Nastasya Nunki, Yetti Hernaningsih, Puspa Wardhani, Asih Herawati, Narazah Mohd Yusoff, Emmanuel Jairaj Moses, Bambang Pujo Semedi
{"title":"血小板和单核细胞微泡作为 COVID-19 严重程度的潜在生物标志物:横断面分析","authors":"Nastasya Nunki, Yetti Hernaningsih, Puspa Wardhani, Asih Herawati, Narazah Mohd Yusoff, Emmanuel Jairaj Moses, Bambang Pujo Semedi","doi":"10.3343/alm.2023.0395","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Coronavirus disease (COVID-19) induces inflammation, coagulopathy following platelet and monocyte activation, and fibrinolysis, resulting in elevated D-dimer levels. Activated platelets and monocytes produce microvesicles (MVs). We analyzed the differences in platelet and monocyte MV counts in mild, moderate, and severe COVID-19, as well as their correlation with D-dimer levels.</p><p><strong>Methods: </strong>In this cross-sectional study, blood specimens were collected from 90 COVID-19 patients and analyzed for D-dimers using SYSMEX CS-2500. Platelet MVs (PMVs; PMVCD42b<sup>+</sup> and PMVCD41a<sup>+</sup>), monocyte MVs (MMVs; MMVCD14<sup>+</sup>), and phosphatidylserine-binding annexin V (PS, AnnV<sup>+</sup>) were analyzed using a BD FACSCalibur instrument.</p><p><strong>Results: </strong>PMV and MMV counts were significantly increased in COVID-19 patients. AnnV<sup>+</sup> PMVCD42b<sup>+</sup> and AnnV<sup>+</sup> PMVCD41a<sup>+</sup> cell counts were higher in patients with severe COVID-19 than in those with moderate clinical symptoms. The median (range) of AnnV<sup>+</sup> PMVCD42b<sup>+</sup> (MV/μL) in mild, moderate, and severe COVID-19 was 1,118.3 (328.1-1,910.5), 937.4 (311.4-2,909.5), and 1,298.8 (458.2-9,703.5), respectively (<i>P</i> =0.009). The median (range) for AnnV<sup>+</sup> PMVCD41a<sup>+</sup> (MV/μL) in mild, moderate, and severe disease was 885.5 (346.3-1,682.7), 663.5 (233.8-2,081.5), and 1,146.3 (333.3-10,296.6), respectively (<i>P</i> =0.007). D-dimer levels (ng/mL) weak correlated with AnnV<sup>+</sup> PMVCD41a<sup>+</sup> (<i>P</i> =0.047, r=0.258).</p><p><strong>Conclusions: </strong>PMV PMVCD42b<sup>+</sup> and PMVCD41a<sup>+</sup> counts were significantly increased in patients with severe clinical symptoms, and PMVCD41a<sup>+</sup> counts correlated with D-dimer levels. Therefore, MV counts can be used as a potential biomarker of COVID-19 severity.</p>","PeriodicalId":8421,"journal":{"name":"Annals of Laboratory Medicine","volume":" ","pages":"392-400"},"PeriodicalIF":4.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11169774/pdf/","citationCount":"0","resultStr":"{\"title\":\"Platelet and Monocyte Microvesicles as Potential Biomarkers of COVID-19 Severity: A Cross-Sectional Analysis.\",\"authors\":\"Nastasya Nunki, Yetti Hernaningsih, Puspa Wardhani, Asih Herawati, Narazah Mohd Yusoff, Emmanuel Jairaj Moses, Bambang Pujo Semedi\",\"doi\":\"10.3343/alm.2023.0395\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Coronavirus disease (COVID-19) induces inflammation, coagulopathy following platelet and monocyte activation, and fibrinolysis, resulting in elevated D-dimer levels. Activated platelets and monocytes produce microvesicles (MVs). We analyzed the differences in platelet and monocyte MV counts in mild, moderate, and severe COVID-19, as well as their correlation with D-dimer levels.</p><p><strong>Methods: </strong>In this cross-sectional study, blood specimens were collected from 90 COVID-19 patients and analyzed for D-dimers using SYSMEX CS-2500. Platelet MVs (PMVs; PMVCD42b<sup>+</sup> and PMVCD41a<sup>+</sup>), monocyte MVs (MMVs; MMVCD14<sup>+</sup>), and phosphatidylserine-binding annexin V (PS, AnnV<sup>+</sup>) were analyzed using a BD FACSCalibur instrument.