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.
Endothelial Nitric Oxide Synthase (-786T>C) and Endothelin-1 (5665G>T) Gene Polymorphisms as Vascular Dysfunction Risk Factors in Sickle Cell Anemia.
内皮型一氧化氮合酶 (-786T>C) 和内皮素-1 (5665G>T) 基因多态性作为镰状细胞贫血血管功能障碍的危险因素
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作者:Vilas-Boas Wendell, Figueiredo Camylla V B, Pitanga Thassila N, Carvalho Magda O S, Santiago Rayra P, Santana Sânzio S, Guarda Caroline C, Zanette Angela M D, Cerqueira Bruno A V, Gonçalves Marilda S
| 期刊: | Gene Regul Syst Bio | 影响因子: | 0.000 |
| 时间: | 2016 | 起止号: | 2016 Jul 28; 10:67-72 |
| doi: | 10.4137/GRSB.S38276 | 研究方向: | 细胞生物学 |
| 疾病类型: | 贫血 | ||
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