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Table of Contents
Vol. 86, No. 4, 2012
Issue release date: January 2013
Section title: Original Paper
Digestion 2012;86:309–314
(DOI:10.1159/000341416)

Factors Associated with Dietary Adherence in Celiac Disease: A Nationwide Study

Kurppa K.a · Lauronen O.b · Collin P.b, d · Ukkola A.a · Laurila K.a · Huhtala H.c · Mäki M.a · Kaukinen K.b, d
aPediatric Research Center, University of Tampere and Tampere University Hospital, bSchool of Medicine and cSchool of Health Sciences, University of Tampere, and dDepartment of Gastroenterology and Alimentary Tract Surgery, Tampere University Hospital, Tampere, Finland
email Corresponding Author

Abstract

Aims: Diagnostics and follow-up of celiac disease have gradually shifted from tertiary centers to secondary and primary health care. In order to establish whether this has affected the success of treatment, and to identify predictors for dietary non-adherence, we carried out a study in a nationwide cohort of treated celiac patients. Patients and Methods: 843 biopsy-proven patients, 94 children and 749 adults, were enrolled and interviewed. Adherence to a gluten-free diet was determined by means of an interview and serological testing. Results: Altogether, 88% were on a strict gluten-free diet; the rest had occasional dietary transgressions. Younger age at diagnosis, being currently a teenager, and current symptoms were associated with non-adherence. There was no association between non-adherence and place of diagnosis, gender, disease phenotype or severity of symptoms before diagnosis, presence of comorbidities, family history of celiac disease, smoking, duration of diet, use of oats, self-efficacy for the diet or lack of follow-up. Conclusions: Good dietary adherence can be achieved also in patients diagnosed and followed in primary health care. In a country with a high prevalence and good general knowledge of celiac disease, only age at diagnosis and age at present would appear to be major determinants for adherence.

© 2012 S. Karger AG, Basel


  

Key Words

  • Celiac disease
  • Adherence
  • Gluten-free diet

 Introduction

Currently, the treatment of celiac disease is based on life-long exclusion of wheat, rye and barley and other gluten-containing food products from the diet. Adherence to a gluten-free diet is crucial not only for intestinal mucosal recovery and alleviation of symptoms, but also for the prevention of complications such as anemia, osteoporotic fractures and small-bowel lymphoma [1,2,3]. However, due to the expense and restrictive nature of the treatment, changing eating habits for life may constitute a formidable challenge for many celiac disease patients, and hence compliance with the diet easily remains inadequate [4]. It has been found in clinical practice that 20–80% of patients adhere only partially to the diet, and especially those detected by screening are thought to be at risk of poor adherence [5,6,7,8,9,10,11]. Nevertheless, data on factors affecting the long-term dietary control of celiac disease are scant. As non-adherence wastes health-care resources and may cause significant morbidity and even increased mortality [2,12], it is important to characterize individuals most likely to be non-adherent, and offer them advice and assist them better to follow their diet.

In recent years, active case-finding in at-risk groups and among subjects with atypical symptoms has resulted in an increasing diagnostic rate, and the prevalence of clinically detected celiac disease in Finland is 0.7% [13]. Simultaneously, the diagnostics and follow-up have shifted from tertiary centers to secondary and primary health care [14]. It is not known whether these changes in clinical practice have affected the success of the treatment. To identify factors associated with non-adherence, we carried out a cross-sectional study in a large, nationwide cohort of celiac disease children and adults.

 

 Materials and Methods


 Patients and Study Design

The study was conducted in the Departments of Gastroenterology and Alimentary Tract Surgery and Pediatrics, Tampere University Hospital and in the School of Medicine, University of Tampere. Volunteer children (age below 18 years) and adults diagnosed with celiac disease were enrolled in study investigating different clinical, pathogenic and genetic aspects of celiac disease. The participants were recruited by a nationwide search using newspaper advertisements and via national and local celiac disease societies. Approximately 70% of celiac patients in our country are members of celiac societies. Subjects with biopsy-proven celiac disease diagnosed more than one year ago were considered eligible. All participants or in the case of young children their parents were interviewed by phone either by a physician or by a study nurse with expertise in celiac disease, and blood samples were drawn for celiac disease serology. All diagnoses, presenting symptoms and the presence of celiac disease-associated disorders or other comorbidities were confirmed from the patients’ medical records. In the present study, particular attention was paid to place of diagnosis, family history of the disease, severity and duration of symptoms at diagnosis, presence of comorbidities, smoking, baseline dietary counseling, duration and strictness of gluten-free diet, possible current symptoms and regular follow-up. Patients were asked to rate the severity of their previous and current symptoms as follows: no symptoms, slight symptoms, moderate symptoms and serious symptoms.

