Journal
WORLD JOURNAL OF SURGICAL ONCOLOGY
Volume 19, Issue 1, Pages -Publisher
BMC
DOI: 10.1186/s12957-021-02302-6
Keywords
Iodine intake; Universal salt iodization; Papillary thyroid cancer; Papillary thyroid microcarcinoma; Central lymph node metastasis
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An increase in iodine intake has been associated with the rising incidence of papillary thyroid cancer (PTC). However, lower iodine intake was found to be a protective factor for central lymph node metastasis (CLNM) in PTC, particularly in cases with tumors smaller than 1 cm. These results suggest that iodine may play a dual role in PTC development, both as an initiator and a promoter of tumorigenesis.
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 mu g/L) was associated with decreased CLNM risk in PTC. And after defining insufficient iodine intake as <= 109 mu g/L and above requirements as >= 190 mu g/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.
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