Abstract
Numerous problematic disorders such as vitamin D (Vit-D) deficiency subsequent to large iron loading can be developed in patients with β-thalassemia. The study aimed to estimate Vit-D insufficiency and its risk factors in patients with β-thalassemia. In this multicenter and observational study, all β-thalassemia patients, who referred to 14 hospital-based thalassemia divisions or clinics in Mazandaran province, Iran were included in the study. The data belong to December 2015 until December 2019. The study population was made of transfusion dependent thalassemia (TDT) and non-transfusion-dependent thalassemia (NTDT) patients. Serum levels of 25-OHD3 have been measured by high performance liquid chromatography (HPLC) method as ng/mL. Demographic and clinical information along with some biological tests, as well as the results of T2*-weighted magnetic resonance imaging were analyzed. Of 1959 registered patients, 487 (24.9%) patients had Vit-D-related data. The prevalence of Vit-D insufficiency (< 30 ng/mL) was 41.9, 95% CI 37.5–46.3. The adjusted risks of moderate to severe liver siderosis and raised AST (aspartate aminotransferase) for Vit-D insufficiency (< 30 ng/mL) were 2.31, 95% CI 1.38–3.89 and 2.62, 95% CI 1.43–4.79, respectively. The receiver operating characteristic (ROC) curve analysis showed that the predictive accuracy of ferritin for Vit-D insufficiency status was 0.61, 95% CI 0.54–0.68 with a cutoff point of 1,078 ng/mL (P = 0.03, sensitivity 67%, specificity 49%, positive predictive value [PPV] 47% and negative predictive value [NPV] 68%). In spite of the national programs for treating Vit-D deficiency and our previous efforts for giving supplements to all patients, Vit-D insufficiency/deficiency is still common in our patients. Also, moderate to severe liver siderosis and raised AST were the independent risk factors for the Vit-D insufficiency.
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Introduction
β-Thalassemia, a congenital defect in the synthesis of the β-globin chains of the hemoglobin, is the most common genetic disease worldwide. It is estimated that 3% of the world population carries one of β-thalassemia phenotype characteristics1,2. Based on data obtained from the Thalassemia Association in Iran, the number of patients with thalassemia in 2005 was 18,616, and this number was enhanced to 20,000 in 2016. The majority of thalassemia patients have been scattered in the Mazandaran and Fars provinces3,4,5.
Low hemoglobin levels in patients with β-thalassemia major—so-called transfusion-dependent β-Thalassemia (TDT)—cause a need to chronic blood transfusion in the rest of their life6. Every blood unit includes near 200–250 mg iron7,8,9. Although the repeated blood transfusion plays a life-saving role in thalassemic patients, an iron toxicity would happen in these cases10,11,12. Many problematic disorders such as vitamin D (Vit-D) deficiency subsequent to large iron loading can be developed in TDT patients. The deficiency in Vit-D is associated with rickets/ osteomalacia and also a decrease in heart activity, muscle fatigue and insulin resistance5,13,14. Moreover, Vit-D deficiency is correlated with numerous mental and physical complications15,16,17,18,19,20,21.
Checking serum levels of 25-OHD3 is not recommended for general population due to the cost. In thalassemia wards, however, serum 25-OHD3 would be measured at least yearly and Vit-D supplements are being administered according to the results. To the best of our knowledge, there has not been any study in Iran aiming to investigate Vit-D status in patients with β-thalassemia with such a sample size. Based on the role of genetic diversities in the incidence of thalassemic complications22, and because of the lack of enough studies in Iranian population, the current study aimed to estimate Vit-D insufficiency and its risk factors in patients with β-thalassemia.
Materials and methods
Ethics statement
Mazandaran Thalassemia Registry (MTR) was approved by the Vice Chancellor of Research and Technology, the Ethics Committee and Institutional Review Board (IRB) of Mazandaran University of Medical Sciences in 2015. The university vouched the study protocol and all methods were performed in accordance with the relevant guidelines and regulations. Before data registration, all patients got informed and oriented by all physicians and care providers who were working with these patients throughout the province. The informed written consent was obtained from all the participants in the current study. All patients were assured that their information will be confidentially kept. The online website is available at thr.mazums.ac.ir.
Study design
The thalassemia registry is an online data bank for a quick and on time assessment of epidemiological and clinical aspects of patients with β-thalassemia in the province, working since 2015. This multicenter and observational study was based on recorded data and a census method. All patients with β-thalassemia, who referred to 14 hospital-based thalassemia divisions or clinics under Mazandaran University of Medical Sciences, between December 2015 and December 2019 were included into the study. The thalassemia research center (TRC) of Bu-Ali Sina hospital was the core center to establish the study.
