Cited by 51Blood Coagulation and Thrombosis MechanismsBlood properties and coagulationPlatelet Disorders and Treatments

Abnormally Short Activated Partial Thromboplastin Times Are Related to Elevated Plasma Levels of TAT, F1+2, D-Dimer and FVIII:C

ten Boekel, Edwin, Bartels, Piet·2002·Pathophysiology of Haemostasis and Thrombosis

Abstract

Abnormally short activated partial thromboplastin times (APTTs) are associated with an increased risk of thrombotic disorders. We have examined the status of coagulation activity in subjects with short APTTs. In addition, the presence of the thrombotic risk factors G1691A-factor V, G20210A-prothrombin gene mutation and factor VIII coagulant activity (FVIII:C) was determined. Plasma levels of TAT, F1+2, D-dimer and FVIII:C were markedly higher in subjects with short APTTs compared with subjects with normal APTTs. APTTs were inversely related to TAT, F1+2, D-dimer and FVIII:C levels. The prevalence of G1691A-factor V and G20210A-prothrombin gene mutation between the group with short APTTs and the control group was not significantly different. Hence, these gene polymorphisms do not contribute to the increased risk of thrombosis associated with short APTTs. In conclusion, short APTTs are indicative of marked coagulation activity and elevated FVIII:C levels. Elevated FVIII:C levels may play a pathogenic role in the increased risk of thrombosis associated with abnormally short APTTs.

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Crossref · 10.1159/000065217

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1 of 1 references verified0 citation errors · 0 not checkable

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  • During an acute thrombotic event, raised factor VIII levels can shorten activated partial thromboplastin time (aPTT), producing false-negative LA screening by aPTT tests.

    “During an acute thrombotic event, the raising of factor VIII levels can shorten activated partial thromboplastin time (aPTT), producing false-negative LA screening by aPTT tests [19]”

    From Lupus Anticoagulant Detection under the Magnifying Glass (2023) · cites this paper as [19]

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Authors
ten Boekel, E., & Bartels, P.
Venue
Pathophysiology of Haemostasis and Thrombosis
Publisher
S. Karger AG
Published
2002
Volume
32
Issue
3
Pages
137-142
ISSN
  • 1424-8832 (ISSN-L)
  • 1424-8840
OpenAlex
W2001692920
Cited by
51
References
1
Citations by year
2026: 2 · 2024: 3 · 2023: 3 · 2022: 1 · 2021: 5 · 2020: 2 · 2018: 1 · 2016: 3 · 2015: 5 · 2014: 2 · 2013: 1 · 2012: 3
FWCI
0.62
Type
journal article
Language
en
Open access
closed
Locations
  • Pathophysiology of Haemostasis and Thrombosis (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Hematology › Blood Coagulation and Thrombosis Mechanisms
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Blood properties and coagulation
  • Health Sciences › Medicine › Hematology › Platelet Disorders and Treatments
Keywords
activated partial thromboplastin time, thrombosis risk, tissue factor, factor Xa, D-dimer, factor VIII coagulant activity, factor V Leiden, prothrombin G20210A, coagulation activation, thrombotic disorders
MeSH terms
Antithrombin III, Factor V, Factor VIII, Fibrin Fibrinogen Degradation Products, Gene Frequency, Humans, Partial Thromboplastin Time, Peptide Fragments, Peptide Hydrolases, Promoter Regions, Genetic, Prospective Studies, Prothrombin, Risk Factors, Cohort Studies, Prevalence, Thrombophilia, Activated Protein C Resistance, Genetic Predisposition to Disease, 3' Untranslated Regions

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