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Serum resolvin E1 levels and its relationship with thyroid autoimmunity in Hashimoto’s thyroiditis: a preliminary study

BMC Endocrine Disorders volume 21, Article number: 66 (2021) Cite this article

Abstract

Background

Omega-3 polyunsaturated fatty acids (PUFAs) produce lipid mediators with both anti-inflammatory and pro-resolution properties, including resolvins. The purpose of this study was to detect serum resolvin E1 (RVE1) levels in Hashimoto’s thyroiditis (HT) patients and healthy controls (HCs) and to evaluate the relationship of RVE1 with thyroid autoimmunity.

Methods

A total of 57 participants were recruited, including 30 untreated HT patients and 27 age- and sex‐matched HCs. The levels of RVE1 in serum were measured via enzyme-linked immunosorbent assay (ELISA). An electrochemiluminescence immunoassay was used for the measurement of thyroid-stimulating hormone (TSH), total T4 (TT4), TT3, free T4 (FT4), FT3, anti-thyroid peroxidase antibody (TPOAb) and anti-thyroglobulin antibody (TgAb) levels. Hemogram tests and routine biochemical analyses were performed on each sample.

Results

The serum level of RVE1 of HT patients (24.09, 15.76–34.38 pg/mL) was significantly lower than that of healthy controls (28.51, 20.76–51.23 pg/mL) (P = 0.027). RVE1 levels showed a downward trend with increasing TgAb levels (P for trend = 0.001). Multivariable ordinal logistic regression analysis showed that RVE1 levels were negatively correlated with increasing TgAb levels in both the unadjusted (OR = 0.9446, 95 % CI = 0.9111–0.9782, P = 0.002) and adjusted models (OR = 0.9380, 95 % CI = 0.8967–0.9811, P = 0.005).

Conclusions

Decreased RVE1 levels might be a sign that HT is associated with inflammatory resolution dysfunction. RVE1 may serve as a protective factor against increased TgAb levels.

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Introduction

Hashimoto’s thyroiditis (HT), which is also known as chronic lymphocytic thyroiditis, is now considered the most common autoimmune disease. HT is characterized by the production of autoantibodies against thyroid peroxidase (TPO) and thyroglobulin (Tg) in the serum and the presence of infiltrating lymphocytes in the thyroid. Most HT patients will eventually develop primary hypothyroidism [1]. A cross-sectional study of 31 provinces in mainland China showed that the anti-TPO antibody (TPOAb) and the anti-Tg antibody (TgAb) positivity rates in Chinese adults were 10.19 and 9.70 %, respectively [2]. Recent studies have confirmed that TgAb and TPOAb can increase the risk of thyroid cancer and thyroid nodules [3, 4]. High levels of thyroid autoantibodies not only cause hypothyroidism but also are an essential factor in HT disease progression. Studying euthyroid HT patients revealed that high levels of thyroid autoantibodies can lead to a lower quality of life score and vestibular dysfunction [5, 6]. Given that euthyroid HT patients already bear the above burden, early diagnosis and intervention are particularly important. HT is currently considered an autoimmune disease affected by genetic and environmental factors. Among these factors, some nutritional factors have been confirmed to be related to HT, such as selenium and vitamin D [7, 8]. Selenium supplementation can significantly reduce thyroid autoantibody levels in patients with HT [9]; however, the clinical efficacy of selenium supplementation is controversial. Therefore, it is necessary to further study nutritional factors that have a protective effect on HT.

Chronic inflammation is the underlying mechanism of disease progression in many autoimmune diseases. Recent research suggests that the progression of chronic inflammatory diseases may be due to impaired resolution and has revealed the protective effect of endogenous lipid mediators [10]. Once thought to be a passive process, acute inflammation has now been shown to involve an active inflammatory resolution process and promote the restoration of inflamed tissue to a steady state [11]. The resolution process involves the following steps: remove the harmful substances that trigger the inflammatory response, stop the synthesis of proinflammatory mediators and promote their decomposition and metabolism, and then terminate leukocyte recruitment. Neutrophils and lymphocytes undergo apoptosis or necrosis and are finally cleared by macrophages [12]. In addition, the resolution of inflammation is an active process induced via endogenous specialized pro-resolving mediators (SPMs). SPMs are downstream derivatives of polyunsaturated fatty acids (PUFAs), which include resolvins, maresins, lipoxins and protectins [13].

