Low-grade inflammation is associated with an increased risk of chronic degenerative disease, but its relationship with mortality is less well explored. We aimed at evaluating, at a large epidemiological level, the possible association of low-grade inflammation, as measured by a composite score, with overall mortality risk. We conducted a population-based prospective investigation on 20, 337 adult subjects free from major hematological disease and acute inflammatory status, randomly recruited from the general population of the Moli-sani study. A low-grade inflammation score was obtained from the sum of 10-tiles of plasmatic (C-reactive protein) and cellular (leukocyte and platelet counts, granulocyte/lymphocyte ratio) biomarkers of low-grade inflammation; higher levels indicated increased low-grade inflammation. Hazard ratios were calculated using multivariable Cox proportional hazard models with 95% confidence intervals. At the end of follow-up (median 7.6 years), 837 all-cause deaths were recorded. As compared to subjects in the lowest quartile of the low-grade inflammation score, those in the highest category had a significantly increased risk in overall mortality (HR=1.44; 1.17-1.77), independently of possible confounders, including the presence of chronic diseases and a number of health-related behaviors. The magnitude of the association of low-grade inflammation with mortality was relatively higher in type 2 diabetic patients (HR=2.90; 1.74-4.84) and in individuals with a history of cardiovascular disease (HR=2.48; 1.50-4.11) as compared to their counterparts who were free from the disease. In conclusion, an elevated degree of lowgrade inflammation, as measured by a composite score of inflammatory biomarkers, is an independent risk factor for total mortality in an apparently healthy adult general population.

A score of low-grade inflammation and risk of mortality: prospective findings from the Moli-sani study.

Iacoviello L.;Gianfagna F.;
2016-01-01

Abstract

Low-grade inflammation is associated with an increased risk of chronic degenerative disease, but its relationship with mortality is less well explored. We aimed at evaluating, at a large epidemiological level, the possible association of low-grade inflammation, as measured by a composite score, with overall mortality risk. We conducted a population-based prospective investigation on 20, 337 adult subjects free from major hematological disease and acute inflammatory status, randomly recruited from the general population of the Moli-sani study. A low-grade inflammation score was obtained from the sum of 10-tiles of plasmatic (C-reactive protein) and cellular (leukocyte and platelet counts, granulocyte/lymphocyte ratio) biomarkers of low-grade inflammation; higher levels indicated increased low-grade inflammation. Hazard ratios were calculated using multivariable Cox proportional hazard models with 95% confidence intervals. At the end of follow-up (median 7.6 years), 837 all-cause deaths were recorded. As compared to subjects in the lowest quartile of the low-grade inflammation score, those in the highest category had a significantly increased risk in overall mortality (HR=1.44; 1.17-1.77), independently of possible confounders, including the presence of chronic diseases and a number of health-related behaviors. The magnitude of the association of low-grade inflammation with mortality was relatively higher in type 2 diabetic patients (HR=2.90; 1.74-4.84) and in individuals with a history of cardiovascular disease (HR=2.48; 1.50-4.11) as compared to their counterparts who were free from the disease. In conclusion, an elevated degree of lowgrade inflammation, as measured by a composite score of inflammatory biomarkers, is an independent risk factor for total mortality in an apparently healthy adult general population.
2016
Bonaccio, M.; Di Castelnuovo, A.; Pounis, G.; De Curtis, A.; Costanzo, S.; Persichillo, M.; Cerletti, C.; Donati, M. B.; De Gaetano, G.; Iacoviello, L.; Vermylen, J.; Carrasco, I. P.; Giampaoli, S.; Spagnuolo, A.; Assanelli, D.; Centritto, V.; Spagnuolo, P.; Staniscia, D.; Zito, F.; Bonanni, A.; Lorenzet, R.; Mascioli, A.; Olivieri, M.; Rotilio, D.; Gianfagna, F.; Giacci, M.; Padulo, A.; Petraroia, D.; Marracino, F.; Spinelli, M.; Silvestri, C.; De Lucia, F.; Vohnout, B.; Coordinator, G.; Verna, A.; Di Lillo, M.; Di Stefano, I.; Pannichella, A.; Vizzarri, A. R.; Pampuch, A.; Arcari, A.; Barbato, D.; Bracone, F.; Di Giorgio, C.; Magnacca, S.; Panebianco, S.; Chiovitti, A.; Caccamo, S.; Caruso, V.; Rago, L.; Cugino, D.; Ferri, A.; Castaldi, C.; Mignogna, M.; Guszcz, T.; Di Giuseppe, R.; Barisciano, P.; Buonaccorsi, L.; Centritto, F.; Cutrone, A.; Fanelli, F.; Santimone, I.; Sciarretta, A.; Sorella, I.; Plescia, E.; Molinaro, A.; Cavone, C.; Galuppo, G.; D'Angelo, D.; Ramacciato, R.; Molise, A. S. R. D.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11383/2060778
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