A Comparative Analysis of Hydroxyurea Treatment on Coagulation Profile Among Sickle Cell Anaemia Children in Lagos, Nigeria.

Q3 Medicine Advances in Hematology Pub Date : 2024-11-23 eCollection Date: 2024-01-01 DOI:10.1155/ah/5002373
Blessing E Kene-Udemezue, Abideen O Salako, Adeseye M Akinsete, Oluwatosin O Odubela, Titilope A Adeyemo
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Abstract

Background: Hydroxyurea (HU) is a disease-modifying therapy with significant clinical and laboratory efficacy among individuals living with sickle cell anaemia (SCA). This is evident through increased fetal haemoglobin, higher packed cell volume, improved red cell hydration, reduced leukocytes, and platelet function. The effect on the coagulation pathway and pathophysiologic mechanism remains unclear, especially in children living with SCA. This study evaluated the coagulation profile using D-dimer and thrombin antithrombin complex (TAT) in children with SCA. Methods: The cross-sectional study was conducted over three months at LUTH among 80 children living with SCA in steady state aged 2-18 years (40 HU exposed and 40 HU naïve, respectively). Blood samples were assayed for D-dimer, TAT, and complete blood count. Descriptive analysis such as mean and standard deviation for normally distributed variables or median and interquartile range for skewed data were used to summarize continuous variables, while proportion or percentages for categorical variables. Univariate analysis and bivariate analysis were done and statistical significance was set at p < 0.05. Results: The mean age (±SD) of study participants in both groups was 11.35 (±4.6 years). D-dimer levels (23.27 ng/mL) and TAT (29.79 pg/mL) were significantly lower among HU exposed compared to HU naïve children (62.73 ng/mL and 109.34 pg/mL, respectively) p < 0.001. There was a negative correlation between D-dimer and TAT with the duration of HU use (r = -0.499, p=0.001, and r = -0.401, p=0.010), respectively. There was a positive correlation between D-dimer and TAT with total WBC (r = 0.368, p=0.019, and r = 0.385, p=0.014, respectively) among the HU naïve participants and a negative correlation between D-dimer and TAT with haemoglobin level (r = -0.303, p=0.047, and r = -0.311, p=0.041, respectively) among HU exposed children. Conclusion: HU modulates the D-dimer and TAT levels of children living with SCA toward the normal reference range, thus reducing the risk of hypercoagulability and associated sequelae. Therefore, continuous advocacy for HU use should entail close monitoring of adverse effects.

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羟基脲治疗尼日利亚拉各斯镰状细胞贫血儿童凝血状况的比较分析。
背景:羟基脲(HU)是一种对镰状细胞贫血(SCA)患者具有显著临床和实验室疗效的疾病改善疗法。胎儿血红蛋白增加,堆积细胞体积增大,红细胞水合作用增强,白细胞减少,血小板功能降低。对凝血途径和病理生理机制的影响尚不清楚,特别是在SCA患儿中。本研究评估了d -二聚体和凝血酶抗凝血酶复合物(TAT)在SCA患儿中的凝血情况。方法:在LUTH对80名2-18岁的稳定状态SCA儿童(分别暴露40 HU和40 HU naïve)进行了为期3个月的横断面研究。血液样本检测d -二聚体、TAT和全血细胞计数。描述性分析,如正态分布变量的平均值和标准差或偏态数据的中位数和四分位数范围,用于总结连续变量,而比例或百分比用于分类变量。进行单因素分析和双因素分析,p < 0.05为差异有统计学意义。结果:两组研究对象的平均年龄(±SD)为11.35岁(±4.6岁)。HU暴露儿童的d -二聚体水平(23.27 ng/mL)和TAT水平(29.79 pg/mL)显著低于HU naïve儿童(分别为62.73 ng/mL和109.34 pg/mL), p < 0.001。d -二聚体和TAT分别与HU使用时间呈负相关(r = -0.499, p=0.001, r = -0.401, p=0.010)。在HU naïve参与者中,d -二聚体和TAT与总WBC呈正相关(r = 0.368, p=0.019, r = 0.385, p=0.014),在HU暴露儿童中,d -二聚体和TAT与血红蛋白水平呈负相关(r = -0.303, p=0.047, r = -0.311, p=0.041)。结论:HU可将SCA患儿d -二聚体和TAT水平调节至正常参考范围,从而降低高凝血症及相关后遗症的发生风险。因此,持续倡导使用胡拉素应密切监测不良影响。
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来源期刊
Advances in Hematology
Advances in Hematology Medicine-Hematology
CiteScore
3.30
自引率
0.00%
发文量
10
审稿时长
15 weeks
期刊最新文献
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