Assessment of Serum Vitamin D in Transfusion-Dependent -Thalassemia Patients: Single-Center Observational Study
Keywords:
Thalassemia, Iron overload, Ferritin, Vitamin D.Abstract
Background: Earlier surveys found that thalassemic patients on repeated blood transfusions unveiled substantial falls in vitamin D concentrations. This observational study aimed to assess vitamin D status among transfusion-dependent [3-thalassemia major patients in Babylon City.Materials and methods: This is a single¬ center observational study comprising 304 patients with |3-thalassemia major (184 males and 120 females) aged between 2.3-17.9 years. The next records were taken from all candidates: demographic features, age at first diagnosis, socioeconomic state, family history, residency, frequency of blood transfusions per month, types of chelating therapy; and laboratory examinations of serum vitamin D and ferritin. The statistical inspection had finished using the SPSS software version23. The qualitative parameters had stated as count +/- percentage, whereas the quantitative parameters had expressed as means +/- SD. A P-value of less than or equal to 5% reflected a significant value.Results: The mean ages of the patients were 12.8 ± 9.9 years, with the predominant male sex (60.5%), and around 2/3rd of them lived in rural areas and (62.1%) have a positive family history of thalassemia among the siblings. The main finding was a high frequency of hypovitaminosis D among thalassemia subjects (40.4%). As well, there was a nonsignificant association between the serum vitamin D levels and ferritin (P-0.3, r-0.11), a highly-significant negative association between vitamin D levels and the ages (P-0.3, r -0.3), and a highly-significant positive association between levels of ferritin and the ages (P-0.006, r-0.2) among the thalassemia patients.Conclusions: Our results suggest a high incidence of hypovitaminosis D among thalassemia subjects with a non-significant correlation between serum vitamin D levels and ferritin. As well, there was a highly significant correlation between ferritin levels and age among the thalassemia patients.
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References
Al-hindy HA-a, Mousa MJ, & Shaker AK (2020) No
Significant Relationship of Ferritin Levels to
the Levels of Platelet-derived Growth Factor
(PDGF) in the Peripheral Blood of
Transfusion-dependent -Thalassemia Major
Patients with Growth Retardation.
International Journal of Pharmaceutical
Research (09752366) 12 (3): 568-575. DOI:
https://doi.Org/10.31838./iipr/2020.12.03.0
Al-Hindy HA-AM, Mousa MJ, Shaker AK, AlSaad RZ, & Al-Dujaili WHS (2020)
Relationship of levels of transforming
growth factorbetal (TGF- 1 ) to the levels
of ferritin in blood of transfusion
dependent -thalassemia major patients
with growth retardation: A case-control
study. EurAsian Journal of BioSciences 14
(1): 521-527. URL:
https://www.researchgate.net/publicatio
n/339816593
AlbayrakC,&AlbayrakD (2013)MtaminD Deficiencyin
Children with Beta Thalassemia Major and
Intermedia/Beta Talasemi Majorve Intermediali
Qocuklaida Vitamin D Eksikligi. Tiirkiye
Klinikleri. Tip Bilimleri Dergisi 33 (4): 1058-
DOI:
https://doi.org/10.5336/medsci.2012-32270Almosawi RHN, & Al-Rashedi NA (2009) Low
Serum 25-Hydroxyvitamin D among
Beta-Thalassemia Patients in Iraq.
Journal of Global Pharma Technology 10
(8): 331-335 URL:
https://www.researchgate.net/publicatio
n/328967692
Arabi A, Khoury N, Zahed L, Birbari A, & El-Hajj
Fuleihan G (2006) Regression of skeletal
manifestations of hyperparathyroidism
with oral vitamin D. The Journal of
Clinical Endocrinology & Metabolism 91
(7): 2480-2483. DOI:
https://doi.org/10.1210/jc.2005-2518
Chow L-H, Frei J, Hodsman A, & Valberg L (1985)
Low serum 25-hydroxyvitamin in hereditary
hemochromatosis: relation to iron status.
Gastroenterology 88 (4): 865-869. DOI:
https://doi.org/10.1016/S0016-
(85)80001-9
Darvishi-Khezri H, Karami H, Naderisorki M,
Zahedi M, Razavi A et al. (2020)
Moderate to severe liver siderosis and
raised AST are independent risk factors for
vitamin D insufficiency in -thalassemia
patients. Scientific Reports 10 (1): 21164.
DOI: https://doi.org/10.1038/s41598-
-78230-4
Dleikh FS, Al-Aaraji AJ, Mohin R, Mousa MJ,
Al-Hindy HA-AM et al. (2020) Possible
cause-and-effect linkage of transforming
growth factor-beta1 and platelets derived
growth factor-AB with delayed
anthropometric parameters in adolescent
patients with Cooley's anemia: Cases vis
control research strategy. EurAsian
Journal of BioSciences 14 (1): 1119-1125.
URL:
https://www.researchgate.net/publicatio
n/341736056
Fahim FM, Saad K, Askar EA, Eldin EN, &
Thabet AF (2013) Growth parameters and
vitamin D status in children with
thalassemia major in upper Egypt.
