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Article

Unrecognized Celiac Disease in Children Presenting for Rheumatology Evaluation

Yekaterina Sherman, Rose Karanicolas, Brittany DiMarco, Nancy Pan, Alexa B. Adams, Laura V. Barinstein, L. Nandini Moorthy and Thomas J. A. Lehman
Pediatrics July 2015, 136 (1) e68-e75; DOI: https://doi.org/10.1542/peds.2014-2379
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Abstract

BACKGROUND AND OBJECTIVES: Current clinical guidelines do not consider patients with rheumatic conditions to be at high risk for celiac disease (CD) despite numerous reported associations between the two in adults and children. The objective of this study was to evaluate the prevalence of CD among patients presenting for pediatric rheumatology evaluation.

METHODS: A total of 2125 patients presenting for initial evaluation by the Division of Pediatric Rheumatology at the Hospital for Special Surgery between June 2006 and December 2013 were screened for CD as a part of the standard initial serologic evaluation. The charts of these patients were evaluated retrospectively at the end of this period.

RESULTS: 36 patients (30 girls, 6 boys, mean age 9.4 ± 4.3 years, range 2–16 years) received a diagnosis of CD after serologic testing and evaluation by pediatric gastroenterology. Eight additional patients with known diagnoses of CD presented during this time period. The total prevalence of CD over this 6.5-year period was 2.0%. The most common presenting complaints among patients diagnosed with CD were myalgias, arthralgias, and rash. Less frequently, patients reported gastrointestinal complaints including abdominal pain, nausea, and diarrhea. All patients reported improvement or complete resolution of their musculoskeletal symptoms after initiation of a gluten-free diet.

CONCLUSIONS: This study identified 36 new cases of CD among children presenting for rheumatology evaluation, for an overall prevalence rate of 2.0%. The majority of patients who ultimately received a diagnosis of CD presented with extraintestinal manifestations. These results underscore the importance of screening children presenting for rheumatology evaluation for CD.

  • Abbreviations:
    AGA —
    antigliadin antibody
    ANA —
    antinuclear antibody
    CD —
    celiac disease
    EMA —
    antiendomysial antibody
    GFD —
    gluten-free diet
    GI —
    gastrointestinal
    Ig —
    immunoglobulin
    JIA —
    juvenile idiopathic arthritis
    NASPGHN —
    North American Society for Pediatric Gastroenterology, Hepatology and Nutrition
    SLE —
    systemic lupus erythematosus
    TTG —
    anti–tissue transglutaminase antibody

    • What’s Known on This Subject:

    Associations have been reported between celiac disease (CD) and numerous autoimmune conditions in adults and children. However, current screening guidelines do not consider patients with rheumatic diseases to be at high risk for CD.

    What This Study Adds:

    The prevalence of CD in children presenting for rheumatology evaluation was found to be 2% by routine serologic screening. The majority of screening-detected CD cases had no CD-associated symptoms. Gluten restriction was found to relieve some musculoskeletal complaints.

    Celiac disease (CD) is a T-cell mediated immune disorder resulting in inflammation of the small intestine after the ingestion of dietary gluten and related proteins in genetically susceptible people. The prevalence of CD in the general US population has been reported as ∼0.7%, similar to that found in several European countries.1 In children ages 2.5 to 15 years this prevalence has been reported as between 0.3% and 1.3%.2–4 Studies have shown an association between CD and numerous autoimmune and rheumatic conditions including rheumatoid arthritis,5,6 juvenile idiopathic arthritis (JIA),7–10 autoimmune thyroiditis,10–12 autoimmune thrombocytopenic purpura, hemolytic anemia,6 vasculitis,5,6 polymyositis and dermatomyositis,13,14 systemic lupus erythematosus (SLE),5,6,15,16 scleroderma,5,6 mixed connective tissue disease,5 diabetes mellitus,17–22 Sjögren syndrome,6,10,23,24 and dermatitis herpetiformis.24 Among the connective tissue disorders, only Sjögren syndrome appears to share the HLA DQ2/DQ8 haplotype with CD.25 Additionally, a link has been reported between gene locus 4q27 and CD, rheumatoid arthritis, psoriatic arthritis, and JIA.26 The prevalence of autoimmune disease in patients with CD is known to increase with age at time of CD diagnosis,27 suggesting that these conditions may be interrelated. However, there are conflicting reports as to whether maintenance of a gluten-free diet (GFD) confers protection against the development of additional autoimmune diseases in patients with CD.28

    Despite the reported links between rheumatologic conditions and CD, current clinical guidelines for CD screening published by the American College of Gastroenterology and the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition (NASPGHN) do not consider such patients to be a high-risk group and do not specifically recommend screening of this population.29,30 At this time, little information is available about the coexistence of CD and rheumatic diseases in the US pediatric population. The aim of this study was to investigate the prevalence of CD in patients presenting to the pediatric rheumatology practice.

    Methods

    A total of 2125 new patients without preexisting rheumatic diagnoses who presented to the Division of Pediatric Rheumatology at the Hospital for Special Surgery, a tertiary care center in a major metropolitan area, were screened for CD by serologic testing as a standard part of the initial workup. The charts of all such patients seen between June 2006 and December 2013 were reviewed retrospectively at the end of this period. Laboratory results were reviewed for the presence of antigliadin antibodies (AGA IgA and IgG), anti–tissue transglutaminase antibodies (TTG IgA), and antiendomysial antibodies (EMA IgA). The EMA and TTG tests are highly sensitive and specific, with values for both parameters reportedly >95% in most studies.31 Sensitivities and specificities for the AGA tests are highly variable but are generally thought to be less reliable than TTG and EMA.31 A low positive AGA IgA or IgG titer alongside a negative TTG test was not considered suggestive of CD. Deamidated gliadin peptide testing was not routinely ordered, and results of this test, if available, were not recorded for the purposes of this study.

    Additional data recorded included age at initial visit, gender, presenting complaints, family history, ultimate diagnosis or diagnoses, antinuclear antibody (ANA) status, and total serum IgA. Patients who were suspected to have CD based on serologic testing were referred to pediatric gastroenterology for additional evaluation. For the purposes of this retrospective review, a patient must have had appropriate findings on serologic tests and have received a diagnosis of CD from a gastroenterologist. Patients were not referred to one particular practice, but rather the reports of several gastroenterology specialists were reviewed over the course of this study. Additional testing conducted by gastroenterology specialists involved endoscopies, tissue biopsies, and genetic testing as appropriate.

    For patients recorded as having CD, additional symptoms were collected from the review of systems elicited from all new patients: presence of abdominal pain, nausea, vomiting, diarrhea, constipation, blood in stool, weight loss, growth parameters, and a thorough review of musculoskeletal complaints. A comprehensive review of systems, including detailed gastrointestinal (GI) complaints, is standardized among the authors.

    Patients were excluded from analysis if they presented with a known diagnosis of inflammatory bowel disease (because they would have already had a complete GI review conducted) or were >18 years old at the time of presentation. Patients who presented with known CD must have already been under the care of a gastroenterologist. Reference ranges for CD serologies varied between local laboratories, and tests were recorded as positive if they fell above the reference range.

    We conducted statistical analyses by using SAS software SAS version 9.3 (SAS Institute, Inc, Cary, NC). This study was approved by the institutional review board of the Hospital for Special Surgery, New York.

    Results

    We reviewed the charts of 2125 new patients. Forty patients were referred to pediatric gastroenterology based on suspicion of CD. Of these, 4 had negative GI evaluations for CD and 36 (30 girls, 6 boys; mean age 9.4 ± 4.3 years, range 2–16 years) were confirmed as having CD (Fig 1). Among these patients, 30 cases of CD were confirmed by endoscopy (with or without intestinal biopsy, as per gastroenterology). The remaining 6 refused the procedure but demonstrated significant mitigation of symptoms upon initiation of a GFD and were considered to have CD by a gastroenterologist. Thirteen additional patients were found to have positive serologies but were lost to rheumatology follow-up, did not follow up with gastroenterology referrals, or started a GFD without a diagnosis of CD by a physician. Additionally, 8 patients (7 girls, 1 boy; mean age 11.4 ± 4.6 years, range 3–17 years) presented during this time period with an existing diagnosis of CD established on the basis of serologic or endoscopic evidence. All patients were under the care of gastroenterologists and reported well-controlled CD at the time of presentation.

    FIGURE 1
    FIGURE 1

    Patient demographics.

    The majority of new patients with a diagnosis of CD (32/36) had a positive TTG-IgA test. Among all 44 patients with CD (both newly and previously diagnosed), we diagnosed many concurrent rheumatologic and autoimmune diseases; most common among these were JIA (including all subtypes per established International League of Associations for Rheumatology classification criteria),32 morphea, uveitis, and thyroid disease. Several patients received a sole diagnosis of CD (Table 1).

