Write your message
Volume 10, Issue 1 (February 2023)                   IJML 2023, 10(1): 57-66 | Back to browse issues page

XML Print

Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
gharehdaghi Z, Rostami S. Hematological and Biochemical Parameters of β-Thalassemia Major Patients in Bushehr City: A Comparative Analysis. IJML 2023; 10 (1) :57-66
URL: http://ijml.ssu.ac.ir/article-1-468-en.html
Hematological and Biochemical Parameters of β-Thalassemia Major Patients in Bushehr City: A Comparative Analysis
Zeynab Gharehdaghi , Shaghayegh Rostami *
Department of Hematology, School of Para Medicine, Bushehr University of Medical Sciences, Bushehr, Iran
Keywords: Hematological characteristics, Iron overload, Serum ferritin, β-thalassemia major
Full-Text [PDF 423 kb]   (149 Downloads)     |   Abstract (HTML)  (217 Views)
Full-Text:   (140 Views)

Introduction
β-thalassemia is an inherited autosomal recessive disorder related to the deficiency of the production of beta-globin chains. The homozygous form of β-thalassemia may lead to either thalassemia major or thalassemia intermedia [1]. Thalassemia major is the most common genetic disorder worldwide, resulting in severe anemia requiring regular red blood cell transfusions [2, 3]. β-thalassemia is so highly prevalent in Iran that it has been shown that there are more than three million beta-thalassemia carriers (4-8%) and approximately 20,000 patients [4]. The disease is prevalent along the margins of the Caspian Sea, the Persian Gulf, and coastal cities in general [5]. These patients have been managed based on systematic blood transfusions to retain a hemoglobin level above 9 mg/dl [6]. Due to a long time necessity of repeated transfusion, excess iron gets accumulates in different organs of the body, namely, the liver, kidney, pancreas, and heart, implicating in excessive generation of free radicals which are capable of inducing damage to cellular membranes, protein, and DNA that consequently leads to wide-ranging impairment in cellular function. The manifestations include cirrhosis, cardiomyo-pathies, diabetes mellitus, secondary hypogo-nadism, and primary hypothyroidism [7-9]. Also, previous studies have reported a high outbreak of endocrine disorders in major thalassemia patients. That deficiency of trace minerals may be suggested as a causative agent in endocrinopathies. Besides, the estimation of trace minerals such as calcium, sodium, and potassium is valuable in these patients [10]. Due to the high prevalence of thalassemia in Bushehr and the lack of a comprehensive study on this disease, the present study has been designed to evaluate biochemical and hematological aspects of β-thalassemia major patients hoping to improve or modify the management and treatment protocols.
Materials and Methods
This study was performed on patients referred to the thalassemia center of Bushehr province from March 2018 to November 2018. The statistical population included 94 β-thalassemia major patients (female: 54 and male: 40) aged 12-46. In contrast, the control group included 94 healthy persons in the same age range. Demographic data of the patients, including age, gender, and medical history, was collected through their medical and laboratory records. The diagnosis of β-thalassemia major in early life has been accomplished via peripheral blood smear and electrophoresis of hemoglobin. Patients of thalassemia intermedia and minor and patients with acute illness were excluded from the study. The Human Ethics Committee of Bushehr University of medical sciences approved the study protocol.
Sample collecting and evaluation
About 5 mL of every patient’s blood was collected, aliquoted 2.0 ml into the K2 Ethylenediaminetetraacetic acid (EDTA) tube, and mixed completely. Hematological assays such as hemoglobin, hematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC) were evaluated by a blood cell counter (Sysmex XP-300, Germany) before 2 hours. The remaining samples (3 mL) were transferred to the clotting tube and centrifuged for 10 min at 3,000 rpm. Plasma samples were used for assessing biochemical factors such as fasting blood sugar (FBS), blood urea nitrogen (Bun), creatinine (Cr), uric acid (UA), triglyceride (TG), cholesterol (Chol), high-density lipoprotein (HDL), low-density lipoprotein (LDL), calcium (Ca), phosphor (Ph), aspartate aminotransferase (AST), alanine transaminase (ALT), alkaline phosphatase (ALP), albumin, total and direct Bilirubin by using DIRUI CS-400 auto analyzer and commercial kits according to the manufacturer's instruction (Pars Azmoon, Iran). Ferritin and thyroid function tests such as thyroxin (T4) and thyroid stimulating hormone (TSH) were assessed by Enzyme-linked immunosorbent assay (ELISA) kits (Monobind INC, USA). Sodium (Na) and potassium (K) levels were determined according to the manufacturer's instruction (Pars Azmoon, Iran) by the JOKOH EX-D electrolyte analyzer (JOKOH, Japan).