The study protocol was approved by the Ethical Committee of Tampere University Hospital. All study subjects, or in the case of young children their parents, gave written informed consent.

 Dietary Assessment

A history of occasional or regular consumption of gluten-containing products and oats was assessed by means of a structured dietary interview [6]. Serologic tests were employed to further monitor disease activity. Serum IgA class endomysial antibodies were measured using an indirect immunofluorescence method with human umbilical cord as substrate [15], and serum IgA class tissue transglutaminase antibodies by enzyme-linked immunosorbent assay (QUANTA Lite h-tTG IgA, INOVA Diagnostics, San Diego, Calif., USA); a dilution 1:≥5 and a unit value ≥30 were considered positive, respectively. In the case of selective IgA deficiency, the corresponding IgG class antibodies were determined. Patients who reported maintaining a strict gluten-free diet in a structured interview and were found to have negative serology after 2 years on the diet were regarded as strictly adherent [6,8]. Further, patients who had been on a gluten-free diet less than 2 years were considered adherent if they reported a strict diet upon interview and serum antibody values had decreased from the level found at diagnosis. When possible, the self-assessed adherence was further confirmed from the patients’ medical reports; the reported diet was considered strict only if there was inadvertent gluten ingestion less than once in a month [16].

 Statistics

Fisher’s exact test was used in cross-tabulation in statistical evaluations, and a p value <0.05 was considered significant. All statistical calculations were performed using Predictive Analytic Software for Windows (version 18).

 

 Results

Altogether, 94 children and 749 adults with celiac disease were eligible. At the time of the study, their median age was 51 years (range 2–89 years); 76% were female. At diagnosis, gastrointestinal complaints had been the main presenting symptom in 62%, while 16% had suffered from extraintestinal symptoms and 22% were detected by screening in celiac disease at-risk groups. Eight percent of the patients had experienced severe symptoms at diagnosis, 36% moderate symptoms, and in 56% symptoms had been mild or absent. Among adults, 18% of the diagnoses had been established in tertiary centers, 47% in secondary health care and 35% in primary care. In contrast, among children 70% of the diagnoses had been still made in tertiary care and the remainder in secondary care.

In total, 69% of the celiac disease adults were not under any kind of follow-up for their disease, while 95% of the children were being followed. Subjects with celiac disease-associated or other comorbidities were followed no more often than others (data not shown). Of those under regular surveillance, 59% were followed up in primary health care (adults 71%, children 5%). In total, 88% of the patients were found to be keeping to a strict gluten-free diet (adults 90%, children 81%). The rest reported occasional dietary transgressions, but none was completely non-adherent. Altogether, the patients had been a median of 7 years (range 1–48 years) on a gluten-free diet.

Younger age at diagnosis and current age were related to dietary non-adherence. In particular, those currently in their teens were likely to be non-adherent (table 1). In contrast, neither the place of diagnosis, gender, clinical presentation of the disease, duration and severity of symptoms before diagnosis, presence of comorbidities, family history of celiac disease, smoking, duration of gluten-free diet, dietary counseling from a dietitian, regular follow-up, self-efficacy for the diet nor consumption of oats were associated with adherence (tables 1, 2, 3). Although there was no significant difference, patients with osteoporotic fracture or malignancy showed particularly good adherence (table 2). Of note, subjects betraying frequent dietary transgressions also experienced more clinical symptoms (table 3); in a separate analysis, this could be seen only in adults. Otherwise, there were no differences between children and adults in the factors related to dietary adherence.

TAB01
Table 1. Demographic data, duration of gluten-free diet, clinical presentation and duration and severity of symptoms at diagnosis and dietary adherence (n = 843)

TAB02
Table 2. Family history of celiac disease, presence of celiac disease-associated conditions or other comorbidities and smoking and adherence to gluten-free diet (n = 843)

TAB03
Table 3. Place of celiac disease diagnosis, dietary counseling, maintenance and place of follow-up, use of oats, current symptoms, self-efficacy for the diet and adherence to gluten-free diet (n = 843)

 

