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Inflammatory cytokines in type 2 diabetes mellitus as facilitators of hypercoagulation and abnormal clot formation

机译:2型糖尿病的炎症细胞因子可促进高凝和异常血凝块形成

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The global burden of type 2 diabetes mellitus (T2DM), together with the presence of cardiovascular risk in this population, is reaching pandemic levels. A prominent feature of T2DM is chronic and systemic inflammation, with the accompanying presence of circulating and dysregulated inflammatory biomarkers; which in turn is associated with abnormal clot formation. Here, we investigate the correlation between abnormal blood clotting, using thromboelastography (TEG), clot ultrastructure using scanning electron microscopy (SEM) and the presence of a dysregulated inflammatory cytokine profile, by examining various circulating biomarkers. Our results show that many biomarkers, across TEG, cytokine and lipid groups, were greatly dysregulated in the T2DM sample. Furthermore, our T2DM sample’s coagulation profiles were significantly more hypercoagulable when compared to our heathy sample, and ultrastructural analysis confirmed a matted and denser clot structure in the T2DM sample. We suggest that dysregulated circulating molecules may in part be responsible for a hypercoagulable state and vascular dysfunction in the T2DM sample. We propose further that a personalized approach could be of great value when planning treatment and tracking the patient health status after embarking on a treatment regimes, and that looking to novel inflammatory and vascular biomarkers might be crucial.
机译:2型糖尿病(T2DM)的全球负担以及该人群中存在心血管疾病的风险正在达到大流行水平。 T2DM的显着特征是慢性和全身性炎症,并伴有循环性和失调的炎症生物标记物的存在。这又与异常的血凝块形成有关。在这里,我们通过检查各种循环生物标记物,研究了使用血栓弹力描记术(TEG)的异常凝血,使用扫描电子显微镜(SEM)的血凝块超微结构与炎症细胞因子分布失调之间的相关性。我们的结果表明,跨TEG,细胞因子和脂质组的许多生物标志物在T2DM样品中大大失调。此外,与我们的健康样本相比,我们的T2DM样本的凝结曲线具有更高的高凝性,并且超微结构分析证实T2DM样本中的凝块结构杂乱且致密。我们建议,T2DM样本中循环分子失调可能部分导致了高凝状态和血管功能异常。我们进一步提出,个性化方法在计划治疗方案并开始采用治疗方案后跟踪患者的健康状况时可能具有重要价值,并且寻找新颖的炎症和血管生物标志物可能至关重要。

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