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Screening for coeliac disease in adult patients with type 1 diabetes mellitus: myths, facts and controversy
Diabetology & Metabolic Syndrome volume 8, Article number: 51 (2016)
This review aims at summarizing the present knowledge on the clinical consequences of concomitant coeliac disease (CD) in adult patients with type 1 diabetes mellitus (T1DM). The cause of the increased prevalence of CD in T1DM patients is a combination of genetic and environmental factors. Current screening guidelines for CD in adult T1DM patients are not uniform. Based on the current evidence of effects of CD on bone mineral density, diabetic complications, quality of life, morbidity and mortality in patients with T1DM, we advise periodic screening for CD in adult T1DM patients to prevent delay in CD diagnosis and subsequent CD and/or T1DM related complications.
Coeliac disease (CD) is a permanent intolerance to ingested gluten resulting in immune mediated inflammatory damage to the small intestinal mucosa and a subsequent malabsorption syndrome . Diagnosis of CD requires duodenal biopsy when the patient is on a gluten-containing diet and for the vast majority of adult patients also positive serology . CD is one of the commonest lifelong disorders encountered in Western countries with a prevalence of about 0.6 % in the general population  and is, in particular in genetically susceptible individuals, associated with other autoimmune disorders including type 1 diabetes mellitus (T1DM) and autoimmune thyroiditis . T1DM is characterized by T-cell mediated destruction of the insulin-producing β-cells in the pancreas leading to hyperglycaemia and diabetic ketoacidosis . Diabetes is diagnosed based on 1) plasma glucose criteria, either the fasting plasma glucose (FPG) or the 2-h plasma glucose (2-h PG) value after a 75-g oral glucose tolerance test (OGTT) or 2) on a glycated haemoglobin (HbA1c) value of >6.5 % . Long term diabetic complications consist of micro- and macrovascular disease, which account for the major morbidity and mortality associated with T1DM . Up to one-third of patients with T1DM have thyroid antibodies, and half of these patients may progress to clinical autoimmune thyroid disease . The need for annual screening for thyroid disease in T1DM patients has therefore been recommended.
The over all prevalence of CD in T1DM patients is about 6 % . The association between CD and T1DM was first noted over 40 years ago in children . Therefore, screening in paediatric T1DM patients is advocated. However, international paediatric consensus based guidelines differ in the need and frequency of screening for CD . Some recommend an annual screening interval by testing antibodies against tissue transglutaminase 2 (TG2A), others advice to perform these tests in the presence of typical CD symptoms only . However, despite the high prevalence of CD in T1DM patients there is no consensus on screening adult T1DM patients for CD.
In this review it is discussed whether screening for CD should be performed in adult T1DM patients and at which interval. For this purpose, the current literature was screened with respect to the clinical features of patients with both diseases as compared to patients with T1DM alone.
Association between CD and T1DM
T1DM and CD are auto-immune, inflammatory diseases for which the major genetic contribution arises from the major histocompatibility complex . These so-called HLA-DQ heterodimers enable the presentation of peptides that are derived from otherwise innocuous self- or non-self antigens (proteins from insulin producing beta cells in T1DM, gliadins in CD) and activate pathogenic effector T-cells . Besides the genetic overlap in the major histocompatibility complex, genome wide association studies (GWAS) in these two diseases have revealed a large number of well validated, non-HLA genetic risk loci providing an opportunity to explore the possibility of overlapping susceptibility between them .
Thus, genetic overlap exists between CD and T1DM consisting of both HLA and non-HLA genes [14–16]. Both disorders are associated with the major histocompatibility complex (MHC) class 2 antigen DQ encoded by the alleles DQA1*05 with DQB1*02 (DQ2.5) and DQA1*03 with DQB1*03:02 (DQ8) [1, 17].
In patients with CD, individuals who are HLA-DQ 2.5 homozygous have a greater risk of developing CD and the gluten specific T-cell response is more vigorous when gluten peptides are presented by antigen presenting cells homozygous for HLA-DQ 2.5 [18, 19]. In European Caucasian populations, more than 90 % of CD patients carry the HLA-DQ 2.5 heterodimer and the majority of CD patients who do not carry this HLA-DQ 2.5 heterodimer are HLA-DQ8 or HLA-DQ2.2 positive .
The main determinant of risk of developing T1DM is HLA-DQ8 and to a lesser extent HLA-DQ 2.5 [21, 22]. In a recent study, we compared the frequency of HLA-DQ haplotypes between 2472 T1DM patients versus 483 T1DM + CD patients . In patients with T1DM, the HLA-DQ 2.5 haplotype showed a significant association and provided the highest risk for developing double autoimmunity (OR = 1.44, p-value = 0.0003, Table 1). As expected, the absence of the haplotypes HLA-DQ 2.5, DQ8 and DQ 2.2 (which is classified as “other” which is present in about 25 % of T1DM patients), showed the strongest protection (OR = 0.66, p = 0.0001, Table 1). Therefore, an HLA-DQ 2.5 negative T1DM patient does not require monitoring for CD.
In addition to the overlap between T1DM and CD in HLA genes, it was revealed that non-HLA genes overlap as well [12, 16]. CTLA-4 and IL2RA loci are more strongly associated with double autoimmunity than with either T1DM or CD alone . The combination of HLA and non-HLA variants might improve risk prediction for potential CD .
