Coagulation profile of Sudanese children with homozygous sickle cell disease and the effect of treatment with omega-3 fatty acid on the coagulation parameters.

Q2 Medicine BMC Hematology Pub Date : 2017-11-09 eCollection Date: 2017-01-01 DOI:10.1186/s12878-017-0089-5
Shiekh Awoda, Ahmed A Daak, Nazik Elmalaika Husain, Kebreab Ghebremeskel, Mustafa I Elbashir
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引用次数: 3

Abstract

Background: 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.

Methods: Homozygous SCD patients untreated (n = 52), omega-3 treated (n = 44), hydroxyurea (HU) treated (n = 8) and healthy (HbAA) controls (n = 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.

Results: 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,(p < 0.05). In comparison to untreated HbSS, treatment with neither omega-3 nor HU had effect on the WBC, plasma proteins C and S, (p > 0.05). HU treated group had a lower PLTs count compared to HbSS untreated group (p < 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, (p < 0.05). Patients treated with omega-3 had lowered D-dimer levels in comparison to HU-treated and untreated HbSS patients, (p < 0.001).

Conclusion: 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.

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苏丹纯合子镰状细胞病患儿凝血特征及omega-3脂肪酸治疗对凝血参数的影响
背景:据报道,SCD患者确实存在凝血功能异常。凝血功能障碍被认为是导致镰状细胞病(SCD)血管闭塞危象的关键因素之一。在这项研究中,我们调查了苏丹镰状细胞患者是否有异常的凝血特征。此外,还评估了omega-3脂肪酸或羟基脲治疗对凝血功能的影响。方法:纳入未经治疗(n = 52)、omega-3治疗(n = 44)、羟基脲治疗(n = 8)和健康(HbAA)对照组(n = 52),年龄(4-20岁)、性别和社会经济地位相匹配。服用omega-3脂肪酸的患者,根据年龄,服用一到四粒含有277.8毫克DHA和39.0毫克二十碳五烯酸的胶囊。羟基脲剂量大于20mg /kg/d。研究了凝血参数的稳态水平以及HU或omega-3脂肪酸对凝血指标的影响。结果:与健康对照组相比,治疗组和未治疗组HbSS患者血红蛋白、血浆蛋白C、蛋白S均降低,白细胞计数(WBC)、血小板计数(PLTs)和血浆d -二聚体水平升高,差异均有统计学意义(p > 0.05)。与HbSS治疗组相比,HU治疗组plt计数较低(p p p)结论:本研究提供证据表明苏丹患者存在凝血功能异常,HU或omega-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。
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来源期刊
BMC Hematology
BMC Hematology Medicine-Hematology
CiteScore
4.10
自引率
0.00%
发文量
0
期刊介绍: BMC Hematology is an open access, peer-reviewed journal that considers articles on basic, experimental and clinical research related to hematology. The journal welcomes submissions on non-malignant and malignant hematological diseases, hemostasis and thrombosis, hematopoiesis, stem cells and transplantation.
期刊最新文献
Correction to: Rapid and reliable detection of α-globin copy number variations by quantitative real-time PCR Correction to: Patterns of bone marrow aspiration confirmed hematological malignancies in Eritrean National Health Laboratory. Correction to: The impact of helicobacter pylori eradication on platelet counts of adult patients with idiopathic thrombocytopenic purpura. Assessment of knowledge, attitude and practice and associated factors of blood donation among health care workers in Ethiopia: a cross-sectional study. Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study.
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