Suzan L. Carmichael, Wei Yang, Chen Ma, Eric Roberts, Susan Kegley, Paul English, Edward J. Lammer, John S. Witte, Gary M. Shaw
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{"title":"基因变异和居住地邻近农药使用对尿道下裂风险的共同影响","authors":"Suzan L. Carmichael, Wei Yang, Chen Ma, Eric Roberts, Susan Kegley, Paul English, Edward J. Lammer, John S. Witte, Gary M. Shaw","doi":"10.1002/bdra.23508","DOIUrl":null,"url":null,"abstract":"<div>\n \n <section>\n \n <h3> Background</h3>\n \n <p>We examined risks associated with joint exposure of gene variants and pesticides.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Analyses included 189 cases and 390 male controls born from 1991 to 2003 in California's San Joaquin Valley. We used logistic regression to examine risks associated with joint exposures of gene variants and pesticides that our previous work identified as associated with hypospadias. Genetic variables were based on variants in <i>DGKK</i>, genes involved in sex steroid synthesis/metabolism, and genes involved in genital tubercle development. Pesticide exposure was based on residential proximity to commercial agricultural pesticide applications.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Odds ratios (ORs) were highest among babies with joint exposures, who had two- to fourfold increased risks; for example, the OR was 3.7 (95% confidence interval [CI], 0.8–16.5) among subjects with the risk-associated <i>DGKK</i> haplotype <i>and</i> pesticide exposure; OR, 1.5 (95% CI, 0.7–3.1) among subjects with the haplotype and no pesticide exposure; and OR, 0.9 (95% CI, 0.5–1.6) among subjects without the haplotype but with pesticide exposure, relative to subjects with neither. However, results did not provide statistical evidence that these risks were significantly greater than expected on an additive scale, relative to risks associated with one exposure at a time.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>We observed elevated risks associated with joint exposures to selected pesticides and genetic variants but no statistical evidence for interaction. Birth Defects Research (Part A) 106:653–658, 2016. © 2016 Wiley Periodicals, Inc.</p>\n </section>\n </div>","PeriodicalId":8983,"journal":{"name":"Birth defects research. Part A, Clinical and molecular teratology","volume":"106 8","pages":"653-658"},"PeriodicalIF":0.0000,"publicationDate":"2016-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/bdra.23508","citationCount":"14","resultStr":"{\"title\":\"Joint effects of genetic variants and residential proximity to pesticide applications on hypospadias risk\",\"authors\":\"Suzan L. Carmichael, Wei Yang, Chen Ma, Eric Roberts, Susan Kegley, Paul English, Edward J. Lammer, John S. Witte, Gary M. Shaw\",\"doi\":\"10.1002/bdra.23508\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>We examined risks associated with joint exposure of gene variants and pesticides.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Analyses included 189 cases and 390 male controls born from 1991 to 2003 in California's San Joaquin Valley. We used logistic regression to examine risks associated with joint exposures of gene variants and pesticides that our previous work identified as associated with hypospadias. Genetic variables were based on variants in <i>DGKK</i>, genes involved in sex steroid synthesis/metabolism, and genes involved in genital tubercle development. Pesticide exposure was based on residential proximity to commercial agricultural pesticide applications.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Odds ratios (ORs) were highest among babies with joint exposures, who had two- to fourfold increased risks; for example, the OR was 3.7 (95% confidence interval [CI], 0.8–16.5) among subjects with the risk-associated <i>DGKK</i> haplotype <i>and</i> pesticide exposure; OR, 1.5 (95% CI, 0.7–3.1) among subjects with the haplotype and no pesticide exposure; and OR, 0.9 (95% CI, 0.5–1.6) among subjects without the haplotype but with pesticide exposure, relative to subjects with neither. However, results did not provide statistical evidence that these risks were significantly greater than expected on an additive scale, relative to risks associated with one exposure at a time.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>We observed elevated risks associated with joint exposures to selected pesticides and genetic variants but no statistical evidence for interaction. Birth Defects Research (Part A) 106:653–658, 2016. © 2016 Wiley Periodicals, Inc.</p>\\n </section>\\n </div>\",\"PeriodicalId\":8983,\"journal\":{\"name\":\"Birth defects research. Part A, Clinical and molecular teratology\",\"volume\":\"106 8\",\"pages\":\"653-658\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-04-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/bdra.23508\",\"citationCount\":\"14\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Birth defects research. Part A, Clinical and molecular teratology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/bdra.23508\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Birth defects research. Part A, Clinical and molecular teratology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bdra.23508","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q","JCRName":"Medicine","Score":null,"Total":0}
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