About this Biochemistry, Genetics and Molecular Biology article
Multi-population Genome-wide Association Study Implicates Immune and Non-immune Factors in Pediatric Steroid-sensitive Nephrotic Syndrome by Alexandra Barry; Michelle T. McNulty; Xiaoyuan Jia; Yask Gupta; Hanna Debiec; Yang Luo; China Nagano; Tomoko Horinouchi; Seulgi Jung; Manuela Colucci; Dina F. Ahram; Adele Mitrotti; Aditi Sinha; Nynke Teeninga; Gina Jin; Shirlee Shril; Gianluca Caridi; Monica Bodria; Tze Y. Lim; Rik Westland; Francesca Zanoni; Maddalena Marasa; Daniel Turudic; Mario Giordano; Loreto Gesualdo; Riccardo Magistroni; Isabella Pisani; Enrico Fiaccadori; Jana Reiterova; Silvio Maringhini; William Morello; Giovanni Montini; Patricia L. Weng; Francesco Scolari; Marijan Saraga; Velibor Tasic; Domenica Santoro; Joanna A. E. van Wijk; Danko Milošević; Yosuke Kawai; Krzysztof Kiryluk; Martin R. Pollak; Ali Gharavi; Fangmin Lin; Ana Cristina Simœs e Silva; Ruth J. F. Loos; Eimear E. Kenny; Michiel F. Schreuder; Aleksandra Zurowska; Claire Dossier; Gema Ariceta; Magdalena Drozynska-Duklas; Julien Hogan; Augustina Jankauskiene; Friedhelm Hildebrandt; Larisa Prikhodina; Kyuyoung Song; Arvind Bagga; Hae Cheong; Gian Marco Ghiggeri; Prayong Vachvanichsanong; Kandai Nozu; Dongwon Lee; Marina Vivarelli; Soumya Raychaudhuri; Katsushi Tokunaga; Simone Sanna-Cherchi; Pierre Ronco; Kazumoto Iijima; Matthew G. Sampson is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
Pediatric steroid-sensitive nephrotic syndrome (pSSNS) is the most common childhood glomerular disease. Previous genome-wide association studies (GWAS) identified a risk locus in the HLA Class II region and three additional independent risk loci. But the genetic architecture of pSSNS, and its genetically driven pathobiology, is largely unknown. Here, we conduct a multi-population GWAS meta-analysis in 38,463 participants (2440 cases). We then conduct conditional analyses and population specific GWAS. We discover twelve significant associations—eight from the multi-population meta-analysis (four novel), two from the multi-population conditional analysis (one novel), and two additional novel loci from the European meta-analysis. Fine-mapping implicates specific amino acid haplotypes in __HLA-DQA1__ and __HLA-DQB1__ driving the HLA Class II risk locus. Non-HLA loci colocalize with eQTLs of monocytes and numerous T-cell subsets in independent datasets. Colocalization with kidney eQTLs is lacking but overlap with kidney cell open chromatin suggests an uncharacterized disease mechanism in kidney cells. A polygenic risk score (PRS) associates with earlier disease onset. Altogether, these
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- Author
- Alexandra Barry; Michelle T. McNulty; Xiaoyuan Jia; Yask Gupta; Hanna Debiec; Yang Luo; China Nagano; Tomoko Horinouchi; Seulgi Jung; Manuela Colucci; Dina F. Ahram; Adele Mitrotti; Aditi Sinha; Nynke Teeninga; Gina Jin; Shirlee Shril; Gianluca Caridi; Monica Bodria; Tze Y. Lim; Rik Westland; Francesca Zanoni; Maddalena Marasa; Daniel Turudic; Mario Giordano; Loreto Gesualdo; Riccardo Magistroni; Isabella Pisani; Enrico Fiaccadori; Jana Reiterova; Silvio Maringhini; William Morello; Giovanni Montini; Patricia L. Weng; Francesco Scolari; Marijan Saraga; Velibor Tasic; Domenica Santoro; Joanna A. E. van Wijk; Danko Milošević; Yosuke Kawai; Krzysztof Kiryluk; Martin R. Pollak; Ali Gharavi; Fangmin Lin; Ana Cristina Simœs e Silva; Ruth J. F. Loos; Eimear E. Kenny; Michiel F. Schreuder; Aleksandra Zurowska; Claire Dossier; Gema Ariceta; Magdalena Drozynska-Duklas; Julien Hogan; Augustina Jankauskiene; Friedhelm Hildebrandt; Larisa Prikhodina; Kyuyoung Song; Arvind Bagga; Hae Cheong; Gian Marco Ghiggeri; Prayong Vachvanichsanong; Kandai Nozu; Dongwon Lee; Marina Vivarelli; Soumya Raychaudhuri; Katsushi Tokunaga; Simone Sanna-Cherchi; Pierre Ronco; Kazumoto Iijima; Matthew G. Sampson
- Publisher
- Springer Science and Business Media LLC
- Published
- 2023
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)