Atopic dermatitis and association of risk for Henoch-Schönlein purpura (IgA vasculitis) and renal involvement among children: results from a
population-based cohort study in Taiwan
Short title: Henoch-Schönlein purpura in atopic dermatitis
Chang-Ching Wei, MDa,b; Cheng-Li Lin, MSc,d; Te-Chun Shen, MDb,e; Tsai-Chung Li,
PhDd, An-Chyi Chen, MDa,b
aChildren’s Hospital, China Medical University Hospital, Taichung, Taiwan; bSchool of Medicine, China Medical University, Taichung, Taiwan;
cManagement Office for Health Data, China Medical University Hospital, Taichung,
Taiwan;
dDepartment of Public Health, China Medical University, Taichung, Taiwan;
eDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine,
China Medical University Hospital, Taichung, Taiwan Correspondence to:
An-Chyi Chen, MD
Children’s Hospital, China Medical University Hospital, Taichung, Taiwan School of Medicine, China Medical University, Taichung, Taiwan
No2, Yu-Der Road Taichung 40402, Taiwan
Tel.: +886-4-22052121-4639; Fax: 886-4-2203-2798 E-mail: [email protected]
Key words: atopic dermatitis; children; Henoch-Schönlein purpura; IgA vasculitis; population study; retrospective cohort study
Abbreviations: atopic dermatitis (AD), confidence intervals (CIs), hazard ratios (HRs), Henoch-Schönlein purpura (HSP)
Word counts: abstract 323; text 2574 Table 5, Figure 1
Funding Sources The study was supported in part by Taiwan Ministry of Health and Welfare Clinical Trial and Research Center of Excellence (MOHW104-TDU-B-212-113002), China Medical University Hospital, Academia Sinica Taiwan Biobank,
Stroke Biosignature Project (BM104010092), NRPB Stroke Clinical Trial Consortium (MOST 103-2325-B-039 -006), Tseng-Lien Lin Foundation, Taichung, Taiwan, Taiwan Brain Disease Foundation, Taipei, Taiwan, and Katsuzo and Kiyo Aoshima Memorial Funds, Japan.
Financial Disclosure: The authors indicate that they have no financial relationships relevant to this article.
Conflict of Interest: None.
Contributor’s Statement:
Chang-Ching Wei and Te-Chun Shen conceptualized and designed the study, drafted the initial manuscript, and approved the final manuscript as submitted.
Cheng-Li Lin and Tsai-Chung Li carried out the initial analysis, reviewed and revised the manuscript, and approved the final manuscript as submitted.
An-Chyi Chen and Chang-Ching Wei coordinated and supervised data collection, critically reviewed the manuscript, and approved the final manuscript as submitted.
Abstract: Elevation of Th2 cytokine driven inflammatory mediators have been
reported in acute stage of Henoch–Schönlein purpura (HSP). However, the temporal interaction between Th2 mediated allergic diseases and HSP with renal involvement remains unknown. Herein, we conducted a population-based cohort analysis to investigate the risk of HSP and renal involvement in children with atopic dermatitis (AD) as one of the first steps in the atopic march.
From 2000 to 2007, 95 208 children with newly diagnosed AD and 190 416 randomly selected non-AD controls were included in the study. By the end of 2008, incidences of HSP in both cohorts and the AD cohort to non-AD cohort hazard ratios (HRs) and confidence intervals (CIs) were measured. Comparison of renal
involvement in HSP between children with and without AD was analyzed.
The incidence of HSP during the study period was 1.75-fold greater (95% CI: 1.27–2.42) in the AD cohort than in the non-AD cohort (14.2 vs. 8.11 per 100,000 person-years). The AD to non-AD HR of HSP was greater for girls (1.92, 95% CI: 1.18–3.13), children older than 6 years (2.54, 95% CI: 1.15–5.59), and those living in less urbanized area (2.74, 95% CI: 1.10–6.82). Concurrent allergic rhinitis or asthma did not increase the HR of HSP further. The HR for HSP in AD children increased from 0.67 (95% CI: 0.41–1.11) for those with ≤2 AD related visits to 9.77 (95% CI: 6.44–14.8) for those with >4 visits (P < 0.0001, by the trend test). The risk of
developing HSP in the AD cohort was highest within first year after AD diagnosis (HR: 3.99; 95% CI: 1.61–9.89). AD cohort with HSP had higher occurrence rate of renal involvement, particular hematuria, than non-AD cohort with HSP.
