PO01 | Diagnosis of inherited platelet function disorders by platelet aggregometry using a fully automated coagulation analyzer
Background and Aims: Inherited platelet-function disorders (IPFD) are qualitative platelet disorders with variable bleeding tendencies due to impaired platelet aggregation. Light-transmission aggregometry (LTA) represents the gold standard for their laboratory diagnosis. LTA is time-consuming, requ...
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PAGEPress Publications
2025-08-01
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| Series: | Bleeding, Thrombosis and Vascular Biology |
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| Online Access: | https://www.btvb.org/btvb/article/view/311 |
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Background and Aims: Inherited platelet-function disorders (IPFD) are qualitative platelet disorders with variable bleeding tendencies due to impaired platelet aggregation. Light-transmission aggregometry (LTA) represents the gold standard for their laboratory diagnosis. LTA is time-consuming, requires large blood-volumes and specialized personnel. In recent years, attempts have been made toward automation to overcome some limitations of manual LTA. Sysmex CN-6500 is a new haemostasis analyser that performs platelet aggregation with small volume samples (140 μl instead of 250 μl necessary for manual LTA or 300 μl for Multiplate) and automates reagent dilution. Aim of our study was to test the agreement between automated Sysmex CN-6500, manual LTA and multiple electrode aggregometry (MEA) in the study of IPFD.
Methods: IPFD patients were studied for platelet aggregation comparing 3 different methods: LTA with APACT 4 aggregometer (Helena), whole blood impedance aggregometry with Multiplate (Roche) and the automated LTA with Sysmex CN-6500 analyser using ADP, arachidonic acid, collagen and epinephrine as agonists.
Results: 50 patients affected by different forms of IPFD (Glanzmann thrombasthenia, PT-VWD, Filamin A defect, TAR, FPD/AML, TxA2 receptor defect, HPS, delta-SPD, COX-1 like defect) were tested. The platelet count in PRP ranged from 176 to 369×109/L, with three samples between 100 and 150×109/L. No significant differences in maximal aggregation amplitude were found between conventional LTA and the Sysmex CN-6500 using all agonists. Only ADP 10 μM performed with LTA gave slightly, but significantly, lower values compared to Sysmex CN-6500 (48.2±5.9% vs. 61±4.6%, p<0.05). Passing-Bablok regression analysis showed good agreement between Sysmex CN-6500, LTA and MEA, with significant correlations with all agonists, the highest with AA for MEA (Pearson r=0.67, p<0.0001) and with ADP for LTA (Person r=0.84, p<0.0001) (Figure 1A, B). Moreover, the percentage of patients with abnormal platelet aggregation in response to the different agonists did not differ significantly when comparing aggregation performed with Sysmex CN-6500 and with APACT 4 aggregometer or with Multiplate (Figure 1C, D).
Conclusions: Automated platelet aggregometry with Sysmex CN-6500 provides comparable results to two widely used and validated platelet aggregation assays, allowing the reliable measurement of platelet aggregation and the correct identification of patients with IPFD, with the advantage of full automation, smaller sample volume and shorter turnaround time.
Figure 1.
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| format | Article |
| id | doaj-art-6ec309d2f2954a7fa34f30b9de4edaad |
| institution | Kabale University |
| issn | 2785-5309 |
| language | English |
| publishDate | 2025-08-01 |
| publisher | PAGEPress Publications |
| record_format | Article |
| series | Bleeding, Thrombosis and Vascular Biology |
| spelling | doaj-art-6ec309d2f2954a7fa34f30b9de4edaad2025-08-20T04:00:45ZengPAGEPress PublicationsBleeding, Thrombosis and Vascular Biology2785-53092025-08-014s110.4081/btvb.2025.311PO01 | Diagnosis of inherited platelet function disorders by platelet aggregometry using a fully automated coagulation analyzer Background and Aims: Inherited platelet-function disorders (IPFD) are qualitative platelet disorders with variable bleeding tendencies due to impaired platelet aggregation. Light-transmission aggregometry (LTA) represents the gold standard for their laboratory diagnosis. LTA is time-consuming, requires large blood-volumes and specialized personnel. In recent years, attempts have been made toward automation to overcome some limitations of manual LTA. Sysmex CN-6500 is a new haemostasis analyser that performs platelet aggregation with small volume samples (140 μl instead of 250 μl necessary for manual LTA or 300 μl for Multiplate) and automates reagent dilution. Aim of our study was to test the agreement between automated Sysmex CN-6500, manual LTA and multiple electrode aggregometry (MEA) in the study of IPFD. Methods: IPFD patients were studied for platelet aggregation comparing 3 different methods: LTA with APACT 4 aggregometer (Helena), whole blood impedance aggregometry with Multiplate (Roche) and the automated LTA with Sysmex CN-6500 analyser using ADP, arachidonic acid, collagen and epinephrine as agonists. Results: 50 patients affected by different forms of IPFD (Glanzmann thrombasthenia, PT-VWD, Filamin A defect, TAR, FPD/AML, TxA2 receptor defect, HPS, delta-SPD, COX-1 like defect) were tested. The platelet count in PRP ranged from 176 to 369×109/L, with three samples between 100 and 150×109/L. No significant differences in maximal aggregation amplitude were found between conventional LTA and the Sysmex CN-6500 using all agonists. Only ADP 10 μM performed with LTA gave slightly, but significantly, lower values compared to Sysmex CN-6500 (48.2±5.9% vs. 61±4.6%, p<0.05). Passing-Bablok regression analysis showed good agreement between Sysmex CN-6500, LTA and MEA, with significant correlations with all agonists, the highest with AA for MEA (Pearson r=0.67, p<0.0001) and with ADP for LTA (Person r=0.84, p<0.0001) (Figure 1A, B). Moreover, the percentage of patients with abnormal platelet aggregation in response to the different agonists did not differ significantly when comparing aggregation performed with Sysmex CN-6500 and with APACT 4 aggregometer or with Multiplate (Figure 1C, D). Conclusions: Automated platelet aggregometry with Sysmex CN-6500 provides comparable results to two widely used and validated platelet aggregation assays, allowing the reliable measurement of platelet aggregation and the correct identification of patients with IPFD, with the advantage of full automation, smaller sample volume and shorter turnaround time. Figure 1. https://www.btvb.org/btvb/article/view/311Poster. |
| spellingShingle | PO01 | Diagnosis of inherited platelet function disorders by platelet aggregometry using a fully automated coagulation analyzer Bleeding, Thrombosis and Vascular Biology Poster. |
| title | PO01 | Diagnosis of inherited platelet function disorders by platelet aggregometry using a fully automated coagulation analyzer |
| title_full | PO01 | Diagnosis of inherited platelet function disorders by platelet aggregometry using a fully automated coagulation analyzer |
| title_fullStr | PO01 | Diagnosis of inherited platelet function disorders by platelet aggregometry using a fully automated coagulation analyzer |
| title_full_unstemmed | PO01 | Diagnosis of inherited platelet function disorders by platelet aggregometry using a fully automated coagulation analyzer |
| title_short | PO01 | Diagnosis of inherited platelet function disorders by platelet aggregometry using a fully automated coagulation analyzer |
| title_sort | po01 diagnosis of inherited platelet function disorders by platelet aggregometry using a fully automated coagulation analyzer |
| topic | Poster. |
| url | https://www.btvb.org/btvb/article/view/311 |