dc.date.accessioned2022-02-17T19:23:11Z
dc.date.available2022-02-17T19:23:11Z
dc.date.created2022-02-17T19:23:11Z
dc.date.issued2022
dc.identifierhttps://hdl.handle.net/20.500.12866/11366
dc.identifierhttps://doi.org/10.1016/j.annepidem.2021.12.007
dc.description.abstractPurpose: To assess the association between all-cause mortality and hs-CRP, based mainly on the cumulative burden approach. Methods: Cohort study with adults ≥35 years from general population, using hs-CRP at two timepoints: at baseline and 30 months later to establish different exposures: change over time, cumulative, and weighted cumulative hs-CRP. The outcome was all-cause mortality assessed 7 years later. Cox models were generated to quantify the association. Results: Data from 3,119 participants (mean age 55.6 years, and 51.2% females), were analyzed. During follow-up, 164 (5.6%) deaths occurred over 20,314.5 person-years, indicating an overall mortality rate of 8.1 per 1,000 person-years. In multivariable model, hs-CRP at baseline was associated with high risk of mortality (HR = 1.77; 95%CI: 1.28–2.46). Similarly, hs-CRP change over time (HR = 2.50; 95%CI: 1.46–4.29), as well as cumulative and weighted cumulative hs-CRP (HR = 2.05; 95%CI: 1.31–3.20) were associated with greater risk of all-cause mortality. The weighted cumulative hs-CRP had the best goodness-of-fit for mortality prediction. Conclusions: In this cohort across diverse geographical low-resource settings, high levels of hs-CRP were strongly associated with all-cause mortality. Two measurements of hs-CRP are better than one to predict mortality, and the weighted cumulative approach had the best prognostic fit.
dc.languageeng
dc.publisherElsevier
dc.relationAnnals of Epidemiology
dc.relation1873-2585
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectMortality
dc.subjectInflammation
dc.subjectC-reactive protein
dc.subjectCohort Studies
dc.subjectPeru
dc.titleHigh-sensitivity C-reactive protein and all-cause mortality in four diverse populations: The CRONICAS Cohort Study
dc.typeinfo:eu-repo/semantics/article


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