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ORIGINAL RESEARCH article

Front. Endocrinol., 31 August 2023
Sec. Cancer Endocrinology
This article is part of the Research Topic Micronutrients and Metabolic Diseases View all 23 articles

Association between iodine nutrition and cervical lymph node metastasis of papillary thyroid microcarcinoma

Hengqiang Zhao*Hengqiang Zhao1*Jin HuJin Hu1Le CuiLe Cui1Yiping Gong*Yiping Gong1*Tao Huang*Tao Huang2*
  • 1Department of Breast and Thyroid Surgery, Renmin Hospital of Wuhan University, Wuhan, China
  • 2Department of Breast and Thyroid Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

We aimed to investigate the association between iodine intake and nodal metastasis stratified by central lymph node metastasis (CLNM) and lateral lymph node metastasis (LLNM) of papillary thyroid microcarcinoma (PTMC). Urinary iodine concentration (UIC) and clinicopathological characteristics were used to identify factors associated with CLNM and LLNM using logistic regression analysis. A sum of 3,858 PTMC patients were enrolled. The median UIC (MUI) of patients with CLNM or LLNM was not statistically different from those without nodal metastasis. Male patients had a higher MUI than females (183.4 μg/L vs. 173.6 μg/L). Female patients with extracapsular extension had a higher MUI than those without it (210.0 μg/L vs. 172.1 μg/L). Male patients with LLNM had a significantly lower MUI than those without LLNM (134.7 μg/L vs. 187.9 μg/L). Female patients with more than adequate iodine intake were more likely to present with CLNM and extrathyroidal extension than those with adequate iodine intake with an odds ratio (95% confidence interval) of 1.23 (1.01–1.51) and 1.59 (1.09–2.32) after adjustment. Iodine nutrition was not found to be associated with LLNM. In addition, patients with a younger age, larger tumors, extrathyroidal extension, and intrathyroidal spread were more likely to be CLNM, whereas nodular goiter presented with a protective factor; CLNM was the only factor associated with LLNM of PTMC in both genders. In conclusion, iodine nutrition has a much closer association with female than male patients, and high iodine intake may be associated with CLNM and extrathyroidal extension in female PTMC patients.

Introduction

The overall incidence of thyroid cancer increased by 3% annually in the United States from 1974 to 2013 (1). In China, the age-standardized incidence of thyroid cancer was 3.21/105 in 2005 and 9.61/105 in 2015 (2). The increasing incidence of thyroid cancer is due in large part to the epidemiology of surveillance and overdiagnosis but that there also appears to be a true increase in new cases of thyroid cancer (3). The increased incidence mainly attributes to papillary thyroid cancer (PTC), especially papillary thyroid microcarcinoma (PTMC) with its maximum tumor diameter ≤1 cm (4).

Iodine is an indispensable element for synthesis of thyroxine and is closely associated with thyroid diseases (5). High iodine intake was associated with the occurrence of Hashimoto thyroiditis, nodular goiter, and hyperthyroidism (6). However, the association between iodine intake and thyroid cancer remains controversial (7). Some studies reported that mild iodine deficiency may contribute to the exceptionally high incidence of thyroid cancer (8), whereas others reported that excessive iodine nutrition was associated with PTC and PTMC occurrence compared with adequate iodine intake (9, 10). We previously found that high iodine intake was not associated with PTC incidence in the general population and in patients with thyroid nodules (11). However, more than adequate iodine intake was independently associated with a larger tumor size of PTC patients (11). Thus, we expected that high iodine intake may be associated with the progression of PTC.

Central lymph node metastasis (CLNM) was not uncommon in PTMC patients with its incidence up to 51.7% (12). In addition, approximately 4.4% of patients with PTMC presented with lateral lymph node metastasis (LLNM) at presentation (13). Accumulating evidence suggested that cervical lymph node metastasis was a risk factor for PTC recurrence (14). Some scholars hold that low iodine intake was inversely associated with CLNM of PTC, particularly for PTMC (15). However, others reported that high iodine nutrition seemed to be associated with CLNM of PTC (16). We previously found that excessive iodine intake was marginally associated with CLNM in female PTC patients after defining CLNM as metastatic lymph nodes ≥2 (12). However, we failed to investigate the effect of iodine nutrition on PTMC progression.

