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Leaf, D.E.* ; Body, S.C.* ; Muehlschlegel, J.D.* ; McMahon, G.M.* ; Lichtner, P. ; Collard, C.D.* ; Shernan, S.K.* ; Fox, A.A.* ; Waikar, S.S.*

Length polymorphisms in heme oxygenase-1 and AKI after cardiac surgery.

J. Am. Soc. Nephrol. 27, 3291-3297 (2016)
Verlagsversion DOI PMC
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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Heme oxygenase-1 (HO-1) catalyzes the degradation of heme, which may be involved in the pathogenesis of AKI. Length polymorphisms in the number of GT dinucleotide repeats in the HO-1 gene (HMOX1) promoter inversely associate with HMOX1 mRNA expression. We analyzed the association between allelic frequencies of GT repeats in the HMOX1 gene promoter and postoperative AKI in 2377 white patients who underwent cardiac surgery with cardiopulmonary bypass. We categorized patients as having the short allele (S; <27 GT repeats) or long allele (L; ≥27 GT repeats), and defined AKI as an increase in serum creatinine ≥0.3 mg/dl within 48 hours or ≥50% within 5 days, or the need for RRT. Compared with patients with the SS genotype, patients with the LL genotype had 1.58-fold (95% confidence interval, 1.06 to 2.34; P=0.02) higher odds of AKI. After adjusting for baseline and operative characteristics, the odds ratio for AKI per L allele was 1.26 (95% confidence interval, 1.05 to 1.50; P=0.01). In conclusion, longer GT repeats in the HMOX1 gene promoter associate with increased risk of AKI after cardiac surgery, consistent with heme toxicity as a pathogenic feature of cardiac surgery-associated AKI, and with HO-1 as a potential therapeutic target.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Acute Renal Failure ; Heme Oxygenase ; Human Genetics; Acute Kidney Injury; Acute-renal-failure; Coronary-artery-disease; Microsatellite Polymorphism; Ischemia-reperfusion; Rheumatoid-arthritis; Promoter; Iron; Mortality; Heme-oxygenase-1
ISSN (print) / ISBN 1046-6673
e-ISSN 1533-3450
Zeitschrift Journal of the American Society of Nephrology
Quellenangaben Band: 27, Heft: 11, Seiten: 3291-3297 Artikelnummer: , Supplement: ,
Verlag American Society of Nephrology
Verlagsort Washington
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Human Genetics (IHG)