Higher levels of circulating desphospho-uncarboxylated matrix Gla protein over time are associated with worse survival: the prospective Maastricht Intensive Care COVID cohort

IF 3.8 2区 医学 Q1 CRITICAL CARE MEDICINE
Mark M. G. Mulder, Joep Schellens, Jan-Willem E. M. Sels, Frank van Rosmalen, Anne-Marije Hulshof, Femke de Vries, Ruud Segers, Casper Mihl, Walther N. K. A. van Mook, Aalt Bast, Henri M. H. Spronk, Yvonne M. C. Henskens, Iwan C. C. van der Horst, Hugo ten Cate, Leon J. Schurgers, Marjolein Drent, Bas C. T. van Bussel
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引用次数: 0

Abstract

Extra-hepatic vitamin K-status, measured by dephosphorylated uncarboxylated matrix Gla protein (dp-ucMGP), maintains vascular health, with high levels reflecting poor vitamin K status. The occurrence of extra-hepatic vitamin K deficiency throughout the disease of COVID-19 and possible associations with pulmonary embolism (PE), and mortality in intensive care unit (ICU) patients has not been studied. The aim of this study was to investigated the association between dp-ucMGP, at endotracheal intubation (ETI) and both ICU and six months mortality. Furthermore, we studied the associations between serially measured dp-ucMGP and both PE and mortality. We included 112 ICU patients with confirmed COVID-19. Over the course of 4 weeks after ETI, dp-ucMGP was measured serially. All patients underwent computed tomography pulmonary angiography (CTPA) to rule out PE. Results were adjusted for patient characteristics, disease severity scores, inflammation, renal function, history of coumarin use, and coronary artery calcification (CAC) scores. Per 100 pmol/L dp-ucMGP, at ETI, the odds ratio (OR) was 1.056 (95% CI: 0.977 to 1.141, p = 0.172) for ICU mortality and 1.059 (95% CI: 0.976 to 1.059, p = 0.170) for six months mortality. After adjustments for age, gender, and APACHE II score, the mean difference in plasma dp-ucMGP over time of ICU admission was 167 pmol/L (95% CI: 4 to 332, p = 0.047). After additional adjustments for c-reactive protein, creatinine, and history of coumarin use, the difference was 199 pmol/L (95% CI: 50 to 346, p = 0.010). After additional adjustment for CAC score the difference was 213 pmol/L (95% CI: 3 to 422, p = 0.051) higher in ICU non-survivors compared to the ICU survivors. The regression slope, indicating changes over time, did not differ. Moreover, dp-ucMGP was not associated with PE. ICU mortality in COVID-19 patients was associated with higher dp-ucMGP levels over 4 weeks, independent of age, gender, and APACHE II score, and not explained by inflammation, renal function, history of coumarin use, and CAC score. No association with PE was observed. At ETI, higher levels of dp-ucMGP were associated with higher OR for both ICU and six month mortality in crude and adjusted modes, although not statistically significantly.
随着时间的推移,较高水平的循环脱磷脱羧基质 Gla 蛋白与较差的存活率有关:马斯特里赫特重症监护 COVID 前瞻性队列
通过去磷酸化非羧化基质 Gla 蛋白(dp-ucMGP)测定的肝外维生素 K 状态可维持血管健康,高水平反映了维生素 K 状态不佳。关于在 COVID-19 的整个病程中出现肝外维生素 K 缺乏以及与肺栓塞(PE)和重症监护病房(ICU)患者死亡率之间可能存在的关联,尚未进行研究。本研究旨在调查气管插管(ETI)时 dp-ucMGP 与重症监护室和六个月死亡率之间的关系。此外,我们还研究了连续测量的 dp-ucMGP 与 PE 和死亡率之间的关系。我们纳入了 112 名确诊为 COVID-19 的 ICU 患者。在 ETI 后的 4 周内,对 dp-ucMGP 进行了连续测量。所有患者均接受了计算机断层扫描肺血管造影术(CTPA)以排除 PE。结果根据患者特征、疾病严重程度评分、炎症、肾功能、香豆素使用史和冠状动脉钙化(CAC)评分进行了调整。在 ETI 时,每 100 pmol/L dp-ucMGP 与 ICU 死亡率的比值比 (OR) 为 1.056(95% CI:0.977 至 1.141,P = 0.172),与 6 个月死亡率的比值比 (OR) 为 1.059(95% CI:0.976 至 1.059,P = 0.170)。对年龄、性别和 APACHE II 评分进行调整后,血浆 dp-ucMGP 与入住 ICU 时间的平均差异为 167 pmol/L(95% CI:4 至 332,p = 0.047)。在对 c 反应蛋白、肌酐和香豆素使用史进行额外调整后,差异为 199 pmol/L(95% CI:50 至 346,p = 0.010)。在对 CAC 评分进行额外调整后,ICU 非存活者与 ICU 存活者相比,差异为 213 pmol/L(95% CI:3 至 422,p = 0.051)。表示随时间变化的回归斜率没有差异。此外,dp-ucMGP 与 PE 无关。COVID-19患者的ICU死亡率与4周内较高的dp-ucMGP水平有关,与年龄、性别和APACHE II评分无关,炎症、肾功能、香豆素使用史和CAC评分也无法解释其原因。与 PE 无关。在 ETI 时,dp-ucMGP 水平越高,ICU 和 6 个月死亡率的粗略模式和调整模式的 OR 越高,但在统计学上并不显著。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Intensive Care
Journal of Intensive Care Medicine-Critical Care and Intensive Care Medicine
CiteScore
11.90
自引率
1.40%
发文量
51
审稿时长
15 weeks
期刊介绍: "Journal of Intensive Care" is an open access journal dedicated to the comprehensive coverage of intensive care medicine, providing a platform for the latest research and clinical insights in this critical field. The journal covers a wide range of topics, including intensive and critical care, trauma and surgical intensive care, pediatric intensive care, acute and emergency medicine, perioperative medicine, resuscitation, infection control, and organ dysfunction. Recognizing the importance of cultural diversity in healthcare practices, "Journal of Intensive Care" also encourages submissions that explore and discuss the cultural aspects of intensive care, aiming to promote a more inclusive and culturally sensitive approach to patient care. By fostering a global exchange of knowledge and expertise, the journal contributes to the continuous improvement of intensive care practices worldwide.
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