Pregled bibliografske jedinice broj: 1049691
New loci associated with kidney function and chronic kidney disease
New loci associated with kidney function and chronic kidney disease // Nature genetics, 42 (2010), 5; 376-384 doi:10.1038/ng.568 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1049691 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
New loci associated with kidney function and chronic kidney disease
Autori
Koettgen, Anna ; Pattaro, Cristian ; Boeger, Carsten A ; Fuchsberger, Christian ; Olden, Matthias ; Glazer, Nicole L. ; Parsa, Afshin ; Gao, Xiaoyi ; Yang, Qiong ; Smith, Albert V. ; O'Connell, Jeffrey R. ; Li, Man ; Schmidt, Helena ; Tanaka, Toshiko ; Isaacs, Aaron ; Ketkar, Shamika ; Hwang, Shih-Jen ; Johnson, Andrew D. ; Dehghan, Abbas ; Teumer, Alexander ; Pare, Guillaume ; Atkinson, Elizabeth J. ; Zeller, Tanja ; Lohman, Kurt ; Cornelis, Marilyn C. ; Probst-Hensch, Nicole M. ; Kronenberg, Florian ; Toenjes, Anke ; Hayward, Caroline ; Aspelund, Thor ; Eiriksdottir, Gudny ; Launer, Lenore J. ; Harris, Tamara B. ; Rampersaud, Evadnie ; Mitchell, Braxton D. ; Arking, Dan E. ; Boerwinkle, Eric ; Struchalin, Maksim ; Cavalieri, Margherita ; Singleton, Andrew ; Giallauria, Francesco ; Metter, Jeffrey ; de Boer, Ian H. ; Haritunians, Talin ; Lumley, Thomas ; Siscovick, David ; Psaty, Bruce M. ; Zillikens, M. Carola ; Oostra, Ben A. ; Feitosa, Mary ; Province, Michael ; de Andrade, Mariza ; Turner, Stephen T. ; Schillert, Arne ; Ziegler, Andreas ; Wild, Philipp S. ; Schnabel, Renate B. ; Wilde, Sandra ; Munzel, Thomas ; Leak, Tennille S. ; Illig, Thomas ; Klopp, Norman ; Meisinger, Christa ; Wichmann, H-Erich ; Koenig, Wolfgang ; Zgaga, Lina ; Zemunik, Tatijana ; Kolcic, Ivana ; Minelli, Cosetta ; Hu, Frank B. ; Johansson, Asa ; Igl, Wilmar ; Zaboli, Ghazal ; Wild, Sarah H. ; Wright, Alan F. ; Campbell, Harry ; Ellinghaus, David ; Schreiber, Stefan ; Aulchenko, Yurii S. ; Felix, Janine F. ; Rivadeneira, Fernando ; Uitterlinden, Andre G. ; Hofman, Albert ; Imboden, Medea ; Nitsch, Dorothea ; Brandstaetter, Anita ; Kollerits, Barbara ; Kedenko, Lyudmyla ; Maegi, Reedik ; Stumvoll, Michael ; Kovacs, Peter ; Boban, Mladen ; Campbell, Susan ; Endlich, Karlhans ; Voelzke, Henry ; Kroemer, Heyo K. ; Nauck, Matthias ; Voelker, Uwe ; Polasek, Ozren ; Vitart, Veronique ; Badola, Sunita ; Parker, Alexander N. ; Ridker, Paul M. ; Kardia, Sharon L. R. ; Blankenberg, Stefan ; Liu, Yongmei ; Curhan, Gary C. ; Franke, Andre ; Rochat, Thierry ; Paulweber, Bernhard ; Prokopenko, Inga ; Wang, Wei ; Gudnason, Vilmundur ; Shuldiner, Alan R. ; Coresh, Josef ; Schmidt, Reinhold ; Ferrucci, Luigi ; Shlipak, Michael G. ; van Duijn, Cornelia M. ; Borecki, Ingrid ; Kraemer, Bernhard K. ; Rudan, Igor ; Gyllensten, Ulf ; Wilson, James F. ; Witteman, Jacqueline C. ; Pramstaller, Peter P. ; Rettig, Rainer ; Hastie, Nick ; Chasman, Daniel I. ; Kao, W. H. ; Heid, Iris M. ; Fox, Caroline S.
Izvornik
Nature genetics (1061-4036) 42
(2010), 5;
376-384
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
GENOME-WIDE ASSOCIATION ; SERUM CREATININE ; PROTEIN ; GENE ; MUTATIONS ; VARIANTS ; POPULATION ; CANDIDATE ; HOMOLOG ; MEGALIN
Sažetak
Chronic kidney disease (CKD) is a significant public health problem, and recent genetic studies have identified common CKD susceptibility variants. The CKDGen consortium performed a meta-analysis of genome-wide association data in 67, 093 individuals of European ancestry from 20 predominantly population-based studies in order to identify new susceptibility loci for reduced renal function as estimated by serum creat-inine (eGFRcrea), serum cystatin c (eGFRcys) and CKD (eGFRcrea < 60 ml/min/ 1.73 m(2) ; n = 5, 807 individuals with CKD (cases)). Follow-up of the 23 new genome-wide-significant loci (P < 5 x 10(-8)) in 22, 982 replication samples identified 13 new loci affecting renal function and CKD (in or near LASS2, GCKR, ALMS1, TFDP2, DAB2, SLC34A1, VEGFA, PRKAG2, PIP5K1B, ATXN2, DACH1, UBE2Q2 and SLC7A9) and 7 loci suspected to affect creatinine production and secretion (CPS1, SLC22A2, TMEM60, WDR37, SLC6A13, WDR72 and BCAS3). These results further our understanding of the biologic mechanisms of kidney function by identifying loci that potentially influence nephrogenesis, podocyte function, angiogenesis, solute transport and metabolic functions of the kidney.
Izvorni jezik
Engleski
POVEZANOST RADA
Profili:
Mladen Boban
(autor)
Tatijana Zemunik
(autor)
Ozren Polašek
(autor)
Lina Zgaga
(autor)
Ivana Kolčić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE