The Evaluation of serum fucose and fucose related parameters in beta- thalassemia major

Heba Hasan Jalal
Department of Clinical Biochemistry, College of Health Science , Hawler Medical University, Erbil, Kurdistan region, Iraq.
Bakhtiar Muhialdin Ahmad
Department of Basic Science, College of Dentistry, Hawler Medical University, Erbil, Kurdistan region, Iraq.
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Abstract

Background and objective: Beta-thalassemia syndrome is characterized by either absent or lower-than-normal production of the beta-globin chain in hemoglobin, which can cause various health problems. α- L-fucose is a methyl pentose sugar, which is a part of the glycan’s of a significant category of compounds referred to as glycoconjugates; glycoproteins and glycolipids. The major aim of the current study is to evaluate using serum fucose parameters as biomarkers or indicators for beta- thalassemia disease.

Methods: The current study was materialized on 45 Beta-thalassemia major patients and 45 healthy volunteer individuals. Blood sample collections were performed at Thalassemia Center (Akre and Erbil). Serum Fucose and related parameters total fucose (TF), protein bound fucose (PBF), protein bound hexose (PBH), lipid associated fucose (LAF), and free fucose (FF) were measured using UV/VIS spectrophotometry.

Results: Beta-thalassemia major (BTM) patients had a significantly higher serum levels of TF and FF compared to the controls. A significant reduction in serum PBF was observed in patients. However, differences in PBH and LAF were not statistically significant. The PBH mean and standard deviation in patients were 6.421 and 3.085, respectively, compared to 6.817 and 3.758 in controls (P = 0.5858). For LAF, patient values were 3.281 and 2.225, versus 2.452 and 1.960 in controls (P = 0.0640).

Conclusion: The results inferred significant increase in serum TF and FF, and a significant decrease in serum (PBF) in Beta-thalassemia major patients. The results suggest that TF, FF and PBF parameters can be used as diagnostic markers for the disease.

