Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

• Main Authors: Gorski, Mathias, Jung, Bettina, Li, Yong, Matias-Garcia, Pamela R., Wuttke, Matthias, Coassin, Stefan, Thio, Chris H. L., Kleber, Marcus E., Winkler, Thomas W., Wanner, Veronika, Chai, Jin-Fang, Chu, Audrey Y., Cocca, Massimiliano, Feitosa, Mary F., Ghasemi, Sahar, Hoppmann, Anselm, Horn, Katrin, Li, Man, Nutile, Teresa, Scholz, Markus, Sieber, Karsten B., Teumer, Alexander, Tin, Adrienne, Wang, Judy, Tayo, Bamidele O., Ahluwalia, Tarunveer S., Almgren, Peter, Bakker, Stephan J. L., Banas, Bernhard, Bansal, Nisha, Biggs, Mary L., Boerwinkle, Eric, Bottinger, Erwin P., Brenner, Hermann, Carroll, Robert J., Chalmers, John, Chee, Miao-Li, Chee, Miao-Ling, Cheng, Ching-Yu, Coresh, Josef, de Borst, Martin H., Degenhardt, Frauke, Eckardt, Kai-Uwe, Endlich, Karlhans, Franke, Andre, Freitag-Wolf, Sandra, Gampawar, Piyush, Gansevoort, Ron T., Ghanbari, Mohsen, Gieger, Christian, Hamet, Pavel, Ho, Kevin, Hofer, Edith, Holleczek, Bernd, Xian Foo, V.H., Hutri-Kähönen, N., Hwang, Shih-Jen, Ikram, M. Arfan, Josyula, Navya Shilpa, Kähönen, M., Khor, Chiea-Chuen, Koenig, Wolfgang, Kramer, Holly, Krämer, B.K., Kühnel, B., Lange, Leslie A., Lehtimäki, T., Lieb, Wolfgang, Alizadeh, B.Z., Boezen, H.M., Franke, L., van der Harst, Pim, Navis, G., Rots, M., Snieder, Harold, Swertz, M., Wolffenbuttel, B.H.R., Wijmenga, C., Abecasis, G., Baras, A., Cantor, M., Coppola, G., Economides, A., Lotta, L.A., Overton, J.D., Reid, J.G., Shuldiner, A., Beechert, C., Forsythe, C., Fuller, E.D., Gu, Z., Lattari, M., Lopez, A., Schleicher, T.D., Padilla, M.S., Toledo, K., Widom, L., Wolf, S.E., Pradhan, M., Manoochehri, K., Ulloa, R.H., Bai, X., Balasubramanian, S., Barnard, L., Blumenfeld, A., Eom, G., Habegger, L., Hawes, A., Khalid, S., Maxwell, E.K., Salerno, W., Staples, J.C., Jones, M.B., Mitnaul, L.J., Loos, Ruth J. F., Lukas, Mary Ann, Lyytikäinen, L.-P., Meisinger, Christa, Meitinger, Thomas, Melander, Olle, Milaneschi, Yuri, Mishra, Pashupati P., Mononen, Nina, Mychaleckyj, Josyf C., Nadkarni, Girish N., Nauck, Matthias, Nikus, Kjell, Ning, Boting, Nolte, Ilja M., O'Donoghue, Michelle L., Orho-Melander, Marju, Pendergrass, Sarah A., Penninx, Brenda W. J. H., Preuss, Michael H., Psaty, Bruce M., Raffield, Laura M., Raitakari, Olli T., Rettig, Rainer, Rheinberger, Myriam, Rice, Kenneth M., Rosenkranz, Alexander R., Rossing, Peter, Rotter, Jerome, I, Sabanayagam, Charumathi, Schmidt, Helena, Schmidt, Reinhold, Schöttker, B., Schulz, Christina-Alexandra, Sedaghat, Sanaz, Shaffer, Christian M., Strauch, Konstantin, Szymczak, Silke, Taylor, Kent D., Tremblay, Johanne, Chaker, Layal, van der Most, Peter J., Verweij, Niek, Völker, U., Waldenberger, Melanie, Wallentin, Lars, Waterworth, Dawn M., White, Harvey D., Wilson, James G., Wong, Tien-Yin, Woodward, Mark, Yang, Qiong, Yasuda, Masayuki, Yerges-Armstrong, Laura M., Zhang, Yan, Wanner, Christoph, Böger, C.A., Köttgen, A., Kronenberg, Florian, Pattaro, Cristian, Heid, Iris M., Lifelines Cohort Study., Regeneron Genetics Center.
• Other Authors: SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
• Format: Article
• Published: Elsevier B.V. 2022
• Subjects: acute kidney injury; end-stage kidney disease; genome-wide association study; rapid eGFRcrea decline
• Online Access: https://scholarbank.nus.edu.sg/handle/10635/233321
• Institution: National University of Singapore

10.1016/j.kint.2020.09.030