Several environmental factors have been investigated as precipitating factors for the development of T1DM or CD. A popular theory, based on possible molecular mimicry, is the association between autoimmune diseases and viral infections. Prime viral candidates that have been shown to cause precipitation to T1DM are enteroviruses, more specifically Coxsackie viruses . Moreover, rotavirus infection increases the risk for developing T1DM and an association between rotavirus and increased risk for CD has been described as well [25, 26]. Furthermore, an altered composition of bacteria in the gut, altered gut permeability and intestinal inflammation seem to be factors that contribute to the development of T1DM . Exposure to cereals has been described as a risk factor for the development of both T1DM and CD related autoantibodies. However, these studies show conflicting results [28–30].
Many studies have investigated the prevalence of CD in paediatric and adult T1DM patients by different serological screening methods (gliadin, anti endomysium (EMA), anti tissue transglutaminase (TG2A) and anti reticulin antibodies). The prevalence of CD in T1DM patients (children and/or adults) is reported to vary between 0.8 % and 16.4 % with a mean prevalence of 6 % [4, 9, 31]. A large meta-analysis identified 27 studies, which included in total 26 605 individuals with T1DM . Seventeen studies were performed in Europe, 4 in North America, 1 in South America, 1 in Australia, 3 in the Middle East and 1 in India (Fig. 1) . A remarkable high prevalence of CD in T1DM patients is seen in studies performed in Algeria (16.4 %), India (11.1 %) and Saudi Arabia (11.3 %) [32–34]. The relatively high frequency of HLA-DQ 2.5 in the Middle East and India possibly contributes to the high prevalence of CD in T1DM . Furthermore, these countries have a per capita wheat consumption that ranks among the highest in the world . This high prevalence still needs to be confirmed in additional studies. Data from East-Asian and African T1DM cohorts and CD screening are lacking in current literature.
The clinical presentation of CD in T1DM patients resembles that in non-T1DM patients and consists of gastrointestinal complaints (diarrhoea, constipation, vomiting, abdominal distension, anorexia) or extra-intestinal complaints such as growth failure, anaemia, decreased bone mass or osteoporosis, and dental enamel defects . However, CD patients might also be asymptomatic and may have subtle complaints indicative of CD and may only be recognized in retrospect following the benefits of a GFD . Previous studies have reported that 45–60 % of patients with T1DM and CD did not have any complaints of CD indicating a diagnostic challenge [37, 38].
Furthermore, gastrointestinal complaints are common in T1DM patients and a broad differential diagnosis exists for these patients (Table 2) [39, 40]. Furthermore, the fact that a large part of patients presents only with mild symptoms or seem to be asymptomatic provides difficulties for detecting CD . Often, a reduced health is only recognized retrospectively, following the benefits conferred to a GFD .
It has been demonstrated that the risk of CD in T1DM patients is associated with age of onset of T1DM. Children with age of onset of T1DM younger than 4 years are at higher risk to develop CD than those with older age of onset . Regarding clinical practice, we observed two peaks in the age of CD diagnosis in T1DM patients: around 10 and 45 years of age . T1DM diagnosis precedes CD diagnosis in about 90 % of patients and females with T1DM have a higher risk of the additional diagnosis of CD than males [41, 42].
A new syndrome of gluten intolerance, non coeliac gluten sensitivity (NCGS), has been described. NCGS can be diagnosed in those patients with gluten intolerance who do not develop antibodies that are typical neither of CD nor of wheat allergy and who do not suffer from lesions in the duodenal mucosa . Although disease characteristics of NCGS are overlapping with irritable bowel syndrome (IBS), a recent study observed that an associated autoimmune disease was present in 14 % of patients with NCGS, which was mainly autoimmune thyroiditis and sporadically T1DM .
Adherence to a GFD
In T1DM, dietary interventions aim to maintain blood glucose, blood pressure, lipid levels and body mass index in the normal range . A GFD together with an insulin therapy integrated into an individual’s dietary and physical activity pattern imposes practical limitations and leads to restrictions in the lifestyle of a child or adolescent. Therefore, it may not be surprising that non adherence to a GFD in T1DM patients with CD is more common than in CD patients [47, 48]. Another problem that arises is the availability of gluten free food. In 5 different US states it was found to be significantly less available than food containing gluten . The increased cost of GFD products may have an impact on compliance in T1DM patients with CD as well . Therefore, we advise that patients with both conditions are guided by a skilled dietitian.
Clinical consequences of CD in adult patients with T1DM
So far, studies addressing the consequences of CD in adult T1DM patients differ in methodology, study size and prospective/retrospective design. Therefore, these results are difficult to compare and interpret. An overview of these results is given in Table 3.
In adult patients with T1DM, no significant change of HbA1c levels was found, when comparing before CD diagnosis, at CD diagnosis and after treatment of CD by a GFD [50, 51]. This data is confirmed in a recent population based cohort study which found that having a diagnosis of CD does not influence the risk of hospital admission due to hypoglycaemia, keto-acidosis or coma in T1DM patients .
Undetected CD in the general population is associated with lower cholesterol levels, which is thought to contribute to a favourable cardiovascular risk profile in untreated CD patients . Accordingly, lower levels of cholesterol and triglycerides were found in newly detected, untreated CD patients with T1DM . The assumed mechanism that may contribute to the lower cholesterol levels in undetected CD patients is malabsorption.
