Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
Détails
Télécharger: BIB_53B973F55248.P001.pdf (1161.56 [Ko])
Etat: Public
Version: Final published version
Etat: Public
Version: Final published version
ID Serval
serval:BIB_53B973F55248
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
Périodique
Nature Communications
Collaborateur⸱rice⸱s
ICBP Consortium, AGEN Consortium, CHARGe-Heart Failure Group, ECHOGen Consortium
Contributeur⸱rice⸱s
CARDIOGRAM , Abecasis GR., Adair LS., Alexander M., Altshuler D., Amin N., Arking DE., Arora P., Aulchenko Y., Bakker SJ., Bandinelli S., Barroso I., Beckmann JS., Beilby JP., Bergman RN., Bergmann S., Bis JC., Boehnke M., Bonnycastle LL., Bornstein SR., Bots ML., Bragg-Gresham JL., Brand SM., Brand E., Braund PS., Brown MJ., Burton PR., Casas JP., Caulfield MJ., Chakravarti A., Chambers JC., Chandak GR., Chang YP., Charchar FJ., Chaturvedi N., Shin Cho Y., Clarke R., Collins FS., Collins R., Connell JM., Cooper JA., Cooper MN., Cooper RS., Corsi AM., Dörr M., Dahgam S., Danesh J., Davey Smith G., Day IN., Deloukas P., Denniff M., Dominiczak AF., Dong Y., Doumatey A., Elliott P., Elosua R., Erdmann J., Eyheramendy S., Farrall M., Fava C., Forrester T., Fowkes FG., Fox ER., Frayling TM., Galan P., Ganesh SK., Garcia M., Gaunt TR., Glazer NL., Go MJ., Goel A., Grässler J., Grobbee DE., Groop L., Guarrera S., Guo X., Hadley D., Hamsten A., Han BG., Hardy R., Hartikainen AL., Heath S., Heckbert SR., Hedblad B., Hercberg S., Hernandez D., Hicks AA., Hilton G., Hingorani AD., Bolton JA., Hopewell JC., Howard P., Humphries SE., Hunt SC., Hveem K., Ikram MA., Islam M., Iwai N., Jarvelin MR., Jackson AU., Jafar TH., Janipalli CS., Johnson T., Kathiresan S., Khaw KT., Kim HL., Kinra S., Kita Y., Kivimaki M., Kooner JS., Kumar MJ., Kuh D., Kulkarni SR., Kumari M., Kuusisto J., Kuznetsova T., Laakso M., Laan M., Laitinen J., Lakatta EG., Langefeld CD., Larson MG., Lathrop M., Lawlor DA., Lawrence RW., Lee JY., Lee NR., Levy D., Li Y., Longstreth WT., Luan£££Jian'an£££ J. , Lucas G., Ludwig B., Mangino M., Mani KR., Marmot MG., Mattace-Raso FU., Matullo G., McArdle WL., McKenzie CA., Meitinger T., Melander O., Meneton P., Meschia JF., Miki T., Milaneschi Y., Mohlke KL., Mooser V., Morken MA., Morris RW., Mosley TH., Najjar S., Narisu N., Newton-Cheh C., Nguyen KD., Nilsson P., Nyberg F., O'Donnell CJ., Ogihara T., Ohkubo T., Okamura T., Ong RT., Ongen H., Onland-Moret NC., O'Reilly PF., Org E., Orru M., Palmas W., Palmen J., Palmer LJ., Palmer ND., Parker AN., Peden JF., Peltonen L., Perola M., Pihur V., Platou CG., Plump A., Prabhakaran D., Psaty BM., Raffel LJ., Rao DC., Rasheed A., Ricceri F., Rice KM., Rosengren A., Rotter JI., Rudock ME., Sõber S., Salako T., Saleheen D., Salomaa V., Samani NJ., Schwartz SM., Schwarz PE., Scott LJ., Scott J., Scuteri A., Sehmi JS., Seielstad M., Seshadri S., Sharma P., Shaw-Hawkins S., Shi G., Shrine NR., Sijbrands EJ., Sim X., Singleton A., Sjögren M., Smith NL., Soler Artigas M., Spector TD., Staessen JA., Stancakova A., Steinle NI., Strachan DP., Stringham HM., Sun YV., Swift AJ., Tabara Y., Tai ES., Talmud PJ., Taylor A., Terzic J., Thelle DS., Tobin MD., Tomaszewski M., Tripathy V., Tuomilehto J., Tzoulaki I., Uda M., Ueshima H., Uiterwaal CS., Umemura S., van der Harst P., van der Schouw YT. , van Gilst WH. , Vartiainen E., Vasan RS., Veldre G., Verwoert GC., Viigimaa M., Vinay DG., Vineis P., Voight BF., Vollenweider P., Wagenknecht LE., Wain LV., Wang X., Wang TJ., Wareham NJ., Watkins H., Weder AB., Whincup PH., Wiggins KL., Witteman JC., Wong A., Wu Y., Yajnik CS., Yao J., Young JH., Zelenika D., Zhai G., Zhang W., Zhang F., Zhao JH., Zhu H., Zhu X., Zitting P., Zukowska-Szczechowska E., Okada Y., Wu JY., Gu D., Takeuchi