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  1. Article ; Online: The ABCG2 Q141K hyperuricemia and gout associated variant illuminates the physiology of human urate excretion.

    Hoque, Kazi Mirajul / Dixon, Eryn E / Lewis, Raychel M / Allan, Jordyn / Gamble, Gregory D / Phipps-Green, Amanda J / Halperin Kuhns, Victoria L / Horne, Anne M / Stamp, Lisa K / Merriman, Tony R / Dalbeth, Nicola / Woodward, Owen M

    Nature communications

    2020  Volume 11, Issue 1, Page(s) 2767

    Abstract: The pathophysiological nature of the common ABCG2 gout and hyperuricemia associated variant Q141K (rs2231142) remains undefined. Here, we use a human interventional cohort study (ACTRN12615001302549) to understand the physiological role of ABCG2 and find ...

    Abstract The pathophysiological nature of the common ABCG2 gout and hyperuricemia associated variant Q141K (rs2231142) remains undefined. Here, we use a human interventional cohort study (ACTRN12615001302549) to understand the physiological role of ABCG2 and find that participants with the Q141K ABCG2 variant display elevated serum urate, unaltered FEUA, and significant evidence of reduced extra-renal urate excretion. We explore mechanisms by generating a mouse model of the orthologous Q140K Abcg2 variant and find male mice have significant hyperuricemia and metabolic alterations, but only subtle alterations of renal urate excretion and ABCG2 abundance. By contrast, these mice display a severe defect in ABCG2 abundance and function in the intestinal tract. These results suggest a tissue specific pathobiology of the Q141K variant, support an important role for ABCG2 in urate excretion in both the human kidney and intestinal tract, and provide insight into the importance of intestinal urate excretion for serum urate homeostasis.
    MeSH term(s) ATP Binding Cassette Transporter, Subfamily G, Member 2/genetics ; ATP Binding Cassette Transporter, Subfamily G, Member 2/metabolism ; Alleles ; Animals ; Disease Models, Animal ; Epithelium/metabolism ; Epithelium/pathology ; Glucose Transport Proteins, Facilitative/genetics ; Glucose Transport Proteins, Facilitative/metabolism ; Gout/genetics ; Gout/metabolism ; Gout/pathology ; Homeostasis ; Humans ; Hyperuricemia/metabolism ; Intestines/pathology ; Kidney/metabolism ; Kidney/pathology ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Neoplasm Proteins ; Phenotype ; Uric Acid/blood ; Uric Acid/metabolism
    Chemical Substances ABCG2 protein, human ; ATP Binding Cassette Transporter, Subfamily G, Member 2 ; Abcg2 protein, mouse ; Glucose Transport Proteins, Facilitative ; Neoplasm Proteins ; SLC2A9 protein, human ; Uric Acid (268B43MJ25)
    Language English
    Publishing date 2020-06-02
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-020-16525-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Implementation of a pooled surveillance testing program for asymptomatic SARS-CoV-2 infections in K-12 schools and universities.

    Mendoza, Rachelle P / Bi, Chongfeng / Cheng, Hui-Ting / Gabutan, Elmer / Pagaspas, Guillerre Jan / Khan, Nadia / Hoxie, Helen / Hanna, Stephen / Holmes, Kelly / Gao, Nicholas / Lewis, Raychel / Wang, Huaien / Neumann, Daniel / Chan, Angela / Takizawa, Meril / Lowe, James / Chen, Xiao / Kelly, Brianna / Asif, Aneeza /
    Barnes, Keena / Khan, Nusrat / May, Brandon / Chowdhury, Tasnim / Pollonini, Gabriella / Gouda, Nourelhoda / Guy, Chante / Gordon, Candice / Ayoluwa, Nana / Colon, Elvin / Miller-Medzon, Noah / Jones, Shanique / Hossain, Rauful / Dodson, Arabia / Weng, Meimei / McGaskey, Miranda / Vasileva, Ana / Lincoln, Andrew E / Sikka, Robby / Wyllie, Anne L / Berke, Ethan M / Libien, Jenny / Pincus, Matthew / Premsrirut, Prem K

    EClinicalMedicine

    2021  Volume 38, Page(s) 101028

    Abstract: Background: The negative impact of continued school closures during the height of the COVID-19 pandemic warrants the establishment of cost-effective strategies for surveillance and screening to safely reopen and monitor for potential in-school ... ...

