Immature reticulocyte fraction and erythrocyte indices in children with homozygous sickle cell disease during the interictal phase: A cross-sectional study in Lubumbashi.
DOI:
https://doi.org/10.51168/crzncv75Cuvinte cheie:
Sickle cell disease, Immature reticulocyte fraction (IRF), Compensatory erythropoiesis, Cross-sectional study, Interictal phase, Erythrocyte indicesRezumat
Introduction:
Homozygous sickle cell disease (SS) is a hemoglobinopathy characterized by chronic hemolytic anemia and vaso -occlusive crises. In Lubumbashi (DRC), routine laboratory evaluation is often limited to a complete blood count, neglecting advanced reticulocyte parameters. This study aims to evaluate the profile of the immature reticulocyte fraction (IRF) and erythrocyte constants in children with SS sickle cell disease during the intercritical phase.
Methods:
A descriptive cross-sectional study was conducted on 49 children with SS sickle cell disease, aged 1 to 12 years, followed at the DeeServices Medical Laboratory. Hematological parameters, including hemoglobin, mean corpuscular volume (MCV), and IRF (sum of medium and high fluorescence fractions), were measured using the URIT 5160 analyzer. Statistical analysis was based on Spearman's rank correlation coefficient to assess the relationships between variables, in accordance with the principles of the Declaration of Helsinki.
Results:
The cohort presented with severe anemia, with a mean hemoglobin concentration of 7.33 g/ dL and impaired erythrocyte indices. The median IRF was 23.30%, reflecting significant reticulocyte stress and sustained compensatory erythropoietic activity. A positive and highly significant correlation ( rho = 0.923, p < 0.001 ) was found between IRF and the absolute reticulocyte count.
Conclusion:
The intercritical phase in children with sickle cell disease (SS) does not correspond to a state of biological rest, but rather to active bone marrow regeneration. The IRF (erythropoietic response index) proves to be a relevant indicator for documenting the erythropoietic response in a cross-sectional setting.
Recommendation: It is recommended that hospital laboratories in Haut-Katanga routinely integrate automated hematological analyzers capable of measuring IRF alongside absolute reticulocyte counts to accurately assess bone marrow regenerative activity during the interictal phase of pediatric sickle cell disease.Referințe
1. Adane, T., Asrie, F., & Getaneh, Z. (2021). Clinical utility of immature reticulocyte fraction. Journal of Clinical Chemistry and Laboratory Medicine, 4(9), 1000p172.
2. Bossuyt, X., & Boeynaems, JM (2001). Benchmarks in laboratory diagnosis. Guarantor.
3. Bouklouze, A., & Cherrah, Y. (2012). Validation of analytical procedures according to the new approach based on total error. Les Technologies de Laboratoire , 4(14).
4. Bouyer, J. (2017). Statistical methods: Medicine, biology. Vuibert.
5. Dahmani , F., Benkirane , S., Kouzih , J., Woumki , A., Mamad , H., & Masrar , A. (2016). Study of the complete blood count in homozygous sickle cell disease: a study of 87 patients. Pan African Medical Journal, 25, Article 240. https://doi.org/10.11604/pamj.2016.25.240.11118
6. Diagne, I. (2018). Management guide: Sickle cell disease in Africa. Gaston Berger University.
7. Diallo, DA (2008). Sickle cell disease in Africa. Bulletin of the National Academy of Medicine, 192(7), 1361-1373. https://doi.org/10.1016/S0001-4079(19)32686-X
8. Doupa, D., Djite, M., Gueye, PM, Seck, M., Faye, BF, Seck, SM, Diallo, F., Ndiaye, A., Samba, A., Cisse, F., Diatta, A., Diagne, I., & Diop, S. (2017). Biochemical and hematological profile of homozygous sickle cell patients in the stationary phase at the National Blood Transfusion Center of Dakar. International Journal of Biological and Chemical Sciences, 11(4), 1706-1715. https://doi.org/10.4314/ijbcs.v11i4.23
9. El Youssoufi , Y. (2016). Reticulocyte parameters: Meanings and applications. Moroccan Journal of Pharmacy, 11, 55-61.
10. Kaur, P., Stoltzfus, J., & Yellapu, V. (2018). Descriptive statistics. International Journal of Academic Medicine, 4(1), 60. https://doi.org/10.4103/IJAM.IJAM_7_18
11. Kocko , I., Ngolet , LO, Atipo Galiba , FO, Ocko , LT, Malanda , F., & Elira Dokekias , A. (2016). Blood count values of Congolese adult sickle cell patients during the intercritical period. Health Sciences and Disease, 17(4), 63-66.
12. Lévy, J.-P., Varet , B., Clauvel , J.-P., Lefrere , F., Bezaud , A., & Guillin , M.-C. (2001). Hematology and transfusion (2nd ed.). Masson.
13. Mbenga Tampwo , B., Panzi Kalunda , E., Twum , D., Luhata , J., Lukisa Kulembama , P., Emina , J., & Ngianga-Bakwin , K. (2025). Evaluation of public awareness of sickle cell disease in the National Program for the Fight Against Sickle Cell Disease (PNLCD) in the Democratic Republic of Congo. Congolese Journal of Science & Technology, 4(4), 840-851.
14. Mounkaila , B., Oumarou Hamido , K., Garba , M., Abdoulaye Maiga , R., Akpona , SA, & Sanogo , I. (2015). Chronic hemolysis in SS and SC sickle cell patients in the stationary phase: A comparative study at the National Reference Center for Sickle Cell Disease in Niamey. CAMES Health Review, 3(1), 25-29.
15. World Health Organization. (2023). Sickle cell disease: Global epidemiological data. WHO.
16. Thiam, L., Dramé, A., Coly, IZ, Diouf, FN, Seck, N., Boiro, D., Ndongo, AA, Basse, I., Niang, B., Deme /Ly, NI, Sylla, A., Diagne, I., & Ndiaye, O. (2017). Epidemiological, clinical, and hematological profiles of homozygous SS sickle cell disease in the intercritical phase in children in Ziguinchor, Senegal. Pan African Medical Journal, 28, Article 208. https://doi.org/10.11604/pamj.2017.28.208.14006
17. URIT Medical Electronic Co., Ltd. (2024). URIT 5160 PLC technical manual. URIT.
18. Varet, B. (2012). The Intern's Book: Hematology (3rd ed.). Lavoisier
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