    View this table:
    TABLE 1

    Clinical Features and Diagnoses of Newly Identified Cases of CD

    Interestingly, 19 out of 36 also had a positive ANA (ranging between 1:40 and 1:640). Additional serologic workup was done at the discretion of the treating physician and was not done for all patients. Of 8 patients presenting with known CD, 4 had a positive ANA (ranging between 1:160 and 1:640), and none had positive celiac serologies at the time of presentation, suggesting good adherence to the GFD (Table 2).

    View this table:
    TABLE 2

    Clinical Features and Diagnoses of Patients Presenting With Known CD

    Notable is that the majority of the patients with newly diagnosed CD (22/36) presented with musculoskeletal complaints in the absence of GI symptoms. Five patients with CD presented with GI complaints without musculoskeletal complaints, and 7 presented with both GI and musculoskeletal complaints. Two patients had only symptoms (including rash, fever, and headaches) that fit neither category (patients 16 and 35). All 8 of the patients with existing CD presented with musculoskeletal complaints. Four of these 8 patients additionally reported GI symptoms that had not resolved upon the restriction of gluten (Table 3).

    View this table:
    TABLE 3

    Presenting Symptoms of Patients Ultimately Diagnosed With CD

    Among all patients with CD (both known and newly diagnosed cases), 35 out of 44 reported a family history of autoimmunity or rheumatic conditions when prompted. (Patients were specifically asked about JIA, rheumatoid arthritis, osteoarthritis, SLE, mixed connective tissue disease, back pain, ankylosing spondylitis, inflammatory bowel disease (Crohn disease and ulcerative colitis), psoriasis, diabetes mellitus type 1, thyroid disease, acute rheumatic fever, and Lyme disease). Six patients reported a family history of CD when prompted (although only 3 were in first-degree relatives). All patients in whom CD was diagnosed by endoscopy were started on a GFD. Patients who refused the procedure but were suspected of having CD on the basis of positive serologies were also initiated on the GFD by their gastroenterologists. All patients reported either partial or complete resolution of their complaints (including musculoskeletal symptoms) upon initiation of the GFD. Ten of the 36 newly diagnosed patients (patients 14, 19, 20, 21, 24, 26, 28, 31, 34, and 36) never needed any medications and reported complete resolution of their symptoms with the restriction of gluten.

    Discussion

    To our knowledge, this study represents one of the largest pediatric cohorts ever evaluated for CD in the United States.3 We diagnosed 36 previously unrecognized cases of CD by standardized serologic screening of 2125 new patients who presented to our pediatric rheumatology practice. Along with the 8 preexisting cases of CD, this indicates a period prevalence of 2.0% (over 6.5 years), or approximately 1:48 patients over that period. Our data suggest that children presenting for rheumatology evaluation are at an elevated risk for CD, and standard screening of these patients should be considered.

    We may have underestimated the prevalence of CD in our cohort because of the criteria required for diagnosis: Any patient with positive titers who did not follow up with gastroenterology or rheumatology or who started a GFD without an official diagnosis of CD was excluded from our study. Additionally, it is possible that some patients who were tested for CD serologies were already on self-initiated GFDs at the time of presentation and would not have been identified in this retrospective review.

    The majority of the newly diagnosed CD cases, 22 out of 36 (61.1%), presented with musculoskeletal complaints alone and none of the classic symptoms of CD, such as abdominal pain, short stature, weight loss, and failure to thrive. In fact, only 12 patients reported a history of GI-related complaints. This is consistent with 2 recent reports that similarly found a low correlation between GI symptoms and CD positivity. These studies both concluded that symptom-based case finding is insufficient to identify a majority of children with CD.33,34

    The current clinical guidelines provided by the NASPGHN recommend screening children with failure to thrive, persistent diarrhea, recurrent abdominal pain, constipation, and vomiting for CD. Screening is currently recommended for the following extraintestinal symptoms: dermatitis herpetiformis, dental enamel hypoplasia, osteoporosis, short stature, delayed puberty, iron deficient anemia, asymptomatic children with diabetes mellitus, autoimmune thyroiditis, Down syndrome, Turner syndrome, Williams syndrome, selective IgA deficiency, and a history of first-degree relative with CD.35 If applied, these recommendations would have missed all but 6 of the asymptomatic cases (patients 2, 9, 10, 11, 16, and 22) we identified by standardized screening. Given the potential association between CD and musculoskeletal complaints that our data suggest, patients with musculoskeletal complaints may need to be given special consideration with regards to CD testing.