Intensive insulin therapy to normalize blood glucose levels effectively delays the onset and slows the progression of microvascular complications including diabetic retinopathy, nephropathy and neuropathy in T1DM patients [55–57]. Several studies investigated the influence of (newly diagnosed) CD with or without treatment by a GFD on long term diabetic complications and found CD to be either protective [51, 54, 58] or aggravating [59–61]. A recent large nationwide study in Sweden revealed that the duration of CD is important for the eventual effect . They showed that individuals with T1DM and CD were at a lower risk of diabetic retinopathy in the first 5 years after CD diagnosis (adjusted hazard ratio (HR) 0.57 [95 % CI 0.36–0.91]), followed by a neutral risk in years 5 to <10 years (1.03 [0.68–1.57]). With longer follow-up, coexisting CD was a risk factor for diabetic retinopathy (10 to <15 years of follow-up, adjusted HR 2.83 [95 % CI 1.95–4.11]; ≥15 years of follow-up, 3.01 [1.43–6.32]) . They ascribe the protective effect in the first 5 years to lower cholesterol levels and lower body mass index (BMI). However, this study lacks individual-based information on GFD adherence.
In a study of our group we found less diabetic retinopathy in a T1DM population with a mean CD duration of 3 years+ treatment by GFD compared to T1DM patients without CD . Also, a previous study by Pitocco et al. showed more subclinical atherosclerosis in T1DM patients with a mean duration of treated CD of 9.9 years . These studies suggest that a short duration of CD is protective and a longer duration of CD may aggravate diabetic complications [51, 60].
CD is associated with a higher risk of end-stage renal disease (ESRD) with a Hazard Ratio (HR) for ESRD of 2.87 (95 % CI 2.22 to 3.71, p < 0.001) . The cumulative prevalence of end-stage renal disease in T1DM patients without CD, is 2.2 % at 20 years and 7.7 % at 30 years . Interestingly, in T1DM patients with CD it was found that non-adherence to a GFD was associated with early elevation of albumin excretion in urine, a recognized factor for diabetic nephropathy . Skovbjerg et al. found that there was a higher prevalence of CD in T1DM patients with nephropathy (2.6 %) than in T1DM patients without nephropathy (1 %) . A recent study found a positive association between longstanding CD in T1DM patients and chronic renal disease in T1DM . For chronic renal disease, this excess risk was present after more than 10 years of CD (HR 2.03, 95 % CI 1.08, 3.79) . However, data about GFD adherence was lacking. These studies suggest that concomitant CD in T1DM patients might lead to more nephropathy in case of longstanding CD, in particular in case of poor adherence to a GFD . The underlying mechanisms need, however, to be elucidated.
Bone mineral density
Decreased bone mineral density (BMD) is observed both in T1DM patients  and in CD patients . In the latter group of patients, this is especially related to the intestinal malabsorption of vitamin D, necessary for healthy bone metabolism . Reports have shown that bone mineral density is lower in paediatric T1DM patients with undiagnosed CD than in T1DM patients without CD [69, 70]. As expected, also in adults with both T1DM and active CD, a decreased BMD was found, but whether CD or T1DM was the cause remains unclear . A study by Sategna-Guidetti showed that treatment by a GFD results in an improvement of lumbar spine BMD in adults with CD .
In summary, BMD in T1DM + CD patients is generally decreased and follow-up of BMD with possible treatment is warranted. Besides maintaining a GFD, data is scarce whether calcium and vitamin D supplementation in CD patients is mandatory . Lifestyle changes as regular exercise and smoking cessation should be advised, and in the case of osteoporosis, calcium, vitamin D and bisphosphonates should be prescribed .
Quality of life
Both T1DM and CD are chronic illnesses which influence the quality of life (QOL) since the treatments are burdensome and the complications can be debilitating and life threatening. T1DM patients have a diminished QOL which is partly caused by the development of vascular complications . The lower QOL in CD patients is reported especially in the social aspects of life and in those with symptoms, women being mostly affected . In adult T1DM patients with both T1DM and treated CD, we described a compromised QOL particularly in women and both social functioning and general health perception was affected . This is of importance since patients with T1DM are at increased risk of depression . The additional diagnosis of CD further increases the risk of depression, and this should be taken into account in the clinical support of these patients .
Comorbidity and mortality
T1DM is, beside CD, associated with autoimmune thyroid diseases (Hashimoto’s or Graves’ disease) (AIT), autoimmune gastritis, Addison’s disease, and vitiligo . The presence of a third autoimmune disease in T1DM + CD patients is frequently found. A study by Kaspers et al. found a higher incidence of AIT in patients with T1DM and CD (6.3 %) when compared to those with CD alone (2.3 %) . Our clinical practice study in adults revealed that 28 % of T1DM + CD patients were diagnosed with a third autoimmune disease, mainly autoimmune thyroiditis (22 %) .
A small group of patients with CD fail to improve clinically and histologically upon elimination of dietary gluten and this complication is referred to as refractory coeliac disease (RCD) . RCD imposes a serious risk of developing enteropathy-associated T-cell lymphoma (EATL). The prevalence of RCD and EATL in the general population is very rare and studies investigating the risk of developing RCD or malignancy in T1DM + CD patients are currently lacking .
The question whether CD influences the mortality in T1DM patients was recently investigated in Sweden . These authors described that having a CD diagnosis for more than 15 years was associated with a 2.8-fold increased risk of death in individuals with T1DM . They hypothesized that the excess mortality was caused by persistent low grade inflammation due to CD or poor adherence to a GFD while using insulin therapy.
