Department of Respiratory Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands.
Department of Internal Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands.
Thromb Haemost. 2020 May;120(5):768-775. doi: 10.1055/s-0040-1709523. Epub 2020 May 5.
Cardiovascular events are associated with low circulating vitamin D concentrations, although the underlying mechanisms are poorly understood. This study investigated associations between 25-hydroxyvitamin D concentrations, platelet function, and single-nucleotide polymorphisms (SNPs) in genes influencing vitamin D biology in the 500 Functional Genomics (500FG) cohort.
In this observational study, platelet activation and function were measured by flow cytometry by binding of fibrinogen to the activated fibrinogen receptor integrin αIIbβ3 and expression of P-selectin, markers of platelet aggregation and degranulation, respectively. These parameters were correlated to serum 25-hydroxyvitamin D and genotyping was performed to investigate SNPs in genes important for vitamin D biology.
Circulating 25-hydroxyvitamin D concentrations correlated inversely with baseline platelet binding of fibrinogen to integrin αIIbβ3 (Pearson's = -0.172, = 0.002) and platelet responses to platelet agonist cross-linked collagen-related peptide (CRP-XL) (Pearson's = -0.196, = 0.002). This effect was due to circulating vitamin D levels ≤50nmol/L, since no differences in platelet fibrinogen binding were observed between subjects with normal 25-hydroxyvitamin D concentrations (>75nmol/L) and a 25-hydroxyvitamin D insufficiency (50-75 nmol/L). No correlations between 25-hydroxyvitamin D concentrations and platelet P-selectin expression were found. Several SNPs in the GC region of the vitamin D binding proteingene were associated with platelet responses to CRP-XL.
Low circulating vitamin D concentrations are associated with increased platelet fibrinogen binding to integrin αIIbβ3 in unstimulated samples and after stimulation with CRP-XL. These findings may contribute to the increased incidence of cardiovascular events in vitamin D deficient adults and its seasonal variation. Further studies are needed to investigate causality.
心血管事件与循环中维生素 D 浓度较低有关,尽管其潜在机制尚不清楚。本研究在 500 个功能基因组(500FG)队列中,调查了 25-羟维生素 D 浓度、血小板功能与影响维生素 D 生物学的基因单核苷酸多态性(SNP)之间的关系。
在这项观察性研究中,通过纤维蛋白原与激活的纤维蛋白原受体整合素αIIbβ3 的结合以及血小板聚集和脱颗粒的标志物 P-选择素的表达,通过流式细胞术测量血小板的激活和功能。这些参数与血清 25-羟维生素 D 相关,并进行基因分型以研究对维生素 D 生物学重要的基因中的 SNP。
循环 25-羟维生素 D 浓度与纤维蛋白原与整合素αIIbβ3 的基线血小板结合呈负相关(Pearson's = -0.172,= 0.002),与血小板对血小板激动剂交联胶原相关肽(CRP-XL)的反应呈负相关(Pearson's = -0.196,= 0.002)。这种作用是由于循环维生素 D 水平≤50nmol/L,因为在具有正常 25-羟维生素 D 浓度(>75nmol/L)和 25-羟维生素 D 不足(50-75nmol/L)的受试者之间,血小板纤维蛋白原结合没有差异。25-羟维生素 D 浓度与血小板 P-选择素表达之间无相关性。维生素 D 结合蛋白基因 GC 区的几个 SNP 与 CRP-XL 刺激后血小板对 CRP-XL 的反应相关。
低循环维生素 D 浓度与未刺激样本中纤维蛋白原与整合素αIIbβ3 的结合增加以及 CRP-XL 刺激后的结合增加有关。这些发现可能导致维生素 D 缺乏的成年人心血管事件发生率增加及其季节性变化。需要进一步研究以调查因果关系。