Resolvins include E series (RVE1-RVE3) and D series (RVD1-RVD6), which are produced from eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), respectively. Among them, RVE1 triggers all aspects of the pro-resolution cascade from inhibiting lymphocyte aggregation at the inflammation site to inflammatory fragment efferocytosis or removal [14]. Notably, RVE1 has a protective effect in many chronic inflammatory disease models. RVE1 induces the expression of its specific receptor chemR23 on the surface of dendritic cells and inhibits the release of IL-12, thus hindering inflammation progression [15]. RVE1 inhibits bone resorption in the inflammatory environment by controlling the ratio of RANKL/OPG and downstream genetic factors [16]. Additionally, omega-3 PUFAs are upstream substances of RVE1 and have a therapeutic effect on some autoimmune diseases. EPA significantly alleviates the disease progression of experimental autoimmune encephalomyelitis (EAE) [17]. The application of omega-3 PUFAs and fish oil has a beneficial effect on reducing the recurrence rate and inflammatory indicator levels and improving the quality of life in patients with multiple sclerosis [18]. Supplementation with omega-3 fatty acids (EPA and DHA) improves type 1 diabetes by regulating autoimmunity and suppressing inflammation [19, 20]. Similarly, omega-3 PUFAs display potential protective effects in thyroid disease; a case report described a female HT patient who refused thyroid replacement therapy but was eventually cured clinically through dietary management (including omega-3 PUFAs) [21]. Therefore, we infer that the omega-3 PUFA downstream derivative RVE1 may also play an important role in the development of HT.

To date, no studies have investigated the changes in RVE1 in HT patients and HCs. Therefore, this study mainly measured the serum RVE1 levels of HT patients and HCs and further analysed the correlations between RVE1 and thyroid autoantibodies and other clinical indicators.

Methods

Study groups

We recruited 57 participants from the endocrinology clinic of Beijing Luhe Hospital, namely, 30 untreated HT patients and 27 age- and sex‐matched HCs. All participants had no history of other autoimmune diseases, any acute or chronic illness, smoking, or alcohol intake and no current use of medications or pregnancy. The diagnostic criteria for HT were diffuse goitre, TPOAb and/or TgAb positivity, and B ultrasound examination revealing uneven hypoechoic changes and diffuse thyroid enlargement. All participants fasted, and blood samples were collected between 8 and 10 AM.

An electrochemiluminescence immunoassay was used to detect serum TgAb, TPOAb, free T3 (FT3), FT4, total T3 (TT3), TT4, and TSH levels. Moreover, routine blood examination (neutrophil, leukocyte, haemoglobin, and platelet levels) and biochemical detection were performed on each sample. Biochemical detection included analysis of liver function markers (aspartate aminotransferase (AST) and alanine aminotransferase (ALT)), albumin, blood glucose, electrolytes (sodium and potassium), creatinine, blood urea nitrogen (BUN), total cholesterol (TC), high-density lipoprotein (HDL), triglycerides (TG), low-density lipoprotein (LDL), C-reactive protein (CRP) and uric acid.

Assay of serum RVE1 levels

A RVE1 ELISA kit (Signalway Antibody, USA) was applied to measure serum RVE1 levels according to the manufacturer’s instructions. All serum samples were assayed on the same day. The inter-assay and intra-assay coefficients of variation (CVs) for RVE1 were < 10 %.

Statistical analysis

SPSS 23.0 software (SPSS, Chicago, IL, USA) was used for the statistical analysis. Normally distributed data are expressed as the mean ± standard deviation (M ± SD), and comparisons were performed with independent samples t tests. Data with abnormal distributions are expressed as the median and interquartile range (IQR), and the distributions between groups were compared using the nonparametric Mann-Whitney U test. The Spearman correlation coefficient (r) was used to analyse the correlation between RVE1 and other variables.

According to the interquartile range, TPOAb levels were divided into Q1: <13.6 U/mL, Q2: 13.6–10.6 U/mL, Q3: 10.6–431 U/mL, and Q4: >431 U/mL and TgAb levels were divided into Q1: <12.9 U/mL, Q2: 12.9–79.1 U/mL, Q3: 79.1–361 U/mL, and Q4: >361 U/mL. Multivariable ordinal logistic regression models were used to evaluate the relationships between RVE1 and thyroid autoantibodies. The Jonckheere-Terpstra test was used to evaluate trends. All P-values were two-sided, and P < 0.05 was defined as statistically significant.