Rationale for screening for CD in adult T1DM patients
CD fulfills many of the WHO criteria for screening in patients with T1DM but not all of them . CD is common and well defined, screening tests are simple + safe + accurate, screening seems to be culturally acceptable, treatment is available and clinical detection of CD can be difficult. However, studies are lacking whether screening for CD in T1DM patients is cost effective and it is currently unknown whether screen detected asymptomatic CD patients benefit from starting with a GFD. The latter will be investigated by the CD-DIET study  which is designed as a prospective controlled trial in which asymptomatic screen detected CD patients will be treated with or without a GFD. The results of the efficacy and safety of a GFD in patients with T1DM with asymptomatic CD will add significant data to the discussion about screening for CD in T1DM patients .
Consequently, there is still no consensus on screening adult patients with T1DM for CD. International guidelines for adult CD and T1DM differ in their recommendations for screening of CD in T1DM patients [2, 6, 85–91] (Table 4). At present, a case-finding approach in adult T1DM patients is most acceptable, ethically and financially [2, 92]. However, a recent study in the United States and Canada underscores the need for an uniform screening program. This study revealed a high variability in testing for CD in T1DM patients together with an inconsistency of management of CD . In addition, we have recently reported that approximately 20 % of patients with T1DM and CD reported to have had CD related complaints for at least 5 years before CD diagnosis was made . The long term consequences of a diagnostic delay are currently unknown. The high prevalence of several complications as reported in Table 3 in T1DM + CD patients, together with improvement of BMD after start of a GFD provides a strong rationale for an uniform screening program together with careful monitoring. Further, a recent randomized study showed that screen-detected and apparently asymptomatic EmA-positive patients at risk for CD benefit from a GFD as measured by extensive clinical, serologic, and histologic parameters . Hypothetically, this data might be extrapolated to asymptomatic CD in T1DM patients. Another argument for screening is the fact that the incidence of T1DM and CD is rising over time [95, 96].
We propose the following screening algorithm (Fig. 2) for CD in adult T1DM patients. CD should be diagnosed by serology and duodenal biopsy with the patient on a gluten-containing diet . Serology is by TG2A and if patients are IgA deficient, IgG-TG2A can be used. Villous atrophy (Marsh IIIa- IIIc) is required for diagnosis of CD . Due to the high sensitivity and specificity of TG2A, this test is used for screening in T1DM patients . In case of IgA deficient individuals, or in patients with high probability of CD, IgG TG2A should be tested as 2 % of CD patients are IgA deficient . As T1DM patients might have transient elevations of TG2A, a confirmatory small intestinal biopsy is recommended [98, 99]. In case of a biopsy with Marsh I-II, a serological repetition in 5 year is recommended. Further, another differential diagnosis for intraepithelial lymphocytosis should be considered (e.g. Giardia, olmesartan induced, small intestinal bacterial overgrowth). So far, only retrospective data is available and prospective studies are needed to determine a screening interval for CD in T1DM patients. As proposed by DeMelo et al. , we suggest to repeat TG2A testing every 5 years in case of negative serology. A recent systematic review found that most cases of CD are diagnosed within 5 years of T1D diagnosis and they advise screening at T1D diagnosis and within 2 and 5 years thereafter . Only the Australian Diabetes Society recommends screening for CD after 5 years of T1DM diagnosis (Table 4). As studies are lacking investigating the screening frequency in T1DM patients, we advocate continuing screening every 5 years for CD in T1DM patients. In the presence of CD a clinical work-up should be performed to evaluate and possibly treat bone mineral density and vitamin deficiencies (Fig. 2). Based on current data, this screening algorithm is not applicable to all countries as studies about prevalence of CD in T1DM patients are lacking from several countries (Fig. 1).
The European Society for Paediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) guidelines recommend assessing the HLA-DQ2.5/DQ8 genotype in patients with T1DM, as an initial approach for CD screening. A recent study investigated the clinical relevance and cost-effectiveness of human leukocyte antigen (HLA)-genotyping in T1DM patients as a screening tool . They found that HLA-DQ typing in T1DM patients is neither distinctive nor cost-effective in screening for CD . This might be due to the fact that only 25 % of T1DM patients is HLA-DQ 2.5 or DQ 8 negative [14, 16]. Thus, in our algorithm HLA-DQ typing is excluded.
According to recent guidelines for symptomatic children who have high antibody titres, a duodenal biopsy is not needed anymore for diagnosing CD . Indeed, a recent study showed that none of the T1DM children with high TG2A titres would have needed a biopsy for diagnosis . Whether this is also the case in symptomatic adult T1DM patients with high TG2A titres remains to be established.
CD fulfills many of the WHO criteria for screening as it is common, simple to diagnose, and treatment is available. Detection of CD in T1DM patients is important as morbidity and mortality is increased in patients with both T1DM and CD. Furthermore, several clinical consequences are present in both disorders as decreased BMD, nephropathy, retinopathy and decreased QOL which need careful follow-up. We propose an algorithm for periodic screening and advise a multidisciplinary approach for these complex patients.
autoimmune thyroid diseases
body mass index
bone mineral density
dual X-ray absorptiometry
enteropathy-associated T cell lymphoma
European Society for Paediatric Gastroenterology, Hepatology and Nutrition
end-stage renal disease
fasting plasma glucose
genome wide association studies
irritable bowel syndrome
non coeliac gluten sensitivity
oral glucose tolerance test
quality of life
refractory coeliac disease
tissue transglutaminase 2
type 1 diabetes mellitus
World Health Organization
Abadie V, Sollid LM, Barreiro LB, Jabri B. Integration of genetic and immunological insights into a model of celiac disease pathogenesis. Annu Rev Immunol. 2011;29:493–525.
