Vitamin D and survival in COVID-19 patients: A quasi-experimental study

被引:158
|
作者
Annweiler, Cedric [1 ,2 ,3 ,4 ]
Hanotte, Berangere [5 ]
de l'Eprevier, Claire Grandin [6 ]
Sabatier, Jean-Marc [7 ]
Lafaie, Ludovic [5 ]
Celarier, Thomas [5 ,8 ,9 ]
机构
[1] Univ Hosp, Res Ctr Auton & Longev, Dept Geriatr Med, Angers, France
[2] Univ Hosp, Res Ctr Auton & Longev, Memory Clin, Angers, France
[3] Univ Angers, UPRES EA 4638, Angers, France
[4] Univ Western Ontario, Schulich Sch Med & Dent, Robarts Res Inst, Dept Med Biophys, London, ON, Canada
[5] Univ Hosp St Etienne, Dept Clin Gerontol, St Etienne, France
[6] Geriatr Hosp St Laurent de Chamousset, St Laurent De Chamousset, France
[7] Univ Aix Marseille, Fac Pharm, Inst Neurophysiopathol INP, UMR 7051, 27 Bd Jean Moulin, F-13385 Marseille, France
[8] Univ Jean Monnet, Chaire Sante Aines, St Etienne, France
[9] Gerontopole Auvergne Rhone Alpes, St Etienne, France
关键词
COVID-19; SARS-CoV-2; Vitamin D; Therapeutics; Quasi-experimental study; Older adults; GUIDELINES; HEALTH;
D O I
10.1016/j.jsbmb.2020.105771
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vitamin D may be a central biological determinant of COVID-19 outcomes. The objective of this quasi experimental study was to determine whether bolus vitamin D3 supplementation taken during or just before COVID-19 was effective in improving survival among frail elderly nursing-home residents with COVID-19. Sixtysix residents with COVID-19 from a French nursing-home were included in this quasi-experimental study. The "Intervention group" was defined as those having received bolus vitamin D3 supplementation during COVID-19 or in the preceding month, and the "Comparator group" corresponded to all other participants. The primary and secondary outcomes were COVID-19 mortality and Ordinal Scale for Clinical Improvement (OSCI) score in acute phase, respectively. Age, gender, number of drugs daily taken, functional abilities, albuminemia, use of corticosteroids and/or hydroxychloroquine and/or antibiotics (i.e., azithromycin or rovamycin), and hospitalization for COVID-19 were used as potential confounders. The Intervention (n = 57; mean +/- SD, 87.7 +/- 9.3years; 79 % women) and Comparator (n = 9; mean, 87.4 +/- 7.2years; 67 %women) groups were comparable at baseline, as were the COVID-19 severity and the use of dedicated COVID-19 drugs. The mean follow-up time was 36 +/- 17 days. 82.5 % of participants in the Intervention group survived COVID-19, compared to only 44.4 % in the Comparator group (P = 0.023). The full-adjusted hazard ratio for mortality according to vitamin D3 supplementation was HR = 0.11 [95 %CI:0.03;0.48], P = 0.003. Kaplan-Meier distributions showed that Intervention group had longer survival time than Comparator group (log-rank P = 0.002). Finally, vitamin D3 supplementation was inversely associated with OSCI score for COVID-19 (beta=-3.84 [95 %CI:-6.07;-1.62], P = 0.001). In conclusion, bolus vitamin D3 supplementation during or just before COVID-19 was associated in frail elderly with less severe COVID-19 and better survival rate.
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页数:6
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