Which blood tests does Nutrafol (biotin supplement) interfere with?

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Last updated: August 28, 2025View editorial policy

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Nutrafol (Biotin) Interference with Blood Tests

Nutrafol, which contains biotin, primarily interferes with streptavidin-biotin-based immunoassays, most notably causing false results in cardiac troponin tests, thyroid function tests (TSH, fT3, fT4), and other hormone assays. 1, 2, 3

Key Blood Tests Affected by Biotin Interference

Cardiac Biomarkers

  • Cardiac Troponin T (high-sensitivity): False-negative results can occur with biotin supplementation, potentially missing myocardial infarction 1, 4
  • Other cardiac markers: Tests using biotin-streptavidin technology may be affected

Thyroid Function Tests

  • Thyroid Stimulating Hormone (TSH): Falsely lowered results 3
  • Free T4 (fT4): Falsely elevated results 3
  • Total T3 (TT3): Falsely elevated results 3
  • Thyroglobulin (Tg): Falsely lowered results 3

Other Hormone Tests

  • Prostate Specific Antigen (PSA): Potential for interference 5
  • Various other hormone assays: Any using streptavidin-biotin technology 2

Mechanism of Interference

Biotin interference occurs due to:

  • Assay design: Depends on whether the test uses a competitive or sandwich immunoassay method 1
  • In competitive assays: Biotin causes falsely elevated results
  • In sandwich assays: Biotin causes falsely decreased results

Factors Affecting Interference Severity

  1. Biotin dose: Higher doses create greater interference
  2. Time since last biotin ingestion: Maximum interference occurs approximately 2 hours after biotin intake 3
  3. Assay platform: Different manufacturers have varying susceptibility to biotin interference
    • Roche Cobas platforms are particularly susceptible 3, 4
    • Abbott Architect platforms show less interference 3
    • Siemens IMMULITE platforms show interference with certain tests 3

Clinical Implications

  • Cardiac testing: False-negative troponin results could lead to missed diagnosis of myocardial infarction 1, 4
  • Thyroid testing: Pattern of falsely low TSH with falsely high T4 can mimic hyperthyroidism 3
  • Cancer monitoring: False-negative tumor markers could affect cancer surveillance 3

Recommendations for Clinicians

  1. Ask about supplement use: Specifically inquire about Nutrafol, biotin supplements, or multivitamins containing biotin
  2. Timing of blood draws: If possible, instruct patients to stop biotin supplementation:
    • At least 8 hours before blood draws for standard doses (≤5 mg/day)
    • At least 72 hours before blood draws for high doses (>5 mg/day)
  3. Consider alternative assays: When biotin interference is suspected, use:
    • Mass spectrometry-based methods which are not affected by biotin 3
    • Newer generation immunoassays designed to be less susceptible to biotin interference 4
    • Alternative assay platforms with different detection methods

Prevalence and Risk Assessment

  • Risk of clinically significant interference varies by population:
    • UK study found extremely low prevalence of biotin levels high enough to cause interference 6
    • US studies show higher prevalence (7.4%) of potentially interfering biotin levels 5
  • Nutrafol contains biotin at doses that could potentially cause interference, especially if taken shortly before blood testing

Important Caveats

  • Newer assay generations: Some manufacturers have developed updated assays with higher tolerance to biotin interference (up to 1200 ng/mL) 4
  • Laboratory notification: Always inform the laboratory when a patient is taking biotin supplements
  • Unexpected results: Consider biotin interference when laboratory results don't match clinical presentation

Remember that biotin interference is dose and time-dependent, with maximum interference typically occurring 2 hours after ingestion and diminishing over time as biotin is cleared from circulation.

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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