Considering the limited and inconsistent results, we aimed to comprehensively investigate the association between iodine nutrition and clinicopathologic characteristics of PTMC. We divided patients into CLNM and LLNM subgroups and explored their associations with urinary iodine concentration (UIC). This study may provide new evidence of the effect of iodine nutrition on PTMC progression.

Patients and methods

Study population

Patients with PTMC were retrospectively enrolled from 2013 to 2018 in Union hospital, Wuhan, China. This study was approved by the Ethics Committee of Union hospital. The enrolled patients underwent thyroidectomy with central lymph node dissection (CLND), and lateral lymph nodes dissection (LLND) or not for the first time. CLND was routinely performed on PTMC patients. LLND was performed based on preoperative imaging suspicious for malignancy and/or fine-needle aspiration cytology preoperatively. Solitary focus means only one tumor in the thyroid, whereas multiple foci mean two or more foci limited to the thyroid. Bilaterality is defined as the presence of PTC foci in the left and right lobes of the thyroid. Capsular invasion means that one tumor invades the thyroid capsule but does not penetrate it, whereas one tumor penetrates the capsule into the strap muscle or perithyroidal fibrofatty tissues, which will be defined as extracapsular or extrathyroidal extension. Intrathyroidal spread means that the primary tumor spreads to the other parts of the thyroid through intrathyroidal lymph vessels. Intraoperative frozen section was routinely performed to determine thyroid malignancy. The final pathological types, tumor number, intrathyroidal spread, capsular invasion and extrathyroidal extension, central lymph node metastasis (CLNM), and lateral lymph node metastasis (LLNM) were determined by postoperative specimen. Hematoxylin and eosin staining with or without immunohistochemistry was performed to determine the pathology or nodal metastasis of PTMC. The pathological types included PTC, PTC and nodular goiter, PTC and Hashimoto’s thyroiditis, and PTC and nodular goiter, and Hashimoto’s thyroiditis. Patients with iodine pretreatment for hyperthyroidism, pathology other than PTC, and reoperation for PTC were excluded.

Iodine nutritional status

Every patient was asked to collect a fasting urine specimen (6). Urinary iodine concentration (UIC) was measured using Direction of Quantitative Test Kit type AR for urinary iodine (Wuhan, China) as previously described (11). Median UIC (MUI) was recommended to assess iodine nutritional status in population according to World Health Organization, and iodine nutritional status was divided into four categories: iodine deficiency (UIC <100 μg/L), adequate iodine intake (UIC: 100–199 μg/L), more than adequate iodine intake (UIC: 200–299 μg/L), and excessive iodine intake (UIC ≥300 μg/L).

Statistical analysis

Variables with skewed distribution were expressed as median (upper and lower quartile) and analyzed using the Mann–Whitney U test. Categorical data were analyzed with the chi-square test. Multivariate logistic regression analysis was performed to identify factors associated with nodal metastasis. All the analyses were performed using SPSS 22.0 software. A two-sided P value <0.05 was considered significant.

Results

The iodine nutrition of PTMC patients

Of the 3,858 patients enrolled, iodine deficiency was more common in female than male PTMC patients (20.0% vs. 13.4%). Adequate iodine intake accounted for 39.7% of the total population. More than adequate and excessive iodine intake accounted for 41.4% (Figure 1).

FIGURE 1
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Figure 1 Iodine status of the study population. Iodine nutrition was classified into four categories: iodine deficiency (UIC <100.0 μg/L), adequate iodine intake (UIC: 100.0–199.9 μg/L), more than adequate iodine intake (UIC: 200.0–299.9), and excessive iodine intake (UIC ≥300.0 μg/L). Data were expressed as percentage (%). UIC, urinary iodine concentration.

The MUI was significantly higher in males than in females (MUI: 183.4 μg/L vs. 173.6 μg/L; P = 0.038). In addition, patients with extrathyroidal extension had a significantly higher MUI than those without it (MUI: 199.7 μg/L vs. 174.3 μg/L; P = 0.024). Patients with a younger age (<55 years) and intrathyroidal spread had a marginally higher MUI than the corresponding counterparts. The MUI in the CLNM and non-CLNM groups was 177.9 μg/L and 173.9 μg/L, respectively (P = 0.554). The MUI in the LLNM and non-LLNM groups of PTMC patients was 157.9 μg/L and 176.5 μg/L, respectively (P = 0.132) (Table 1).

