Lipemia Reject
Gross icterus OK

Clinical Information

Vitamin K1, or phylloquinone, is part of a group of similar fat-soluble vitamins in which the 2-methyl-1,4- naphthoquinone ring is common. Phylloquinone is found in high amounts in leafy green vegetables and some fruits (avocado, kiwi). It is a required cofactor involved in the gamma-carboxylation of glutamate residues of several proteins. Most notably, the inactive forms of the coagulation factors prothrombin (factor II), factors VII, IX, and X, as well as protein S and protein C are converted to their active forms by the transformation of glutamate residues to gamma-carboxyglutamic acid (Gla). Other proteins such as those involved in bone metabolism, cell growth and apoptosis also undergo this Gla transformation. Thus, vitamin K plays a critical role in hemostasis (blood clotting) and acute deficiency is characterized by defective blood coagulation. In neonates, low vitamin K levels in breast milk, inadequate placental transport, and hepatic immaturity leading to insufficient synthesis of coagulation proteins can result in the bleeding disorder hemorrhagic disease of the newborn. To minimize this risk, Vitamin K is commonly administered prophylactically immediately after birth. Other at-risk groups for vitamin K deficiency include those with insufficient dietary intake, malabsorption disorders, cystic fibrosis, cholestasis, and alcoholism, as well as liver and pancreatic disease. Several drugs such as coumarin anticoagulants (ie, warfarin) and antibiotics (ie, cephalosporin) have also been shown to interfere with vitamin K metabolism. High doses of vitamin K have not been shown to produce toxicity. Direct measurement of vitamin K1 by liquid chromatography tandem mass spectrometry has been established as a highly effective strategy to assess status and intake.

Reference Values

<18 years: Not established

≥18 years: 0.10-2.20 ng/mL

Interpretation

Low vitamin K1 concentrations in the serum are indicative of insufficiency and poor vitamin K1 status.

Cautions

Testing of nonfasting specimens or the use of vitamin K1 supplementation can result in elevated serum vitamin K1 concentrations.

Method Description

Deuterated stable isotope (vitamin K1-d7) is added to a serum sample as an internal standard. Protein is precipitated from the mixture by the addition of ethanol. Vitamin K1 and internal standard are extracted from the resulting supernatant by solid-phase extraction. Vitamin K1 and internal standard are then separated utilizing high-throughput liquid chromatography with analysis on a tandem mass spectrometer equipped with a heated nebulizer ion source using multiple-reaction monitoring.(Unpublished Mayo method)

Day(s) Performed

Monday through Friday

Report Available

2 to 5 days

Specimen Retention Time

14 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

84597

LOINC Code Information

Test ID Test Order Name Order LOINC Value
VITK1 Vitamin K1, S 9622-2

 

Result ID Test Result Name Result LOINC Value
62167 Vitamin K1, S 9622-2

Forms

If not ordering electronically, complete, print, and send a General Request (T239) with the specimen.