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Albumin Levels: Normal Range & Clinical Meaning

Complete reference for normal serum albumin levels, causes and consequences of low albumin (hypoalbuminemia), and why albumin matters for liver function, prognosis, and patient outcomes.

Normal Albumin Range
3.4–5.4
g/dL (34–54 g/L)
Mild low: 3.0–3.4 g/dL
Moderate low: 2.5–3.0 g/dL
Severe low: <2.5 g/dL

What Is Albumin?

Albumin is the most abundant protein in human blood plasma, accounting for approximately 50–60% of total serum protein. It is synthesized exclusively by the liver at a rate of approximately 10–15 g/day and has a serum half-life of about 20 days. Normal serum albumin concentration ranges from 3.4 to 5.4 g/dL (34–54 g/L).

Albumin serves several critical physiological functions: it maintains oncotic pressure (the force that keeps fluid within blood vessels), transports a wide variety of substances (bilirubin, fatty acids, hormones, drugs, calcium, and medications including warfarin, phenytoin, and benzodiazepines), acts as an antioxidant and buffer, and modulates inflammation. About 60% of total body albumin is in the extravascular space.

Serum albumin is one of the most commonly measured laboratory values and is a powerful prognostic marker. Low albumin independently predicts poor surgical outcomes, increased length of hospital stay, higher complication rates, and mortality across nearly all clinical settings — from elective surgery to critical illness to chronic disease. However, interpreting albumin requires understanding that it is primarily a marker of disease severity and inflammation rather than nutritional status.

Normal Albumin Levels & Severity Classification

Classification Conventional (g/dL) SI Units (g/L) Clinical Significance
Normal 3.4–5.4 34–54 Normal range; adequate liver synthetic function
Mild hypoalbuminemia 3.0–3.4 30–34 Common in acute illness; investigate if persistent
Moderate hypoalbuminemia 2.5–3.0 25–30 Clinically significant; expect peripheral edema, impaired healing
Severe hypoalbuminemia <2.5 <25 High morbidity/mortality; anasarca, ascites, poor prognosis
High albumin >5.4 >54 Almost always from dehydration (hemoconcentration)

Note: Reference ranges may vary slightly between laboratories. SI conversion: albumin g/dL × 10 = g/L. Albumin has a half-life of approximately 20 days — changes in albumin reflect processes occurring over weeks, not hours.

What Does a High Albumin Level Mean?

Elevated serum albumin (>5.4 g/dL) is uncommon and essentially always reflects hemoconcentration from dehydration rather than true albumin overproduction. The liver does not upregulate albumin synthesis to supranormal levels.

Causes of High Albumin

  • Dehydration (hemoconcentration) — the predominant and nearly exclusive cause. Reduced plasma water volume concentrates all serum proteins, including albumin
  • Prolonged tourniquet application — a specimen collection artifact that can falsely elevate albumin and other proteins
  • Upright posture — albumin is ~0.3 g/dL higher in ambulatory samples compared to supine samples due to fluid redistribution

Clinical Significance

An elevated albumin is primarily a signal to assess hydration status. It does not indicate a disease of albumin excess. If total protein and albumin are both elevated, dehydration is the most likely explanation. Treat the underlying cause — typically fluid resuscitation.

What Does a Low Albumin Level Mean?

Hypoalbuminemia (<3.4 g/dL) is extremely common in hospitalized patients and is one of the strongest non-specific prognostic markers in medicine. Understanding the mechanism helps guide workup.

Common Causes of Low Albumin

  • Liver disease (decreased synthesis) — cirrhosis is the classic cause. The liver must lose ~75% of its synthetic capacity before albumin falls significantly. Albumin is a component of the Child-Pugh and MELD scores for liver disease staging
  • Nephrotic syndrome (urinary loss) — glomerular damage allows massive albuminuria (>3.5 g/day). Severe hypoalbuminemia with edema, hyperlipidemia, and lipiduria is the hallmark presentation
  • Inflammation and sepsis (negative acute-phase response) — pro-inflammatory cytokines (IL-6, TNF-α) suppress hepatic albumin synthesis and increase capillary permeability, redistributing albumin to the extravascular space. This is the most common cause of hypoalbuminemia in hospitalized patients
  • Malnutrition — prolonged protein-calorie malnutrition (kwashiorkor, anorexia nervosa) reduces substrate for albumin synthesis. However, albumin's long half-life makes it a late and insensitive marker of nutritional depletion
  • Burns — direct protein loss through damaged capillaries and skin; severe burns can cause precipitous albumin decline
  • Protein-losing enteropathy — gastrointestinal protein loss in conditions such as inflammatory bowel disease, celiac disease, lymphangiectasia, and Ménétrier disease
  • Heart failure — hemodilution, hepatic congestion impairing synthesis, and inflammatory activation all contribute
  • Critical illness — capillary leak syndrome in sepsis and ARDS redistributes albumin to the interstitial space; levels can fall dramatically within 24–48 hours of ICU admission