International journal of hematology¬
oncology and stem cell research 7 (4): 10-
URL:
https://pubmed.ncbi.nlm.nih.gov/245055
Fung EB, Aguilar C, Micaily I, Haines D, & Lal
A (2011) Treatment of vitamin D
deficiency in transfusion dependent
thalassemia. American journal of
Hematology 86 (10): 871-873. DOI:
https://doi.org/10.1002/ajh.22117
Gaudio A, Morabito N, Catalano A, Rapisarda R,
Xourafa A et al. (2019) Pathogenesis of
thalassemia major-associated
osteoporosis: a review with insights from
clinical experience. Journal of clinical
research in Pediatric Endocrinology 11
(2): 110-117. DOI:
https://doi.org/10.4274/jcrpe.galenos.20
2018.0074
Hamayun T (2017) Assessment of Vitamin D and
Calcium Levels in Multi Transfused -
thalassemia Syndrome Patients of District
Peshawar. Advances in Basic Medical
Sciences 1 (2). URL:
https://www.abms.kmu.edu.pk/index.php/a
bms/article/view/37
Izzah A, Rofinda Z, & Arbi F (2017) Mtamin D and
parathyroid hormone levels and their relation to
serum ferritin levels in children with thalassemia
major: One-Center Study in Western Indonesia.
Journal of Advances in Medical and
Pharmaceutical Sciences 15 (1): 1-5. DOI:
https://doi.oig/10.9734/JAMPS/2017/35473
Kuo KH, & Mrkobrada M (2014) A systematic review
and meta-analysis of deferiprone
monotherapy and in combination with
deferoxaminefor reduction ofiron overloadin
chronically transfused patients with
thalassemia. Hemoglobin 38 (6): 409-421.
DOI:https://doi.org/10.3109/03630269.2014.9657
Lertsuwan K, Wongdee K, Teerapornpuntakit J,
& Charoenphandhu N (2018) Intestinal
calcium transport and its regulation in
thalassemia: interaction between calcium
and iron metabolism. The journal of
physiological sciences 68 (3): 221-232.
DOI: https://doi.org/10.1007/sl2576-
-0600-1
Masser JA-H, Mousa MJ, Makki Al-Hindy HAA, Al-Khafaji NS, Al-Dahmoshi HO et al.
(2021) Calcium and Phosphate
Homeostasis in Patients with Recurrent
Nephrolithiasis. Journal of Contemporary
Medical Sciences 7 (6): 368-372. URL:
https://www.iasj.net/iasj/download/8cb4
e78a9e416001
Munasinghe LL, EkwaruJP, Mastroeni MF, Mastroeni SS,
&VeugelersPJ (2019)Theassociationofserum 25-
hydroxyvitamin D concentrations with elevated
semm ferritin levels in normal weight, overweight
and obese Canadians. PLoS One 14 (3): e0213260.
DOI:
https://doi.oig/10.1371/ioumal.pone.0213260
Napoli N, Carmina E, Bucchieri S, Sferrazza C, Rini G
et al. (2006) Low serum levels of 25-hydroxy
vitamin D in adults affected by thalassemia
major or intermedia. Bone 38 (6): 888-892.
DOI:
https://doi.Org/10.1016/i.bone.2005.l1.018
Piga A (2017) Impact of bone disease and pain in
thalassemia. Hematology 2017 (1): 272-277.
DOI:
https://doi.org/10.1182/asheducation-
1.272
Saad BH, Abdul-AM A-HH, Hussein A-MB, &
Mazin J (2021) The study of semm ferritin
level as a predictor of growth retardation in
thalassemia-major. Archives Venezolanos de
Farmacologia y Terapeutica 40 (5): 492-501.
DOI:
https://doi.org/10.5281/zenodo.544980
Shaykhbaygloo R, Moradabadi A, Taherahmadi
H, Rafiei M, Lotfi F et al. (2020)
Correlation of cardiac and liver iron level
with T2* MRI and vitamin D3 serum level
in patients with thalassemia major.
Journal of Blood Medicine 11: 83-87.
DOI:
https://doi.org/10.2147/JBM.S227012
Tharwat RI, Balilah S, Habib HM, Mahmoud NH,
Beek FS et al. (2019) Ferritin and Vitamin D
levels and its relation to bone diseases in
thalassemic adults: A hospital-based
retrospective cohort study. Journal of Applied
Hematology 10 (1): 15-22. DOI:
https://doi.org/10.4103/ioah.joah 56 18
Toumba M, & Skordis N (2010) Osteoporosis
syndrome in thalassaemia major: an
overview. Journal of osteoporosis 2010: 51
DOI:
https://doi.org/10.4061/2010/537673
Wood JC, Claster S, Carson S, Menteer J, Hofstra T et
al. (2008) Vitamin D deficiency, cardiac iron
and cardiac function in thalassaemia major.
British journal of haematology 141 (6): 891-
DOI: https://doi.oig/10.1111/i.1365-
2008.07135.x
Yu U, Chen L, Wang X, Zhang X, Li Y et al.
(2019) Evaluation of the vitamin D and
biomedical statuses of young children with
-thalassemia major at a single center in
southern China. BMC pediatrics 19 (1): 1-
DOI: https://doi.org/10.1186/sl2887-
-1744-8
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