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. 2022 Nov 15;11:e2397. doi: 10.31661/gmj.v11i.2397

Changes in Serum Alkaline Phosphatase, Calcium, and Parathyroid Hormone with Different Doses of Iodine Therapy

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Mohammad Mehdi Movahedi 1,2, Gholam Reza Karimaghaei 3, Ahmad Noori 4, Mohammad Atefi 2,5, Tahereh Mahmoudi 1, Farshid Gheisari 2,6,✉
PMCID: PMC9838107  PMID: 36698694

Abstract

Background: Despite the benefits of radioactive iodine (RAI) therapy as an adjunctive treatment for thyroid cancer, it can be associated with several side effects. The main purpose of this study was to determine the changes in serum alkaline phosphatase (ALP), calcium (Ca), and parathyroid hormone (PTH) at different doses of RAI therapy among patients who were referred to the nuclear medicine department of Namazi Hospital, Shiraz. Materials and Methods: This cross-sectional study was conducted on 60 patients with papillary thyroid cancer who underwent RAI therapy at different doses of 100, 150, and 200 mCi. The ALP, Ca, and PTH levels of patients were measured before and 60 days after RAI therapy. Results: Our study revealed that RAI therapy at all doses significantly increased ALP level in comparison with baseline amounts (P≤0.05). However, changes in PTH and Ca levels were not significant among patients who received different doses of RAI (P˃0.05). Conclusion: RAI therapy could affect important hormones and enzymes such as ALP and PTH. This issue can be considered in diagnostic and therapeutic prescriptions of RAI for the treatment of thyroid cancer.[GMJ.2022;11:e2397]

Keywords: Nuclear Medicine, Thyroid Cancer, Radioactive Iodine, Alkaline Phosphatase, Serum Calcium, Parathyroid Hormone

Introduction

One of the most important effects of radiation on various organs is their late effects, which occur at different and long intervals after irradiation from low doses. In such effects, there is a noticeable time interval between exposure and the time of symptoms onset. These effects include an imperceptible reduction in the life span, the emergence of genetic impacts on future generations, and the occurrence of various cancers [1][2][3]. Cancer affects more than one-third of the population, accounting for more than 20% of all deaths, and it is responsible for more than 10% of total health care costs in developed countries [4]. In 2000, there were 10 million new cases of cancer and 6 million cases of cancer-related deaths worldwide [5]. Each year, approximately 1.5 million people in the United States are diagnosed with some cancers for the first time [6]. According to reports, in 2003, about 556,000 people died related to malignancies, which is equivalent to 1,500 daily deaths, and only deaths caused by cardiovascular diseases are more prevalent than this amount [7]. The most common cancers are prostate, lung, and colon cancers in men, and breast, lung, and colon cancers in women. Lung, breast, prostate, and colon cancers caused more than 50% of cancers diagnosed, as well as cancer deaths in the United States [8][9].

Regarding applications of ionizing radiation, including radiology, nuclear medicine, and computed tomography scans, in addition to the benefits of diagnosing and treating diseases, the risk of radiation should also be considered [10]. Iodine 131 is a radioactive substance widely used to diagnose and treat diseases. The dose of iodine 131 used for the diagnostic cases is 5 millicurie (mCi), but the doses used for therapeutic purposes are much higher (about 20 to 250 mCi) and even more in some cases [11]. One of the major differences between radioactive iodine (RAI) 131 and other radiopharmaceuticals used in nuclear medicine is the confirmed type of radiation, which is a beta type that has a greater practical biological effect than gamma rays [12]. Recently, many studies have been conducted on the extent of biological damage following treatment with RAI. This substance is used to treat thyroid cancers with doses above 100 mCi and in the treatment of hyperthyroidism with lower doses [13][14]. One of the biological effects of beta radiation is chromosomal abnormalities that can be measured in different ways in individuals who have undergone diagnostic or therapeutic studies with RAI [15][16]. One of the indicators of the harmful effects of the medical application of ionizing radiation, including radioactive substances, is the changes in the levels of enzymes and hormones among patients. The aim of this study was to evaluate the changes in serum alkaline phosphatase (ALP), Calcium (Ca), and parathyroid hormone (PTH) at different doses of RAI therapy in patients with papillary thyroid cancer.

Materials and Methods

Patients

This cross-sectional study was performed on 60 patients with papillary thyroid cancer who were referred to the RAI therapy division of the nuclear medicine department of Namazi Hospital, Shiraz, Iran, during 2013-2019.

