Jinping Yuan
Shibin Jiang
Yansong Lu
Yuhui Zhang
Yan Wu- Key Lab of Immunodermatology, Ministry of Health, Department of Dermatology, The First Hospital of China Medical University, Shenyang, China
Background: Associations between vitiligo and thyroid disorders have been suggested, However, the prevalence of thyroid disorders in vitiligo vary widely.
Purpose: To conduct a systematic review and meta-analysis assessing the prevalence of thyroid disorders in patients with vitiligo.
Method: The PubMed, Cochrane Library, EMBASE, CNKI (China National Knowledge Infrastructure), Chongqing VIP database, and Wanfang database from inception to August 2, 2018 were systematically searched. The pooled prevalence and its 95% confidence interval (CI) were calculated.
Results: A total of 77 eligible studies were identified and included, published from 1968 to 2018. Six thyroid disorders including subclinical hyperthyroidism, overt hyperthyroidism, subclinical hypothyroidism, overt hypothyroidism, Graves disease, and Hashimoto thyroiditis were described. The numbers of relative studies were 54 in overt hypothyroidism, 50 in overt hyperthyroidism, 25 in subclinical hypothyroidism, 19 in Hashimoto thyroiditis, 16 in Graves disease, and 10 in subclinical hyperthyroidism. The highest prevalence was 0.06 (95% CI: 0.04–0.07) in subclinical hypothyroidism, and the lowest was 0.01 in subclinical hyperthyroidism (95% CI: 0.00–0.01) or Graves disease (95% CI: 0.01–0.02).
Conclusion: Six thyroid disorders showed various prevalence in vitiligo. The highest prevalence was in subclinical hypothyroidism, and the lowest was in subclinical hyperthyroidism or Graves disease. Screening vitiligo patients for thyroid disorders seem plausible, in an effort to detect potential thyroid diseases or to assess the risk of future onset.
Introduction
Vitiligo is characterized by the loss of functional skin and mucosal melanocytes, the estimated prevalence is 0.5–2% (1, 2). Currently, the exact pathogenesis of vitiligo remains obscure. The most accredited hypothesis is the autoimmune theory, being sustained by several epidemiological, clinical, and experimental findings (3–5). These studies indicate that melanocyte defects drive vitiligo pathogenesis by triggering an autoimmune response that leads to melanocyte destruction in susceptible individuals. Patients with vitiligo are more likely to suffer from autoimmune conditions than the general population (6). Several studies have suggested vitiligo is associated with a variety of other autoimmune diseases, including thyroid conditions, alopecia areata, type 1 diabetes mellitus, pernicious anemia, and rheumatoid arthritis. Among these, thyroid disorders are common conditions in vitiligo patients, and a recent study showed one of the most frequently observed autoimmune diseases in autoimmune thyroiditis patients was vitiligo (7, 8). A genetic co-localization between vitiligo and thyroid autoantibodies has also been proposed (9). The British guidelines suggested to check the thyroid function for adult patients with vitiligo, the Dutch guidelines recommend that when patients with vitiligo have clinical symptoms of thyroid disease, thyroid function should be tested (10, 11) Herein, we conducted a systematic review and meta-analysis to explore the prevalence of various kind of thyroid disorders in patients with vitiligo.
Methods
Electronic Search
The PubMed, Cochrane Library, EMBASE, CNKI (China National Knowledge Infrastructure), Chongqing VIP database, and Wanfang database were systematically searched with different combinations of key words to identify studies on thyroid disorders in vitiligo. The studies published in the period from inception to August 2, 2018 were identified. The search keywords were [vitiligo] AND [thyroid] with [“prevalence” OR “incidence” OR “epidemiology”]. A manual search was performed by checking the reference lists of key studies and review articles before they were excluded to identify additional studies.
