Key result
Insulin glargine did not significantly reduce the annualized progression of maximum carotid intima-media thickness compared to standard care (difference -0.0030 mm/year, p=0.145), and n-3FA supplementation had no effect compared to placebo.
Why the study?
Does insulin glargine and n-3FA reduce CIMT progression in people with dysglycemia at high risk for cardiovascular events?
RCT (n=1,184)
PROBE (open-label) for insulin glargine, double-blind for n-3FA
Automated telephone randomization system (varying block sizes, stratified by center)
Yes
Does insulin glargine and n-3FA reduce CIMT progression in people with dysglycemia at high risk for cardiovascular events?
Mean Difference: -0.003
Absolute Event Rate: 0.0234% vs 0.0264%
p-value: p=0.145
No support for insulin glargine or n-3FA to slow CIMT progression; confirms neutral effects on this surrogate in high-risk dysglycemia.
OBJECTIVE: To evaluate the effects of insulin glargine and n-3 polyunsaturated fatty acid (n-3FA) supplements on carotid intima-media thickness (CIMT). RESEARCH DESIGN AND METHODS: We enrolled 1,184 people with cardiovascular (CV) disease and/or CV risk factors plus impaired fasting glucose, impaired glucose tolerance, or early type 2 diabetes in a randomized multicenter 2 × 2 factorial design trial. Participants received open-label insulin glargine (targeting fasting glucose levels ≤ 5.3 mmol/L [95 mg/dL]) or standard glycemic care and double-blind therapy with a 1-g capsule of n-3FA or placebo. The primary trial outcome was the annualized rate of change in maximum CIMT for the common carotid, bifurcation, and internal carotid artery segments. Secondary outcomes were the annualized rates of change in maximum CIMT for the common carotid and the common carotid plus bifurcation, respectively. Baseline followed by annual ultrasounds were obtained during a median follow-up of 4.9 years. RESULTS: Compared with standard care, insulin glargine reduced the primary CIMT outcome, but the difference was not statistically significant (difference = 0.0030 ± 0.0021 mm/year; P = 0.145) and significantly reduced the secondary CIMT outcomes (differences of 0.0033 ± 0.0017 mm/year [P = 0.049] and 0.0045 ± 0.0021 mm/year [P = 0.032], respectively). There were no differences in the primary and secondary outcomes between the n-3FA supplement and placebo groups. CONCLUSIONS: In people with CV disease and/or CV risk factors and dysglycemia, insulin glargine used to target normoglycemia modestly reduced CIMT progression, whereas daily supplementation with n-3FA had no effect on CIMT progression.
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Lonn et al. (2013) conducted an RCT in Dysglycemia at high risk for cardiovascular events (n=1,184). Insulin glargine and n-3 polyunsaturated fatty acids vs. Standard glycemic care and placebo was evaluated on Annualized rate of change in maximum carotid intima-media thickness (CIMT) for 12 carotid artery segments (MD -0.0030 mm/year, p=0.145). Insulin glargine did not significantly reduce the annualized progression of maximum carotid intima-media thickness compared to standard care (difference -0.0030 mm/year, p=0.145), and n-3FA supplementation had no effect compared to placebo.
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