Patients and data collection
The study population was made of TDT and non-transfusion-dependent thalassemia (NTDT) patients. All patients were diagnosed and documented by their responsible physicians based on the results of CBC (complete blood count) after birth, hemoglobin electrophoresis and genetic test for mutations of the β-globin gene. Transfusion dependent thalassemia cases were on a regular red-cell transfusion.
The information sources comprise demographic, bio-clinical and therapeutic data in thalassemic wards in the north of Iran (n = 1959). The patients' information was extracted from the MTR with ethical points using a self-made checklist. The checklist contains variables, including demographic and clinical features, transfusion dependency and information about iron chelation therapy. Also, we used medical history and laboratory data such as AST (aspartate aminotransferase), ALT (alanine aminotransferase), serum ferritin, calcium, phosphor, parathyroid hormone (PTH) and use of Vit-D supplementation.
Magnetic resonance imaging (MRI)
A MRI without contrast was performed on a 1.5 T MR scanner (Symphony; Siemens, Germany) to calculate the T2*-weighted magnetic resonance imaging (MRI T2*, millisecond [ms]) for all patients. Cardiac MRI was carried out based on the Brompton protocol23. To measure myocardial T2*-weighted, scans were coordinated to the cardiac cycle by use of standard electrocardiography gating. A standard radio frequency body coil was also applied in all measurements. The region of interest (ROI) was determined in mid-ventricle. The center of the liver was imaged at 12 diverse echo times (1.29 to 23 ms, increasing in 2.2 ms increments) by a single trans-axial slice24.
The results of heart and liver MRI T2* were registered as normal to severe25. Cardiac siderosis was characterized by cardiac MRI T2* index, a myocardial loading, as follows: ≥ 20 ms (normal), 19.99–14 ms (mild), 13.99–10 ms (moderate) and < 10 ms (severe). The classification of hepatic siderosis severity was based on hepatic MRI T2* index, a hepatic loading, as normal (≥ 6.3 ms), mild (6.3–2.80 ms), moderate (2.79–1.4 ms) and severe (< 1.4 ms)25.
Echocardiography
According to the American Society of Echocardiography, a transthoracic Echocardiography, M-mode, 2D, color Doppler was used to prepare the echocardiograms and GE Vivid S5 echocardiographic machine (General Electric, Boston, MA, USA) at rest and in supine and left lateral decubitus position. To measure the left ventricular ejection fraction (LVEF), the biplane Simpson technique was applied26,27. Pulmonary artery pressure (PAP) was also valued by use of the Bernoulli equation to estimate the pressure gradient between the right ventricle and the right atrium28. Reduced LVEF was also considered as LVEF lower than 55%29.
Biochemical parameters
Serum levels of 25-OHD3 have been measured by high performance liquid chromatography (HPLC) method as ng/mL. A categorical scale was also used for Vit-D insufficiency as follows: insufficient/ deficient (< 30 ng/mL), insufficient (30–20 ng/mL), deficient (< 20 ng/mL), moderately deficient (20–10 ng/mL) and severe deficiency (< 10 ng/mL)30,31. The serum AST and ALT levels higher than 40 and 56 U/L were defined as abnormal ranges32. Serum ferritin 800 ≥ ng/mL and 2000 ≥ ng/mL were demarcated as iron overload condition in NTDT and TDT cases, respectively33,34.
Statistical analysis
All statistical procedures were performed by SPSS software package (version 20.0, SPSS Inc., Chicago, IL, USA) and STATA version 13 (StataCorp, College Station, TX, USA). Data have been expressed as mean ± standard deviation (M ± SD) or number (percent). The normal distribution of quantitative variables was checked through histogram plot and Shapiro–Wilk test. We utilized the independent student's t- and chi-square tests to compare the variables between two groups, insufficient versus non-insufficient in 25-OHD3 level. The risk of different grades of Vit-D insufficiency was computed as crude and adjusted. To calculate the adjusted odds ratio (OR), the effects of multiple potential confounders including age, gender, transfusion dependency, calcitriol, Vit-D and calcium supplementations were controlled. The correlation between 25-OHD3 and serum ferritin was estimated using Pearson correlation coefficient. A logistic regression model was lastly applied to sort the risk factors based on their strength in this study. The goodness of fit of the model was assessed by means of Hosmer and Lemeshow test. We also checked multicollinearity between independent variables for the final model with the LMCOL command, based on VIF index (variance inflation factor). A receiver operating characteristic (ROC) curve analysis was operated to determine an optimal statistically significant threshold value of ferritin in discriminating Vit-D insufficiency. The prevalence of Vit-D insufficiency grades, with 95% confidence interval (CI), were also estimated using the binomial exact method by STATA 13 software. A P value lower than 0.05 was chosen as the threshold of statistical significance. A correction on the estimated ORs was performed in our study by an online web calculator (https://clincalc.com/Stats/ConvertOR.aspx).