Statistical analysis
Statistical analysis was conducted using SPSS 16.0, and a p-value < 0.05 was considered significant. Data are presented as Mean ± standard deviation (SD). The results were analyzed using analysis of variance (ANOVA) followed by the independent t-test. Correlations were calculated by Pearson's correlation coefficients.
Results
The average ages of β-thalassemia major cases and the control group were 27.2 and 29.8 years, respectively. Most patients were taken iron chelation with deferoxamine. In this section, the age and gender of β-thalassemia major patients versus the corresponding control group are represented (Table 1). No significant difference was found between the patients and the control regarding age or sex (p > 0.05). The highest percentage of patients was observed in the age range of 21 to 30 (Fig. 1). On average, blood transfusions were prescribed for patients from the age of 2.9 years. The overall mean transfusion interval was 20.90 days, but it was 20.61 days for males and 21.20 days for females. The mean height and weight were 158 ± 10.34 cm and 49.24 ± 9.49 Kg, respectively. Pre-transfusion hemoglobin in males and females was 8.7 ± 0.9 (g/dL) and 8.1 ± 1.0 (g/dL), respectively.
According to one-way ANOVA and two-tailed Dunnet’s test, as shown in Table 2, all hematological parameters in patients such as Hb (p < 0.01), HCT (p < 0.01), MCV (p < 0.05) and MCH (p < 0.05) were significantly reduced compared to the control group except MCHC which was insignificant (p > 0.05).
As shown in Table 3, the average of T4 and TSH was close to normal range values. All thyroid function tests in β-thalassemia major patients were not significantly different from controls (p > 0.05). According to the Pearson correlation test, there was a significant correlation between age and T4 value (R = -.44; p < 0.05 ).

 Fig. 1. Percentage of four age groups in studied thalassemia patients
Table 1. Age and sex of β-thalassemia major patients and control group (n=94)
Indices (Unit) Sex β-thalassemia Control
Sex Female  54 54
Male 40 40
Age (yr) Female 12-45 12-46
Male 13-46 12-46
Table 2. Hematological characteristics in β-thalassemia major patients and controls (n=94)
Indices
(Unit)		 Case
 Mean ± SD		 Control
Mean ± SD		 P-value
                    Female Male Female Male
Hemoglobin (g/dL) 8.1 ± 1.0 8.7 ± 0.9 12.8 ± 1.2 13.4 ± 1.6 P< 0.01
Hematocrit (%) 27.0 ± 2.6 27.1 ± 2.6 38.1 ± 7.9 43.1 ± 8.4 P < 0.01
Mean corpuscular volume (μm3) 73.9 ± 6.0 75.9 ± 5.5 83.6 ± 11.1 84.5 ± 12.0 P < 0.05
Mean corpuscular hemoglobin (pg) 25.9 ± 2.4 25.8 ± 1.0 29.1 ± 2.5 31.9 ± 2.0 P < 0.05
Mean corpuscular hemoglobin concentration (g/dL) 31.8 ± 1.3 31.9 ± 1.5 32.8 ± 1.4 33.1 ± 2.3 P > 0.05
Ferritin (μg/L) 3407 ± 2553 3674 ± 2730 38 ± 19 52 ± 21 P < 0.01
P-value < 0.05: Significant
Table 3. Thyroid function tests in β-thalassemia major patients and controls (n=94)
Indices (Unit) Sex Case
Mean ± SD		 Control
Mean ± SD		 P value