 Discussion

Our main finding was that the decentralization of celiac disease diagnostics and follow-up from tertiary centers to primary health care in recent decades has not affected the success of treatment. We also showed that, in a country with a good general knowledge and a high prevalence of celiac disease, only current age and age at diagnosis were major factors associated with dietary adherence. In particular, teenage patients showed more non-adherence than others. Previously, poor coping among adolescents has also been noted in a small Italian study [5], and in some adult studies older patients have been more adherent than younger [17,18,19,20]. Elsewhere, no such association has been found [6,8,21,22]. Besides current teenagers, in our study patients diagnosed in childhood also showed more dietary non-adherence. Ciacci et al. [23] detected better adherence in patients diagnosed after 20 years of age, whereas in another study the same applied to children diagnosed before the age of 4 years [24]. Again, there are studies where no association has been observed between age at diagnosis and dietary adherence [6,8,21]. Though somewhat inconsistent, the results indicate that adolescence in particular is a sensitive period to adapt and maintain a gluten-free diet. At that age, parents may still have a major role in the treatment, and it may be challenging for a teenager to take more self-responsibility. Also, considerable changes such as new place of education and residence often occur at the same time. With this in mind, health care professionals should pay particular attention to adolescent celiac patients. In accord with most previous studies [17,18,23], we observed no significant difference between genders in adherence.

In line with our previous observations in screen-detected patients [6,25], the clinical presentation of celiac disease at diagnosis had no effect on adherence, and also some other groups have obtained corresponding results [8,21]. In contrast, Fabiani et al. [5] detected poorer adherence in screen- than in symptom-detected celiac adolescents, but the study in question was small, and both patient groups showed very poor adherence. There is usually a particular reason why a person is screened for celiac disease, for example belonging to an at-risk group. In such cases, even asymptomatic patients might be motivated to adapt a strict diet, for example in order to prevent possible complications of untreated disease. In any case, the fact that good adherence can be achieved in screen-detected subjects in at-risk groups supports intensified serological screening for such individuals. Consistently with Edwards et al. [26], non-adherent adults here evinced more current symptoms, this probably a being consequence rather than a cause. This would imply that many celiac patients may tolerate a certain amount of symptoms produced by inadvertent or deliberate gluten ingestion.

There was no association between celiac disease-related or other comorbidities and dietary adherence. Similarly, Leffler et al. [8] detected no effect of autoimmune or psychological comorbidities on adherence in celiac adults. However, in contrast to the present observations, they found higher adherence among patients with other food intolerance; this discrepancy might in fact be explained by differences in study cohorts. In a study by Addolorato et al. [27], psychological support reduced depression and dietary non-adherence in celiac patients; in the present and in two other studies [8,17], no association was seen between psychiatric comorbidities and non-adherence. Interestingly, patients with osteoporotic fracture or malignancy showed very high adherence. This may reflect an aim to optimize celiac disease treatment in the presence of severe complication or comorbidity.

Somewhat surprisingly, lack of dietary counseling was not associated with dietary non-adherence; this was also observed in a recent adult study [8]. Nowadays, information regarding gluten-free products is easy to obtain in the internet and via different advocacy groups; better labeling and availability of products in food stores and restaurants may also have reduced the impact of dietary counseling. In addition, health care professionals may sometimes provide limited information on the treatment of celiac disease [28,29]. Interestingly, in one earlier study dietetic counseling proved beneficial in white Caucasian but not in South Asian patients [30], this suggesting that cultural factors may have a significant influence on the outcome. Such results emphasize that dietary counseling should be individually tailored and given by dietitians with expertise in celiac disease. Whether the counseling is implemented in primary care or in specialized centers seems to be less important.

Neither the maintenance nor duration of regular follow-up of celiac disease was associated with dietary adherence, indicating that, once achieved, good adherence remains [6,8]. These results suggest that the follow-up of celiac disease in adults might be focused predominantly on subjects with coping problems. In children, the situation is different; due to rapid changes in development even short-term dietary transgressions can lead to permanent complications, and regular follow-up is thus mandatory [31,32]. Interestingly, in our study adult patients diagnosed and followed in primary care evinced adherence equal to that in subjects who were under hospital care. This is important, since it will in the future be impossible to manage the increasing number of celiac patients only in tertiary and secondary centers. These observations cannot be directly generalized to pediatric patients, since here only 5% of them were being followed in primary care settings. In one recent study, children followed by primary care physicians showed poorer adherence than those followed by specialists [33], and this issue remains to be addressed in future studies. When interpreting our results, it is important to realize that in Finland there have been nationwide celiac disease care guidelines already since 1997 [34]. According to the guidelines, adult patients can be diagnosed in primary centers by general practitioners who themselves perform endoscopies. In contrast, all celiac children are diagnosed in secondary and tertiary centers by pediatric gastroenterologists.