Results

A total of 57 participants (30 HT patients and 27 HCs) were included in our research. As shown in Table 1, no significant difference in age or sex was noted between HT patients and HCs. The levels of thyroid-specific antibodies (TPOAb and TgAb) in the HT group were significantly greater than those in the HCs group (P < 0.001 for all). No differences in thyroid parameters (TSH, TT4, FT4, TT3, and FT3), blood cells and routine biochemical indicators were noted between the two groups (P > 0.05 for all).

Table 1 Clinical and demographic characteristics of the HT patients and HCs
Full size table

The serum level of RVE1 of HT patients (24.09, 15.76–34.38 pg/mL) was significantly reduced compared with those of healthy controls (28.51, 20.76–51.23 pg/mL) (P = 0.027) (Fig. 1).

Fig. 1
figure 1

Comparison of serum resolvin E1 (RVE1) levels in patients with Hashimoto’s thyroiditis (n = 30) and healthy controls (n = 27). Data were expressed as median and interquartile intervals. HT: Hashimoto’s thyroiditis. HCs: Healthy controls

Full size image

We performed Spearman correlation analysis to assess the relationships between serum RVE1 and other variables for all participants. RVE1 was significantly negatively correlated with TgAb (r=-0.426, P = 0.001), TT3 (r=-0.348, P = 0.008) and FT3 (r=-0.339, P = 0.010) (Table 2).

Table 2 Spearman correlation analysis between RVE1 levels and clinical characteristics in all the participants
Full size table

To evaluate the relationship between RVE1 and thyroid autoantibodies, we divided the TPOAb and TgAb levels into four categories according to the interquartile range. As shown in Table 3, the RVE1 level showed a downward trend with increasing TgAb levels (P for trend = 0.001). The RVE1 content in the Q4 (TgAb > 361 IU/mL) group (19.21, 13.81–27.34 pg/mL) was significantly lower than that in the Q1 (TgAb < 34 IU/mL) group (37.70, 24.66–99.16 pg/mL) (P = 0.005). Multivariable ordinal logistic regression analysis showed that RVE1 was negatively correlated with TgAb in both the unadjusted (OR = 0.9446, 95 % CI = 0.9111–0.9782, P = 0.002) and adjusted models (OR = 0.9475, 95 % CI = 0.9166–0.9792, P = 0.001 and OR = 0.9380, 95 % CI = 0.8967–0.9811,

P = 0.005). As shown in Table 4, we also assessed the relationship between RVE1 and TPOAb levels. As TPOAb levels increased, RVE1 levels exhibited an inverted U-shaped trend (P for trend = 0.036). The RVE1 content reached the highest value in the Q2 group. Moreover, the RVE1 content in the Q4 group (19.21, 15.11–26.01 pg/mL) was significantly lower than that in the Q2 group (31.39, 23.79–62.31 pg/mL) (P = 0.019). Multivariable ordinal logistic regression analysis showed that RVE1 was negatively correlated with TPOAb in both the unadjusted (OR = 0.9762, 95 % CI = 0.9559–0.9970, P = 0.028) and adjusted models (OR = 0.9772, 95 % CI = 0.9567–0.9980, P = 0.011, adjusted for age and sex). However, when the model was adjusted for age, sex, and TT3, TT4, TSH, FT3, FT4, and TgAb levels, RVE1 levels showed no significant correlation with increasing TPOAb levels (OR = 0.9860, 95 % CI = 0.9627-1.010, P = 0.244).

Table 3 Multivariable ordinal logistic regression to investigate the association between RVE1 and TgAb
Full size table
Table 4 Multivariable ordinal logistic regression to investigate the association between RVE1 and TPOAb
Full size table

Discussion

To the best of our knowledge, this is the first study investigating serum RVE1 levels in HT patients. In the present study, we found that serum RVE1 levels in the HT group was significantly lower than that in the control group, potentially indicating dysregulation of inflammation resolution in HT patients.