TABLE 1
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Table 1 Comparison of MUI in PTMC patients (n = 3,858).

We then evaluated the iodine nutrition in male and female PTMC patients, separately. We found that male patients with LLNM had a significantly lower MUI than those without LLNM (MUI: 134.7 μg/L vs. 187.9 μg/L; P = 0.002). In addition, female patients with extrathyroidal extension had a significantly higher MUI than those without it (MUI: 210.0 μg/L vs. 172.1 μg/L; P = 0.010) (Table 2).

TABLE 2
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Table 2 Comparison of MUI in PTMC patients stratified by gender (n = 3,858).

We divided UIC into four categories: iodine deficiency, adequate iodine intake, more than adequate iodine intake, and excessive iodine intake. Similarly, we found that iodine nutrition status was not significantly different between patients with CLNM or LLNM and those without nodal metastasis (Supplementary Table 1). In addition, males were more likely to be adequate iodine intake and more than adequate iodine intake compared with females (70.1% vs. 63.0%). Additionally, patients with extrathyroidal extension were more likely to be more than adequate iodine intake and excessive iodine intake than those without it (50% vs. 40.9%) (Supplementary Table 1).

Association between iodine intake and CLNM in male PTMC

In the univariate analysis, iodine deficiency and more than adequate and excessive iodine intake were not associated with CLNM compared with adequate iodine intake. After adjustment, iodine nutrition status was not found to be associated with CLNM in male PTMC patients. In the multivariate model, a younger age, larger tumor size, extrathyroidal extension, intrathyroidal spread, and LLNM were associated with CLNM. Of note, PTMC patients accompanied by nodular goiter were inversely associated with CLNM compared with PTMC alone (Table 3).

TABLE 3
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Table 3 Association between iodine intake and CLNM in male PTMC patients (n = 650).

Association between iodine intake and CLNM in female PTMC

In the univariate analysis, more than adequate iodine intake was associated with CLNM compared with adequate iodine intake with OR (95% CI) of 1.25 (1.04–1.50) in female PTMC patients. After adjustment, patients with more than adequate iodine intake were associated with CLNM than those with adequate iodine intake with OR (95% CI) of 1.23 (1.01–1.51). In addition, a younger age, lager tumor size, bilaterality, capsular invasion, intrathyroidal spread, and LLNM were positively associated with CLNM in female PTMC after adjustment. Of note, PTMC patients accompanied by nodular goiter, or nodular goiter and Hashimoto’s thyroiditis were inversely associated with CLNM compared with PTMC alone (Table 4).

TABLE 4
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Table 4 Association between iodine intake and CLNM in female PTMC patients (n = 3208).

Association between iodine intake and LLNM in male PTMC

In the univariate analysis, more than adequate iodine intake was inversely associated with LLNM compared with adequate iodine intake with OR (95% CI) of 0.45 (0.21–0.96) in male PTMC patients. After adjustment, iodine nutrition status was not found to be associated with LLNM in male PTMC patients. In the multivariate model, results showed that multifocality, CLNM, and PTMC and nodular goiter, and Hashimoto’s thyroiditis were independently associated with LLNM in male PTMC patients (Table 5).

TABLE 5
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Table 5 Association between iodine intake and LLNM in male PTMC patients (n = 650).

Association between iodine intake and LLNM in female PTMC

Iodine nutrition status was not found to be associated with LLNM in female PTMC patients in the univariate and multivariate logistic regression analyses. After adjustment, larger tumor size, extrathyroidal extension, intrathyroidal spread, CLNM, and PTMC and Hashimoto’s thyroiditis were independently associated with LLNM in female PTMC patients (Table 6).

TABLE 6
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Table 6 Association between iodine intake and LLNM in female PTMC patients (n = 3208).

Association between iodine nutrition and extrathyroidal extension in PTMC patients

In the univariate analysis, more than adequate iodine intake was associated with extrathyroidal extension with OR (95% CI) of 1.70 (1.18–2.44) in female PTMC patients. After adjustment, more than adequate iodine intake predicted a higher possibility for extrathyroidal extension with OR (95% CI) of 1.59 (1.09–2.32) compared with adequate iodine intake (Supplementary Table 2).