    For patients with a known diagnosis of rheumatic disease who have not demonstrated satisfactory clinical improvement with appropriate treatment, CD may be considered as a potential concomitant diagnosis. Furthermore, given that ≥2 of our patients with newly diagnosed CD had previously tested negative for celiac antibodies, retesting may be considered for patients who have not had a satisfactory response to medical therapy. However, it should be noted that we did not routinely screen patients who presented with preexisting rheumatologic diagnoses for CD.

    In our cohort, gender and CD were shown to not be independent by χ2 analysis (P = .036). When we adjusted for age, thyroiditis, and JIA (each of which had a statistical association with both gender and CD) by logistical regression, girls were 2.25 times more likely to be diagnosed with CD (95% confidence interval, 1.01–5.05) compared with boys (P = .048). Previous studies have reported that CD is female predominant by a female-to-male ratio of 3:1 or 2:1 in adults.36,37

    Interestingly, 23 of all 44 patients with CD were found to be ANA positive. The presence of serologic abnormalities in CD has not been comprehensively studied. The increased presence of antigliadin antibodies in patients with SLE has been considered to represent false positivity, which is consistent with the presence of false positive autoantibodies for numerous other conditions in patients with SLE.15 One study by Lerner et al38 observed that in a group of patients with CD, 23% had anti-dsDNA and 14% had anticardiolipin antibodies. However, a study by Caglar et al39 found no significant differences in the frequency of a number of anticytoplasmic and antinuclear antibodies between patients with CD and healthy controls. Additional studies are necessary to clarify the significance, if any, of these serologic abnormalities.

    Untreated CD in adults has been linked to an elevated risk of malignancy35,40–42 (although no such link has been found in children, presumably because of earlier initiation of a GFD),43 cardiovascular disease,40 and mortality.44 Prompt recognition of CD is essential to the early initiation of a GFD and the avoidance of unnecessary immunosuppressive therapies. Interestingly, 10 of our 36 patients with newly diagnosed CD reported complete resolution of their GI and non-GI symptoms upon initiating the GFD and needed no additional medications. However, we acknowledge that this improvement was self-reported by patients and was not systematically evaluated. Although there have been no studies confirming the benefit of treating asymptomatic CD in patients with other autoimmune conditions, 1 case report showed that in a patient with idiopathic hypoparathyroidism and CD, parathyroid immunoreactivity disappeared in parallel with a decrease in serum celiac antibodies during a period of gluten restriction.45 However, another report demonstrated that successful treatment of CD in patients with primary Sjögren syndrome did not relieve sicca symptoms.46 It has been calculated that the prevalence of autoimmune diseases is 5.3 per 1000 patient-years during a period of adherence to a GFD, compared with 11.3 per 1000 patient-years during nonadherence to a GFD,47 suggesting an elevated risk for additional autoimmune conditions in patients with untreated CD. This finding again underscores the importance of prompt CD screening for patients with suspected rheumatic conditions. Although it was not the intention of this study to identify the number of patients needed to test for CD to have favorable financial and clinically significant outcomes, these types of calculations have been conducted by other groups.33,48

    Finally, patients with concurrent diagnoses of JIA and CD who report clinical improvement of musculoskeletal complaints on the GFD alone raise an intriguing question: Can patients such as these really be considered to have “idiopathic” arthritis if it resolves with the treatment of the CD? Deposition of immune complexes originating from the small intestinal mucosa in other organs was proposed to explain the association between CD and a range of autoimmune diseases as early as 1975,49 but this connection has not yet been satisfactorily clarified. Our data suggest that there may be a subset of patients with “silent” CD who present with isolated musculoskeletal symptoms and that perhaps JIA is not an appropriate diagnosis in these cases. Clinicians must be vigilant in cases such as these to evaluate appropriately for CD.

    Conclusions

    Currently, the American College of Gastroenterology and NASPGHN recommendations for CD screening do not consider children with rheumatic disease to be a high-risk group, despite numerous reported associations between autoimmune diseases and CD and despite the positive effect of GFD on the development and treatment of autoimmune conditions. Among patients presenting for initial pediatric rheumatology evaluation, we found an unexpectedly high number of previously unrecognized CD cases compared with the general population (2% vs 0.7%). Furthermore, the most common presenting complaints among patients with an ultimate diagnosis of CD were musculoskeletal rather than GI. Although this finding is not surprising given that the cohort is from a pediatric rheumatology practice, where patients would be expected to present with musculoskeletal rather than GI symptoms, we discovered a surprising number of “silent” cases of CD that presented with no GI complaints at all. Because of the potential benefits of early initiation of a GFD in patients with CD, along with the dangers of unnecessary immunosuppressive therapies in unidentified celiac cases, we believe that children presenting for rheumatologic evaluation should be considered a high-risk population and screened for CD as part of the standard initial laboratory evaluation.

