Acquired vitamin K-dependent carboxylation deficiency in liver disease

N Engl J Med. 1981 Jul 30;305(5):242-8. doi: 10.1056/NEJM198107303050502.

Abstract

gamma-Carboxyglutamic acid residues on prothrombin are synthesized from glutamic acid on a prothrombin precursor in the liver through a vitamin K-dependent carboxylase. In the absence of vitamin K or in the presence of vitamin K antagonists, an inert form of prothrombin - abnormal prothrombin - circulates in the blood. We have developed specific immunoassays for native and abnormal human prothrombin. The prothrombin concentration in our normal subjects was 108 +/- 19 microgram per milliliter. The abnormal-prothrombin concentration varied over four orders of magnitude between the limits of detection in normal plasma and the level in patients with cirrhosis (0 to 5 microgram per milliliter), acute hepatitis (0 to 33 microgram per milliliter), or vitamin K deficiency (32 to 100 microgram per milliliter) and in those treated with sodium warfarin (12 to 65 microgram per milliliter). These studies indicate that abnormal prothrombin is not a component of normal plasma but appears in a variety of hepatic and nutritional disorders characterized by impaired hepatic vitamin-K-dependent carboxylation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Carbon-Carbon Ligases*
  • Epitopes
  • Female
  • Hepatitis / enzymology
  • Humans
  • Ligases / deficiency*
  • Liver / enzymology
  • Liver Cirrhosis / enzymology
  • Liver Diseases / blood
  • Liver Diseases / enzymology*
  • Male
  • Middle Aged
  • Prothrombin / biosynthesis*
  • Prothrombin / immunology
  • Prothrombin / isolation & purification
  • Prothrombin Time
  • Vitamin K Deficiency / enzymology
  • Warfarin / adverse effects

Substances

  • Epitopes
  • Warfarin
  • Prothrombin
  • Ligases
  • Carbon-Carbon Ligases
  • glutamyl carboxylase