The aim of this study was to investigate the role of the interleukin-18 +105A/C and interleukin-10 -1082A/G germline polymorphisms in the development and outcome of differentiated thyroid carcinoma associated or not with concurrent thyroiditis.
METHODS:We studied 346 patients with differentiated thyroid carcinomas, comprising 292 papillary carcinomas and 54 follicular carcinomas, who were followed up for 12-298 months (mean 76.10±68.23 months) according to a standard protocol. We genotyped 200 patients and 144 control individuals for the interleukin-18 +105A/C polymorphism, and we genotyped 183 patients and 137 controls for the interleukin-10 -1082A/G polymorphism.
RESULTS:Interleukin-18 polymorphisms were not associated with chronic lymphocytic thyroiditis or any clinical or pathological feature of tumor aggressiveness. However, there was an association between the presence of interleukin-10 variants and chronic lymphocytic thyroiditis. Chronic lymphocytic thyroiditis was present in 21.74% of differentiated thyroid carcinoma patients, most frequently affecting women previously diagnosed with Hashimoto's thyroiditis who had received a lower 131I cumulative dose and did not present lymph node metastases.
CONCLUSIONS:We conclude that the inheritance of a G allele at the interleukin-10 -1082A/G polymorphism may favor a concurrent thyroid autoimmunity in differentiated thyroid carcinoma patients, and this autoimmunity may favor a better prognosis for these patients.
An association between chronic lymphocytic thyroiditis (CLT), also known as Hashimoto's thyroiditis, and differentiated thyroid carcinoma (DTC), especially the papillary histotype, has long been recognized and supported by a series of epidemiological studies.1,2 Chronic inflammatory infiltrates and chronic inflammatory thyroiditis are observed in 20-50% of papillary thyroid carcinoma (PTC) cases.3,4 Moreover, autoimmune thyroid diseases and DTC share numerous morphological and molecular traits.5,6 However, the relationship between autoimmune thyroid diseases and DTC remains controversial. On the one hand, chronic inflammation related to Hashimoto's thyroiditis might predispose individuals to neoplastic transformation and cancer development.6 Several cytokines, including interleukin (IL)-1, IL-6 and tumor necrosis factor (which are produced by tumor cells), and tumor-associated leukocytes and platelets have been found to contribute to the invasive phenotype.7 On the other hand, genetic alterations implicated in PTC, such as RET/PTC, BRAFV600E and RASG12V, have been demonstrated to help promote a proinflammatory environment characterized by high levels of proinflammatory cytokines that provide a protumorigenic condition.8 Thyroid cancer cells also secrete several cytokines and chemokines necessary to sustain cancer cell growth and recruit leukocytes to tumor sites.7,9
Interleukin-18 has multiple functions, including the induction of interferon-gamma synthesis by T cells and natural killer cells,10 the promotion of T-helper (Th) 1-type immune responses, the augmentation of the proliferative response, and activated T-cell cytokine production.11 The IL-18 gene is located on chromosome 11q22.2-q22.3 and consists of six exons and five introns. The promoter region of the gene can harbor nucleotide variations that affect IL-18 synthesis.12 An IL-18 gene polymorphism at position +105 has been linked to increased production of this cytokine.13
Interleukin-10 is a pleiotropic cytokine with both anti-inflammatory and anti-angiogenic properties that may be involved in the pathogenesis of autoimmune thyroid diseases.14 It is normally produced by activated T cells, monocytes, B cells, and thymocytes, contributing to antigen- or mitogen-driven B cell differentiation, acting as a growth factor, and stimulating the humoral immune response.15 The IL-10 gene is located on chromosome 1q31-q32. Thyroid cancer cells of all histological variants produce considerable amounts of IL-10, which might be important in the pathological features of thyroid cancer and/or outcome.16 A polymorphism at codon -1082 has been associated with increased IL-10 protein production.17
The aim of this study was to investigate the roles of the IL-18 +105A/C and IL-10 -1082A/G germline polymorphisms in the development and outcome of DTC associated or not with concurrent thyroiditis.
