Awoda Shiekh, Daak Ahmed A, Husain Nazik Elmalaika, Ghebremeskel Kebreab, Elbashir Mustafa I
Department of Medical Biochemistry, Faculty of Medicine, University of Khartoum, Alghasr Street, Khartoum, Sudan.
College of Medical Laboratory Sciences, Sudan University of Science& Technology, Khartoum, Sudan.
BMC Hematol. 2017 Nov 9;17:18. doi: 10.1186/s12878-017-0089-5. eCollection 2017.
It has been reported that patients with SCD do have an abnormal coagulation profile. Coagulopathy is thought to be one of the key factors that contribute to the vaso-occlusive crisis that characterises sickle cell disease (SCD). In this study, we investigated whether Sudanese sickle cell patients have an abnormal coagulation profile. In addition, the effect of treatment with either omega-3 fatty acids or hydroxyurea on coagulation profile was assessed.
Homozygous SCD patients untreated ( = 52), omega-3 treated ( = 44), hydroxyurea (HU) treated ( = 8) and healthy (HbAA) controls ( = 52) matched for age (4-20 years), gender and socioeconomic status were enrolled. Patients on omega-3 fatty acids, according to age, received one to four capsules containing 277.8 mg DHA and 39.0 mg eicosapentnoic. Patients on Hydroxyurea were in on dosage more than 20 mg/kg/day. The steady state levels of the coagulation parameters and the effect of the treatments with either HU or omega-3 fatty acids on markers of coagulation were investigated.
Compared to the healthy controls, treated and untreated HbSS patients had lower hemoglobin, plasma Protein C, proteins S and higher white blood cell count (WBC), platelets count (PLTs) and plasma D-dimer levels,( < 0.05). In comparison to untreated HbSS, treatment with neither omega-3 nor HU had effect on the WBC, plasma proteins C and S, ( > 0.05). HU treated group had a lower PLTs count compared to HbSS untreated group ( < 0.5). The prothrombin and activated partial thromboplastin times and international normalized ratio (INR) of untreated patients are significantly higher than n-3 treated, HU-treated patients and health controls, ( < 0.05). Patients treated with omega-3 had lowered D-dimer levels in comparison to HU-treated and untreated HbSS patients, ( < 0.001).
This study provides evidence that Sudanes patients have abnormal coagulation profile and treatment with either HU or omega-3 fatty acids might partially ameliorate SCD-associated chronic coagulopathic state.
据报道,镰状细胞病(SCD)患者确实存在凝血指标异常。凝血功能障碍被认为是导致镰状细胞病(SCD)特征性血管闭塞性危机的关键因素之一。在本研究中,我们调查了苏丹镰状细胞病患者是否存在凝血指标异常。此外,还评估了ω-3脂肪酸或羟基脲治疗对凝血指标的影响。
纳入年龄(4 - 20岁)、性别和社会经济地位相匹配的未治疗的纯合子SCD患者(n = 52)、ω-3治疗组(n = 44)、羟基脲(HU)治疗组(n = 8)和健康(HbAA)对照组(n = 52)。根据年龄,服用ω-3脂肪酸的患者每天服用1至4粒胶囊,每粒含277.8毫克DHA和39.0毫克二十碳五烯酸。服用羟基脲的患者剂量超过20毫克/千克/天。研究了凝血参数的稳态水平以及HU或ω-3脂肪酸治疗对凝血标志物的影响。
与健康对照组相比,接受治疗和未接受治疗的HbSS患者血红蛋白、血浆蛋白C、蛋白S水平较低,白细胞计数(WBC)、血小板计数(PLTs)和血浆D - 二聚体水平较高(P < 0.05)。与未治疗的HbSS相比,ω-3和HU治疗对WBC、血浆蛋白C和S均无影响(P > 0.05)。与未治疗的HbSS组相比,HU治疗组的PLTs计数较低(P < 0.5)。未治疗患者的凝血酶原时间、活化部分凝血活酶时间和国际标准化比值(INR)显著高于ω-3治疗组、HU治疗组患者和健康对照组(P < 0.05)。与HU治疗组和未治疗的HbSS患者相比,ω-3治疗的患者D - 二聚体水平降低(P < 0.001)。
本研究提供了证据表明苏丹患者存在凝血指标异常,HU或ω-3脂肪酸治疗可能部分改善SCD相关的慢性凝血功能障碍状态。