Biological Effects of Intravenous Vitamin C on Neutrophil Extracellular Traps and the Endothelial Glycocalyx in Patients with Sepsis-Induced ARDS.
Biological Effects of Intravenous Vitamin C on Neutrophil Extracellular Traps and the Endothelial Glycocalyx in Patients with Sepsis-Induced ARDS.
复制标题
静脉内维生素C对嗜中性粒细胞外陷阱和内皮糖脂的生物学作用对脓毒症诱导的ARDS患者的生物学作用。
DOI:
10.3390/nu14204415
复制
发表时间:
2022-10-21
期刊:
影响因子:
5.9
通讯作者:
Fowler AA
中科院分区:
文献类型:
--
作者:
Qiao X;Kashiouris MG;L'Heureux M;Fisher BJ;Leichtle SW;Truwit JD;Nanchal R;Hite RD;Morris PE;Martin GS;Sevransky J;Fowler AA
(1) Background: The disease-modifying mechanisms of high-dose intravenous vitamin C (HDIVC) in sepsis induced acute respiratory distress syndrome (ARDS) is unclear. (2) Methods: We performed a post hoc study of plasma biomarkers from subjects enrolled in the randomized placebo-controlled trial CITRIS-ALI. We explored the effects of HDIVC on cell-free DNA (cfDNA) and syndecan-1, surrogates for neutrophil extracellular trap (NET) formation and degradation of the endothelial glycocalyx, respectively. (3) Results: In 167 study subjects, baseline cfDNA levels in HDIVC (84 subjects) and placebo (83 subjects) were 2.18 ng/µL (SD 4.20 ng/µL) and 2.65 ng/µL (SD 3.87 ng/µL), respectively, p = 0.45. At 48-h, the cfDNA reduction was 1.02 ng/µL greater in HDIVC than placebo, p = 0.05. Mean baseline syndecan-1 levels in HDIVC and placebo were 9.49 ng/mL (SD 5.57 ng/mL) and 10.83 ng/mL (SD 5.95 ng/mL), respectively, p = 0.14. At 48 h, placebo subjects exhibited a 1.53 ng/mL (95% CI, 0.96 to 2.11) increase in syndecan-1 vs. 0.75 ng/mL (95% CI, 0.21 to 1.29, p = 0.05), in HDIVC subjects. (4) Conclusions: HDIVC infusion attenuated cell-free DNA and syndecan-1, biomarkers associated with sepsis-induced ARDS. Improvement of these biomarkers suggests amelioration of NETosis and shedding of the vascular endothelial glycocalyx, respectively.
登录
查看更多内容
影响因子:
4.5
作者:
Reitsma, Sietze;Slaaf, Dick W.;Vink, Hans;van Zandvoort, Marc A. M. J.;Egbrink, Mirjam G. A. oude
通讯作者:
Egbrink, Mirjam G. A. oude
影响因子:
3.7
作者:
Hirose T;Hamaguchi S;Matsumoto N;Irisawa T;Seki M;Tasaki O;Hosotsubo H;Yamamoto N;Yamamoto K;Akeda Y;Oishi K;Tomono K;Shimazu T
通讯作者:
Shimazu T
影响因子:
3.2
作者:
O'Brien XM;Biron BM;Reichner JS
通讯作者:
Reichner JS
影响因子:
2
作者:
Paul, Prabasaj;Pennell, Michael L.;Lemeshow, Stanley
通讯作者:
Lemeshow, Stanley
影响因子:
11.1
作者:
Rannikko, J.;Seiskari, T.;Aittoniemi, J.
通讯作者:
Aittoniemi, J.