Results
Out of 1959 registered data, 487 patients had Vit-D-related data in the thalassemia registry (24.9%). Basic characteristics, clinico-biological and therapeutic status of β-thalassemia patients are also shown in Table 1.
The mean ± SD of Vit-D was 38.31 ± 41.20 ng/mL (3 to 786, median = 32.20 ng/mL). The prevalence of Vit-D insufficiency (< 30 ng/mL) in all β-thalassemia patients was 41.9, 95% CI 37.5–46.3. The difference in the prevalence of Vit-D insufficiency between TDT and NTDT patients was significantly found in the severe Vit-D deficiency category. The results of a subgroup analysis for the prevalence of Vit-D insufficiency in all grades according to blood transfusion dependency are shown in Table 2.
Of 19 registered data regarding LVEF, the percentage of reduced LVEF in Vit-D insufficient patients (< 30 ng/mL) was 60% (three cases, n = 5) compared with 28.6% (four cases, n = 14) among non-Vit-D insufficient patients (OR 3.75, 95% CI 0.44–31.62, P = 0.21). The mean ± SD of LVEF in Vit-D insufficient patients (< 30 ng/mL) versus non- insufficient individuals was 51.0 ± 8.94% and 53.9 ± 5.25%, respectively (P = 0.4). The difference of PAP among patients with Vit-D insufficiency (< 30 ng/mL) and without Vit-D insufficiency was not significant (M ± SD, 38.3 ± 2.89 mmHg versus 34.2 ± 9.67 mmHg; P = 0.5, respectively.
The OR of iron overload (ferritin 800 ≥ ng/mL) for Vit-D insufficiency (< 30 ng/mL) in cases with NTDT was 1.84, 95% CI 1.17–2.90. In TDT patients, the risk of iron overload (ferritin 2000 ≥ ng/mL) was calculated 1.5, 95% CI 0.52–4.34 for Vit-D insufficiency.
The adjusted risks of moderate to severe liver siderosis and raised AST for Vit-D insufficiency (< 30 ng/mL) were 2.31, 95% CI 1.38–3.89 and 2.62, 95% CI 1.43–4.79, respectively. The adjusted risk in patients with raised AST for severe Vit-D insufficiency (< 10 ng/mL) has been significantly valued at 6.49, 95% CI 2.39–17.62. The potential risk factors for Vit-D insufficiency in β-thalassemia patients are shown in Table 3.
After converting ORs to risk ratio (RR) index, the modified risk of Vit-D insufficiency (< 30 ng/mL) for patients with cardiac siderosis changed to a risk of 18% (RR = 1.18). The adjusted risk of 16% was also found for Vit-D insufficiency (< 30 ng/mL) in cases who had moderate to severe cardiac siderosis, RR = 1.16. The risk of Vit-D insufficiency (< 30 ng/mL), 12% raised in patients with liver siderosis after a bias correction (RR = 1.12). A 31% escalation in the risk of Vit-D insufficiency (< 30 ng/mL) was computed for patients with moderate to severe liver siderosis (RR = 1.31). In iron overloaded cases (ferritin 2000 ≥ ng/mL), the risk of Vit-D insufficiency (< 30 ng/mL) decreased to 25% after the correction of upward bias (RR = 1.25). The modified risk of Vit-D insufficiency (< 30 ng/mL) for patients with raised ALT and cases with raised AST changed to the risk of 19% and 39%, respectively (RR = 1.19 and RR = 1.39).
The multivariate logistic regression analysis presented a significant association between raised AST and also moderate to severe liver siderosis with Vit-D insufficiency (< 30 ng/mL). The results of the multivariate logistic regression model have been provided in Table 4. The ROC curve analysis showed that the predictive accuracy of ferritin for Vit-D insufficiency status was 0.61, 95% CI 0.54–0.68 with a cutoff point of 1,078 ng/mL (P = 0.03, sensitivity 67%, specificity 49%, positive predictive value [PPV] 47% and negative predictive value [NPV] 68%). There was a significant negative association between 25-OHD3 and serum ferritin (r = − 0.2; P < 0.01).