    Acknowledgment

    We thank Kara G. Fields, MS of the Hospital for Special Surgery Healthcare Research Institute for help with statistical analysis.

    Footnotes

      • Accepted April 17, 2015.
    • Address correspondence to Thomas J. A. Lehman, MD, Division of Pediatric Rheumatology, Hospital for Special Surgery, 535 East 70th St, New York, NY 10021. E-mail: goldscout{at}aol.com

    • Ms Sherman and Dr Karanicolas carried out the data acquisition and analysis, drafted the initial manuscript, and reviewed and revised the manuscript; Ms DiMarco carried out the data acquisition; Drs Pan, Adams, Barinstein, Moorthy, and Lehman conceptualized and designed the study, contributed to the interpretation of the data, and reviewed and revised the manuscript; and all authors approved the final manuscript as submitted.

    • FINANCIAL DISCLOSURE: The authors have indicated they have no financial relationships relevant to this article to disclose.

    • FUNDING: No external funding.

    • POTENTIAL CONFLICT OF INTEREST: The authors have indicated they have no potential conflicts of interest to disclose.

    References

    1. ↵
      1. Rubio-Tapia A,
      2. Ludvigsson JF,
      3. Brantner TL,
      4. Murray JA,
      5. Everhart JE
      . The prevalence of celiac disease in the United States. Am J Gastroenterol. 2012;107:1538–1544; quiz 7, 45
      OpenUrlCrossRefPubMed
    2. ↵
      1. Guandalini S,
      2. Assiri A
      . Celiac disease: a review. JAMA Pediatr. 2014;168(3):272–278pmid:24395055
      OpenUrlCrossRefPubMed
    3. ↵
      1. Fasano A,
      2. Berti I,
      3. Gerarduzzi T,
      4. et al
      . Prevalence of celiac disease in at-risk and not-at-risk groups in the United States: a large multicenter study. Arch Intern Med. 2003;163(3):286–292pmid:12578508
      OpenUrlCrossRefPubMed
    4. ↵
      1. Korponay-Szabó IR,
      2. Kovács JB,
      3. Czinner A,
      4. Gorácz G,
      5. Vámos A,
      6. Szabó T
      . High prevalence of silent celiac disease in preschool children screened with IgA/IgG antiendomysium antibodies. J Pediatr Gastroenterol Nutr. 1999;28(1):26–30pmid:9890464
      OpenUrlCrossRefPubMed
    5. ↵
      1. Collin P,
      2. Reunala T,
      3. Pukkala E,
      4. Laippala P,
      5. Keyriläinen O,
      6. Pasternack A
      . Coeliac disease–associated disorders and survival. Gut. 1994;35(9):1215–1218pmid:7959226
      OpenUrlAbstract/FREE Full Text
    6. ↵
      1. Bizzaro N,
      2. Villalta D,
      3. Tonutti E,
      4. Tampoia M,
      5. Bassetti D,
      6. Tozzoli R
      . Association of celiac disease with connective tissue diseases and autoimmune diseases of the digestive tract. Autoimmun Rev. 2003;2(6):358–363pmid:14550877
      OpenUrlCrossRefPubMed
    7. ↵
      1. Andersson Gäre B,
      2. Fasth A,
      3. Andersson J,
      4. et al
      . Incidence and prevalence of juvenile chronic arthritis: a population survey. Ann Rheum Dis. 1987;46(4):277–281pmid:3592782
      OpenUrlAbstract/FREE Full Text
      1. Lepore L,
      2. Martelossi S,
      3. Pennesi M,
      4. et al
      . Prevalence of celiac disease in patients with juvenile chronic arthritis. J Pediatr. 1996;129(2):311–313pmid:8765635
      OpenUrlCrossRefPubMed
      1. von Koskull S,
      2. Truckenbrodt H,
      3. Holle R,
      4. Hörmann A
      . Incidence and prevalence of juvenile arthritis in an urban population of southern Germany: a prospective study. Ann Rheum Dis. 2001;60(10):940–945pmid:11557650
      OpenUrlAbstract/FREE Full Text
    10. ↵
      1. Neuhausen SL,
      2. Steele L,
      3. Ryan S,
      4. et al
