| Online-Ressource |
Verfasst von: | Brandenburg, Vincent [VerfasserIn]  |
| Kleber, Marcus E. [VerfasserIn]  |
| Delgado Gonzales de Kleber, Graciela [VerfasserIn]  |
| Grammer, Tanja B. [VerfasserIn]  |
| März, Winfried [VerfasserIn]  |
Titel: | Soluble klotho and mortality |
Titelzusatz: | the Ludwigshafen Risk and Cardiovascular Health Study |
Verf.angabe: | Vincent M. Brandenburg, Marcus E. Kleber, Marc G. Vervloet, Tobias E. Larsson, Andreas Tomaschitz, Stefan Pilz, Tatjana Stojakovic, Graciela Delgado, Tanja B. Grammer, Nikolaus Marx, Winfried März, Hubert Scharnagl |
E-Jahr: | 2015 |
Jahr: | October 2015 |
Umfang: | 7 S. |
Fussnoten: | Gesehen am 25.01.2018 |
Titel Quelle: | Enthalten in: Atherosclerosis |
Ort Quelle: | Amsterdam [u.a.] : Elsevier Science, 1970 |
Jahr Quelle: | 2015 |
Band/Heft Quelle: | 242(2015), 2, Seite 483-489 |
ISSN Quelle: | 1879-1484 |
Abstract: | Background: Experimental evidence suggests that soluble klotho (s-klotho), a co-receptor for fibroblast growth factor 23 (FGF23), may modulate cardiovascular risk through multiple mechanisms. However, the predictive value of s-klotho in patients remains unclear. Therefore, the present study examined in a large cohort of patients referred for coronary angiography whether s-klotho is associated with cardiovascular and total mortality. Methods: The longitudinal associations between baseline s-klotho and FGF23 concentrations and mortality were evaluated in 2948 participants of the Ludwigshafen Risk and Cardiovascular Health Study (LURIC), referred for coronary angiography. Results: Mean age of participants was: 63 ± 10 years. Patients with diabetes mellitus (n = 1136) had elevated s-klotho: [440 (430-449) versus 414 (406-421) pg/mL, p < 0.001]. S-klotho decreased in parallel to glomerular filtration rate (GFR) and increased in parallel to FGF23. During a median follow-up of 9.9 years, 874 deaths (30%) occurred, 539 (18%) of which were cardiovascular. After adjustment for cardiovascular risk factors, the hazard ratios in the fourth quartile compared to the first quartile of s-klotho were 1.14 (95%CI, 0.94-1.38; p = 0.187) for all-cause mortality and 1.03 (95%CI, 0.80-1.31; p = 0.845) for cardiovascular mortality. Excess mortality prediction by high levels of baseline FGF23 was not modified by adjustment for baseline s-klotho levels. Conclusions: Klotho does not add predictive power to cardiovascular and mortality risk assessment in patients with normal renal function. |
DOI: | doi:10.1016/j.atherosclerosis.2015.08.017 |
URL: | Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.
Volltext: http://dx.doi.org/10.1016/j.atherosclerosis.2015.08.017 |
| Volltext: http://www.sciencedirect.com/science/article/pii/S0021915015300800 |
| DOI: https://doi.org/10.1016/j.atherosclerosis.2015.08.017 |
Datenträger: | Online-Ressource |
Sprache: | eng |
Sach-SW: | Coronary artery disease |
| Cardiovascular events |
| Coronary angiography |
| Fibroblast growth factor 23, FGF23 |
| Outcome |
K10plus-PPN: | 1567607098 |
Verknüpfungen: | → Zeitschrift |
Soluble klotho and mortality / Brandenburg, Vincent [VerfasserIn]; October 2015 (Online-Ressource)