Inclusion and Exclusion Criteria

A definitive diagnosis of papillary thyroid cancer was confirmed by nuclear medicine professors and pathology reports (in cases in which the diagnosis was based on biopsy). Patients with other thyroid pathologies, previous history of radiation, pregnancy, and breastfeeding were excluded from the study.

Data Collection

Baseline characteristics of patients, such as age, sex, weight, height, and body mass index were recorded. The serum levels of Ca, ALP, and PTH before and 60 days after RAI therapy were obtained. Also, the patients were divided into three groups based on received doses of iodine as 100, 150, and 200 mCi. The subjects’ demographics and clinical characteristics are reported in Table-1.

Table - 1 . Changes in Serum Alkaline Phosphatase (ALP), Parathyroid Hormone (PTH), and Calcium (Ca) Levels before and after Radioactive Iodine (RAI) with Different Doses.

Variables RAI Therapy P-Value
Before (mean±SD) After (mean±SD)
ALP (U/L)
100 mCi 287.3±73.09 330.1± 61.3 0.002
150 mCi 247.9±72.79 281.5±68.4 0.001
200 mCi 243.9±57.7 289.1±74.38 0.004
PTH (pg/ml)
100 mCi 37±13.65 37.2±14.69 0.88
150 mCi 44.7±15.19 41.8±12.39 0.24
200 mCi 39.4±11.16 42.4±13.37 0.2
Ca (mmol/l)
100 mCi 7.33±0.71 7.29±0.55 0.65
150 mCi 7.68±1.06 7.55±0.86 0.35
200 mCi 7.8±0.92 7.58±0.85 0.31
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ALP:Alkaline phosphatase; Ca:Calcium; PTH:Parathyroid hormone; RAI: Radioactive iodine

Ethical Approval

This study was approved by the Shiraz University of Medical Sciences Institutional Review Board (IR.SUMS.MED.REC.1400.234). The declaration of Helsinki was considered during the study, and written informed consents were obtained from the patients.

Data Analysis

Data analysis was performed using SPSS software (The IBM® SPSS® software), and t-test and chi-squared test were applied. A P-value of <0.05 was considered statistically significant.

Results

The mean age of patients was 38 (63.3%) were female. According to Table-1, the changes in serum ALP level at a dose of 100 mCi were statistically significant (P=0.002) and increased from 287.3±73.09 to 330.1±30.3 U/L. However, there were no significant changes in Ca and PTH levels among patients who received a dose of 100 mCi (P=0.65 and P=0.88, respectively).

As shown in Table-1, among patients who received doses of 150 and 200 mCi, serum ALP levels were significantly increased after RAI therapy compared to the baseline levels (P=0.001 and P=0.004, respectively). The Ca and PTH levels of patients in groups 150 and 200 mCi were decreased after RAI therapy. However, findings showed Ca and PTH levels were not significantly changed after RAI therapy with doses of 150 and 200 mCi (Table-2).

Table 2. Changes in Variables before and after RAI with Dose of 100, 150 and 200 mCi for Three Groups of Patients .

Variable Before RAI (mean±SD) After RAI (mean±SD) RAI dose (mCi) aP-value
287.3±73.09 330.1±61.3 100 0.002
ALP (U/L) 247.9±72.79 281.5±68.4 150 0.001
243.9±57.7 289.1 ±74.38 200 0.004
7.33±0.71 7.29±0.55 100 0.65
Ca (mmol/l) 7.68±1.06 7.55±0.86 150 0.35
7.8±0.92 7.58±0.85 200 0.31
0.37±13.65 37.2±14.69 100 0.88
PTH (pg/ml) 44.7±15.19 41.8±12.39 150 0.24
11.16±39.4 42.4±13.37 200 0.2
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ALP: Alkaline phosphatase; Ca: Calcium; PTH: Parathyroid hormone; RAI: Radioactive iodine.aComparison of changes between baseline and follow-up

Discussion

The results of the present study were in line with the results obtained by Wang et al. that evaluated changes in liver enzymes following RAI therapy [17]. Changes in PTH and ALP were mentioned as consequences of RAI therapy [18], while in our study, only changes in ALP level were significant. Guven et al. [19] evaluated the effect of a high dose of RAI therapy on the parathyroid function of patients with various types of thyroid cancer. They studied biochemical parameters, such as serum Ca, phosphate, creatinine, ALP, intact PTH (iPTH), and urinary Ca levels [19]. The results indicated no significant changes in serum Ca levels, while the changes in iPTH and ALP levels were significant [19].

