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首页> 外文期刊>European journal of clinical nutrition >Assessment of three levels of folic acid on serum folate and plasma homocysteine: a randomised placebo-controlled double-blind dietary intervention trial.
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Assessment of three levels of folic acid on serum folate and plasma homocysteine: a randomised placebo-controlled double-blind dietary intervention trial.

机译:评估血清叶酸和血浆同型半胱氨酸上的三叶酸水平:一项随机安慰剂对照的双盲饮食干预试验。

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OBJECTIVE: To determine the minimum effective dose of folic acid required to appreciably increase serum folate and to produce a significant reduction in plasma total homocysteine (tHcy). DESIGN: Double-blind, randomised placebo-controlled intervention trial. SETTING: Community-based project in a New Zealand city. SUBJECTS: Seventy free living men and women with tHcy>/=10 micromol/l. Mean age (range) was 58 (29-90) y. INTERVENTIONS: Daily consumption over 4 weeks of 20 g breakfast cereal either unfortified (placebo) or fortified with 100, 200 or 300 microg folic acid. Dietary intake was determined by weighed diet records and consumption of commercially fortified products was avoided. MAIN OUTCOME MEASURES: Plasma tHcy and serum folate concentrations. RESULTS: Average serum folate concentrations (95% CI) increased significantly in the treatment groups relative to the control group by 28(9-51)%, 60(37-87)% and 79(51-114)% for supplementation with 100, 200 and 300 microg folic acid, respectively. A reduction in tHcy was observed, being 16(8-22)%, 12(4-18)% and 17(9-24)% in the three treatment groups, respectively. CONCLUSIONS: A regular intake of as little as 100 microg folic acid per day was sufficient to lower tHcy in persons at the upper end of the normal range for tHcy. Low-level fortification may also be appropriate for lowering the risk of neural tube defects given that, when aggregated from all sources, the total intake of folic acid may be sufficiently high to adequately improve the folate status of young women. FUNDING: The breakfast cereals were supplied and the study partially funded by Kellogg Company. doi:10.1038/sj.ejcn.1601388
机译:目的:确定叶酸的最低有效剂量,以显着增加血清叶酸并显着降低血浆总同型半胱氨酸(tHcy)。设计:双盲,随机安慰剂对照干预试验。地点:一个新西兰城市的社区项目。受试者:70名生活中的男性和女性,tHcy> / = 10 micromol / l。平均年龄(范围)为58(29-90)岁。干预措施:在4周内每天食用20克早餐麦片,其中不添加(安慰剂)或用100、200或300微克叶酸强化。通过称重饮食记录确定饮食摄入量,避免食用商业强化产品。主要观察指标:血浆tHcy和血清叶酸浓度。结果:与对照组相比,治疗组的平均血清叶酸浓度(95%CI)显着增加了28(9-51)%,60(37-87)%和79(51-114)%分别为200和300微克的叶酸。在三个治疗组中观察到的tHcy降低,分别为16(8-22)%,12(4-18)%和17(9-24)%。结论:每天摄入少至100微克叶酸足以降低tHcy正常范围上限患者的tHcy。考虑到从各种来源汇总得出的叶酸总摄入量可能足够高,足以充分改善年轻女性的叶酸状况,低水平的强化可能也适合降低神经管畸形的风险。资金:早餐谷物由凯洛格公司提供,部分研究由凯洛格公司提供。 doi:10.1038 / sj.ejcn.1601388

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