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Gene-environment interactions between CD14 C-260T and endotoxin exposure on Foxp3+ and Foxp3- CD4+ lymphocyte numbers and total serum IgE levels in early childhood.儿童早期CD14 C-260T基因与内毒素暴露之间的基因-环境相互作用对Foxp3+和Foxp3- CD4+淋巴细胞数量及血清总IgE水平的影响。
Ann Allergy Asthma Immunol. 2008 Feb;100(2):128-36. doi: 10.1016/S1081-1206(10)60421-8.
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Race, genetics and medicine: does the color of a leopard's spots matter?种族、遗传学与医学:豹身上斑点的颜色重要吗?
Curr Opin Pediatr. 2007 Dec;19(6):613-8. doi: 10.1097/MOP.0b013e3282f163ca.
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The structure of common genetic variation in United States populations.美国人群中常见基因变异的结构。
Am J Hum Genet. 2007 Dec;81(6):1221-31. doi: 10.1086/522239. Epub 2007 Oct 16.
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Indoor environmental differences between inner city and suburban homes of children with asthma.患有哮喘的儿童居住的市中心和郊区家庭的室内环境差异。
J Urban Health. 2007 Jul;84(4):577-90. doi: 10.1007/s11524-007-9205-3.
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Gene-environment interactions with CD14 C-260T and their relationship to total serum IgE levels in adults.成人中CD14 C-260T的基因-环境相互作用及其与血清总IgE水平的关系。
J Allergy Clin Immunol. 2006 Oct;118(4):851-7. doi: 10.1016/j.jaci.2006.07.007. Epub 2006 Aug 30.
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PSMIX: an R package for population structure inference via maximum likelihood method.PSMIX:一个用于通过最大似然法进行群体结构推断的R软件包。
BMC Bioinformatics. 2006 Jun 22;7:317. doi: 10.1186/1471-2105-7-317.
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Applying epidemiologic concepts of primary, secondary, and tertiary prevention to the elimination of racial disparities in asthma.将一级、二级和三级预防的流行病学概念应用于消除哮喘方面的种族差异。
J Allergy Clin Immunol. 2006 Feb;117(2):233-40; quiz 241-2. doi: 10.1016/j.jaci.2005.11.004.
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Self-reported race and genetic admixture.自我报告的种族和基因混合情况。
N Engl J Med. 2006 Jan 26;354(4):421-2. doi: 10.1056/NEJMc052515.
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Variation in total and specific IgE: effects of ethnicity and socioeconomic status.总IgE和特异性IgE的变异:种族和社会经济地位的影响
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自我报告的种族和遗传血统在过敏致敏方面的差异。

Differences in allergic sensitization by self-reported race and genetic ancestry.

作者信息

Yang James J, Burchard Esteban G, Choudhry Shweta, Johnson Christine C, Ownby Dennis R, Favro David, Chen Justin, Akana Matthew, Ha Connie, Kwok Pui-Yan, Krajenta Richard, Havstad Suzanne L, Joseph Christine L, Seibold Max A, Shriver Mark D, Williams L Keoki

机构信息

Department of Biostatistics and Research Epidemiology, Henry Ford Health System, Detroit, Mich.

Department of Medicine, University of California San Francisco, San Francisco, Calif; Department of Biopharmaceutical Sciences, University of California San Francisco, San Francisco, Calif.

出版信息

J Allergy Clin Immunol. 2008 Oct;122(4):820-827.e9. doi: 10.1016/j.jaci.2008.07.044.

DOI:10.1016/j.jaci.2008.07.044
PMID:19014772
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2951327/
Abstract

BACKGROUND

Many allergic conditions occur more frequently in African American patients when compared with white patients; however, it is not known whether this represents genetic predisposition or disparate environmental exposures.

OBJECTIVE

We sought to assess the relationship of self-reported race and genetic ancestry to allergic sensitization.

METHODS

We included 601 women enrolled in a population-based cohort study whose self-reported race was African American or white. Genetic ancestry was estimated by using markers that differentiate West African and European ancestry. We assessed the relationship between allergic sensitization (defined as > or =1 allergen-specific IgE results) and both self-reported race and genetic ancestry. Regression models adjusted for sociodemographic variables, environmental exposures, and location of residence.

RESULTS

The average proportion of West African ancestry in African American participants was 0.69, whereas the mean proportion of European ancestry in white participants was 0.79. Self-reported African American race was associated with allergic sensitization when compared with those who reported being white (adjusted odds ratio, 2.19; 95% CI, 1.22-3.93), even after adjusting for other variables. Genetic ancestry was not significantly associated with allergic sensitization after accounting for location of residence (adjusted odds ratio, 2.09 for urban vs suburban residence; 95% CI, 1.32-3.31).

CONCLUSION

Self-reported race and location of residence appeared to be more important predictors of allergic sensitization when compared with genetic ancestry, suggesting that the disparity in allergic sensitization by race might be primarily a result of environmental factors rather than genetic differences.

摘要

背景

与白人患者相比,许多过敏病症在非裔美国患者中更为常见;然而,尚不清楚这是代表遗传易感性还是不同的环境暴露。

目的

我们试图评估自我报告的种族和遗传血统与过敏致敏之间的关系。

方法

我们纳入了601名参与基于人群的队列研究的女性,她们自我报告的种族为非裔美国人或白人。通过使用区分西非和欧洲血统的标记来估计遗传血统。我们评估了过敏致敏(定义为≥1种过敏原特异性IgE结果)与自我报告的种族和遗传血统之间的关系。回归模型对社会人口统计学变量、环境暴露和居住地点进行了调整。

结果

非裔美国参与者中西非血统的平均比例为0.69,而白人参与者中欧洲血统的平均比例为0.79。与报告为白人的人相比,自我报告为非裔美国人的种族与过敏致敏相关(调整后的优势比为2.19;95%置信区间为1.22 - 3.93),即使在对其他变量进行调整之后。在考虑居住地点后,遗传血统与过敏致敏无显著关联(城市与郊区居住的调整后优势比为2.09;95%置信区间为1.32 - 3.31)。

结论

与遗传血统相比,自我报告的种族和居住地点似乎是过敏致敏更重要的预测因素,这表明种族间过敏致敏的差异可能主要是环境因素而非遗传差异导致的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eb9/2951327/f9d5caabb522/nihms232434f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eb9/2951327/f88b8740dd9f/nihms232434f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eb9/2951327/f9d5caabb522/nihms232434f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eb9/2951327/f88b8740dd9f/nihms232434f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eb9/2951327/f9d5caabb522/nihms232434f2.jpg