What is the relationship between total energy and protein intake and malnutrition status in patients undergoing maintenance hemodialysis?

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Association of Total Energy and Protein Intake with Malnutrition Status in Maintenance Hemodialysis Patients

Malnutrition represents a critical and highly prevalent complication in maintenance hemodialysis patients, affecting 28-54% of this population, with inadequate protein and energy intake serving as the primary modifiable driver of nutritional decline. 1 The relationship between nutrient intake and malnutrition status in hemodialysis patients is characterized by a vicious cycle where inadequate dietary protein and energy consumption—often falling below the recommended 1.2 g/kg/day for protein and 35 kcal/kg/day for energy—directly correlates with progressive depletion of protein and energy stores, leading to protein-energy wasting that independently predicts increased morbidity and mortality. 1 Multiple large-scale studies have demonstrated that dietary protein intake in maintenance hemodialysis patients frequently averages only 0.94-1.0 g/kg/day, meaning approximately half of patients consume less than this amount, falling substantially short of the 1.2 g/kg/day threshold necessary to maintain neutral or positive nitrogen balance. 1 This inadequate intake occurs through multiple mechanisms: uremia-induced anorexia, dialysis-related amino acid losses (10-12 g per session), chronic inflammation with elevated pro-inflammatory cytokines that suppress appetite, metabolic acidosis, insulin resistance, and inappropriate dietary restrictions. 1, 2 The metabolic consequences extend beyond simple nutrient deficiency, as hemodialysis itself induces a persistent catabolic state with negative nitrogen balance on dialysis days, compounded by dialysis-induced losses of glucose (12-25 g per session with glucose-free dialysate), peptides, and small amounts of protein (1-3 g per dialysis). 1 Critically, nutritional status markers—particularly serum albumin below 35 g/L, prealbumin below 300 mg/L, and normalized protein nitrogen appearance (nPNA) below 1 g/kg/day—have been consistently validated as powerful predictors of survival, with low albumin at dialysis initiation independently associated with significantly increased relative risk of death. 1 The pathophysiology involves not only inadequate intake but also altered metabolism characterized by resistance to anabolic factors such as growth hormone and insulin-like growth factor-1, chronic inflammation (often reflected by elevated C-reactive protein), and the systemic effects of a "kidney-centered" inflammatory syndrome affecting protein, carbohydrate, and lipid metabolism. 1, 3 Recent evidence emphasizes that nutritional deterioration begins even before dialysis initiation when glomerular filtration rate falls below 50 mL/min, with spontaneous reductions in dietary protein and energy intake playing a central role in the progressive nutritional decline observed as kidney function deteriorates. 4 The clinical significance of this association is underscored by data showing that correction of inadequate intake through nutritional interventions—including oral nutritional supplements that increase serum albumin by 2.3 g/L and targeted enteral nutrition—can improve nutritional status and potentially reduce the 20-36% of hemodialysis patients who fall below high-risk nutritional thresholds. 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Nutritional aspects in hemodialysis.

Kidney international. Supplement, 2000

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This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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