Brief Report

Serological Screening of Celiac Disease in Patients with Juvenile Idiopathic Arthritis

Cite this article as: Sadeghi P, Salari K, Ziaee V, Rezaei N, Eftekhari K. Serological screening of celiac disease in patients with juvenile idiopathic arthritis. Arch Iran Med. 2021;24(10):783-785. doi: 10.34172/aim.2021.116

Introduction

Juvenile idiopathic arthritis (JIA), the most common cause of non-infectious chronic arthritis in children younger than 16 years, is occasionally associated with extra-articular symptoms, such as growth retardation (weight or height) and gastrointestinal manifestations.¹

Celiac disease (CD) can cause gastrointestinal and joint involvement. Therefore, CD should be considered in patients with arthritis associated with failure to thrive (FTT) and gastrointestinal symptoms.¹ CD is a gluten-sensitive enteropathy which leads to autoimmune reactions and production of autoantibodies in genetically susceptible individuals.² The association between CD and JIA has been reported in some studies and its prevalence is reported at 1%–10%.³ Therefore, CD should be considered in patients with JIA when unexplained extra-articular symptoms occur.³ There are still some questions about the association of these diseases; for example, whether CD should be screened in all patients with JIA before initiation of treatment. Is this association due to the common background of two different diseases with different treatments^3,4? The results of different studies are not similar and the relationship between these two diseases is currently unclear. In Iran, only one study was conducted on children and adults with JIA and it did not show a higher incidence of CD in these patients.⁵ In another study, the prevalence of CD was higher in adults with JIA.⁶

Our aim was to screen CD in patients with JIA at the pediatric rheumatology centers of Tehran University of Medical Sciences.

Materials and Methods

This was a cross-sectional study performed in children with JIA from July 2017 to March 2019 at the Pediatric Rheumatology Centers of Tehran University of Medical Sciences. The patients were classified into different subgroups according to the ILAR- JIA criteria.

Inclusion criteria were the following: children under the age of 16 with JIA, whose disease did not respond appropriately to treatment (resistant after one year of treatment) or relapsed after undergoing remission.

Exclusion criteria were the following: known immune deficiencies, renal failure, liver failure, and known malabsorption syndromes such as CD or inflammatory bowel disease.

Seventy-eight patients were enrolled after obtaining informed consent from them or their parents. All data were recorded in a checklist which included demographic information (age, gender), clinical information such as type of the disease, duration of disease, type of medication used, and control degree of disease (according to clinical and laboratory findings). Also, the growth status, presence and type of gastrointestinal symptoms, and laboratory findings were recorded. Weight and height were measured and compared with standard growth charts of WHO and CDC. Growth classification was done as follows: growth retardation or FTT [type I (weight retardation), type II (height and weight retardation)], and obesity.

Then 5 mL venous blood samples were taken and analyzed for Anti-tissue transglutaminase antibodies (IgA) (Anti TTG-IgA) by means of enzyme-linked immunosorbent assay (ELISA). Anti TTG Antibody levels of 20 (U/mL) and above were considered positive according to the kit manufacturer’s reference. Cases with Anti TTG antibody levels ranging from 5 to 20 (U/mL) were considered suspicious and re-measured. Since selective immunoglobulin A deficiency is more common in the celiac patients, total immunoglobulin A levels (Total IgA) were measured by nephelometry method, to confirm the true negative results of the Anti-TTG antibody. The cutoff point of this test was considered to be less than 33 mg/dL according to the kit manufacturer’s reference. If the primary serologic results were abnormal, the patients were referred to a pediatric gastroenterologist for the definite diagnosis of CD (by upper GI endoscopy and biopsy). The samples were classified on the basis of “March criteria” by a pathologist. Finally, the diagnosis of CD was confirmed or rejected by pediatric gastroenterologists. In case of low total serum IgA, the patient was referred to a pediatric immunologist for further immune deficiency evaluations.

Data Analysis

The data were analyzed using SPSS version 25. The descriptive data were reported by descriptive statistics (median, standard deviation, frequency, relative frequency). For comparison of qualitative variables between two groups, the chi-square test (Fisher’s exact test) was done and for quantitative variables, the student sample t test in case of normal distribution and Mann-Whitney test in case of abnormal distribution were done. P-values less than 0.05 were considered statistically significant.