AD children had a greater risk of developing HSP and HSP with renal involvement. Further research is needed to clarify the role of allergy in the pathogenesis of HSP and renal involvement.
INTRODUCTION
Henoch–Schönlein purpura (HSP), nowadays called IgA vasculitis, is an immune complex vasculitis affecting small vessels with dominant IgA deposits.1 HSP is a
systemic vasculitis commonly seen in children.1 HSP is characterized by
non-thrombocytopenic purpura, abdominal pain and bleeding, arthritis, and renal involvement.1 The manifestations of renal involvement vary from asymptomatic
hematuria and/or proteinuria to nephritic syndrome, nephrotic syndrome, and rapidly progressive glomerulonephritis.2 The long term outcome of HSP depends primarily on
the extent of renal manifestations.2-4
HSP had been termed anaphylactoid purpura because HSP was reported to develop after exposure to allergens in drugs or food, immunization, and insect bites.5-8
Although the exact etiology and pathogenesis of HSP remain unclear, elevated serum IgA levels, vascular deposition of IgA-containing immune complexes, and increased proinflammatory cytokine levels were observed during its acute stage.9 Moreover,
previous studies revealed elevated soluble IL-2 receptor levels and a shift towards increased Th1 lymphocyte production in children with HSP, indicating a Th1 polarized disease.10,11 However, Davin et al. reported that plasma IgE levels were
significantly higher in patients with HSP, indicating a shift towards Th2 immune response.12 The complexity of Th1/Th2 interaction of HSP raises an research interest
whether Th2-mediated allergic diseases have any influence on the development of HSP and HSP with renal involvement.
Atopic dermatitis (AD) is a Th2 driven chronic relapsing inflammatory skin disease.13 AD is classically the first clinical manifestation of allergic disease,
presenting early in infancy, followed by the development of allergic airway diseases in some children.13-15 This so-called atopic march suggests a common etiology for the
different atopic diseases.15-17 The peak age of HSP occurrence is 4 to 6 yr. Hence, AD
children are an appropriate cohort to assess the temporal interaction between allergy and HSP. We conducted a population-based cohort study to investigate the incidence and subsequent risk of HSP and HSP with renal involvement in Taiwan children with AD so that we could provide better insights into the common immunological
aberrancies of both disorders. We hypothesized AD children had higher risk of HSP and HSP with renal involvement.
METHODS Data Sources
The National Health Insurance Research database (NHIRD), maintained by the National Health Research Institutes, contains population-based claims data from the National Health Insurance program, a mandatory-enrollment, single-payment system created in 1995, now covering over 99% of Taiwan's population
(http://www.nhi.gov.tw/english/index.aspx).18 The high reliability of the diagnostic
data from the NHIRD has been evaluated in previous studies.19,20 This study utilized a
data file derived from the NHIRD, containing information from half of all insured children in Taiwan, chosen at random. The dataset provided a sufficient sample size to pursue the objectives addressed in this study. Because of personal electronic data-privacy regulations, identifying information was encrypted before being sent to the researcher. The study was approved the Institutional Review Board of China Medical University Hospital (CMU-REC-101-012). Diseases were coded based on the
International Classification of Diseases, 9th Revision, Clinical Modification (ICD-9-CM).
