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Clinical Rheumatology

, Volume 32, Issue 9, pp 1357–1364 | Cite as

Derangement of hemostasis in rheumatoid arthritis: association with demographic, inflammatory and metabolic factors

  • Theodoros DimitroulasEmail author
  • Karen M. J. Douglas
  • Vasileios F. Panoulas
  • Tracey Toms
  • Jacqueline P. Smith
  • Gareth J. Treharne
  • Peter Nightingale
  • James Hodson
  • George D Kitas
Original Article

Abstract

Disturbance of fibrinolysis is common in rheumatoid arthritis (RA), and it may be associated with the increased cardiovascular risk observed in this population. We aimed to assess coagulation derangement and investigate whether abnormalities are influenced by demographic, inflammatory or metabolic factors in patients with RA. Levels of tissue plasminogen activator (tPA), plasminogen activator inhibitor (PAI-1), fibrinogen, prothrombin fragment 1 + 2 (PF1 + 2), thrombomodulin (TM), protein C and Von Willebrand factor (vWF) were compared between 141 RA patients and 50 healthy hospital controls. Within RA, coagulation factors were assessed alongside several demographic, inflammation and metabolic indicators. RA patients had higher levels of coagulation factors than controls. After correction for age and sex, having RA predicted increased tPA (B = 0.15, P < 0.001), PAI-1 (B = 0.21, P < 0.001), fibrinogen (B = 0.86, P < 0.001), PF1 + 2 (B = 0.20, P < 0.001), and TM (B = 0.01, P = 0.03) levels. CRP correlated positively with tPA (P < 0.05), fibrinogen (P < 0.001), TM (P < 0.05), PF1 + 2 (P < 0.001) and vWF (P < 0.001). Metabolic factors linked with coagulation factors were hypertriglyceridaemia (tPA, P < 0.05; PAI-1, P < 0.05; protein C, P < 0.05) and insulin resistance (tPA, P < 0.01; PAI-1, P < 0.01; vWF, P < 0.05). Imbalance of coagulation and fibrinolytic mechanisms is common in RA and associates with age, inflammation, and metabolic factors. Further studies may determine whether these abnormalities are the consequence of acute inflammation or markers of vascular dysfunction.

Keywords

Blood coagulation Cardiovascular disease Fibrinolysis Rheumatoid arthritis 

Notes

Acknowledgments

Dr Theodoros Dimitroulas has been supported by the Rheumatology Society of Northern Greece and the Hellenic Society for Rheumatology.

Disclosures

None

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Copyright information

© Clinical Rheumatology 2013

Authors and Affiliations

  • Theodoros Dimitroulas
    • 1
    • 5
    Email author
  • Karen M. J. Douglas
    • 1
  • Vasileios F. Panoulas
    • 1
  • Tracey Toms
    • 1
  • Jacqueline P. Smith
    • 1
  • Gareth J. Treharne
    • 2
  • Peter Nightingale
    • 3
  • James Hodson
    • 3
  • George D Kitas
    • 1
    • 4
  1. 1.Department of RheumatologyDudley Group of HospitalsDudleyUK
  2. 2.Department of PsychologyUniversity of OtagoDunedinNew Zealand
  3. 3.Wolfson Computer LabaratoryUniversity Hospitals of BirminghamBirminghamUK
  4. 4.Arthritis Research UK Epidemiology Unit, School of Translational MedicineUniversity of Manchester Rutherford HouseManchesterUK
  5. 5.Department of Rheumatology, Russells Hall HospitalDudley Group of HospitalsDudleyUK

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