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临床试验/NCT02135393
NCT02135393已完成不适用

Folic Acid Handling by the Human Gut: Implications for Food Fortification and Supplementation

Newcastle-upon-Tyne Hospitals NHS Trust4 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2009年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
6
试验地点
4
主要终点
The percentage of folate in un-modified and modified form in the portal vein for each of the different oral folate dosing formulations

研究概览

简要总结

The aim of this study is to test the assumption that, in humans, folic acid, a dietary supplement is biotransformed (reduced and methylated) to the natural circulating plasma folate 6S-5Methyltetrahydrofolic acid (5-MTHF) in the intestinal mucosa.

详细描述

Current thinking, based mainly on rodent studies, is that physiological doses of folic acid (pteroylmonoglutamic acid), like dietary vitamin folates, are biotransformed in the intestinal mucosa and transferred to the portal vein as the natural circulating plasma folate, 5-methyltetrahydrofolic acid (5-MTHF), before entering the liver and the wider systemic blood supply.

Study design:Open labelled study that samples portal and peripheral veins for labelled folate concentrations following oral ingestion with physiological doses of dietary supplements stable-isotope-labelled folic acid, or, the reduced folate, 5-formyltetrahydrofolic acid (5-FormylTHF). The study was performed in subjects with a Transjugular Intrahepatic Porto Systemic Shunt (TIPSS) in situ at the time of a routine annual patency check to allow blood samples to be taken from the portal vein. The aim of this study is to test the assumption that, in humans, folic acid is biotransformed (reduced and methylated) to 5-MTHF in the intestinal mucosa.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Stable, synthetic liver function without recent evidence of decompensation (defined as liver function inadequacy or active complications of portal hypertension)
  • Abstinent from alcohol
  • Free from malignant disease
  • Normal gut permeability (as assessed by the lactulose/mannitol test)
  • Patent TIPSS on their last surveillance

排除标准

  • Taking Vitamin B supplements
  • Taking Folic Acid supplementation
  • Unable to provide informed consent

研究组 & 干预措施

13C5-folic acid or 13C5-6S-5-FormylTHF

Experimental

Physiological 500 nmol (220 µg folic acid equivalent) dose of dietary supplement 13C5-folic acid or 13C5-6S-5-FormylTHF given to subjects with in situ transjugular intrahepatic portosystemic stent at the time of routine venography patency check followed by regular portal venous sampling for 85 minutes at pre determined intervals and then physiological 500 nmol dose of 13C-6S-5-FormylTHF or 13C5-folic acid respectively at the next annual routine venography patency check followed by portal venous sampling for 85 minutes

干预措施: 13C5-folic acid or 13C5-6S-5-FormylTHF (Dietary Supplement)

结局指标

主要结局

The percentage of folate in un-modified and modified form in the portal vein for each of the different oral folate dosing formulations

时间窗: 85 minutes

次要结局

未报告次要终点

研究者

发起方
Newcastle-upon-Tyne Hospitals NHS Trust
申办方类型
Other
责任方
Sponsor

研究点 (4)

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