Discussion

In the present study, we comprehensively investigated the association between iodine intake and nodal metastasis of PTMC patients for the first time. The present evidence suggested that more than adequate iodine intake was associated with CLNM and extrathyroidal extension compared with adequate iodine intake in female PTMC patients. Iodine nutrition was not found to be associated with CLNM in males and was not associated with LLNM in either gender.

The association between iodine intake and PTC has been controversial. Some hold that a higher exposure to iodine intake was associated with PTC incidence (9, 10, 1721). However, some scholars hold that high iodine intake was not associated with PTC occurrence and high UIC was just a specific characteristic of the disease (22). Fan et al. reported that the areas with a low consumption rate of qualified iodized salt and areas with a high incidence of thyroid goiter had a relatively high incidence of thyroid cancer (8). We previously found that the MUI was not significantly different between patients with benign thyroid nodules and PTC, which was consistent with other reports (23). However, more than adequate iodine intake might be associated with the growth of PTC (≥1 cm vs. <1 cm) compared with adequate iodine intake (11). We thus expected that a high iodine intake might be associated with the progression of PTC.

Extrathyroidal extension and intrathyroidal spread were aggressive features of PTC. Huang et al. found that excessive iodine exposure was associated with capsular invasion and extrathyroidal metastases of PTC (19). Similarly, we previously reported that more than adequate and excessive iodine intake were marginally associated with capsular invasion of PTC (12). In this study, the MUI of patients with extrathyroidal extension and intrathyroidal spread was higher than that in the corresponding patients. In addition, more than adequate iodine intake was associated with extrathyroidal extension of PTMC. Accumulating evidence suggested that extrathyroidal extension and intrathyroidal spread were positively associated with CLNM of PTC (24, 25). We can expect that high iodine intake may induce CLNM via promoting the aggressiveness of PTMC. High iodine intake within a certain concentration may promote PTC cell proliferation via upregulating growth signaling pathways (26). However, the potential mechanisms remain explored in vivo.

Cervical nodal metastasis was common in PTC, as well as in PTMC (12). However, the available data failed to find a definitive association between iodine take and CLNM. Fan et al. reported that the proportions of UIC >300 μg/L and of serum iodine concentration >90 μg/L were higher in the CLNM (n = 167) than that in the non-CLNM (n = 235) PTC patients (16). However, we did not find a statistical difference in MUI between CLNM (n = 1517) and non-CLNM (n = 2341) patients with PTMC. Similarly, Huang et al. found that iodine nutrition was not associated with CLNM with a sum of 97 PTC patients via UIC determination (19). We found that more than adequate iodine intake was associated with CLNM, but not excessive iodine intake. In our opinion, it may be easier to be more than adequate iodine status than excessive iodine intake. The recommended intake of iodine for adults is 150 μg/day, and the maximum tolerable iodine intake is 1,000 μg/day. In addition, the high iodine intake status will take a long time to produce adverse effects. The occasionally excessive iodine intake may not cause adverse results. Therefore, studies on the relationship between excessive iodine intake like high iodine area and thyroid cancer should be investigated. We found that patients with LLNM (n = 235) had a lower MUI than those without LLNM for the first time, whereas iodine intake was not found to be associated with LLNM, which should be validated in the following studies.

The MUI of male patients was significantly higher than that in female patients. In general, women’s demand for iodine is greater than men’s. This will lead to a higher proportion of women with iodine deficiency than men (11), which was consistent with the present result. However, we found that high iodine intake was associated with extrathyroidal extension and CLNM in women, but not in men. This indicated that women were more vulnerable to iodine nutrition than men. A recent study revealed that more than adequate and excessive iodine intake had an inverse relationship with thyroid peroxidase antibody, and they were predictors for elevated thyrotropin (27). Furthermore, the higher thyrotropin level was associated with extrathyroidal extension and cervical lymph node metastasis of PTMC (28). Therefore, we speculated that high iodine intake might induce thyroid antibody production, leading to elevated thyrotropin levels and contributing to the progression of thyroid cancer. In addition, the average serum thyrotropin concentration and prevalence of antithyroid antibodies are greater in women relative to men in the general population (29). This suggested that thyroid disease should be considered during routine evaluation of this susceptible population and should be followed by appropriate detection and treatment.