Study Design and Subjects
AD is a chronic, relapsing, inflammatory skin disorder. Hence, AD was defined as at least one inpatient claim record or two ambulatory claims containing ICD-9-CM code 691.8 in the primary diagnosis field. A total of 95,208 patients (aged <18 years) newly diagnosed with AD between 2000 and 2007 were identified as the AD cohort. The baseline index date was the date of AD diagnosis. For each child with AD, we randomly selected 2 children without AD (never having ICD-9-CM code 691.8 in any diagnosis field) matched by sex, age (within 1 year), urbanized residence area, parental occupation, and baseline year. We used the method of 1:2 matching to
increase statistical power and to control for potential confounders. Children with missing data regarding sex or date of birth and those with preexisting HSP (ICD-9-CM 287.0) before or within 1 month after the baseline index date were excluded. We also identified and compared the differences of the subjects who were diagnosed with allergic rhinitis (ICD-9 code: 477) and asthma (ICD-9 codes: 493) in both the AD and non-AD cohorts. Diagnoses of HSP were based on clinical manifestations, including non-thrombocytopenic purpura located predominantly on dependent areas, such as the lower extremities and buttocks, and at least one of the following findings: arthralgia or arthritis, abdominal pain, or nephritis, according to the 1990 criteria of the
American College of Rheumatology (ACR). In this study, IgA vasculitis and allergic diseases were diagnosed by physicians and were defined as at least one inpatient claim record or two ambulatory claims in any diagnosis field with the respective ICD-9-CM codes. IgA vasculitis with renal involvement was defined as occurrence of any one of the following: hematuria, proteinuria, nephritis, and nephrotic syndrome (ICD-9 codes 5(ICD-9(ICD-9.7, 7(ICD-91.0, and 580-585) within 1 year after IgA vasculitis was diagnosed. Each child was followed from the index date until the development of IgA vasculitis, withdrawal of insurance, or conclusion of follow-up on December 31, 2008. This study’s design is summarized in the flow chart shown in figure 1.
Statistical Analysis
The sociodemographic variables included in this study were sex, age,
urbanization, and parental occupation. Urbanization was categorized into 4 levels based on the population density of the residential area: level 1 was the most urbanized and level 4 was the least urbanized. All data analyses were performed using SAS software version 9.1 (SAS Institute Inc., Carey, NC). Statistical significance was set at P < 0.05 in 2-tailed tests. To describe the baseline distributions of the AD and
non-AD cohorts, mean and standard deviations (SD) were used for continuous variables and counts and percentages were used for categorical variables.
Differences were examined using the chi-square test for categorical variables and
t test for continuous variables. Kaplan–Meier method was used to estimate the
proportion of study subjects in both cohorts who did not develop IgA vasculitis during the follow-up period. The incidence was calculated for each cohort. Hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated using multivariate Cox proportional hazard regression models, with the non-AD cohort as the reference group, to assess the association between AD and the risk of developing IgA vasculitis.
RESULTS
This study evaluated 95 208 AD cases and 190 416 non-AD cases. No
differences in the sociodemographic variables were noted between groups. Majority of AD children were boy (54.1%), aged ≤2 years (62.3%), and lived in higher urbanization regions (33.8%) (Table 1). AD cohort had higher occurrence rate of allergic rhinitis (18.5% vs 4.92%) and asthma (11.4% vs 2.64%) than no-AD cohort (Table 1). There were no differences in age group, sex, urbanization of living areas, or follow-up period between the 2 cohorts. Kaplan–Meier analysis showed that the accumulated incidence rate of HSP was significantly greater in the AD cohort than in the non-AD cohort (log-rank test P< 0.0001; Figure 2).
The incidence of HSP in both cohorts and the AD to non-AD HRs of HSP by sociodemographic status are presented in Table 2. Overall, the HSP incidence was 1.75-fold greater (95% CI: 1.27–2.42) in the AD cohort than in the non-AD cohort (14.2 vs. 8.11 per 100,000 person-years) at the end of follow-up period. The increased AD to non-AD HRs of HSP was consistent regardless of age, sex, and urbanization. The AD to non-AD HRs were increasing with age, from 1.65 for HSP (95% CI: 1.08– 2.52) for the children aged <2 years to 2.54 (95% CI: 1.15–2.51) for the children aged >6 years. The sex-specific AD to non-AD HRs was greater for girls 1.92 (95% CI: 1.18–3.13) than for boys 1.63 (95% CI: 1.05–2.51). The urbanization-specific AD to
non-AD HRs decreased with the higher level of urbanization. Concurrent allergic rhinitis or asthma did not increase the risk of HSP further in AD cohort (Table 2). The HR for HSP in AD children increased from 0.67 (95% CI: 0.41–1.11) for those with ≤2 AD related visits to 9.77 (95% CI: 6.44–14.8) for those with >4 visits (P < 0.0001, by the trend test) and the trend was consistent in both sex (Table 3). The risk of developing HSP in the AD cohort was highest within first year after AD diagnosis (HR: 3.99; 95% CI: 1.61–9.89) and declined with follow-up time (Table 4). AD cohort with HSP had higher occurrence rate of renal involvement, particular hematuria (P = 0.04), than non-AD cohort with HSP (Table 5).
