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Relation of Alcohol Intake to Kidney Function and Mortality Observational, Population-Based, Cohort Study

Data are conflicting about the effects of alcohol intake on kidney function. This population-based study investigated associations of alcohol intake with kidney function and mortality. The study cohort included adult participants in Exam-1, Exam-2 (6-year follow-up), and Exam-3 (20-year follow-up) o...

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Autores principales: Cirillo, Massimo, Bilancio, Giancarlo, Secondulfo, Carmine, Iesce, Gennaro, Ferrara, Carmela, Terradura-Vagnarelli, Oscar, Laurenzi, Martino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954827/
https://www.ncbi.nlm.nih.gov/pubmed/35334954
http://dx.doi.org/10.3390/nu14061297
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author Cirillo, Massimo
Bilancio, Giancarlo
Secondulfo, Carmine
Iesce, Gennaro
Ferrara, Carmela
Terradura-Vagnarelli, Oscar
Laurenzi, Martino
author_facet Cirillo, Massimo
Bilancio, Giancarlo
Secondulfo, Carmine
Iesce, Gennaro
Ferrara, Carmela
Terradura-Vagnarelli, Oscar
Laurenzi, Martino
author_sort Cirillo, Massimo
collection PubMed
description Data are conflicting about the effects of alcohol intake on kidney function. This population-based study investigated associations of alcohol intake with kidney function and mortality. The study cohort included adult participants in Exam-1, Exam-2 (6-year follow-up), and Exam-3 (20-year follow-up) of the Gubbio study. Kidney function was evaluated as estimated glomerular filtration rate (eGFR, CKD-Epi equation, mL/min × 1.73 m(2)). Daily habitual alcohol intake was assessed by questionnaires. Wine intake accounted for >94% of total alcohol intake at all exams. Alcohol intake significantly tracked over time (R > 0.66, p < 0.001). Alcohol intake distribution was skewed at all exams (skewness > 2) and was divided into four strata for analyses (g/day = 0, 1–24, 25–48, and >48). Strata of alcohol intake differed substantially for lab markers of alcohol intake (p < 0.001). In multivariable regression, strata of alcohol intake related cross-sectionally to eGFR at all exams (Exam-1: B = 1.70, p < 0.001; Exam-2: B = 1.03, p < 0.001; Exam-3: B = 0.55, p = 0.010) and related longitudinally to less negative eGFR change from Exam-1 to Exam-2 (B = 0.133, p = 0.002) and from Exam-2 to Exam-3 (B = 0.065, p = 0.004). In multivariable Cox models, compared to no intake, intakes > 24 g/day were not associated with different mortality while an intake of 1–24 g/day was associated with lower mortality in the whole cohort (HR = 0.77, p = 0.003) and in the subgroup with eGFR < 60 mL/min × 1.73 m(2) (HR = 0.69, p = 0.033). These data indicate a positive independent association of alcohol intake with kidney function not due to a mortality-related selection.
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spelling pubmed-89548272022-03-26 Relation of Alcohol Intake to Kidney Function and Mortality Observational, Population-Based, Cohort Study Cirillo, Massimo Bilancio, Giancarlo Secondulfo, Carmine Iesce, Gennaro Ferrara, Carmela Terradura-Vagnarelli, Oscar Laurenzi, Martino Nutrients Article Data are conflicting about the effects of alcohol intake on kidney function. This population-based study investigated associations of alcohol intake with kidney function and mortality. The study cohort included adult participants in Exam-1, Exam-2 (6-year follow-up), and Exam-3 (20-year follow-up) of the Gubbio study. Kidney function was evaluated as estimated glomerular filtration rate (eGFR, CKD-Epi equation, mL/min × 1.73 m(2)). Daily habitual alcohol intake was assessed by questionnaires. Wine intake accounted for >94% of total alcohol intake at all exams. Alcohol intake significantly tracked over time (R > 0.66, p < 0.001). Alcohol intake distribution was skewed at all exams (skewness > 2) and was divided into four strata for analyses (g/day = 0, 1–24, 25–48, and >48). Strata of alcohol intake differed substantially for lab markers of alcohol intake (p < 0.001). In multivariable regression, strata of alcohol intake related cross-sectionally to eGFR at all exams (Exam-1: B = 1.70, p < 0.001; Exam-2: B = 1.03, p < 0.001; Exam-3: B = 0.55, p = 0.010) and related longitudinally to less negative eGFR change from Exam-1 to Exam-2 (B = 0.133, p = 0.002) and from Exam-2 to Exam-3 (B = 0.065, p = 0.004). In multivariable Cox models, compared to no intake, intakes > 24 g/day were not associated with different mortality while an intake of 1–24 g/day was associated with lower mortality in the whole cohort (HR = 0.77, p = 0.003) and in the subgroup with eGFR < 60 mL/min × 1.73 m(2) (HR = 0.69, p = 0.033). These data indicate a positive independent association of alcohol intake with kidney function not due to a mortality-related selection. MDPI 2022-03-18 /pmc/articles/PMC8954827/ /pubmed/35334954 http://dx.doi.org/10.3390/nu14061297 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cirillo, Massimo
Bilancio, Giancarlo
Secondulfo, Carmine
Iesce, Gennaro
Ferrara, Carmela
Terradura-Vagnarelli, Oscar
Laurenzi, Martino
Relation of Alcohol Intake to Kidney Function and Mortality Observational, Population-Based, Cohort Study
title Relation of Alcohol Intake to Kidney Function and Mortality Observational, Population-Based, Cohort Study
title_full Relation of Alcohol Intake to Kidney Function and Mortality Observational, Population-Based, Cohort Study
title_fullStr Relation of Alcohol Intake to Kidney Function and Mortality Observational, Population-Based, Cohort Study
title_full_unstemmed Relation of Alcohol Intake to Kidney Function and Mortality Observational, Population-Based, Cohort Study
title_short Relation of Alcohol Intake to Kidney Function and Mortality Observational, Population-Based, Cohort Study
title_sort relation of alcohol intake to kidney function and mortality observational, population-based, cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954827/
https://www.ncbi.nlm.nih.gov/pubmed/35334954
http://dx.doi.org/10.3390/nu14061297
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