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强化饮料对改善老年人B族维生素生物标志物的有效性:一项对照干预试验。

Effectiveness of a fortified drink in improving B vitamin biomarkers in older adults: a controlled intervention trial.

作者信息

Heffernan Maria, Doherty Leanne C, Hack Mendes Roberta, Clarke Michelle, Hodge Stephanie, Clements Michelle, McAnena Liadhan, Rivelsrud Mari, Ward Mary, Strain J J, McNulty Helene, Brennan Lorraine

机构信息

UCD School of Agriculture and Food Science, Institute of Food and Health, Conway Institute, University College Dublin, Belfield, Dublin 4, Ireland.

Nutrition Innovation Centre for Food and Health (NICHE), School of Biomedical Sciences, Ulster University, Coleraine, Northern Ireland, UK.

出版信息

Nutr Metab (Lond). 2021 Dec 7;18(1):104. doi: 10.1186/s12986-021-00630-8.

Abstract

BACKGROUND

Older adults are reported to have sub-optimal B vitamin status; targeted food-based solutions may help to address this. The objectives of the OptiAge food intervention study were to develop and investigate the effectiveness of a B vitamin-fortified drink in improving B vitamin biomarkers in older Irish adults with a primary outcome of change in the B vitamin biomarker status.

METHODS

A double-blinded randomised controlled trial was performed in parallel at University College Dublin and Ulster University. Participants aged > 50 years were recruited following screening for exclusion criteria (i.e. taking medications known to interfere with B vitamin metabolism, supplements containing B vitamins, consuming > 4 portions of B vitamin-fortified foods per week or diagnosed with gastrointestinal, liver or pulmonary disease). Recruited participants meeting the inclusion criteria were randomised (by sex and study centre) to receive daily for 16 weeks either B vitamin-fortified or placebo drinks as developed by Smartfish, Norway. Each B vitamin-fortified drink (200 ml) contained 200 µg folic acid, 10 µg vitamin B12, 10 mg vitamin B6 and 5 mg riboflavin, while the placebo was an identical, isocaloric formulation without added B vitamins. Fasting blood samples were collected pre- and post-intervention which were used to measure the primary outcome of change in B vitamin biomarker levels.

RESULTS

A total of 95 participants were randomised, of which 81 commenced the trial. Of these, 70 completed (37 in the active and 33 in the placebo groups). Intention to treat (ITT) analysis of the B vitamins demonstrated a significant improvement in all B vitamin biomarkers in the active compared to placebo groups: p < 0.01 for each of serum folate, serum vitamin B12 and plasma pyridoxal 5'-phosphate (vitamin B6) and the functional riboflavin biomarker, erythrocyte glutathione reductase activation coefficient (EGRac). Correspondingly, a significant lowering of serum homocysteine from 11.9 (10.3-15.1) µmol/L to 10.6 (9.4-13.0) µmol/L was observed in response to the active treatment (P < 0.001). Similar results were seen in a per-protocol analysis.

CONCLUSIONS

The results demonstrate that a B vitamin-fortified drink was effective in optimising B vitamin status, making this a useful intervention option to improve B vitamin status in older adults. Trial registration ISRCTN, ISRCTN61709781-Retrospectively registered, https://www.isrctn.com/ISRCTN61709781.

摘要

背景

据报道,老年人的B族维生素状态欠佳;有针对性的基于食物的解决方案可能有助于解决这一问题。OptiAge食物干预研究的目的是开发并研究一种B族维生素强化饮料在改善爱尔兰老年人体内B族维生素生物标志物方面的有效性,主要观察指标为B族维生素生物标志物状态的变化。

方法

都柏林大学学院和阿尔斯特大学同时进行了一项双盲随机对照试验。对年龄大于50岁的参与者进行筛查,排除标准包括(即正在服用已知会干扰B族维生素代谢的药物、含有B族维生素的补充剂、每周食用超过4份B族维生素强化食品或被诊断患有胃肠道、肝脏或肺部疾病)。符合纳入标准的招募参与者按性别和研究中心随机分组,每天饮用挪威Smartfish公司研发的B族维生素强化饮料或安慰剂饮料,持续16周。每瓶B族维生素强化饮料(200毫升)含有200微克叶酸、10微克维生素B12、10毫克维生素B6和5毫克核黄素,而安慰剂是不含添加B族维生素的相同等热量配方。干预前后采集空腹血样,用于测量B族维生素生物标志物水平变化这一主要观察指标。

结果

共有95名参与者被随机分组,其中81人开始试验。在这些人中,70人完成了试验(活性组37人, 安慰剂组33人)。对B族维生素的意向性分析表明,与安慰剂组相比,活性组所有B族维生素生物标志物均有显著改善:血清叶酸、血清维生素B12、血浆磷酸吡哆醛(维生素B6)以及功能性核黄素生物标志物红细胞谷胱甘肽还原酶激活系数(EGRac),每组的p值均<0.01。相应地,活性治疗后血清同型半胱氨酸从11.9(10.3 - 15.1)微摩尔/升显著降至10.6(9.4 - 13.0)微摩尔/升(P < 0.001)。在符合方案分析中也观察到了类似结果。

结论

结果表明,B族维生素强化饮料能有效优化B族维生素状态,使其成为改善老年人B族维生素状态的有用干预选项。试验注册号ISRCTN,ISRCTN61709781 - 回顾性注册,https://www.isrctn.com/ISRCTN61709781

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eae/8650259/70bee27166c6/12986_2021_630_Fig1_HTML.jpg

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