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ORIGINAL ARTICLE |
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Year : 2017 | Volume
: 37
| Issue : 2 | Page : 50-55 |
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An association between rheumatoid arthritis and scabies infection: A population-based study in Taiwan
Ren-Jun Hsu1, Jui-Ming Liu2, Her-Young Su3, Cheng-Ping Yu4, Mu-Hsien Yu3, Jih-Chin Lee5, Fung-Wei Chang3
1 National Defense Medical Center, Graduate Institute of Life Sciences; Department of Pathology, National Defense Medical Center, Graduate Institute of Pathology and Parasitology, The Tri-Service General Hospital; National Defense Medical Center, Biobank Management Center of the Tri-Service General Hospital, Taipei, Taiwan, Republic of China 2 National Defense Medical Center, Graduate Institute of Life Sciences, Taipei; Department of Surgery, Division of Urology, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan; Faculty of Medicine, National Yang-Ming University, Taipei, Taiwan, Republic of China 3 Department of Obstetrics and Gynecology, National Defense Medical Center, Tri-Service General Hospital, Taipei, Taiwan, Republic of China 4 Department of Pathology, National Defense Medical Center, Graduate Institute of Pathology and Parasitology, The Tri-Service General Hospital, Taipei, Taiwan, Republic of China 5 Department of Otolaryngology, Head and Neck Surgery, National Defense Medical Center, Tri-Service General Hospital, Taipei, Taiwan, Republic of China
Date of Web Publication | 21-Apr-2017 |
Correspondence Address: Dr. Fung-Wei Chang Department of Obstetrics and Gynecology, National Defense Medical Center, Tri-Service General Hospital, Taipei, Taiwan Republic of China
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/jmedsci.jmedsci_95_16
Background: Scabies is an infectious inflammatory skin disease, and rheumatoid arthritis (RA) is also an immune-medicated inflammatory disease. Immune-mediated inflammatory processes result in the pathophysiologic mechanism in both diseases. Only a few studies have investigated the possible association between scabies and RA. Methods: This nationwide population-based study included 5135 patients with scabies as the study group; 19,115 people chosen from the National Health Insurance Research Database of Taiwan formed a control group. We tracked patients in both groups for 7 years to identify newly diagnosed cases of RA. Demographic characteristics and comorbidities were analyzed. Cox proportional hazards regressions were performed to calculate the hazard ratio (HR) of RA during the 7-year follow-up period. Results: Of the 24,250 patients enrolled in this study, 217 (0.9%) were diagnosed with RA during the 7-year follow-up period; 61 (1.2%) were from the scabies group and 156 (0.8%) were from the control group. The data showed that patients with scabies had a higher risk of subsequent RA, with an HR of 1.46 (95% confidence interval = 1.09–1.96). Conclusions: The results indicated an increased risk for RA among the patients with scabies infections. The data also showed that the assessment of RA symptoms should be included in the long-term follow-up of patients with scabies. Keywords: Rheumatoid arthritis, scabies, National Health Insurance Research Database
How to cite this article: Hsu RJ, Liu JM, Su HY, Yu CP, Yu MH, Lee JC, Chang FW. An association between rheumatoid arthritis and scabies infection: A population-based study in Taiwan. J Med Sci 2017;37:50-5 |
How to cite this URL: Hsu RJ, Liu JM, Su HY, Yu CP, Yu MH, Lee JC, Chang FW. An association between rheumatoid arthritis and scabies infection: A population-based study in Taiwan. J Med Sci [serial online] 2017 [cited 2023 Dec 4];37:50-5. Available from: https://www.jmedscindmc.com/text.asp?2017/37/2/50/204987 |
Ren-Jun Hsu, Jui-Ming Liu
These authors contributed equally to this work.
Introduction | |  |
Scabies is a pruritic disease caused by a parasitic skin infection. Scabies is easily spread by contact with the mite Sarcoptes scabiei.[1],[2],[3] About 300 million people worldwide are infected with scabies each year.[4] Those with a lower quality of life have a greater chance of having intensely itchy skin lesions caused by scabies infection. In developing countries, the prevalence rate is high among preschool children, adolescents, and the elderly.[5] However, scabies infection is also more common among nursing home residents, institutionalized patients, and immunocompromised persons.[6],[7],[8] The pathophysiology of scabies infection is generated by hypersensitivity-like reactions, followed by immune responses.[9]
Rheumatoid arthritis (RA) is a chronic autoimmune disorder that primarily involves cartilage and bone. It can also affect other organs, including the kidneys, blood vessels, and the lungs. RA affects approximately 0.5%–1.0% of the world's population.[10] RA patients suffer from fatigue, chronic pain, and functional disability, which leads to a tremendous mental and physical burden.[11],[12]
However, a few studies have assessed an association between RA and scabies.[13],[14] Our aim during our 14-year study has been to investigate the possible relationship between scabies and RA.