T4 (μg/dl) Female 7.8± 2.2 8.2 ± 1.5 P > 0.05
Male 6.8 ± 1.7 7.5 ± 2.2 P > 0.05
Thyroid stimulating hormone (mIU/l) Female 2.9 ± 1.7 2.3 ± 1.2 P > 0.05
Male 3.3 ± 2.3  2.6 ± 1.1 P > 0.05
P-value < 0.05: Significant

Table 4. Sugar, lipid, and kidney function test in β-thalassemia major male and female patients as compared to control
Parameters (Unit) Sex Case (Mean ± SD) Control (Mean ± SD) P value
Sugar and lipid (mg/dL)
Fasting blood sugar F 121± 70 95± 12 P<0.05
M 128 ± 65 98 ± 9
Triglyceride F 151 ± 70 98 ± 17 P < 0.05
M 132 ± 72 93 ± 13
Cholesterol F 127 ± 31 151 ± 28 P < 0.05
M 108 ± 31 162 ± 20
High-density lipoprotein F 30.3 ± 10.3 69.1 ± 9.8 P < 0.05
M 26.5 ± 9.2 70.6 ± 11
Low-density lipoprotein F 61.4 ± 19.6 86.8 ± 10.4 P < 0.05
M 54.1 ± 22.0 90.4 ± 13.0
Kidney Function Test (mg/dL)
Blood urea nitrogen F 15.3± 7.9 14.9± 8.4 P>0.05
M 17.1± 7.2 16.4± 6.7
Creatinine F 0.81± 0.33 0.80± 0.31 P>0.05
M 0.82± 0.17 0.79 ± 0.2
Uric acid F 4.8± 1.1 3.4± 0.6 P<0.05
M 5.3± 1.2 3.2± 0.7
Electrolytes
Sodium (mEq/L) F 135.5± 1.6 136± 2.4 P>0.05
M 135.2± 2.0 137± 2.7
Potassium (mEq/L) F 4.2± 0.15 4.0± 0.1 P>0.05
M 4.2± 0.2 4.0± 0.3
Calcium (mg/dL) F 9.9± 0.6 9.6± 1.2 P>0.05
M 9.9± 0.68 9.7± 1.6
Phosphorus (mg/dL) F 5.5± 0.75 4.2± 0.5 P<0.05
M 5.3± 0.9 3.99± 0.6
M= Male, F= Female, pvalue< 0.05: Significant
Table 5. Liver function tests and vitamin D3 in β-thalassemia major male and female patients as compared to control
Parameters (Unit) Sex Case (Mean± SD) Control (Mean± SD) P value
Aspartate aminotransferase F 41.4± 18.8 21.3± 6.7 P<0.05
M 45.8± 20.7 20.2± 8.9
Alanine transaminase (U/L) F 44.2± 21.4 19.1± 7.4 P<0.05
M 47.4± 23.1 21.2± 5.9
Alkaline phosphatase (U/L) F 305± 165 186± 122 P<0.05
M 338± 116 201± 117
Total bilirubin (mg/dL) F 1.7± 0.9 0.4± 0.2 P<0.05
M 2.9± 1.1 0.5± 0.2
Direct bilirubin (mg/dL) F 0.61± 0.21 0.2± 0.1 P<0.05
M 0.57± 0.21 0.2± 0.1
Albumin( g/dL) F 3.9± 0.3 3.7±  0.2 P>0.05
M 4.1± 0.4 3.8± 0.3
M= Male; F= Female, pvalue< 0.05: Significant

As shown in Table 4, the patients have shown significantly high serum FBS levels compared to the control group (p < 0.05). Also, the FBS level was more than 105 mg/dL in 35 patients (37.2%). The lipid profile in patients was significantly different from the control group (p < 0.05). Eighteen patients (19.1%) had over 200 mg/dL serum TG. Serum HDL was less than 30 mg/dL in 68 patients (72.3%). Moreover, cholesterol was reported to be less than 200 mg/dL in all patients and below 110 mg/dL in 48 patients (51%). A significant difference between patients and the control group was observed for uric acid (p <0.05), whereas serum creatinine and Bun were not significantly different from the control group (p > 0.05) . In Table 4, the examination of some biochemical indices levels in β-thalassemia major patients and controls has been presented. Serum Na, K, and Ca were not significantly different from the control group (p > 0.05), while high serum PH was observed in 82.9% of the patients.
