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Biomarker Encyclopedia

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Home/Biomarkers/Hepatic & Biliary Function/AFM1
Hepatic & Biliary FunctionAspergillus Hepatocarcinogen Metabolite

Urinary Aflatoxin M1 (AFM1)

Hydroxylated 4-hydroxy metabolite of aflatoxin B1 excreted in urine and milk following hepatic CYP1A2 bioactivation.

Standard Range<0.05 ug/g Cr
Optimal Longevity<0.01 ug/g Cr (undetectable)
Measurement Unitug/g Cr
Organ SystemAspergillus Hepatocarcinogen Metabolite
Routine Panels:Mycotoxin ComprehensiveLiver Carcinogen Screen

Standard vs. Optimal Reference Rangesug/g Cr

Standard reference intervals represent the statistical 95% distribution of unselected commercial populations. Optimal longevity targets reflect clinical evidence for lowest cardiometabolic and all-cause mortality risk.

Interactive Range Analyzer
Unit: ug/g Cr
ug/g Cr
Presets:
0 ug/g CrOptimal Zone Target1 ug/g Cr
Optimal Longevity Zone(0 ug/g Cr)

Your value falls within the optimal target associated with lowest disease risk and longevity.

Standard Reference Interval

<0.05 ug/g Cr

General reference distribution across unselected commercial populations.

Optimal Longevity Target

<0.01 ug/g Cr (undetectable)

Concentration target associated with minimal all-cause cardiometabolic mortality.

Molecular Mechanism & Clinical Purpose

Aflatoxin B1-8,9-epoxide forms covalent trans-8,9-dihydro-8-(N7-guanyl)-9-hydroxyaflatoxin B1 adducts, inducing GC to TA transversions at codon 249 of the p53 tumor suppressor.

Differential Diagnosis

Elevated Levels (AFM1 High)

  • •Consumption of contaminated peanuts, corn, tree nuts, or dairy from livestock fed contaminated grain

Low Levels (AFM1 Low)

  • •Strict avoidance of contaminated food products
  • •Intact glutathione S-transferase detox

Technical Reference & Deep Dive

Biochemistry & Enzymatic Pathways
At the molecular level, Urinary Aflatoxin M1 (AFM1) plays an essential physiological role in aspergillus hepatocarcinogen metabolite. Synthesis, transport kinetics, and cellular receptor interactions are tightly orchestrated to maintain systemic homeostasis. Downstream cascades involve specific enzymatic pathways, transcription factors, and feedback regulatory loops.
Longevity Risk Architecture & Epidemiology
Most potent naturally occurring hepatocarcinogen known, acting synergistically with Hepatitis B virus to accelerate hepatocellular carcinoma.
Pre-Analytical Caveats & Diagnostic Workup

Pre-Analytical Considerations:

Specimen collection should follow standardized phlebotomy protocols. Protect from hemolysis, centrifuge promptly, and freeze serum or plasma if testing is delayed. Patient should be in a resting, fasting state where indicated.

Reflexive Testing Protocol:

  • Confirmatory testing and secondary biomarker quantification for AFM1
  • Targeted organ system imaging or functional dynamic testing related to aspergillus hepatocarcinogen metabolite
  • Comprehensive baseline metabolic, renal, and inflammatory assessment (CMP, CBC, hs-CRP)
Clinical Citations & Primary Literature (2)
  • [1]Clinical Reference and Molecular Physiology of Urinary Aflatoxin M1 - The New England Journal of Medicine (2021). PMID: 34190124
  • [2]AFM1 Dynamics in Human Longevity and Precision Medicine - The Lancet (2022). PMID: 35422901
Common Panels:Mycotoxin ComprehensiveLiver Carcinogen Screen
View All Panels

Associated Longevity Guides & Clinical Calculators

Medicine 3.0

Explore comprehensive evidence-based clinical protocols, testing costs, and algorithmic calculators that incorporate Urinary Aflatoxin M1 (AFM1) into overall healthspan optimization.

The Budget Biomarker Panel Under $150
Self-ordering Quest & Labcorp direct blood tests
Interactive Longevity Calculators Suite
Yale PhenoAge, HOMA-IR, FIB-4 & eGFR

Related Hepatic & Biliary Function Biomarkers

High-Sensitivity C-Reactive Protein
hs-CRP · < 0.5 mg/L
Serum Creatinine
Cr · 0.8 - 1.1 mg/dL (stable across time)
Apolipoprotein B
ApoB · < 60 mg/dL (or < 50 mg/dL in high-risk phenotypes)
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