Methods | |  |
Data collection
This nationwide population-based study was authorized by the Institutional Review Board of the Tri-Service General Hospital in Taiwan (approval number: TSGHIRB NO. B-105-06). The data were collected from the National Health Insurance Research Database (NHIRD) of Taiwan. The National Health Insurance (NHI) is a special health and medical insurance system program that provides broad health-care coverage to residents of Taiwan. The NHI program was begun in 1995, and covered 99.9% of the 23 million residents until the end of 2013.[15] The NHIRD includes the data of people who have sought medical help; these data include, for example, medical records, prescription records, demographic data, and medical procedures. We randomly selected one million people from the Longitudinal Health Insurance Database 2000 (LHID2000), which is a sub-dataset of the NHIRD.
Study sample
The study population was selected from the LHID2000 from January 2000 to December 2013. All newly diagnosed patients with scabies infection (The International Classification of Diseases, Ninth Revision, Clinical Modification [ICD-9-CM]: 133.0)[16] from January 2001 to December 2006 were enrolled in the study, and the clinical diagnoses were based on the ICD-9-CM [Figure 1]. Those younger than 20 years of age (n = 1348), those with incomplete medical records (n = 67), those with a previous history of scabies or RA (n = 62), and subjects diagnosed with scabies before January 1, 2001 (n = 345) were excluded from the study. | Figure 1: Flowchart of recruitment of subjects from the 1-million random sample of the National Health Insurance Research Database from 2001 to 2006 in Taiwan
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There were 24,250 subjects enrolled in this study, who were assigned to one of two groups, a study group or a control group. A total of 5135 patients with scabies infections were enrolled in the scabies group. The 19,115 nonscabies control subjects were randomized with a ratio of 1:4 by matching them to the subjects with scabies. The nonscabies control subjects were matched to those in the scabies group by gender, age, insured region, and urbanization.
We tracked each subject for 7 years, starting with his or her index date, to identify and evaluate those diagnosed with RA (ICD-9-CM: 714.0). The diagnosis of RA and scabies was determined by physicians according to the results of the patient history and physical examination. We identified RA patients according to (ICD-9-CM) Code 714.0 and included only patients with RA who had received a catastrophic illness certificate, to ensure that RA diagnoses were valid. Several studies have been published that have examined the epidemiology of systemic autoimmune diseases, particularly RA, by using data from the NHIRD.[17],[18] Typical symptoms of scabies, such as inflammatory pruritic papules, severe pruritus, especially at night, burrows, nodules or generalized itching sparing the face, were required for the clinical diagnoses of scabies.[1]
Outcome measures
The results of this study were evaluated by the occurrence and severity of newly diagnosed RA. We analyzed all the medical procedures, medical diagnoses, and prescriptions each subject had received during the 7 years. The diagnosis of RA (ICD-9-CM: 714.0) was made by dermatologists when a patient was admitted to the hospital at least once or if at least two consistent diagnoses of RA had been made in the outpatient department. Covariates such as age, monthly income, urbanization, and comorbidities were analyzed in both groups. Comorbidities selected in this study included diabetes mellitus (ICD-9-CM: 250), hyperlipidemia (ICD-9-CM: 272), hypertension (ICD-9-CM: 401-405), chronic liver disease (ICD-9-CM: 456, 571, 572), chronic obstructive pulmonary disease (ICD-9-CM: 491, 492, 496), cerebrovascular accident (ICD-9-CM: 430-438), chronic kidney disease (ICD-9-CM: 585,586,588), and coronary heart disease (ICD-9-CM: 410-414). Age was categorized in a 10-year interval into 6 groups, as mentioned before. The monthly income, in New Taiwan Dollars (NTD), was divided into four categories: <NTD $20,000; NTD $20,000 through NTD $39,999; NTD $40,000 through NTD $59,999; and >NTD $60,000. Urbanization in Taiwan was classified into four groups. The geographic residential areas of Taiwan were divided into four regions, Northern region, Central region, Southern region, and “other” regions (eastern and outlying islands).
Statistical analysis
The Chi-square test and Student's t-test were used to analyze categorical descriptive data, including income, age, demographic characteristics, geography, comorbidities between the scabies patients and nonscabies control subjects, and level of urbanization. The Cox proportional hazards regression model was performed to obtain the effects of potential confounders on the hazard ratios (HRs) of the incidence of RA during the 7-year follow-up period between both study groups. We listed HR accompanying with 95% confidence intervals (CIs). A two-sided P < 0.05 was determined to be statistically significant. We used SPSS software version 19.0 (SPSS Inc., Chicago, IL, USA) for statistical analysis and Microsoft ® SQL Server ® 2008 software for data management.
