2018
Higher spermidine intake is linked to lower mortality: a prospective population-based study
KIECHL, Stefan; Raimund PECHLANER; Peter WILLEIT; Marlene NOTDURFTER; Bernhard PAULWEBER et al.Základní údaje
Originální název
Higher spermidine intake is linked to lower mortality: a prospective population-based study
Autoři
KIECHL, Stefan; Raimund PECHLANER; Peter WILLEIT; Marlene NOTDURFTER; Bernhard PAULWEBER; Karin WILLEIT; Philipp WERNER; Christoph RUCKENSTUHL; Bernhard IGLSEDER; Siegfried WEGER; Barbara MAIRHOFER; Markus GARTNER; Ludmilla KEDENKO; Monika CHMELÍKOVÁ; Slaven STEKOVIC; Hermann STUPPNER; Friedrich OBERHOLLENZER; Guido KROEMER; Manuel MAYR; Tobias EISENBERG; Herbert TILG; Frank MADEO a Johann WILLEIT
Vydání
American Journal of Clinical Nutrition, Bethesda, American Society for Nutrition, 2018, 0002-9165
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30308 Nutrition, Dietetics
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 6.568
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/18:00104191
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
polyamines; spermidine; life span; cancer; vascular disease
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 10. 2. 2019 13:30, Soňa Böhmová
Anotace
V originále
Background: Spermidine administration is linked to increased survival in several animal models. Objective: The aim of this study was to test the potential association between spermidine content in diet and mortality in humans. Design: This prospective community-based cohort study included 829 participants aged 45-84 y, 49.9% of whom were male. Diet was assessed by repeated dietitian-administered validated food-frequency questionnaires (2540 assessments) in 1995, 2000, 2005, and 2010. During follow-up between 1995 and 2015, 341 deaths occurred. Results: All-cause mortality (deaths per 1000 person-years) decreased across thirds of increasing spermidine intake from 40.5 (95% CI: 36.1, 44.7) to 23.7 (95% CI: 20.0, 27.0) and 15.1 (95% CI: 12.6, 17.8), corresponding to an age-, sex-and caloric intake-adjusted 20-y cumulative mortality incidence of 0.48 (95% CI: 0.45, 0.51), 0.41 (95% CI: 0.38, 0.45), and 0.38 (95% CI: 0.34, 0.41), respectively. The age-, sex-and caloric ratio-adjusted HR for all-cause death per 1-SD higher spermidine intake was 0.74 (95% CI: 0.66, 0.83; P < 0.001). Further adjustment for lifestyle factors, established predictors of mortality, and other dietary features yielded an HR of 0.76 (95% CI: 0.67, 0.86; P < 0.001). The association was consistent in subgroups, robust against unmeasured confounding, and independently validated in the Salzburg Atherosclerosis Prevention Program in Subjects at High Individual Risk (SAPHIR) Study (age-, sex-, and caloric ratioadjusted HR per 1-SD higher spermidine intake: 0.71; 95% CI: 0.53, 0.95; P = 0.019). The difference in mortality risk between the top and bottom third of spermidine intakes was similar to that associated with a 5.7-y (95% CI: 3.6, 8.1 y) younger age. Conclusion: Our findings lend epidemiologic support to the concept that nutrition rich in spermidine is linked to increased survival in humans.