MATERIALS AND METHODSSubjectsThis retrospective case-control study was approved by the Research Ethics Committee of the Faculty of Medical Sciences – University of Campinas (FCM-Unicamp), and informed written consent was obtained from all individuals. The study was designed and conducted in accordance with good clinical practice guidelines, the relevant laws regarding the conduct of clinical studies, and the Declaration of Helsinki. The study population comprised 346 patients with DTC (292 PTC cases and 54 follicular carcinoma [FTC] cases) who underwent surgery between 1999 and 2007 in Hospital das Clínicas – Faculty of Medical Sciences – Unicamp. Thyroid carcinoma had been either diagnosed or suspected in these patients for clinical or epidemiological reasons, including the results of fine-needle aspiration cytology and/or histological analysis. All of the patients underwent total or near-total thyroidectomy. Patients with preoperatively or intraoperatively palpable neck node metastases underwent regional neck dissection. The stage and grade of tumor differentiation were obtained from surgical and pathological records. Experienced pathologists of the Hospital das Clínicas – Faculty of Medical Sciences – Unicamp confirmed all diagnoses. All the cases were managed according to a standard protocol. Total body 131I scans were performed 4-6 weeks after the operations. A total of 27 patients who were classified as very low-risk – patients with unifocal microcarcinoma (T1≤1 cm, according to the International Union Against Cancer [AJCC/UICC] staging system) and no extension beyond the thyroid capsule or distant metastases (N0M0) – did not receive any actinic dose after ablation; all other patients received at least 100 mCi of 131I. Long-term levothyroxine therapy at suppressive doses was administered following total body scans to keep serum thyrotropin (TSH) at low-normal levels.
Data on lifetime occupational history, dietary habits, alcohol and drug consumption, medical history with an emphasis on previous and/or current thyroid diseases, family history of DTC, and other anamnestic data were obtained by interviews, using a structured questionnaire. Individuals with a history of accidental or medical radiation exposure or other antecedent malignancies were excluded. Skin color was determined by the interviewer in accordance with the Brazilian Institute of Geography and Statistics (http://www.ibge.gov.br/english/); however, due to the difficulty in classifying our highly heterogeneous population, we grouped it into Caucasian and non-Caucasian. Cigarette smoking habits were recorded; however, due to the limited reliable data obtained on smoking duration, the age at which smoking began, the quantity smoked, and the time elapsed since smoking cessation, the patients were grouped into never smokers and ever smokers. The latter group comprised individuals who had consumed at least 20 packs (at 20 cigarettes per pack) for 1 of the prior 5 years. All data, including nodule size, tumor histological features, and the results of laboratory examinations, were confirmed by the patients' records.
Follow-upAccording to a routine protocol based on American Thyroid Association and Latin American Thyroid Society recommendations,18,19 the follow-up of cancer patients included periodic total body scans, serum TSH and thyroglobulin (Tg) measurements and other eventual procedures for detecting distant metastases for a period of 1-336 months (76.10±68.23 months). Patients presenting with or suspected of high non-stimulated serum Tg levels (>2 mg/dl) underwent total body scans. We defined tumors as recurrent and/or presenting long-distance metastasis according to the above parameters.
According to the total actinic ablation received prior to this study, the patients were divided into two groups: (a) patients with cumulative doses bellow 250 mCi and (b) patients with cumulative doses above 250 mCi.
ControlsWe selected 416 healthy controls from the general population of our region; we considered these individuals to have a normal iodine intake, and they were matched to the patients on the basis of gender, age, ethnicity, and environmental exposure risk. Hence, the 200 DTC patients genotyped for the IL-18 polymorphism were compared with 144 control individuals, and the 183 patients genotyped for the IL-10 polymorphism were compared with 137 controls. The history obtained from these control subjects included demographic and ethnic background, diet, lifetime occupational history, smoking and drinking history, general health conditions, and disease history. Individuals with a history of thyroid disease, radiation exposure, specific environmental or occupational exposure risks, or antecedent malignancy were excluded.
