Landburg Precious P, Teerlink Tom, Muskiet Frits A J, Duits Ashley J, Schnog John-John B
Immunology Laboratory Department, Red Cross Blood Bank Foundation Curaçao, Curaçao, Netherlands Antilles.
Am J Hematol. 2008 Jul;83(7):577-9. doi: 10.1002/ajh.21184.
Plasma concentrations of asymmetric dimethylarginine (ADMA), an endogenous nitric oxide synthase inhibitor, are elevated in the clinically asymptomatic state of sickle cell disease (SCD). However, the role of ADMA during vaso-occlusive complications has not been defined. ADMA concentrations were determined in HbSS (n = 43) and HbSC (n = 25) patients with healthy blood donors (HbAA) as controls. In the clinically asymptomatic state ADMA concentrations were elevated in sickle cell patients as compared to healthy controls (HbSS 0.70 micromol/L, HbSC 0.54 micromol/L, HbAA 0.39 micromol/L) (P < 0.001). Yet plasma ADMA concentrations did not increase further at presentation with a painful crisis implicating no role of primary importance during vaso-occlusive crises.
内源性一氧化氮合酶抑制剂不对称二甲基精氨酸(ADMA)的血浆浓度在镰状细胞病(SCD)的临床无症状状态下会升高。然而,ADMA在血管闭塞性并发症期间的作用尚未明确。以健康献血者(HbAA)作为对照,测定了HbSS(n = 43)和HbSC(n = 25)患者的ADMA浓度。在临床无症状状态下,与健康对照相比,镰状细胞病患者的ADMA浓度升高(HbSS为0.70微摩尔/升,HbSC为0.54微摩尔/升,HbAA为0.39微摩尔/升)(P < 0.001)。然而,在出现疼痛危象时,血浆ADMA浓度并未进一步升高,这表明其在血管闭塞性危象期间没有至关重要的作用。