DISCUSSION
This is the first population-based cohort study investigating the incidence and risk of HSP and HSP with renal involvement in AD cohort compared to non-AD cohort. Our results showed AD was a risk factor for HSP and HSP with renal involvement in children. The risks for HSP were constantly increased regardless of age, sex, and urbanization of residential area. The elevated risk of HSP was greater for girls, older children, and those living in less urbanized area.
Previous epidemiological studies revealed the annual incidence of HSP 13.5– 18/100 000 children with slight male predominance and peak age between 4 years and 6 years .1,24,25 Current study demonstrated the incidence rate of HSP 8.1/100 000
person-years in non-AD children and 14.2/100 000 person-years in AD children in Taiwan between 2000 and 2008. In addition, boys had a higher incidence in non-AD cohort and had a slightly lower incidence than girls in AD cohort, indicating that the impact of AD is greater for girls than for boys. The incidence of HSP is generally inversely associated with age in both AD and non-AD cohorts. However, the risk of HSP in AD to non-AD cohort increased as children grew. The discrepancy between sexes and age groups was not well documented in previous studies.1,24,25
Concurrent allergic rhinitis or asthma seems not related to a further increase of risk for HSP. The risk of HSP increased with more clinical burden of AD and was highest
within first year after AD was diagnosed. AD cohort with HSP had higher occurrence rate of renal involvement, particular hematuria, than non-AD cohort with HSP. Although most of the children with HSP have a good outcome, long-term prognosis of HSP depends on the severity of renal involvement. Previous studies reported that severe abdominal symptoms, older age, and persistent purpura, decreased factor XIII activity increased the risk of renal involvement. 26,27 However, no any study except
ours investigated whether AD increased risk of HSP with renal involvement. Our data indicate that AD is a risk factor for HSP and HSP with renal involvement.
AD is a chronic inflammatory skin disorder that develops in early infancy, often preceding asthma and allergic disorders, and representing the beginning of the atopic march.15 Therefore, the AD cohort is a useful model to study the impact of atopy on
certain diseases. In this study, 62.3% of children were diagnosed with AD before age 2, and boys had a slightly higher AD prevalence. This age and sex distribution is similar to previous reports in Asian populations.25 Recent advances in our knowledge
of the pathogenesis of AD have posited the relationship between immune
dysregulation, and skin barrier abnormalities.13,14 Exposure to irritants and allergens
from barrier-defective skin in patients with AD may lead to a specific Th2 cell
activation and IgE production in a subset of these patients. Elevated serum IgE is also commonly found in children with HSP.12 The genetic predisposition of an individual
to make IgE antibody responses to common environmental allergens and triggers may be associated with the development of AD and IgA vasculitis.