HistopathologyExperienced pathologists confirmed the diagnosis of PTC in 292 patients (159 with the classical form of the disease, 88 with follicular variants, 23 with tall-cell variants, and 22 with less-differentiated variants) and FTC in 54 cases (all clearly invasive tumors). CLT was investigated in the non-malignant thyroid parenchyma of all the DTC patients. The presence of thyroiditis was confirmed by extensive diffuse lymphocytic infiltration with the formation of lymphoid follicles or reactive germinal centers and scarring, as well as follicular regenerative activity in the form of numerous small follicles frequently lined by Hurthle cells. The Hurthle cells had abundant eosinophilic cytoplasm, enlarged hyperchromatic nuclei, mildly to moderately pleomorphic nuclei, and prominent nucleoli. Peritumoral inflammatory response was not considered chronic lymphocytic thyroiditis.
Identification of Genotypic ProfilesBlood specimens were obtained from patients and controls. Genomic DNA was extracted from frozen specimens, and leukocytes were separated from whole blood using a standard proteinase K-phenol-chloroform protocol. Both the IL-18 (+105A/C) and IL-10 (-1082A/G) genotypes were analyzed by the polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) methods. Genotyping was conducted with blinding to case/control status. The primers for IL-18 +105A/C were forward 5′- AGA TTT AAT GTT TAT TGT AGA AAA CCT GGA CTC -3′ and reverse 5′- CAG TCA TAT CTT CAA ATA GAG GCC G-3′ , which produced a 141-bp fragment. The primers for IL-10 -1082A/G were forward 5′- CTG GCT GCA ACC CAA CTG GC -3′ and reverse 5′- TCT TAC CTA TCC CTA CTT CC -3′, which generated a 139-bp fragment. These fragments were amplified separately under similar conditions in 25-μl volumes of a mixture containing 100 ng of DNA, 10 μM of each primer, 10 mM Tris-HCl (pH 8.0), 0.1 mM of each dNTP, 2.0 mM MgCl2, and 0.5 U Taq DNA polymerase. The samples were amplified for 35 cycles at 94°C for 55 sec followed by 72°C for 1 min, with an initial denaturation step at 94°C for 5 min and a final extension step at 72°C for 10 min, using a Thermocycler MJ PTC-200 PCR System (Harlow Scientific, Arlington, USA). The PCR fragments were visualized in ethidium bromide-stained gels. The DdeI restriction enzyme was used to identify the IL-18 polymorphism according to the manufacturer's protocol (Fermentas, Vilnius, Lithuania). The IL-18 A allele generated a double band representing 109- and 32-bp fragments, and the IL-18 C variant allele produced one fragment of 141 bp. The MnlI restriction enzyme was used to identify the IL-10 polymorphism according to the manufacturer's protocol (Fermentas, Vilnius, Lithuania). The IL-10 A allele generated a single band representing a 139-bp fragment, and the IL-10 G variant allele produced two fragments of 106 and 33 bp. The restriction products were analyzed by electrophoresis in 3% agarose gels containing ethidium bromide.
