Effect of vitamin D deficiency treatment on thyroid function and autoimmunity markers in hashimoto's thyroiditis: A double-blind randomized placebo-controlled clinical trial
Parichehr Vahabi Anaraki, Ashraf Aminorroaya, Massoud Amini, Fatemeh Momeni, Awat Feizi, Bijan Iraj, Azamosadat Tabatabaei
Isfahan Endocrine and Metabolism Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
|Date of Submission||16-Jan-2017|
|Date of Decision||15-Apr-2017|
|Date of Acceptance||20-Jun-2017|
|Date of Web Publication||26-Sep-2017|
Isfahan Endocrine and Metabolism Research Center, Sedigheh Tahereh Research Complex, Khorram Street, Isfahan
Source of Support: None, Conflict of Interest: None
Background: The link between autoimmune thyroid diseases and Vitamin D deficiency has been reported. However, there are controversies in this regard. We conducted a double-blind randomized placebo-controlled clinical trial to investigate the effect of Vitamin D deficiency treatment on thyroid function and autoimmunity marker (thyroid peroxidase antibody [TPO-Ab]) in patients with Hashimoto's thyroiditis. Materials and Methods: Fifty-six patients with Hashimoto's thyroiditis and Vitamin D deficiency (25-hydroxyvitamin D level ≤20 ng/mL) were randomly allocated into two groups to receive Vitamin D (50000 IU/week, orally) or placebo for 12 weeks, as Vitamin D-treated (n = 30) and control (n = 26) groups, respectively. TPO-Ab, thyroid-stimulating hormone (TSH), parathormone, calcium, albumin, and creatinine concentrations were compared before and after trial between and within groups. The data were presented as mean (standard error [SE]) and analyzed by appropriate tests. Results: Mean (SE) of Vitamin D was increased in Vitamin D-treated group (45.5 [1.8] ng/mL vs. 12.7 [0.7] ng/mL, P = 0.01). Mean (SE) of TPO-Ab did not significantly change in both groups (734 [102.93] IU/mL vs. 820.25 [98.92] IU/mL, P = 0.14 in Vitamin D-treated and 750.03 [108.7] [IU/mL] vs. 838.07 [99.4] [IU/mL] in placebo-treated group, P = 0.15). Mean (SE) of TSH was not changed in both groups after trial, P = 0.4 and P = 0.15 for Vitamin D-treated and control groups, respectively. No significant difference was observed between two study groups in none studied variables (P > 0.05). Conclusion: Vitamin D treatment in Vitamin D deficient patients with Hashimoto's thyroiditis could not have significant effect on thyroid function and autoimmunity.
Keywords: Autoimmune thyroiditis, clinical trial, Iran, peroxidase, thyroid-stimulating hormone, Vitamin D deficiency
|How to cite this article:|
Vahabi Anaraki P, Aminorroaya A, Amini M, Momeni F, Feizi A, Iraj B, Tabatabaei A. Effect of vitamin D deficiency treatment on thyroid function and autoimmunity markers in hashimoto's thyroiditis: A double-blind randomized placebo-controlled clinical trial. J Res Med Sci 2017;22:103
|How to cite this URL:|
Vahabi Anaraki P, Aminorroaya A, Amini M, Momeni F, Feizi A, Iraj B, Tabatabaei A. Effect of vitamin D deficiency treatment on thyroid function and autoimmunity markers in hashimoto's thyroiditis: A double-blind randomized placebo-controlled clinical trial. J Res Med Sci [serial online] 2017 [cited 2020 Feb 24];22:103. Available from: http://www.jmsjournal.net/text.asp?2017/22/1/103/215653
| Introduction|| |
Vitamin D deficiency is a common medical condition and an important focus of research. Vitamin D has been known for its role in regulation of calcium and bone development since many years ago. Recently, the receptors of 1,25-dihydroxyvitamin D have been found on many cells, including immune cells., The expression of 1α hydroxylase (cyp27B1) activity in many of these cells supports ,, the idea that the Vitamin D has immunomodulating effects. Several genetic studies have shown an association between gene polymorphism of Vitamin D receptor and of 1α hydroxylase (cyp27B1),,, with autoimmune thyroid diseases (AITDs). However, some papers do not support these associations.