Omega-3 PUFAs produce lipid mediators with both anti-inflammatory and pro-resolution properties, including resolvins [22]. The anti-inflammatory actions indicate that pro-inflammatory mediators are suppressed, whereas pro-resolution actions indicate activation of the inflammation termination process, such as apoptotic cell removal by macrophages [23]. Dysregulation of resolution increases the risk of autoimmune diseases. Although anti-inflammatory drugs can improve the symptoms of autoimmune diseases, they cannot cure the disease and are even ineffective in most patients. Therefore, the combination of anti-inflammation and pro-resolution effects may represent a superior treatment method. Moreover, pro-resolution pathways themselves do not increase the body’s susceptibility to infection [24]. Omega-3 PUFAs have shown therapeutic potential in some autoimmune diseases, including rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and type 1 diabetes mellitus (T1DM) [25]. After treatment with omega-3 PUFAs in patients with inflammatory arthritis, RVE1 levels in the knee effusion and plasma were significantly higher than that in HCs, suggesting that RVE1 may be a mediator of omega-3 PUFAs [26]. In the present study, the serum RVE1 levels in HT patients were significantly lower than those in HCs. We inferred that this difference might indicate that HT is associated with inflammatory resolution dysfunction. Similarly, RVE1 is also a marker of inflammatory resolution defects in other diseases, such as cardiovascular diseases [27], periodontitis [28], and type 2 diabetes mellitus [29].

In this study, we also analysed the correlation between levels of RVE1 and thyroid autoantibodies. The HT patients recruited in our study were euthyroid, so the interference of thyroid hormones can be excluded. Spearman correlation analysis showed that RVE1 levels were negatively correlated with TgAb levels (r=-0.426, P = 0.001). As the TgAb level increased, the RVE1 content showed a decreasing trend (P for trend = 0.001). Moreover, multivariable ordinal logistic regression analysis showed that RVE1 was negatively correlated with TgAb in both the unadjusted (OR = 0.9446, 95 % CI = 0.9111–0.9782, P = 0.002) and adjusted models (OR = 0.9380, 95 % CI = 0.8967–0.9811, P = 0.005). We also assessed the relationship between RVE1 and TPOAb levels. As TPOAb levels increased, the RVE1 levels showed an inverted U-shaped trend (P for trend = 0.036). However, when the logistic model was adjusted for age, sex, and TT3, TT4, TSH, FT3, FT4, and TgAb levels, RVE1 levels showed no significant correlation with increasing TPOAb levels (OR = 0.9860, 95 % CI = 0.9627-1.010, P = 0.244). Although it is currently believed that TgAb is not as specific and sensitive as TPOAb, some studies have confirmed that TgAb and TPOAb may represent two different aspects of thyroid autoimmunity. TgAb represents the initial or innate immune response, and TPOAb represents the later adaptive immune response [1]. Studies have confirmed a significant positive correlation between TgAb and clinical symptoms (fragile hair, face oedema, oedema of the eyes and harsh voice) in untreated HT patients [29]. Therefore, we hypothesize that RVE1 may serve as a protective factor against increased TgAb levels. However, further research is needed to verify the relationship between RVE1 and TgAb.

A recent study confirmed that topical application of RVE1 alleviates inflammation-induced tissue damage and reduce bone loss in an animal model of periodontitis [30]. Similarly, RVE1 administration reverses experimental periodontitis and malnutrition [31]. RVE1 inhibits the activation of dental pulp fibroblasts in a ChemR23-dependent manner and inflammation in the early stages of pulpitis [32]. The pathogeneses of autoimmune thyroid disease and periodontitis are different. The former is an autoimmune-driven disease, and the latter is an infection-driven disease. However, the two diseases have many common pathological and immunological characteristics, such as autoimmune antibodies, apoptosis, inflammation, and oxidative stress. Therefore, we infer that RVE1 may also have a protective effect on HT [33]. Further longitudinal studies are needed to verify our hypothesis. In some other diseases, the application of RVE1 has also been shown to promote inflammation resolution. RVE1 reduces airway responsiveness and inflammation in asthmatic mice [34]. Moreover, RVE1 reduces neutrophil infiltration, pro-inflammatory cytokine expression, and inflammatory pain [35]. Oral or topical application of RVE1 prevents vascular inflammation and arteriosclerosis and reduces systemic CRP levels [36]. RVE1 reduces the levels of lipopolysaccharide (LPS)-induced pro-inflammatory factors (IL-8, MCP-1) in isolated human pancreatic islets and exhibits antiapoptotic effects in a pro-inflammatory environment [37].