Statistical AnalysisStatistical analyses were conducted using SAS statistical software (Statistical Analysis System, version 8.1, Cary, NC, USA, 1999-2000). Associations were assessed using 2X2 or 2Xn contingency table analysis; the chi-squared (χ2) or Fisher's (F) exact test was used to examine homogeneity between cases and controls in terms of gender, race, previous thyroid disease, thyroid nodule size, medication use, cigarette smoking, disease extent, and genotypes. The Kruskal-Wallis (KW) test was used to compare age among the groups. The Mann-Whitney or Wilcoxon test was used to compare age among the different genotype groups. The observed genotype frequencies were compared with those calculated using Hardy-Weinberg equilibrium theory. The 95% CI odds ratio (OR) provided a measure of strength of association. To further explore the significance of the studied genotypes in different age ranges, we performed a univariate logistic regression analysis in patients under and over 45 years old after adjusting for gender. The 23 tall-cell variant cases and the 22 samples of less-differentiated variants were excluded from all comparisons concerning DTC. Logistic regression analysis was used to evaluate the effects of all genotypes after adjusting for potential confounders, such as age, gender, race, tobacco use, and alcohol use. A multivariate logistic regression model was applied using the presence/absence of CLT as the dependent variable and all genotypes and clinical risk factors, including gender, age, and cumulative radioiodine doses, as explicative variables. The Cox regression model was used to search for associations between risk factors and disease-free survival in thyroid cancer patients. All tests were conducted at a 5% significance level (p<0.05).
RESULTSTable 1 summarizes the demographics, pathological features, and follow-up characteristics of the 346 patients with DTC, including the 200 patients genotyped for the IL-18 +105A/C polymorphism and the 183 patients genotyped for the IL-10 -1082A/G polymorphism. As expected, the DTC patients were predominantly female (85%). There were no differences between the control individuals and the cancer patients in terms of ethnicity (78.06% Caucasian and 21.94% non-Caucasian versus 82.82% Caucasian and 17.18% non-Caucasian patients, respectively; p = 0.117) or smoking habits (70.95% non-smokers and 29.05% smokers versus 72.17% non-smokers and 27.82% smokers, respectively; p = 0.729). The mean age at the time of diagnosis was 41.62±14.89 years (range of 5-87 years). According to the pathologic TNM staging system, 210 (60.58%) patients were stage I, 84 (24.36%) stage II, 30 (8.65%) stage III, and 22 (6.41%) stage IV. Most DTC cases were classified as differentiated tumors (88.26%), 42.28% were multicentric, and 86 (24.85%) presented lymph node metastasis at the time of diagnosis. Lymph node metastases were more frequent in patients with multifocal tumors (36.64%) than in patients with a single tumor focus (19.25%; p = 0.0007).
