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. 2024 Aug 1;7(8):e2426577.
doi: 10.1001/jamanetworkopen.2024.26577.

Protein Intake and Mortality in Older Adults With Chronic Kidney Disease

Affiliations

Protein Intake and Mortality in Older Adults With Chronic Kidney Disease

Adrián Carballo-Casla et al. JAMA Netw Open. .

Abstract

Importance: Avoiding high protein intake in older adults with chronic kidney disease (CKD) may reduce the risk of kidney function decline, but whether it can be suboptimal for survival is not well known.

Objective: To estimate the associations of total, animal, and plant protein intake with all-cause mortality in older adults with mild or moderate CKD and compare the results to those of older persons without CKD.

Design, setting, and participants: Data from 3 cohorts (Study on Cardiovascular Health, Nutrition and Frailty in Older Adults in Spain 1 and 2 and the Swedish National Study on Aging and Care in Kungsholmen [in Sweden]) composed of community-dwelling adults 60 years or older were used. Participants were recruited between March 2001 and June 2017 and followed up for mortality from December 2021 to January 2024. Those with no information on diet or mortality, with CKD stages 4 or 5, or undergoing kidney replacement therapy and kidney transplant recipients were excluded. Data were originally analyzed from June 2023 to February 2024 and reanalyzed in May 2024.

Exposures: Cumulative protein intake, estimated via validated dietary histories and food frequency questionnaires.

Main outcomes and measures: The study outcome was 10-year all-cause mortality, ascertained with national death registers. Chronic kidney disease was ascertained according to estimated glomerular filtration rates, urine albumin excretion, and diagnoses from medical records.

Results: The study sample consisted of 8543 participants and 14 399 observations. Of the 4789 observations with CKD stages 1 to 3, 2726 (56.9%) corresponded to female sex, and mean (SD) age was 78.0 (7.2) years. During the follow-up period, 1468 deaths were recorded. Higher total protein intake was associated with lower mortality among participants with CKD; adjusted hazard ratio (HR) for 1.00 vs 0.80 g/kg/d was 0.88 (95% CI, 0.79-0.98); for 1.20 vs 0.80 g/kg/d, 0.79 (95% CI, 0.66-0.95); and for 1.40 vs 0.80 g/kg/d, 0.73 (95% CI, 0.57-0.92). Associations with mortality were comparable for plant and animal protein (HRs, 0.80 [95% CI, 0.65-0.98] and 0.88 [95% CI, 0.81-0.95] per 0.20-g/kg/d increment, respectively) and for total protein intake in participants younger than 75 years vs 75 years or older (HRs, 0.94 [95% CI, 0.85-1.04] and 0.91 [95% CI, 0.85-0.98] per 0.20-g/kg/d increment in total protein intake, respectively). However, the hazards were lower among participants without CKD than in those with CKD (HRs, 0.85 [95% CI, 0.79-0.92] and 0.92 [95% CI, 0.86-0.98] per 0.20-g/kg/d increment, respectively; P = .02 for interaction).

Conclusions and relevance: In this multicohort study of older adults, higher intake of total, animal, and plant protein was associated with lower mortality in participants with CKD. Associations were stronger in those without CKD, suggesting that the benefits of proteins may outweigh the downsides in older adults with mild or moderate CKD.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Avesani reported serving on the advisory board for Fresenius-Kabi SE & Co KGaA and receiving speaker honoraria from Fresenius Medical Care, Abbott Laboratories, and AstraZeneca outside the submitted work. Dr Stenvinkel reported receiving grant funding from AstraZeneca and Bayer AG, lecture fees from AstraZeneca, Novo Nordisk A/S, Baxter International Inc, Astellas Pharma, and Pfizer Inc, and serving on the scientific advisory board of Boehringer Mannheim, Invizius, and FMC Corporation outside the submitted work. Dr Lindholm reported receiving grant funding to institution from Baxter Healthcare Corporation and previous employment by Baxter Healthcare Corporation outside the submitted work. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Association of Total Protein Intake With 10-Year All-Cause Mortality, Stratified by Chronic Kidney Disease and Age
Analyses used Cox proportional hazards regression models. Protein intake was modeled as a 3-knot restricted cubic spline. Hazard ratios (HRs) and 95% CIs were plotted for protein intake above the 1st percentile and below the 99th percentile and obtained from models with interaction terms among protein intake, chronic kidney disease, and age. Models were adjusted for cohort, sex, age, living arrangement, previous occupation, educational level, tobacco smoking, light physical activity, moderate-to-vigorous physical activity, body mass index, diabetes, cardiovascular disease, chronic lung disease, musculoskeletal disease, cancer, depression and mood disorders, and intake of energy, monounsaturated fat, sugar, alcohol, and sodium.
Figure 2.
Figure 2.. Associations of Animal and Plant Protein Intake With 10-Year All-Cause Mortality, Stratified by Chronic Kidney Disease and Age
Analyses used Cox proportional hazards regression models. Protein intake was modeled as a 3-knot restricted cubic spline. Hazard ratios (HRs) and 95% CIs were plotted for protein intake above the 1st percentile and below the 99th percentile and obtained from models integrating interaction terms among animal protein intake, chronic kidney disease, and age and among plant protein intake, chronic kidney disease, and age. Models were adjusted for cohort, sex, age, living arrangement, previous occupation, educational level, tobacco smoking, light physical activity, moderate-to-vigorous physical activity, body mass index, diabetes, cardiovascular disease, chronic lung disease, musculoskeletal disease, cancer, depression and mood disorders, and intake of energy, monounsaturated fat, sugar, alcohol, and sodium.

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