Some research indicated that the therapeutic effect of RAI on toxic and non-toxic goiter is based on the fact that it emits strong beta-ionizing radiation, which causes damage to thyrocytes [20]. The maximum range of beta radiation from iodine 131 decay is about 2.4 mm [21]. Hence, the RAI radiation not only affects the tissue of the thyroid gland but also reaches more than 2 mm of its surroundings, and by increasing the radiation dose, its effect also increases [22][23][24]. Anatomically, it has been shown that the parathyroid glands are located in the vicinity of the posterior thyroid gland in the vicinity of thyrocytes and can therefore penetrate the thyroid gland by beta radiation from iodine 131 [25]. It should be considered whether this type of radiation may lead to parathyroid defects or not. Although various researchers have studied this issue, the available results mainly based on a limited number of patients- are often contradictory [26][27][28]. Some authors believe that radiation from the thyroid uptake of iodine 131 causes temporary damage to the parathyroid glands, leading to temporary dysfunction [29]. However, other researchers believe that the same radiation causes parathyroid dysfunction [30, 31]. Also, there are studies that indicated radiation from iodine 131 thyroid uptake might lead to parathyroid adenoma, as well as cases indicating no evidence regarding the risk of such phenomenon [32]. The results of our study represented a slightly decreased trend in the serum PTH and Ca levels.

In addition, the cause of parathyroid dysfunction in patients with differentiated thyroid cancer (DTC) after RAI therapy is still unknown. It has been reported that a non-targeted effect of ionizing radiation may reduce parathyroid function after RAI therapy, which is called the "bystander effect" in adjacent cells [27]. Guven et al. reported that PTH decreased temporarily but generally did not lead to hypocalcemia [13]. However, some studies have shown that RAI therapy does not affect parathyroid function in patients with DTC [28]. Szumowski et al. [31] stated that RAI therapy for hyperthyroidism induces transient hyperparathyroidism. They believe that inflammation of the parathyroid glands after radiation may cause excessive release of PTH in parathyroid cells [31]. Also, they found that the higher the dose of thyroid absorption have the greater effect on the parathyroid function [31]. Evidence showed that the dose of RAI therapy was higher for patients with hyperthyroidism than for patients with thyroid cancer [28]. High doses of thyroid absorption in patients with hyperthyroidism may cause transient hyperparathyroidism after RAI treatment [28].

Regarding the stability of serum Ca values, it is worthwhile to mention that the thyroid hormones could increase the absorption and release the Ca from bones; hence, they contribute to a higher concentration of serum Ca [32]. Exogenous thyroxine normalizes levels of the thyroid-stimulating hormone leading to increased Ca and decreased PTH. Thus, the previous authors emphasize the effect of thyroid hormones and PTH on bone metabolism and Ca levels in the body [33]. Meanwhile, our study has indicated that the increase in PTH was not the consequence of the hormonal dysfunction of the thyroid gland. It is noteworthy that serum Ca concentrations were stable, probably related to high PTH level for a short time and other mechanisms that regulate Ca homeostasis.

Conclusion

The changes in serum ALP level were significant in all three different doses, and despite the changes in serum Ca and PTH levels, the results were not significant. The changes in PTH and ALP levels may be due to changes in hepatocytes and parathyroid cells due to gamma iodine and radioactive beta energy. So, antioxidant therapy is recommended before and after RAI therapy.

Conflict of Interest

The authors declare no conflicts of interest.

Acknowledgments

The authors would like to thank Shiraz University of Medical Sciences for its support.