Ludvigsson JF, Bai JC, Biagi F, et al. Diagnosis and management of adult coeliac disease: guidelines from the British Society of Gastroenterology. Gut. 2014;63:1210–28.
Biagi F, Klersy C, Balduzzi D, Corazza GR. Are we not over-estimating the prevalence of coeliac disease in the general population? Ann Med. 2010;42:557–61.
Holmes GK. Coeliac disease and type 1 diabetes mellitus—the case for screening. Diabet Med. 2001;18:169–77.
van Belle TL, Coppieters KT, von Herrath MG. Type 1 diabetes: etiology, immunology, and therapeutic strategies. Physiol Rev. 2011;91:79–118.
American Diabetes Association. Standards of medical care in diabetes–2014. Diabetes Care. 2014;37 (Suppl 1):S14–S80.
Daneman D. Type 1 diabetes. Lancet. 2006;367:847–58.
Van den Driessche A, Eenkhoorn V, Van GL, De BC. Type 1 diabetes and autoimmune polyglandular syndrome: a clinical review. Neth J Med. 2009;67:376–87.
Elfstrom P, Sundstrom J, Ludvigsson JF. Systematic review with meta-analysis: associations between coeliac disease and type 1 diabetes. Aliment Pharmacol Ther. 2014;40:1123–32.
Walker-Smith JA, Vines R, Grigor W. Coeliac disease and diabetes. Lancet. 1969;2:650.
Sud S, Marcon M, Assor E, Palmert MR, Daneman D, Mahmud FH. Celiac disease and pediatric type 1 diabetes: diagnostic and treatment dilemmas. Int J Pediatr Endocrinol. 2010;2010:161285.
Smyth DJ, Plagnol V, Walker NM, et al. Shared and distinct genetic variants in type 1 diabetes and celiac disease. N Engl J Med. 2008;359:2767–77.
Busch R, De RA, Hadjinicolaou AV, Jiang W, Hou T, Mellins ED. On the perils of poor editing: regulation of peptide loading by HLA-DQ and H2-A molecules associated with celiac disease and type 1 diabetes. Expert Rev Mol Med. 2012;14:e15.
Sumnik Z, Cinek O, Bratanic N, et al. Risk of celiac disease in children with type 1 diabetes is modified by positivity for HLA-DQB1*02-DQA1*05 and TNF -308A. Diabetes Care. 2006;29:858–63.
Larizza D, Calcaterra V, Klersy C, et al. Common immunogenetic profile in children with multiple autoimmune diseases: the signature of HLA-DQ pleiotropic genes. Autoimmunity. 2012;45:470–5.
Gutierrez-Achury J, Romanos J, Bakker SF, et al. Contrasting the genetic background of type 1 diabetes and celiac disease autoimmunity. Diabetes Care. 2015;38(Suppl 2):S37–44.
Polychronakos C, Li Q. Understanding type 1 diabetes through genetics: advances and prospects. Nat Rev Genet. 2011;12:781–92.
Mearin ML, Biemond I, Pena AS, et al. HLA-DR phenotypes in Spanish coeliac children: their contribution to the understanding of the genetics of the disease. Gut. 1983;24:532–7.
Vader W, Stepniak D, Kooy Y, et al. The HLA-DQ2 gene dose effect in celiac disease is directly related to the magnitude and breadth of gluten-specific T cell responses. Proc Natl Acad Sci USA. 2003;100:12390–5.
Karell K, Louka AS, Moodie SJ, et al. HLA types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac Disease. Hum Immunol. 2003;64:469–77.
Koeleman BP, Lie BA, Undlien DE, et al. Genotype effects and epistasis in type 1 diabetes and HLA-DQ trans dimer associations with disease. Genes Immun. 2004;5:381–8.
Thomson G, Valdes AM, Noble JA, et al. Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: a meta-analysis. Tissue Antigens. 2007;70:110–27.
Romanos J, Rosen A, Kumar V, et al. Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants. Gut. 2014;63:415–22.
Filippi CM, von Herrath MG. Viral trigger for type 1 diabetes: pros and cons. Diabetes. 2008;57:2863–71.
Honeyman MC, Coulson BS, Stone NL, et al. Association between rotavirus infection and pancreatic islet autoimmunity in children at risk of developing type 1 diabetes. Diabetes. 2000;49:1319–24.
Stene LC, Honeyman MC, Hoffenberg EJ, et al. Rotavirus infection frequency and risk of celiac disease autoimmunity in early childhood: a longitudinal study. Am J Gastroenterol. 2006;101:2333–40.
Vaarala O, Atkinson MA, Neu J. The “perfect storm” for type 1 diabetes: the complex interplay between intestinal microbiota, gut permeability, and mucosal immunity. Diabetes. 2008;57:2555–62.
Norris JM, Barriga K, Hoffenberg EJ, et al. Risk of celiac disease autoimmunity and timing of gluten introduction in the diet of infants at increased risk of disease. JAMA. 2005;293:2343–51.
Vriezinga SL, Auricchio R, Bravi E, et al. Randomized feeding intervention in infants at high risk for celiac disease. N Engl J Med. 2014;371:1304–15.
Ziegler AG, Schmid S, Huber D, Hummel M, Bonifacio E. Early infant feeding and risk of developing type 1 diabetes-associated autoantibodies. JAMA. 2003;290:1721–8.
Volta U, Tovoli F, Caio G. Clinical and immunological features of celiac disease in patients with type 1 diabetes mellitus. Expert Rev Gastroenterol Hepatol. 2011;5:479–87.
