Whole-body protein kinetics in critically ill patients during 50 or 100% energy provision by enteral nutrition: A randomized cross-over study

PLoS One. 2020 Oct 5;15(10):e0240045. doi: 10.1371/journal.pone.0240045. eCollection 2020.

Abstract

Background: Enteral nutrition (EN) is a ubiquitous intervention in ICU patients but there is uncertainty regarding the optimal dose, timing and importance for patient-centered outcomes during critical illness. Our research group has previously found an improved protein balance during normocaloric versus hypocaloric parenteral nutrition in neurosurgical ICU patients. We now wanted to investigate if this could be demonstrated in a general ICU population with established enteral feeding, including patients on renal replacement therapy.

Methods: Patients with EN >80% of energy target as determined by indirect calorimetry were randomized to or 50% or 100% of current EN rate. After 24 hours, whole-body protein kinetics were determined by enteral and parenteral stable isotope tracer infusions. Treatment allocation was then switched, and tracer investigations repeated 24 hours later in a crossover design with patients serving as their own controls.

Results: Six patients completed the full protocol. During feeding with 100% EN all patients received >1.2 g/kg/day of protein. Mean whole-body protein balance increased from -6.07 to 2.93 µmol phenylalanine/kg/h during 100% EN as compared to 50% (p = 0.044). The oxidation rate of phenylalanine was unaltered (p = 0.78).

Conclusions: It is possible to assess whole-body protein turnover using a stable isotope technique in critically ill patients during enteral feeding and renal replacement therapy. Our results also suggest a better whole-body protein balance during full dose as compared to half dose EN. As the sample size was smaller than anticipated, this finding should be confirmed in larger studies.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Carbon Isotopes / chemistry
  • Critical Illness
  • Cross-Over Studies
  • Energy Intake
  • Energy Metabolism*
  • Enteral Nutrition / methods*
  • Female
  • Humans
  • Intensive Care Units
  • Isotope Labeling
  • Kinetics
  • Male
  • Middle Aged
  • Parenteral Nutrition
  • Phenylalanine / chemistry
  • Phenylalanine / metabolism
  • Proteins / metabolism*
  • Whole-Body Counting / methods

Substances

  • Carbon Isotopes
  • Proteins
  • Phenylalanine
  • Carbon-13

Grants and funding

This study was funded by grants to JW from Stockholm City Council (https://www.sll.se/), grant #563170, and the Swedish Research Council (https://www.vr.se/english.html), grant #04210. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.