The main strengths of our study were its nationwide coverage and the large number of celiac disease patients participating. In addition, adherence was defined meticulously by both dietary interview and serological testing, which is important in that patients may easily underestimate their inadvertent gluten intake when approached trough questionnaires only [8,21,35]. Limitation of the study was that a substantial number of participants were recruited via celiac societies. This may cause selection bias to the results and limit the accessible patient population [29]. In theory, the high overall adherence noted in this study might also have caused false-negative associations by a ceiling effect, but due to the large cohort size, we still had more than a hundred non-adherent participants.

To conclude, our results showed that good dietary adherence in celiac disease can be attained irrespective of place of diagnosis and subsequent follow-up of the disease. In addition, in a country with a high prevalence, there are only a few major determinants for adherence, the most important being age at diagnosis and age at present.

 

 Acknowledgements

This study and the Celiac Disease Study Group are supported by the Academy of Finland Research Council for Health, the Competitive Research Funding of the Pirkanmaa Hospital District, the Sigrid Juselius Foundation, the Foundation for Paediatric Research, the Maud Kuistila Foundation, the Ehrnrooth Foundation, the Finnish Gastroenterology Society and the Finnish Celiac Society.

 

 Disclosure Statement

None of the authors declare a conflict of interest.


References

  1. Holmes GKT, Prior P, Lane MR, Pope D, Allan RN: Malignancy in coeliac disease – effect of a gluten free diet. Gut 1989;30:333–338.
  2. Haines ML, Anderson RP, Gibson PR: Systematic review: the evidence base for long-term management of coeliac disease. Aliment Pharmacol Ther 2008;28:1042–1066.
  3. Olmos M, Antelo M, Vazquez H, Smecuol E, Maurino E, Bai JC: Systematic review and meta-analysis of observational studies on the prevalence of fractures in coeliac disease. Dig Liver Dis 2008;40:46–53.
  4. Hall NJ, Rubin G, Charnock A: Systematic review: adherence to a gluten-free diet in adult patients with coeliac disease. Aliment Pharmacol Ther 2009;30:315–330.
  5. Fabiani E, Taccari LM, Rätsch I-M, DiGiuseppe S, Coppa GV, Catassi C: Compliance with gluten-free diet in adolescents with screening-detected celiac disease: a 5-year follow-up study. J Pediatr 2000;136:841–843.
  6. Viljamaa M, Collin P, Huhtala H, Sievanen H, Mäki M, Kaukinen K: Is coeliac disease screening in risk groups justified? A fourteen-year follow-up with special focus on compliance and quality of life. Aliment Pharmacol Ther 2005;22:317–324.
  7. Shamir R, Yehezkely-Schildkraut V, Hartman C, Eliakim R: Population screening for celiac disease: follow-up of patients identified by positive serology. J Gastroenterol Hepatol 2007;22:532–535.

    External Resources

  8. Leffler DA, Edwards-George J, Dennis M, Schuppan D, Cook F, Franko DL, Blom-Hoffman J, Kelly CP: Factors that influence adherence to a gluten-free diet in adults with celiac disease. Dig Dis Sci 2008;53:1573–1581.
  9. Errichiello S, Esposito O, Di Mase R, Camarca ME, Natale C, Limongelli MG, Marano C, Coruzzo A, Lombardo M, Strisciuglio P, Greco L: Celiac disease: predictors of compliance with a gluten-free diet in adolescents and young adults. J Pediatr Gastroenterol Nutr 2010;50:54–60.
  10. Roma E, Roubani A, Kolia E, Panayiotou J, Zellos A, Syriopoulou VP: Dietary compliance and life style of children with coeliac disease. J Hum Nutr Diet 2010;23:176–182.
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  12. Corrao G, Corazza GR, Bagnardi V, Brusco G, Ciacci C, Cottone M, Sategna Guidetti C, Usai P, Cesari P, Pelli MA, Loperfido S, Volta U, Calabro A, Certo M: Mortality in patients with coeliac disease and their relatives: a cohort study. Lancet 2001;358:356–361.
  13. Virta L, Kaukinen K, Collin P: Incidence and prevalence of diagnosed coeliac disease in Finland: results of effective case finding in adults. Scand J Gastroenterol 2009;44:933–938.

