冠状动脉微血管功能障碍中的单核苷酸多态性
Single Nucleotide Polymorphisms in Coronary Microvascular Dysfunction.
作者信息
Stein Andrew P, Harder Jonathan, Holmes Henry R, Merz C Noel Bairey, Pepine Carl J, Keeley Ellen C
机构信息
Department of Medicine University of Florida Gainesville FL USA.
Barbra Streisand Women's Heart Center Smidt Heart Institute, Cedars-Sinai Medical Center Los Angeles CA USA.
出版信息
J Am Heart Assoc. 2024 Feb 20;13(4):e032137. doi: 10.1161/JAHA.123.032137. Epub 2024 Feb 13.
Coronary microvascular dysfunction is an underdiagnosed pathologic process that is associated with adverse clinical outcomes. There are data to suggest that coronary microvascular dysfunction, in some cases, may be genetically determined. We present an updated review of single nucleotide polymorphisms in coronary microvascular dysfunction.
冠状动脉微血管功能障碍是一种诊断不足的病理过程，与不良临床结局相关。有数据表明，在某些情况下，冠状动脉微血管功能障碍可能由基因决定。我们对冠状动脉微血管功能障碍中的单核苷酸多态性进行了最新综述。
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