Demographics, pathological features and follow-up characteristics of the differentiated thyroid cancer patients according to their genotypic distribution of interleukin-18 +105A/C (IL-18 +105A/C) and interleukin-10 -1082A/G (IL-10 -1082A/G) polymorphic profiles. PTC = papillary thyroid carcinoma; N = absolute number of patients; pTNM = International Union Against Cancer (AJCC/UICC) staging system.
| Demographic/Pathological/Follow-up Factors | IL-18 genotype | IL-10 genotype | ||||||
|---|---|---|---|---|---|---|---|---|
| AA | AC | CC | AA | AG | GG | |||
| N (%) | N (%) | N (%) | p-value | N (%) | N (%) | N (%) | p-value | |
| Gender | ||||||||
| Female | 69 (42.86) | 75 (46.58) | 17 (10.56) | 0.279 | 63 (42.86) | 61 (41.50) | 23 (15.64) | 0.330 |
| Male | 9 (28.12) | 18 (56.25) | 5 (15.63) | 10 (32.26) | 13 (41.93) | 8 (25.81) | ||
| Ethnicity | ||||||||
| White | 77 (40.96) | 90 (47.87) | 21 (11.17) | 0.684 | 54 (38.57) | 60 (42.86) | 26 (18.57) | 0.453 |
| Non-white | 17 (44.74) | 16 (42.10) | 5 (13.16) | 18 (50.00) | 13 (36.11) | 5 (13.89) | ||
| Smoking | ||||||||
| Smoker | 21 (35.00) | 33 (55.00) | 6 (10.00) | 0.435 | 23 (41.81) | 21 (38.18) | 11 (20.01) | 0.694 |
| Non-smoker | 56 (43.41) | 58 (44.96) | 15 (11.63) | 48 (40.00) | 53 (44.17) | 19 (15.83) | ||
| Age | ||||||||
| <40 | 33 (39.29) | 43 (51.90) | 8 (8.81) | 0.745 | 35 (45.45) | 32 (41.56) | 10 (12.99) | 0.336 |
| ≥40 | 45 (40.90) | 51 (46.36) | 14 (12.74) | 38 (37.62) | 42 (41.58) | 21 (20.80) | ||
| Tumor Type | ||||||||
| Papillary (PTC) | 62 (38.99) | 80 (50.31) | 17 (10.70) | 0.429 | 62 (40.00) | 67 (43.23) | 26 (16.77) | 0.504 |
| Follicular (FTC) | 16 (47.06) | 13 (38.23) | 5 (14.71) | 11 (47.83) | 7 (30.43) | 5 (21.74) | ||
| PTC histological variants | ||||||||
| Classical | 33 (38.82) | 43 (50.58) | 9 (10.60) | 0.622 | 30 (36.14) | 40 (48.19) | 13 (15.67) | 0.409 |
| Follicular | 14 (31.81) | 23 (52.27) | 7 (15.92) | 22 (51.16) | 14 (32.56) | 7 (16.28) | ||
| Others | 25 (46.29) | 23 (42.59) | 6 (11.12) | 19 (40.42) | 18 (38.30) | 10 (21.28) | ||
| Concurrent thyroiditis | ||||||||
| Yes | 18 (40.90) | 24 (54.54) | 2 (4.56) | 0.241 | 13 (31.71) | 22 (53.66) | 6 (14.63) | 0.208 |
| No | 57 (39.04) | 69 (47.26) | 20 (13.70) | 60 (44.12) | 52 (38.23) | 24 (17.65) | ||
| Multifocality | ||||||||
| Multinodular | 26 (37.68) | 36 (52.17) | 7 (10.15) | 0.740 | 30 (46.15) | 27 (41.54) | 8 (12.31) | 0.447 |
| Uninodular | 46 (40.00) | 54 (46.95) | 15 (13.05) | 41 (38.68) | 45 (42.45) | 20 (18.87) | ||
| Extrathyroidal invasion | ||||||||
| Yes | 33 (37.50) | 47 (53.41) | 8 (9.09) | 0.527 | 31 (39.24) | 34 (43.04) | 14 (17.72) | 0.725 |
| No | 39 (41.49) | 43 (45.74) | 12 (12.77) | 40 (44.94) | 36 (40.45) | 13 (14.61) | ||
| pTNM stage | ||||||||
| I | 43 (41.35) | 51 (49.04) | 10 (9.61) | 0.653 | 44 (44.90) | 39 (39.80) | 15 (15.30) | 0.705 |
| II | 19 (39.58) | 22 (45.83) | 7 (14.59) | 15 (34.09) | 20 (45.45) | 9 (20.46) | ||
| III | 6 (27.27) | 12 (54.54) | 4 (18.19) | 9 (42.86) | 8 (38.09) | 4 (19.05) | ||
| IV | 5 (41.66) | 7 (58.34) | 0 (0.00) | 2 (22.22) | 6 (66.67) | 1 (11.11) | ||
| Microcarcinoma | ||||||||
| Yes | 23 (48.93) | 19 (40.42) | 5 (10.65) | 0.230 | 20 (43.48) | 18 (39.13) | 8 (17.44) | 0.946 |
