Literature DB >> 24683503

Matching on Race and Ethnicity in Case-Control Studies as a Means of Control for Population Stratification.

Anand P Chokkalingam1, Melinda C Aldrich2, Karen Bartley1, Ling-I Hsu1, Catherine Metayer1, Lisa F Barcellos1, Joseph L Wiemels3, John K Wiencke4, Patricia A Buffler1, Steve Selvin1.   

Abstract

Some investigators argue that controlling for self-reported race or ethnicity, either in statistical analysis or in study design, is sufficient to mitigate unwanted influence from population stratification. In this report, we evaluated the effectiveness of a study design involving matching on self-reported ethnicity and race in minimizing bias due to population stratification within an ethnically admixed population in California. We estimated individual genetic ancestry using structured association methods and a panel of ancestry informative markers, and observed no statistically significant difference in distribution of genetic ancestry between cases and controls (P=0.46). Stratification by Hispanic ethnicity showed similar results. We evaluated potential confounding by genetic ancestry after adjustment for race and ethnicity for 1260 candidate gene SNPs, and found no major impact (>10%) on risk estimates. In conclusion, we found no evidence of confounding of genetic risk estimates by population substructure using this matched design. Our study provides strong evidence supporting the race- and ethnicity-matched case-control study design as an effective approach to minimizing systematic bias due to differences in genetic ancestry between cases and controls.

Entities:  

Keywords:  Case-control; Genetic susceptibility; Matching; Population stratification

Year:  2011        PMID: 24683503      PMCID: PMC3966291          DOI: 10.4172/2161-1165.1000101

Source DB:  PubMed          Journal:  Epidemiology (Sunnyvale)


  13 in total

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Journal:  J Genet       Date:  2010-12       Impact factor: 1.166

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4.  Control selection strategies in case-control studies of childhood diseases.

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5.  Examination of ancestry and ethnic affiliation using highly informative diallelic DNA markers: application to diverse and admixed populations and implications for clinical epidemiology and forensic medicine.

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Journal:  Hum Genet       Date:  2005-09-29       Impact factor: 4.132

Review 6.  Accounting for ancestry: population substructure and genome-wide association studies.

Authors:  Chao Tian; Peter K Gregersen; Michael F Seldin
Journal:  Hum Mol Genet       Date:  2008-10-15       Impact factor: 6.150

7.  Self-reported ethnicity, genetic structure and the impact of population stratification in a multiethnic study.

Authors:  Hansong Wang; Christopher A Haiman; Laurence N Kolonel; Brian E Henderson; Lynne R Wilkens; Loïc Le Marchand; Daniel O Stram
Journal:  Hum Genet       Date:  2010-05-25       Impact factor: 4.132

8.  CYP1A1/2 haplotypes and lung cancer and assessment of confounding by population stratification.

Authors:  Melinda C Aldrich; Steve Selvin; Helen M Hansen; Lisa F Barcellos; Margaret R Wrensch; Jennette D Sison; Karl T Kelsey; Patricia A Buffler; Charles P Quesenberry; Michael F Seldin; John K Wiencke
Journal:  Cancer Res       Date:  2009-03-10       Impact factor: 12.701

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Journal:  PLoS One       Date:  2008-07-02       Impact factor: 3.240

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2.  Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children.

Authors:  Ling-I Hsu; Anand P Chokkalingam; Farren B S Briggs; Kyle Walsh; Vonda Crouse; Cecilia Fu; Catherine Metayer; Joseph L Wiemels; Lisa F Barcellos; Patricia A Buffler
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4.  Variation in xenobiotic transport and metabolism genes, household chemical exposures, and risk of childhood acute lymphoblastic leukemia.

Authors:  Anand P Chokkalingam; Catherine Metayer; Ghislaine A Scelo; Jeffrey S Chang; Kevin Y Urayama; Melinda C Aldrich; Neela Guha; Helen M Hansen; Gary V Dahl; Lisa F Barcellos; John K Wiencke; Joseph L Wiemels; Patricia A Buffler
Journal:  Cancer Causes Control       Date:  2012-06-07       Impact factor: 2.506

5.  Genetic variants in ARID5B and CEBPE are childhood ALL susceptibility loci in Hispanics.

Authors:  Anand P Chokkalingam; Ling-I Hsu; Catherine Metayer; Helen M Hansen; Stacy R Month; Lisa F Barcellos; Joseph L Wiemels; Patricia A Buffler
Journal:  Cancer Causes Control       Date:  2013-07-09       Impact factor: 2.506

6.  SNP association mapping across the extended major histocompatibility complex and risk of B-cell precursor acute lymphoblastic leukemia in children.

Authors:  Kevin Y Urayama; Anand P Chokkalingam; Catherine Metayer; Helen Hansen; Suzanne May; Patricia Ramsay; Joseph L Wiemels; John K Wiencke; Elizabeth Trachtenberg; Pamela Thompson; Yasushi Ishida; Paul Brennan; Kent W Jolly; Amanda M Termuhlen; Malcolm Taylor; Lisa F Barcellos; Patricia A Buffler
Journal:  PLoS One       Date:  2013-08-22       Impact factor: 3.240

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Journal:  Genes (Basel)       Date:  2019-02-18       Impact factor: 4.096

8.  A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal Evolution.

Authors:  Kyle M Walsh; Adam J de Smith; Helen M Hansen; Ivan V Smirnov; Semira Gonseth; Alyson A Endicott; Jianqiao Xiao; Terri Rice; Cecilia H Fu; Lucie S McCoy; Daniel H Lachance; Jeanette E Eckel-Passow; John K Wiencke; Robert B Jenkins; Margaret R Wrensch; Xiaomei Ma; Catherine Metayer; Joseph L Wiemels
Journal:  Cancer Res       Date:  2015-11-02       Impact factor: 13.312

  8 in total

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