In this study, PTMC patients accompanied by nodular goiter (NG) were inversely associated with CLNM compared with PTMC alone in both men and women. Similarly, some reported that PTC patients with NG had a lower incidence of CLNM compared with those of PTC alone (30). We previously found that patients with NG had an obviously higher MUI than healthy controls, and high iodine intake was associated with a larger tumor size of NG (11). We expected that PTMC patients with NG may be treated at an earlier stage compared with patients with PTMC alone. Thus, these patients were more likely to be negative for cervical lymph nodes.

The mutation rate of BRAFV600E in PTC was up to 86.7%, whereas it was not found to be associated with CLNM (31), and LLNM of PTMC (13). However, some reported that BRAFV600E mutation was independently associated with CLNM when PTMC ≤5 mm (32). It was reported that low iodine intake (UIC <300 μg/L) and more than excessive iodine intake (UIC ≥500 μg/L) were associated with BRAFV600E mutation of PTC (33). However, some reported that there were no significant differences in the prevalence of BRAFV600E mutation between PTC patients in iodine-rich areas and those in iodine-deficient areas (34). In addition, some researchers found that the MUI was not significantly different in patients with BRAFV600E mutation or not (21). Therefore, the relationship between iodine nutrition and BRAFV600E should be investigated further.

CLNM was positively associated with LLNM in both male and female PTMC patients, which was consistent with previous reports (24, 25). As far as we know, this is the largest study focusing on the association between iodine nutrition and PTMC progression. However, some shortcomings should be acknowledged. First, the retrospective study nature cannot demonstrate the cause and effect between iodine nutrition and nodal metastasis of PTMC. Second, the iodine nutrition of patients may not be evaluated accurately by a single determination of UIC. Third, we failed to assess the genetic alterations of PTMC. Last but not least, we cannot explore the underlying mechanisms between iodine intake and PTC initiation and progression.

In conclusion, we investigated the association between iodine nutrition and cervical lymph node metastasis of PTMC patients. We found that more than adequate iodine intake was associated with CLNM and extrathyroidal extension compared with adequate iodine intake in female PTMC patients. Iodine nutrition was more closely associated with tumor progression in female patients. The following studies with a larger sample size should be done to further illuminate the association between iodine nutrition and PTC progression.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding authors.

Ethics statement

The studies involving humans were approved by Ethics Committee of Union hospital. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation was not required from the participants or the participants’ legal guardians/next of kin in accordance with the national legislation and institutional requirements.

Author contributions

HZ and JH contributed the design of the study and writing of the manuscript. HZ, JH and LC collected the data and performed the analyses. YG and TH supervised the work. All authors reviewed and approved the final version of the manuscript.

Funding

This study was supported by the Open Foundation of Hubei Key Laboratory of Renmin Hospital of Wuhan University (grant number 2021KFY009).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fendo.2023.1164069/full#supplementary-material

References

1. Lim H, Devesa SS, Sosa JA, Check D, Kitahara CM. Trends in thyroid cancer incidence and mortality in the United States, 1974-2013. JAMA (2017) 317:1338–48. doi: 10.1001/jama.2017.2719

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Wang J, Yu F, Shang Y, Ping Z, Liu L. Thyroid cancer: incidence and mortality trends in China, 2005-2015. Endocrine (2020) 68:163–73. doi: 10.1007/s12020-020-02207-6

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Seib CD, Sosa JA. Evolving understanding of the epidemiology of thyroid cancer. Endocrinol Metab Clin North Am (2019) 48:23–35. doi: 10.1016/j.ecl.2018.10.002

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Du L, Wang Y, Sun X, Li H, Geng X, Ge M, et al. Thyroid cancer: trends in incidence, mortality and clinical-pathological patterns in Zhejiang Province, Southeast China. BMC Cancer (2018) 18:291. doi: 10.1186/s12885-018-4081-7

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Li Y, Teng D, Ba J, Chen B, Du J, He L, et al. Efficacy and safety of long-term universal salt iodization on thyroid disorders: epidemiological evidence from 31 provinces of mainland China. Thyroid (2020) 30:568–79. doi: 10.1089/thy.2019.0067

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Zhao H, Tian Y, Liu Z, Li X, Feng M, Huang T. Correlation between iodine intake and thyroid disorders: a cross-sectional study from the South of China. Biol Trace Elem Res (2014) 162:87–94. doi: 10.1007/s12011-014-0102-9