| No | 49 (35.00) | 74 (52.86) | 17 (12.14) | 53 (41.08) | 54 (41.86) | 22 (17.06) | ||
| Differentiation grade | ||||||||
| Well differentiated | 64 (40.76) | 72 (45.86) | 21 (13.38) | 0.128 | 64 (43.84) | 57 (39.04) | 25 (17.12) | 0.283 |
| Poorly differentiated | 4 (28.57) | 10 (71.43) | 0 (0.00) | 4 (26.67) | 9 (60.00) | 2 (13.33) | ||
| Lymph node metastasis | ||||||||
| Yes | 16 (31.37) | 30 (58.82) | 5 (9.80) | 0.176 | 22 (43.14) | 23 (45.10) | 6 (11.76) | 0.485 |
| No | 66 (44.59) | 65 (43.92) | 17 (11.49) | 54 (41.22) | 52 (39.69) | 25 (19.09) | ||
| Distant metastasis | ||||||||
| Yes | 7 (30.43) | 15 (65.22) | 1 (4.35) | 0.171 | 6 (30.00) | 12 (60.00) | 2 (10.00) | 0.181 |
| No | 76 (42.94) | 80 (45.20) | 21 (11.86) | 70 (42.94) | 63 (38.65) | 30 (18.41) | ||
| Familial cases | ||||||||
| Yes | 2 (40.00) | 2 (40.00) | 1 (20.00) | 0.652 | 2 (50.00) | 2 (50.00) | 0 (0.00) | 1.000 |
| No | 81 (41.54) | 93 (47.69) | 21 (10.77) | 74 (41.34) | 73 (40.78) | 32 (17.88) | ||
| Hashimoto's thyroiditis | ||||||||
| Yes | 2 (50.00) | 2 (50.00) | 0 (0.00) | 1.000 | 2 (50.00) | 2 (50.00) | 0 (0.00) | 1.000 |
| No | 73 (39.67) | 89 (48.37) | 22 (11.96) | 71 ( 41.52) | 70 (40.94) | 30 (17.54) | ||
| Basedow-Graves' disease | ||||||||
| Yes | 3 (42.86) | 3 (42.86) | 1 (14.28) | 1.000 | 3 (37.50) | 1 (12.50) | 4 (50.00) | 0.053 |
| No | 72 (39.78) | 88 (48.62) | 21 (11.60) | 70 (41.92) | 71 (42.51) | 26 (15.57) | ||
| Metastasis during follow-up | ||||||||
| Yes | 6 (50.00) | 5 (41.67) | 1 (8.33) | 0.909 | 7 (53.85) | 5 (38.46) | 1 (7.69) | 0.522 |
| No | 77 (40.96) | 90 (47.87) | 21 (11.17) | 69 (40.59) | 70 (41.18) | 31 (18.23) | ||
| Cumulative 131I dose | ||||||||
| <250 mCi | 16 (41.03) | 20 (51.28) | 3 (7.69) | 0.753 | 13 (37.14) | 16 (45.71) | 6 (17.15) | 0.353 |
| ≥250 mCi | 10 (32.26) | 19 (61.29) | 2 (6.45) | 15 (50.00) | 13 (43.33) | 2 (6.67) | ||
A total of 24 DTC patients had previously been diagnosed with autoimmune disease, including eight cases (8 PTC) of Hashimoto's thyroiditis and 16 cases (14 PTC and 2 FTC) of Basedow-Graves' disease.
The IL-18 and IL-10 genotype profiles were according to a Hardy-Weinberg equilibrium (IL-18: χ2 = 0.210, gl = 2, p = 0.900; IL-10: χ2 = 1.616, gl = 2, p = 0.445). We were unable to find any differences in IL-18 or IL-10 genotype distribution between the controls and patients (p = 0.342 and p = 0.665, respectively). Further investigation into possible associations among IL-18 and IL-10 polymorphism profiles, tumor features, and patient outcomes, as shown in Table 1, did not reveal any association between genotype and aggressive clinical characteristics at diagnosis or during follow-up. Moreover, there was no relationship between IL-18 or IL-10 genotype and previous diagnosis of autoimmune disease. There were no differences in IL-18 polymorphism profiles between patients with or without CLT. However, a multivariate regression analysis showed that CLT was more frequent in patients with the IL-10 variant allele than in patients with the wild-type AA genotype (p = 0.039).