References

  1. Lenzi M, Bassani G. The effect of radiation on the lymph and on the lymph vessels. Radiol. 1963;5(80):814–7. doi: 10.1148/80.5.814. [DOI] [PubMed] [Google Scholar]
  2. Partington M, Craig AW, Jackson H. The effect of radiation on spermatogenic cells in the rat and mouse. Br J Radiol. 1962;418(35):713–8. doi: 10.1259/0007-1285-35-418-713. [DOI] [PubMed] [Google Scholar]
  3. Kobayashi K, Usami N, Porcel E, Lacombe S, Le Sech. Enhancement of radiation effect by heavy elements. Mutat Res. 2010;1-3(704):123–31. doi: 10.1016/j.mrrev.2010.01.002. [DOI] [PubMed] [Google Scholar]
  4. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, Bray F. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2021;3(71):209–49. doi: 10.3322/caac.21660. [DOI] [PubMed] [Google Scholar]
  5. Parkin DM. Global cancer statistics in the year 2000. Lancet Oncol. 2001;9(2):533–43. doi: 10.1016/S1470-2045(01)00486-7. [DOI] [PubMed] [Google Scholar]
  6. Siegel RL, Miller KD, Fuchs HE, Jemal A. Cancer statistics, 2022. CA Cancer J Clin. 2022;1(72):7–33. doi: 10.3322/caac.21708. [DOI] [PubMed] [Google Scholar]
  7. Sturgeon KM, Deng L, Bluethmann SM, Zhou S, Trifiletti DM, Jiang C, et al. A population-based study of cardiovascular disease mortality risk in US cancer patients. Eur Heart J. 2019;48(40):3889–97. doi: 10.1093/eurheartj/ehz766. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Li LB, Wang JP, Yu XR, He SS, Yu FH, Ding CH. Medical radiation usage and exposures from medical X ray diagnosis in Shandong province of China. Radia Protect Dosi. 2001;3(93):261–6. doi: 10.1093/oxfordjournals.rpd.a006437. [DOI] [PubMed] [Google Scholar]
  9. Creach KM, Siegel BA, Nussenbaum B, Grigsby PW. Radioactive iodine therapy decreases recurrence in thyroid papillary microcarcinoma. ISRN Endocrinol. 2012;(2012):81638–81638. doi: 10.5402/2012/816386. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Donya M, Radford M, ElGuindy A, Firmin D, Yacoub MH. Radiation in medicine: Origins, risks and aspirations. Glob Cardiol Sci Pract. 2014;4(2014):437–48. doi: 10.5339/gcsp.2014.57. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Siegel R, Naishadham D, Jemal A. Cancer statistics, 2012. CA Cancer J Clin. 2012;1(62):10–29. doi: 10.3322/caac.20138. [DOI] [PubMed] [Google Scholar]
  12. Ahmad T, Khoja A, Rashid NH, Ashfaq MA. Outcome of radioactive iodine therapy in Toxic Nodular Goiter in Pakistan. Pak J Med Sci. 2018;5(34):1146–51. doi: 10.12669/pjms.345.15244. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. La Perle, Kim DC, Hall NC, Bobbey A, Shen DH, Nagy RS, et al. Modulation of sodium/iodide symporter expression in the salivary gland. Thyroid. 2013;8(23):1029–36. doi: 10.1089/thy.2012.0571. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Petrich T, Widjaja A, Musholt TJ, Hofmann M, Brunkhorst T, Ehrenheim C, et al. Outcome after radioiodine therapy in 107 patients with differentiated thyroid carcinoma and initial bone metastases: side-effects and influence of age. Europ J Nucl Med. 2001;2(28):203–8. doi: 10.1007/s002590000420. [DOI] [PubMed] [Google Scholar]
  15. O’connor MK. New York: Churchill Livingstone; 1996. [Google Scholar]
  16. Frans JT, Berman DS, Maddahi J, Watson DD, Beller GA, Strauss HW, et al. Technetium-99m hexakis 2-methoxyisobutyl isonitrile: human biodistribution, dosimetry, safety, and preliminary comparison to thallium-201 for myocardial perfusion imaging. J Nucl Med. 1989;3(30):301–11. [PubMed] [Google Scholar]
  17. Wang S, Liang C, Zhao L, Meng Z, Zhang C, Jia Q, et al. Influence of radioactive iodine therapy on liver function in patients with differentiated thyroid cancer. Nucl Med Commun. 2018;12(39):1113–20. doi: 10.1097/MNM.0000000000000919. [DOI] [PubMed] [Google Scholar]
