Genetic Variants and Iron Absorption
2014年7月21日 更新者:Cornell University
Metabolic Adaptation to Plant-based Diets in Asian Populations
The two specific aims of this study are: 1) to assess the impact of a genetic variant on iron status; 2) to assess the impact of a genetic variant on non-heme absorption among Asian women.
The investigators hypothesize that the genetic variant could enhance iron status and iron absorption in Asian women.
研究概览
地位
完全的
条件
详细说明
To determine the HFE genotype of female Asian study volunteers, we collected venous blood samples and extracted DNA from these blood samples.
HFE genotype was determined as CC, CT, and TT and used to assess possible differences in iron status as a function of genotype.
To measure the impact of genotype on non-heme Fe absorption, a sub-group of women with the CC (n=10) or TT (n=11) genotype were invited to return for an Fe absorption study.
Each volunteer consumed stable 57Fe (as ferrous sulfate).
Two weeks after ingesting this tracer, a blood sample was collected from each woman and the amount of non-heme (57Fe) iron incorporated into red blood cells was measured with magnetic sector thermal ionization mass spectrometry.
Possible associations between iron status and iron absorption as a function of genotypes were explored.
Data from this study will provide information that aims to improve human health by better understanding the iron requirements of individuals with different genetic background.
研究类型
观察性的
注册 (实际的)
57
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
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New York
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Ithaca、New York、美国、14853
- Human Metabolic Research Unit, Cornell University
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 35年 (成人)
接受健康志愿者
是的
有资格学习的性别
女性
取样方法
非概率样本
研究人群
Women were eligible for the study if they met the following criteria: 1) non-pregnant and between the ages of 18~35 y; 2) of East Asian descent with both maternal and paternal grandparents from East Asia, including China, Japan, South Korea, Vietnam, Thailand, Malaysia and Singapore; 3) not taking any vitamin or mineral supplements for at least 1 month before the study and during the 2-week study interval; 4) no pre-existing medical problems including malabsorption, blood disorders, ulcers, joint diseases or asthma that might impact inflammation or Fe status; 5) not taking any prescribed medications known to affect iron homeostasis.
描述
Inclusion Criteria:
- non-pregnant and between the ages of 18~35 y
- East Asian descent with both maternal and paternal grandparents from East Asia, including China, Japan, South Korea, Vietnam, Thailand, Malaysia and Singapore
Exclusion Criteria:
- taking or planing to take any vitamin or mineral supplements during the study period
- pre-existing medical problems that might impact inflammation or Fe status, including malabsorption, blood disorders, ulcers, joint diseases and asthma
- taking any prescribed medications known to affect iron homeostasis
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
---|---|---|
Genotype at SNP rs9366637
大体时间:2 weeks after the participant's visit to the laboratory
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At the participant's visit to the laboratory, a 10 mL blood sample was collected.
The blood sample was used for determining genotype.
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2 weeks after the participant's visit to the laboratory
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Hemoglobin
大体时间:Up to 2 days after the participant's visit to the laboratory
|
At the participant's visit to the laboratory, a 10 mL blood sample was collected.
The blood sample was used for determining the concentration of hemoglobin.
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Up to 2 days after the participant's visit to the laboratory
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Serum Ferritin
大体时间:Up to 6 months after the participant's visit to the laboratory
|
At the participant's visit to the laboratory, a 10 mL blood sample was collected.
The blood sample was used for determining the concentration of serum ferritin.
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Up to 6 months after the participant's visit to the laboratory
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Serum transferrin receptor
大体时间:Up to 6 months after the participant's visit to the laboratory
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At the participant's visit to the laboratory, a 10 mL blood sample was collected.
The blood sample was used for determining the concentration of serum transferrin receptor.
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Up to 6 months after the participant's visit to the laboratory
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Non-heme Iron absorption in women with 2 HFE genotypes
大体时间:one month for screening with genotype then 2 weeks for iron absorption study
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Women donated a blood sample for genotyping.
Women with particular HFE genotypes were invited to return for an absorption study.
Two weeks after women consume the iron tracer, a blood sample was obtained to measure the amount of iron absorbed.
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one month for screening with genotype then 2 weeks for iron absorption study
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
---|---|---|
Folate
大体时间:Up to 6 months after the participant's visit to the laboratory
|
At the participant's visit to the laboratory, a 10 mL blood sample was collected.
The blood sample was used for determining the concentration of folate.
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Up to 6 months after the participant's visit to the laboratory
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Vitamin B-12
大体时间:Up to 6 months after the participant's visit to the laboratory
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At the participant's visit to the laboratory, a 10 mL blood sample was collected.
The blood sample was used for determining the concentration of vitamin B-12.
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Up to 6 months after the participant's visit to the laboratory
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C-reactive protein
大体时间:Up to 6 months after the participant's visit to the laboratory
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At the participant's visit to the laboratory, a 10 mL blood sample was collected.
The blood sample was used for determining the concentration of C-reactive protein.
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Up to 6 months after the participant's visit to the laboratory
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2012年6月1日
初级完成 (实际的)
2013年4月1日
研究完成 (实际的)
2014年5月1日
研究注册日期
首次提交
2014年7月16日
首先提交符合 QC 标准的
2014年7月21日
首次发布 (估计)
2014年7月23日
研究记录更新
最后更新发布 (估计)
2014年7月23日
上次提交的符合 QC 标准的更新
2014年7月21日
最后验证
2014年7月1日
更多信息
与本研究相关的术语
其他研究编号
- IRB #: 1206003117
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.