Al-Hussaini A, Sulaiman N, Al-Zahrani M, Alenizi A, Haj I. High prevalence of celiac disease among Saudi children with type 1 diabetes: a prospective cross-sectional study. BMC Gastroenterol. 2012;12:180.
Bhadada SK, Kochhar R, Bhansali A, et al. Prevalence and clinical profile of celiac disease in type 1 diabetes mellitus in north India. J Gastroenterol Hepatol. 2011;26:378–81.
Boudraa G, Hachelaf W, Benbouabdellah M, Belkadi M, Benmansour FZ, Touhami M. Prevalence of coeliac disease in diabetic children and their first- degree relatives in west Algeria: screening with serological markers. Acta Paediatr Suppl. 1996;412:58–60.
Cummins AG, Roberts-Thomson IC. Prevalence of celiac disease in the Asia-Pacific region. J Gastroenterol Hepatol. 2009;24:1347–51.
Holmes GK. Screening for coeliac disease in type 1 diabetes. Arch Dis Child. 2002;87:495–8.
Mahmud FH, Murray JA, Kudva YC, et al. Celiac disease in type 1 diabetes mellitus in a North American community: prevalence, serologic screening, and clinical features. Mayo Clin Proc. 2005;80:1429–34.
Remes-Troche JM, Rios-Vaca A, Ramirez-Iglesias MT, et al. High prevalence of celiac disease in Mexican Mestizo adults with type 1 diabetes mellitus. J Clin Gastroenterol. 2008;42:460–5.
Schvarcz E, Palmer M, Ingberg CM, Aman J, Berne C. Increased prevalence of upper gastrointestinal symptoms in long-term type 1 diabetes mellitus. Diabet Med. 1996;13:478–81.
Lodefalk M, Aman J. Gastrointestinal symptoms in adolescents with type 1 diabetes. Pediatr Diabetes. 2010;11:265–70.
Bakker SF, Tushuizen ME, Stokvis-Brantsma WH, et al. Frequent delay of coeliac disease diagnosis in symptomatic patients with type 1 diabetes mellitus: clinical and genetic characteristics. Eur J Intern Med. 2013;24:456–60.
Cerutti F, Bruno G, Chiarelli F, Lorini R, Meschi F, Sacchetti C. Younger age at onset and sex predict celiac disease in children and adolescents with type 1 diabetes: an Italian multicenter study. Diabetes Care. 2004;27:1294–8.
Lundin KE, Alaedini A. Non-celiac gluten sensitivity. Gastrointest Endosc Clin N Am. 2012;22:723–34.
Volta U, Bardella MT, Calabro A, Troncone R, Corazza GR. An Italian prospective multicenter survey on patients suspected of having non-celiac gluten sensitivity. BMC Med. 2014;12:85.
Green PH, Cellier C. Celiac disease. N Engl J Med. 2007;357:1731–43.
Bantle JP, Wylie-Rosett J, Albright AL, et al. Nutrition recommendations and interventions for diabetes: a position statement of the American Diabetes Association. Diabetes Care. 2008;31(Suppl 1):S61–78.
Valerio G, Maiuri L, Troncone R, et al. Severe clinical onset of diabetes and increased prevalence of other autoimmune diseases in children with coeliac disease diagnosed before diabetes mellitus. Diabetologia. 2002;45:1719–22.
Errichiello S, Esposito O, Di MR, et al. Celiac disease: predictors of compliance with a gluten-free diet in adolescents and young adults. J Pediatr Gastroenterol Nutr. 2010;50:54–60.
Lee AR, Ng DL, Zivin J, Green PH. Economic burden of a gluten-free diet. J Hum Nutr Diet. 2007;20:423–30.
Kaukinen K, Salmi J, Lahtela J, et al. No effect of gluten-free diet on the metabolic control of type 1 diabetes in patients with diabetes and celiac disease. Retrospective and controlled prospective survey. Diabetes Care. 1999;22:1747–8.
Bakker SF, Tushuizen ME, von Blomberg ME, Mulder CJ, Simsek S. Type 1 diabetes and celiac disease in adults: glycemic control and diabetic complications. Acta Diabetol. 2013;50:319–24.
Kurien M, Mollazadegan K, Sanders DS, Ludvigsson JF. A nationwide population-based study on the risk of coma, ketoacidosis and hypoglycemia in patients with celiac disease and type 1 diabetes. Acta Diabetol. 2015;52:1167–74.
Lewis NR, Sanders DS, Logan RF, Fleming KM, Hubbard RB, West J. Cholesterol profile in people with newly diagnosed coeliac disease: a comparison with the general population and changes following treatment. Br J Nutr. 2009;102:509–13.
Picarelli A, Di TM, Sabbatella L, et al. Type 1 diabetes mellitus and celiac disease: endothelial dysfunction. Acta Diabetol. 2013;50:497–503.
Tesfaye S, Stevens LK, Stephenson JM, et al. Prevalence of diabetic peripheral neuropathy and its relation to glycaemic control and potential risk factors: the EURODIAB IDDM Complications Study. Diabetologia. 1996;39:1377–84.
Paterson AD, Rutledge BN, Cleary PA, Lachin JM, Crow RS. The effect of intensive diabetes treatment on resting heart rate in type 1 diabetes: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications study. Diabetes Care. 2007;30:2107–12.
The Diabetes Control and Complications Trial Research Group. Effect of intensive diabetes treatment on the development and progression of long-term complications in adolescents with insulin-dependent diabetes mellitus: Diabetes Control and Complications Trial. Diabetes Control and Complications Trial Research Group. J Pediatr 1994; 125:177–188.
