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Plasma levels of platelet-derived microvesicles are associated with risk of future venous thromboembolism.
Snir, Omri; Wilsgård, Line; Latysheva, Nadezhda; Wahlund, Casper J E; Braekkan, Sigrid K; Hindberg, Kristian; Hansen, John-Bjarne.
Afiliación
  • Snir O; Thrombosis Research Center (TREC), Department of Clinical Medicine, UiT-The Arctic University of Norway, Tromsø, Norway.
  • Wilsgård L; Thrombosis Research Center (TREC), Department of Clinical Medicine, UiT-The Arctic University of Norway, Tromsø, Norway.
  • Latysheva N; Thrombosis Research Center (TREC), Department of Clinical Medicine, UiT-The Arctic University of Norway, Tromsø, Norway.
  • Wahlund CJE; Thrombosis Research Center (TREC), Department of Clinical Medicine, UiT-The Arctic University of Norway, Tromsø, Norway.
  • Braekkan SK; Thrombosis Research Center (TREC), Department of Clinical Medicine, UiT-The Arctic University of Norway, Tromsø, Norway.
  • Hindberg K; Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway.
  • Hansen JB; Thrombosis Research Center (TREC), Department of Clinical Medicine, UiT-The Arctic University of Norway, Tromsø, Norway.
J Thromb Haemost ; 20(4): 899-908, 2022 04.
Article en En | MEDLINE | ID: mdl-35000275
ABSTRACT

BACKGROUND:

Microvesicles (MVs) are small double-membrane encapsulated particles shed from cells. Case-control studies have reported elevated plasma levels of platelet-derived MVs (PDMVs) in patients with venous thromboembolism (VTE). However, it is not known whether high PDMV levels is a risk factor or a consequence of the acute VTE event.

OBJECTIVES:

To investigate the association between PDMVs in plasma and risk of future incident VTE.

METHODS:

We performed a population-based nested case-control study with 314 VTE cases and 705 age- and sex-matched controls (from The Tromsø Study) to investigate the association between the proportion of PDMVs (PDMVs%) in plasma and risk of future incident VTE. MVs isolated from plasma sampled at baseline (i.e., before VTE) were stained for platelet markers and analyzed by flow cytometry. PDMVs% were defined as the number of PDMVs divided by the total number of MVs. Odds ratios (ORs) with 95% confidence intervals (CI) for VTE risk were estimated across quartiles of PDMVs%.

RESULTS:

Subjects with PDMVs% in the highest quartile had an OR for VTE of 1.78 (95% CI 1.21-2.64) and 1.99 (95% CI 1.24-3.26) for provoked VTE, compared to those in the lowest quartile. The association was moderately affected by multivariable adjustment for age, sex, body mass index, C-reactive protein, platelet count, and cancer. The OR for VTE was higher when the time between blood sampling and event was shorter.

CONCLUSIONS:

Our results show that high proportions of PDMVs are associated with future risk of incident VTE and imply a role of platelet activation in the pathogenesis of VTE.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tromboembolia Venosa Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Thromb Haemost Asunto de la revista: HEMATOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Noruega

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tromboembolia Venosa Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Thromb Haemost Asunto de la revista: HEMATOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Noruega