F., Takahashi A., Maeda S., Tsunoda T., Chen P., Lim SC., Wong TY., Liu J., Young TL., Aung T., Teo YY., Kim YJ., Kang D., Chen CH., Tsai FJ., Chang LC., Fann SJ., Mei H., Hixson JE., Chen S., Katsuya T., Isono M., Albrecht E., Yamamoto K., Kubo M., Nakamura Y., Kamatani N., Kato N., He J., Chen YT., Tanaka T., Reilly MP., Schunkert H., Assimes TL., Hall A., Hengstenberg C., König IR., Laaksonen R., McPherson R., Thompson JR., Thorsteinsdottir U., Ziegler A., Absher D., Chen L., Cupples LA., Halperin E., Li M., Musunuru K., Preuss M., Schillert A., Thorleifsson G., Wells GA., Holm H., Roberts R., Stewart AF., Fortmann S., Go A., Hlatky M., Iribarren C., Knowles J., Myers R., Quertermous T., Sidney S., Risch N., Tang H., Blankenberg S., Schnabel R., Sinning C., Lackner KJ., Tiret L., Nicaud V., Cambien F., Bickel C., Rupprecht HJ., Perret C., Proust C., Münzel TF., Barbalic M., Chen IY., Demissie-Banjaw S., Folsom A., Lumley T., Marciante K., Taylor KD., Volcik K., Gretarsdottir S., Gulcher JR., Kong A., Stefansson K., Thorgeirsson G., Andersen K., Fischer M., Grosshennig A., Linsel-Nitschke P., Stark K., Schreiber S., Aherrahrou Z., Bruse P., Doering A., Klopp N., Diemert P., Loley C., Medack A., Nahrstedt J., Peters A., Wagner AK., Willenborg C., Böhm BO., Dobnig H., Grammer TB., Hoffmann MM., Meinitzer A., Winkelmann BR., Pilz S., Renner W., Scharnagl H., Stojakovic T., Tomaschitz A., Winkler K., Guiducci C., Burtt N., Gabriel SB., Dandona S., Jarinova O., Qu L., Wilensky R., Matthai W., Hakonarson HH., Devaney J., Burnett MS., Pichard AD., Kent KM., Satler L., Lindsay JM., Waksman R., Knouff CW., Waterworth DM., Walker MC., Epstein SE., Rader DJ., Nelson CP., Wright BJ., Balmforth AJ., Ball SG., Loehr LR., Rosamond WD., Benjamin E., Haritunians T., Couper D., Murabito J., Wang YA., Stricker BH., Chang PP., Willerson JT., Felix SB., Watzinger N., Aragam J., Zweiker R., Lind L., Rodeheffer RJ., Greiser KH., Deckers JW., Stritzke J., Ingelsson E., Kullo I., Haerting J., Reffelmann T., Redfield MM., Werdan K., Mitchell GF., Arnett DK., Gottdiener JS., Blettner M., Friedrich N.
ISSN
2041-1723 (Electronic)
ISSN-L
2041-1723
Statut éditorial
Publié
Date de publication
2016
Peer-reviewed
Oui
Volume
7
Pages
10023
Langue
anglais
Notes
Publication types: Journal Article ; Meta-Analysis ; Research Support, N.I.H., Extramural
Publication Status: epublish
Publication Status: epublish
Résumé
Reduced glomerular filtration rate defines chronic kidney disease and is associated with cardiovascular and all-cause mortality. We conducted a meta-analysis of genome-wide association studies for estimated glomerular filtration rate (eGFR), combining data across 133,413 individuals with replication in up to 42,166 individuals. We identify 24 new and confirm 29 previously identified loci. Of these 53 loci, 19 associate with eGFR among individuals with diabetes. Using bioinformatics, we show that identified genes at eGFR loci are enriched for expression in kidney tissues and in pathways relevant for kidney development and transmembrane transporter activity, kidney structure, and regulation of glucose metabolism. Chromatin state mapping and DNase I hypersensitivity analyses across adult tissues demonstrate preferential mapping of associated variants to regulatory regions in kidney but not extra-renal tissues. These findings suggest that genetic determinants of eGFR are mediated largely through direct effects within the kidney and highlight important cell types and biological pathways.
Mots-clé
Gene Expression Regulation, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, Renal Insufficiency, Chronic/genetics
Pubmed
Web of science
Open Access
Oui
Création de la notice
19/02/2016 15:56
Dernière modification de la notice
20/08/2019 14:08