      . Co-occurrence of celiac disease and other autoimmune diseases in celiacs and their first-degree relatives. J Autoimmun. 2008;31(2):160–165pmid:18692362
      OpenUrlCrossRefPubMed
      1. Valentino R,
      2. Savastano S,
      3. Tommaselli AP,
      4. et al
      . Prevalence of coeliac disease in patients with thyroid autoimmunity. Horm Res. 1999;51(3):124–127pmid:10461017
      OpenUrlCrossRefPubMed
    12. ↵
      1. Berti I,
      2. Trevisiol C,
      3. Tommasini A,
      4. et al
      . Usefulness of screening program for celiac disease in autoimmune thyroiditis. Dig Dis Sci. 2000;45(2):403–406pmid:10711459
      OpenUrlCrossRefPubMed
    13. ↵
      1. Volta U,
      2. De Franceschi L,
      3. Molinaro N,
      4. Tetta C,
      5. Bianchi FB
      . Organ-specific autoantibodies in coeliac disease: do they represent an epiphenomenon or the expression of associated autoimmune disorders? Ital J Gastroenterol Hepatol. 1997;29(1):18–21pmid:9265573
      OpenUrlPubMed
    14. ↵
      1. Marie I,
      2. Lecomte F,
      3. Hachulla E,
      4. et al
      . An uncommon association: celiac disease and dermatomyositis in adults. Clin Exp Rheumatol. 2001;19(2):201–203pmid:11326486
      OpenUrlPubMed
    15. ↵
      1. Rensch MJ,
      2. Szyjkowski R,
      3. Shaffer RT,
      4. et al
      . The prevalence of celiac disease autoantibodies in patients with systemic lupus erythematosus. Am J Gastroenterol. 2001;96(4):1113–1115pmid:11316156
      OpenUrlCrossRefPubMed
    16. ↵
      1. Ludvigsson JF,
      2. Rubio-Tapia A,
      3. Chowdhary V,
      4. Murray JA,
      5. Simard JF
      . Increased risk of systemic lupus erythematosus in 29,000 patients with biopsy-verified celiac disease. J Rheumatol. 2012;39(10):1964–1970pmid:22859356
      OpenUrlAbstract/FREE Full Text
    17. ↵
      1. Cronin CC,
      2. Feighery A,
      3. Ferriss JB,
      4. Liddy C,
      5. Shanahan F,
      6. Feighery C
      . High prevalence of celiac disease among patients with insulin-dependent (type I) diabetes mellitus. Am J Gastroenterol. 1997;92(12):2210–2212pmid:9399754
      OpenUrlPubMed
      1. Gillett PM,
      2. Gillett HR,
      3. Israel DM,
      4. et al
      . High prevalence of celiac disease in patients with type 1 diabetes detected by antibodies to endomysium and tissue transglutaminase. Can J Gastroenterol. 2001;15(5):297–301pmid:11381296
      OpenUrlPubMed
      1. Koletzko S,
      2. Bürgin-Wolff A,
      3. Koletzko B,
      4. et al
      . Prevalence of coeliac disease in diabetic children and adolescents. A multicentre study. Eur J Pediatr. 1988;148(2):113–117pmid:3069470
      OpenUrlCrossRefPubMed
      1. Jaeger C,
      2. Hatziagelaki E,
      3. Petzoldt R,
      4. Bretzel RG
      . Comparative analysis of organ-specific autoantibodies and celiac disease–associated antibodies in type 1 diabetic patients, their first-degree relatives, and healthy control subjects. Diabetes Care. 2001;24(1):27–32pmid:11194235
      OpenUrlAbstract/FREE Full Text
      1. Holmes GK
      . Screening for coeliac disease in type 1 diabetes. Arch Dis Child. 2002;87(6):495–498pmid:12456547
      OpenUrlAbstract/FREE Full Text
    22. ↵
      1. Simmons JH,
      2. Klingensmith GJ,
      3. McFann K,
      4. et al.
      Celiac autoimmunity in children with type 1 diabetes: a two-year follow-up. J Pediatr. 2011;158:276–281, e1
      OpenUrlCrossRefPubMed
    23. ↵
      1. Iltanen S,
      2. Collin P,
      3. Korpela M,
      4. et al
      . Celiac disease and markers of celiac disease latency in patients with primary Sjögren’s syndrome. Am J Gastroenterol. 1999;94(4):1042–1046pmid:10201480
      OpenUrlPubMed
    24. ↵
