3,327 results match your criteria: "Genetics of Venous Thromboembolism"

Genetic correlation between genes targeted by lipid-lowering drugs and venous thromboembolism: A drug-target Mendelian randomization study.

Medicine (Baltimore)

December 2024

National Clinical Research Center for Chinese Medicine Cardiology, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

Dyslipidemia has been established as a potential risk factor for venous thromboembolism (VTE) in several observational studies. Statins and novel lipid-modifying agents are being explored for their potential in VTE prevention, encompassing deep vein thrombosis (DVT), and pulmonary embolism (PE). Nonetheless, conclusive evidence supporting the effectiveness remains uncertain.

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Comprehensive Mendelian Randomization Analysis of Smoking and Its Effects on Venous Thromboembolism.

Semin Thromb Hemost

December 2024

Department of Trauma Hand and Foot Surgery, The First Affiliated Hospital of Yangtze University, the First People's Hospital of Jingzhou, Jingzhou, Hubei Province, People's Republic of China.

An increasing number of Mendelian randomization (MR) studies have evaluated the causal link between smoking and venous thromboembolism (VTE). However, previous studies often rely on single genetic variants related to smoking quantity and exhibit various other shortcomings, making them prone to pleiotropy and potentially leading to imprecise causal estimates. Thus, the deeper causal mechanisms remain largely unexplored.

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Direct Oral Anticoagulants (DOACs) have transformed the management of thrombotic disorders, offering a more convenient and effective alternative to traditional vitamin K antagonists (VKAs). However, assessing thrombotic risk in patients treated with DOACS remains crucial due to the potential for recurrent events. Current clinical risk scores have limitations in predicting and monitoring venous thromboembolism (VTE) risk in specific DOAC populations.

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Glioblastoma multiforme (GBM) is a malignant primary brain tumor categorized as a Grade 4 astrocytic glioma by the World Health Organization (WHO). Some of the established risk factors of GBM include inherited genetic syndromes, body mass index, alcohol consumption, use of non-steroidal anti-inflammatory drugs (NSAIDs), and therapeutic ionizing radiation. Vascular anomalies, including local and peripheral thrombosis, are common features of GBM.

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Unlabelled: Venous thromboembolism (VT) is a frequent (annual incidence of 1 to 2 per 1,000) and potentially life-threatening (case-fatality rate up to 10%) disease. VT is associated with serious short-term and long-term complications including a recurrence rate of approximately 20% within five years. Anticoagulant therapy, the mainstay of VT treatment, drastically reduces the risk of early VT recurrence, but it exposes patients to a substantial risk of bleeding.

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Psychiatric patients face a significantly shorter life expectancy than the general population due to a complex interplay of medical, behavioral, and social factors. Venous thromboembolism (VTE), encompassing both pulmonary embolism and deep vein thrombosis, is an underrecognized yet critical contributor to morbidity and mortality in this population. Evidence suggests a two to three times higher prevalence of VTE in psychiatric patients compared to the general population, with incidence rates up to 4.

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Relationship of Serum 25-Hydroxyvitamin D Concentrations, Diabetes, Vitamin D Receptor Gene Polymorphisms and Incident Venous Thromboembolism.

Diabetes Metab Res Rev

January 2025

Division of Nephrology, Nanfang Hospital, Southern Medical University, National Clinical Research Center for Kidney Disease, State Key Laboratory of Organ Failure Research, Guangdong Provincial Institute of Nephrology, Guangdong Provincial Key Laboratory of Renal Failure Research, Guangzhou, China.

Aims: The association between vitamin D and the risk of venous thromboembolism (VTE) remains inconclusive. We aimed to explore the association of serum 25-hydroxyvitamin D (25OHD) with incident VTE among participants with and without diabetes, and examine the modifying effect of genetic susceptibility of VTE and vitamin D receptor (VDR) gene polymorphisms on this association.

Materials And Methods: A total of 378,082 participants free of VTE at baseline from the UK Biobank were included.

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Purpose: Studies consistently show abnormally high levels of lactate acid in cardiovascular disease patients, suggested that targeting lactate production may serve as potential strategies for the treatment in the future. However, observational results may be subject to residual confounding and bias.

Methods: This study used the dataset from GWAS database to examine confounding in epidemiologic associations between lactate and cardiovascular diseases.

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Reassessing the Risk of Venous Thromboembolism (VTE) Events in Women.

Clin Appl Thromb Hemost

December 2024

Department of Vascular Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

This research aims to reassess women's risk of venous thromboembolism (VTE) events. We conducted an in-depth analysis of the environmental risk factors associated with VTE and their interactions with gender while also exploring the genetic underpinnings of the disease. VTE is identified as a multifactorial condition influenced by a combination of genetic, non-predisposing, and predisposing environmental factors.

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Background: Long-term outcome after a first venous thromboembolism (VTE) might be optimized by tailoring anticoagulant treatment duration on individual risks of recurrence and major bleeding. The L-TRRiP models (A-D) were previously developed in data from the Dutch Multiple Environment and Genetic Assessment of Risk Factors for Venous thrombosis study to predict VTE recurrence.

Objectives: We aimed to externally validate models C and D using data from the United States Heart and Vascular Health (HVH) study.

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Background: Several studies indicated that C-reactive protein (CRP) is associated with the risk of venous thromboembolism (VTE) in general population. But CRP appears to be unrelated to VTE events in newly diagnosed cancer patients. However, as the survival time of cancer patients increases, the effect of CRP on the long-term risk of VTE may change.

