6
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Biomarkers, menopausal hormone therapy and risk of venous thrombosis: The Women's Health Initiative

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Essentials

          • Venous thrombosis is the most common vascular complication of menopausal hormone use.

          • We studied biomarkers to predict thrombosis with hormones in the Women's Health Initiative.

          • Lower proteins C and S, and higher D‐dimer were related to thrombosis risk.

          • The 25% of women with high D‐dimer had a six‐times greater risk of thrombosis with hormones.

          Background

          Oral menopausal hormone therapy causes venous thrombosis but whether biomarkers of thrombosis risk can identify women at risk is unknown.

          Methods

          We completed a nested case control study in the two Women's Health Initiative hormone trials; 27 347 women aged 50‐79 were randomized to hormone therapy (conjugated equine estrogen with or without medroxyprogesterone acetate) or placebo. With 4 years follow‐up, biomarkers were measured using stored baseline samples prior to starting treatment, and one‐year later, in 215 women who developed thrombosis and 867 controls.

          Results

          Overall, lower protein C and free protein S, and higher D‐dimer, prothrombin fragment 1.2 and plasmin‐antiplasmin complex were associated with risk of future thrombosis with odds ratios ranging from 1.9 to 3.2. Compared to women with normal biomarkers assigned to placebo, the risk of thrombosis with hormone therapy was increased among women with abnormal biomarkers, especially elevated D‐dimer, elevated plasmin‐antiplasmin, and low free protein S; the largest association was for D‐dimer: odds ratio 6.0 (95% CI 3.6‐9.8). Differences in associations by hormone use were not significant on the multiplicative scale. Considering a multi‐marker score of eight biomarkers, women with three or more abnormal biomarkers had 15.5‐fold increased odds of VT (95% CI 6.8‐35.1). One‐year changes in biomarkers were not robustly associated with subsequent thrombosis risk.

          Conclusion

          Abnormal levels of biomarkers of thrombosis risk identified women at increased risk of future venous thrombosis with oral menopausal hormone therapy. Findings support the potential for clinical use of D‐dimer testing in advance of hormone therapy prescription.

          Related collections

          Most cited references29

          • Record: found
          • Abstract: found
          • Article: not found

          Design of the Women's Health Initiative clinical trial and observational study. The Women's Health Initiative Study Group.

          The Women's Health Initiative (WHI) is a large and complex clinical investigation of strategies for the prevention and control of some of the most common causes of morbidity and mortality among postmenopausal women, including cancer, cardiovascular disease, and osteoporotic fractures. The WHI was initiated in 1992, with a planned completion date of 2007. Postmenopausal women ranging in age from 50 to 79 are enrolled at one of 40 WHI clinical centers nationwide into either a clinical trial (CT) that will include about 64,500 women or an observational study (OS) that will include about 100,000 women. The CT is designed to allow randomized controlled evaluation of three distinct interventions: a low-fat eating pattern, hypothesized to prevent breast cancer and colorectal cancer and, secondarily, coronary heart disease; hormone replacement therapy, hypothesized to reduce the risk of coronary heart disease and other cardiovascular diseases and, secondarily, to reduce the risk of hip and other fractures, with increased breast cancer risk as a possible adverse outcome; and calcium and vitamin D supplementation, hypothesized to prevent hip fractures and, secondarily, other fractures and colorectal cancer. Overall benefit-versus-risk assessment is a central focus in each of the three CT components. Women are screened for participation in one or both of the components--dietary modification (DM) or hormone replacement therapy (HRT)--of the CT, which will randomize 48,000 and 27,500 women, respectively. Women who prove to be ineligible for, or who are unwilling to enroll in, these CT components are invited to enroll in the OS. At their 1-year anniversary of randomization, CT women are invited to be further randomized into the calcium and vitamin D (CaD) trial component, which is projected to include 45,000 women. The average follow-up for women in either CT or OS is approximately 9 years. Concerted efforts are made to enroll women of racial and ethnic minority groups, with a target of 20% of overall enrollment in both the CT and OS. This article gives a brief description of the rationale for the interventions being studied in each of the CT components and for the inclusion of the OS component. Some detail is provided on specific study design choices, including eligibility criteria, recruitment strategy, and sample size, with attention to the partial factorial design of the CT. Some aspects of the CT monitoring approach are also outlined. The scientific and logistic complexity of the WHI implies particular leadership and management challenges. The WHI organization and committee structure employed to respond to these challenges is also briefly described.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            D-dimer and prothrombin fragment 1 + 2 predict venous thromboembolism in patients with cancer: results from the Vienna Cancer and Thrombosis Study.

            Venous thromboembolism (VTE) is a well-recognized complication of cancer. Laboratory parameters might be useful to assess the VTE risk in patients with cancer. The aim of this study was to investigate D-dimer and prothrombin fragment 1 + 2 (F 1 + 2), which reflect activation of blood coagulation and fibrinolysis, for prediction of cancer-associated VTE. In a prospective, observational, cohort study of 821 patients with newly diagnosed cancer or progression of disease who did not recently receive chemotherapy, radiotherapy, or surgery were enrolled and followed for a median of 501 days (interquartile range, 255 to 731 days). The malignancies in these patients were as follows: breast (n = 132), lung (n = 119), stomach (n = 35), lower gastrointestinal tract (n = 106), pancreas (n = 46), kidney (n = 22), and prostate (n = 101) cancers; high-grade glioma (n = 102); malignant lymphoma (n = 94); multiple myeloma (n = 17); and other tumor types (n = 47). The study end point was occurrence of objectively confirmed symptomatic or fatal VTE. VTE occurred in 62 patients (7.6%). The cutoff level for elevated D-dimer and elevated F 1 + 2 was set at the 75th percentile of the total study population. In multivariable analysis that included elevated D-dimer, elevated F 1 + 2, age, sex, surgery, chemotherapy, and radiotherapy, the hazard ratios (HRs) of VTE in patients with elevated D-dimer (HR, 1.8; 95% CI, 1.0 to 3.2; P = .048) and elevated F 1 + 2 (HR, 2.0; 95% CI, 1.2 to 3.6; P = .015) were statistically significantly increased. The cumulative probability of developing VTE after 6 months was highest in patients with both elevated D-dimer and elevated F 1 + 2 (15.2%) compared with patients with nonelevated D-dimer and nonelevated F 1 + 2 (5.0%; P < .001). High D-dimer and F 1 + 2 levels independently predict occurrence of VTE in patients with cancer.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Venous thrombosis risk associated with plasma hypofibrinolysis is explained by elevated plasma levels of TAFI and PAI-1.

