The effect of recombinant and plasma-derived prothrombin on prothrombin time in human plasma

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The effect of recombinant and plasma-derived prothrombin on prothrombin time in human plasma. / Hansson, K M; Björkqvist, J; Deinum, J.

In: INT J LAB HEMATOL, Vol. 37, No. 3, 06.2015, p. 357-64.

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@article{14d5ab9c69a4480d90c0761375e5437e,
title = "The effect of recombinant and plasma-derived prothrombin on prothrombin time in human plasma",
abstract = "INTRODUCTION: When investigating coagulation assays to measure the effect of infused prothrombin (FII) in in vivo coagulopathy models, we found that addition of FII, plasma-derived human FII (pd-hFII) or recombinant human FII (r-hFII), to normal plasma resulted in a concentration-dependent increase in prothrombin time (PT) initiated with Innovin({\textregistered}) .METHODS: The effect on PT by addition to plasma of either pd-hFII or r-hFII, using different commercial PT reagents, was studied both by turbidimetry and viscometry.RESULT: Addition of FII to plasma resulted in increased PT when initiated with Innovin({\textregistered}) : PT increased with 20% by doubling the concentration. The prolongation of PT became more pronounced with 2-6000 times diluted Innovin({\textregistered}) . However, by adjustment of the final free Ca(2+) concentration in the assay with diluted Innovin({\textregistered}) from 8.3 to 1.3 mmol/L, no FII-dependent increase in PT was found. In contrast, no prolongation of PT was found with other commercial PT reagents. A KM = 3 nmol/L was obtained with pd-hFII, respectively, r-hFII with FII-depleted plasma using Thromborel({\textregistered}) to initiate PT.CONCLUSION: At normal plasma concentration of FII, addition of FII should not have an effect on PT. The prolonged PT with Innovin({\textregistered}) , but not with other PT reagents, at supranormal FII concentration is an artefact.",
keywords = "Blood Proteins, Calcium, Humans, Prothrombin, Prothrombin Time, Recombinant Proteins, Thromboplastin",
author = "Hansson, {K M} and J Bj{\"o}rkqvist and J Deinum",
note = "{\textcopyright} 2014 John Wiley & Sons Ltd.",
year = "2015",
month = jun,
doi = "10.1111/ijlh.12293",
language = "English",
volume = "37",
pages = "357--64",
journal = "INT J LAB HEMATOL",
issn = "1751-5521",
publisher = "Wiley-Blackwell",
number = "3",

}

RIS

TY - JOUR

T1 - The effect of recombinant and plasma-derived prothrombin on prothrombin time in human plasma

AU - Hansson, K M

AU - Björkqvist, J

AU - Deinum, J

N1 - © 2014 John Wiley & Sons Ltd.

PY - 2015/6

Y1 - 2015/6

N2 - INTRODUCTION: When investigating coagulation assays to measure the effect of infused prothrombin (FII) in in vivo coagulopathy models, we found that addition of FII, plasma-derived human FII (pd-hFII) or recombinant human FII (r-hFII), to normal plasma resulted in a concentration-dependent increase in prothrombin time (PT) initiated with Innovin(®) .METHODS: The effect on PT by addition to plasma of either pd-hFII or r-hFII, using different commercial PT reagents, was studied both by turbidimetry and viscometry.RESULT: Addition of FII to plasma resulted in increased PT when initiated with Innovin(®) : PT increased with 20% by doubling the concentration. The prolongation of PT became more pronounced with 2-6000 times diluted Innovin(®) . However, by adjustment of the final free Ca(2+) concentration in the assay with diluted Innovin(®) from 8.3 to 1.3 mmol/L, no FII-dependent increase in PT was found. In contrast, no prolongation of PT was found with other commercial PT reagents. A KM = 3 nmol/L was obtained with pd-hFII, respectively, r-hFII with FII-depleted plasma using Thromborel(®) to initiate PT.CONCLUSION: At normal plasma concentration of FII, addition of FII should not have an effect on PT. The prolonged PT with Innovin(®) , but not with other PT reagents, at supranormal FII concentration is an artefact.

AB - INTRODUCTION: When investigating coagulation assays to measure the effect of infused prothrombin (FII) in in vivo coagulopathy models, we found that addition of FII, plasma-derived human FII (pd-hFII) or recombinant human FII (r-hFII), to normal plasma resulted in a concentration-dependent increase in prothrombin time (PT) initiated with Innovin(®) .METHODS: The effect on PT by addition to plasma of either pd-hFII or r-hFII, using different commercial PT reagents, was studied both by turbidimetry and viscometry.RESULT: Addition of FII to plasma resulted in increased PT when initiated with Innovin(®) : PT increased with 20% by doubling the concentration. The prolongation of PT became more pronounced with 2-6000 times diluted Innovin(®) . However, by adjustment of the final free Ca(2+) concentration in the assay with diluted Innovin(®) from 8.3 to 1.3 mmol/L, no FII-dependent increase in PT was found. In contrast, no prolongation of PT was found with other commercial PT reagents. A KM = 3 nmol/L was obtained with pd-hFII, respectively, r-hFII with FII-depleted plasma using Thromborel(®) to initiate PT.CONCLUSION: At normal plasma concentration of FII, addition of FII should not have an effect on PT. The prolonged PT with Innovin(®) , but not with other PT reagents, at supranormal FII concentration is an artefact.

KW - Blood Proteins

KW - Calcium

KW - Humans

KW - Prothrombin

KW - Prothrombin Time

KW - Recombinant Proteins

KW - Thromboplastin

U2 - 10.1111/ijlh.12293

DO - 10.1111/ijlh.12293

M3 - SCORING: Journal article

C2 - 25212252

VL - 37

SP - 357

EP - 364

JO - INT J LAB HEMATOL

JF - INT J LAB HEMATOL

SN - 1751-5521

IS - 3

ER -