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Tytuł pozycji:

The effects of fructose diphosphate on routine coagulation tests in vitro.

Tytuł:
The effects of fructose diphosphate on routine coagulation tests in vitro.
Autorzy:
Chen T; Blood Transfusion Department, Anhui No. 2 Provincial People's Hospital, Hefei, Anhui, China.
Chen D; Clinical Medicine (5+3 Integration) 2020 Year 4 Class, School of Basic Medical Sciences, Wuhan University Medical School, Wuhan, Hubei, China.
Chen L; Blood Transfusion Department, Anhui No. 2 Provincial People's Hospital, Hefei, Anhui, China.
Chen Z; Clinical Laboratory Department, The Second People's Hospital of Hefei, Anhui, China.
Wang B; Clinical Laboratory Department, The First Hospital of the University of Science and Technology of China, Hefei, Anhui, China.
Zhou D; Department of Oncology, Anhui No. 2 Provincial People's Hospital, 6nd Floor,Building B, Hefei, Anhui, China. .
Źródło:
Scientific reports [Sci Rep] 2022 Jan 07; Vol. 12 (1), pp. 304. Date of Electronic Publication: 2022 Jan 07.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Original Publication: London : Nature Publishing Group, copyright 2011-
MeSH Terms:
Blood Coagulation Tests*
Blood Coagulation/*drug effects
Fructosediphosphates/*pharmacology
Dose-Response Relationship, Drug ; Humans ; Partial Thromboplastin Time ; Platelet Aggregation/drug effects ; Platelet Function Tests ; Prothrombin Time ; Thrombin Time
References:
Cardioscience. 1991 Sep;2(3):161-5. (PMID: 1660321)
Metab Eng. 2017 Jul;42:168-174. (PMID: 28624535)
Am J Clin Pathol. 2011 Dec;136(6):848-54. (PMID: 22095369)
Nature. 2017 Aug 3;548(7665):112-116. (PMID: 28723898)
Biometals. 2015 Aug;28(4):687-91. (PMID: 25940829)
J Thromb Thrombolysis. 2010 May;29(4):387-94. (PMID: 19705256)
Stroke. 1990 Apr;21(4):606-13. (PMID: 2326842)
Int J Clin Pract. 2011 Jul;65(7):784-9. (PMID: 21564449)
Curr Med Chem. 2016;23(39):4396-4417. (PMID: 27758716)
Antimicrob Agents Chemother. 2017 Jan 24;61(2):. (PMID: 27956417)
Acta Pharm. 2015 Jun;65(2):147-57. (PMID: 26011931)
Biochim Biophys Acta. 1991 Aug 13;1094(1):121-9. (PMID: 1883850)
Res Pract Thromb Haemost. 2018 Aug 30;2(4):778-789. (PMID: 30349897)
Arch Pathol Lab Med. 2004 Oct;128(10):1142-5. (PMID: 15387708)
Biochem Soc Trans. 2014 Dec;42(6):1792-5. (PMID: 25399608)
Biochem Pharmacol. 1992 Apr 1;43(7):1539-44. (PMID: 1314605)
Grant Information:
2020ZR12925B008 Program of Natural Science Research of Anhui Provincial Education Department
Substance Nomenclature:
0 (Fructosediphosphates)
M7522JYX1H (fructose-1,6-diphosphate)
Entry Date(s):
Date Created: 20220108 Date Completed: 20220224 Latest Revision: 20231105
Update Code:
20240104
PubMed Central ID:
PMC8741944
DOI:
10.1038/s41598-021-04263-y
PMID:
34997135
Czasopismo naukowe
To evaluate the effects of fructose diphosphate (FDP) on routine coagulation tests in vitro, we added FDP into the mixed normal plasma to obtain the final concentration of 0, 1, 2, 3, 4, 5, 6, 10, 15, 20, 25, 30 and 35 mg/mL of drug. Prothrombin time (PT), activated partial thromboplastin time (aPTT), fibrinogen (FBG) and thrombin time (TT) of samples were analyzed with blood coagulation analyzers from four different manufacturers(Sysmex, Stago, SEKISUI and Werfen) and their corresponding reagents, respectively. Before the experiment, we also observed whether there were significant differences in coagulation test results of different lots of reagents produced by each manufacturer. At the same time as the four routine clotting tests, the Sysmex blood coagulation analyzer and its proprietary analysis software were used to detect the change of maximum platelet aggregation rate in platelet-rich plasma after adding FDP (0, 1, 2, 3, 4, 5 and 6 mg/mL). The results of PT, aPTT and TT showed a FDP (0-35 mg/mL) concentration-dependent increase and a FBG concentration-dependent decrease. The degree of change (increase or decrease) varied depending on the assay system, with PT and aPTT being more affected by the Sysmex blood coagulation testing instrument reagent system and less affected by CEKISUI, TT less affected by CEKISUI and more affected by Stago, and FBG less affected by Stago and more affected by Sysmex. The results of PT, aPTT and TT were statistically positively correlated with their FDP concentrations, while FBG was negatively correlated. The correlation coefficients between FDP and the coagulation testing systems of Sysmex, Stago, Werfen and SEKISUI were 0.975, 0.988, 0.967, 0.986 for PT, and 0.993, 0.989, 0.990 and 0.962 for aPTT, 0.994, 0.960, 0.977 and 0.982 for TT, - 0.990, - 0.983, - 0.989 and - 0.954 for FBG, respectively. Different concentrations of FDP (0, 1, 2, 3, 4, 5 and 6 mg/mL) had different effects on the maximum aggregation rate of platelet induced by the agonists of adenosine diphosphate (ADP, 5 µmol/L), arachidonic acid (Ara, 1 mmol/L), collagen (Col, 2.5 µg/mL) and epinephrine (Epi,10 µmol/L), but the overall downward trend was consistent, that is, with the increase of FDP concentration, the platelet aggregation rate decreased significantly. Our experimental study demonstrated a possible effect of FDP on the assays of coagulation and Platelet aggregation, which may arise because the drug interferes with the coagulation and platelet aggregation detection system, or it may affect our in vivo coagulation system and Platelet aggregation function, the real mechanism of which remains to be further verified and studied.
(© 2022. The Author(s).)
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