TY - JOUR
T1 - Magnetic Resonance Imaging of Intraplaque Hemorrhage and Plaque Lipid Content with Continued Lipid-Lowering Therapy
T2 - Results of a Magnetic Resonance Imaging Substudy in AIM-HIGH
AU - for the AIM-HIGH Carotid MRI Substudy Investigators
AU - Zhao, Xue Qiao
AU - Sun, Jie
AU - Hippe, Daniel S.
AU - Isquith, Daniel A.
AU - Canton, Gador
AU - Yamada, Kiyofumi
AU - Balu, Niranjan
AU - Crouse, John R.
AU - Anderson, Todd J.
AU - Huston, John
AU - O'Brien, Kevin D.
AU - Hatsukami, Thomas S.
AU - Yuan, Chun
N1 - Funding Information:
This study was supported in part by the NIH (R01 HL088214, R01 HL089504, R01 HL103609, R01 NS083503, R01 NS092207, UL1 TR002319) and the American Heart Association (17MCPRP33671077). Carotid coils were provided by GE Healthcare and Philips Healthcare. The content is solely the responsibilities of the authors and do not necessarily represent the official views of the NIH or the US Government.
Funding Information:
Mr. Hippe has received research grants from GE Healthcare, Philips Healthcare, and Toshiba America Medical Systems. Dr. Balu has received research grants from Philips Healthcare. Dr. Hatsukami has received research grants from Philips Healthcare. Dr. Yuan has received research grants from Philips Healthcare. All other authors have reported that they have no relationships relevant to the contents of this article to disclose.
Publisher Copyright:
© 2022 Lippincott Williams and Wilkins. All rights reserved.
PY - 2022/11/1
Y1 - 2022/11/1
N2 - Background: Intraplaque hemorrhage (IPH) is associated with plaque progression and ischemic events, and plaque lipid content (% lipid core) predicts the residual atherosclerotic cardiovascular disease risk. This study examined the impact of IPH on lipid content change in the setting of intensive lipid-lowering therapy. Methods: In total, 214 AIM-HIGH (Atherothrombosis Intervention in Metabolic Syndrome with Low High-Density Lipoprotein/High Triglycerides: Impact on Global Health Outcomes) participants with clinically established ASCVD and low high-density lipoprotein cholesterol received cartoid MRI at baseline and 2 years to assess changes in carotid morphology and composition. Patients were randomized to extended-release niacin or placebo, and all received simvastatin with optional ezetimibe as necessary to lower low-density lipoprotein cholesterol to 40 to 80 mg/dL. Changes in lipid content and carotid morphology were tested using the Wilcoxon signed-rank test. Differences between subjects with and without IPH and between subjects assigned extended-release niacin or placebo were tested using the Wilcoxon rank-sum test. Linear regression was used to test the association of IPH and lipid content changes after adjusting for clinical risk factors. Results: Among 156 patients (61±9 years; 81% men) with complete MRI, prior statin use: <1 year, 26%; 1 to 5 years, 37%; >5 years, 37%. Triglycerides and ApoB decreased significantly, whereas high-density lipoprotein cholesterol and ApoA1 increased significantly over time. Plaque lipid content was significantly reduced (-0.5±2.4 %/year, P = 0.017) without a significant difference between the 2 treatment groups. However, the lipid content increased in plaques with IPH but regressed in plaques without IPH (1.2±2.5 %/year versus -1.0±2.2, P = 0.006). Additionally, IPH was associated with a decrease in lumen area (-0.4±0.9 mm2/year versus 0.3±1.4, P = 0.033). IPH remained significantly associated with increase in lipid content in multivariable analysis (54.4%, 95% CI: 26.8, 88.0, P < 0.001). Conclusions: Carotid plaques under continued intensive lipid-lowering therapy moved toward stabilization. However, plaques with IPH showed greater increases in lipid content and greater decreases in lumen area than plaques without IPH. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01178320.
AB - Background: Intraplaque hemorrhage (IPH) is associated with plaque progression and ischemic events, and plaque lipid content (% lipid core) predicts the residual atherosclerotic cardiovascular disease risk. This study examined the impact of IPH on lipid content change in the setting of intensive lipid-lowering therapy. Methods: In total, 214 AIM-HIGH (Atherothrombosis Intervention in Metabolic Syndrome with Low High-Density Lipoprotein/High Triglycerides: Impact on Global Health Outcomes) participants with clinically established ASCVD and low high-density lipoprotein cholesterol received cartoid MRI at baseline and 2 years to assess changes in carotid morphology and composition. Patients were randomized to extended-release niacin or placebo, and all received simvastatin with optional ezetimibe as necessary to lower low-density lipoprotein cholesterol to 40 to 80 mg/dL. Changes in lipid content and carotid morphology were tested using the Wilcoxon signed-rank test. Differences between subjects with and without IPH and between subjects assigned extended-release niacin or placebo were tested using the Wilcoxon rank-sum test. Linear regression was used to test the association of IPH and lipid content changes after adjusting for clinical risk factors. Results: Among 156 patients (61±9 years; 81% men) with complete MRI, prior statin use: <1 year, 26%; 1 to 5 years, 37%; >5 years, 37%. Triglycerides and ApoB decreased significantly, whereas high-density lipoprotein cholesterol and ApoA1 increased significantly over time. Plaque lipid content was significantly reduced (-0.5±2.4 %/year, P = 0.017) without a significant difference between the 2 treatment groups. However, the lipid content increased in plaques with IPH but regressed in plaques without IPH (1.2±2.5 %/year versus -1.0±2.2, P = 0.006). Additionally, IPH was associated with a decrease in lumen area (-0.4±0.9 mm2/year versus 0.3±1.4, P = 0.033). IPH remained significantly associated with increase in lipid content in multivariable analysis (54.4%, 95% CI: 26.8, 88.0, P < 0.001). Conclusions: Carotid plaques under continued intensive lipid-lowering therapy moved toward stabilization. However, plaques with IPH showed greater increases in lipid content and greater decreases in lumen area than plaques without IPH. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01178320.
KW - atherosclerotic plaque
KW - cardiovascular disease
KW - carotid artery disease
KW - hemorrhage
KW - lipids
KW - magnetic resonance imaging
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U2 - 10.1161/CIRCIMAGING.122.014229
DO - 10.1161/CIRCIMAGING.122.014229
M3 - Article
C2 - 36378778
AN - SCOPUS:85141941356
SN - 1941-9651
VL - 15
SP - E014229
JO - Circulation: Cardiovascular Imaging
JF - Circulation: Cardiovascular Imaging
IS - 11
ER -