Malalasekera V, Cameron F, Grixti E, Thomas MC. Potential reno-protective effects of a gluten-free diet in type 1 diabetes. Diabetologia. 2009;52:798–800.
Leeds JS, Hopper AD, Hadjivassiliou M, Tesfaye S, Sanders DS. High prevalence of microvascular complications in adults with type 1 diabetes and newly diagnosed celiac disease. Diabetes Care. 2011;34:2158–63.
Mollazadegan K, Kugelberg M, Montgomery SM, Sanders DS, Ludvigsson J, Ludvigsson JF. A population-based study of the risk of diabetic retinopathy in patients with type 1 diabetes and celiac disease. Diabetes Care. 2013;36:316–21.
Pitocco D, Giubilato S, Martini F, et al. Combined atherogenic effects of celiac disease and type 1 diabetes mellitus. Atherosclerosis. 2011;217:531–5.
Welander A, Prutz KG, Fored M, Ludvigsson JF. Increased risk of end-stage renal disease in individuals with coeliac disease. Gut. 2012;61:64–8.
Finne P, Reunanen A, Stenman S, Groop PH, Gronhagen-Riska C. Incidence of end-stage renal disease in patients with type 1 diabetes. JAMA. 2005;294:1782–7.
Pham-Short A, Donaghue C, Ambler G, et al. Early elevation of albumin excretion rate is associated with poor gluten-free diet adherence in young people with coeliac disease and diabetes. Diabet Med. 2014;31:208–12.
Skovbjerg H, Tarnow L, Locht H, Parving HH. The prevalence of coeliac disease in adult Danish patients with type 1 diabetes with and without nephropathy. Diabetologia. 2005;48:1416–7.
Mollazadegan K, Fored M, Lundberg S, et al. Risk of renal disease in patients with both type 1 diabetes and coeliac disease. Diabetologia. 2014;57:1339–45.
Gunczler P, Lanes R, Paoli M, Martinis R, Villaroel O, Weisinger JR. Decreased bone mineral density and bone formation markers shortly after diagnosis of clinical type 1 diabetes mellitus. J Pediatr Endocrinol Metab. 2001;14:525–8.
Larussa T, Suraci E, Nazionale I, Abenavoli L, Imeneo M, Luzza F. Bone mineralization in celiac disease. Gastroenterol Res Pract. 2012;2012:198025.
Diniz-Santos DR, Brandao F, Adan L, Moreira A, Vicente EJ, Silva LR. Bone mineralization in young patients with type 1 diabetes mellitus and screening-identified evidence of celiac disease. Dig Dis Sci. 2008;53:1240–5.
Artz E, Warren-Ulanch J, Becker D, Greenspan S, Freemark M. Seropositivity to celiac antigens in asymptomatic children with type 1 diabetes mellitus: association with weight, height, and bone mineralization. Pediatr Diabetes. 2008;9:277–84.
Lunt H, Florkowski CM, Cook HB, Whitehead MR. Bone mineral density, type 1 diabetes, and celiac disease. Diabetes Care. 2001;24:791–2.
Sategna-Guidetti C, Grosso SB, Grosso S, et al. The effects of 1-year gluten withdrawal on bone mass, bone metabolism and nutritional status in newly-diagnosed adult coeliac disease patients. Aliment Pharmacol Ther. 2000;14:35–43.
Rubin RR, Peyrot M. Quality of life and diabetes. Diabetes Metab Res Rev. 1999;15:205–18.
Kurppa K, Collin P, Maki M, Kaukinen K. Celiac disease and health-related quality of life. Expert Rev Gastroenterol Hepatol. 2011;5:83–90.
Bakker SF, Pouwer F, Tushuizen ME, Hoogma RP, Mulder CJ, Simsek S. Compromised quality of life in patients with both Type 1 diabetes mellitus and coeliac disease. Diabet Med. 2013;30:835–9.
Anderson RJ, Freedland KE, Clouse RE, Lustman PJ. The prevalence of comorbid depression in adults with diabetes: a meta-analysis. Diabetes Care. 2001;24:1069–78.
Garud S, Leffler D, Dennis M, et al. Interaction between psychiatric and autoimmune disorders in coeliac disease patients in the Northeastern United States. Aliment Pharmacol Ther. 2009;29:898–905.
Kaspers S, Kordonouri O, Schober E, Grabert M, Hauffa BP, Holl RW. Anthropometry, metabolic control, and thyroid autoimmunity in type 1 diabetes with celiac disease: a multicenter survey. J Pediatr. 2004;145:790–5.
Bakker SF, Tushuizen ME, Stokvis-Brantsma WH, et al. Frequent delay of coeliac disease diagnosis in symptomatic patients with type 1 diabetes mellitus: clinical and genetic characteristics. Eur J Intern Med. 2013;24:456–60.
Tack GJ, Verbeek WH, Schreurs MW, Mulder CJ. The spectrum of celiac disease: epidemiology, clinical aspects and treatment. Nat Rev Gastroenterol Hepatol. 2010;7:204–13.
Ilus T, Kaukinen K, Virta LJ, et al. Refractory coeliac disease in a country with a high prevalence of clinically-diagnosed coeliac disease. Aliment Pharmacol Ther. 2014;39:418–25.
Mollazadegan K, Sanders DS, Ludvigsson J, Ludvigsson JF. Long-term coeliac disease influences risk of death in patients with type 1 diabetes. J Intern Med. 2013;274:273–80.