Inclusion and Exclusion Criteria
Studies were included if they met the following eligibility criteria: (1) provided sufficient information to estimate the prevalence of thyroid disorders in patients with vitiligo; (2) published in either English or Chinese language; (3) had the exact diagnosis of thyroid disorders. The exclusion criteria were duplicate data, irrelevant to vitiligo, review, data mistake, not providing sufficient information. Obscure terms, such as thyroid disfunction, thyroid disease, and autoimmune thyroid disease, or no categorical diagnoses were excluded.
Data Extraction
Data was extracted from each article using a standardized data-abstraction form, designed in advance. All the potentially relevant papers were reviewed independently by two investigators. Disagreements were resolved through discussion. The following characteristics were extracted: first authors' name, year of publication, country area, number of vitiligo patients, number of different type, or stage of vitiligo patients who have thyroid disorders, number of male and female patients, number, or prevalence of thyroid disorders in vitiligo patients, duration of vitiligo, survey age, adults or children.
Data Analysis
All statistical analyses were carried out in Stata software (v15.0; Stata Corp, College Station, TX, USA) and a p < 0.05 was deemed statistically significant. To explore the prevalence of each thyroid disorder in vitiligo patients, the pooled prevalence and its 95%CI were calculated. Random-effects models were used, if the p < 0.05, I2 > 50%, otherwise, a fixed-effect model was selected (p > 0.05, I2 < 50%). Subgroup analyses based on areas, gender, age, vitiligo type, and vitiligo stage were done to assess sources of heterogeneity. Sensitivity analysis was performed by eliminating individual studies one by one. The effect of publication bias was assessed by Egger's test.
Results
Study Flow and Characteristics
A total of 3,643 articles were screened. Of these, 3,566 were excluded for the following reasons: not relevant to our topic, duplication, review, not English or Chinese, not providing sufficient information or data mistake, no categorical diagnoses (for example, thyroid goiter). Finally, 77 studies met the inclusion criteria, and were included in this systematic review and meta-analysis (12–88). Of these studies, 2 studies were reported by one author in the same year, sharing the common basic data, but respectively provided some different data. The detailed selection process was shown in Figure 1.
Figure 1. Flow diagram of the study selection process.
The characteristics of included studies were described in Table 1. The publication years were from 1968 to 2018. The countries covered France, Netherland, Greece, Serbia, Bulgaria, FRG (the Federal Republic of Germany), Italy, Spain, Austria, England, Denmark, USA, Washington, Colorado, California, Canada, Brazil, China, India, Turkey, Korea, Japan, Iran, Thailand, and Nigeria. The areas covered Europe (France, Netherland, Greece, Serbia, Bulgaria, FRG, Italy, Spain, Austria, England, Denmark), North America (USA, Washington, Colorado, California, Canada), South America (Brazil), Asia (China, India, Turkey, Korea, Japan, Iran, Thailand), and Africa (Nigeria). The number of patients with thyroid disorders ranged from 35 to 73,336.
Table 1. Characteristics of studies on the prevalence of thyroid disorders in patients with vitiligo.
Six thyroid disorders were described in the study. They were subclinical hyperthyroidism, overt hyperthyroidism, subclinical hypothyroidism, overt hypothyroidism, Graves disease, and Hashimoto thyroiditis. The number of studies on the 6 above mentioned thyroid disorders in vitiligo patients were 54 on overt hypothyroidism, 50 on overt hyperthyroidism, 25 on subclinical hypothyroidism, 19 on Hashimoto thyroiditis, 16 on Graves disease, and 10 on subclinical hyperthyroidism (Table 2). The data of vitiligo patients who accompanied with one of the following 5 thyroid disorders including thyroid cancer, toxic nodular goiter, thyroid adenoma or asymptomatic atrophic thyroiditis, was not extracted as only 1 study was reported in each disorder.
Table 2. The pooled prevalence and subgroup analysis of thyroid disorders in vitiligo patients.
