Abstract

To accommodate the loss of the plethora of functions of the kidneys, patients with chronic kidney disease require many dietary adjustments, including restrictions on the intake of protein, phosphorus, sodium and potassium. Plant-based foods are increasingly recommended as these foods contain smaller amounts of saturated fatty acids, protein and absorbable phosphorus than meat, generate less acid and are rich in fibers, polyunsaturated fatty acids, magnesium and potassium. Unfortunately, these dietary recommendations cannot prevent the occurrence of many symptoms, which typically include fatigue, impaired cognition, myalgia, muscle weakness, and muscle wasting. One threat coming with the recommendation of low-protein diets in patients with non-dialysis-dependent chronic kidney disease (CKD) and with high-protein diets in patients with dialysis-dependent CKD, particularly with current recommendations towards proteins coming from plant-based sources, is that of creatine deficiency. Creatine is an essential contributor in cellular energy homeostasis, yet on a daily basis 1.6–1.7% of the total creatine pool is degraded. As the average omnivorous diet cannot fully compensate for these losses, the endogenous synthesis of creatine is required for continuous replenishment. Endogenous creatine synthesis involves two enzymatic steps, of which the first step is a metabolic function of the kidney facilitated by the enzyme arginine:glycine amidinotransferase (AGAT). Recent findings strongly suggest that the capacity of renal AGAT, and thus endogenous creatine production, progressively decreases with the increasing degree of CKD, to become absent or virtually absent in dialysis patients. We hypothesize that with increasing degree of CKD, creatine coming from meat and dairy in food increasingly becomes an essential nutrient. This phenomenon will likely be present in patients with CKD stages 3, 4 and 5, but will likely be most pronouncedly present in patients with dialysis-dependent CKD, because of the combination of lowest endogenous production of creatine and unopposed losses of creatine into the dialysate. It is likely that these increased demands for dietary creatine are not sufficiently met. The result of which, may be a creatine deficiency with important contributions to the sarcopenia, fatigue, impaired quality of life, impaired cognition, and premature mortality seen in CKD.

Highlights

  • More than 10% of the world’s population is currently suffering from non-dialysis-dependent chronic kidney disease (CKD) [1,2], and almost one out of every two adults aged 30–64 years is expected to develop CKD during their lifetime [3,4]

  • With an increasing focus on a plant-based intake, it is likely that these increased demands for dietary creatine are not sufficiently met

  • This would result in a creatine deficiency, with important contributions to sarcopenia, fatigue, impaired quality of life, impaired cognition, and premature mortality seen in CKD

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Summary

Introduction

More than 10% of the world’s population is currently suffering from non-dialysis-dependent chronic kidney disease (CKD) [1,2], and almost one out of every two adults aged 30–64 years is expected to develop CKD during their lifetime [3,4]. The comorbidities that accompany CKD are for a large part the progressive loss of the plethora of functions displayed by the kidneys, including maintenance of protein homeostasis, acid-base homeostasis, volume homeostasis, and bone and mineral homeostasis [7,8]. This requires many dietary adjustments, including restriction of intake of protein, phosphorus, sodium and potassium. The National Kidney Foundation website names a plant-based diet as being beneficial to CKD patients [16,17,18] These dietary recommendations cannot prevent the occurrence of many symptoms, which typically include fatigability, muscle weakness, muscle wasting, and sarcopenia [7,8,19]

Compromised Creatine Intake
Contribution of the Kidney to Endogenous
Effectinof
Most Susceptible Patient Group
Hypothesis
Effects on on International
Safety of Creatine Supplementation
Limitations
Findings
10. Conclusions
Full Text
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