Kidney Res Clin Pract > Volume 38(1); 2019 > Article
Bolasco: Very low protein plus ketoacid analogs of essential aminoacids do not confirm superiority of a low protein diet to retard chronic kidney disease progression
To the Editor:
I read with great interest the original work of Satirapoj et al [1], particularly with regard to the number of cases seen in patients affected by chronic kidney disease (CKD III and CKD IV). However, in spite of the use of an amino acid supplement, this study seems to lack clarity and provides no firm evidence by which to evaluate and confirm the aims of the study. In particular, I should like to emphasize the following: 1) There is no explanation as to how glomerular filtration rate (GFR) was calculated. 2) Generally, when assessing the outcome of residual renal function, patient adherence to a very limited diet such as the very low protein diet (VLPD) should be monitored, particularly if the patient is required to take approximately 13 tablets a day of steroids over an extended period of time. Conversely, the compliance assessments cited in this study are based solely on diet records and tables of standard food composition. This type of adherence assessment has never been viewed as a reliable method due to the need to associate it with a strict educational program and to implement monthly or three-monthly checks by an expert nutritionist [25]. Furthermore, in routine clinical practice, the deceptive and misleading nature of patient recall is widely acknowledged, and also takes into account poor patient evaluation and failure to introduce specific foods and liquids. 3) A further serious bias of this study is due to omitting to report the amount of energy provided by the kilocalories prescribed and introduced. Evaluation of the latter is a mandatory skill for a renal dietician. Without a strict prescription [6], no comparisons or evaluations of GFR outcome between the two groups can be obtained, as energy intake has a marked effect on anabolism and protein catabolism. 4) No assurance is provided that patients suffering from acute, subacute, or chronic intestinal diseases that exacerbate the microbiota, already severely affected by the uremic milieu and amino acid adsorption, were excluded from the study [7]. 5) Finally, the sole method to have been deemed reliable since 1985, still in use today, is assessment of urea nitrogen appearance, which takes into account the output of urinary and non-urinary nitrogen, in addition to the differences detected in urea distribution volume; indeed, the presence of azoturia did not seem to be assessed in the patients studied, although this simple evaluation yields the protein catabolic rate that provides considerably more reliable information, corresponding to actual protein intake [8,9]. Should the authors not be in a position to provide these data, no firm conclusions may be drawn from this paper.

Notes

Conflicts of interest

The author has no conflicts of interest to declare.

References

1. Satirapoj B, Vongwattana P, Supasyndh O. Very low protein diet plus ketoacid analogs of essential amino acids supplement to retard chronic kidney disease progression. Kidney Res Clin Pract 2018;37:384–392.
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7. Prokopienko AJ, Nolin TD. Microbiota-derived uremic retention solutes: perpetrators of altered nonrenal drug clearance in kidney disease. Expert Rev Clin Pharmacol 2018;11:71–82.
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8. Maroni BJ, Steinman TI, Mitch WE. A method for estimating nitrogen intake of patients with chronic renal failure. Kidney Int 1985;27:58–65.
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9. Weiner ID, Mitch WE, Sands JM. Urea and ammonia metabolism and the control of renal nitrogen excretion. Clin J Am Soc Nephrol 2015;10:1444–1458.
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