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标题:在新冠病毒病背景下理解维生素D水平低的状态

Title: Understanding a Low Vitamin D State in the Context of COVID-19.

作者信息

Walsh James Bernard, McCartney Daniel M, Laird Éamon, McCarroll Kevin, Byrne Declan G, Healy Martin, O'Shea Paula M, Kenny Rose Anne, Faul John L

机构信息

Mercer's Institute for Successful Ageing, St James's Hospital, Dublin, Ireland.

Department of Medical Gerontology, School of Medicine, Trinity College Dublin, Dublin, Ireland.

出版信息

Front Pharmacol. 2022 Mar 4;13:835480. doi: 10.3389/fphar.2022.835480. eCollection 2022.

DOI:10.3389/fphar.2022.835480
PMID:35308241
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8931482/
Abstract

While a low vitamin D state has been associated with an increased risk of infection by SARS-CoV-2 in addition to an increased severity of COVID-19 disease, a causal role is not yet established. Here, we review the evidence relating to i) vitamin D and its role in SARS-CoV-2 infection and COVID-19 disease ii) the vitamin D status in the Irish adult population iii) the use of supplemental vitamin D to treat a deficient status and iv) the application of the Bradford-Hill causation criteria. We conclude that reverse causality probably makes a minimal contribution to the presence of low vitamin D states in the setting of COVID-19. Applying the Bradford-Hill criteria, however, the collective literature supports a causal association between low vitamin D status, SARS-CoV-2 infection, and severe COVID-19 (respiratory failure, requirement for ventilation and mortality). A biologically plausible rationale exists for these findings, given vitamin D's role in immune regulation. The thresholds which define low, deficient, and replete vitamin D states vary according to the disease studied, underscoring the complexities for determining the goals for supplementation. All are currently unknown in the setting of COVID-19. The design of vitamin D randomised controlled trials is notoriously problematic and these trials commonly fail for a number of behavioural and methodological reasons. In Ireland, as in most other countries, low vitamin D status is common in older adults, adults in institutions, and with obesity, dark skin, low UVB exposure, diabetes and low socio-economic status. Physiological vitamin D levels for optimal immune function are considerably higher than those that can be achieved from food and sunlight exposure alone in Ireland. A window exists in which a significant number of adults could benefit from vitamin D supplementation, not least because of recent data demonstrating an association between vitamin D status and COVID-19. During the COVID pandemic, we believe that supplementation with 20-25ug (800-1000 IU)/day or more may be required for adults with apparently normal immune systems to improve immunity against SARS-CoV-2. We expect that higher monitored doses of 37.5-50 ug (1,500-2,000)/day may be needed for vulnerable groups (e.g., those with obesity, darker skin, diabetes mellitus and older adults). Such doses are within the safe daily intakes cited by international advisory agencies.

摘要

虽然低维生素D状态除了会增加新冠病毒疾病的严重程度外,还与感染新冠病毒的风险增加有关,但因果关系尚未确立。在此,我们回顾了以下相关证据:i)维生素D及其在新冠病毒感染和新冠病毒疾病中的作用;ii)爱尔兰成年人群的维生素D状态;iii)使用补充维生素D来治疗缺乏状态;iv)应用布拉德福德-希尔因果关系标准。我们得出结论,在新冠病毒感染的情况下,反向因果关系可能对低维生素D状态的存在贡献极小。然而,应用布拉德福德-希尔标准,现有文献支持低维生素D状态、新冠病毒感染和严重新冠病毒疾病(呼吸衰竭、需要通气和死亡率)之间存在因果关联。鉴于维生素D在免疫调节中的作用,这些发现存在生物学上合理的依据。定义低、缺乏和充足维生素D状态的阈值因所研究的疾病而异,这凸显了确定补充目标的复杂性。在新冠病毒感染的情况下,所有这些目前都尚不清楚。维生素D随机对照试验的设计存在众所周知的问题,这些试验通常因多种行为和方法学原因而失败。在爱尔兰,与大多数其他国家一样,老年人、机构中的成年人、肥胖者、皮肤黝黑者、紫外线B暴露量低者、糖尿病患者以及社会经济地位低者中,维生素D水平低的情况很常见。在爱尔兰,仅通过食物和阳光照射所能达到的维生素D水平,远低于实现最佳免疫功能所需的生理水平。存在一个窗口期,大量成年人可能会从补充维生素D中受益,尤其是因为最近的数据表明维生素D状态与新冠病毒感染之间存在关联。在新冠疫情期间,我们认为,对于免疫系统看似正常的成年人,可能需要每天补充20 - [25微克(800 - 1000国际单位)]或更多,以提高对新冠病毒的免疫力。我们预计,弱势群体(如肥胖者、皮肤较黑者、糖尿病患者和老年人)可能需要每天监测剂量更高的37.5 - 50微克(1500 - 2000国际单位)。这些剂量在国际咨询机构引用的每日安全摄入量范围内。 (注:原文中“20-25ug (800-1000 IU)/day”括号内的“800-1000 IU”前面少了右括号,翻译时补充完整)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0719/8931482/cfd41097d5e8/fphar-13-835480-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0719/8931482/26a8400b8414/fphar-13-835480-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0719/8931482/53609dd69d09/fphar-13-835480-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0719/8931482/8587ab49b40e/fphar-13-835480-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0719/8931482/cfd41097d5e8/fphar-13-835480-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0719/8931482/26a8400b8414/fphar-13-835480-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0719/8931482/53609dd69d09/fphar-13-835480-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0719/8931482/8587ab49b40e/fphar-13-835480-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0719/8931482/cfd41097d5e8/fphar-13-835480-g004.jpg

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