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References

  1. Iyevhobu KO, Okobi TJ, Usoro ER, Ivie AA, Ken-Iyevhobu BA, Victoria OO. Overview of beta-thalassemia. Thalassemia Syndromes-New Insights and Transfusion Modalities: Intech Open. 2023.
  2. DOI: 10.5772/intechopen.111682
  3. De Sanctis V, Kattamis C, Canatan D, Soliman AT, Elsedfy H, Karimi M, et al. β-thalassemia distribution in the old world: an ancient disease seen from a historical standpoint. Med J Hematol Infect Dis. 2017;9(1):e2017018. https://doi.org/10.4084/mjhid.2017.018
  4. Kuo KH. Fast Facts for Patients: Scientific Basis and Practical Guidelines. 2023. http://digital.casalini.it/9783318073447
  5. Origa R. β-Thalassemia. Genet Med. 2017;19(6):609-19. https://doi.org/10.1038/gim.2016.173
  6. Allen A, Perera S, Mettananda S, Rodrigo R, Perera L, Darshana T, et al. Oxidative status in the β-thalassemia syndromes in Sri Lanka; a cross-sectional survey. Free Radic Biol Med. 2021;166:337-47. DOI: 10.1016/j.freeradbiomed.2021.02.028
  7. Reily C, Stewart TJ, Renfrow MB, Novak J. Glycosylation in health and disease. Nat Rev Nephrol. 2019;15(6):346-66. https://doi.org/10.1038/s41581-019-0129-4
  8. Lauc G, Pezer M, Rudan I, Campbell H. Mechanisms of disease: The human N-glycome. Biochim Biophys Acta Gen Subj. 2016;1860(8):1574-82. https://doi.org/10.1016/j.bbagen.2015.10.016
  9. Adhikari E, Liu Q, Burton C, Mockabee‐Macias A, Lester DK, Lau E. L‐fucose, a sugary regulator of antitumor immunity and immunotherapies. Mol Carcinog. 2022;61(5):439-53.
  10. https://doi.org/10.1002/mc.23394
  11. Schneider M, Al-Shareffi E, Haltiwanger RS. Biological functions of fucose in mammals. Glycobiology. 2017;27(7):601-18. https://doi.org/10.1093/glycob/cwx034
  12. Xu X, Fukuda T, Takai J, Morii S, Sun Y, Liu J, et al. Exogenous l-fucose attenuates neuroinflammation induced by lipopolysaccharide. J Biol Chem. 2024;300(1).
  13. https://doi.org/10.1016/j.jbc.2024.107558
  14. Wu H, Owen CD, Juge N. Structure and function of microbial α-l-fucosidases: a mini review. Essays Biochem. 2023;67(3):399-414. https://doi.org/10.1042/EBC20220158
  15. Wan L, Zhu Y, Zhang W, Mu W. α-L-Fucosidases and their applications for the production of fucosylated human milk oligosaccharides. Appl Microbiol Biotechnol. 2020;104:5619-31.
  16. https://doi.org/10.1007/s00253-020-10635-7
  17. Miyoshi E, Fujita K, Morishita K, Ouchida T, Nakagawa T, Takamatsu S, et al. Fucosylated Proteins as Cancer Biomarkers. In: Glycosignals in Cancer: Molecular Assembly and Recognition. 2023:19-32. https://doi.org/10.1007/978-981-19-7732-9_2
  18. Olejnik B, Kratz EM, Zimmer M, Ferens-Sieczkowska M. Glycoprotein fucosylation is increased in seminal plasma of subfertile men. Asian J Androl. 2015;17(2):274-80. DOI: 10.4103/1008-682X.138187
  19. Shan M, Yang D, Dou H, Zhang L. Fucosylation in cancer biology and its clinical applications. Prog Mol Biol Transl Sci. 2019;162:93-119. https://doi.org/10.1016/bs.pmbts.2019.01.002
  20. Yaseen NA, Ahmed BM. Effect of cigarette smoking on serum α-L-fucose and its related parameters.Zanco J Med Sci. 2014;18(1):596-603.
  21. http://dx.doi.org/10.15218/zjms.2014.0002
  22. Kumar S, Saxena M, Srinivas K, Singh VK. Fucose: A biomarker in grading of oral cancer. Natl J Maxillofac Surg. 2015;6(2):176-9. DOI: 10.4103/0975-5950.183869
  23. Wsoo MA, Ahmed BM. Evaluation of salivary α-L-Fucose and its related parameters in periodontitis. Zanco J Med Sci. 2013;17(3):563-9. http://dx.doi.org/10.15218/zjms.2013.0049
  24. Ali DR, Mahmoud TJ, Hassan HG. Evaluation of serum fucose and protein bound fucose on myocardial infarction patients in Erbil city.Zanco J Med Sci. 2012;16(1):40-4. https://doi.org/10.15218/zjms.2012.0007
  25. Dordevic A, Mrakovcic-Sutic I, Pavlovic S, Ugrin M, Roganovic J. Beta thalassemia syndromes: New insights. World J Clin Cases. 2025;13(10):100223. doi: 10.12998/wjcc.v13.i10.100223
  26. Fatima T, Khan S, Khan MM, Kamran R, Uddin MW, Sohrab S. Oxidative stress in Beta-thalassemia Patients: Role of enzymatic and non-enzymatic modulators.Protein Pept Lett. 2023;30(12):1030-7. https://doi.org/10.2174/0109298665246270231020062048
  27. Khalid A, Siddiqui AJ, Ansari SH, Musharraf SG. Reflection of treatment proficiency of hydroxyurea treated β-thalassemia serum samples through nuclear magnetic resonance based metabonomics. Sci Rep. 2019;9(1):2041. https://doi.org/10.1038/s41598-019-38823-0
  28. Al-Hakeem T, Hasan HG, Ali ZA. Levels of Total Fucose and Total Protein in Sera of Blood Groups and RBCs of Control, Minor and Major Thalassemic Patients.Middle East J Intern Med. 2013;6(2). DOI: 10.5742/mejim.2013.62219
  29. Fibach E, Dana M. Oxidative stress in β-thalassemia. Mol Diagn Ther 2019;23:245-61. https://doi.org/10.1007/s40291-018-0373-5
  30. Doltchinkova V, Lozanova S, Rukova B, Nikolov R, Ivanova E, Roumenin C. Electrokinetic properties of healthy and β-thalassemia erythrocyte membranes under in vitro exposure to static magnetic field. Front Chem. 2023;11:1197210. https://doi.org/10.3389/fchem.2023.1197210
  31. Assi MA. Estimation of α-L-fucose and vitamin D 3 levels in β thalassemia patients in Al-Najaf Province. J Glob Pharma Technol. 2019;11:192-5.
  32. Mirlohi MS, Yaghooti H, Shirali S, Aminasnafi A, Olapour S. Increased levels of advanced glycation end products positively correlate with iron overload and oxidative stress markers in patients with β-thalassemia major. Ann Hematol. 2018;97:679-84. https://doi.org/10.1007/s00277-017-3223-3
  33. Hirsch RE, Sibmooh N, Fucharoen S, Friedman JM. HbE/β-thalassemia and oxidative stress: the key to pathophysiological mechanisms and novel therapeutics. Antioxid Redox Signal. 2017;26(14):794-813. https://doi.org/10.1089/ars.2016.6806
  34. Rivella S. Iron metabolism under conditions of ineffective erythropoiesis in β-thalassemia. Blood. 2019;133(1):51-8. https://doi.org/10.1182/blood-2018-07-815928
  35. Al-Zuhairy SH, Darweesh MA, Othman MA. Relation of Serum Ferritin Level with Serum Hepcidin and Fucose Levels in Children with β-Thalassemia Major. Hemoglobin. 2021;45(1):69-73. https://doi.org/10.1080/03630269.2021.1898419
  36. Wang M, Liu R, Liang Y, Yang G, Huang Y, Yu C, et al. Iron overload correlates with serum liver fibrotic markers and liver dysfunction: Potential new methods to predict iron overload-related liver fibrosis in thalassemia patients. United Eur Gastroenterol J. 2017;5(1):94-103. https://doi.org/10.1177/2050640616646525
  37. Fibach E, Rachmilewitz EA. Pathophysiology and treatment of patients with beta-thalassemia–an update. F1000Res. 2017;6:2156. doi: 10.12688/f1000research.12688.1
How to Cite
Jalal, H. H., & Muhialdin Ahmad, B. . (2026). The Evaluation of serum fucose and fucose related parameters in beta- thalassemia major. Zanco Journal of Medical Sciences (ZJMS), 30(2), 345–356. https://doi.org/10.15218/zjms.2026.024

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