There are some limitations in our research. One major limitation was its cross-sectional design, as we could not observe whether RVE1 undergoes dynamic alterations related to changes in thyroid autoimmunity and thyroid function. In view of our small sample size, a follow-up longitudinal study with a larger sample size is needed to verify the role of RVE1 in HT development.

Conclusions

Our study showed for the first time that serum RVE1 levels in HT patients were significantly reduced. Moreover, RVE1 may protect against increased TgAb levels.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

HT:

Hashimoto’s thyroiditis

Tg:

Thyroglobulin

TPO:

Thyroid peroxidase

TPOAb:

Anti-TPO antibody

TgAb:

Anti-Tg antibody

SPMs:

Specialized pro-resolving mediators

PUFAs:

Polyunsaturated fatty acids

EPA:

Eicosapentaenoic acid

References

  1. Caturegli P, De Remigis A, Rose NR. Hashimoto thyroiditis: clinical and diagnostic criteria. Autoimmun Rev. 2014;13(4–5):391–6.

    Article  CAS  Google Scholar 

  2. Li Y, Teng D, Ba J, Chen B, Du J, He L, Lai X, Teng X, Shi X, Li Y, 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(4):568–11.

    Article  CAS  Google Scholar 

  3. Wu X, Lun Y, Jiang H, Gang Q, Xin S, Duan Z, Zhang J. Coexistence of thyroglobulin antibodies and thyroid peroxidase antibodies correlates with elevated thyroid-stimulating hormone level and advanced tumor stage of papillary thyroid cancer. Endocrine. 2014;46(3):554–6.

    Article  CAS  Google Scholar 

  4. Xu W, Huo L, Chen Z, Huang Y, Jin X, Deng J, Zhu S, Yu Y. The Relationship of TPOAb and TGAb with Risk of Thyroid Nodules: A Large Epidemiological Study. Int J Environ Res Public Health. 2017; 14(7).

  5. Bektas Uysal H, Ayhan M. Autoimmunity affects health-related quality of life in patients with Hashimoto’s thyroiditis. Kaohsiung J Med Sci. 2016;32(8):427–6.

    Article  Google Scholar 

  6. Chiarella G, Russo D, Monzani F, Petrolo C, Fattori B, Pasqualetti G, Cassandro E, Costante G. Hashimoto Thyroiditis and Vestibular Dysfunction. Endocr Pract. 2017;23(7):863–8.

    Article  Google Scholar 

  7. Hu S, Rayman MP. Multiple Nutritional Factors and the Risk of Hashimoto’s Thyroiditis. Thyroid. 2017;27(5):597–3.

    Article  CAS  Google Scholar 

  8. Rayman MP. Multiple nutritional factors and thyroid disease, with particular reference to autoimmune thyroid disease. Proc Nutr Soc. 2019;78(1):34–10.

    Article  CAS  Google Scholar 

  9. Wichman J, Winther KH, Bonnema SJ, Hegedus L. Selenium Supplementation Significantly Reduces Thyroid Autoantibody Levels in Patients with Chronic Autoimmune Thyroiditis: A Systematic Review and Meta-Analysis. Thyroid. 2016;26(12):1681–11.

    Article  CAS  Google Scholar 

  10. Fredman G, Serhan CN. Specialized proresolving mediator targets for RvE1 and RvD1 in peripheral blood and mechanisms of resolution. Biochem J. 2011;437(2):185–12.

    Article  CAS  Google Scholar 

  11. Serhan CN, Chiang N, Van Dyke TE. Resolving inflammation: dual anti-inflammatory and pro-resolution lipid mediators. Nat Rev Immunol. 2008;8(5):349–12.

    Article  CAS  Google Scholar 

  12. Fullerton JN, Gilroy DW. Resolution of inflammation: a new therapeutic frontier. Nat Rev Drug Discov. 2016;15(8):551–16.

    Article  CAS  Google Scholar 

  13. Basil MC, Levy BD. Specialized pro-resolving mediators: endogenous regulators of infection and inflammation. Nat Rev Immunol. 2016;16(1):51–16.

