What is the S-CDT (Serum Carbohydrate-Deficient Transferrin) lab test?

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Serum Carbohydrate-Deficient Transferrin (S-CDT) Lab Test

S-CDT is a biomarker used primarily to detect chronic excessive alcohol consumption, with high specificity but limited sensitivity, requiring alcohol intake of 50-80g daily for 1-2 weeks to become positive. 1

Definition and Mechanism

  • S-CDT refers to specific isoforms of transferrin (the second most abundant glycosylated protein in human serum) that are deficient in sialic acid groups, primarily asialo, monosialo, and disialo transferrin 1
  • Chronic alcohol consumption inhibits transferrin glycosylation, leading to increased carbohydrate-deficient isoforms that can be measured in serum 1
  • After alcohol cessation, CDT levels normalize within approximately 2-3 weeks 1

Clinical Applications

  • Primary use is to detect and monitor chronic excessive alcohol consumption, particularly in:

    • Patients with suspected alcohol-related liver disease 1
    • Monitoring abstinence in alcohol addiction programs 1
    • Evaluating patients prior to liver transplantation 1
    • License reapplication after driving under alcohol influence 2
    • Differentiating alcohol-induced liver disease from other causes 2
  • Secondary use is in screening for congenital disorders of glycosylation (CDGs), where it serves as a common screening test to detect aberrant glycosylation 1

Testing Methodology

  • Modern laboratories typically use one of these methods:

    • High-performance liquid chromatography (preferred method) 1
    • Capillary zone electrophoresis 3, 4
    • Mass spectrometry techniques:
      • Liquid chromatography-electrospray ionization 1
      • Matrix-assisted laser desorption/ionization time of flight (MALDI-TOF) 1
  • Results are typically expressed as percentage of CDT per total transferrin (%CDT) to account for individual variations in transferrin levels 1

Interpretation and Clinical Significance

  • Positive results indicate chronic excessive alcohol consumption (typically >50-80g ethanol daily for at least 1-2 weeks) 1, 2
  • CDT has higher specificity for chronic alcohol abuse compared to other markers like GGT, AST, ALT, and MCV 1, 5
  • Normal values do not exclude significant alcohol use due to limited sensitivity (25-50% in some studies) 1

Limitations and Confounding Factors

  • Limited sensitivity (25-50%) compared to its high specificity 1

  • False-positive results can occur in:

    • Patients with severe liver disease even without alcohol use 1
    • Congenital disorders of glycosylation 2
    • Patients treated for galactosemia 2
  • False-negative results are more common in:

    • Patients with cirrhosis 1
    • Women (who generally show less elevated CDT values after alcohol intake) 2
    • Immunosuppressed patients 2

Comparison with Other Alcohol Biomarkers

  • CDT is more specific but less sensitive than GGT for detecting alcohol consumption 1
  • Direct alcohol markers (ethyl glucuronide, ethyl sulfate, phosphatidylethanol) have higher specificity than CDT 1
  • Combining CDT with other markers (GGT, MCV) improves diagnostic accuracy 5, 2

Best Practice Recommendations

  • CDT should be expressed as percent of total transferrin to improve reliability 1
  • Specifically measure the disialotransferrin glycoform using high-performance liquid chromatography for best results 1
  • Use in combination with other biomarkers and clinical assessment rather than as a standalone test 1, 5
  • Consider that CDT is a better marker for chronic alcohol misuse than for recent high alcohol consumption alone 6

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Carbohydrate-deficient transferrin (CDT)--a biomarker for long-term alcohol consumption.

Journal of toxicology and environmental health. Part B, Critical reviews, 2004

Guideline

Evaluating Alcoholism as the Cause of Abnormal LFTs and Blood Cell Counts

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

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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