ஜர்னல் ஆஃப் ஹெமாட்டாலஜி & த்ரோம்போம்போலிக் நோய்கள்

ஜர்னல் ஆஃப் ஹெமாட்டாலஜி & த்ரோம்போம்போலிக் நோய்கள்
திறந்த அணுகல்

ஐ.எஸ்.எஸ்.என்: 2329-8790

சுருக்கம்

The Main Causes of Thrombotic Events in Carriage of Leiden Mutation in Women of Reproductive Age

Momot AP, Nikolaeva MG and Zainulina MS

The article defines the role of a combination of several acquired thrombogenic risk factors with Activated Protein C (APC) resistance which is due to carriage of FVL (1691)GA genotype to develop Venous Thromboembolic Complications (VTEC). In this regard, a prospective clinical study of 1100 women of reproductive age was conducted. The patients were divided into two groups. The main group–500 patients with FVL (1691)GA genotype, and the control group–600 women with FVL(1691)GG genotype. Based on the findings of the conducted study, it was concluded that carriage of FVL (1691)GA genotype is associated with VTEC development compared to the normozygous genotype. The highest incidence of primary thrombotic events was identified on the background of combined hormonal contraceptive administration. In the event of VTEC, carriers of Factor V Leiden (FVL (1691)GA) mutation often suffer from hypertensive disorders, varicose disease of the lower extremities, overweight and/or combinations of these pathology types. It was defined that in all cases of thrombosis episode, the value of APC resistance was ≤ 0.49 according to Normalized Ratio (NR), while episodes of VTEC were not observed in NR ≥ 0.5.

மறுப்பு: இந்த சுருக்கமானது செயற்கை நுண்ணறிவு கருவிகளைப் பயன்படுத்தி மொழிபெயர்க்கப்பட்டது மற்றும் இன்னும் மதிப்பாய்வு செய்யப்படவில்லை அல்லது சரிபார்க்கப்படவில்லை.
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