    Abstract Background: The negative impact of continued school closures during the height of the COVID-19 pandemic warrants the establishment of cost-effective strategies for surveillance and screening to safely reopen and monitor for potential in-school transmission. Here, we present a novel approach to increase the availability of repetitive and routine COVID-19 testing that may ultimately reduce the overall viral burden in the community.
    Methods: We implemented a testing program using the SalivaClear࣪ pooled surveillance method that included students, faculty and staff from K-12 schools (student age range 5-18 years) and universities (student age range >18 years) across the country (Mirimus Clinical Labs, Brooklyn, NY). The data analysis was performed using descriptive statistics, kappa agreement, and outlier detection analysis.
    Findings: From August 27, 2020 until January 13, 2021, 253,406 saliva specimens were self-collected from students, faculty and staff from 93 K-12 schools and 18 universities. Pool sizes of up to 24 samples were tested over a 20-week period. Pooled testing did not significantly alter the sensitivity of the molecular assay in terms of both qualitative (100% detection rate on both pooled and individual samples) and quantitative (comparable cycle threshold (Ct) values between pooled and individual samples) measures. The detection of SARS-CoV-2 in saliva was comparable to the nasopharyngeal swab. Pooling samples substantially reduced the costs associated with PCR testing and allowed schools to rapidly assess transmission and adjust prevention protocols as necessary. In one instance, in-school transmission of the virus was determined within the main office and led to review and revision of heating, ventilating and air-conditioning systems.
    Interpretation: By establishing low-cost, weekly testing of students and faculty, pooled saliva analysis for the presence of SARS-CoV-2 enabled schools to determine whether transmission had occurred, make data-driven decisions, and adjust safety protocols. We provide strong evidence that pooled testing may be a fundamental component to the reopening of schools by minimizing the risk of in-school transmission among students and faculty.
    Funding: Skoll Foundation generously provided funding to Mobilizing Foundation and Mirimus for these studies.
    Language English
    Publishing date 2021-07-17
    Publishing country England
    Document type Journal Article
    ISSN 2589-5370
    ISSN (online) 2589-5370
    DOI 10.1016/j.eclinm.2021.101028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.

    Tin, Adrienne / Marten, Jonathan / Halperin Kuhns, Victoria L / Li, Yong / Wuttke, Matthias / Kirsten, Holger / Sieber, Karsten B / Qiu, Chengxiang / Gorski, Mathias / Yu, Zhi / Giri, Ayush / Sveinbjornsson, Gardar / Li, Man / Chu, Audrey Y / Hoppmann, Anselm / O'Connor, Luke J / Prins, Bram / Nutile, Teresa / Noce, Damia /
    Akiyama, Masato / Cocca, Massimiliano / Ghasemi, Sahar / van der Most, Peter J / Horn, Katrin / Xu, Yizhe / Fuchsberger, Christian / Sedaghat, Sanaz / Afaq, Saima / Amin, Najaf / Ärnlöv, Johan / Bakker, Stephan J L / Bansal, Nisha / Baptista, Daniela / Bergmann, Sven / Biggs, Mary L / Biino, Ginevra / Boerwinkle, Eric / Bottinger, Erwin P / Boutin, Thibaud S / Brumat, Marco / Burkhardt, Ralph / Campana, Eric / Campbell, Archie / Campbell, Harry / Carroll, Robert J / Catamo, Eulalia / Chambers, John C / Ciullo, Marina / Concas, Maria Pina / Coresh, Josef / Corre, Tanguy / Cusi, Daniele / Felicita, Sala Cinzia / de Borst, Martin H / De Grandi, Alessandro / de Mutsert, Renée / de Vries, Aiko P J / Delgado, Graciela / Demirkan, Ayşe / Devuyst, Olivier / Dittrich, Katalin / Eckardt, Kai-Uwe / Ehret, Georg / Endlich, Karlhans / Evans, Michele K / Gansevoort, Ron T / Gasparini, Paolo / Giedraitis, Vilmantas / Gieger, Christian / Girotto, Giorgia / Gögele, Martin / Gordon, Scott D / Gudbjartsson, Daniel F / Gudnason, Vilmundur / Haller, Toomas / Hamet, Pavel / Harris, Tamara B / Hayward, Caroline / Hicks, Andrew A / Hofer, Edith / Holm, Hilma / Huang, Wei / Hutri-Kähönen, Nina / Hwang, Shih-Jen / Ikram, M Arfan / Lewis, Raychel M / Ingelsson, Erik / Jakobsdottir, Johanna / Jonsdottir, Ingileif / Jonsson, Helgi / Joshi, Peter K / Josyula, Navya Shilpa / Jung, Bettina / Kähönen, Mika / Kamatani, Yoichiro / Kanai, Masahiro / Kerr, Shona M / Kiess, Wieland / Kleber, Marcus E / Koenig, Wolfgang / Kooner, Jaspal S / Körner, Antje / Kovacs, Peter / Krämer, Bernhard K / Kronenberg, Florian / Kubo, Michiaki / Kühnel, Brigitte / La Bianca, Martina / Lange, Leslie A / Lehne, Benjamin / Lehtimäki, Terho / Liu, Jun / Loeffler, Markus / Loos, Ruth J F / Lyytikäinen, Leo-Pekka / Magi, Reedik / Mahajan, Anubha / Martin, Nicholas G / März, Winfried / Mascalzoni, Deborah / Matsuda, Koichi / Meisinger, Christa / Meitinger, Thomas / Metspalu, Andres / Milaneschi, Yuri / O'Donnell, Christopher J / Wilson, Otis D / Gaziano, J Michael / Mishra, Pashupati P / Mohlke, Karen L / Mononen, Nina / Montgomery, Grant W / Mook-Kanamori, Dennis O / Müller-Nurasyid, Martina / Nadkarni, Girish N / Nalls, Mike A / Nauck, Matthias / Nikus, Kjell / Ning, Boting / Nolte, Ilja M / Noordam, Raymond / O'Connell, Jeffrey R / Olafsson, Isleifur / Padmanabhan, Sandosh / Penninx, Brenda W J H / Perls, Thomas / Peters, Annette / Pirastu, Mario / Pirastu, Nicola / Pistis, Giorgio / Polasek, Ozren / Ponte, Belen / Porteous, David J / Poulain, Tanja / Preuss, Michael H / Rabelink, Ton J / Raffield, Laura M / Raitakari, Olli T / Rettig, Rainer / Rheinberger, Myriam / Rice, Kenneth M / Rizzi, Federica / Robino, Antonietta / Rudan, Igor / Krajcoviechova, Alena / Cifkova, Renata / Rueedi, Rico / Ruggiero, Daniela / Ryan, Kathleen A / Saba, Yasaman / Salvi, Erika / Schmidt, Helena / Schmidt, Reinhold / Shaffer, Christian M / Smith, Albert V / Smith, Blair H / Spracklen, Cassandra N / Strauch, Konstantin / Stumvoll, Michael / Sulem, Patrick / Tajuddin, Salman M / Teren, Andrej / Thiery, Joachim / Thio, Chris H L / Thorsteinsdottir, Unnur / Toniolo, Daniela / Tönjes, Anke / Tremblay, Johanne / Uitterlinden, André G / Vaccargiu, Simona / van der Harst, Pim / van Duijn, Cornelia M / Verweij, Niek / Völker, Uwe / Vollenweider, Peter / Waeber, Gerard / Waldenberger, Melanie / Whitfield, John B / Wild, Sarah H / Wilson, James F / Yang, Qiong / Zhang, Weihua / Zonderman, Alan B / Bochud, Murielle / Wilson, James G / Pendergrass, Sarah A / Ho, Kevin / Parsa, Afshin / Pramstaller, Peter P / Psaty, Bruce M / Böger, Carsten A / Snieder, Harold / Butterworth, Adam S / Okada, Yukinori / Edwards, Todd L / Stefansson, Kari / Susztak, Katalin / Scholz, Markus / Heid, Iris M / Hung, Adriana M / Teumer, Alexander / Pattaro, Cristian / Woodward, Owen M / Vitart, Veronique / Köttgen, Anna

