Key result
ApoB reduction in statin-treated diabetic CAD is linked to maxLCBI 4mm regression in ~61% of patients.
Why the study?
Because apolipoprotein B is present on both triglyceride-rich lipoproteins and LDL particles, circulating ApoB may associate with diabetic coronary atherosclerosis.
Does a reduction in ApoB levels improve coronary atheroma progression and instability in statin-treated type 2 diabetic patients with CAD?
RCT (n=78)
randomized
Does a reduction in ApoB levels improve coronary atheroma progression and instability in statin-treated type 2 diabetic patients with CAD?
Odds Ratio: 0.92 (95% CI 0.87–0.98)
Absolute Event Rate: 61.1% vs 31%
p-value: p=0.01
In statin-treated type 2 diabetic patients with CAD, a reduction in ApoB levels is associated with greater delipidation of coronary atherosclerosis, suggesting a potential anti-atherosclerotic effect.
ApoB reduction was associated with greater plaque regression in this cohort; hypothesis-generating for targeted ApoB therapy in statin-treated diabetic CAD.
BACKGROUND Type 2 diabetic patients exhibited an increased secretion of triglyceride-rich lipoproteins and low HDL-C levels with a greater amount of small dense LDL. Given that apolipoprotein B (ApoB), a proatherogenic lipoprotein, exists at both triglyceride-rich lipoproteins and LDL particles, circulating ApoB may associate with diabetic coronary atherosclerosis. METHODS The OPTIMAL study was a prospective randomized-controlled study which employed serial NIRS/IVUS imaging to evaluate the efficacy of glycemic control on coronary atherosclerosis in 94 statin-treated type 2 diabetic patients with CAD (UMIN000036721). Of these, 78 patients with both serial ApoB levels and NIRS/IVUS images at baseline and week 48 were analyzed. NIRS/IVUS-derived plaque measures were compared in those with and without any reduction of ApoB levels. RESULTS All of study subjects received a statin, and 60.6% of study subjects exhibited any reduction of ApoB levels. There was no significant difference in the atheroma progression rate between two groups (-0.27±0.15% vs. -0.33±0.51%, p=0.44). However, patients with any reduction of ApoB levels exhibited a greater frequency of change in maxLCBI 4mm (-13.4±22.2% vs. 70.3±28.7%, p=0.03) and maxLCBI 4mm regression (61.1±0.08 vs. 31.0±0.09%, p=0.02). Multivariate analysis demonstrated change in ApoB as an independent factor associated with maxLCBI 4mm regression (OR=0.92, 95%CI=0.87-0.98, p=0.01). CONCLUSIONS In statin-treated type 2 diabetic patients with CAD, a greater delipidation of coronary atherosclerosis was observed in association with a reduction of ApoB levels. The current findings indicate a potential anti-atherosclerotic effect of lowering ApoB levels, which may ultimately mitigate a future coronary events' risks in statin-treated type 2 diabetic patients with CAD.
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Funabashi et al. (2025) conducted an RCT in Type 2 diabetes with coronary artery disease (n=78). Reduction of ApoB levels vs. No reduction of ApoB levels was evaluated on maxLCBI 4mm regression (OR 0.92, 95% CI 0.87-0.98, p=0.01).
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