Liver Fibrosis and 8-Year All-Cause Mortality Trajectories in the Aging Cohort of the Salus in Apulia Study - PubMed (original) (raw)
doi: 10.3390/biomedicines9111617.
Fabio Castellana [ 1](#full-view-affiliation-1 "Unit of Data Sciences and Technology Innovation for Population Health, National Institute of Gastroenterology "Saverio de Bellis", Research Hospital, Castellana Grotte, 70013 Bari, Italy."), Sara De Nucci [ 1](#full-view-affiliation-1 "Unit of Data Sciences and Technology Innovation for Population Health, National Institute of Gastroenterology "Saverio de Bellis", Research Hospital, Castellana Grotte, 70013 Bari, Italy."), Giovanni De Pergola [ 2](#full-view-affiliation-2 "Unit of Geriatrics and Internal Medicine, National Institute of Gastroenterology "Saverio de Bellis", Research Hospital, Castellana Grotte, 70013 Bari, Italy."), Madia Lozupone [ 1](#full-view-affiliation-1 "Unit of Data Sciences and Technology Innovation for Population Health, National Institute of Gastroenterology "Saverio de Bellis", Research Hospital, Castellana Grotte, 70013 Bari, Italy."), Ilaria Bortone [ 1](#full-view-affiliation-1 "Unit of Data Sciences and Technology Innovation for Population Health, National Institute of Gastroenterology "Saverio de Bellis", Research Hospital, Castellana Grotte, 70013 Bari, Italy."), Marco Castellana [ 1](#full-view-affiliation-1 "Unit of Data Sciences and Technology Innovation for Population Health, National Institute of Gastroenterology "Saverio de Bellis", Research Hospital, Castellana Grotte, 70013 Bari, Italy."), Giancarlo Sborgia [ 3](#full-view-affiliation-3 "Department of Basic Medical Sciences, Neuroscience and Sense Organs, University of Bari "Aldo Moro", 70124 Bari, Italy."), Luisa Lampignano [ 1](#full-view-affiliation-1 "Unit of Data Sciences and Technology Innovation for Population Health, National Institute of Gastroenterology "Saverio de Bellis", Research Hospital, Castellana Grotte, 70013 Bari, Italy."), Gianluigi Giannelli [ 4](#full-view-affiliation-4 "Scientific Direction, National Institute of Gastroenterology "Saverio de Bellis", Research Hospital, Castellana Grotte, 70124 Bari, Italy."), Francesco Panza [ 1](#full-view-affiliation-1 "Unit of Data Sciences and Technology Innovation for Population Health, National Institute of Gastroenterology "Saverio de Bellis", Research Hospital, Castellana Grotte, 70013 Bari, Italy."), Rodolfo Sardone [ 1](#full-view-affiliation-1 "Unit of Data Sciences and Technology Innovation for Population Health, National Institute of Gastroenterology "Saverio de Bellis", Research Hospital, Castellana Grotte, 70013 Bari, Italy.")
Affiliations
- PMID: 34829846
- PMCID: PMC8615636
- DOI: 10.3390/biomedicines9111617
Liver Fibrosis and 8-Year All-Cause Mortality Trajectories in the Aging Cohort of the Salus in Apulia Study
Roberta Zupo et al. Biomedicines. 2021.
Abstract
Age is a major contributor to the liver fibrosis rate and its adverse health-related outcomes, including mortality, but older populations are still under-explored. We investigated multimorbidity and inflammatory biomarkers in relation to the increasing liver fibrosis risk to delineate 8-year all-cause mortality trajectories in 1929 older adults from the population-based Salus in Apulia Study. Liver fibrosis risk was assumed using the fibrosis-4 (FIB-4) score, assigned to three liver fibrosis risk groups (low, intermediate, high). In the secondary analyses, the APRI score was also calculated to allow for comparisons. Male subjects (prevalence difference: -13.49, 95% confidence interval (CI): -18.96 to -8.03), a higher multimorbidity burden (effect size, ES: -0.14, 95% CI: -0.26 to -0.02), a higher prevalence of physical frailty (ES: 6.77, 95% CI: 0.07 to 13.47), and a more pronounced inflammatory pattern as indicated by tumor growth factor-α circulating levels (ES: -0.12, 95% CI: -0.23 to -0.01) were significantly more common in the highest-risk FIB-4 score group. Liver function characterized by lipid profile and platelet levels worsened with increasing FIB-4 risk score. The 8-year risk of death was nearly double in subjects in the highest-risk FIB-4 score group, even after controlling for possible confounders. Furthermore, a steeper mortality curve was clearly observed for FIB-4 scores as compared with the APRI scoring system with respect to liver fibrosis risk. In conclusion, using a scoring tool based on simple routine biomarkers to detect liver fibrosis risk may enhance biological knowledge of age-related outcomes of chronic liver disease and be helpful in the clinical setting to identify subjects at risk for adverse health-related outcomes, including mortality.
Keywords: biomarkers; chronic liver disease; frailty; liver fibrosis; survival.
Conflict of interest statement
The authors declare no conflict of interest.
Figures
Figure 1
Kaplan–Meier survival probability curves for the three categories of fibrosis-4 (FIB-4) score (low-, intermediate-, and high-risk).
Figure 2
Kaplan–Meier survival curves for the probable fibrosis according to APRI scores: fibrosis-free (APRI < 0.50), liver fibrosis (APRI < 1.50) and probable cirrhosis (APRI ≥ 1.50).
References
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