Results

The ratio of girls to boys was 2/1 and the mean age was 7.9 ± 3.9 years (1.6 – 16 years), the age at disease onset was 5 ± 2.3 (0.3–12) years, and duration of the disease was 33 ± 34 (1–144) months. In these patients, 32% had growth retardation [type 1 (14.1%, n = 11) and type 2 (17.9%, n = 14)] and 6.4% were overweight. Twenty-five patients (32%) had gastrointestinal symptoms including anorexia, abdominal pain, constipation, and flatulence in decreasing order of frequency. None of the patients had low levels of total serum IgA. Seven patients had anti-TTG Ab (IgA) levels above 5 in the primary screening which was considered suspicious according the laboratory kit. However, after repeating the test, only three patients (8.3%) had antibody levels above 20 which were considered positive. The antibody level in two patients was higher than 200 and the third patient had 133 IU/mL (in this patient, the primary screening test was 7). The mean age in these sero-positive children was 6.7 and the mean age of onset of disease was 5 years. The clinical and laboratory characteristic of the positive serologic tests are summarized in Table 1. All had a normal growth pattern with no gastrointestinal complaints.

There were no significant statistical differences in terms of growth disorders [P value = 1.00, 95% CI: 1.0 (1.00–1.00)], sex distribution (P value = 0.700), and different subtypes of JIA [P value = 0.620, 95% CI: 0.6 (0.60–0.63)] between the two groups of positive and negative anti-TTG. A gluten-free diet was started in the patient with a definitive diagnosis of CD based on the pathology result (March III_b). After two months of diet, all clinical (including musculoskeletal) manifestations subsided completely. The drugs were tapered gradually and then discontinued. The patient had no recurrence after 12 months, continues on gluten-free diet and has been monitored by the Anti-TTG level.

Discussion

The aim of this study was serological screening of JIA patients for CD. Based on the findings, the prevalence of high serum Anti TTG Antibody is 8.3%. The prevalence of CD in healthy asymptomatic children has been reported at 0.5–2%.^7,8 In our study, the mean age was lower than those studies. The prevalence of CD was higher in our study and the sex dominancy was female/male ratio of 2/1, in contrast to Farahmand and colleagues’ study.⁷ Concerning the similarities of lab kits, geographic region and the population between our study and Farahmand and colleagues’ study, this difference could be valuable.

The prevalence of CD among JIA patients was reported differently among several studies (1.8%–6.6%).^5,9 The reason for the false-positive result of Anti-TTG IgA could be the presence of some antibodies due to other conditions or to increased polyclonal IgA levels.^9,10 Sometimes, in spite of a positive serologic result for CD, the inflammation of small bowel mucosa could be improved by corticosteroids or immunosuppressive drugs. In such cases, despite a biopsy, a definitive diagnosis can be very challenging especially in JIA patients under treatment.¹¹ Selective IgA deficiency and use of immunosuppressive drugs could be important reasons for false-negative results of the Anti-TTG test.² In these situations, measuring endomysial antibody is useful, and if there is a high suspicion, biopsy is recommended. One negative result of anti-TTG Ab IgA cannot definitively rule out the disease (a CD with negative Anti-TTG Ab is called sero-negative CD).² On the basis of multiple studies including ours, absence of clinical manifestation or growth failure in JIA patients cannot exclude CD.^3,5 Therefore, patients with rheumatological complaints are considered to be at higher risk for CD. Also, the presence of symptoms such as inadequate response to routine treatments of JIA can raise the suspicion of the CD. In different studies, a gluten-free diet could reduce joint involvement,^9,12 musculoskeletal complaints,⁴ and improve growth rate.⁹ In our study, this method helped to discontinue the drug therapy.

Study Limitations

Among the limitations of our study are the following: lack of consent of some patients, unwillingness of some positive serologic patients to undergo endoscopy regarding lack of obvious gastrointestinal complaints or aggressive nature of the medical procedure, the patient’s unwillingness to repeat the test.

In conclusion,CD can be asymptomatic and only be diagnosed by screening. In JIA patients with concomitant growth disorders or even failure to respond to appropriate treatment for underlying disease, screening for concomitant CD is necessary.

References

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