@article{b921fe77d5334d6e99fa376bba7765b6,
title = "Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation Syndrome",
abstract = "Biliary atresia (BA) is the most common cause of end-stage liver disease in children and the primary indication for pediatric liver transplantation, yet underlying etiologies remain unknown. Approximately 10% of infants affected by BA exhibit various laterality defects (heterotaxy) including splenic abnormalities and complex cardiac malformations—a distinctive subgroup commonly referred to as the biliary atresia splenic malformation (BASM) syndrome. We hypothesized that genetic factors linking laterality features with the etiopathogenesis of BA in BASM patients could be identified through whole-exome sequencing (WES) of an affected cohort. DNA specimens from 67 BASM subjects, including 58 patient–parent trios, from the National Institute of Diabetes and Digestive and Kidney Diseases–supported Childhood Liver Disease Research Network (ChiLDReN) underwent WES. Candidate gene variants derived from a prespecified set of 2,016 genes associated with ciliary dysgenesis and/or dysfunction or cholestasis were prioritized according to pathogenicity, population frequency, and mode of inheritance. Five BASM subjects harbored rare and potentially deleterious biallelic variants in polycystic kidney disease 1 like 1 (PKD1L1), a gene associated with ciliary calcium signaling and embryonic laterality determination in fish, mice, and humans. Heterozygous PKD1L1 variants were found in 3 additional subjects. Immunohistochemical analysis of liver from the one BASM subject available revealed decreased PKD1L1 expression in bile duct epithelium when compared to normal livers and livers affected by other noncholestatic diseases. Conclusion: WES identified biallelic and heterozygous PKD1L1 variants of interest in 8 BASM subjects from the ChiLDReN data set; the dual roles for PKD1L1 in laterality determination and ciliary function suggest that PKD1L1 is a biologically plausible, cholangiocyte-expressed candidate gene for the BASM syndrome.",
author = "{for the Childhood Liver Disease Research Network (ChiLDReN)} and Berauer, {John Paul} and Mezina, {Anya I.} and Okou, {David T.} and Aniko Sabo and Muzny, {Donna M.} and Gibbs, {Richard A.} and Hegde, {Madhuri R.} and Pankaj Chopra and Cutler, {David J.} and Perlmutter, {David H.} and Bull, {Laura N.} and Thompson, {Richard J.} and Loomes, {Kathleen M.} and Spinner, {Nancy B.} and Ramakrishnan Rajagopalan and Guthery, {Stephen L.} and Barry Moore and Mark Yandell and Sanjiv Harpavat and Magee, {John C.} and Kamath, {Binita M.} and Molleston, {Jean P.} and Bezerra, {Jorge A.} and Murray, {Karen F.} and Alonso, {Estella M.} and Philip Rosenthal and Squires, {Robert H.} and Wang, {Kasper S.} and Finegold, {Milton J.} and Pierre Russo and Sherker, {Averell H.} and Sokol, {Ronald J.} and Karpen, {Saul J.}",
note = "Funding Information: Hospital of Pittsburgh of UPMC; DK062456, to The University of Michigan; DK062453, to Children{\textquoteright}s Hospital Colorado and University of Colorado; DK062452, to Washington University School of Medicine; DK062445, to Icahn School of Medicine at Mount Sinai; and DK062436, to Ann & Robert H. Lurie Children{\textquoteright}s Hospital of Chicago); by UL1 grants from the National Institutes of Health Clinical and Translational Sciences Award program through the National Center for Advancing Translational Sciences (TR001872, to University of California San Francisco Benioff Children{\textquoteright}s Hospital; TR001857, to Children{\textquoteright}s Hospital of Pittsburgh of UPMC; TR001108, to Riley Hospital for Children at Indiana University; TR002535, to University of Colorado; TR002378, to Emory University School of Medicine; TR000423 and RR025014, to Seattle Children{\textquoteright}s Hospital; and TR000077, to Cincinnati Children{\textquoteright}s Hospital Medical Center; TR000003, to Children{\textquoteright}s Hospital of Philadelphia]); by the American Gastroenterological Association Research Foundation (U54 HG003273, to A.S., D.M., R.G.; Student Research Fellowship Award and TL1TR000456, to A.I.M.); and by the Cade R. Alpard Foundation for Pediatric Liver Disease, the Spain Foundation, and the Meredith Brown Foundation (to S.J.K.). {\textcopyright} 2019 by the American Association for the Study of Liver Diseases. View this article online at wileyonlinelibrary.com. DOI 10.1002/hep.30515 Potential conflict of interest: Dr. Kamath consults for Retrophin, Shire, and Mirum. Dr. Karpen consults for Intercept, Albireo, Retrophin, Mirum, and Gemphire. Dr. Molleston consults for Lilly and received grants from AbbVie, Gilead, and Shire. Dr. Murray received grants from and owns stock in Merck. She received grants from Gilead and Shire. Dr. Rosenthal consults for and is on the speakers{\textquoteright} bureau of Retrophin. He consults for and received grants from Gilead and AbbVie. He consults for Intercept, Alexion, Albireo, and Audentes. He received grants from Bristol-Myers Squibb and Roche. Dr. Thompson consults for, advises, and owns stock in Generation Bio and Qing Bile. He consults for Albireo, Shire, Mirum, and Arcturus. Funding Information: Received May 3, 2018; accepted January 2, 2019. Additional Supporting Information may be found at onlinelibrary.wiley.com/doi/10.1002/hep.30515/suppinfo. A portion of this work was presented as an oral abstract at the 68th Annual Meeting of the American Association for the Study of Liver Diseases: The Liver Meeting in Washington, DC, on October 23, 2017 (Hepatology 2017;66:1258A-1259A). Supported by U01 grants from the National Institute of Diabetes and Digestive and Kidney Diseases (DK103149, to Texas Children{\textquoteright}s Hospital; DK103140, to University of Utah; DK103135, to The Hospital for Sick Children; DK084575, to Seattle Children{\textquoteright}s Hospital; DK084538, to Children{\textquoteright}s Hospital of Los Angeles; DK084536, to Indiana University/Riley Hospital for Children; DK062503, to Johns Hopkins Children{\textquoteright}s Center; DK062500, to University of California San Francisco Children{\textquoteright}s Hospital; DK062497, to Cincinnati Children{\textquoteright}s Hospital Medical Center; DK062481 to The Children{\textquoteright}s Hospital of Philadelphia; DK062470 to Emory University School of Medicine; DK062466 to Children{\textquoteright}s Publisher Copyright: {\textcopyright} 2019 by the American Association for the Study of Liver Diseases.",
year = "2019",
month = sep,
doi = "10.1002/hep.30515",
language = "English (US)",
volume = "70",
pages = "899--910",
journal = "Hepatology",
issn = "0270-9139",
publisher = "John Wiley and Sons Ltd",
number = "3",
}