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Verfasst von:Brandenburg, Vincent [VerfasserIn]   i
 Kleber, Marcus E. [VerfasserIn]   i
 Delgado Gonzales de Kleber, Graciela [VerfasserIn]   i
 Grammer, Tanja B. [VerfasserIn]   i
 März, Winfried [VerfasserIn]   i
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

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