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Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
Plaque volume and plaque risk profile in diabetic vs. non-diabetic patients undergoing lipid-lowering therapy: a
Tomas Kovarnik1, Zhi Chen2, Gary S Mintz3
12nd Department of Medicine-Department of Cardiovascular Medicine, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, II. interni klinika VFN a 1. LF UK, U nemocnice 2, 128 08, Praha 2, Czech Republic. tomas.kovarnik@vfn.cz.
Insights
Patients with diabetes mellitus (DM) show faster coronary atherosclerosis progression and more advanced plaque phenotypes than non-diabetics, even with similar LDL cholesterol levels. Advanced plaque analysis reveals significant differences in disease progression between DM and non-DM patients.
Area of Science:
- Cardiovascular Medicine
- Diabetology
- Medical Imaging
Background:
- Coronary atherosclerosis progresses more rapidly in patients with diabetes mellitus (DM).
- DM patients experience higher morbidity and mortality from coronary atherosclerosis compared to non-diabetic (non-DM) patients.
- Lipid-lowering therapy is crucial for managing atherosclerosis, but its differential effects in DM versus non-DM patients require detailed investigation.
Purpose of the Study:
- To quantify and compare changes in coronary plaque volume and phenotype during lipid-lowering therapy in DM versus non-DM patients.
- To utilize advanced intracoronary imaging techniques for precise assessment of atherosclerosis progression.
- To identify specific plaque characteristics that differ between DM and non-DM patients under treatment.
Main Methods:
- Analysis of data from 61 stable angina patients in the PREDICT trial receiving intensive lipid-lowering therapy (40 mg rosuvastatin daily).
- Fusion of two-plane angiography and intravascular ultrasound virtual histology (IVUS-VH) for 3-D vascular wall reconstruction and tissue characterization.
- Calculation of frame-based plaque morphology indices and virtual histology analyses, including the Liverpool active plaque score (LAPS), in 698 vessel segments.
Main Results:
- DM patients showed significantly higher progression in mean plaque area (0.47 vs. 0.21 mm², p=0.001) and percent atheroma volume (0.7% vs. -1.4%, p=0.007) compared to non-DM patients.
- DM patients exhibited a greater increase in LAPS (0.23 vs. 0.13, p=0.018) and more Thin-Cap Fibro-Atheroma (TCFA) locations (20.3% vs. 12.5%, p=0.01).
- Despite similar LDL cholesterol levels achieved, plaque changes were more pronounced in pathological intimal thickening (PIT) and TCFA phenotypes in DM patients.
Conclusions:
- DM patients demonstrate advanced plaque phenotypes and accelerated atherosclerosis progression compared to non-DM patients, even when achieving similar LDL cholesterol levels.
- Detailed 3D analysis reveals significant differences in plaque dynamics between DM and non-DM individuals under lipid-lowering therapy.
- These findings underscore the need for tailored therapeutic strategies for atherosclerosis management in diabetic patients.
Background:
Coronary atherosclerosis progresses faster in patients with diabetes mellitus (DM) and causes higher morbidity and mortality in such patients compared to non-diabetics ones (non-DM). We quantify changes in plaque volume and plaque phenotype during lipid-lowering therapy in DM versus non-DM patients using advanced intracoronary imaging.
Methods:
We analyzed data from 61 patients with stable angina pectoris included to the PREDICT trial searching for prediction of plaque changes during intensive lipid-lowering therapy (40 mg rosuvastatin daily). Geometrically correct, fully 3-D representation of the vascular wall surfaces and intravascular ultrasound virtual histology (IVUS-VH) defined tissue characterization was obtained via fusion of two-plane angiography and IVUS-VH. Frame-based indices of plaque morphology and virtual histology analyses were computed and averaged in 5 mm long baseline/follow-up registered vessel segments covering the entire length of the two sequential pullbacks (baseline, 1-year). We analyzed 698 5-mm-long segments and calculated the Liverpool active plaque score (LAPS).
Results:
Despite reaching similar levels of LDL cholesterol (DM 2.12 ± 0.91 mmol/l, non-DM 1.8 ± 0.66 mmol/l, p = 0.21), DM patients experienced, compared to non-DM ones, higher progression of mean plaque area (0.47 ± 1.15 mm2 vs. 0.21 ± 0.97, p = 0.001), percent atheroma volume (0.7 ± 2.8% vs. - 1.4 ± 2.5%, p = 0.007), increase of LAPS (0.23 ± 1.66 vs. 0.13 ± 1.79, p = 0.018), and exhibited more locations with TCFA (Thin-Cap Fibro-Atheroma) plaque phenotype in 5 mm vessel segments (20.3% vs. 12.5%, p = 0.01). However, only non-DM patients reached significant decrease of LDL cholesterol. Plaque changes were more pronounced in PIT (pathologic intimal thickening) compared to TCFA with increased plaque area in both phenotypes in DM patients.
Conclusion:
Based on detailed 3D analysis, we found advanced plaque phenotype and further atherosclerosis progression in DM patients despite the same reached levels of LDLc as in non-DM patients. Trial registration ClinicalTrials.gov identifier: NCT01773512.
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