A study of vitamin D concentration and some physiological variables among patients with beta thalassemia in Kirkuk city

Authors

  • Ismail Rajaa Mosa Biology Dept.,College of Education for Pure Science, Kirkuk University, Iraq Author
  • Muhammad Ektifa Abdul Hamid Biology Dept.College of Education for Girls, Tikrit University, Iraq. Author

Keywords:

Thalassemia, liver enzymes, ferritin, D dimer, oxidative stress

Abstract

 The current study aimed to estimate vitamin D concentration and some physiological variables in patients with beta thalassemia. 150 subjects with thalassemia were taken from both Azadi Teaching Hospital and Al Jumhuri Hospital from November 2021 to April 2022. The experimental work was carried out in private laboratories in Kirkuk, Iraq. The volunteers in the current study were divided as follows: 50 healthy volunteers as a control group. 150 thalassemia patients as a second group. The results showed that the activity of liver enzymes showed a significant increase (P < 0.05) in thalassemia patients with beta thalassemia compared to the control group. the ferritin and D dimer concentrations showed a significant increase (P < 0.05) in patients compared to the control group. For oxidative stress, malondialdehyde (MDA) level showed a significant increase (P < 0.05) in patients compared to the control group. The glutathione (GSH), catalase and superoxide dismutase (SOD) concentration showed a significant decrease (P < 0.05) in the patients (0.284 ± 0.025) compared to the control group. the concentration of vitamin D showed a significant decrease (P < 0.05) in patients compared to the control group. It is concluded from the current study that there is a link between thalassemia and liver enzymes, and this indicates the direct effect of beta-thalassemia on the liver. On the other hand, it was found that both ferritin and D dimer can be considered as indicators for the detection of thalassemia. The results of the current study also showed that there is an association between vitamin D deficiency and beta thalassemia. 

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References

ossio MLT, Giesen LF. Araya G. (2016) Hoffbrands Essential

Haematologica 7th Hoffbrand AV Moss PAH editor. Vol. xxxlll.

Wiley Blackwell John Wiely and sons LTD. 73-85 p.

Makroo RN. Bhatia A (2014) provision of ideal transfusions support The

essences of thalassemia care Apollo medicine 11(3):184- 90.

Maria DomenicaCappellini. Alan Cohen, John Porter Ali Taher

VV(2014) guidelines for the management of transfusions dependent

thalassemia 3th. Edit.thalassemia international federations pl-16.

Skirton H, O’Connor A, Humphreys A. Nurses’ competence in genetics:

a mixed method systematic review. J AdvNurs. 2012 Nov; 68(11):

-98.

Aimiuwu E, Thomas A, Roheemun N, Khairallah T, Nacouzi NA,

Georgiou A et al. A Guide for the haemoglobinopathy nurse.

Thalassaemia International Federation. Teamup Creations Ltd. 2012

Awjagh, I. S. A. (2018). Study of zinc and copper in patients with Beta

Thalassemia major and splenctomized in Kirkuk city. Kirkuk

University J. Sci. Stu. 13(1): 239-248.

AHMED, N. H.; AZAD H. F.; NASIR A. and SANA D. J. (2009).

PREVALENCE OF HAEMOGLOBINOPATHIES IN SULAIMANI

- IRAQ. DuhokMedical J. 2(1):71-79

Bashir N, Barkawi M, Sharif L, Momani A, Gharaibeh N. Prevalence of

hemoglobinopathies in North Jordan.Trop GeogrMed 1992; 44(1- 2):122-5.

Yildiz S, Atalay A, Baci H, Atalay EO. Beta -thalassaemiamuations in

Denizili Province of Turkey. Turk J Haematol 2005;22(l):181-5.

El- Hazami MA, Warsy AS. Appraisal of sickle cell and thalassaemia

genes in Saudi Arabia. East Mediterr Health J 1999;5(6):1147-53.

Hassan MK, Taha JY Al-Nama, Widad NM, Jasim SN(2003) frequency

of haemoglobinopthies and glucose 6 phosphate dehydrogenase

deficiency in Basra. East. Med. health J 9:45-54

Al-Nood H(2009)Thalassemia trait in outpatients clinics of Sana city,

Yemen. Hemoglobin 33:242-246. 8. Aydinok (2012)Thalassemia

Hematology 17:28-31.

Khaleel K.J, Hameed AH, Fadhil AM, and Yassin NY.(2009) prevalence

of thalassemia genes in Mousul. Iraqi. J. Of Sci, Supp. 8-10.

Ameli M, Besharati S, Nemati K, Zamani F. Relationship between elevated liver

enzyme with iron overload and viral hepatitis in thalassemia major patients

in Northern Iran.SaudiMed J.2008; 29(11):1611-5.

