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Statin therapy and inflammation in patients with diabetes treated with high dose aspirin
Rahul Chaudhary1, Kevin P Bliden2, Jalaj Garg3
1Johns Hopkins University/Sinai Hospital of Baltimore, Baltimore, MD, USA.
Insights
Statin and aspirin therapy in diabetic patients with coronary artery disease (CAD) reduces blood thrombogenicity and inflammation. Urinary 11-dehydrothromboxane B2 (11-dh-TxB2) may help personalize statin treatment for better outcomes.
Area of Science:
- Cardiology
- Pharmacology
- Biomarkers
Background:
- Statin and aspirin are standard treatments for coronary artery disease (CAD) in diabetic patients.
- The impact of statins on blood thrombogenicity and inflammation in this population is not well understood.
Purpose of the Study:
- To investigate the effects of statin therapy on blood thrombogenicity and inflammation markers in diabetic patients with suspected CAD.
- To explore the relationship between statin use and specific biomarkers like urinary 11-dehydrothromboxane B2 (11-dh-TxB2).
Main Methods:
- 209 diabetic patients with suspected CAD undergoing cardiac catheterization were grouped by statin use.
- Measurements included urinary 11-dh-TxB2, lipid profiles, oxidized-LDL/β2GPI, and thrombogenicity assays (thrombelastography, aggregometry).
- Coronary artery disease severity was classified based on diameter stenosis.
Main Results:
- Patients on statins showed significantly lower levels of 11-dh-TxB2, collagen-induced aggregation, total cholesterol, LDL, oxidized-LDL, Apo B100, and ApoB100/A1 ratio.
- A lower proportion of statin users had high urinary 11-dh-TxB2 levels compared to non-users (25% vs. 57%, p=0.01).
- CAD severity was distributed as 66% severe, 19% moderate, and 15% no/minor CAD.
Conclusions:
- Statin therapy, in addition to aspirin, provides significant anti-inflammatory and antithrombotic benefits in diabetic patients with CAD.
- Urinary 11-dh-TxB2 emerges as a potential biomarker for tailoring statin therapy in this patient group.
Background:
Statin and aspirin form the therapeutic cornerstone in patients with coronary artery disease (CAD) and diabetes. Little is known about relationship of statins with blood thrombogenicity and inflammation in these patients.
Methods:
Two hundred nine consecutive patients with diabetes and suspected CAD undergoing elective cardiac catheterization were divided in groups based on statin treatment in the Multi-Analyte, Thrombogenic, and Genetic Markers Atherosclerosis study. Urinary 11-dehydrothromboxane B2 (11-dh-TxB2), lipid profile and oxLDL/β2GPI were measured by AspirinWorks™ ELISA assay, vertical density gradient ultracentrifugation and immunoassay respectively. Thrombelastography, and ADP- and collagen-induced light transmittance aggregometry assessed thrombogenicity. CAD was classified as none/minor [<20% diameter stenosis (DS)], moderate (20-75% DS), or severe (>75% DS).
Results:
Severe, moderate, and no CAD was observed in 66, 19, and 15% of patients respectively. Patients on statins had significantly lower 11-dh-TxB2, collagen-induced aggregation, total cholesterol, total LDL, LDL3, oxidized-LDL, Apo B100, and ApoB100/A1 ratio (p<0.01 for all). Statin therapy demonstrated a lower proportion of patients with high urinary 11-dh-TxB2 (>1500pg 11-dh-TxB2/mg creatinine) (25 vs. 57%, p=0.01).
Conclusion:
Statins along with aspirin, confers additional anti-inflammatory and antithrombotic effect in diabetics with CAD. Urinary 11-dh-TxB2 may be a useful biomarker for personalizing statin therapy.
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