Discussion
This study was designed to evaluate the prevalence and risk factors of Vit-D insufficiency in β-thalassemia patients. Although the majority of patients—roughly 68 percent—received Vit-D supplementation, the prevalence of Vit-D insufficiency is not ignorable. The prevalence of the majority of Vit-D insufficiency was highly detected among TDT patients. Cardiac siderosis, moderate to severe cardiac siderosis, liver siderosis, moderate to severe liver siderosis, iron overload (ferritin 2000 ≥ ng/mL) and the raise of ALT and AST levels were introduced as the risk factors for Vit-D insufficiency in this population. After controlling potential confounders, the multivariate logistic regression analysis presented that raised AST and moderate to severe liver siderosis as the outstanding risk factors had the maximum strength of association with Vit-D insufficiency in β-thalassemia patients.
Some evidence has shown that Vit D deficiency has been seen in 12.8 to 82% of TDT patients35,36. Progressive accumulation of iron37, parenchymal hemosiderosis38, insufficient hydroxylation in the liver39, malabsorption of Vit-D intestinal, and impaired synthesis of Vit D in the skin subsequent to jaundice37 have been reported as the plausible causes of Vit-D insufficiency in TDT patients. Elevated serum iron levels ensues from blood transfusions and hyperabsorption of dietary iron by the gastrointestinal tract—especially in NTDT alongside reduced hepcidin as the hepatic peptide hormone regulating iron homeostasis40—are conducive to the iron siderosis in several organs such as tissue, cardiac, liver and also endocrine system glands, which harm their natural physiology. Subsequently, endocrinopathy and Vit-D deficiency as the adverse consequences resulting from superfluous iron burden can occur in patients with TDT41,42.
Previous studies have shown that Vit-D levels were significantly reduced in thalassemia patients who had chronic blood transfusions31,37,43. In current study, the greatest prevalence of Vit-D insufficiency belongs to TDT, except one subgroup of Vit-D insufficiency (20 to 10 ng/mL). In other words, the prevalence of the majority of Vit-D insufficiency was highly detected among TDT patients.
Repeated blood transfusions can cause secondary iron overload conditions which may disturb the 25-hepatic hydroxylation and synthesis of Vit D, causing Vit D deficiency31. Also, an iron deposition in the intestinal epithelium may interrupt the gastrointestinal absorption of Vit-D which can contribute to develop a comparatively resistant to Vit D supplementations in β-thalassemia patients44. It has been stated that the darkening of the skin due to iron siderosis seems to interfere with Vit-D synthesized in the skin in TDT patients44. Given this, we speculate that iron overload also contributed to Vit-D deficiency in these patients.
Recently, the results of a cross-sectional on 61 patients with TDT have shown that there has been an relationship between Vit-D deficiency and cardiac MRI T2* in these patients. The mean (range) of 25-OHD3 levels in patients with cardiac siderosis was 15.9 ng/mL (11.7 to 20.0 ng/mL) compared to 20.2 ng/mL (15.85 to 22.3 ng/mL) in patients without siderosis (P = 0.06). The reported prevalence of Vit-D deficiency was also 50.8%45. In another cross-sectional study on 40 TDT patients, there was no correlation between serum 25-OHD3 and liver and cardiac MRI T2*. The mean of 25-OHD3 serum levels was 16.1 ± 8.1 ng/dl5.
Patients with moderate to severe liver siderosis and/or iron-overload had a greater tendency to Vit-D insufficiency than those without moderate to severe liver siderosis and/or iron-overload. Transfusional iron burden in TDT patients leads to an increase in ferritin and the formation of iron siderosis in liver46. In other findings confirmed in β-thalassemia population, serum ferritin levels are significantly higher in patients with Vit-D deficiency35,37,44. Excessive accumulation of iron can help to promote Vit-D deficiency resultant a disturbance in Vit-D-PTH axis.
A study aimed to examine the association of hepatic siderosis with Vit-D-PTH axis in TDT patients. That results demonstrated that ferritin levels of > 2500 μg/L were an independent risk factor for Vit-D insufficiency in the patients with TDT (OR 5.3, 95% CI 2.3–12.3; P < 0.01)46. In a recent study, the patients deprived of Vit-D supplements with ferritin levels of > 9000 ng/mL had multiple endocrinopathies including osteoporosis and low levels of 25-OHD3 (17.1 ± 7.9 ng/mL)47.