Results | |  |
A total of 24,250 people were enrolled in this study from January 2001 to December 2006. A total of 5135 patients with scabies infection formed the study group, and 19,115 subjects were controls, in a 1:4 ratio matched with members of the study group. The demographic characteristics of all subjects are illustrated in [Table 1]. There were 2195 female patients and 2940 male patients with scabies infections. There is no significant difference in gender in this study. The two peak incidences occurred in the age group who were older than 70 years of age, and in the 20–29-year age group. Most patients with scabies infections had low incomes, and those who lived in northern Taiwan and urbanized areas had a higher proportion of scabies infections. The most common comorbidities in patients with scabies were chronic obstructive pulmonary disease, diabetes mellitus, cerebrovascular accident, and hypertension.
There were 217 newly diagnosed cases of RA among the 24,250 study subjects during the 7-year study. Of these, 61 (1.2%) occurred in scabies group and 156 (0.8%) in the control group [Table 2]. The incidence of RA was significantly higher among those in the scabies infection group than among those in the control group. Moreover, the results also indicated that an increased risk of RA in scabies infection was noted with HR 1.46 (95% CI = 1.09–1.96) [Table 3]. After adjusting for gender, age, income, geography, urbanization, and comorbidities, the adjusted HR (aHR) of scabies was 1.09 (95% CI = 1.02–1.47). Male patients (aHR: 0.49; 95% CI = 0.37–0.65) had a lower aHR than female patients. Hypertension (aHR: 1.68; 95% CI = 1.16–2.24), coronary heart disease (aHR: 1.75; 95% CI = 1.27–2.4), chronic liver disease (aHR: 1.71; 95% CI = 1.27–2.4), and chronic obstructive pulmonary disease (aHR: 1.46; 95% CI = 1.07–1.99) were significantly all associated with RA [Table 3]. | Table 2: Individuals with and without scabies as predictors of rheumatoid arthritis identified by Cox regression
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 | Table 3: Cox regression analysis of independent predictors of rheumatoid arthritis among scabies patients
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Discussion | |  |
This is the first study to investigate the relationship between RA and scabies. There were 5135 subjects with scabies and 19,115 controls studied for 7 years, with a 7-year follow-up. We found that patients with scabies infections had a 46% increased risk of developing RA.
One of the possible reasons for this increased risk is chronic inflammation. Scabies is an infectious, inflammatory disease, and increasing evidence implicates inflammation as a critical mediator of RA. RA is a chronic immune disorder. The inflamed synovium is infiltrated with CD4+ T-cells, and most of them express several activation markers.[19] RA is thought to be a kind of Th1 disease because peripheral blood or T-cell clones from synovium usually contain the Th1-like phenotype.[20] A Th1 cell generates interleukin 2 (IL-2) and interferon-r (IFN-r), which causes delayed-type hypersensitivity and activation of macrophages.[21] Scabies infection had also involved those inflammatory processes after infestation by S. scabiei.[22],[23],[24],[25] Accordingly, it seems that elevations of IL-2 and IFN-r have been discovered both in patients with RA and in those with scabies in most studies.
The causal relationship between scabies and RA is still unknown. Pipitone et al. reported a case of crusted scabies in a 17-year-old female patient with juvenile RA who was treated with infliximab.[13] Baccouche et al. also had reported a case of an 80-year-old woman who had crusted scabies with RA and was treated with tocilizumab.[14] The use of immunomodulatory agents to treat RA may become a risk factor for severe scabies infection. Future studies will be needed to further evaluate the relationship between RA and scabies.
Limitation
One strength of our study is that it was a large, nationwide, population-based, longitudinal study of the association between scabies and RA. Despite this, there are several limitations. First, all the diagnoses in this study were made with an ICD-9 coding system that was sourced from an administrative database; thus, the database diagnoses may be less accurate than diagnoses made with standardized procedures. Second, we were unable to do further evaluation of inflammatory markers, and laboratory test results are not available in the NHIRD. Laboratory tests may provide more useful information to help researchers find the mechanism involved in the relationship of RA and scabies, although the diagnoses of RA and scabies are established based on the physician's clinical diagnosis under diagnostic criteria. Third, our study using NHIRD data were retrospective in nature; NHIRD data are available for approximately 99% of the 23 million residents currently living in Taiwan. Furthermore, the relationship between RA and scabies is not fully established, due to limitations of the population-based cohort study design. Further prospective studies are warranted to investigate the relationship between scabies and RA, and such studies are essential.
Conclusions | |  |
This nationwide population-based study demonstrated a possible relationship between RA and scabies. The risk of developing RA increased up to 46% among those with scabies infections. In addition, IFN-r and IL-2 were identified in both RA patients and those with scabies. In the past, the positive treatment of scabies may have decreased the subsequent risk of RA. In the future, long-term follow-up of patients with scabies will be needed to better assess their RA symptoms.
Acknowledgments
This study was supported by grants from the Ministry of Health and Welfare (10,510) and Taoyuan General Hospital in the analysis and interpretation of data.
The results and conclusions in this study do not represent the opinions of the Bureau of NHI, the Department of Health, or the National Health Research Institute.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
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[Figure 1]
[Table 1], [Table 2], [Table 3]
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