Lipid-lowering Therapies in Myositis

被引:4
作者
Mizus, Marisa C. [1 ]
Tiniakou, Eleni [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Div Rheumatol, Ctr Tower,5200 Eastern Ave, Baltimore, MD 21224 USA
关键词
Lipid-lowering therapy; Myositis; Idiopathic inflammatory myopathy; Statins; PCSK9; inhibitors; Atherosclerotic cardiovascular disease; HMGCR; DENSITY-LIPOPROTEIN CHOLESTEROL; CORONARY-ARTERY-DISEASE; HEALED MYOCARDIAL-INFARCTION; STATIN-ASSOCIATED MYOPATHY; CARDIOVASCULAR RISK; RHEUMATOID-ARTHRITIS; MONOCLONAL-ANTIBODY; ADVERSE EVENTS; PRIMARY HYPERCHOLESTEROLEMIA; METABOLIC SYNDROME;
D O I
10.1007/s11926-020-00942-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of Review The use of lipid-lowering therapies in patients with idiopathic inflammatory myopathies (IIM) is complicated and there are no guidelines for diagnosing, monitoring, or treating atherosclerotic cardiovascular disease (ASCVD) in this group of patients. Recent Findings The use of lipid-lowering therapies, especially statins, is recommended in patients with increased risk for ASCVD, which includes patients with inflammatory diseases, based on recent American College of Cardiology/American Heart Association (ACC/AHA) guidelines for ASCVD management. Summary There is accumulating evidence that patients with IIM are at increased risk for ASCVD, similar to other inflammatory diseases. Lipid-lowering therapies have side effects that may be pronounced or confounding in myositis patients, potentially limiting their use. Statins are specifically contraindicated in patients with anti 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR) antibodies. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors have been shown to be safe and potentially beneficial in patients with IIM. Here, we propose a framework for (1) ASCVD risk assessment and treatment based on ACC/AHA ASCVD primary prevention guidelines; (2) myositis disease monitoring while undergoing lipid-lowering therapy; and (3) management of statin intolerance, including, indications for the use of PCSK9 inhibitors.
引用
收藏
页数:13
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