Department of Systems Medicine, Diabetes Research Institute Federation (DRIF), CTO Hospital ASL Roma 2, University of Rome Tor Vergata, Rome, Italy.
UniCamillus, Saint Camillus International University of Health Sciences, Rome, Italy.
J Am Nutr Assoc. 2022 Mar-Apr;41(3):250-265. doi: 10.1080/07315724.2021.1877580. Epub 2021 Feb 18.
Preliminary findings suggest a relationship between lower serum 25-hydroxyvitamin D [25(OH)D] levels and incidence and severity of COVID-19. The aim of this study was to evaluate the relationship between vitamin D status at admission and different markers of inflammation, coagulation, and sepsis in hospitalized patients with COVID-19.
We conducted a retrospective study on 137 consecutive patients with SARS-CoV-2 infection and available data on serum 25(OH)D levels, who were admitted to our Institution between March 1 and April 30, 2020. Patients were divided into two groups: survivors (n = 78; 57%) and non-survivors (n = 59; 43%).
At admission, all patients showed hypovitaminosis D. Median total serum 25(OH)D levels at admission were significantly higher in survivors than non-survivors (12 ng/mL vs 8 ng/mL; < 0.01). Non-survivors exhibited significantly higher median levels of white blood cell (WBC) count, neutrophil-to-lymphocyte count ratio (NLR), high-sensitivity C-reactive protein (hsCRP), ferritin, interleukin 6 (IL-6), D-dimer, fibrinogen, and procalcitonin (PCT) compared to survivors at three different time points during hospitalization. In a multivariate analysis performed by a logistic regression model, serum 25(OH)D levels were significantly inversely associated with risk of COVID-19-related in-hospital mortality (odds ratio, 0.91; 95% confidence interval, 0.85-0.98; = 0.01). According to receiver operating characteristic curve analysis, hsCRP, NLR, ferritin, and D-dimer were the best predictive biomarkers for poor prognosis of COVID-19, whereas IL-6, PCT, fibrinogen, 25(OH)D, WBC count, and tumor necrosis factor alpha (TNF-α) may serve as supportive biomarkers for worse clinical course of the disease.
We found a markedly high prevalence (100%) of hypovitaminosis D in patients admitted to hospital with COVID-19, suggesting a possible role of low vitamin D status in increasing the risk of SARS-CoV-2 infection and subsequent hospitalization. The inverse association between serum 25(OH)D levels and risk of in-hospital mortality observed in our cohort suggests that a lower vitamin D status upon admission may represent a modifiable and independent risk factor for poor prognosis in COVID-19.
初步研究结果表明,血清 25-羟维生素 D [25(OH)D] 水平与 COVID-19 的发病率和严重程度之间存在关系。本研究旨在评估入院时维生素 D 状态与 COVID-19 住院患者不同炎症、凝血和脓毒症标志物之间的关系。
我们对 2020 年 3 月 1 日至 4 月 30 日期间我院收治的 137 例连续 SARS-CoV-2 感染患者进行了回顾性研究,这些患者的血清 25(OH)D 水平数据可用。患者分为两组:幸存者(n=78;57%)和非幸存者(n=59;43%)。
入院时,所有患者均表现出维生素 D 缺乏症。幸存者的中位总血清 25(OH)D 水平明显高于非幸存者(12ng/mL 与 8ng/mL;<0.01)。非幸存者在住院期间三个不同时间点的白细胞(WBC)计数、中性粒细胞与淋巴细胞比值(NLR)、高敏 C 反应蛋白(hsCRP)、铁蛋白、白细胞介素 6(IL-6)、D-二聚体、纤维蛋白原和降钙素原(PCT)水平均明显高于幸存者。在通过逻辑回归模型进行的多变量分析中,血清 25(OH)D 水平与 COVID-19 相关住院死亡率的风险呈显著负相关(比值比,0.91;95%置信区间,0.85-0.98;=0.01)。根据接受者操作特征曲线分析,hsCRP、NLR、铁蛋白和 D-二聚体是 COVID-19 预后不良的最佳预测生物标志物,而白细胞介素 6、PCT、纤维蛋白原、25(OH)D、白细胞计数和肿瘤坏死因子-α(TNF-α)可能是疾病严重程度恶化的支持性生物标志物。
我们发现 COVID-19 住院患者维生素 D 缺乏症的患病率(100%)非常高,这表明维生素 D 状态较低可能增加 SARS-CoV-2 感染和随后住院的风险。我们的队列观察到血清 25(OH)D 水平与住院死亡率风险之间的负相关关系表明,入院时维生素 D 水平较低可能是 COVID-19 预后不良的一个可改变和独立的危险因素。