    Nature genetics

    2019  Volume 51, Issue 10, Page(s) 1459–1474

    Abstract: Elevated serum urate levels cause gout and correlate with cardiometabolic diseases via poorly understood mechanisms. We performed a trans-ancestry genome-wide association study of serum urate in 457,690 individuals, identifying 183 loci (147 previously ... ...

    Abstract Elevated serum urate levels cause gout and correlate with cardiometabolic diseases via poorly understood mechanisms. We performed a trans-ancestry genome-wide association study of serum urate in 457,690 individuals, identifying 183 loci (147 previously unknown) that improve the prediction of gout in an independent cohort of 334,880 individuals. Serum urate showed significant genetic correlations with many cardiometabolic traits, with genetic causality analyses supporting a substantial role for pleiotropy. Enrichment analysis, fine-mapping of urate-associated loci and colocalization with gene expression in 47 tissues implicated the kidney and liver as the main target organs and prioritized potentially causal genes and variants, including the transcriptional master regulators in the liver and kidney, HNF1A and HNF4A. Experimental validation showed that HNF4A transactivated the promoter of ABCG2, encoding a major urate transporter, in kidney cells, and that HNF4A p.Thr139Ile is a functional variant. Transcriptional coregulation within and across organs may be a general mechanism underlying the observed pleiotropy between urate and cardiometabolic traits.
    MeSH term(s) ATP Binding Cassette Transporter, Subfamily G, Member 2/genetics ; Cardiovascular Diseases/blood ; Cardiovascular Diseases/epidemiology ; Cardiovascular Diseases/genetics ; Cohort Studies ; Genetic Loci ; Genetic Markers ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Gout/blood ; Gout/epidemiology ; Gout/genetics ; Hepatocyte Nuclear Factor 1-alpha/genetics ; Hepatocyte Nuclear Factor 4/genetics ; Humans ; Kidney/metabolism ; Kidney/pathology ; Liver/metabolism ; Liver/pathology ; Metabolic Diseases/blood ; Metabolic Diseases/epidemiology ; Metabolic Diseases/genetics ; Neoplasm Proteins/genetics ; Organ Specificity ; Polymorphism, Single Nucleotide ; Signal Transduction ; Uric Acid/blood
    Chemical Substances ABCG2 protein, human ; ATP Binding Cassette Transporter, Subfamily G, Member 2 ; Genetic Markers ; HNF1A protein, human ; HNF4A protein, human ; Hepatocyte Nuclear Factor 1-alpha ; Hepatocyte Nuclear Factor 4 ; Neoplasm Proteins ; Uric Acid (268B43MJ25)
    Language English
    Publishing date 2019-10-02
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1108734-1
    ISSN 1546-1718 ; 1061-4036
    ISSN (online) 1546-1718
    ISSN 1061-4036
    DOI 10.1038/s41588-019-0504-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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