Vitamin D deficiency contributes directly to the acute respiratory distress syndrome (ARDS).
Vitamin D deficiency contributes directly to the acute respiratory distress syndrome (ARDS).
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DOI:
10.1136/thoraxjnl-2014-206680
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发表时间:
2015-07
期刊:
影响因子:
10
通讯作者:
Thickett DR
中科院分区:
文献类型:
--
作者:
Dancer RC;Parekh D;Lax S;D'Souza V;Zheng S;Bassford CR;Park D;Bartis DG;Mahida R;Turner AM;Sapey E;Wei W;Naidu B;Stewart PM;Fraser WD;Christopher KB;Cooper MS;Gao F;Sansom DM;Martineau AR;Perkins GD;Thickett DR
Vitamin D deficiency has been implicated as a pathogenic factor in sepsis and intensive therapy unit mortality but has not been assessed as a risk factor for acute respiratory distress syndrome (ARDS). Causality of these associations has never been demonstrated. To determine if ARDS is associated with vitamin D deficiency in a clinical setting and to determine if vitamin D deficiency in experimental models of ARDS influences its severity. Human, murine and in vitro primary alveolar epithelial cell work were included in this study. Vitamin D deficiency (plasma 25(OH)D levels <50 nmol/L) was ubiquitous in patients with ARDS and present in the vast majority of patients at risk of developing ARDS following oesophagectomy. In a murine model of intratracheal lipopolysaccharide challenge, dietary-induced vitamin D deficiency resulted in exaggerated alveolar inflammation, epithelial damage and hypoxia. In vitro, vitamin D has trophic effects on primary human alveolar epithelial cells affecting >600 genes. In a clinical setting, pharmacological repletion of vitamin D prior to oesophagectomy reduced the observed changes of in vivo measurements of alveolar capillary damage seen in deficient patients. Vitamin D deficiency is common in people who develop ARDS. This deficiency of vitamin D appears to contribute to the development of the condition, and approaches to correct vitamin D deficiency in patients at risk of ARDS should be developed. UKCRN ID 11994.
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影响因子:
10
作者:
Perkins, G. D.;Gao, F.;Thickett, D. R.
通讯作者:
Thickett, D. R.
影响因子:
2
作者:
Mohamed, W. A. Wahab;Al-Shehri, M. A.
通讯作者:
Al-Shehri, M. A.
影响因子:
6.9
作者:
Leow, Leong;Simpson, Talia;Hancox, Robert J.
通讯作者:
Hancox, Robert J.
影响因子:
10
作者:
Calfee, C. S.;Ware, L. B.;Matthay, M. A.
通讯作者:
Matthay, M. A.
影响因子:
7
作者:
Hewison, Martin
通讯作者:
Hewison, Martin