Methionine
metaboliteMethionine metabolism is altered in CAD and associated with acute MI risk through systemic metabolic derangement.
Pathway placement
Cascade stepOff-pathway / systemic markers
Confidencelow
RationaleAmino acid biomarker in CAD; metabolic pathway marker not plaque-specific.
Druggability
Not assessed (no mapped human gene target).
Type I vs Type II discrimination
ScoresType-I-specific
R — rupture / Type-I67
C — confounder / Type-II25
A — assay feasibility42
E — evidence strength60
T1DI (composite)18
Specificity differential (R−C)+41.7
Confounder panel (Type-II drivers)
1sepsis / systemic inflammationmag 1
2anemia / acute blood lossn/a
3hypovolemia / dehydrationmag 0
4tachyarrhythmiamag 1
5hypoxemia / respiratory failuren/a
6hypertensive emergencyn/a
7high-demand / peri-operative stressmag 1
Coverage: 4/7 confounders with evidence
Tier: deep-scored (abstract-extracted) · 16 supporting references. See the discrimination table for all markers.
Assay & specimen
Class-level default (no specific cleared assay)— generic method inferred from analyte class; confirm against a specific product insert before use.
Specimen
Serum, plasma or urine
Collection tube
Serum separator (gold/red-top, SST) · Lithium heparin (green-top) · Sterile urine container
Method / principle
LC-MS/MS (targeted metabolomics) or enzymatic colorimetric where available
Reagent / substrate
Stable-isotope-labeled internal standard (MS); or enzyme-coupled Trinder reagent
Platform
LC-MS/MS; some automated chemistry
Turnaround · availability
Send-out / research · Specialized / research
Literature evidence(1)
- Improved Risk Prediction of Acute Myocardial Infarction in Patients With Stable Coronary Artery Disease Using an Amino Acid-Assisted Model.Cardiovascular therapeutics · 2024 · PMID 39742009 · doi