  18. Fard-Esfahani A, Emami-Ardekani A, Fallahi B, Fard-Esfahani P, Beiki D, Hassanzadeh-Rad A, Eftekhari M. Adverse effects of radioactive iodine-131 treatment for differentiated thyroid carcinoma. Nucl Med Commun. 2014;8(35):808–17. doi: 10.1097/MNM.0000000000000132. [DOI] [PubMed] [Google Scholar]
  19. Guven A, Salman S, Boztepe H, Yarman S, Tanakol R, Azizlerli H, Alagol F. Parathyroid changes after high dose radioactive iodine in patients with thyroid cancer. Ann Nucl Med. 2009;5(23):437–41. doi: 10.1007/s12149-009-0270-4. [DOI] [PubMed] [Google Scholar]
  20. Lin Y. Internal radiation therapy: a neglected aspect of nuclear medicine in the molecular era. J Biomed Res. 2015;5(29):345–55. doi: 10.7555/JBR.29.20140069. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Wyszomirska A. Iodine-131 for therapy of thyroid diseases. Nucl Med Rev. 2012;2(15):120–3. [PubMed] [Google Scholar]
  22. Rosen IB, Palmer JA, Rowen J, Luk SC. Induction of hyperparathyroidism by radioactive iodine. Amj Surg. 1984;4(148):441–5. doi: 10.1016/0002-9610(84)90366-0. [DOI] [PubMed] [Google Scholar]
  23. Kawamura J, Tobisu K, Sanada S, Okada Y, Yoshida O, Minami S, et al. Hyperparathyroidism after radioactive iodine therapy for Graves' disease: a case report. Acta Urologica Japonica. 1983;11(29):1513–9. [PubMed] [Google Scholar]
  24. Esselstyn Jr, Schumacher OP, Eversman J, Sheeler L, Levy WJ. Hyperparathyroidism after radioactive iodine therapy for Graves disease. Surg. 1982;5(92):811–3. [PubMed] [Google Scholar]
  25. Ehrhardt JD, Güleç S. A Review of the History of Radioactive Iodine Theranostics: The Origin of Nuclear Ontology. Mol Imaging Radionucl Ther. 2020;3(29):88–97. doi: 10.4274/mirt.galenos.2020.83703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Haugen BR, Alexander EK, Bible KC, Doherty GM, Mandel SJ, Nikiforov YE, et al. 2015 American Thyroid Association management guidelines for adult patients with thyroid nodules and differentiated thyroid cancer: the American Thyroid Association guidelines task force on thyroid nodules and differentiated thyroid cancer. Thyroid. 2016;1(26):1–33. doi: 10.1089/thy.2015.0020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Sokolov M, Neumann R. Changes in gene expression as one of the key mechanisms involved in radiation induced bystander effect. Bio Med Rep. 2018;2(9):99–111. doi: 10.3892/br.2018.1110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Mattar E, Salih MA, Alsafi K, Suliman II. Radiation Protection in The Release of Patients Receiving 131I Treatment. Radiat Prot Dosi. 2019;4(187):499–508. doi: 10.1093/rpd/ncz190. [DOI] [PubMed] [Google Scholar]
  29. Lu L, Shan F, Li W, Lu H. Short-Term Side Effects after Radioiodine Treatment in Patients with Differentiated Thyroid Cancer. Biomed Res Int. 2016;(2016):4376720–4376720. doi: 10.1155/2016/4376720. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Wei S, Baloch ZW, LiVolsi VA. Parathyroid adenoma in patients with Graves’ disease: a report of 21 cases. Endocr Pathol. 2015;1(26):71–4. doi: 10.1007/s12022-014-9349-0. [DOI] [PubMed] [Google Scholar]
  31. Szumowski P, Abdelrazek S, Mojsak M, Rogowski F, Kociura-Sawicka A, Myśliwiec J. Parathyroid gland function after radioiodine (131I) therapy for toxic and non-toxic goitre. Endokrynol Pol. 2013;5(64):340–5. doi: 10.5603/EP.2013.0015. [DOI] [PubMed] [Google Scholar]
  32. Iqbal AA, Burgess EH, Gallina DL, Nanes MS, Cook CB. Hypercalcemia in hyperthyroidism: patterns of serum calcium, parathyroid hormone, and 1,25-dihydroxyvitamin D3 levels during management of thyrotoxicosis. Endocr Pract. 2003;6(9):517–21. doi: 10.4158/EP.9.6.517. [DOI] [PubMed] [Google Scholar]
  33. Bassett JH, Williams GR. Role of Thyroid Hormones in Skeletal Development and Bone Maintenance. Endocr Rev. 2016;2(37):135–87. doi: 10.1210/er.2015-1106. [DOI] [PMC free article] [PubMed] [Google Scholar]

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