scholarly journals New evidence on the potential role of the metabolic syndrome as a risk factor for venous thromboembolism

2009 ◽  
Vol 7 (5) ◽  
pp. 736-738 ◽  
Author(s):  
W. AGENO ◽  
F. DENTALI ◽  
A. M. GRANDI
2009 ◽  
Vol 5 (7) ◽  
pp. 71-92 ◽  
Author(s):  
Francesca Fava ◽  
Julie A. Lovegrove ◽  
Kieran M. Tuohy ◽  
Glenn R. Gibson

2020 ◽  
Vol 135 ◽  
pp. 240-251
Author(s):  
Anuar Salazar-Gómez ◽  
Julio C. Ontiveros-Rodríguez ◽  
Saudy S. Pablo-Pérez ◽  
M. Elena Vargas-Díaz ◽  
Leticia Garduño-Siciliano

2004 ◽  
Vol 91 (02) ◽  
pp. 255-258 ◽  
Author(s):  
Ezio Zanon ◽  
Graziella Saggiorato ◽  
Roberto Ramon ◽  
Antonio Girolami ◽  
Antonio Pagnan ◽  
...  

SummaryThe role of antiprothrombin (aPT) antibodies in the development of venous thromboembolism (VTE) is still uncertain. The aim of this study was to evaluate the potential role of aPT antibodies in the development of recurrent thromboembolism. Out of 236 consecutive symptomatic patients with an episode of acute VTE, antiphospholipid antibodies were found in 85 (36.0%), of whom 24 were carriers of aPT antibodies (10.2% of the entire cohort). A history of previous thromboembolism was identified in 56 patients (23.7%). The prevalence of previous thromboembolism was significantly higher in carriers than in non-carriers of antiphospholipid antibodies (OR=2.4; 95% CI, 1.3 to 4.4). Of the 24 patients with aPT antibodies, 12 had a history of previous thromboembolism. In a multivariate logistic regression analysis, in which the other categories of antiphospholipid antibodies were taken into account, as well as the patient’s age, sex, and the modality of clinical presentation, it was found that the presence of aPT antibodies was significantly associated with the prevalence of prior thromboembolism (OR=3.3; 95% CI, 1.3 to 8.6). Since aPT antibodies are more commonly identifiable in patients with multiple thrombotic episodes, they are a likely risk factor for recurrent thromboembolism.


Author(s):  
Elena Korneeva ◽  
Mikhail Voevoda ◽  
Sergey Semaev ◽  
Vladimir Maksimov

Results of the study related to polymorphism of ACE gene (rs1799752)‎, integrin αIIbβ3, and CSK gene (rs1378942) influencing development of arterial hypertension in young patients with metabolic syndrome are presented. Hypertension as a component of the metabolic syndrome was detected in 15.0% of young patients. Prevalence of mutant alleles of the studied genes among the examined patients was quite high, so homozygous DD genotype was found in 21.6%, and mutant D allele of the ACE gene in 47.4%. A high risk of hypertension in patients with MS was detected in carriers of the T allele of the CSK (rs1378942) gene – 54.8%, which was most often observed in a combination of polymorphic ACE and CSK gene loci (p = 0.0053).


2016 ◽  
Vol 22 (7) ◽  
pp. 859-869 ◽  
Author(s):  
Bianca Martins Gregório ◽  
Diogo Benchimol De Souza ◽  
Fernanda Amorim de Morais Nascimento ◽  
Leonardo Matta ◽  
Caroline Fernandes-Santos

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