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  14. Collin P, Huhtala H, Virta L, Kekkonen L, Reunala T: Diagnosis of celiac disease in clinical practice. Physician’s alertness to condition essential. J Clin Gastroenterol 2007;41:152–156.

    External Resources

  15. Sulkanen S, Halttunen T, Laurila K, Kolho K-L, Korponay-Szabo I, Sarnesto A, Savilahti E, Collin P, Mäki M: Tissue transglutaminase autoantibody enzyme-linked immunosorbent assay in detecting celiac disease. Gastroenterology 1998;115:1322–1328.
  16. Lanzini A, Lanzarotto F, Villanacci V, Mora A, Bertolazzi S, Turini D, Carella G, Malagoli A, Ferrante G, Cesana BM, Ricci C: Complete recovery of intestinal mucosa occurs very rarely in adult coeliac patients despite adherence to gluten-free diet. Aliment Pharmacol Ther 2009;29:1299–1308.
  17. Ciacci C, Iavarone A, Mazzacca G, De Rosa A: Depressive symptoms in adult coeliac disease. Scand J Gastroenterol 1998;33:247–250.
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  22. Vahedi K, Mascart F, Mary JY, Laberenne JE, Bouhnik Y, Morin MC, Ocmant A, Velly C, Colombel JF, Matuchansky C: Reliability of antitransglutaminase antibodies as predictors of gluten-free diet compliance in adult celiac disease. Am J Gastroenterol 2003;98:1079–1087.
  23. Ciacci C, D’Agate C, De Rosa A, Franzese C, Errichiello S, Gasperi V, Pardi A, Quagliata D, Visentini S, Greco L: Self-rated quality of life in celiac disease. Dig Dis Sci 2003;48:2216–2220.
  24. Högberg L, Grodzinsky E, Stenhammar L: Better dietary compliance in patients with coeliac disease diagnosed in early childhood. Scand J Gastroenterol 2003;38:751–754.
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  27. Addolorato G, De Lorenzi G, Abenavoli L, Leggio L, Capristo E, Gasbarrini G: Psychological support counselling improves gluten-free diet compliance in coeliac patients with affective disorders. Aliment Pharmacol Ther 2004;20:777–782.
  28. Parakkal D, Du H, Semer R, Ehrenpreis ED, Guandalini S: Do gastroenterologists adhere to diagnostic and treatment guidelines for celiac disease? J Clin Gastroenterol 2012;46:e12–20.

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  30. Butterworth JR, Banfield LM, Iqbal TH, Cooper BT: Factors relating to compliance with a gluten-free diet in patients with coeliac disease: comparison of white Caucasian and South Asian patients. Clin Nutr 2004;23:1127–1134.
  31. Aine L, Mäki M, Collin P, Keyriläinen O: Dental enamel defects in celiac disease. J Oral Pathol Med 1990;19:241–245.
  32. Troncone R, Kosova R: Short stature and catch-up growth in celiac disease. J Pediatr Gastroenterol Nutr 2010;51(suppl 3):S137–S138.

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  33. Mozer-Glassberg Y, Zevit N, Rosenbach Y, Hartman C, Morgenstern S, Shamir R: Follow-up of children with celiac disease – lost in translation? Digestion 2011;83:283–287.

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  34. Collin P, Kaukinen K, Mäki M, Vuorio A, Working group appointed by the Finnish Medical Society Duodecim and the Finnish Society of Gastroenterology: Update on current care guidelines. Celiac disease. www.kaypahoito.fi.
  35. Dipper CR, Maitra S, Thomas R, Lamb CA, McLean-Tooke AP, Ward R, Smith D, Spickett G, Mansfield JC: Anti-tissue transglutaminase antibodies in the follow-up of adult coeliac disease. Aliment Pharmacol Ther 2009;30:236–244.

  

Author Contacts

Katri Kaukinen, MD, PhD
University of Tampere
School of Medicine
FI–33014 University of Tampere (Finland)
E-Mail katri.kaukinen@uta.fi

  

Article Information

Received: March 12, 2012
Accepted: June 10, 2012
Published online: October 23, 2012
Number of Print Pages : 6
Number of Figures : 0, Number of Tables : 3, Number of References : 35

  

Publication Details

Digestion (International Journal of Gastroenterology)

Vol. 86, No. 4, Year 2012 (Cover Date: January 2013)

Journal Editor: Göke B. (Munich), Shinomura Y. (Sapporo)
ISSN: 0012-2823 (Print), eISSN: 1421-9867 (Online)

For additional information: http://www.karger.com/DIG


Copyright / Drug Dosage / Disclaimer

Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher or, in the case of photocopying, direct payment of a specified fee to the Copyright Clearance Center.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in goverment regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.