The diagnoses of subclinical hyperthyroidism were based on the presence of a low TSH level with both normal FT3 value and normal FT4 value and the diagnosis of overt hyperthyroidism was based on the presence of a low TSH level with both raised FT3 value and raised FT4 value (52, 82). The diagnosis of overt hypothyroidism required low FT3 and FT4 values no matter what the TSH level was. Subclinical hypothyroidism was diagnosed on the basis of a raised TSH level with normal T3 and T4 values. Hashimoto's thyroiditis was diagnosed based on the demonstration of circulating thyroid antibodies and diffuse thyroid enlargement or reduced echogenicity on thyroid ultrasonography. And the diagnosis of Graves' disease relies on persistent hyperthyroidism together with positive thyroid antibody and/or increase vascularization on thyroid sonogram, thyroid-stimulating antibodies and diffuse hypercaptation at scintigraphy. Thyroid ophthalmopathy and/or dermopathy are characteristic features of Graves' disease (13).
Pooled Result of the Prevalence of Thyroid Disorders in Patients With Vitiligo
The pooled prevalence of thyroid disorders in patients with vitiligo were showed in Table 2. The highest prevalence of thyroid disorder accompanying vitiligo was 0.06 (95% CI: 0.04–0.07) for subclinical hypothyroidism (Figure 2A). The lowest prevalence was 0.01 (95% CI: 0.00–0.01) for subclinical hyperthyroidism and 0.01 (95% CI: 0.01–0.02) for Graves disease.
Figure 2. The forest plot of three thyroid disorders in vitiligo patients. The highest prevalence was reported in (A) subclinical hypothyroidism, and a majority of investigators paid attention to (B) overt hypothyroidism, and (C) overt hyperthyroidism in vitiligo patients.
Subgroup Analysis of the Prevalence of Each Thyroid Disorder in Patients With Vitiligo
Potentially distorting factors, including area, vitiligo type, the stage of vitiligo, gender, and age were investigated for subgroup analysis. The areas covered Europe, North America, South America, Asia, Africa. For vitiligo type, segmental vitiligo (SV), non-segmental vitiligo (NSV), generalized vitiligo, acrofacial vitiligo, vulgaris vitiligo were classified. When stratified by the stage, it was divided into active vitiligo and stable vitiligo. For the gender, it was divided into male and female. When stratified by age, the groups were children (<18 years) and adults (≥18 years). The results of subgroup analysis were listed in Table 2.
Overt hypothyroidism in vitiligo patients was reported in 54 studies. The pooled prevalence was 0.03 (95% CI: 0.03–0.04) (Figure 2B). The prevalence in Europe, North America, South America and Asia were found to be 0.06 (95% CI: 0.04–0.09), 0.09 (95% CI: 0.07–0.11), 0.14 (95% CI: 0.07–0.22), and 0.01 (95% CI: 0.01–0.02), respectively. The highest prevalence was 0.14 (95% CI: 0.07–0.22) in South America. Male and female subgroups were 0.02 (95% CI: 0.01–0.03) and 0.06 (95% CI: 0.04–0.08), respectively. The prevalence of overt hypothyroidism in the male population was lower than in females. When stratified by age, the prevalence was higher in children 0.04 (95% CI: 0.02–0.06) than adults 0.02 (95% CI: 0.01–0.04). Pooled prevalence of segmental vitiligo, non-segmental vitiligo, generalized vitiligo, and acrofacial vitiligo were 0.00 (95% CI: −0.00 to 0.01), 0.03 (95% CI: 0.01 to 0.05), 0.10 (95% CI: −0.03 to 0.22), and 0.01 (95% CI: −0.00 to 0.02), respectively. The prevalence in generalized vitiligo was the highest.
