Prealbumin: Normal Range and Clinical Interpretation
Direct Answer
The normal serum prealbumin range is ≥30 mg/dL, and values below this threshold warrant evaluation for protein-energy malnutrition, but prealbumin should never be interpreted in isolation without considering inflammatory status, renal function, and hepatic function. 1, 2
Normal Reference Range
- Target threshold: ≥30 mg/dL is the recommended outcome goal for prealbumin when monitoring nutritional status 1, 2
- Some research suggests 135 mg/L (13.5 mg/dL) or greater reflects return to stable nutritional status in patients receiving nutritional support 3
- Normal population mean is approximately 29.6 ± 4.82 mg/dL 4
Critical Limitations That Override Nutritional Interpretation
Inflammation (Most Important Confounder)
Prealbumin is a negative acute-phase reactant that declines during inflammation, infection, or critical illness regardless of actual nutritional intake. 1, 5, 2
- Inflammatory cytokines directly downregulate hepatic synthesis even when protein and caloric intake are adequate 5
- An elevated C-reactive protein negates the relationship between prealbumin and actual protein intake 5, 6
- The American College of Cardiology recommends that prealbumin should not be used as a primary marker of nutritional status in critically ill adults with suspected malnutrition 5
Renal Dysfunction (Artificial Elevation)
Prealbumin levels are artificially elevated in renal failure due to impaired kidney degradation, making interpretation unreliable in patients with impaired kidney function. 1, 5, 2
- This elevation occurs because the kidney normally degrades prealbumin, and when renal function is impaired, clearance is reduced 1
- Despite this limitation, values <30 mg/dL in dialysis patients are still associated with increased mortality risk 1
Hepatic Dysfunction
- Prealbumin is synthesized by the liver and is significantly decreased when liver function is impaired 7
- In acute viral hepatitis, prealbumin drops to approximately 15.3 ± 7.4 mg/dL, and in chronic liver diseases (cirrhosis, chronic active hepatitis), it drops to approximately 10 mg/dL 4
- Prealbumin may be more sensitive than albumin for detecting acute liver dysfunction 4
Clinical Interpretation Algorithm
Step 1: Check for Confounders FIRST
Before interpreting prealbumin as a nutritional marker, you must:
- Measure C-reactive protein alongside prealbumin to assess inflammatory status 5, 6
- Assess renal function (if impaired, prealbumin is unreliable for nutrition assessment) 1, 5
- Assess hepatic function (if impaired, low prealbumin reflects liver dysfunction, not just malnutrition) 7, 4
Step 2: Interpret Based on Clinical Context
If inflammation is present (elevated CRP):
- Low prealbumin reflects inflammation, not necessarily malnutrition 5, 6
- Do not use prealbumin to guide nutritional intervention decisions 5
- Use alternative assessment tools instead (see below) 5
If renal failure is present:
- Prealbumin values are artificially elevated and unreliable 1, 5
- However, in dialysis patients, values <30 mg/dL still predict increased mortality risk 1
If no inflammation and normal renal/hepatic function:
- Prealbumin <30 mg/dL warrants evaluation for protein-energy malnutrition 1, 2
- Prealbumin can complement clinical assessment but should not be used alone 8
Step 3: Use Superior Assessment Tools
The American Society for Parenteral and Enteral Nutrition recommends using Nutritional Risk Screening 2002 (NRS-2002), which incorporates BMI, weight loss, food intake, and disease severity. 5
- Subjective Global Assessment (SGA) is more reliable than albumin or prealbumin in detecting protein-energy wasting 5
- Body composition assessment should be preferred to biochemical markers when diagnosing and monitoring malnutrition 5
- Monitor food intake daily using semi-quantitative methods in malnourished patients 5
- Trigger nutritional intervention when intake is ≤50% of energy requirements over 3 days 5
Comparison to Albumin
There is insufficient evidence to conclude that prealbumin is a more sensitive or accurate index of malnutrition than serum albumin. 1, 2
- Prealbumin has a shorter half-life (2-3 days) compared to albumin (20 days), theoretically making it more responsive to acute changes 1, 5, 2
- However, prealbumin does not consistently correlate with changes in other nutritional parameters 1, 5
- Both are negative acute-phase reactants limited by the same confounding factors 1
Prognostic Value
Low prealbumin levels are strongly associated with increased mortality risk, particularly in dialysis patients. 1, 2
- Prealbumin levels at initiation of dialysis or during maintenance dialysis predict future mortality risk 1, 2
- Values <30 mg/dL correlate with other indices of protein-energy malnutrition 1
Common Pitfalls to Avoid
- Never interpret low prealbumin as malnutrition without ruling out inflammation first 5, 6
- Never use prealbumin to assess nutritional status in renal failure patients 1, 5, 2
- Never assume hypoprealbuminemia is solely due to malnutrition when inflammation may be the primary driver 5
- Never wait for laboratory confirmation to begin nutritional support if clinical signs of malnutrition are present 6
- Never interpret prealbumin in isolation without considering inflammatory status, renal function, and hepatic function 5, 6
Monitoring Nutritional Intervention
- Prealbumin changes more rapidly and accurately reflect current nutritional status compared to albumin when monitoring response to nutritional support 3
- In patients receiving enteral or parenteral nutrition with adequate caloric/protein goals, prealbumin concentration changes can guide effectiveness of intervention 3
- However, this utility is only valid in the absence of inflammation and normal renal/hepatic function 5, 9