Intraindividual consistency of the activated protein C resistance phenotype

Br J Haematol. 2004 Aug;126(3):405-9. doi: 10.1111/j.1365-2141.2004.05059.x.

Abstract

Resistance to activated protein C (APC) has been demonstrated to be a risk factor for venous thromboembolism, but it is not known whether this phenotype is consistent over time. We reinvestigated 2580 subjects from the Vicenza Thrombophilia and Atherosclerosis (VITA) Project to evaluate the prevalence of a consistent APC resistance phenotype in the population. Among the 433 subjects with an APC resistance at first visit, the phenotype was confirmed in all the 74 factor V (FV) Leiden carriers and in 124 of 359 FV Leiden negative subjects (34%). The prevalence of a confirmed phenotype, not associated with FV Leiden, was 4.8% in our population. In a subgroup of subjects previously investigated for heritability of the APC resistance, we confirmed the APC resistance phenotype in seven of 39 (17.9%) subjects with an APC resistant sibling but only in 20 of 408 (4.9%) subjects without a sibling with the same phenotype (P = 0.005). Among the 124 FV Leiden negative subjects with a persistent APC resistance phenotype, 40 (32%) had a plasma factor VIII coagulant activity level above 150 IU/dl and eight (6.4%) were carriers of the G20210A prothrombin allele. APC resistance not due to FV Leiden is a frequent and consistent phenotype in the general population, with a possibly strong genetic influence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activated Protein C Resistance / blood
  • Activated Protein C Resistance / genetics*
  • Adolescent
  • Adult
  • Alleles
  • Analysis of Variance
  • Blood Coagulation Tests
  • Cross-Sectional Studies
  • Factor V / analysis
  • Factor VIII / analysis
  • Female
  • Humans
  • Italy
  • Male
  • Middle Aged
  • Phenotype
  • Protein C / analysis
  • Prothrombin / genetics
  • Thrombophilia / blood
  • Thrombophilia / genetics*
  • Time Factors

Substances

  • Protein C
  • factor V Leiden
  • Factor V
  • Prothrombin
  • Factor VIII