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. 2020 Jan-Dec:26:1076029619895111.
doi: 10.1177/1076029619895111.

Effect of Hydroxyurea Treatment on the Inflammatory Markers Among Children With Sickle Cell Disease

Affiliations

Effect of Hydroxyurea Treatment on the Inflammatory Markers Among Children With Sickle Cell Disease

Asmaa M Zahran et al. Clin Appl Thromb Hemost. 2020 Jan-Dec.

Abstract

Background: Neutrophil-to-lymphocyte ratio (NLR) was introduced as a potential inflammatory marker in sickle cell disease (SCD). This study aimed to evaluate the impact of hydroxyurea (HU) treatment on the value of NLR and some inflammatory mediators in SCD.

Methods: The hematological parameters and clinical events were analyzed in 35 children with SCD under HU treatment and followed up for 1 year and in 20 healthy controls. Enzyme-linked immunosorbent assay was performed for the evaluation of proinflammatory cytokines, including interleukin (IL) 6, IL-8, high-sensitivity C-reactive protein (hs-CRP), and tumor necrosis factor α (TNF-α).

Results: Hydroxyurea significantly improves most of the hematological parameters in children with SCD. The percentages of hemoglobin fraction S, serum levels of TNF-α and IL-6 were significantly decreased when compared to baseline value but did not reach the value of the healthy control. The HU treatment led to a significant decrease in NLR compared to the baseline values and reached healthy control values. Neutrophil-to-lymphocyte ratio was positively correlated with hs-CRP, TNF-α, and IL-8 serum levels and negatively correlated with percentage of fetal hemoglobin and hematocrit values. The cutoff value of NLR to expect a response to HU among SCD was 3.0, with 76% specificity and 85% sensitivity (area under the curve: 0.85, P < .0001). In conclusion, hydroxyurea induced a decrease in NLR and inflammatory cytokines, which represent a biomarker of inflammation in SCD. The calculation of NLR is a straightforward and cheap method for SCD outcome prediction in young children.

Keywords: hydroxyurea; neutrophil-to-lymphocyte ratio; sickle cell disease.

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Conflict of interest statement

Declaration of Conflicting Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figure 1.
Figure 1.
Difference in the values of NLR between patients with SCD at baseline (black bars) and after 1 year of HU treatment (plotted bars) and healthy control group (grey bars). HU indicates hydroxyurea; NLR, neutrophil-to-lymphocyte ratio; SCD, sickle cell disease.
Figure 2.
Figure 2.
Receiver Operating Characteristic (ROC) curve analysis of NLR to predict the presence of sickle cell disease (SCD). NLR indicates neutrophil-to-lymphocyte ratio.
Figure 3.
Figure 3.
Association between NLR and (a) the percentage of fetal hemoglobin (HbF) and hematocrit (b). NLR indicates neutrophil-to-lymphocyte ratio.
Figure 4.
Figure 4.
Association between NLR and serum levels of (a) hs-CRP, (b) TNF-α, and (c) IL-8. hs-CRP indicates high-sensitivity C-reactive protein; IL-8, interleukin 8; NLR, neutrophil-to-lymphocyte ratio; TNF-α, tumor necrosis factor α.

References

    1. Zahran AM, Elsayh KI, Saad K, et al. Circulating microparticles in children with sickle cell anemia in a tertiary center in upper Egypt. Clin Appl Thromb Hemost. 2019;25:1076029619828839. - PMC - PubMed
    1. Zahran AM, Elsayh KI, Saad K, Embaby M, Ali AM. Regulatory B cells (CD19+ CD38hiCD24hi) in alloimmunized and non-alloimmunized children with β-thalassemia major. Blood Cells Mol Dis. 2016;57:91–96. - PubMed
    1. Strouse JJ, Lanzkron S, Beach MC, et al. Hydroxyurea for sickle cell disease: a systematic review for efficacy and toxicity in children. Pediatrics. 2008;122(6):1332–1342. - PubMed
    1. Akohoue SA, Shankar S, Milne GL, et al. Energy expenditure, inflammation, and oxidative stress in steady-state adolescents with sickle cell anemia. Pediat Res. 2007;61(2):233–238. - PubMed
    1. Makis AC, Hatzimichael EC, Bourantas KL. The role of cytokines in sickle cell disease. Ann Hematol. 2000;79(8):407–413. - PubMed