    Article  CAS  Google Scholar 

  14. Gilroy DW, Bishop-Bailey D. Lipid mediators in immune regulation and resolution. Br J Pharmacol. 2019;176(8):1009–14.

    Article  CAS  Google Scholar 

  15. Arita M, Bianchini F, Aliberti J, Sher A, Chiang N, Hong S, Yang R, Petasis NA, Serhan CN. Stereochemical assignment, antiinflammatory properties, and receptor for the omega-3 lipid mediator resolvin E1. J Exp Med. 2005;201(5):713–9.

    Article  CAS  Google Scholar 

  16. El Kholy K, Freire M, Chen T, Van Dyke TE. Resolvin E1 Promotes Bone Preservation Under Inflammatory Conditions. Front Immunol. 2018;9:1300.

    Article  Google Scholar 

  17. Unoda K, Doi Y, Nakajima H, Yamane K, Hosokawa T, Ishida S, Kimura F, Hanafusa T. Eicosapentaenoic acid (EPA) induces peroxisome proliferator-activated receptors and ameliorates experimental autoimmune encephalomyelitis. J Neuroimmunol. 2013;256(1–2):7–5.

    Article  CAS  Google Scholar 

  18. AlAmmar WA, Albeesh FH, Ibrahim LM, Algindan YY, Yamani LZ, Khattab RY. Effect of omega-3 fatty acids and fish oil supplementation on multiple sclerosis: a systematic review. Nutr Neurosci. 2019:1–10.

  19. Cadario F, Pozzi E, Rizzollo S, Stracuzzi M, Beux S, Giorgis A, Carrera D, Fullin F, Riso S, Rizzo AM, et al. Vitamin D and omega-3 Supplementations in Mediterranean Diet During the 1st Year of Overt Type 1 Diabetes: A Cohort Study. Nutrients. 2019; 11(9).

  20. Bi X, Li F, Liu S, Jin Y, Zhang X, Yang T, Dai Y, Li X, Zhao AZ. omega-3 polyunsaturated fatty acids ameliorate type 1 diabetes and autoimmunity. J Clin Invest. 2017;127(5):1757–14.

    Article  Google Scholar 

  21. Dolan K, Finley H, Gasta M, Houseman S. Managing Hashimoto’s Thyroiditis Through Personalized Care: A Case Report. Altern Ther Health Med. 2018;24(3):56–61.

    PubMed  Google Scholar 

  22. Serhan CN. Resolution phase of inflammation: novel endogenous anti-inflammatory and proresolving lipid mediators and pathways. Annu Rev Immunol. 2007;25:101–36.

    Article  CAS  Google Scholar 

  23. Schwab JM, Chiang N, Arita M, Serhan CN. Resolvin E1 and protectin D1 activate inflammation-resolution programmes. Nature. 2007;447(7146):869–5.

    Article  CAS  Google Scholar 

  24. Feehan KT, Gilroy DW. Is Resolution the End of Inflammation? Trends Mol Med. 2019;25(3):198–16.

    Article  CAS  Google Scholar 

  25. Li X, Bi X, Wang S, Zhang Z, Li F, Zhao AZ. Therapeutic Potential of omega-3 Polyunsaturated Fatty Acids in Human Autoimmune Diseases. Front Immunol. 2019;10:2241.

    Article  CAS  Google Scholar 

  26. Barden AE, Moghaddami M, Mas E, Phillips M, Cleland LG, Mori TA. Specialised pro-resolving mediators of inflammation in inflammatory arthritis. Prostaglandins Leukot Essent Fatty Acids. 2016;107:24–5.

    Article  CAS  Google Scholar 

  27. Carracedo M, Artiach G, Arnardottir H, Back M. The resolution of inflammation through omega-3 fatty acids in atherosclerosis, intimal hyperplasia, and vascular calcification. Semin Immunopathol. 2019;41(6):757–9.

    Article  CAS  Google Scholar 

  28. Balta MG, Loos BG, Nicu EA. Emerging Concepts in the Resolution of Periodontal Inflammation: A Role for Resolvin E1. Front Immunol. 2017;8:1682.

