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健康成年人补充维生素D3:在冬季进行的一项随机、开放标签、交叉研究中,比较胶囊和口服喷雾溶液作为给药方式的效果。

Vitamin D3 supplementation in healthy adults: a comparison between capsule and oral spray solution as a method of delivery in a wintertime, randomised, open-label, cross-over study.

作者信息

Todd Joshua J, McSorley Emeir M, Pourshahidi L Kirsty, Madigan Sharon M, Laird Eamon, Healy Martin, Magee Pamela J

机构信息

1Northern Ireland Centre for Food and Health,University of Ulster,Coleraine BT52 1SA,UK.

2Irish Institute of Sport,Sports Campus Ireland,Dublin 15,Ireland.

出版信息

Br J Nutr. 2016 Oct;116(8):1402-1408. doi: 10.1017/S0007114516003470. Epub 2016 Oct 11.

Abstract

Vitamin D is typically supplied in capsule form, both in trials and in clinical practice. However, little is known regarding the efficacy of vitamin D administered via oral sprays - a method that primarily bypasses the gastrointestinal absorption route. This study aimed to compare the efficacy of vitamin D3 liquid capsules and oral spray solution in increasing wintertime total 25-hydroxyvitamin D (25(OH)D) concentrations. In this randomised, open-label, cross-over trial, healthy adults (n 22) received 3000 IU (75 µg) vitamin D3 daily for 4 weeks in either capsule or oral spray form. Following a 10-week washout phase, participants received the opposite treatment for a final 4 weeks. Anthropometrics and fasted blood samples were obtained before and after supplementation, with samples analysed for total 25(OH)D, creatinine, intact parathyroid hormone and adjusted Ca concentrations. At baseline, vitamin D sufficiency (total 25(OH)D>50 nmol/l), insufficiency (31-49 nmol/l) and clinical deficiency (<30 nmol/l) were evident in 59, 23 and 18 % of the participants, respectively. Overall, baseline total mean 25(OH)D concentration averaged 59·76 (sd 29·88) nmol/l, representing clinical sufficiency. ANCOVA revealed no significant difference in the mean and standard deviation change from baseline in total 25(OH)D concentrations between oral spray and capsule supplementation methods (26·15 (sd 17·85) v. 30·38 (sd 17·91) nmol/l, respectively; F=1·044, adjusted r 2 0·493, P=0·313). Oral spray vitamin D3 is an equally effective alternative to capsule supplementation in healthy adults.

摘要

在试验和临床实践中,维生素D通常以胶囊形式提供。然而,对于通过口服喷雾剂给药的维生素D的疗效知之甚少,口服喷雾剂这种给药方式主要绕过了胃肠道吸收途径。本研究旨在比较维生素D3软胶囊和口服喷雾溶液在提高冬季总25-羟维生素D(25(OH)D)浓度方面的疗效。在这项随机、开放标签、交叉试验中,22名健康成年人以胶囊或口服喷雾形式每天接受3000 IU(75 μg)维生素D3,持续4周。经过10周的洗脱期后,参与者接受为期4周的相反治疗。在补充前后测量人体测量学指标并采集空腹血样,对样本进行总25(OH)D、肌酐、完整甲状旁腺激素和校正钙浓度分析。在基线时,分别有59%、23%和18%的参与者维生素D充足(总25(OH)D>50 nmol/l)、不足(31 - 49 nmol/l)和临床缺乏(<30 nmol/l)。总体而言,基线时总平均25(OH)D浓度为59.76(标准差29.88)nmol/l,表明临床充足。协方差分析显示,口服喷雾和胶囊补充方法之间,总25(OH)D浓度从基线开始的均值和标准差变化无显著差异(分别为26.15(标准差17.85)和30.38(标准差17.91)nmol/l;F = 1.044,校正r² = 0.493,P = 0.313)。对于健康成年人,口服喷雾维生素D3是胶囊补充剂的同等有效替代品。

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