Beyond early LDL cholesterol lowering to prevent coronary atherosclerosis in familial hypercholesterolaemia

被引:16
作者
Ibrahim, Shirin [1 ]
Reeskamp, Laurens F. [1 ]
de Goeij, Jim N. [1 ]
Hovingh, G. Kees [1 ]
Planken, R. Nils [2 ]
Bax, Willem A. [3 ]
Min, James K. [4 ]
Earls, James P. [4 ,5 ]
Knaapen, Paul [6 ]
Wiegman, Albert [7 ]
Stroes, Erik S. G. [1 ]
Nurmohamed, Nick S. [1 ,5 ,6 ]
机构
[1] Univ Amsterdam, Dept Vasc Med, Amsterdam UMC, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Dept Radiol & Nucl Med, Amsterdam UMC, Amsterdam, Netherlands
[3] Northwest Clin, Dept Internal Med, Alkmaar, Netherlands
[4] Cleerly Inc, Denver, CO USA
[5] George Washington Univ, Sch Med, 2150 Penn Ave NW, Washington, DC 20037 USA
[6] Vrije Univ Amsterdam, Dept Cardiol, Amsterdam UMC, Boelelaan 1117, NL-1081 HV Amsterdam, Netherlands
[7] Univ Amsterdam, Dept Paediat, Amsterdam UMC, Amsterdam, Netherlands
关键词
Familial hypercholesterolaemia; Cumulative LDL cholesterol exposure; Coronary plaque burden; CCTA; AI-QCT; COMPUTED-TOMOGRAPHY; CARDIOVASCULAR-DISEASE; ASYMPTOMATIC PATIENTS; STATIN THERAPY; RISK; CHILDREN; ANGIOGRAPHY; EZETIMIBE; ADULTHOOD; EXPOSURE;
D O I
10.1093/eurjpc/zwae028
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Familial hypercholesterolaemia (FH) patients are subjected to a high lifetime exposure to low density lipoprotein cholesterol (LDL-C), despite use of lipid-lowering therapy (LLT). This study aimed to quantify the extent of subclinical atherosclerosis and to evaluate the association between lifetime cumulative LDL-C exposure and coronary atherosclerosis in young FH patients. Methods and results Familial hypercholesterolaemia patients, divided into a subgroup of early treated (LLT initiated <25 years) and late treated (LLT initiated >= 25 years) patients, and an age- and sex-matched unaffected control group, underwent coronary CT angiography (CCTA) with artificial intelligence-guided analysis. Ninety genetically diagnosed FH patients and 45 unaffected volunteers (mean age 41 +/- 3 years, 51 (38%) female) were included. Familial hypercholesterolaemia patients had higher cumulative LDL-C exposure (181 +/- 54 vs. 105 +/- 33 mmol/L & lowast; years) and higher prevalence of coronary plaque compared with controls (46 [51%] vs. 10 [22%], OR 3.66 [95%CI 1.62-8.27]). Every 75 mmol/L & lowast; years cumulative exposure to LDL-C was associated with a doubling in per cent atheroma volume (total plaque volume divided by total vessel volume). Early treated patients had a modestly lower cumulative LDL-C exposure compared with late treated FH patients (167 +/- 41 vs. 194 +/- 61 mmol/L & lowast; years; P = 0.045), without significant difference in coronary atherosclerosis. Familial hypercholesterolaemia patients with above-median cumulative LDL-C exposure had significantly higher plaque prevalence (OR 3.62 [95%CI 1.62-8.27]; P = 0.001), compared with patients with below-median exposure. Conclusion Lifetime exposure to LDL-C determines coronary plaque burden in FH, underlining the need of early as well as potent treatment initiation. Periodic CCTA may offer a unique opportunity to monitor coronary atherosclerosis and personalize treatment in FH.
引用
收藏
页码:892 / 900
页数:9
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