Whereas CLT was present in 21.41% of the DTC samples, 257 (78.59%) patients did not present with CLT, and histological characteristics were ambiguous in the remaining 19 cases, which were therefore excluded from further analysis. We also evaluated the influence of CLT on DTC presentation and outcome, as shown in Table 2. CLT was more frequent in women (p = 0.020) previously diagnosed with Hashimoto's thyroiditis (p<0.001) and who had received a lower 131I cumulative dose (p = 0.005). A multivariate regression analysis confirmed significant associations among the presence of CLT, female gender (p = 0.013) and the absence of lymph node metastasis at diagnosis (p = 0.012).
Demographics, pathological features and follow-up characteristics of 327 differentiated thyroid carcinoma patients presenting concurrent lymphocytic thyroiditis (N = 70 patients) or not (N = 257 patients). The data were obtained using a multivariate regression analysis. IL = interleukin; N = absolute number of patients.
| Thyroiditis | |||
|---|---|---|---|
| Present | Absent | p-value | |
| Demographic/Pathological/ | N (%) | N (%) | |
| Follow-up Factors | |||
| Gender | |||
| Female | 66 (23.57) | 214 (76.43) | 0.013 |
| Male | 4 (8.51) | 43 (91.49) | |
| Ethnicity | |||
| White | 60 (22.56) | 206 (77.44) | 0.475 |
| Non-white | 10 (18.18) | 45 (81.82) | |
| Smoking | |||
| smoker | 15 (16.67) | 75 (83.33) | 0.175 |
| non-smoker | 55 (23.61) | 178 (76.39) | |
| Age | |||
| <40 | 32 (21.48) | 117 (78.52) | 0.978 |
| ≥40 | 38 (21.35) | 140 (78.65) | |
| Extrathyroidal invasion | |||
| Yes | 28 (19.31) | 117 (80.69) | 0.377 |
| No | 38 (23.46) | 124 (76.54) | |
| pTNM stage | |||
| I | 42 (22.46) | 145 (77.54) | 0.678 |
| II | 20 (26.32) | 56 (73.68) | |
| III | 5 (18.52) | 22 (81.48) | |
| IV | 3 (15.00) | 17 (85.00) | |
| Microcarcinoma | |||
| Yes | 20 (27.03) | 54 (72.97) | 0.209 |
| No | 50 (20.16) | 198 (79.84) | |
| Differentiation grade | |||
| Well differentiated | 54 (20.61) | 208 (79.39) | 0.282 |
| Poorly differentiated | 10 (28.57) | 25 (71.43) | |
| Lymph node metastasis | |||
| Yes | 12 (14.12) | 73 (85.88) | 0.012 |
| No | 58 (24.17) | 182 (75.83) | |
| Distant metastasis | |||
| Yes | 5 (14.71) | 29 (85.29) | 0.310 |
| No | 65 (22.26) | 227 (77.74) | |
| Familial cases of thyroid cancer | |||
| Yes | 3 (33.33) | 6 (66.67) | 0.409 |
| No | 67 (21.07) | 251 (78.93) | |
| Preoperative Hashimoto's thyroiditis | |||
| Yes | 7 (87.5) | 1 (12.50) | <0.001 |
| No | 63 (20.00) | 252 (80.00) | |
| Metastasis during follow-up | |||
| Yes | 2 (10.00) | 18 (90.00) | 0.267 |
| No | 68 (22.15) | 239 (77.85) | |
| Cumulative radioiodine dose | |||
| <250 mCi | 18 (36.73) | 31 (63.27) | 0.005 |
| ≥250 mCi | 6 (12.24) | 43 (87.76) | |
| IL-10 genotype | |||
| AA | 13 (17.81) | 60 (82.19) | 0.039 |
| AG/GG | 28 (26.92) | 76 (73.08) | |
| IL-18 genotype | |||
| AA | 18 (24.00) | 57 (76.00) | 0.969 |
| AC/CC | 26 (22.61) | 89 (77.39) | |
To further explore the influence of autoimmunity on DTC prognosis, we grouped all the DTC patients with lymphocytic infiltration surrounding neoplastic tissue and/or circulating autoantibodies and/or preoperative diagnosis of Graves' disease or Hashimoto's thyroiditis. These 89 patients (83 women and 6 men, mean age ± SD 41.45±14.84) were then compared with 239 DTC patients (198 women and 41 men, mean age ± SD 41.62±14.89) without any histological or serological evidence of thyroid autoimmunity. Eighteen patients with ambiguous data were excluded from further analysis. Again, the presence of autoimmunity was correlated with female gender (p = 0.020), absence of lymph node metastasis at diagnosis (p = 0.017), and lower 131I cumulative dose (p = 0.025).