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Zhang X, Zhang F, Li Q, Feng C, Teng W. Iodine nutrition and papillary thyroid cancer. Front Nutr (2022) 9:1022650. doi: 10.3389/fnut.2022.1022650

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Fan L, Meng F, Gao Y, Liu P. Insufficient iodine nutrition may affect the thyroid cancer incidence in China. Br J Nutr (2021) 126:1852–60. doi: 10.1017/s0007114521000593

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Kim K, Cho SW, Park YJ, Lee KE, Lee DW, Park SK. Association between iodine intake, thyroid function, and papillary thyroid cancer: A case-control study. Endocrinol Metab (Seoul) (2021) 36:790–99. doi: 10.3803/EnM.2021.1034

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Inoue K, Leung AM, Sugiyama T, Tsujimoto T, Makita N, Nangaku M, et al. Urinary iodine concentration and mortality among U.S. Adults. Thyroid (2018) 28:913–20. doi: 10.1089/thy.2018.0034

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Zhao H, Li H, Huang T. High urinary iodine, thyroid autoantibodies, and thyroid-stimulating hormone for papillary thyroid cancer risk. Biol Trace Elem Res (2018) 184:317–24. doi: 10.1007/s12011-017-1209-6

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Zhao H, Li H, Huang T. High iodine intake and central lymph node metastasis risk of papillary thyroid cancer. J Trace Elem Med Biol (2019) 53:16–21. doi: 10.1016/j.jtemb.2019.01.015

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Kim K, Zheng X, Kim JK, Lee CR, Kang SW, Lee J, et al. The contributing factors for lateral neck lymph node metastasis in papillary thyroid microcarcinoma (PTMC). Endocrine (2020) 69:149–56. doi: 10.1007/s12020-020-02251-2

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Siddiqui S, White MG, Antic T, Grogan RH, Angelos P, Kaplan EL, et al. Clinical and pathologic predictors of lymph node metastasis and recurrence in papillary thyroid microcarcinoma. Thyroid (2016) 26:807–15. doi: 10.1089/thy.2015.0429

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Zeng Z, Li K, Wang X, Ouyang S, Zhang Z, Liu Z, et al. Low urinary iodine is a protective factor of central lymph node metastasis in papillary thyroid cancer: a cross-sectional study. World J Surg Oncol (2021) 19:208. doi: 10.1186/s12957-021-02302-6

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Fan L, Tian Q, Xiu C, Wang F, Yuan Z, He Q, et al. High iodine nutrition may be a risk factor for cervical lymph node metastasis in papillary thyroid cancer patients. Ann Nutr Metab (2021) 77:90–9. doi: 10.1159/000513334

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Lee JH, Hwang Y, Song RY, Yi JW, Yu HW, Kim SJ, et al. Relationship between iodine levels and papillary thyroid carcinoma: A systematic review and meta-analysis. Head Neck (2017) 39:1711–18. doi: 10.1002/hed.24797

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Choi JY, Lee JH, Song Y. Evaluation of iodine status among korean patients with papillary thyroid cancer using dietary and urinary iodine. Endocrinol Metab (Seoul) (2021) 36:607–18. doi: 10.3803/EnM.2021.1005

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Huang F, Cong W, Xiao J, Zhou Y, Gong M, Sun J, et al. Association between excessive chronic iodine exposure and the occurrence of papillary thyroid carcinoma. Oncol Lett (2020) 20:189. doi: 10.3892/ol.2020.12051

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Zhang L, Fang C, Liu L, Liu X, Fan S, Li J, et al. A case-control study of urinary levels of iodine, perchlorate and thiocyanate and risk of papillary thyroid cancer. Environ Int (2018) 120:388–93. doi: 10.1016/j.envint.2018.08.024

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Lee JH, Song RY, Yi JW, Yu HW, Kwon H, Kim SJ, et al. Case-control study of papillary thyroid carcinoma on urinary and dietary iodine status in South Korea. World J Surg (2018) 42:1424–31. doi: 10.1007/s00268-017-4287-x

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Yan AR, Zhang X, Shen H, Zhou X, Li R, Yuan Z. Urinary iodine is increased in papillary thyroid carcinoma but is not altered by regional population iodine intake status: a meta-analysis and implications. Endocr J (2019) 66:497–514. doi: 10.1507/endocrj.EJ18-0532

