Peršić Viktor, Raljević Damir, Markova-Car Elitza, Cindrić Leon, Miškulin Rajko, Žuvić Marta, Kraljević Pavelić Sandra
Department of Medical Rehabilitation, Medical Faculty, University of Rijeka, Rijeka, Croatia.
Division of Cardiology, Hospital for Medical Rehabilitation of the Heart and Lung Diseases and Rheumatism "Thalassotherapia-Opatija", Opatija, Croatia.
Ann Transl Med. 2019 Aug;7(16):374. doi: 10.21037/atm.2019.07.49.
Cardiovascular diseases (CVD) are among leading causes of death worldwide and amongst CVD, coronary artery disease (CAD) accounts for almost half of all cardiovascular deaths as the most common cause of death in the developed world. Vitamin D and the vitamin D-binding protein (VDBP) have been studied as possible CAD pathogenesis factors but literature data provide opposing evidence on their role in CAD. Herein we aimed to present novel evidence on the association of two VDBP polymorphisms (rs4588) and (rs7041) with CAD in patients after acute myocardial infarction and study possible correlations of these polymorphisms with 25-hydroxyvitamin D [25(OH)D] serum levels.
The cross-section genotyping study included 155 subjects with CAD upon acute myocardial infarct and 104 control subjects. All patients and control group were Caucasians of European descent. VDBP polymorphisms (rs4588) and (rs7041) were studied by use of RT-PCR. Liquid chromatography, tandem mass spectrometry (LC-MS/MS) method was used for measurement of vitamin D in the serum.
Association of the VDBP (rs4588) T/T genotype with CAD patients after acute MI and correlation of VDBP (rs4588) genotype G/G with higher levels of total vitamin D were found. No correlation of 25(OH)D serum levels with CAD were established but the multivariate logistic regression modelling enabled association of total vitamin D level and VDBP (rs4588) T/T genotype with CAD and anteroseptal myocardial infarction (ASMI) CAD occurrence.
Obtained data speak in favor to the VDBP (rs4588) T/T genotype as a susceptibility factor for anteroseptal myocardial infarction where the same genotype showed to be generally more prevalent in smokers.
心血管疾病(CVD)是全球主要死因之一,在心血管疾病中,冠状动脉疾病(CAD)占所有心血管死亡的近一半,是发达国家最常见的死因。维生素D和维生素D结合蛋白(VDBP)已被作为CAD发病机制的可能因素进行研究,但文献数据对它们在CAD中的作用提供了相互矛盾的证据。在此,我们旨在提供关于两种VDBP多态性(rs4588)和(rs7041)与急性心肌梗死后患者CAD关联的新证据,并研究这些多态性与25-羟基维生素D [25(OH)D]血清水平的可能相关性。
横断面基因分型研究包括155例急性心肌梗死伴CAD的受试者和104例对照受试者。所有患者和对照组均为欧洲血统的白种人。通过RT-PCR研究VDBP多态性(rs4588)和(rs7041)。采用液相色谱-串联质谱(LC-MS/MS)法测定血清中的维生素D。
发现VDBP(rs4588)T/T基因型与急性心肌梗死后CAD患者相关,VDBP(rs4588)基因型G/G与总维生素D水平较高相关。未确定25(OH)D血清水平与CAD的相关性,但多因素逻辑回归模型显示总维生素D水平和VDBP(rs4588)T/T基因型与CAD及前间隔心肌梗死(ASMI)CAD的发生相关。
获得的数据支持VDBP(rs4588)T/T基因型是前间隔心肌梗死的易感因素,同一基因型在吸烟者中通常更为普遍。