SI UNITS (recommended)

CONVENTIONAL UNITS

* The SI units is the recommended method of reporting clinical laboratory results

(Oxidized Dimer of Cysteine – Key Marker for Cystinuria & Amino Acid Metabolism)

Synonyms

  • Cystine
  • Cys–Cys (oxidized cysteine dimer)
  • Dibasic amino acid
  • Sulfur amino acid dimer

Units of Measurement

  • µmol/L
  • mg/L
  • mg/dL
  • mg/100 mL
  • mg%
  • µg/mL

1 mg/L = 0.1 mg/dL
1 µg/mL = 1 mg/L
mg/dL = mg% = mg/100 mL

Description

Cystine is the oxidized dimer of two cysteine molecules linked via a disulfide bond (S–S).
It appears in the blood and urine as part of normal sulfur amino acid metabolism.

Clinically, cystine is most important as a biomarker for cystinuria and cystine kidney stones - one of the few amino acids that forms insoluble crystals in urine.

Physiological Role

  • Formed by oxidation of cysteine
  • Helps stabilize proteins through disulfide bonding
  • Significant structural component of keratin (hair, nails, skin)
  • Present in plasma, tissues, and urine
  • Regulated by cystine/cysteine redox balance

Clinical Significance

High Cystine (Hyper-cystinuria)

The most important clinical condition related to cystine elevation.

1. Cystinuria (Primary Use)

A genetic disorder (SLC3A1 or SLC7A9 mutations) involving defective renal tubular reabsorption of:

  • Cystine
  • Lysine
  • Arginine
  • Ornithine
    Collectively called COLA amino acids.

Cystine is the least soluble, leading to:

  • Recurrent kidney stones
  • Early-onset urolithiasis
  • Staghorn calculi
  • Recurrent UTIs

2. Cystine Stones

High cystine in urine → hexagonal cystine crystals.
Serum cystine may be normal; urine cystine is key for diagnosis.

3. Oxidative Stress Disorders

Increased cystine relative to cysteine indicates:

  • Oxidative stress
  • Systemic inflammation
  • Aging processes

4. Renal Tubular Disorders

Tubular dysfunction may cause elevated urinary cystine.

Low Cystine (Rare)

May be seen in:

  • Malnutrition
  • Severe oxidative stress (cysteine depletion → low cystine)
  • Metabolic disorders involving sulfur metabolism
  • After cystine-binding drug therapy (tiopronin, D-penicillamine)

Usually not clinically significant.

Reference Intervals

(Tietz 8E + LC-MS/MS Amino Acid Panels + Mayo + ARUP)

Fasting Plasma Cystine

  • 40 – 70 µmol/L (typical adult range)

Ranges vary slightly by lab and age.

Urine Cystine (Primary Diagnostic Test)

  • <30 mg/day: Normal
  • >250–300 mg/day: Cystinuria
  • >500 mg/day: Severe cystinuria

Special tests:

  • Sodium nitroprusside test (qualitative)
  • Urinary cystine saturation index

Diagnostic Uses

1. Cystinuria Diagnosis (Primary Use)

  • Detects excess cystine → identifies patients prone to cystine stones.
  • Urine cystine is much more diagnostic than plasma.

2. Kidney Stone Workup

  • Hexagonal crystals on microscopy confirm cystine stones
  • Quantitative urine cystine monitors:
    • Treatment response
    • Thiol therapy effectiveness
    • Hydration adequacy

3. Metabolic Disorders

Cystine levels are assessed in:

  • Aminoacidopathies
  • Oxidative stress studies
  • Disorders of sulfur metabolism

4. Nutritional & Redox Status

Altered cystine-to-cysteine ratio indicates:

  • Poor antioxidant status
  • High oxidative load

Analytical Notes

  • Fasting plasma preferred
  • Plasma must be deproteinized promptly to prevent oxidation/reduction changes
  • LC-MS/MS is gold standard
  • Cystine is sensitive to sample handling and storage
  • Urine tests require acidified samples for stability

Clinical Pearls

  • Cystinuria = high urine cystine, NOT high plasma cystine.
  • Hexagonal crystals in urine are almost pathognomonic for cystine stones.
  • Cystine stones require urine alkalinization, high fluid intake, and sometimes thiol agents (tiopronin, D-penicillamine).
  • Cystine is much less soluble at acidic urine pH - keep urine pH >7.0–7.5 to prevent stone formation.
  • Plasma cystine-to-cysteine ratio is a marker of oxidative stress.

Interesting Fact

Cystine stones are radiodense on CT due to sulfur content - unlike uric acid stones, which are radiolucent.

References

  1. Tietz Clinical Chemistry & Molecular Diagnostics, 8th Edition - Amino Acids.
  2. Mayo Clinic Laboratories - Plasma & Urine Amino Acids.
  3. ARUP Consult - Amino Acid Disorders & Kidney Stone Analysis.
  4. AUA/EAU Kidney Stone Guidelines.
  5. Inborn Errors of Metabolism Clinical Guidelines.
  6. MedlinePlus / NIH - Amino Acids & Kidney Stones.

Last updated: January 26, 2026

Reviewed by : Medical Review Board

Change language

Other Convertors