Birth weight and its relationship with endothelial function and pattern of endothelium-derived microparticles during childhood: New insight about early vascular damage

To investigate whether a specific endothelium-derived microparticles (EMPs) phenotype could be associated with birth weight and microvascular endothelial function in children. A total of 95 children aged 6–14 years were recruited. Anthropometric measurements, blood pressure measurement, microvascula...

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Veröffentlicht in:Life sciences (1973) 2022-06, Vol.298, p.120517-120517, Article 120517
Hauptverfasser: Parizotto, Giovanna Pachele, de Souza, Livia Victorino, Thomazini, Fernanda, Prado, Mônica Simon, Agudelo, Juan Sebastian Henao, de Almeida, Danilo Cândido, do Carmo Franco, Maria
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Sprache:eng
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Zusammenfassung:To investigate whether a specific endothelium-derived microparticles (EMPs) phenotype could be associated with birth weight and microvascular endothelial function in children. A total of 95 children aged 6–14 years were recruited. Anthropometric measurements, blood pressure measurement, microvascular endothelial function testing, and biochemical profile analyses were performed. Standardized flow cytometry methods were used to identify and quantify the circulating CD144+, CD31+/annexin V+, and CD62E+ EMPs. The circulating number of CD31+/annexin V+ EMPs and CD144+ EMP levels were correlated with birth weight, systolic blood pressure, microvascular endothelial function, total cholesterol, and low-density lipoprotein cholesterol (LDL-C) level. In the multivariable logistic regression models, we identified strong evidence of a higher risk of microvascular endothelial dysfunction among children with low birth weight (LBW) and increased levels of both CD31+/annexin V+ EMPs and LDL-C; LBW and elevated LDL-C levels were independent predictors of high circulating numbers of CD31+/annexin V+ and CD144+ > 75th percentile EMPs. Our data provide evidence that children with LBW values showed greater numbers of circulating CD31+/annexin V+ and CD144+ EMPs. In addition, LBW and high levels of CD31+/annexin V+ and LDL-C were significant risk factors for the presence of microvascular endothelial dysfunction.
ISSN:0024-3205
1879-0631
DOI:10.1016/j.lfs.2022.120517