Wilson JMG, Jungner G. Principles and practice of screening for disease. Geneva: WHO; 1968.
Mahmud FH, De Melo EN, Noordin K, et al. The celiac disease and diabetes-dietary intervention and evaluation trial (CD-DIET) protocol: a randomised controlled study to evaluate treatment of asymptomatic coeliac disease in type 1 diabetes. BMJ Open. 2015;5:e008097.
The Digestive Health Foundation. Coeliac disease, 4th edn. Gastroenterological Society of Australia (GESA); 2007.
Nederlandse Vereniging van Maag-Darm-Leverartsen. Richtlijn Coeliakie en Dermatitis Herpetiformis. 2008.
National Clinical Guideline Centre (UK). Type 1 Diabetes in Adults: Diagnosis and Management. London: National Institute for Health and Care Excellence (UK); 2015.
Bai JC, Fried M, Corazza GR, et al. World Gastroenterology Organisation global guidelines on celiac disease. J Clin Gastroenterol. 2013;47:121–6.
Rubio-Tapia A, Hill ID, Kelly CP, Calderwood AH, Murray JA. ACG clinical guidelines: diagnosis and management of celiac disease. Am J Gastroenterol. 2013;108:656–76.
Downey L, Houten R, Murch S, Longson D. Recognition, assessment, and management of coeliac disease: summary of updated NICE guidance. BMJ. 2015;351: h4513.
Craig ME, Twigg SM, Donaghue KC, CheungNW, Cameron FJ, Conn J, Jenkins AJ, Silink M. Australian Type 1 Diabetes Guidelines Expert Advisory Group. National evidence based clinical care guidelines for type 1 diabetes in children, adolescents and adults. Canberra Aust Gov Dep HealthAgeing. 2011.
Ludvigsson JF, Card TR, Kaukinen K, et al. Screening for celiac disease in the general population and in high-risk groups. United European Gastroenterol J. 2015;3:106–20.
Simpson SM, Ciaccio EJ, Case S, et al. Celiac disease in patients with type 1 diabetes: screening and diagnostic practices. Diabetes Educ. 2013;39:532–40.
Kurppa K, Paavola A, Collin P, et al. Benefits of a gluten-free diet for asymptomatic patients with serologic markers of celiac disease. Gastroenterology. 2014;147:610–7.
Dabelea D. The accelerating epidemic of childhood diabetes. Lancet. 2009;373:1999–2000.
Kang JY, Kang AH, Green A, Gwee KA, Ho KY. Systematic review: worldwide variation in the frequency of coeliac disease and changes over time. Aliment Pharmacol Ther. 2013;38:226–45.
Rostom A, Dube C, Cranney A, et al. The diagnostic accuracy of serologic tests for celiac disease: a systematic review. Gastroenterology. 2005;128:S38–46.
Barera G, Bonfanti R, Viscardi M, et al. Occurrence of celiac disease after onset of type 1 diabetes: a 6-year prospective longitudinal study. Pediatrics. 2002;109:833–8.
Husby S, Koletzko S, Korponay-Szabo IR, et al. European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease. J Pediatr Gastroenterol Nutr. 2012;54:136–60.
DeMelo EN, McDonald C, Saibil F, Marcon MA, Mahmud FH. Celiac disease and type 1 diabetes in adults: is this a high-risk group for screening? Can J Diabetes. 2015;39:513–9.
Pham-Short A, Donaghue KC, Ambler G, Phelan H, Twigg S, Craig ME. Screening for celiac disease in type 1 diabetes: a systematic review. Pediatrics. 2015;136:e170–6.
Elias J, Hoorweg-Nijman JJ, Balemans WA. Clinical relevance and cost-effectiveness of HLA genotyping in children with Type 1 diabetes mellitus in screening for coeliac disease in the Netherlands. Diabet Med. 2015;32:834–8.
Husby S, Koletzko S, Korponay-Szabo IR, et al. European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease. J Pediatr Gastroenterol Nutr. 2012;54:136–60.
Popp A, Mihu M, Munteanu M, et al. Prospective antibody case finding of coeliac disease in type-1 diabetes children: need of biopsy revisited. Acta Paediatr. 2013;102:e102–6.
Samsom M, Akkermans LM, Jebbink RJ, van Isselt IH, vanBerge-Henegouwen GP, Smout AJ. Gastrointestinal motor mechanisms in hyperglycaemia induced delayed gastric emptying in type I diabetes mellitus. Gut. 1997;40:641–6.
Horowitz M, Fraser R. Disordered gastric motor function in diabetes mellitus. Diabetologia. 1994;37:543–51.
SB contributed to the design of the review, collected and analyzed the data and wrote the draft of the paper. MT participated in writing of the manuscript and critically reviewed the data of the articles. BB, HB and CM critically reviewed the intellectual content of the study. SS contributed to the concept and design of the study, performed acquisition of data and critically reviewed the paper. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
SB is financially supported by the Coeliac Disease Consortium, The Netherlands.
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Bakker, S.F., Tushuizen, M.E., von Blomberg, B.M.E. et al. Screening for coeliac disease in adult patients with type 1 diabetes mellitus: myths, facts and controversy. Diabetol Metab Syndr 8, 51 (2016). https://doi.org/10.1186/s13098-016-0166-0
- Coeliac disease
- Clinical characteristics
- Gluten free diet
- Quality of life
- Tissue-transglutaminase antibodies
- Complications and type 1 diabetes mellitus