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Адрес редакции и реквизиты

199406, Санкт-Петербург, ул.Гаванская, д. 49, корп.2

ISSN 1999-6314

Российская поисковая система
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«
Vol. 15, Art. 58 (pp. 731-741)    |    2014       
»

The state of hemostasis and the сharacter of allelic polymorphism of genes associated with dysfunction of hemostasis in children with primary and secondary glomerulonephritis
Papayan K. *, Kapustin S. **, Savenkova N.*, Golovina O. **, Tarkovskaya L. **, Papayan L. **, Kachanova T. ***

* The Department of faculty Pediatric, Saint-Petersburg State Pediatric Medical University, e-mail: papayan@inbox.ru;
** Laboratory of blood coagulation, laboratory of biochemistry, Russian Research Institute of Hematology and Transfusiology; Saint-Petersburg
*** Department of automation and control processes, St. Petersburg state Electrotechnical University «LETI»



Brief summary

In 151 patients: 31 with hormone-sensitive nephrotic syndrome (NS); 95 with primary chronic glomerulonephritis (GN) and 25 patients with secondary GN in systemic vasculitis investigated indicators of coagulation hemostasis and the nature of allelic polymorphism of genes associated with dysfunction of hemostasis. As a result of the study, the patients with primary and secondary glomerulonephritis defined some differences in coagulation status and nature of allelic polymorphism of genes associated with dysfunction of hemostasis. Signs of hypercoagulability identified in persons of the 1st and 3rd groups. A large degree of hypercoagulability characterized patients of the 1st group with hormone-sensitive nephrotic syndrome, which is in contrast to the patients of the 3rd group with secondary GN, associated with systemic vasculitis, the activity of antithrombin was significantly reduced. In patients of the 2nd group with chronic GN blood coagulation statistically not significantly different from those of the normal group and were correspondingly lower than in patients with other two groups. A distinctive feature of patients with chronic GN was the increased activity of antithrombin compared with the control group. The greatest intensity of hypercoagulation along with high frequency of occurrence of mutation FV Leiden – 12, 9% (OR=3,2; p=0.07) characterized only patients with NS, which indicates the role of thrombophilic status in the development of the most severe forms of glomerulonephritis.


Key words

children, glomerulonephritis, hemostasis, thrombophilia, the polymorphism of





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