Analytical validation of platelet microparticle quantification in cats

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Analytical validation of platelet microparticle quantification in cats. / Cremer, Signe E.; Koch, Jørgen; Graversen, Nanna; Gravgaard, Anne S.; Langhorn, Rebecca; Kristensen, Annemarie T.; Willesen, Jakob L.; Nielsen, Lise N.

In: Veterinary Clinical Pathology, Vol. 47, No. 3, 2018, p. 386-395.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Cremer, SE, Koch, J, Graversen, N, Gravgaard, AS, Langhorn, R, Kristensen, AT, Willesen, JL & Nielsen, LN 2018, 'Analytical validation of platelet microparticle quantification in cats', Veterinary Clinical Pathology, vol. 47, no. 3, pp. 386-395. https://doi.org/10.1111/vcp.12641

APA

Cremer, S. E., Koch, J., Graversen, N., Gravgaard, A. S., Langhorn, R., Kristensen, A. T., Willesen, J. L., & Nielsen, L. N. (2018). Analytical validation of platelet microparticle quantification in cats. Veterinary Clinical Pathology, 47(3), 386-395. https://doi.org/10.1111/vcp.12641

Vancouver

Cremer SE, Koch J, Graversen N, Gravgaard AS, Langhorn R, Kristensen AT et al. Analytical validation of platelet microparticle quantification in cats. Veterinary Clinical Pathology. 2018;47(3):386-395. https://doi.org/10.1111/vcp.12641

Author

Cremer, Signe E. ; Koch, Jørgen ; Graversen, Nanna ; Gravgaard, Anne S. ; Langhorn, Rebecca ; Kristensen, Annemarie T. ; Willesen, Jakob L. ; Nielsen, Lise N. / Analytical validation of platelet microparticle quantification in cats. In: Veterinary Clinical Pathology. 2018 ; Vol. 47, No. 3. pp. 386-395.

Bibtex

@article{e1dbbae8620c43c9a2732811b26ac594,
title = "Analytical validation of platelet microparticle quantification in cats",
abstract = "Background: Cardiogenic embolism (CE) in cats is a devastating condition primarily associated with hypertrophic cardiomyopathy (HCM). Hypercoagulability may pose a risk for thrombus formation; however, no single test can predict CE development. Platelet microparticles (PMPs) released from platelet membranes are associated with thrombosis in humans. Objectives: The aims were to validate flow cytometric PMP quantification in cats analytically and, in a pilot study, evaluate the procoagulant annexin V (AnV) positive PMP concentration in healthy cats and cats with asymptomatic HCM. Methods: With CD61 as a platelet marker, CD61+AnV+ PMPs (0.3-1.0 μm) were quantified in citrated whole blood (WB) and platelet-poor plasma (PPP) using flow cytometry. Analyses were performed in 6 healthy cats and 5 cats with asymptomatic HCM. The coefficient of variation (CV) for duplicate (intra-assay) and parallel (inter-assay) analyses were calculated. Results: PMP concentrations were quantified with acceptable intra-assay CV for WB (CD61+/AnV-; 2.4%, 0.2%-8.4% (median, range), CD61+/AnV+; 3.8%, 0.1%-12.5%) and PPP (CD61+/AnV-; 5.0%, 0.7%-12.8%, CD61+/AnV+; 7.4%, 0.5%-15.3%), and acceptable inter-assay CV for WB in 10/11 cats (CD61+/AnV-; 6.2%, 1.4%-13.3%, CD61+/AnV+; 6.4%, 0.7%-17.2%), but unacceptable for PPP (CD61+/AnV-; 15.6%, 5.8%-42.7%, CD61+/AnV+; 27.8%, 8.4%-77.1%). For WB PMP concentrations, the pilot data demonstrated no differences between healthy cats and cats with asymptomatic HCM (4/5 with left ventricular outflow obstruction) for either the CD61+/AnV- or the CD61+/AnV+ PMPs. Conclusions: Only WB PMP concentrations could be quantified reliably in cats in a clinical setting. PMP concentrations did not differ between healthy and asymptomatic HCM cats in this pilot study.",
keywords = "Annexin, cardiac, CD61, microvesicles, precision",
author = "Cremer, {Signe E.} and J{\o}rgen Koch and Nanna Graversen and Gravgaard, {Anne S.} and Rebecca Langhorn and Kristensen, {Annemarie T.} and Willesen, {Jakob L.} and Nielsen, {Lise N.}",
year = "2018",
doi = "10.1111/vcp.12641",
language = "English",
volume = "47",
pages = "386--395",
journal = "Veterinary Clinical Pathology",
issn = "0275-6382",
publisher = "Wiley-Blackwell",
number = "3",

}

RIS

TY - JOUR

T1 - Analytical validation of platelet microparticle quantification in cats

AU - Cremer, Signe E.

