The cross-sectional association between vasomotor symptoms and hemostatic parameter levels in postmenopausal women

Menopause. 2017 Apr;24(4):360-370. doi: 10.1097/GME.0000000000000777.

Abstract

Objective: Vasomotor symptoms (VMS) may be a marker of cardiovascular risk. We aimed to evaluate the cross-sectional association of VMS presence and severity with hemostatic parameter levels measured at baseline among Women's Health Initiative (WHI) Hormone Therapy trial postmenopausal participants.

Methods: This cross-sectional analysis included 2,148 postmenopausal women with measures of VMS presence and severity reported in the 4 weeks before WHI baseline, who were not using warfarin or hormone therapy and for whom the following baseline hemostatic parameters were measured within the WHI Cardiovascular Disease Biomarker Case-Control Study: antithrombin, plasminogen activator inhibitor-1, protein C antigen, total and free protein S antigen, total and free tissue factor pathway inhibitor, D-dimer, normalized activated protein C sensitivity ratio, and thrombin generation. Using multiple linear regression, we estimated the adjusted average difference in each hemostatic parameter associated with VMS presence and severity. A multiple comparisons-corrected P value was computed using the P-min procedure to determine statistical significance of our smallest observed P value.

Results: Women were 67 years of age on average and 33% reported VMS presence at baseline. There was some suggestion that VMS presence may be associated with a -0.34 adjusted difference in normalized activated protein C sensitivity ratio compared with no VMS (95% CI, -0.60 to -0.087; P = 0.009), but this association was not significant after correction for multiple comparisons (P = 0.073). VMS presence or severity was not significantly associated with the other hemostatic parameters.

Conclusions: We found no convincing evidence that VMS presence or severity was associated with levels of hemostatic parameters among postmenopausal women.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Antigens / blood
  • Antithrombin Proteins / metabolism
  • Cross-Sectional Studies
  • Female
  • Fibrin Fibrinogen Degradation Products / metabolism
  • Hemostasis
  • Hot Flashes / blood*
  • Humans
  • Lipoproteins / blood
  • Middle Aged
  • Plasminogen Activator Inhibitor 1 / blood
  • Postmenopause / blood*
  • Protein C / immunology
  • Protein S / immunology
  • Severity of Illness Index
  • Sweating*
  • Symptom Assessment
  • Thrombin / biosynthesis

Substances

  • Antigens
  • Antithrombin Proteins
  • Fibrin Fibrinogen Degradation Products
  • Lipoproteins
  • Plasminogen Activator Inhibitor 1
  • Protein C
  • Protein S
  • fibrin fragment D
  • lipoprotein-associated coagulation inhibitor
  • Thrombin