Overt hyperthyroidism in vitiligo patients was reported in 50 studies. The pooled prevalence was 0.02 (95% CI: 0.01–0.02) (Figure 2C). The prevalence in Europe, North America, South America, Asia and Africa were found to be 0.03 (95% CI: 0.02 to 0.05), 0.01 (95% CI: 0.01 to 0.01), 0.02 (95% CI: −0.01 to 0.06) and 0.01 (95% CI: 0.01 to 0.02), 0.01 (95% CI: −0.00 to 0.01), respectively. The pooled prevalence in Europe was the highest. Male and female subgroups were 0.01 (95% CI: 0.00–0.03) and 0.02 (95% CI: 0.01–0.04), respectively. When stratified by age, the prevalence was higher in adults 0.05 (95% CI: 0.03–0.07) than children 0.01 (95% CI: 0.00–0.02). Pooled prevalence of segmental vitiligo, non-segmental vitiligo, generalized vitiligo, and acrofacial vitiligo were 0.00 (95% CI: −0.00 to 0.01), 0.06 (95% CI: 0.02 to 0.09), and 0.04 (95% CI: 0.02 to 0.06), respectively. The prevalence of non-segmental vitiligo was higher than the other vitiligo types.
The subgroup analysis of other 4 thyroid disorders including subclinical hyperthyroidism, subclinical hypothyroidism, Graves disease, Hashimoto thyroiditis in vitiligo patients is reported in Table 2.
Sensitivity Analysis
To examine the stability of the pooled prevalence of thyroid disorders in vitiligo, each study was sequentially excluded for sensitivity analysis. The results demonstrated that some individual studies significantly affected the pooled results in overt hypothyroidism and Hashimoto thyroiditis. The studies of Jian et al. (41) influenced the original results of overt hypothyroidism in vitiligo patients. After removing the study, the pooled prevalence increased by 0.54% (from 3.23 to 3.77%). After removing the study of Bae et al. (15) and Tang et al. (55) of Hashimoto thyroiditis in vitiligo patients, the pooled prevalence increased by 3.47% (from 1.94 to 5.41%).
Publication Bias
No publication bias were found in papers on overt hyperthyroidism (t = 1.16, p = 0.256) (Figure 3A), overt hypothyroidism (t = 0.95, p = 0.350) (Figure 3B), and subclinical hypothyroidism (t = −1.36, p = 0.194) (Figure 3C). Publication bias was found in the prevalence of Graves disease (t = 3.32, p = 0.021) and Hashimoto thyroiditis (t = 2.96, p = 0.012) in patients with vitiligo. Publication bias was not done in subclinical hyperthyroidism in vitiligo patients as there were insufficient observations.
Figure 3. The three thyroid disorders in vitiligo patients with no publication bias (A) overt hyperthyroidism; (B) overt hypothyroidism; (C) subclinical hypothyroidism.
Discussion
Genome-wide association studies suggesting the relationship between vitiligo and thyroid disorders may be explained by the sharing of a subset of susceptibility gene (89–97). For example, genome-wide linkage analysis in families identified an autoimmunity susceptibility locus on chromosome 1 in patients with both vitiligo and Hashimoto's thyroiditis (96–98). In 2012, Vrijmanc et reported a systematic review about the prevalence of abnormal thyroid function test or elevated thyroid antibodies in vitiligo patients, covering 48 studies (99). The study reminds clinicians should be aware of the possibility of thyroid function changes in patients with vitiligo, however, it did not elaborate specific thyroid dysfunction in vitiligo patients. From a different point, the present systematic review summarized the results of the studies which have categorical diagnoses. The present review involving 77 studies with 3,643 vitiligo subjects supports a significant association between vitiligo and at least one thyroid disorders. The thyroid disorders were subclinical hyperthyroidism, overt hyperthyroidism, Graves disease, subclinical hypothyroidism, overt hypothyroidism, Hashimoto thyroiditis. Twenty-five studies reported the prevalence of subclinical hypothyroidism in vitiligo and the prevalence was the highest (6%) among the six thyroid disorders. Subclinical hyperthyroidism or Graves disease had the lowest prevalence (1%) in vitiligo patients, correspondingly, only approximately 10 studies were, respectively reported about these diseases.
