A simple method for measuring fibrinogen and evaluating its functionality

Authors

  • B. B. Shoibonov National Medical Research Center for Preventive Medicine, Moscow, Russia; P.K. Anokhin Institute of Normal Physiology, Moscow, Russia
  • O. M. Drapkina National Medical Research Center for Preventive Medicine, Moscow, Russia http://orcid.org/0000-0002-4453-8430
  • T. P. Baronets I.M. Sechenov First Moscow State Medical University, Moscow, Russia
  • N. Yu. Serebryakova National Medical Research Center for Preventive Medicine, Moscow, Russia
  • M. B. Khudyakov National Medical Research Center for Preventive Medicine, Moscow, Russia
  • D. V. Grigorieva Moscow Regional Research Institute of Obstetrics and Gynecology, Moscow, Russia
  • O. A. Lebedeva National Medical Research Center for Preventive Medicine, Moscow, Russia
  • O. A. Litinskaya National Medical Research Center for Preventive Medicine, Moscow, Russia
  • S. M. Tolpigo P.K. Anokhin Institute of Normal Physiology, Moscow, Russia http://orcid.org/0000-0002-6457-6725
  • L. V. Lagutina P.K. Anokhin Institute of Normal Physiology, Moscow, Russia

DOI:

https://doi.org/10.25557/2310-0435.2020.01.74-81

Keywords:

fibrinogen, plasma recalcification, turbidimetry, fibrinogen functionality

Abstract

Background. The Clauss fibrinogen assay is sensitive to hypo-, dys- and hyper-fibrinogenemia, as well as to fibrin degradation products, which may affect coagulation and cause underestimation of or increase the fibrinogen level.
The aim of this study was to develop a simple turbidimetric test to measure fibrinogen and evaluate its functionality.
Materials and methods. In this study, fibrinogen was measured in citrate plasma from 96 patients using the Clauss assay, a modified Rutberg method, and a new turbidimetric test.
Result. A simple turbidimetric test was developed for measuring fibrinogen. This test is based on measuring coagulated fibrinogen during recalcification of citrate plasma according to the formula, FG (g/l) = ΔА450 × 5.12, where ΔА450 is a change in optical density of the experimental sample; 5.12 is a conversion coefficient ΔА450 in g/l FG. Correlation analysis showed a high degree of agreement between the results (R = 0.843). With a FG difference of more than 10% by the Clauss assay and the developed method, impaired functionality of the FG is stated.

Conclusion. Using a simple, affordable turbidimetric method to determine fibrinogen in routine studies allows accessing the fibrinogen functionality.

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Published

2020-03-05

Issue

Section

New technologies

How to Cite

A simple method for measuring fibrinogen and evaluating its functionality. (2020). Patogenez (Pathogenesis), 18(1), 74-81. https://doi.org/10.25557/2310-0435.2020.01.74-81