In a case–control study46, in a case group of 158 TDT patients with an average of 26.5 ± 1.1 nmol /L for 25-OHD3, Vit D deficiency had a 8.8-fold increase in the patients with liver iron concentration (LIC) above 7 mg/g dry weight (OR 8.8, 95% CI 3.5–10.3; P < 0.01). The prominent role of iron in the overgeneration of reactive oxygen specious (ROS) and the exacerbation of oxidative stress through Fenton and Haber–Weiss reactions are well-documented48,49. Indeed, iron burden can be noxious for vital organs and can expedite the endocrine disorders via an overproduction of ROS, disrupting the ferroportin-hepcidin axis. As liver is a target organ for the iron deposition, the inception of iron siderosis can begin in hepatic tissue in overloaded patients. Eventually, the progressive iron excess and a deleterious iron deposition in the liver can lead to structural and functional damage to hepatocytes through fibrosis46.
Our findings revealed that the patients with increased levels of ALT and AST had a greater risk of severe Vit-D insufficiency versus those without raise of ALT and/or AST levels. Liver damage due to iron overload in the liver can increase liver enzymes such as ALT and AST50. It has been shown that the reduced levels of 25-OHD3 can increase the likelihood of raising ALT and AST levels in β-thalassemia patients51. In a study, the elevated levels of ALT (> 50 IU/L) were significantly connected to Vit-D insufficiency in patients with β-thalassemia (OR 9.7, 95% CI 4.0–23.5; P < 0.001)46. Since the serum ALT levels might be dependent on LIC, a prolonged hepatic iron deposition may be the main cause of decreased 25-OHD3 level in blood circulation among patients with β-thalassemia46.
Regarding some surveys, Vit-D deficiency increases PTH and hyperparathyroidism52 and PTH affects the myocardium both directly and indirectly through G protein-coupled receptors, causing left ventricular hypertrophy and an increased risk of heart failure53. On the other hand, the transfer of iron to the heart myocytes and iron overload are performed by cardiac L-type voltage-dependent calcium channels (LVDCCs) which induce heart dysfunction45. It should also be noted that Vit-D deficiency causes the production of inflammatory cytokines, creating oxidative stress, and accelerating the process of fibrosis of the heart muscle cells. All of these mechanisms are associated with a reduction in LVEF in thalassemia patients with Vit-D deficiency54. In our findings, the risk of decreased LVEF in the cases with Vit-D insufficiency was near twofold higher than those who did not have Vit-D insufficiency. However, more well-defined and large studies to investigate the relationship between reduced LVEF and Vit-D insufficiency in β-thalassemia patients are required in the future.
Study limitations
There have been several limitations in current study. These limitations include other factors that can effect on Vit-D status, comprising sun exposure and outdoor activity that have not been evaluated. In this study, the effects of other nutritional deficiencies on heart function were not investigated. The measure time of Vit-D test and doing cardiac and liver MRI and also echocardiography were not exactly concurrent. Moreover, the ferritin and liver enzyme levels may be affected by the possible existing infectious diseases at the test time in our population. Finally, the quantitative values of LIC, heart and liver MRI T2* were not considered to be registered in our data registry for further analyses.
Conclusion
In spite of the national programs for treating Vit-D deficiency and our previous efforts for giving supplements to all patients, Vit-D insufficiency/deficiency is still common in our patients and needs more attention. Also, moderate to severe liver siderosis and raised AST were the independent risk factors for the Vit-D insufficiency in β-thalassemia.
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Acknowledgements
The authors thanks thalassemic patients for their permission to use their data. Also we thank the nurses who are registering data.
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The Ministry of Health and Medical Education funds the Thalassemia Registry.
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H.D.K, H.K. and M.N.S. contributed to the conception and design of this study. M.Z., A.R. and A.A. acquired the data. H.D.K. analyzed and interpreted the data. H.D.K., H.K. and H.K drafted the manuscript, which M.K. and M.N.S critically revised.
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Darvishi-Khezri, H., Karami, H., Naderisorki, M. et al. Moderate to severe liver siderosis and raised AST are independent risk factors for vitamin D insufficiency in β-thalassemia patients. Sci Rep 10, 21164 (2020). https://doi.org/10.1038/s41598-020-78230-4
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DOI: https://doi.org/10.1038/s41598-020-78230-4
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