      1. Brow JR,
      2. Parker F,
      3. Weinstein WM,
      4. Rubin CE
      . The small intestinal mucosa in dermatitis herpetiformis. I. Severity and distribution of the small intestinal lesion and associated malabsorption. Gastroenterology. 1971;60(3):355–361pmid:5554077
      OpenUrlPubMed
    25. ↵
      1. Dalton TA,
      2. Bennett JC
      . Autoimmune disease and the major histocompatibility complex: therapeutic implications. Am J Med. 1992;92(2):183–188pmid:1543203
      OpenUrlCrossRefPubMed
    26. ↵
      1. Gheita TA,
      2. Fawzy SM,
      3. Nour El-Din AM,
      4. Gomaa HE
      . Asymptomatic celiac sprue in juvenile rheumatic diseases children. Int J Rheum Dis. 2012;15(2):220–226pmid:22212536
      OpenUrlCrossRefPubMed
    27. ↵
      1. Ventura A,
      2. Magazzù G,
      3. Greco L,
      4. SIGEP Study Group for Autoimmune Disorders in Celiac Disease
      . Duration of exposure to gluten and risk for autoimmune disorders in patients with celiac disease. Gastroenterology. 1999;117(2):297–303pmid:10419909
      OpenUrlCrossRefPubMed
    28. ↵
      1. Sategna Guidetti C,
      2. Solerio E,
      3. Scaglione N,
      4. Aimo G,
      5. Mengozzi G
      . Duration of gluten exposure in adult coeliac disease does not correlate with the risk for autoimmune disorders. Gut. 2001;49(4):502–505pmid:11559646
      OpenUrlAbstract/FREE Full Text
    29. ↵
      1. Rubio-Tapia A,
      2. Hill ID,
      3. Kelly CP,
      4. Calderwood AH,
      5. Murray JA,
      6. American College of Gastroenterology
      . ACG clinical guidelines: diagnosis and management of celiac disease. Am J Gastroenterol. 2013;108(5):656–676, quiz 677pmid:23609613
      OpenUrlCrossRefPubMed
    30. ↵
      1. Hill ID,
      2. Dirks MH,
      3. Liptak GS,
      4. et al.,
      5. North American Society for Pediatric Gastroenterology, Hepatology and Nutrition
      . Guideline for the diagnosis and treatment of celiac disease in children: recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. J Pediatr Gastroenterol Nutr. 2005;40(1):1–19pmid:15625418
      OpenUrlCrossRefPubMed
    31. ↵
      1. Hill ID
      . What are the sensitivity and specificity of serologic tests for celiac disease? Do sensitivity and specificity vary in different populations? Gastroenterology. 2005;128(4 suppl 1):S25–S32pmid:15825123
      OpenUrlCrossRefPubMed
    32. ↵
      1. Petty RE,
      2. Southwood TR,
      3. Baum J,
      4. et al
      . Revision of the proposed classification criteria for juvenile idiopathic arthritis: Durban, 1997. J Rheumatol. 1998;25(10):1991–1994pmid:9779856
      OpenUrlPubMed
    33. ↵
      1. Rosén A,
      2. Sandström O,
      3. Carlsson A,
      4. et al
      . Usefulness of symptoms to screen for celiac disease. Pediatrics. 2014;133(2):211–218pmid:24420802
      OpenUrlAbstract/FREE Full Text
    34. ↵
      1. Agardh D,
      2. Lee HS,
      3. Kurppa K,
      4. et al.,
      5. TEDDY Study Group
      . Clinical features of celiac disease: a prospective birth cohort. Pediatrics. 2015;135(4):627–634pmid:25733751
      OpenUrlAbstract/FREE Full Text
    35. ↵
      1. Holmes GK,
      2. Prior P,
      3. Lane MR,
      4. Pope D,
      5. Allan RN
      . Malignancy in coeliac disease: effect of a gluten free diet. Gut. 1989;30(3):333–338pmid:2707633
      OpenUrlAbstract/FREE Full Text
    36. ↵
      American Gastroenterological Association medical position statement: celiac sprue. Gastroenterology. 2001;120(6):1522–1525pmid:11313323
      OpenUrlCrossRefPubMed
    37. ↵
      1. Ciacci C,
      2. Cirillo M,
      3. Sollazzo R,
      4. Savino G,
      5. Sabbatini F,
      6. Mazzacca G