The role of Vitamin D has been suggested in many chronic diseases  and immune disorders such as multiple sclerosis,, rheumatoid arthritis, and type I diabetes mellitus.,, However, the relationship between Vitamin D and AITDs is still a controversial issue. Many studies have already pointed out a relation between low concentration of Vitamin D and AITDs;,,, however, the cause and effect relationship is not known. The findings of one prospective case-control study wer54e performed in Amsterdam  and did not support the association between low Vitamin D level and early stages of thyroid autoimmunity.
Most of the above-mentioned studies have a cross-sectional design, and to our best knowledge, no clinical trials have already been conducted on the effectiveness of Vitamin D treatment among Vitamin D deficient patients with AITDs.
Many of these studies have recommended that interventional clinical trials are necessary to determine the causal effect of Vitamin D deficiency in the pathogenesis of thyroid autoimmune diseases. Therefore, we designed this clinical trial to investigate the effect of Vitamin D deficiency treatment on thyroid function and autoimmunity marker, thyroid peroxidase antibody (TPO-Ab), in patients with Hashimoto's thyroiditis. The results of this study may be helpful to improve the management of AITDs and their prevention in susceptible people.
| Materials and Methods|| |
Study design and participants
In this double-blind placebo-controlled randomized clinical trial which was conducted from February to July 2015 in Isfahan Endocrine and Metabolism Research Center (IEMRC), 120 hypothyroid or euthyroid adults with positive TPO-Ab were selected by consecutive sampling method. Hypothyroid patients were euthyroid and stable on levothyroxine at least for 6 months or had mild hypothyroidism on enrolment (thyroid-stimulating hormone [TSH] <15 mU/L). Serum Vitamin D levels of selected patients were measured. Those people with 25-hydroxyvitamin D (25[OH] D) ≤20 ng/mL were included in the study. Patients with renal or liver disease, cancer, pregnancy, severe weight loss, and those who were on immunosuppressive medication, insulin, sulfonamides, or any supplement were excluded from the study. Those patients who were on levothyroxine, metformin, or statin treatment enrolled if their medications had been started at least 6 months before enrolment, and no dose adjustment was done during the study period. Study design explained for each person and participants knew that they may receive drug or placebo, and if they were in placebo group after completion of the study, their Vitamin D deficiency would be corrected by treatment. Each participant gave and signed a written informed consent. The research protocol was complied with the ethical standards of Helsinki Declaration (Edinburgh 2000) and approved by Regional Ethics Committee of Isfahan University of Medical Sciences.
The trial also was registered in the Iranian Registry of Clinical trials (IRCT) with the registration number IRCT2014120520216N1.
Procedures and variables assessment
Finally, 65 persons enrolled the study. Participants were randomly allocated using simple randomization to intervention (Vitamin D-treated) and control (placebo-treated) groups. Randomization was performed by a third person, and sealed drug boxes with label A or B were given to each person. Neither patients nor researchers knew the content of the boxes. After trial, the codes were broken. Patients in Vitamin D-treated group (n = 33) were assigned to receive pearls of Vitamin D, 50,000 unit weekly and those in control group (n = 32) were received placebo weekly for 12 weeks [Figure 1]. Both Vitamin D and placebo pearls were provided and manufactured by Zahravi's pharmaceutical company, Tehran-Iran.
|Figure 1: Consort diagram of the study in Vitamin D deficient, thyroid peroxidase antibody positive, euthyroid or hypothyroid patients, randomized in Vitamin D and placebo groups|
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Demographic characteristics and medical history of all studied population were recorded. Physical examination was done by an expert endocrinologist. The blood pressure was measure by ERKA sphygmomanometer, weight and height by SECA stadiometer, and waist circumference by tape meter. Body mass index was calculated by dividing weight (kg) by square of height (m2).
