Haybar Habib, Khodadi Elahe, Zibara Kazem, Saki Najmaldin
Atherosclerosis Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Research Center of Thalassemia & Hemoglobinopathy, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Cardiovasc Hematol Disord Drug Targets. 2018;18(2):153-161. doi: 10.2174/1871529X18666180326121239.
Ischemia is a multifactorial disorder in which several genetic and environmental factors are involved. Platelets are the major causative agents of this disease because their elevated activity and aggregation would increase the risk of atherosclerosis and thrombosis, as well as ischemia. A number of polymorphisms in platelet receptors can increase the risk of ischemia and single-nucleotide polymorphisms (SNPs) have been detected in platelets. In addition, polymorphisms in other genes have been shown to cause platelet adhesion and aggregation that plays a role in ischemia. Patients respond differently to anti-platelet drugs which are used to treat patients with ischemia. Polymorphisms affect patients' responses to anti-platelet drugs, for instance, by increasing platelet activity and causing resistance of platelets to these drugs. Diagnosis of these polymorphisms can greatly contribute to better prediction of prognosis and response to treatment of patients, leading to more effective therapeutic strategies and a proper approach to ischemia.
In this review, we have evaluated the role of polymorphisms involved in platelet activation and development of ischemia.
缺血是一种多因素疾病,涉及多种遗传和环境因素。血小板是这种疾病的主要致病因素,因为其活性和聚集性升高会增加动脉粥样硬化、血栓形成以及缺血的风险。血小板受体中的一些多态性可增加缺血风险,并且已在血小板中检测到单核苷酸多态性(SNP)。此外,其他基因中的多态性已被证明可导致血小板黏附和聚集,这在缺血中起作用。患者对用于治疗缺血患者的抗血小板药物反应不同。多态性会影响患者对抗血小板药物的反应,例如,通过增加血小板活性并导致血小板对这些药物产生耐药性。诊断这些多态性可极大地有助于更好地预测患者的预后和对治疗的反应,从而产生更有效的治疗策略和针对缺血的适当方法。
在本综述中,我们评估了参与血小板活化和缺血发展的多态性的作用。