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Admixture mapping of quantitative trait loci for BMI in African Americans: evidence for loci on chromosomes 3q, 5q, and 15q.

作者信息

Basu Analabha, Tang Hua, Arnett Donna, Gu C Charles, Mosley Tom, Kardia Sharon, Luke Amy, Tayo Bamidele, Cooper Richard, Zhu Xiaofeng, Risch Neil

机构信息

Institute for Human Genetics, Department of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.

出版信息

Obesity (Silver Spring). 2009 Jun;17(6):1226-31. doi: 10.1038/oby.2009.24. Epub 2009 Feb 19.


DOI:10.1038/oby.2009.24
PMID:19584881
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2929755/
Abstract

Obesity is a heritable trait and a major risk factor for highly prevalent common diseases such as hypertension and type 2 diabetes. Previously we showed that BMI was positively correlated with African ancestry among the African Americans (AAs) in the US National Heart, Lung, and Blood Institute's Family Blood Pressure Program (FBPP). In a set of 1,344 unrelated AAs, using Individual Ancestry (IA) estimates at 284 marker locations across the genome, we now present a quantitative admixture mapping analysis of BMI. We used a set of unrelated individuals from Nigeria to represent the African ancestral population and the European American (EA) in the FBPP as the European ancestral population. The analysis was based on a common set of 284 microsatellite markers genotyped in all three groups. We considered the quantitative trait, BMI, as the response variable in a regression analysis with the marker location specific excess European ancestry as the explanatory variable. After suitably adjusting for different covariates such as sex, age, and network, we found strong evidence for a positive association with European ancestry at chromosome locations 3q29 and 5q14 and a negative association on chromosome 15q26. To our knowledge, this is the largest quantitative admixture mapping effort in terms of sample size and marker locus involvement for the trait. These results suggest that these regions may harbor genes influencing BMI in the AA population.

摘要

相似文献

[1]
Admixture mapping of quantitative trait loci for BMI in African Americans: evidence for loci on chromosomes 3q, 5q, and 15q.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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[2]
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[3]
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[4]
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[5]
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[6]
Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American families.

Circ Cardiovasc Genet. 2015-2

[7]
Trans-ethnic genome-wide association studies: advantages and challenges of mapping in diverse populations.

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[8]
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[9]
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Hum Hered. 2013

[10]
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本文引用的文献

[1]
Evidence of linkage and association with body fatness and abdominal fat on chromosome 15q26.

Obesity (Silver Spring). 2007-8

[2]
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity.

Science. 2007-5-11

[3]
Genetic ancestry, population sub-structure, and cardiovascular disease-related traits among African-American participants in the CARDIA Study.

Hum Genet. 2007-6

[4]
Heterozygosity for a mutation in the growth hormone-releasing hormone receptor gene does not influence adult stature, but affects body composition.

J Clin Endocrinol Metab. 2007-6

[5]
Genetic factors in human obesity.

Obes Rev. 2007-3

[6]
Genetic markers for ancestry are correlated with body composition traits in older African Americans.

Osteoporos Int. 2007-6

[7]
The human obesity gene map: the 2005 update.

Obesity (Silver Spring). 2006-4

[8]
Racial admixture and its impact on BMI and blood pressure in African and Mexican Americans.

Hum Genet. 2006-7

[9]
Genetics of common forms of obesity: a brief overview.

Am J Clin Nutr. 2005-7

[10]
Sex-specific findings from a genome-wide linkage analysis of human fatness in non-Hispanic whites and African Americans: the HyperGEN study.

Int J Obes (Lond). 2005-6

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