              Elevated plasma clot lysis time (CLT) increases risk of venous and arterial thrombosis. It is unclear which fibrinolytic factors contribute to thrombosis risk. In 743 healthy control subjects we investigated determinants of CLT. By comparison with 770 thrombosis patients, we assessed plasma levels of fibrinolytic proteins as risk factors for a first thrombosis. Plasminogen activator inhibitor-1 (PAI-1) levels were the main determinants of CLT, followed by plasminogen, thrombin-activatable fibrinolysis inhibitor (TAFI), prothrombin, and alpha2-antiplasmin. Fibrinogen, factor VII, X, and XI contributed minimally. These proteins explained 77% of variation in CLT. Levels of the fibrinolytic factors were associated with thrombosis risk (odds ratios, highest quartile vs lowest, adjusted for age, sex, and body mass index: 1.6 for plasminogen, 1.2 for alpha2-antiplasmin, 1.6 for TAFI, 1.6 for PAI-1, and 1.8 for tissue plasminogen activator [t-PA]). Adjusting for acute-phase proteins attenuated the risk associated with elevated plasminogen levels. The risk associated with increased t-PA nearly disappeared after adjusting for acute-phase proteins and endothelial activation. TAFI and PAI-1 remained associated with thrombosis after extensive adjustment. In conclusion, CLT reflects levels of all fibrinolytic factors except t-PA. Plasminogen, TAFI, PAI-1, and t-PA are associated with venous thrombosis. However, plasminogen and t-PA levels may reflect underlying risk factors.
                Bookmark

                Author and article information

                Contributors
                mary.cushman@uvm.edu , https://twitter.com/MaryCushmanMD
                Journal
                Res Pract Thromb Haemost
                Res Pract Thromb Haemost
                10.1002/(ISSN)2475-0379
                RTH2
                Research and Practice in Thrombosis and Haemostasis
                John Wiley and Sons Inc. (Hoboken )
                2475-0379
                17 April 2018
                April 2018
                : 2
                : 2 ( doiID: 10.1002/rth2.2018.2.issue-2 )
                : 310-319
                Affiliations
                [ 1 ] Department of Medicine Larner College of Medicine University of Vermont Burlington VT USA
                [ 2 ] Public Health Sciences Division Fred Hutchinson Cancer Research Center Seattle WA USA
                [ 3 ] Department of Clinical Epidemiology Leiden University Medical Center Leiden the Netherlands
                [ 4 ] Department of Epidemiology Cardiovascular Health Research Unit University of Washington Seattle WA USA
                [ 5 ] Department of Geriatric Medicine University of Hawaii Honolulu HI USA
                [ 6 ] Atlanta VA Medical Center Decatur GA USA
                [ 7 ] Division of Endocrinology and Metabolism Emory University School of Medicine Atlanta GA USA
                [ 8 ] Department of Neurology State University of New York Downstate Medical Center Brooklyn NY USA
                [ 9 ] Department of Family Medicine Alpert Medical School Brown University Providence RI USA
                [ 10 ] Department of Epidemiology School of Public Health Brown University Providence RI USA
                [ 11 ] Program on Prevention Outcomes and Practices Stanford Prevention Research Center Stanford University Palo Alto CA USA
                Author notes
                [*] [* ] Correspondence

                Mary Cushman, Larner College of Medicine at the University of Vermont, Colchester, VT, USA.

                Email: mary.cushman@ 123456uvm.edu

                [†]

                Posthumous author

                Author information
                http://orcid.org/0000-0002-7871-6143
                http://orcid.org/0000-0003-2558-7496
                Article
                RTH212100
                10.1002/rth2.12100
                5974918
                30046733
                e74fc210-5bc8-4b49-99cc-eff88cf0cf26
                © 2018 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals, Inc on behalf of International Society on Thrombosis and Haemostasis.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 03 November 2017
                : 05 March 2018
                Page count
                Figures: 1, Tables: 4, Pages: 10, Words: 7715
                Funding
                Funded by: National Heart, Lung, and Blood Institute of NIH
                Funded by: U.S. Department of Health and Human Services
                Award ID: HHSN268201100046C
                Award ID: HHSN268201100001C
                Award ID: HHSN268201100002C
                Award ID: HHSN268201100003C
                Award ID: HHSN268201100004C
                Award ID: HHSN271201100004C
                Categories
                Original Article
                Original Articles: Thrombosis
                Custom metadata
                2.0
                rth212100
                April 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.3.8.2 mode:remove_FC converted:29.05.2018

                blood coagulation,d‐dimer,menopausal hormone therapy,risk assessment,risk factor,venous thrombosis,venous thromboembolism

                Comments

                Comment on this article