According to one-way ANOVA and two-tailed Dunnet's test, as shown in Table 5, AST, ALT, Alkp, Direct, and total bilirubin levels in patients were significantly higher than the control group (p < 0.05). High serum total and direct bilirubin levels were observed in 63.8% and 80.8% of the patients, respectively. In 96% of patients, Albumin level was observed in the normal range, and there was no significant difference between the study and control groups (p > 0.05).
Discussion
β-Thalassemia, as a genetic disorder, is characterized by ineffective erythropoiesis, leading to chronic anemia and abnormal iron metabolism [11]. In order to prevent complications like chronic anemia and bone changes, these patients need regular blood transfusions, which leads to iron overload in their bodies [12]. In recent years, chelation therapy has progressed to diminish iron overload, but endocrinopathies still threaten the quality of patients' lives [13]. Moreover, various biochemical and hematological abnormalities are other symptoms among these patients [14]. In the present study, the biochemical and hematological factors were investigated among β-thalassemia major patients in Bushehr.
In this study, all hematological parameters such as Hb, HCT, MCV, and MCH have been significantly decreased in patients compared to the control group. However, there was no significant difference in MCHC compared to the control group. Similarly, Fazlul Karim et al. reported that Hematological parameters such as Hb, HCT, MCV, and MCH have been significantly reduced in patients except for MCHC [10].  In the present study, the mean ferritin level in patients was 3540 μg/L, and compared with the control group, serum ferritin was raised significantly (p < 0.01). This is due to the iron overload caused by regular blood transfusion. The findings are consistent with several similar studies. For example, Surchi et al. reported a mean serum ferritin level of 2803.4 μg/L [15], and Eghbali et al. reported a mean serum ferritin level of 1927.1 μg/L [16].
Many studies have assessed the toxic effect of excess iron and peroxidative injuries on liver cells, leading to an increase in liver enzymes[17, 18]. In these patients, the mean ALT, AST, and ALP were 43.6 U/L, 45.8 U/L, and 321.5 U/L, respectively, substantially high due to the developed abnormal liver function. Hashemizadeh et al., in the Sarvar clinic of Mashhad, found that the mean ALT and  AST were 70 U/L and 95 U/L, respectively [2]. In a study in Qatar, Kanbour et al. reported that the mean ALT, AST, and ALP were 61.9 U/L, 52 U/L, and 145.46 U/L, respectively [19]. The serum AST and ALT positively correlated with serum ferritin with correlation coefficients r = +0.45 and r = +0.42, respectively (P<0.05). The study's results correlate well with previous studies [10, 17].
In the present study, the average level of total and direct serum bilirubin in the study group was significantly higher than the control group (P < 0.05), which can be due to the excessive destruction of red blood cell. Sultana et al. reported similar results: mean serum bilirubin of 2.04 ± 0.70 mg/dL in Patients [20]. Moreover, this study showed that most β-thalassemia major patients had lower total cholesterol, LDL-C, and HDL-C levels than the control group. Though, a high level of triglycerides has been observed. These fluctuations may be due to iron overload, liver injury, hormonal disturbances, and aging [21]. Our findings align with the outcome of Shams et al. and Ragab et al. [22, 23]. However, Haghpanah et al. showed that the triglyceride level was not significantly different from the control group [24]. In this study, 14.8% of patients had FBS>126 mg/dl, which agrees with similar studies, such as Chahkandi et al.'s study. In Birjand city, eastern Iran, who reported the mean serum FBS levels in patients were 124.19 mg/dl, and 14.3% of patients had FBS ≥ 126 mg/dl [13]. In studies conducted in Pakistan, research on 124 β-thalassemia major patients showed that 29.4% of patients had FBS ≥ 126 mg/dl [25].
