Progression of vascular calcification is increased with statin use in the Veterans Affairs Diabetes Trial (VADT).

OBJECTIVE: To determine the effect of statin use on progression of vascular calcification in type 2 diabetes (T2DM). RESEARCH DESIGN AND METHODS: Progression of coronary artery calcification (CAC) and abdominal aortic artery calcification (AAC) was assessed according to the frequency of statin use in 197 participants with T2DM.
RESULTS: After adjustment for baseline CAC and other confounders, progression of CAC was significantly higher in more frequent statin users than in less frequent users (mean ± SE, 8.2 ± 0.5 mm(3) vs. 4.2 ± 1.1 mm(3); P < 0.01). AAC progression was in general not significantly increased with more frequent statin use; in a subgroup of participants initially not receiving statins, however, progression of both CAC and AAC was significantly increased in frequent statin users.
CONCLUSIONS: More frequent statin use is associated with accelerated CAC in T2DM patients with advanced atherosclerosis.

The role of statins in prevention of cardiovascular disease (CVD) in type 2 diabetes (T2DM) is well established. Despite the wide use of statins, however, calcific atherosclerosis is accelerated in T2DM and is associated with increased risk of CVD morbidity and mortality in this population (1). The purpose of the current study was to determine the effect of statin use on progression of vascular calcification in T2DM participants with advanced atherosclerosis.

RESEARCH DESIGN AND METHODS

The Risk Factors, Atherosclerosis, and Clinical Events in Diabetes (RACED) study is a seven-site substudy (1) of the Veterans Affairs Diabetes Trial (VADT) (2). The designs of both studies have been previously described (3–5). As part of this study, baseline and follow-up coronary artery calcification (CAC) and abdominal aortic artery calcification (AAC) volumetric scores were assessed by computed tomography, and change was estimated as the difference between square root transformation (SQRT) of the these scores (5,6). Multiple linear regression models of vascular calcium progression were adjusted for age, diabetes duration, ethnicity or race (non-Hispanic whites vs. others), current smoking, baseline CAC or AAC, CVD events (before and during the study), treatment assignment (intensive vs. standard), baseline and change in BMI, HbA1c, systolic and diastolic blood pressures, LDL, HDL, triglycerides, and time in the study. Sex was not included as one of the covariates because only 7% (n = 14) of the study population were women, and the results did not change appreciably with their exclusion from analyses.

RESULTS

The study included 197 participants with T2DM (mean duration, 12 ± 8 years), a mean age of 61 ± 9 years, and extensive atherosclerosis at baseline (median [25th–75th percentile] Agatston score; CAC, 258 [18-872]; AAC, 888 [159-3,831]). Follow-up calcium scans were completed on average 4.6 years later. Optimizing lipid levels was a critical part of the VADT (2); use of statins was therefore encouraged and carefully documented during the study. Participants underwent 14–28 VADT study visits, 3 months apart. At each visit, information regarding concomitant medications, including statin use, was updated. At the baseline examination, 61% (n = 121) of participants were taking statin agents (simvastatin, 70%; lovastatin, 25%; and atorvastatin, 5%). During the study, 82% of subjects (n = 161) reported frequent statin use in >50% of the visits, with a median use of 95% (25th–75th percentile, 85–100%). Eighteen percent (n = 36) reported statin use in ≤50% of the visits (median [25th–75th percentile], 14% [0–38%]).

More frequent statin users had a higher prevalence of previous CVD than did others (41% vs. 19%; P = 0.01). There were no other significant differences between the groups at baseline (Supplementary Table 1). At the end of the study, more frequent statin users had lower total cholesterol (mean ± SD, 151 ± 34 vs. 167 ± 37 mg/dL; P = 0.01), LDL cholesterol (79 ± 28 vs. 91 ± 28 mg/dL; P = 0.01), and total cholesterol/HDL ratio (3.6 ± 1.1 vs. 4.1 ± 1.4 mg/dL; P = 0.05) compared with less frequent users. There were no significant differences in the incidence of CVD events during the study between categories of statin use (30% vs. 19%; P = 0.18); however, progression of CAC was significantly (P < 0.01) greater with more frequent statin use (Fig. 1), and adjustment for relevant covariates did not change the results. Because people with previous or incident CVD events may have accelerated progression of vascular calcification, we evaluated the effect of statins in the cohort after excluding these individuals. In these remaining participants (n = 105), those with frequent statin use had significantly greater CAC progression (7.1 ± 5.9 vs. 4.3 ± 5.4 mm3; P = 0.03). Progression of AAC was not significantly different in the whole group (Fig. 1); however, in those not receiving statins at the baseline examination (n = 76 with CAC and n = 73 with AAC scans, respectively), after adjustment for age and baseline calcium, progressions of both CAC and AAC were significantly higher in those who subsequently reported frequent statin use compared with less frequent users (CAC progression, 7.9 ± 0.8 vs. 3.5 ± 1.0 mm3; P < 0.01; AAC progression, 11.9 ± 1.3 vs. 7.6 ± 1.6 mm3; P = 0.04).

Figure 1

Baseline, follow-up, and progression of CAC (A) and AAC (B) according to reported statin use. Volume scores at baseline and follow-up are SQRT values to stabilize interscan variability across the range of coronary calcium as reported by Hokanson et al. (6). Progression is the difference in SQRT volume scores of follow-up and baseline values. Data presented are means ± SE. White bars represent less frequent statin use (in ≤50% of the visits during the study); black bars represent frequent statin use (in >50% of the visits during the study).

CONCLUSIONS

In this cohort of T2DM patients with advanced atherosclerosis, we found that more frequent statin use was associated with accelerated progression of CAC. These findings are consistent with those reported in a previous study of T2DM participants without previous coronary artery disease (7). Results of this earlier study were believed to result from higher baseline CAC scores and insufficient lowering of LDL at follow-up in the statin users (7). In our study, however, there were no significant differences in baseline CAC or AAC according to statin use (Supplementary Table 1). In addition, at the end of the study more frequent statin users had significantly lower and nearly optimal LDL-cholesterol levels. Moreover, adjustment for baseline and on-trial risk factors, including LDL cholesterol and baseline CAC, did not explain the greater CAC progression in frequent statin users.

Randomized controlled trials in largely nondiabetic populations with no previous coronary artery disease demonstrated that, despite potent lipid-lowering effects, statin agents do not reduce the progression of CAC (8) or AAC (9). In fact, there was a trend toward progression of CAC with statin treatment in several studies (9–11). We now demonstrate that even in a setting of optimal lipid lowering and similar baseline CAC and AAC, statin agents promote calcification in T2DM subjects with advanced atherosclerosis. Because the variation in progression of AAC scores is greater, it is possible that the lack of significantly greater AAC progression with statin use is a sample size issue. Among those not initially on statins at baseline, however, the magnitude of AAC progression in those with subsequent frequent statin use was large enough to achieve statistical significance.

Statins have been implicated in calcification of vascular smooth muscle cells and mesenchymal cells (12,13). Statins also lower the lipid-rich core of atherosclerotic plaques and may enhance the density of calcification (14) as part of a healing process, potentially contributing to plaque stabilization and decreased CVD events. Alternatively, accelerated progression of calcified atherosclerosis in T2DM by statins may have the effect of lessening these medications’ overall benefit. Long-term follow-up in this cohort will help determine whether accelerated CAC and AAC progression in statin users is associated with more or fewer CVD events compared with statin users with less progression.