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1.
Thromb Res ; 133(2): 168-72, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24321417

RESUMO

INTRODUCTION: The role of thrombophilia screening and antithrombotic therapy in unselected women undergone Assisted Reproductive Technologies (ART) is largely unknown. Nonetheless, in many Countries infertile women undergo thrombophilia screening and/or antithrombotic therapy. MATERIALS AND METHODS: We carried out a follow-up study. The original sample (n=1107) consisted of infertile women observed in 13 years. A cohort of 157 women with at least 1 cycle before thrombophilia test and 1 after test was investigated. All underwent thrombophilia screening; an antithrombotic treatment was prescribed in 216 out of 801 cycles. Clinical pregnancy and live birth rates were the main clinical objectives. RESULTS: Overall, 15 (9.6%) women carried thrombophilia. The Cox regression showed that LMWH alone or combined with ASA was significantly associated with the outcome "live birth" "live births" (p: 0.015, HR: 2.8, 95%CI: 1.2-6.6 for combined therapy), independently of the carriership of thrombophilia. Women with a lower number of attempts had a higher likelihood of delivering a live-born child using the combined therapy (p<0.001, HR: 0.7, 95%CI: 0.7-0.8), independently of the presence of thrombophilia. CONCLUSIONS: A potential benefit of LMWH in improving number of live births, independently of the presence of thrombophilia, is suggested. Universal thrombophilia screening before ART is not useful to discriminate women with a worse pregnancy prognosis.


Assuntos
Anticoagulantes/uso terapêutico , Heparina de Baixo Peso Molecular/uso terapêutico , Técnicas de Reprodução Assistida , Trombofilia/diagnóstico , Trombofilia/tratamento farmacológico , Adulto , Feminino , Seguimentos , Humanos , Infertilidade Feminina/diagnóstico , Nascido Vivo , Pessoa de Meia-Idade , Gravidez , Resultado da Gravidez , Trombofilia/complicações , Adulto Jovem
2.
Haemophilia ; 18(6): 1003-7, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-22672258

RESUMO

Development of inhibitory antibodies is perhaps the most serious complication of FVIII replacement therapy, precluding efficient clinical management of patients with haemophilia A (HA). The development and function of immune system are also regulated by microRNAs (miRNAs). Mutations and changes in the level of expression of some miRNA genes have been associated with the onset and progression of immunological disorders. The aim of this study was to investigate new genetic polymorphisms in loci for miRNA and their targets to evaluate whether these SNPs may confer susceptibility to inhibitor development in patients with HA. Italian HA patients with and without inhibitors and healthy controls were recruited in this study. For SNP analysis, standard DNA sequencing method was used. We have studied four SNPs, i.e. rs36101366, rs34683807, rs1803603 and rs3024496 located in the 3'UTR of F8 and IL-10 genes. These SNPs have been checked for their frequencies in patients with and without inhibitors, but no statistically significant differences were found. Then, we have searched for other genetic variants in loci for haematopoietic-specific miRNAs, i.e. hsa-mir-150, hsa-mir-155, hsa-mir-146a, hsa-mir-142, hsa-mir-181a and in a specific miRNA, hsa-mir-1184, i.e. predicted to be located in the intron 22 of F8 gene. For all miRNAs selected, we did not identify any sequence variation in our study population. This is the first study to demonstrate that there was no association between selected SNPs in miRNAs and their targets and the susceptibility to inhibitor development in people affected by HA.


Assuntos
Fator VIII/genética , Hemofilia A/genética , MicroRNAs/metabolismo , Regiões 3' não Traduzidas , Alelos , Bases de Dados Genéticas , Suscetibilidade a Doenças , Fator VIII/antagonistas & inibidores , Humanos , Interleucina-10/genética , Íntrons , MicroRNAs/genética , Polimorfismo de Nucleotídeo Único
4.
Minerva Ginecol ; 60(5): 431-6, 2008 Oct.
Artigo em Italiano | MEDLINE | ID: mdl-18854809

RESUMO

Pregnancy is a condition of excessive clotting due to a decrease of some coagulation factors and a reduction of anticoagulant proteins, such as protein S. It is known that the causes of congenital or acquired thrombophilia may be associated with an increased risk of venous thromboembolism during pregnancy and/or obstetric complications, such early or late fetal loss, intrauterine fetal deaths, pre-eclampsia, fetal growth restriction. During pregnancy the use of a prophylaxis with antithrombotic drugs is considered at present a promising opportunity to significantly reduce the prevalence of thromboembolic complications, improving maternal and fetal outcomes. This article is a review to most recent evidence of pregnant anticoagulant prophylaxis in women with previous thromboembolic events.


Assuntos
Anticoagulantes/uso terapêutico , Complicações Hematológicas na Gravidez/prevenção & controle , Trombofilia/prevenção & controle , Feminino , Humanos , Gravidez , Complicações Hematológicas na Gravidez/fisiopatologia , Fatores de Risco , Trombofilia/fisiopatologia
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