In our study, the mean serum creatinine and Bun were within the normal range and not significantly different from the control group. However, the uric acid level was significantly higher than the control group . Our findings align with the outcome of Aldudak et al. and Sen et al. [26, 27], while in contrast, Ahmadzadeh et al., in their study, found normal range serum uric acid level [28]. Renal damage in patients with β-thalassemia major can be due to long-lasting anemia, iron overload, and deferoxamine toxicity [29]. There was also a slight difference in Na and K in the patients compared to the control group. Similar findings were reported by previous studies [27, 30]. However, in a study carried out in Bangladesh, higher levels of Na and K were found in patients compared to healthy individuals [10].
In this study, the Ph levels in female and male patients were 5.5 ± 0.75 mg/dL, and 5.3 ± 0.9 mg/dL, respectively. In general, 67.8% of phosphorus was above 4.5 mg /dL. Similar results have been observed in other studies [31- 33]. Also, the mean serum calcium of patients was not significantly different from the control group. Our outcomes agree with the result obtained by Surchi et al. [15]. However, Ayyash et al., in their study, showed that the level of Ca in patients was significantly lower than in the control group [17]. One of the main causes of hypothyroidism in β-thalassemia major patients is mentioned poisoning of the thyroid gland with iron overload. The prevalence of hypothyroidism varied in different studies. For example, the highest and lowest prevalence of hypothyroidism was reported (26.7% and 0%) in Najafipour and Mostafavi et al.'s studies, respectively [34, 35]. In this study, the prevalence of primary hypothyroidism (TSH>4.5 mIU/l and T4< 5.6 μg/dl) was reported at 5.31%. The incidence of hypothyroidism varies widely, depending on age, region, and type of remedy, including the number of red-packed cell transfusions per month, chelation therapy, and follow-up intervals of cases. This fact answers why the prevalence of hypothyroidism is so different in different studies [5].
Conclusion
In conclusion, the difference in hematological and biochemical parameters between β-thalassemia major patients and controls has been demonstrated. In this study, the serum ferritin is increased in most patients because of the breakdown of red blood cell and chronic blood transfusion, leading to iron accumulation in the body. Also, it has been indicated that increasing ferritin levels led to a subsequent increase in the serum levels of liver enzymes (ALT, AST, and Alkp). The present study revealed that 52% and 19.1% of patients had hypocholesterolemia and hypertriglyceridemia, respectively, and 5.31% had hypothyroidism. Consequently, due to iron overload in patients with thalassemia major that resulted in permanent tissue damage, this is necessary to evaluate iron toxicity and follow up on the β-thalassemia major patients regularly. We are hopeful that current findings will contribute to developing a guideline concerning the early diagnosis and mode of treatment among β-thalassemia major patients.
Conflicts of Interest
The authors declare that there is no conflict of interest.
Acknowledgement
This study was financially supported by the Bushehr University of Medical Sciences, Bushehr, Iran. We are grateful to all participants and Bushehr Thalassemia Hospital.


References
  1.  Hailan YMA, Sayed G, Yassin MA. COVID‐19 in a pregnant patient with beta‐thalassemia major: A case report. Clinical Case Reports 2021; 9(7): 12-20.
  2.  Hashemizadeh H, Noori R. Assessment hepatomegaly and liver enzymes in 100 patients with beta thalassemia major in Mashhad, Iran. Iranian Journal of Pediatric Hematology and Oncology 2012; 2(4): 171-79.
  3.  Ansari S, Baghersalimi A, Azarkeivan A, Nojomi M, Rad AH. Quality of life in patients with thalassemia major. Iranian Journal of Pediatric Hematology and Oncology 2014; 4(2): 57-69.
  4.  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. Mediterranean Journal of Hematology and Infectious Diseases 2017; 9(1): 78-95.
