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Platelet-Derived Microparticles: A New Index of Monitoring Platelet Activation and Inflammation in Kawasaki Disease

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机构: [1]Nanjing Med Univ, Childrens Hosp, Nanjing, Jiangsu, Peoples R China [2]Southeast Univ, Sch Med, Nanjing Tongren Hosp, Nanjing, Jiangsu, Peoples R China
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关键词: Platelet-derived microparticle Platelet activation Kawasaki disease Inflammation

摘要:
Objective To investigate the dynamic changes of platelet-derived microparticles (PDMP) in Kawasaki disease (KD) and its clinical significance and to study its relationship with intravenous immunoglobulin (IVIG) resistance, inflammatory indicators and aspirin treatment in children with KD. Methods Twenty children with KD were enrolled as the experimental group, while 20 age- and gender-matched children with common febrile disease were included in the control group. Blood samples were drawn before and 7-10 d after IVIG infusion and thereafter at 1, 2, and 3 mo after the onset of KD to estimate the PDMP concentrations by enzyme linked immunosorbent assay (ELISA). C-reactive protein (hs-CRP), erythrocyte sedimentation rate (ESR), procalcitonin (PCT), and cytokines [Interleukin-6 (IL-6), Tumor necrosis factor-alpha (TNF-alpha), and Soluble interleukin-2 (sIL-2R)] were also measured. Results The level of PDMP in KD children before IVIG was significantly higher than that in controls (P < 0.0001). The PDMP level in KD children decreased significantly at 7 to 10 d after IVIG (P < 0.0001) and then decreased to the lowest level in the course of 1 to 2 mo. Some children's PDMP level rebounded in the course of 3 mo (P = 0.047). In addition, the mean level of PDMP in IVIG-resistant children was higher than that in IVIG-effective children; however, there was no significant difference between the two groups (P = 0.1945). Furthermore, PDMP was positively correlated with hs-CRP, IL-6, and sIL-2R levels, but no correlation was observed with ESR, PCT, and TNF-alpha levels. Conclusions PDMP can be used as an index to monitor inflammation in children at the acute stage of KD. And the duration of platelet activation in KD is individualized.

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出版当年[2018]版:
大类 | 4 区 医学
小类 | 4 区 儿科
最新[2023]版:
大类 | 4 区 医学
小类 | 4 区 儿科
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出版当年[2017]版:
Q4 PEDIATRICS
最新[2023]版:
Q2 PEDIATRICS

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第一作者机构: [1]Nanjing Med Univ, Childrens Hosp, Nanjing, Jiangsu, Peoples R China
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