内皮型一氧化氮合酶(-786T>C)和内皮素-1 (5665G>T)基因多态性与镰状细胞性贫血血管功能障碍的关系

Gene regulation and systems biology Pub Date : 2016-07-28 eCollection Date: 2016-01-01 DOI:10.4137/GRSB.S38276
Wendell Vilas-Boas, Camylla V B Figueiredo, Thassila N Pitanga, Magda O S Carvalho, Rayra P Santiago, Sânzio S Santana, Caroline C Guarda, Angela M D Zanette, Bruno A V Cerqueira, Marilda S Gonçalves
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引用次数: 9

摘要

镰状细胞性贫血(SCA)患者存在血管并发症,内皮素-1 (ET-1)和内皮型一氧化氮合酶(eNOS)基因多态性与ET-1和一氧化氮紊乱有关。我们研究ET-1 5665G>T和eNOS -786T>C多态性与可溶性粘附分子(sVCAM-1和sICAM-1)、生化标志物和病史的关系。我们研究了101名SCA患者;eNOS小等位基因(C)携带者sVCAM-1水平最高,ET-1小等位基因携带者急性胸综合征(ACS)发生率较高。多因素分析提示ET-1基因对ACS预后有影响,eNOS基因与上呼吸道感染有关联。我们认为eNOS和ET-1基因多态性可以影响SCA的病理生理,并且SCA患者的eNOS变异可能对一氧化氮活性和血管改变很重要。我们发现ET-1小等位基因在ACS中存在关联,表明遗传筛查在SCA中的重要性。
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Endothelial Nitric Oxide Synthase (-786T>C) and Endothelin-1 (5665G>T) Gene Polymorphisms as Vascular Dysfunction Risk Factors in Sickle Cell Anemia.

Sickle cell anemia (SCA) patients have vascular complications, and polymorphisms in endothelin-1 (ET-1) and endothelial nitric oxide synthase (eNOS) genes were associated with ET-1 and nitric oxide disturbance. We investigate the association of ET-1 5665G>T and eNOS -786T>C polymorphisms with soluble adhesion molecules (sVCAM-1 and sICAM-1), biochemical markers, and medical history. We studied 101 SCA patients; carriers of eNOS minor allele (C) had the highest levels of sVCAM-1, and carriers of ET-1 minor allele had more occurrence of acute chest syndrome (ACS). The multivariate analysis suggested the influence of the ET-1 gene on ACS outcome and an association of the eNOS gene with upper respiratory tract infection. We suggest that eNOS and ET-1 gene polymorphisms can influence SCA pathophysiology and that eNOS variant in SCA patients might be important to nitric oxide activity and vascular alteration. We found an association of the ET-1 minor allele in ACS, showing the importance of genetic screening in SCA.

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