At the beginning and at the end of the trial, two blood samples were taken from each person, one clot and one ethylenediaminetetraacetic acid containing blood sample. Biochemical tests including calcium (Ca), phosphorus (P), albumin, C-reactive protein (CRP), blood urea nitrogen, and creatinine (Cr) were measured on the day of sampling. However, the serum samples taken to measure TPO-Ab, TSH, 25(OH)D, and parathormone (PTH) froze and stored at −20°C to be analyzed at the same time with the second sample at the end of the trial.
All biochemical tests were done by photometric assays (BT 2000) using Pars kit (Tehran, Iran). TPO-Ab, PTH, and TSH were measured by chemiluminescent immunoassay method (Advia Centaur CP, Siemens Healthcare Diagnostic Inc., USA).
Vitamin D measured by enzyme-linked immunosorbent assay kit (Immunodiagnostic Systems Limited, UK).
Continuous quantitative variables were expressed as mean and standard error of the mean (standard error) and qualitative variables as frequency and percentage. Normality of data was evaluated by Kolmogorov–Smirnov test and normal Q-Q plot. Log transformation was used for skewed data (including TSH, TPO-Ab, and CRP). Paired t-test was used for within-group comparisons, and between-group comparison was performed by multivariate analysis of covariance. Box's M-test was used for evaluating homogeneity of covariance matrixes. To compare the qualitative variables, Chi-square test was used. All data analysis was done using SPSS for Windows, version 20 (SPSS Inc., Chicago, IL, USA). P < 0.05 was statistically significant.
| Results|| |
Three persons in Vitamin D-treated group and six persons in placebo-treated group were excluded or dropped. Finally, a total of 30 Vitamin D-treated and 26 placebo-treated participants attended the baseline examination and entered in statistical analysis [Figure 1]. No one developed hypercalcemia during the study.
The clinical characteristics of the study participants are shown in [Table 1]. Demographic, anthropometric, and laboratory data were not significantly different between Vitamin D- and placebo-treated groups at baseline (P > 0.05).
|Table 1: Demographic and clinical characteristics of Vitamin D deficient, thyroid peroxidase antibody positive, euthyroid or hypothyroid patients, randomized in Vitamin D and placebo groups|
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The concentrations of 25(OH)D, TSH, and TPO-Ab at baseline in vitamin D- and placebo-treated groups are presented in [Table 1] and [Figure 2]a,[Figure 2]b,[Figure 2]c. The mean of 25(OH)D was 12.76 (0.74) ng/mL and 13.28 (0.86) in Vitamin D- and placebo-treated groups, respectively, at baseline (P = 0.98) [Table 1].
|Figure 2: (a) Concentrations of Vitamin D 25-hydroxyvitamin D at baseline and after trial in Vitamin D deficient, thyroid peroxidase antibody positive, euthyroid or hypothyroid patients, randomized in Vitamin D and placebo groups. (b) Concentration of thyroid peroxidase antibody at baseline and after trial in Vitamin D deficient, thyroid peroxidase antibody positive, euthyroid or hypothyroid patients, randomized in Vitamin D and placebo groups. (c) Concentrations of thyroid-stimulating hormone at baseline and after trial in Vitamin D deficient, thyroid peroxidase antibody positive, euthyroid or hypothyroid patients, randomized in Vitamin D and placebo groups|
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The mean of the biochemical measurements including TPO-Ab, TSH, PTH, calcium, albumin, and creatinine in Vitamin D- and placebo-treated groups at baseline and after trial are presented in [Table 2].
|Table 2: Mean (standard error) of biochemical parameters at baseline and after trial in Vitamin D deficient, thyroid peroxidase antibody positive, euthyroid or hypothyroid patients, randomized in Vitamin D and placebo groups|
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Within-group comparison in Vitamin D-treated group, showed significant decrease for PTH (P = 0.001) but not for TSH, TPO-Ab, or other variables (P > 0.05). In placebo-treated group, there was not any significant changes in studied variables (P > 0.05).