AU - Koch, Jørgen

AU - Graversen, Nanna

AU - Gravgaard, Anne S.

AU - Langhorn, Rebecca

AU - Kristensen, Annemarie T.

AU - Willesen, Jakob L.

AU - Nielsen, Lise N.

PY - 2018

Y1 - 2018

N2 - Background: Cardiogenic embolism (CE) in cats is a devastating condition primarily associated with hypertrophic cardiomyopathy (HCM). Hypercoagulability may pose a risk for thrombus formation; however, no single test can predict CE development. Platelet microparticles (PMPs) released from platelet membranes are associated with thrombosis in humans. Objectives: The aims were to validate flow cytometric PMP quantification in cats analytically and, in a pilot study, evaluate the procoagulant annexin V (AnV) positive PMP concentration in healthy cats and cats with asymptomatic HCM. Methods: With CD61 as a platelet marker, CD61+AnV+ PMPs (0.3-1.0 μm) were quantified in citrated whole blood (WB) and platelet-poor plasma (PPP) using flow cytometry. Analyses were performed in 6 healthy cats and 5 cats with asymptomatic HCM. The coefficient of variation (CV) for duplicate (intra-assay) and parallel (inter-assay) analyses were calculated. Results: PMP concentrations were quantified with acceptable intra-assay CV for WB (CD61+/AnV-; 2.4%, 0.2%-8.4% (median, range), CD61+/AnV+; 3.8%, 0.1%-12.5%) and PPP (CD61+/AnV-; 5.0%, 0.7%-12.8%, CD61+/AnV+; 7.4%, 0.5%-15.3%), and acceptable inter-assay CV for WB in 10/11 cats (CD61+/AnV-; 6.2%, 1.4%-13.3%, CD61+/AnV+; 6.4%, 0.7%-17.2%), but unacceptable for PPP (CD61+/AnV-; 15.6%, 5.8%-42.7%, CD61+/AnV+; 27.8%, 8.4%-77.1%). For WB PMP concentrations, the pilot data demonstrated no differences between healthy cats and cats with asymptomatic HCM (4/5 with left ventricular outflow obstruction) for either the CD61+/AnV- or the CD61+/AnV+ PMPs. Conclusions: Only WB PMP concentrations could be quantified reliably in cats in a clinical setting. PMP concentrations did not differ between healthy and asymptomatic HCM cats in this pilot study.

AB - Background: Cardiogenic embolism (CE) in cats is a devastating condition primarily associated with hypertrophic cardiomyopathy (HCM). Hypercoagulability may pose a risk for thrombus formation; however, no single test can predict CE development. Platelet microparticles (PMPs) released from platelet membranes are associated with thrombosis in humans. Objectives: The aims were to validate flow cytometric PMP quantification in cats analytically and, in a pilot study, evaluate the procoagulant annexin V (AnV) positive PMP concentration in healthy cats and cats with asymptomatic HCM. Methods: With CD61 as a platelet marker, CD61+AnV+ PMPs (0.3-1.0 μm) were quantified in citrated whole blood (WB) and platelet-poor plasma (PPP) using flow cytometry. Analyses were performed in 6 healthy cats and 5 cats with asymptomatic HCM. The coefficient of variation (CV) for duplicate (intra-assay) and parallel (inter-assay) analyses were calculated. Results: PMP concentrations were quantified with acceptable intra-assay CV for WB (CD61+/AnV-; 2.4%, 0.2%-8.4% (median, range), CD61+/AnV+; 3.8%, 0.1%-12.5%) and PPP (CD61+/AnV-; 5.0%, 0.7%-12.8%, CD61+/AnV+; 7.4%, 0.5%-15.3%), and acceptable inter-assay CV for WB in 10/11 cats (CD61+/AnV-; 6.2%, 1.4%-13.3%, CD61+/AnV+; 6.4%, 0.7%-17.2%), but unacceptable for PPP (CD61+/AnV-; 15.6%, 5.8%-42.7%, CD61+/AnV+; 27.8%, 8.4%-77.1%). For WB PMP concentrations, the pilot data demonstrated no differences between healthy cats and cats with asymptomatic HCM (4/5 with left ventricular outflow obstruction) for either the CD61+/AnV- or the CD61+/AnV+ PMPs. Conclusions: Only WB PMP concentrations could be quantified reliably in cats in a clinical setting. PMP concentrations did not differ between healthy and asymptomatic HCM cats in this pilot study.

KW - Annexin

KW - cardiac

KW - CD61

KW - microvesicles

KW - precision

U2 - 10.1111/vcp.12641

DO - 10.1111/vcp.12641

M3 - Journal article

C2 - 30199121

AN - SCOPUS:85053008443

VL - 47

SP - 386

EP - 395

JO - Veterinary Clinical Pathology

JF - Veterinary Clinical Pathology

SN - 0275-6382

IS - 3

ER -

ID: 203673551