Abstract

BackgroundAn abrupt increase of thyroid cancer has been witnessed paralleling the supplemented iodine intake in formerly iodine-deficient countries. And increased iodine intake has been linked to the rising incidence rate of papillary thyroid cancer (PTC). However, the correlation between iodine and clinicopathological features of PTC has not been well-characterized. This study aimed to investigate the associations between iodine intake and the clinicopathological features of PTC patients.MethodsThree hundred and fifty-nine PTC patients who received surgical treatment in Peking Union Medical College Hospital from May 2015 to November 2020 were retrospectively reviewed. The associations between urinary iodine (UI), urinary iodine/creatinine ratio (UI/U-Cr), and the clinicopathological features of PTC were analyzed. Univariate and multivariate analysis were performed to investigate the relationship between UI level and central lymph node metastasis (CLNM).ResultsThere were no significant differences in UI in different groups according to the variables studied, except that patients with CLNM had higher UI level than CLNM(−) patients. No associations were found between UI/U-Cr and clinicopathological features except variant subtypes (classic/follicular). After dividing patients into high-iodine group and low-iodine group, more patients were found to have CLNM in the high-iodine group (p = 0.02). In addition, younger age, larger tumor size, and classic variant were positively correlated with CLNM (p < 0.05). Univariate analysis showed that insufficient iodine intake (≤ 99 μg/L) was associated with decreased CLNM risk in PTC. And after defining insufficient iodine intake as ≤ 109 μg/L and above requirements as ≥ 190 μg/L, multivariate analysis showed that lower iodine was associated with CLNM in total population of PTC (OR 0.53, 95% CI 0.31–0.91) and in PTC < 1 cm (papillary thyroid microcarcinoma, PTMC) (OR 0.43, 95% CI 0.21–0.87).ConclusionsLow iodine was a protective factor for CLNM in papillary thyroid cancer, particularly in those < 1 cm. These results indicated that iodine may not only be an initiator of tumorigenesis, but also a promoter of the development of PTC.

Highlights

  • An abrupt increase of thyroid cancer has been witnessed paralleling the supplemented iodine intake in formerly iodine-deficient countries

  • urinary iodine (UI) and UI/U-Cr level in different clinicopathologic status among papillary thyroid cancer (PTC) patients Among the 359 patients diagnosed with PTC, UI was not significantly different between different age, sex, or other clinicopathological features, except that UI was significantly higher in central lymph node metastasis (CLNM)(+) patients than in N0 patients (152 μg/L vs 126 μg/L, p = 0.028)

  • Correlations of UI, UI/U-Cr, and clinicopathological features of PTC patients Using the median value as the cutoff, the patients were classified into an iodine-high and an iodine-low group to compare the difference between clinical and histopathological features

Read more

Summary

Introduction

An abrupt increase of thyroid cancer has been witnessed paralleling the supplemented iodine intake in formerly iodine-deficient countries. Increased iodine intake has been linked to the rising incidence rate of papillary thyroid cancer (PTC). Risk factors have been revealed such as radiation exposure [3], industrialized lifestyle such as obesity [4], pollutants [5], and population aging as well as growing scrutiny of thyroid and improved diagnostics [6]. Apart from these known ones, iodine intake has been suggested as an important impact factor for the rise of thyroid cancer. The controversies between studies indicated that more variables should be considered in the analysis of iodine and thyroid cancer

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call