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| Verfasst von: | Verbitsky, Miguel [VerfasserIn]  |
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| | Krithivasan, Priya [VerfasserIn] |
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| | Batourina, Ekaterina [VerfasserIn] |
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| | Khan, Atlas [VerfasserIn] |
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| | Graham, Sarah E. [VerfasserIn] |
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| | Marasà, Maddalena [VerfasserIn] |
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| | Kim, Hyunwoo [VerfasserIn] |
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| | Lim, Tze Y. [VerfasserIn] |
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| | Weng, Patricia L. [VerfasserIn] |
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| | Sánchez-Rodríguez, Elena [VerfasserIn] |
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| | Mitrotti, Adele [VerfasserIn] |
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| | Ahram, Dina F. [VerfasserIn] |
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| | Zanoni, Francesca [VerfasserIn] |
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| | Fasel, David A. [VerfasserIn] |
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| | Westland, Rik [VerfasserIn] |
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| | Sampson, Matthew G. [VerfasserIn] |
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| | Zhang, Jun Y. [VerfasserIn] |
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| | Bodria, Monica [VerfasserIn] |
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| | Kil, Byum Hee [VerfasserIn] |
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| | Shril, Shirlee [VerfasserIn] |
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| | Gesualdo, Loreto [VerfasserIn] |
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| | Torri, Fabio [VerfasserIn] |
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| | Scolari, Francesco [VerfasserIn] |
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| | Izzi, Claudia [VerfasserIn] |
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| | Wijk, Joanna A. E. van [VerfasserIn] |
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| | Saraga, Marijan [VerfasserIn] |
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| | Santoro, Domenico [VerfasserIn] |
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| | Conti, Giovanni [VerfasserIn] |
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| | Barton, David E. [VerfasserIn] |
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| | Dobson, Mark G. [VerfasserIn] |
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| | Puri, Prem [VerfasserIn] |
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| | Furth, Susan L. [VerfasserIn] |
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| | Warady, Bradley A. [VerfasserIn] |
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| | Pisani, Isabella [VerfasserIn] |
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| | Fiaccadori, Enrico [VerfasserIn] |
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| | Allegri, Landino [VerfasserIn] |
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| | Degl'Innocenti, Maria Ludovica [VerfasserIn] |
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| | Piaggio, Giorgio [VerfasserIn] |
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| | Alam, Shumyle [VerfasserIn] |
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| | Gigante, Maddalena [VerfasserIn] |
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| | Zaza, Gianluigi [VerfasserIn] |
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| | Esposito, Pasquale [VerfasserIn] |
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| | Lin, Fangming [VerfasserIn] |
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| | Simões-e-Silva, Ana Cristina [VerfasserIn] |
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| | Brodkiewicz, Andrzej [VerfasserIn] |
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| | Drozdz, Dorota [VerfasserIn] |
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| | Zachwieja, Katarzyna [VerfasserIn] |
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| | Miklaszewska, Monika [VerfasserIn] |
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| | Szczepanska, Maria [VerfasserIn] |
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| | Adamczyk, Piotr [VerfasserIn] |
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| | Tkaczyk, Marcin [VerfasserIn] |
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| | Tomczyk, Daria [VerfasserIn] |
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| | Sikora, Przemyslaw [VerfasserIn] |
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| | Mizerska-Wasiak, Malgorzata [VerfasserIn] |
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| | Krzemien, Grazyna [VerfasserIn] |
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| | Szmigielska, Agnieszka [VerfasserIn] |
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| | Zaniew, Marcin [VerfasserIn] |
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| | Lozanovski, Vladimir J. [VerfasserIn] |
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| | Gucev, Zoran [VerfasserIn] |
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| | Ionita-Laza, Iuliana [VerfasserIn] |
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| | Stanaway, Ian B. [VerfasserIn] |
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| | Crosslin, David R. [VerfasserIn] |
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| | Wong, Craig S. [VerfasserIn] |
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| | Hildebrandt, Friedhelm [VerfasserIn] |
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| | Barasch, Jonathan [VerfasserIn] |
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| | Kenny, Eimear E. [VerfasserIn] |
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| | Loos, Ruth J. F. [VerfasserIn] |
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| | Levy, Brynn [VerfasserIn] |
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| | Ghiggeri, Gian Marco [VerfasserIn] |
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| | Hakonarson, Hakon [VerfasserIn] |