    Article  Google Scholar 

  29. Xia F, He C, Ren M, Xu FG, Wan JB. Quantitative profiling of eicosanoids derived from n-6 and n-3 polyunsaturated fatty acids by twin derivatization strategy combined with LC-MS/MS in patients with type 2 diabetes mellitus. Anal Chim Acta. 2020;1120:24–11.

    Article  CAS  Google Scholar 

  30. Hasturk H, Kantarci A, Ohira T, Arita M, Ebrahimi N, Chiang N, Petasis NA, Levy BD, Serhan CN, Van Dyke TE. RvE1 protects from local inflammation and osteoclast- mediated bone destruction in periodontitis. FASEB J. 2006;20(2):401–2.

    Article  CAS  Google Scholar 

  31. Lee CT, Teles R, Kantarci A, Chen T, McCafferty J, Starr JR, Brito LC, Paster BJ, Van Dyke TE. Resolvin E1 Reverses Experimental Periodontitis and Dysbiosis. J Immunol. 2016;197(7):2796–10.

    Article  CAS  Google Scholar 

  32. Xu H, Chen J, Ge J, Xia K, Tao S, Su Y, Zhang Q. Resolvin E1 Ameliorates Pulpitis by Suppressing Dental Pulp Fibroblast Activation in a Chemerin Receptor 23-dependent Manner. J Endod. 2019;45(9):1126–8.

    Article  Google Scholar 

  33. Patil BS, Patil S, Gururaj TR. Probable autoimmune causal relationship between periodontitis and Hashimotos thyroidits: a systemic review. Niger J Clin Pract. 2011;14(3):253–8.

    Article  CAS  Google Scholar 

  34. Siddiquee A, Patel M, Rajalingam S, Narke D, Kurade M, Ponnoth DS. Effect of omega-3 fatty acid supplementation on resolvin (RvE1)-mediated suppression of inflammation in a mouse model of asthma. Immunopharmacol Immunotoxicol. 2019;41(2):250–7.

    Article  CAS  Google Scholar 

  35. Xu ZZ, Zhang L, Liu T, Park JY, Berta T, Yang R, Serhan CN, Ji RR. Resolvins RvE1 and RvD1 attenuate inflammatory pain via central and peripheral actions. Nat Med. 2010;16(5):592–5.

    Article  CAS  Google Scholar 

  36. Hasturk H, Abdallah R, Kantarci A, Nguyen D, Giordano N, Hamilton J, Van Dyke TE. Resolvin E1 (RvE1) Attenuates Atherosclerotic Plaque Formation in Diet and Inflammation-Induced Atherogenesis. Arterioscler Thromb Vasc Biol. 2015;35(5):1123–10.

    Article  CAS  Google Scholar 

  37. Lund T, Mangsbo SM, Scholz H, Gjorstrup P, Totterman TH, Korsgren O, Foss A. Resolvin E1 reduces proinflammatory markers in human pancreatic islets in vitro. Exp Clin Endocrinol Diabetes. 2010;118(4):237–7.

    Article  CAS  Google Scholar 

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Acknowledgements

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Funding

This work was supported by a grant from the Beijing Luhe Hospital Youth Scientific Research Incubation Project. The funder had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Authors and Affiliations

  1. Beijing Key Laboratory of Diabetes Research and Care, Center for Endocrine Metabolism and Immune Diseases, Lu He Hospital Capital Medical University, Beijing, China

    Jing Song, Rongxin Sun, Yuanyuan Zhang, Jing Ke & Dong Zhao

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Contributions

JS conceived and coordinated the study; designed, performed and analysed the experiments; and wrote the paper. JS, RXS, YYZ, JK and DZ performed data collection and data analysis and revised the paper. All authors reviewed the results and approved the final version of the manuscript.

Corresponding author

Correspondence to Dong Zhao.

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The study was approved by the Ethics Committee of the Beijing Luhe Hospital. After completely explaining the nature and purpose of all procedures utilized, informed written consent was obtained from each participant.

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Song, J., Sun, R., Zhang, Y. et al. Serum resolvin E1 levels and its relationship with thyroid autoimmunity in Hashimoto’s thyroiditis: a preliminary study. BMC Endocr Disord 21, 66 (2021). https://doi.org/10.1186/s12902-021-00730-9

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BMC Endocrine Disorders

ISSN: 1472-6823

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