A majority of investigators paid attention to overt hypothyroidism (54 studies) and overt hyperthyroidism (50 studies) in vitiligo patients, although the prevalence of these two disorders (3 and 2%) were lower than that of subclinical hypothyroidism. Overt hypothyroidism patients may experience weight gain, hair loss, dry skin, cold intolerance, constipation, muscle aches, or impaired memory (100–102). Overt hyperthyroidism patients may present with irritability, nervousness and heat intolerance (101, 103).
Our study investigated the potentially distorting factors, including area, gender, age, vitiligo type and stage of vitiligo. The prevalence of overt hyperthyroidism, overt hypothyroidism, Graves disease, and Hashimoto thyroiditis in Europe were higher than in Asia, in contrast, the prevalence of subclinical hypothyroidism in Europe were lower than in Asia. Genetic factor and iodine intaking habit may explain the disparity. The risk of thyroid dysfunction in female vitiligo patients is equal or greater than male, suggesting a gender-relationship between thyroid disorders and vitiligo. Men and women have sexual dimorphism of the immune response (104, 105). The British vitiligo guideline suggests that adult vitiligo patients should regularly screen for thyroid disorders. The present systematic review supports this recommendation in adult vitiligo patients with subclinical hyperthyroidism and overt hyperthyroidism. However, as for subclinical hypothyroidism, overt hypothyroidism and Hashimoto thyroiditis, children had higher prevalence than adult.
In the present review, all thyroid disorders were found in NSV, but not in SV. SV is characterized by early involvement of follicular melanocyte reservoir, early age of onset, and rapid stabilization (106), whereas NSV typically evolves over time and associates with thyroid disease frequently (107). Ethnic background may explain the disparity (91, 107). Different clinical subtypes of NSV have been described, including generalized, acrofacial, and vulgaris types. However, very few studies were included, so we can't draw a clear conclusion. As for the subgroup analysis between active vitiligo and stable vitiligo, 2 thyroid dysfunctions (overt hyperthyroidism and subclinical hypothyroidism) were studied but no definite results were found.
Several limitations of this meta-analysis must be considered. As there were insufficient studies, publication biases were not done about subclinical hyperthyroidism, and publication bias was found in Graves disease and Hashimoto thyroiditis. Studies about vitiligo type and stage were scant. This may have influenced confidence intervals and limited the generalizability of findings. Besides, 3 studies were not included due to the language restrictions.
In conclusion, the systematic review and meta-analysis showed that 6 thyroid disorders showed various prevalence in vitiligo. The highest prevalence was in subclinical hypothyroidism, and the lowest was in subclinical hyperthyroidism or Graves disease. The results of the current review provide useful estimates of the burden of thyroid disorders in vitiligo patients. Screening vitiligo patients for thyroid disorders seem reasonable, in an effort to detect potential thyroid diseases or to assess the risk of future onset.
Author Contributions
JY and CS conceived, designed and performed the article. SJ, YL, and YZ acquisition of data. H-DC, X-HG, and YW participated in revising the manuscript. All authors contributed to manuscript revision, read and approved the submitted version.
Funding
The study was supported by Liaoning Provincial Natural Science Fund (Code 201602837).
Conflict of Interest Statement
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.
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Keywords: vitiligo, thyroid disorders, prevalence, systematic review, meta-analysis
Citation: Yuan J, Sun C, Jiang S, Lu Y, Zhang Y, Gao X-H, Wu Y and Chen H-D (2019) The Prevalence of Thyroid Disorders in Patients With Vitiligo: A Systematic Review and Meta-Analysis. Front. Endocrinol. 9:803. doi: 10.3389/fendo.2018.00803
Received: 16 September 2018; Accepted: 20 December 2018;
Published: 15 January 2019.
Edited by:
Alessandro Antonelli, University of Pisa, ItalyReviewed by:
Roberto Vita, Università degli Studi di Messina, ItalySilvia Martina Ferrari, University of Pisa, Italy
Copyright © 2019 Yuan, Sun, Jiang, Lu, Zhang, Gao, Wu and Chen. 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: Yan Wu, jlwuyan@126.com
Hong-Duo Chen, hongduochen@hotmail.com