DISCUSSIONWe were unable to find any association between the IL-18 +105A/C polymorphism and DTC with CLT or previous autoimmune thyroid diseases. Neither the IL-18 nor the IL-10 genotype was differentially distributed between patients and controls, indicating that these genotypes are not a risk factor for DTC development. However, there was an association between the presence of IL-10 variants and CLT. In addition, we demonstrated that CLT accompanied by DTC is associated with good prognostic features, including female gender, lower 131I cumulative dose, and absence of lymph node metastasis at diagnosis.
Because IL-10 may be involved in leukocyte recruitment,14,20 and the studied polymorphism increased IL-10 protein levels,17 we could speculate that individuals with the inherited polymorphic variant would be more efficient at increasing their IL-10 levels, leading to thyroid autoimmunity. The IL-10 -1082A/G polymorphism has been associated with the development of various types of cancer, including thyroid cancer.21–24 In a recent work, Erdogan and colleagues21 studied the IL-10 -1082A/G polymorphism in patients with papillary thyroid carcinoma and control individuals using the same genotyping technique as in our study but a smaller cohort. They obtained a genotype profile similar to that reported here. However, patients with a heterozygous genotype were more frequent in the Erdogan cohort (61.9%) than in our cohort (44.53%), which suggests that the genetic backgrounds of different populations may influence DTC development.
Although we confirmed a previously reported association between thyroid autoimmunity and tumor features related to a good prognosis,3,25–30 this issue is still being debated. Although a worse prognosis has been reported for patients with thyroid autoimmunity in a few series,31,32 most studies have shown either a protective effect3,13,14,27,33 or no effect of thyroid autoimmunity on DTC behavior.34
Hashimoto's thyroiditis is characterized by follicular cell depletion due to an immune system reaction against a series of thyroid epithelial cell antigens. DTC cells might also be recognized and destroyed by the immune system, which would explain why DTC patients with concomitant autoimmune thyroid diseases may present a better prognosis.25,35 The immune response is modulated by a complex network of cytokines, and the final output of this interaction can be either the stimulation or the suppression of immunity. Therefore, merely analyzing IL-10 and IL-18 is not sufficient to understand the immune response against thyroid cancer. More studies are warranted to confirm the hypothesis of tumor destruction by immune reaction and to elucidate the mechanisms engaged in this process.
CONCLUSIONSIn conclusion, we suggest that neither the IL-18 +105A/C nor the IL-10 -1082A/G polymorphisms represent risk factors for the development or outcome of DTC. However, the inheritance of the G allele at IL-10 -1082 may favor concurrent autoimmunity in DTC with lymphocyte recruitment and hence modulate an antitumor immune reaction. Further studies are needed to confirm the hypothesis of tumor cell depletion by immune cells and to elucidate the mechanisms engaged in this process.
We thank the team of statisticians of the Faculty of Medical Sciences of University of Campinas for their valuable suggestions and insights. This study was supported by the State of São Paulo Research Foundation (Fapesp) and the Coordination for Higher Level Graduates Improvement (Capes). LSW, JV and FAS are researchers of the National Council for Scientific and Technological Development (CNPq). These institutions had no involvement in the study development.