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phosphatidylethanolamine
Pathway / Platelet adhesion & activation

phosphatidylethanolamine

lipid

Phosphatidylethanolamine dysregulation in platelets and monocytes contributes to platelet dysfunction and pro-thrombotic extracellular vesicle release in Type 1 MI.

Pathway placement
Cascade stepPlatelet adhesion & activation
Confidencehigh
RationalePhospholipid altered in MI monocytes and platelets; extracellular vesicle thrombotic marker; platelet dysfunction in MI.
Also acts inLipid entry/oxidation, Myocardial injury
Druggability
Not assessed (no mapped human gene target).

Type I vs Type II discrimination

ScoresLow-confidence (proxy)
R — rupture / Type-I
71
C — confounder / Type-II
78
A — assay feasibility
40
E — evidence strength
31
T1DI (composite)
6
Specificity differential (R−C)-7
Confounder panel (Type-II drivers)
No confounder evidence retrieved.
Tier: light (literature co-occurrence proxy — lower confidence). 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 or plasma (EDTA to limit oxidation)
Collection tube
K2/K3-EDTA (lavender-top) · Serum separator (gold/red-top, SST)
Method / principle
LC-MS/MS lipidomics (targeted or shotgun)
Reagent / substrate
Deuterated lipid-class internal standards; MS/MS transitions
Platform
LC-MS/MS
Turnaround · availability
Research · Research-only

Literature evidence(11)