  5.   Asad ZT, Ghazanfari M, Naleini SN, Sabagh A, Kooti W. Evaluation of serum levels in T3, T4 and TSH in beta-thalassemic patients referred to the Abuzar hospital in Ahwaz. Electronic Physician 2016; 8(7): 2620-632.
  6.   Lioudaki E, Whyte M. Acute cardiac decompensation in a patient with beta‐thalassemia and diabetes mellitus following cessation of chelation therapy. Clinical Case Reports 2016; 4(10): 992-96.
  7.   Rasool M, Malik A, Jabbar U, Begum I, Qazi MH, Asif M, et al. Effect of iron overload on renal functions and oxidative stress in beta thalassemia patients. Saudi Medical Journal 2016; 37(11): 1239-250.
  8.  Jaidev S, Meena V, Sangeeta P. Study of serum ferritin level, SGOT, SGPT and hepatitis B status in multi transfused thalassemia patients. JARBS 2011; 3(2): 63-5.
  9.  De Sanctis V, Soliman AT, Canatan D, Yassin MA, Daar S, Elsedfy H, et al. Thyroid Disorders in homozygous β-Thalassemia: Current knowledge, emerging issues and Open problems. Mediter-ranean Journal of Hematology and Infectious Diseases 2019; 11(1): 38-59.
  10.   Karim MF, Ismail M, Hasan AM, Shekhar HU. Hematological and biochemical status of Beta-thalassemia major patients in Bangladesh: A comparative analysis. International Journal of Hematology-Oncology and Stem Cell Research 2016; 10(1): 7-20.
  11.  Rivella S. Iron metabolism under conditions of ineffective erythropoiesis in β-thalassemia. Blood 2019; 133(1): 51-8.
  12.   Azami M, Sharifi A, Norozi S, Mansouri A, Sayehmiri K. Prevalence of diabetes, impaired fasting glucose and impaired glucose tolerance in patients with thalassemia major in Iran: A meta-analysis study. Caspian Journal of Internal Medicine 2017; 8(1): 1-15.
  13.  Chahkandi T, Norouziasl S, Farzad M, Ghanad F. Endocrine disorders in beta thalassemia major patients. International Journal of Pediatrics 2017; 5(8): 5531-538.
  14.  Sultan S, Irfan SM, Ahmed SI. Biochemical markers of bone turnover in patients with β-thalassemia major: a single center study from southern Pakistan. Advances in Hematology 2016; 12(5): 167-78.
  15.   Surchi O, Ali S. Biochemical status of beta-thalassemia major patients in Erbil City. Erbil Dental Journal (EDJ) 2018; 1(1): 1-9.
  16.  Eghbali A, Taherahmadi H, Shahbazi M, Bagheri B, Ebrahimi L. Association between serum ferritin level, cardiac and hepatic T2-star MRI in patients with major β-thalassemia. Iranian Journal of Pediatric Hematology and Oncology 2014; 4(1): 17-32.
  17.  Ayyash H, Sirdah M. Hematological and biochemical evaluation of β-thalassemia major (βTM) patients in Gaza Strip: A cross-sectional study. International Journal of Health Sciences 2018; 12(6): 18-30.
  18.   Suman RL, Sanadhya A, Meena P, Goyal S. Correlation of liver enzymes with serum ferritin levels in β-thalassemia major. International Journal of Research in Medical Sciences 2017; 4(8): 3271-274.
  19.   Kanbour I, Chandra P, Soliman A, De Sanctis V, Nashwan A, Abusamaan S, et al. Severe liver iron concentrations (LIC) in 24 patients with β-thalassemia major: correlations with serum ferritin, liver enzymes and endocrine complications. Mediterranean J Hematol Infect Dis. 2018; 10(1): 33-49.
  20.  Sultana N, Sadiya S, Rahman M. Correlation between serum bilirubin and serum ferritin level in thalassaemia patients. Bangladesh Journal of Medical Biochemistry. 2011; 4(2): 6-12.