Between-group analyses showed significant difference only in terms of mean PTH when adjustment was made for baseline values. No significant difference was observed between two study groups in none studied variables (P > 0.05).
| Discussion|| |
We investigated the effect of Vitamin D treatment on autoimmune thyroid marker (TPO-Ab) and thyroid function (TSH) in Vitamin D deficient hypothyroid or euthyroid adult patients with positive TPO-Ab. Our results indicated that Vitamin D did not have a significant effect on thyroid function and autoimmunity of studied population.
Kivity et al. in a cross-sectional study compared the level of Vitamin D in patients with AITDs, non-AITDs, and healthy people. They showed that the prevalence of Vitamin D deficiency was significantly higher in patients with AITDs than healthy persons. The rate of Vitamin D deficiency was also higher in patients with non-AITDs than healthy population.
Shin et al. in Korea studied the association between Vitamin D and TPO-Ab in patients with and without AITDs. They demonstrated that there was a significant negative correlation between Vitamin D level and TPO-Ab in patients with AITDs.
In a study in Turkey, Bozkurt et al. studied the relation between Vitamin D deficiency and Hashimoto's thyroiditis. They compared the level of Vitamin D and severity of Vitamin D deficiency between euthyroid patients with Hashimoto's thyroiditis and a healthy control group. Their results pointed out that there was correlation between severity of Vitamin D deficiency and thyroid volume, level of thyroid autoantibodies as well as duration of Hashimoto's thyroiditis. They concluded that Vitamin D may have potential role both in development and progression of Hashimoto's thyroiditis to hypothyroidism.
In a study in Tehran, Iran, Mansournia et al. reached to the similar conclusions. Furthermore, they showed that by 5 ng/mL increases in the level of Vitamin D, the risk of occurrence of Hashimoto's thyroiditis would be decreased by 19%.
Several other studies also reported similar results regarding the inverse association between Vitamin D level and AITDs.,,,,
On the other hand, some studies did not support the association between Vitamin D and thyroid autoimmunity.,,,, Effraimidis et al. have conducted two case–control researches in the framework of Amsterdam AITD cohort study to determine the association between Vitamin D and early stages of thyroid autoimmunity. In one cross-sectional study, they compared the concentration of serum Vitamin D between euthyroid participants with genetic susceptibility for AITDs and negative thyroid antibodies and controls who were healthy women without family history of AITDs. In another longitudinal study, they compared level of Vitamin D between those euthyroid persons with genetic susceptibility for AITDs who developed TPO-Ab and those who did not. Their findings showed higher Vitamin D level in euthyroid participants with genetic susceptibility to AITDs than control group but not any significant differences between patients with newly diagnosed thyroid autoimmunity than control group. They concluded that Vitamin D is not correlate with early stages of thyroid autoimmunity.
D'Aurizio et al. did not find any association between low Vitamin D levels and AITDs too.
The strength of our clinical trial was its novelty. This was the first randomized controlled clinical trial which evaluated the effects of Vitamin D treatment on thyroid autoimmune disease (Hashimoto's thyroiditis), in a prospective manner. We rely on 25(OH)D measurement to define Vitamin D deficiency (≤20 ng/mL) and assessing treatment efficacy with increasing the concentration of 25(OH)D to more than 30 ng/mL. We measured the baseline autoimmune marker and Vitamin D levels at the same time.
The limitations of this study were small sample size and short duration of follow-up period.
We recommend a larger sample size and longer follow-up and enrolment of people with positive family history of AITDs as they are more prone to AITDs and may benefit from potential prevention protocols.
| Conclusion|| |
The findings of this clinical trial did not support the hypothesis that Vitamin D treatment can improve thyroid autoimmune diseases.
The authors would like to thank the laboratory technicians of IEMRC, especially Ms. Atosa Norozi. We express our great appreciation to Mr. Majid Abyar for his computer assistance, Ms. Mansooreh Kabirzadeh for her help in randomization and intervention blinding, and Dr. Silva Hovsepian and Dr. Meamar for their assistance for their technical comments. We also appreciate Zahravi's pharmaceutical company in providing placebo pearls of Vitamin D for our research and finally with many thanks from all participants that cooperated with us during the study.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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