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Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
Tang, Clara Sze-Man; Gui, Hongsheng; Kapoor, Ashish; Kim, Jeong-Hyun; Luzón-Toro, Berta; Pelet, Anna; Burzynski, Grzegorz; Lantieri, Francesca; So, Man-Ting; Berrios, Courtney; Shin, Hyoung Doo; Fernández, Raquel M; Le, Thuy-Linh; Verheij, Joke B G M; Matera, Ivana; Cherny, Stacey S; Nandakumar, Priyanka; Cheong, Hyun Sub; Antiñolo, Guillermo; Amiel, Jeanne; Seo, Jeong-Meen; Kim, Dae-Yeon; Oh, Jung-Tak; Lyonnet, Stanislas; Borrego, Salud; Ceccherini, Isabella; Hofstra, Robert M W; Chakravarti, Aravinda; Kim, Hyun-Young; Sham, Pak Chung; Tam, Paul K H; Garcia-Barceló, Maria-Mercè.
Afiliación
  • Tang CS; Department of Surgery.
  • Gui H; Centre for Genomic Sciences.
  • Kapoor A; Dr Li Dak-Sum Research Centre, The University of Hong Kong - Karolinska Institutet Collaboration in Regenerative Medicine, Hong Kong SAR, China.
  • Kim JH; Department of Surgery.
  • Luzón-Toro B; Centre for Genomic Sciences.
  • Pelet A; Center for Complex Disease Genomics, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
  • Burzynski G; Research Institute for Basic Science, Sogang University, Seoul 121-742, Republic of Korea.
  • Lantieri F; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.
  • So MT; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.
  • Berrios C; Laboratory of Embryology and Genetics of Congenital Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Institut Imagine, Paris, France.
  • Shin HD; Paris Descartes-Sorbonne Paris Cité University, Institut Imagine, Paris, France.
  • Fernández RM; Department of Clinical Genetic, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Le TL; UOC Genetica Medica, Istituto Giannina Gaslini, 16148 Genova, Italy.
  • Verheij JB; Department of Surgery.
  • Matera I; Center for Complex Disease Genomics, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
  • Cherny SS; Research Institute for Basic Science, Sogang University, Seoul 121-742, Republic of Korea.
  • Nandakumar P; Department of Life Science, Sogang University, Seoul 121-742, Republic of Korea.
  • Cheong HS; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.
  • Antiñolo G; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.
  • Amiel J; Laboratory of Embryology and Genetics of Congenital Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Institut Imagine, Paris, France.
  • Seo JM; Paris Descartes-Sorbonne Paris Cité University, Institut Imagine, Paris, France.
  • Kim DY; Department of Clinical Genetic, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Oh JT; UOC Genetica Medica, Istituto Giannina Gaslini, 16148 Genova, Italy.
  • Lyonnet S; Centre for Genomic Sciences.
  • Borrego S; Department of Psychiatry.
  • Ceccherini I; State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.
  • Hofstra RM; Center for Complex Disease Genomics, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
  • Chakravarti A; Department of Genetic Epidemiology, SNP Genetics, Inc., Seoul 121-742, Republic of Korea.
  • Kim HY; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.
  • Sham PC; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.
  • Tam PK; Laboratory of Embryology and Genetics of Congenital Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Institut Imagine, Paris, France.
  • Garcia-Barceló MM; Paris Descartes-Sorbonne Paris Cité University, Institut Imagine, Paris, France.
Hum Mol Genet ; 25(23): 5265-5275, 2016 12 01.
Article en En | MEDLINE | ID: mdl-27702942
Hirschsprung disease (HSCR) is the most common cause of neonatal intestinal obstruction. It is characterized by the absence of ganglia in the nerve plexuses of the lower gastrointestinal tract. So far, three common disease-susceptibility variants at the RET, SEMA3 and NRG1 loci have been detected through genome-wide association studies (GWAS) in Europeans and Asians to understand its genetic etiologies. Here we present a trans-ethnic meta-analysis of 507 HSCR cases and 1191 controls, combining all published GWAS results on HSCR to fine-map these loci and narrow down the putatively causal variants to 99% credible sets. We also demonstrate that the effects of RET and NRG1 are universal across European and Asian ancestries. In contrast, we detected a European-specific association of a low-frequency variant, rs80227144, in SEMA3 [odds ratio (OR) = 5.2, P = 4.7 × 10-10]. Conditional analyses on the lead SNPs revealed a secondary association signal, corresponding to an Asian-specific, low-frequency missense variant encoding RET p.Asp489Asn (rs9282834, conditional OR = 20.3, conditional P = 4.1 × 10-14). When in trans with the RET intron 1 enhancer risk allele, rs9282834 increases the risk of HSCR from 1.1 to 26.7. Overall, our study provides further insights into the genetic architecture of HSCR and has profound implications for future study designs.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Neurregulina-1 / Semaforina-3A / Proteínas Proto-Oncogénicas c-ret / Enfermedad de Hirschsprung Tipo de estudio: Risk_factors_studies / Systematic_reviews Límite: Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2016 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Neurregulina-1 / Semaforina-3A / Proteínas Proto-Oncogénicas c-ret / Enfermedad de Hirschsprung Tipo de estudio: Risk_factors_studies / Systematic_reviews Límite: Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2016 Tipo del documento: Article Pais de publicación: Reino Unido