  21.   Khubchandani A, Solanki V, Solanki M. Estimation of serum lipid profiles in patients with beta thalassemia major. Int J Res Med. 2014; 3(2): 65-7.
  22.  Shams S, Ashtiani MTH, Monajemzadeh M, Koochakzadeh L, Irani H, Jafari F, et al. Evaluation of serum insulin, glucose, lipid profile, and liver function in β-thalassemia major patients and their correlation with iron overload. Lab Med. 2010; 41(8): 486-89.
  23.   Ragab SM, Safan MA, Sherif AS. Lipid profiles in β thalassemic children. Menoufia Medical Journal 2014; 27(1): 66-74.
  24.  Haghpanah S, Davani M, Samadi B, Ashrafi A, Karimi M. Serum lipid profiles in patients with beta-thalassemia major and intermedia in southern Iran. Journal of Isfahan University of Medical Sciences 2010; 15(3): 150-63.
  25.   Adil A, Sobani ZA, Jabbar A, Adil SN, Awan S. Endocrine complications in patients of beta thalassemia major in a tertiary care hospital in Pakistan. Journal of the Pakistan Medical Association 2012; 62(3): 307-318.
  26.  Aldudak B, Bayazit AK, Noyan A, Özel A, Anarat A, Sasmaz I, et al. Renal function in pediatric patients with β-thalassemia major. Pediatric Nephrology. 2000; 15(1-2): 109-112.
  27.   Şen V, Ece A, Uluca Ü, Söker M, Güneş A, Kaplan İ, et al. Urinary early kidney injury molecules in children with beta-thalassemia major. Renal Failure 2015; 37(4): 607-613.
  28.    Ahmadzadeh A, Jalali A, Assar S, Khalilian H, Zandian K, Pedram M. Renal tubular dysfunction in pediatric patients with beta-thalassemia major. Saudi Journal of Kidney Diseases and Transplantation 2011; 22(3): 497-510.
  29.  Hashemieh M, Radfar M, Azarkeivan A, Tabatabaei SMTH, Nikbakht S, Yaseri M, et al. Renal hemosiderosis among Iranian transfusion dependent β-thalassemia major patients. Int  J Hematology-Oncol nd Stem Cell Res. 2017; 11(2): 133-42.
  30.  Annayev A, Karakaş Z, Karaman S, Yalçıner A, Yılmaz A, Emre S. Glomerular and tubular functions in children and adults with transfusion-dependent thalassemia. Turkish Journal of Hematology 2018; 35(1): 66-78.
  31.  Adly A, Toaima DN, Mohamed N, El Seoud K. Subclinical renal abnormalities in young thalassemia major and intermedia patients and its relation to chelation therapy. Egyptian Journal of Medical Human Genetics. 2014; 15(4): 369-77.
  32.  Ahmed Z. Study of serum calcium, phosphorus and vitamin D status in multitransfused β-thalassemia major children and adolescents of Jharkhand, India. International Journal of Contemporary Pediatrics. 2019; 6(2): 598-610.
  33.   Aslan I, Canatan D, Balta N, Kacar G, Dorak C, Ozsancak A, et al. Bone mineral density in thalassemia major patients from Antalya, Turkey. Int J Endocrinol. 2012; 7(4): 23-31.
  34.  Najafipour F. Evaluation of endocrine disorders in patients with thalassemia major. Int Iran J Endocrinol Metabol. 2008; 6(2): 104-113.
  35.  Mostafavi H, Afkhamizadeh M, Rezvanfar M. Endocrine disorders in patients with thalassemia major. Int Iran J Endocrinol Metabol. 2005; 7(2): 143-47.



 

Type of Study: Research | Subject: Hematology & Blood Banking
Received: 2023/01/9 | Accepted: 2023/03/7 | Published: 2023/03/1
Add your comments about this article : Your username or Email:
CAPTCHA
Send email to the article author

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2024 CC BY-NC 4.0 | International Journal of Medical Laboratory

Designed & Developed by : Yektaweb