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Venous thromboembolism presenting as deep vein thrombosis or pulmonary embolism (PE) remains to be an important cause of mortality and morbidity worldwide. Despite its significance and incidence, compared to many other cardiovascular conditions there are significant gaps in knowledge in many aspects of it, including its pathophysiology. A rare sequela of PE is chronic thromboembolic pulmonary hypertension (CTEPH).

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Association between Genetic Risk and the Renal Function for Developing Venous Thromboembolism.

J Atheroscler Thromb

November 2024

Department of Epidemiology and Biostatistics, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology.

Aims: The impact of a reduced renal function on the risk of venous thromboembolism (VTE) remains controversial. The association between VTE and the renal function, as well as genetic susceptibility, requires further clarification in a large population.

Methods: This study included 358,723 participants with non-renal failure from the UK Biobank.

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Background: The gut microbiota of venous thromboembolism (VTE) patients exhibited significant alterations. However, the causal relationship between gut microbiota and VTE has not been fully understood. This study aimed to assess the causal relationship between gut microbiota and the risk of VTE using a two-sample Mendelian Randomization (MR) study.

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Objective: To assess the effect of contemporary menopausal hormone therapy on the risk of cardiovascular disease according to the route of administration and combination of hormones.

Design: Nationwide register based emulated target trial.

Setting: Swedish national registries.

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Neutrophil count and reduced risk of venous thromboembolism: a Mendelian randomization study.

Hematology

December 2024

Department of Thoracic Surgery, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.

Article Synopsis
  • The study explored the relationship between blood cell traits, especially neutrophils, and venous thromboembolism (VTE) using genetic data from over 173,000 individuals.
  • Researchers utilized various methods, including Mendelian randomization, to analyze genetic variants and their influence on VTE, incorporating data from a larger cohort of nearly 377,000 individuals.
  • The findings revealed that higher neutrophil counts are associated with a reduced risk of VTE, suggesting potential avenues for future prevention and treatment strategies for this condition.
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Article Synopsis
  • - Postpartum venous thromboembolism (VTE) is a serious complication that can occur after childbirth, driven by factors like increased blood clotting, reduced mobility, and injury to blood vessels, leading to high risks for new mothers.
  • - A case study details a 37-year-old woman with a history of recurrent clots and pregnancy issues that ultimately resulted in severe chronic venous obstruction despite various treatments, necessitating advanced procedures like stent implantation.
  • - The patient's medical journey involved multiple challenges, including spontaneous abortions, a pulmonary embolism linked to contraceptive use, and serious complications during and after her last pregnancy, highlighting the importance of careful monitoring and effective prevention strategies for postpartum VTE.
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Article Synopsis
  • A systematic assessment was conducted to evaluate the association between 19 autoimmune diseases (AIDs) and 14 cardiovascular diseases (CVDs) using a method called Mendelian randomization.
  • Significant associations were found, particularly celiac disease and type 1 diabetes mellitus, which increased the risk of peripheral arterial disease, while other AIDs were linked to various heart conditions.
  • The research suggests that immune responses and inflammation play a crucial role in these associations, and it identifies potential therapies, such as TNF-alpha inhibitors, that could be beneficial for treating AID-related CVDs.
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Venous thromboembolism is a multifactorial dis ease and major cause of morbidity and mortality. Absolute risk of venous thromboembolism is less than 1 per 10,000 per year in women of reproductive age. Hormonal contraception is a common risk situation for venous thromboembolism in this part of the population.

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Unlabelled: Inherited antithrombin deficiency is an autosomal dominant thrombophilia, resulting from genetic variations in the serpin family C member 1 (SERPINC1) gene. Antithrombin deficiency increases the risk of venous thromboembolism (VTE) compared to the general population. In this report, a novel missense variant of , c.

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Introduction: Inferior vena cava agenesis (IVCA) is a very uncommon vascular condition, occurring in about 0.0005% to 1% of the population. It is often overlooked as a potential cause of deep venous thrombosis and pulmonary embolism, particularly in younger patients.

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HSYA ameliorates venous thromboembolism by depleting the formation of TLR4/NF-κB pathway-dependent neutrophil extracellular traps.

Int Immunopharmacol

December 2024

Department of General Surgery, Nanjing First Hospital, Nanjing Medical University, No.68 Changle Road, Nanjing, Jiangsu 210006, China. Electronic address:

Neutrophil extracellular traps (NETs), released by activated neutrophils, are implicated in various medical conditions, including venous thromboembolism (VTE). To develop effective therapeutic strategies for VTE, it is crucial to elucidate the mechanisms involved. In this study, we explored the role of NETs in VTE pathogenesis and assessed the impact of hydroxyl safflower yellow pigment A (HSYA) treatment on VTE pathogenesis.

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Article Synopsis
  • The study investigates the causal relationship between chronic venous insufficiency (CVI) and cardiovascular diseases (CVDs) using Mendelian randomization (MR) analysis.
  • Results indicate that while genetically predicted CVI associates with a decreased risk of heart failure and an increased risk of atrial fibrillation, these associations weaken when accounting for other health factors.
  • The findings suggest that monitoring CVI could be important in managing patients with heart failure and atrial fibrillation, but no significant links were found with other cardiovascular conditions like hypertension or coronary artery disease.
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