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| | Latos-Bieleńska, Anna [VerfasserIn] |
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| | Materna-Kiryluk, Anna [VerfasserIn] |
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| | Darlow, John M. [VerfasserIn] |
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| | Tasic, Velibor [VerfasserIn] |
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| | Willer, Cristen [VerfasserIn] |
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| | Kiryluk, Krzysztof [VerfasserIn] |
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| | Sanna-Cherchi, Simone [VerfasserIn] |
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| | Mendelsohn, Cathy L. [VerfasserIn] |
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| | Gharavi, Ali G. [VerfasserIn] |
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| Titel: | Copy number variant analysis and genome-wide association study identify loci with large effect for vesicoureteral reflux |
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| Verf.angabe: | Miguel Verbitsky, Priya Krithivasan, Ekaterina Batourina, Atlas Khan, Sarah E. Graham, Maddalena Marasà, Hyunwoo Kim, Tze Y. Lim, Patricia L. Weng, Elena Sánchez-Rodríguez, Adele Mitrotti, Dina F. Ahram, Francesca Zanoni, David A. Fasel, Rik Westland, Matthew G. Sampson, Jun Y. Zhang, Monica Bodria, Byum Hee Kil, Shirlee Shril, Loreto Gesualdo, Fabio Torri, Francesco Scolari, Claudia Izzi, Joanna A. E. van Wijk, Marijan Saraga, Domenico Santoro, Giovanni Conti, David E. Barton, Mark G. Dobson, Prem Puri, Susan L. Furth, Bradley A. Warady, Isabella Pisani, Enrico Fiaccadori, Landino Allegri, Maria Ludovica Degl'Innocenti, Giorgio Piaggio, Shumyle Alam, Maddalena Gigante, Gianluigi Zaza, Pasquale Esposito, Fangming Lin, Ana Cristina Simões-e-Silva, Andrzej Brodkiewicz, Dorota Drozdz, Katarzyna Zachwieja, Monika Miklaszewska, Maria Szczepanska, Piotr Adamczyk, Marcin Tkaczyk, Daria Tomczyk, Przemyslaw Sikora, Malgorzata Mizerska-Wasiak, Grazyna Krzemien, Agnieszka Szmigielska, Marcin Zaniew, Vladimir J. Lozanovski, Zoran Gucev, Iuliana Ionita-Laza, Ian B. Stanaway, David R. Crosslin, Craig S. Wong, Friedhelm Hildebrandt, Jonathan Barasch, Eimear E. Kenny, Ruth J. F. Loos, Brynn Levy, Gian Marco Ghiggeri, Hakon Hakonarson, Anna Latos-Bieleńska, Anna Materna-Kiryluk, John M. Darlow, Velibor Tasic, Cristen Willer, Krzysztof Kiryluk, Simone Sanna-Cherchi, Cathy L. Mendelsohn, and Ali G. Gharavi |
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| E-Jahr: | 2021 |
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| Jahr: | March 31, 2021 |
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| Umfang: | 16 S. |
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| Fussnoten: | Gesehen am 16.12.2021 |
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| Titel Quelle: | Enthalten in: American Society of NephrologyJournal of the American Society of Nephrology |
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| Ort Quelle: | Washington, DC : American Society of Nephrology, 1990 |
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| Jahr Quelle: | 2021 |
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| Band/Heft Quelle: | 32(2021), 4, Seite 805-820 |
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| ISSN Quelle: | 1533-3450 |
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| Abstract: | Background: Vesicoureteral reflux (VUR) is a common, familial genitourinary disorder, and a major cause of pediatric urinary tract infection (UTI) and kidney failure. The genetic basis of VUR is not well understood. Methods: A diagnostic analysis sought rare, pathogenic copy number variant (CNV) disorders among 1737 patients with VUR. A GWAS was performed in 1395 patients and 5366 controls, of European ancestry.Results: Altogether, 3% of VUR patients harbored an undiagnosed rare CNV disorder, such as the 1q21.1, 16p11.2, 22q11.21, and triple X syndromes ((OR, 3.12; 95% CI, 2.10 to 4.54; P=6.35×10−8) The GWAS identified three study-wide significant and five suggestive loci with large effects (ORs, 1.41–6.9), containing canonical developmental genes expressed in the developing urinary tract (WDPCP, OTX1, BMP5, VANGL1, and WNT5A). In particular, 3.3% of VUR patients were homozygous for an intronic variant in WDPCP (rs13013890; OR, 3.65; 95% CI, 2.39 to 5.56; P=1.86×10–9). This locus was associated with multiple genitourinary phenotypes in the UK Biobank and eMERGE studies. Analysis of Wnt5a mutant mice confirmed the role of Wnt5a signaling in bladder and ureteric morphogenesis. Conclusions: These data demonstrate the genetic heterogeneity of VUR. Altogether, 6% of patients with VUR harbored a rare CNV or a common variant genotype conferring an OR >3. Identification of these genetic risk factors has multiple implications for clinical care and for analysis of outcomes in VUR. |
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| DOI: | doi:10.1681/ASN.2020050681 |
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| URL: | Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.
Volltext ; Verlag: https://doi.org/10.1681/ASN.2020050681 |
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| | Volltext: https://jasn.asnjournals.org/content/32/4/805 |
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| | DOI: https://doi.org/10.1681/ASN.2020050681 |
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| Datenträger: | Online-Ressource |
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| Sprache: | eng |
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| Sach-SW: | genetics and development |
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| | human genetics |
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| | pediatric nephrology |
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| | vesico-ureteral reflux |
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| K10plus-PPN: | 1782355855 |
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| Verknüpfungen: | → Zeitschrift |
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Copy number variant analysis and genome-wide association study identify loci with large effect for vesicoureteral reflux / Verbitsky, Miguel [VerfasserIn]; March 31, 2021 (Online-Ressource)