To date, the exact triggers and pathogenesis of HSP remain unclear. HSP was originally considered a Th1-mediated systemic vasculitis with cytokine cascades and endothelial cell lesions in small vessels in the acute stage.9,11,29 Th1-related serum
receptor expressions are often elevated in the acute phase of HSP.9,11,29 In contrast,
there have also been several reports of elevated Th2-related biomarker levels in children with HSP.10,12,30,31 Allergic diseases are caused by inappropriate Th2
cell-mediated immunological responses to allergens. Th2 cells secrete IL-4 and IL-5, which lead to type 1 hypersensitivity.29 The onset of HSP usually follows viral
infection, bacterial infection, drug allergy, food allergy, insect bites, or immunization, which implies that allergic reactions may participate in the onset of this disease.5-8 In
the presence of IL-4, the majority of B-cells switch immunoglobulin production to produce a vast amount of IgE.30,31 Davin et al., reported that the incidence of increased
plasma IgE levels was significantly higher in patients with HSP and suggested that IgE plays a possible pathogenic role in HSP.12 IL-5 switches the B cell
immunoglobulin to IgA and activates eosinophils30,31 IgA is considered to be the mediating factor in IgA vasculitis.1 Namgoong et al. found that eosinophil cationic
protein (ECP) and soluble IL-2 receptor levels were significantly higher in patients with IgA vasculitis than in a control group, indicating that T-cell and eosinophil activation were involved in the pathogenesis of IgA vasculitis.10 Tsuji et al. found
higher serum IgE and urinary leukotriene E4 levels at the onset of IgA vasculitis in children with AD than in healthy children.27 They also noted IgE deposits in the
Langerhans and mast cells in patients with IgA vasculitis with renal involvement, implying that stimulation of IgE-sensitized mast cells by specific antigens in the presence of circulating IgA immune complexes was associated with the disease cascade.27 In turn, the increased capillary permeability and perivascular deposition of
IgA CIC, which resulted in deposition of IgA and complement C3 in the small vessels of the skin and renal glomeruli.10,28 Kawasaki et al. found elevated serum IL-4 levels
ECP-activated eosinophil levels in patients with IgA vasculitis with renal
involvement.29 These studies support our findings. More recently, Li et al. reported
significantly elevated Th2 and Th17 cell levels in patients with acute IgA vasculitis.16
Dysregulation of the immune response, such as functional imbalance of Th cell subsets and a strongly polarized cytokine milieu in the peripheral blood, to environmental stimuli may contribute to both allergic and autoimmune diseases.16
Therefore, both early-life environmental factors and common immune aberrancy may contribute to the development of allergies and IgA vasculitis.
This study had several limitations. Thorough medical records for each patient are not available from the NHIRD. Therefore, the clinical presentations such as arthritis, bowel angina, complications, and therapeutic strategies in these patients and the clinical information of AD, such as serum IgE level, eosinophil level, skin infection, a family history of allergic diseases were unknown. Another limitation was the lack of data on genetic and environmental factors that might affect the risks of HSP and allergic diseases. In this study, diagnoses of HSP was made by physicians was based on the criteria defined by the 1990 criteria of ACR. The reliability of HSP diagnosis according to the ACR criteria was reported a sensitivity of 87.1% and a specificity of 87.7%.23 Our results showed an incidence of 14.2 vs 8.1 per 100 000 person years of
HSP in the AD vs the non-AD population. Hence, the result of the 1.75 fold greater risk of HSP in the AD cohort versus the non-AD cohort has a quite low clinical relevance taking account to the low prevalence of HSP. Lastly, the ethnic population
in the study was Chinese, which may not yield results generalizable to other populations.
In conclusion, this population-based cohort study reveals an increased incidence and subsequent risk of IgA vasculitis in children with AD. Future studies to clarify the role of allergy in the pathogenesis of IgA vasculitis with or without renal involvement are recommended.
STATEMENT OF FINANCIAL SUPPORT
The study was supported in part by Taiwan Ministry of Health and Welfare Clinical Trial and Research Center of Excellence (MOHW104-TDU-B-212-113002), China Medical University Hospital, Academia Sinica Taiwan Biobank, Stroke Biosignature Project (BM104010092), NRPB Stroke Clinical Trial Consortium (MOST 103-2325-B-039 -006), Tseng-Lien Lin Foundation, Taichung, Taiwan, Taiwan Brain Disease Foundation, Taipei, Taiwan, and Katsuzo and Kiyo Aoshima Memorial Funds, Japan. Disclosure: none
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FIGURE LEGENDS
Figure 1. Cummulative incidence of Henoch-Schönlein purpura for patients with atopic dermatitis (dashed line) or without atopic dermatitis (solid line)