</p><p><strong>Results: </strong>PMV and MMV counts were significantly increased in COVID-19 patients. AnnV<sup>+</sup> PMVCD42b<sup>+</sup> and AnnV<sup>+</sup> PMVCD41a<sup>+</sup> cell counts were higher in patients with severe COVID-19 than in those with moderate clinical symptoms. The median (range) of AnnV<sup>+</sup> PMVCD42b<sup>+</sup> (MV/μL) in mild, moderate, and severe COVID-19 was 1,118.3 (328.1-1,910.5), 937.4 (311.4-2,909.5), and 1,298.8 (458.2-9,703.5), respectively (<i>P</i> =0.009). The median (range) for AnnV<sup>+</sup> PMVCD41a<sup>+</sup> (MV/μL) in mild, moderate, and severe disease was 885.5 (346.3-1,682.7), 663.5 (233.8-2,081.5), and 1,146.3 (333.3-10,296.6), respectively (<i>P</i> =0.007). D-dimer levels (ng/mL) weak correlated with AnnV<sup>+</sup> PMVCD41a<sup>+</sup> (<i>P</i> =0.047, r=0.258).</p><p><strong>Conclusions: </strong>PMV PMVCD42b<sup>+</sup> and PMVCD41a<sup>+</sup> counts were significantly increased in patients with severe clinical symptoms, and PMVCD41a<sup>+</sup> counts correlated with D-dimer levels. Therefore, MV counts can be used as a potential biomarker of COVID-19 severity.</p>\",\"PeriodicalId\":8421,\"journal\":{\"name\":\"Annals of Laboratory Medicine\",\"volume\":\" \",\"pages\":\"392-400\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11169774/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of Laboratory Medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3343/alm.2023.0395\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/3/12 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICAL LABORATORY TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Laboratory Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3343/alm.2023.0395","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/3/12 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
Platelet and Monocyte Microvesicles as Potential Biomarkers of COVID-19 Severity: A Cross-Sectional Analysis.
Background: Coronavirus disease (COVID-19) induces inflammation, coagulopathy following platelet and monocyte activation, and fibrinolysis, resulting in elevated D-dimer levels. Activated platelets and monocytes produce microvesicles (MVs). We analyzed the differences in platelet and monocyte MV counts in mild, moderate, and severe COVID-19, as well as their correlation with D-dimer levels.
Methods: In this cross-sectional study, blood specimens were collected from 90 COVID-19 patients and analyzed for D-dimers using SYSMEX CS-2500. Platelet MVs (PMVs; PMVCD42b+ and PMVCD41a+), monocyte MVs (MMVs; MMVCD14+), and phosphatidylserine-binding annexin V (PS, AnnV+) were analyzed using a BD FACSCalibur instrument.
Results: PMV and MMV counts were significantly increased in COVID-19 patients. AnnV+ PMVCD42b+ and AnnV+ PMVCD41a+ cell counts were higher in patients with severe COVID-19 than in those with moderate clinical symptoms. The median (range) of AnnV+ PMVCD42b+ (MV/μL) in mild, moderate, and severe COVID-19 was 1,118.3 (328.1-1,910.5), 937.4 (311.4-2,909.5), and 1,298.8 (458.2-9,703.5), respectively (P =0.009). The median (range) for AnnV+ PMVCD41a+ (MV/μL) in mild, moderate, and severe disease was 885.5 (346.3-1,682.7), 663.5 (233.8-2,081.5), and 1,146.3 (333.3-10,296.6), respectively (P =0.007). D-dimer levels (ng/mL) weak correlated with AnnV+ PMVCD41a+ (P =0.047, r=0.258).
Conclusions: PMV PMVCD42b+ and PMVCD41a+ counts were significantly increased in patients with severe clinical symptoms, and PMVCD41a+ counts correlated with D-dimer levels. Therefore, MV counts can be used as a potential biomarker of COVID-19 severity.
期刊介绍:
Annals of Laboratory Medicine is the official journal of Korean Society for Laboratory Medicine. The journal title has been recently changed from the Korean Journal of Laboratory Medicine (ISSN, 1598-6535) from the January issue of 2012. The JCR 2017 Impact factor of Ann Lab Med was 1.916.