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Yu Z, Yu Y, Wan Y, Fan J, Meng H, Li S, et al. Iodine intake level and incidence of thyroid disease in adults in Shaanxi province: a cross-sectional study. Ann Transl Med (2021) 9:1567. doi: 10.21037/atm-21-4928

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Kim SK, Park I, Woo JW, Lee JH, Choe JH, Kim JH, et al. Predictive factors for lymph node metastasis in papillary thyroid microcarcinoma. Ann Surg Oncol (2016) 23:2866–73. doi: 10.1245/s10434-016-5225-0

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Sheng L, Shi J, Han B, Lv B, Li L, Chen B, et al. Predicting factors for central or lateral lymph node metastasis in conventional papillary thyroid microcarcinoma. Am J Surg (2020) 220:334–40. doi: 10.1016/j.amjsurg.2019.11.032

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Xiang J, Wang X, Wang Z, Wu Y, Li D, Shen Q, et al. Effect of different iodine concentrations on well-differentiated thyroid cancer cell behavior and its inner mechanism. Cell Biochem Biophys (2015) 71:299–305. doi: 10.1007/s12013-014-0198-8

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Teng D, Yang W, Shi X, Li Y, Ba J, Chen B, et al. An inverse relationship between iodine intake and thyroid antibodies: A national cross-sectional survey in mainland China. Thyroid (2020) 30:1656–65. doi: 10.1089/thy.2020.0037

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Mao A, An N, Wang J, Wu Y, Wang T, Wang Z, et al. Association between preoperative serum TSH and tumor status in patients with papillary thyroid microcarcinoma. Endocrine (2021) 73:617–24. doi: 10.1007/s12020-021-02690-5

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Hollowell JG, Staehling NW, Flanders WD, Hannon WH, Gunter EW, Spencer CA, et al. T(4), and thyroid antibodies in the United States population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III). J Clin Endocrinol Metab (2002) 87:489–99. doi: 10.1210/jcem.87.2.8182

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Huang J, Lin C, Chen Y, Li X. Clinical preliminary study on the correlation between nodular goitre and papillary thyroid carcinoma. Transl Cancer Res (2020) 9:3794–803. doi: 10.21037/tcr-19-2951

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Li X, Li E, Du J, Wang J, Zheng B. BRAF mutation analysis by ARMS-PCR refines thyroid nodule management. Clin Endocrinol (Oxf) (2019) 91:834–41. doi: 10.1111/cen.14079

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Zhou SL, Guo YP, Zhang L, Deng T, Xu ZG, Ding C, et al. Predicting factors of central lymph node metastasis and BRAF(V600E) mutation in Chinese population with papillary thyroid carcinoma. World J Surg Oncol (2021) 19:211. doi: 10.1186/s12957-021-02326-y

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Kim HJ, Park HK, Byun DW, Suh K, Yoo MH, Min YK, et al. Iodine intake as a risk factor for BRAF mutations in papillary thyroid cancer patients from an iodine-replete area. Eur J Nutr (2018) 57:809–15. doi: 10.1007/s00394-016-1370-2

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Vuong HG, Kondo T, Oishi N, Nakazawa T, Mochizuki K, Inoue T, et al. Genetic alterations of differentiated thyroid carcinoma in iodine-rich and iodine-deficient countries. Cancer Med (2016) 5:1883–9. doi: 10.1002/cam4.781

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Keywords: papillary thyroid microcarcinoma, iodine, iodine nutrition, urinary iodine concentration, lymph node metastasis

Citation: Zhao H, Hu J, Cui L, Gong Y and Huang T (2023) Association between iodine nutrition and cervical lymph node metastasis of papillary thyroid microcarcinoma. Front. Endocrinol. 14:1164069. doi: 10.3389/fendo.2023.1164069

Received: 12 February 2023; Accepted: 09 August 2023;
Published: 31 August 2023.

Edited by:

Yongting Luo, China Agricultural University, China

Reviewed by:

Ge Zhao, China Animal Health and Epidemiology Center, China
Junyu Zhao, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, China

Copyright © 2023 Zhao, Hu, Cui, Gong and Huang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Hengqiang Zhao, zhaochewh@whu.edu.cn; Yiping Gong, gongyp@whu.edu.cn; Tao Huang, huangtaowh@163.com

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