Ruhl CE, Everhart JE. Relation of elevated serum alanine

aminotransferase activity with iron and antioxidant levels in the

United States. Gastroenterology. 2003; 124: 1821-1829.

Abdalla M, Fawzi M, Salem R, et al. Increased oxidative stress and iron

overload in jordanian pthaassemic children. Hemoglobin.

;35:67- 79.

Company F , Rezaei N , Pourmohmmad B , Gharibi F. Assessment of thyroid

dysfunction in patients with B- thalassemia major (Text in Persian).

Scientific Journal of Kurdistan University of Medical 2008; 13,4(50):37-44.

Wanachiwanawin W, Luengrojanakul P, Sirangkapracha P, Leowattana

W , Fucharoen S. Prevalence and Clinical Significance of Hepatitis C

Virus Infection in Thai Patients with Thalassemia .International

Journal of Hematology 2003;78( 4): 374-378.

Pootrakul, P.; Vongsmasa, V.; La- ongpanich, P. and Wasi, P. Serum

Ferritin Levels in Thalassemias and the Effect of Splenectomy. Acta.

Haematol. 1981; 66(4): 244-50.

Mishra, A. and Tiwari, A. Iron Overload in Beta Thalassemia Major and

Intermedia Patients. Maedica (Buchar). 2013 Sep; 8(4): 328-332.

Easa, Z. Complications of High Serum Ferritin Level after Splenectomy

in p Thalassemic Patients. Kufa Med. Journal. 2009; 12(1): 138-142.

Hallberg L, Bengtsson C, Lapidus L, Lindstedt G, Lundberg PA, Hulten

L. Screening for iron deficiency: an analysis based on bone-marrow

examinations and serum ferritin determinations in a population

sample of women. Br J Haematol 1993;85:787-98.

Zanella, A.; Gridelli, L.; Berzuini, A.; Colotti, MT.; Mozzi, F. and Milani,

S. Sensitivity and Predictive Value of Serum Ferritin and Free

Erythrocyte Protoporphyrin for Iron Deficiency. J Lab Clin Med.

Jan; 113(1): 73-8Hassan MK, Taha JY Al-Nama, Widad NM, Jasim SN(2003) frequency

of haemoglobinopthies and glucose 6 phosphate dehydrogenase

deficiency in Basra. East. Med. health J 9:45-54

Hadi TK, Mohammad NS, Nooruldin SA (2020). Protein C and protein

S levels in patients with major p-thalassemia in Erbil, Kurdistan

Region. Cell MolBiol (Noisy le Grand); 66 (5):25-28.

Travazzi, D., Duca, L., Graziadei, G., Comino, A., Fiorelli, G., and

Cappellini, M.D; Br. J. Haematol. , 112: 48 ; 2001.

Cighetti, G., Duca, L., Bortone, L., Sala, S., Nava, I., Fiorelli, G., and

Cappellini, M.D. ; Eur. J.Clin. Invest., 32: 55 ; 2002.

Chan, A.C. , Chow, C.K. , and Chiu, D.; Proc-Soc. Exp. Biol. Med., 222:

; 1999.

Hershko, C., Link, G., and Cabantchik, I.; Ann. N.Y. Acad. Sci., 850: 191

; 1998.

Abdulkhader, A.A., B.A. Majeed and A.N (2010). Mahmood The Effects

of Chelating Therapy on the Levels of Serum Ferritin, Zinc, Copper

& its relation with Malondialdehyde in Patients with BThalassemia

Major. Iraqi J. Comm. Med.,. (3):147- 152.

Chatterton B.E., Thomas C.M. and Schultz C.G."Liver Density Measured

by DEXA Correlates with Serum Ferritin in Patients with Beta¬

Thalassemia Major" Journal of Clinical Densitometry, 2003; 6(3)

-288.

Dresner P.R., Rachmilewitz E., Blumenfeld A., Idelson M. and Goldfarb

A.W. "Bone Mineral Metabolism in Adults with Beta-Thalassaemia

Major and Intermedia" British Journal of Haematology, Vol. Ill, No.

, Pp. 902- 907, 2000.

EzzatHatoon M., John W.u., Heather M., Leitch Heather A."Vitamin D

Insufficiency and Liver Iron Concentration in Transfusion

Dependent Hemoglobinop

athies in British Columbia" Open Journal of Hematology, 2015; 6-6

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Published

2023-02-28

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How to Cite

Rajaa Mosa, I., & Ektifa Abdul Hamid , M. (2023). A study of vitamin D concentration and some physiological variables among patients with beta thalassemia in Kirkuk city. History of Medicine, 9(1). http://13.200.237.241/HOM/index.php/medicine/article/view/842