Symptoms and Consequences of Low Albumin

  • Edema — peripheral pitting edema, periorbital edema, ascites, and pleural effusions from reduced oncotic pressure
  • Impaired wound healing — albumin is needed for tissue repair; surgical patients with albumin <3.0 g/dL have significantly higher complication rates
  • Altered drug pharmacokinetics — many drugs are highly albumin-bound (warfarin, phenytoin, diazepam); low albumin increases the free (active) drug fraction, raising toxicity risk
  • Increased infection risk — albumin has immunomodulatory and antioxidant functions
  • Falsely low total calcium — calcium is partially bound to albumin; low albumin causes artificially low total calcium without affecting ionized calcium. Use corrected calcium or measure ionized calcium

Related Tests & Calculators

Albumin influences the interpretation of several other laboratory values and clinical scores:

  • Corrected Calcium Calculator — adjusts total calcium for albumin level; essential when albumin is low to avoid missing true hypercalcemia or diagnosing false hypocalcemia
  • Albumin-Corrected Anion Gap — adjusts the anion gap for low albumin, which unmasks hidden anion gap metabolic acidosis
  • MELD Score Calculator — Model for End-Stage Liver Disease; uses bilirubin, INR, and creatinine (albumin is not in MELD but correlates with severity)
  • Child-Pugh Score — classifies cirrhosis severity using albumin, bilirubin, INR, ascites, and encephalopathy
  • FENa Calculator — fractional excretion of sodium; relevant in the workup of nephrotic syndrome with AKI

About This Test

Methodology

Serum albumin is most commonly measured using the bromocresol green (BCG) dye-binding method or the bromocresol purple (BCP) method. BCG tends to overestimate albumin slightly (especially at low levels) because it binds non-specifically to other proteins, including acute-phase reactants. BCP is more specific for albumin but may underestimate it in some settings. Immunonephelometric methods are the most accurate but are not routinely used for serum albumin measurement.

🔑 Clinical Pearls

  • Albumin is NOT a nutrition marker: Despite decades of misuse, albumin is a marker of inflammation and disease severity, not nutritional intake. ASPEN guidelines explicitly state albumin should not be used to diagnose malnutrition. It is a negative acute-phase reactant — levels drop in response to IL-6, regardless of diet.
  • Prealbumin (transthyretin): With a half-life of 2–3 days, prealbumin responds faster to nutritional changes but is also a negative acute-phase reactant and falls during inflammation. Neither albumin nor prealbumin is a reliable stand-alone nutrition marker.
  • The "albumin gap": In severe hypoalbuminemia, the anion gap falls by approximately 2.5 mEq/L for each 1 g/dL decrease in albumin below 4.0. This means a "normal" anion gap of 12 in a patient with albumin of 2.0 g/dL actually represents a hidden elevated gap. Always correct the anion gap for albumin.
  • Albumin infusion: While IV albumin is widely used, evidence for its benefit is limited to specific settings — large-volume paracentesis (>5L, give 6–8 g albumin per liter removed), spontaneous bacterial peritonitis in cirrhosis, and hepatorenal syndrome. Routine albumin replacement in ICU patients (SAFE trial, 2004) showed no mortality benefit compared to saline.
  • Half-life considerations: Albumin's ~20-day half-life means that even after the underlying cause is treated, albumin may take 2–3 weeks to normalize. Do not expect rapid improvements.
  • Preoperative albumin: Albumin <3.0 g/dL is one of the strongest predictors of postoperative complications. The NSQIP database shows albumin below 3.5 g/dL independently predicts 30-day morbidity and mortality across all surgical specialties.

References

  1. Tietz NW, ed. Tietz Clinical Guide to Laboratory Tests. 4th ed. WB Saunders; 2006.
  2. Don BR, Kaysen GA. Serum albumin: relationship to inflammation and nutrition. Semin Dial. 2004;17(6):432–437.
  3. Goldwasser P, Feldman J. Association of serum albumin and mortality risk. J Clin Epidemiol. 1997;50(6):693–703.
  4. Finfer S, Bellomo R, Boyce N, et al. A comparison of albumin and saline for fluid resuscitation in the intensive care unit (SAFE Study). N Engl J Med. 2004;350(22):2247–2256.
  5. White JV, Guenter P, Jensen G, et al. Consensus statement: Academy of Nutrition and Dietetics and American Society for Parenteral and Enteral Nutrition: characteristics recommended for the identification and documentation of adult malnutrition. JPEN J Parenter Enteral Nutr. 2012;36(3):275–283.

References last verified: February 2026