      . Gender and clinical presentation in adult celiac disease. Scand J Gastroenterol. 1995;30(11):1077–1081pmid:8578167
      OpenUrlCrossRefPubMed
    38. ↵
      1. Lerner A,
      2. Blank M,
      3. Lahat N,
      4. Shoenfeld Y
      . Increased prevalence of autoantibodies in celiac disease. Dig Dis Sci. 1998;43(4):723–726pmid:9558026
      OpenUrlCrossRefPubMed
    39. ↵
      1. Caglar E,
      2. Ugurlu S,
      3. Ozenoglu A,
      4. Can G,
      5. Kadioglu P,
      6. Dobrucali A
      . Autoantibody frequency in celiac disease. Clinics (Sao Paulo). 2009;64(12):1195–1200pmid:20037707
      OpenUrlCrossRefPubMed
    40. ↵
      1. Ludvigsson JF
      . Mortality and malignancy in celiac disease. Gastrointest Endosc Clin N Am. 2012;22(4):705–722pmid:23083988
      OpenUrlCrossRefPubMed
      1. Corrao G,
      2. Corazza GR,
      3. Bagnardi V,
      4. et al.,
      5. Club del Tenue Study Group
      . Mortality in patients with coeliac disease and their relatives: a cohort study. Lancet. 2001;358(9279):356–361pmid:11502314
      OpenUrlCrossRefPubMed
    42. ↵
      1. Logan RF,
      2. Rifkind EA,
      3. Turner ID,
      4. Ferguson A
      . Mortality in celiac disease. Gastroenterology. 1989;97(2):265–271pmid:2744350
      OpenUrlPubMed
    43. ↵
      1. Askling J,
      2. Linet M,
      3. Gridley G,
      4. Halstensen TS,
      5. Ekström K,
      6. Ekbom A
      . Cancer incidence in a population-based cohort of individuals hospitalized with celiac disease or dermatitis herpetiformis. Gastroenterology. 2002;123(5):1428–1435pmid:12404215
      OpenUrlCrossRefPubMed
    44. ↵
      1. Solaymani-Dodaran M,
      2. West J,
      3. Logan RF
      . Long-term mortality in people with celiac disease diagnosed in childhood compared with adulthood: a population-based cohort study. Am J Gastroenterol. 2007;102(4):864–870pmid:17324126
      OpenUrlCrossRefPubMed
    45. ↵
      1. Wortsman J,
      2. Kumar V
      . Case report: idiopathic hypoparathyroidism co-existing with celiac disease: immunologic studies. Am J Med Sci. 1994;307(6):420–427pmid:8198149
      OpenUrlCrossRefPubMed
    46. ↵
      1. Alvarez-Celorio MD,
      2. Angeles-Angeles A,
      3. Kraus A
      . Primary Sjögren’s syndrome and celiac disease: causal association or serendipity? J Clin Rheumatol. 2000;6(4):194–197pmid:19078470
      OpenUrlCrossRefPubMed
    47. ↵
      1. Cosnes J,
      2. Cellier C,
      3. Viola S,
      4. et al.,
      5. Groupe d’Etude et de Recherche sur la Maladie Coeliaque
      . Incidence of autoimmune diseases in celiac disease: protective effect of the gluten-free diet. Clin Gastroenterol Hepatol. 2008;6(7):753–758pmid:18255352
      OpenUrlCrossRefPubMed
    48. ↵
      1. Shamir R,
      2. Hernell O,
      3. Leshno M
      . Cost-effectiveness analysis of screening for celiac disease in the adult population. Med Decis Making. 2006;26(3):282–293pmid:16751327
      OpenUrlAbstract/FREE Full Text
    49. ↵
      1. Scott BB,
      2. Losowsky MS
      . Coeliac disease: a cause of various associated diseases? Lancet. 1975;2(7942):956–957pmid:53436
      OpenUrlPubMed
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    Pediatrics
    Vol. 136, Issue 1
    1 Jul 2015
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    Unrecognized Celiac Disease in Children Presenting for Rheumatology Evaluation
    Yekaterina Sherman, Rose Karanicolas, Brittany DiMarco, Nancy Pan, Alexa B. Adams, Laura V. Barinstein, L. Nandini Moorthy, Thomas J. A. Lehman
    Pediatrics Jul 2015, 136 (1) e68-e75; DOI: 10.1542/peds.2014-2379
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