Abstract

Aims: Diagnostics and follow-up of celiac disease have gradually shifted from tertiary centers to secondary and primary health care. In order to establish whether this has affected the success of treatment, and to identify predictors for dietary non-adherence, we carried out a study in a nationwide cohort of treated celiac patients. Patients and Methods: 843 biopsy-proven patients, 94 children and 749 adults, were enrolled and interviewed. Adherence to a gluten-free diet was determined by means of an interview and serological testing. Results: Altogether, 88% were on a strict gluten-free diet; the rest had occasional dietary transgressions. Younger age at diagnosis, being currently a teenager, and current symptoms were associated with non-adherence. There was no association between non-adherence and place of diagnosis, gender, disease phenotype or severity of symptoms before diagnosis, presence of comorbidities, family history of celiac disease, smoking, duration of diet, use of oats, self-efficacy for the diet or lack of follow-up. Conclusions: Good dietary adherence can be achieved also in patients diagnosed and followed in primary health care. In a country with a high prevalence and good general knowledge of celiac disease, only age at diagnosis and age at present would appear to be major determinants for adherence.

© 2012 S. Karger AG, Basel


  

Author Contacts

Katri Kaukinen, MD, PhD
University of Tampere
School of Medicine
FI–33014 University of Tampere (Finland)
E-Mail katri.kaukinen@uta.fi

  

Article Information

Received: March 12, 2012
Accepted: June 10, 2012
Published online: October 23, 2012
Number of Print Pages : 6
Number of Figures : 0, Number of Tables : 3, Number of References : 35

  

Publication Details

Digestion (International Journal of Gastroenterology)

Vol. 86, No. 4, Year 2012 (Cover Date: January 2013)

Journal Editor: Göke B. (Munich), Shinomura Y. (Sapporo)
ISSN: 0012-2823 (Print), eISSN: 1421-9867 (Online)

For additional information: http://www.karger.com/DIG


Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: 3/12/2012 12:36:00 PM
Accepted: 6/4/2012
Published online: 10/23/2012
Issue release date: January 2013

Number of Print Pages: 6
Number of Figures: 0
Number of Tables: 3

ISSN: 0012-2823 (Print)
eISSN: 1421-9867 (Online)

For additional information: http://www.karger.com/DIG


Copyright / Drug Dosage

Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher or, in the case of photocopying, direct payment of a specified fee to the Copyright Clearance Center.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in goverment regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.

References

  1. Holmes GKT, Prior P, Lane MR, Pope D, Allan RN: Malignancy in coeliac disease – effect of a gluten free diet. Gut 1989;30:333–338.
  2. Haines ML, Anderson RP, Gibson PR: Systematic review: the evidence base for long-term management of coeliac disease. Aliment Pharmacol Ther 2008;28:1042–1066.
  3. Olmos M, Antelo M, Vazquez H, Smecuol E, Maurino E, Bai JC: Systematic review and meta-analysis of observational studies on the prevalence of fractures in coeliac disease. Dig Liver Dis 2008;40:46–53.
  4. Hall NJ, Rubin G, Charnock A: Systematic review: adherence to a gluten-free diet in adult patients with coeliac disease. Aliment Pharmacol Ther 2009;30:315–330.
  5. Fabiani E, Taccari LM, Rätsch I-M, DiGiuseppe S, Coppa GV, Catassi C: Compliance with gluten-free diet in adolescents with screening-detected celiac disease: a 5-year follow-up study. J Pediatr 2000;136:841–843.
  6. Viljamaa M, Collin P, Huhtala H, Sievanen H, Mäki M, Kaukinen K: Is coeliac disease screening in risk groups justified? A fourteen-year follow-up with special focus on compliance and quality of life. Aliment Pharmacol Ther 2005;22:317–324.
  7. Shamir R, Yehezkely-Schildkraut V, Hartman C, Eliakim R: Population screening for celiac disease: follow-up of patients identified by positive serology. J Gastroenterol Hepatol 2007;22:532–535.

    External Resources

  8. Leffler DA, Edwards-George J, Dennis M, Schuppan D, Cook F, Franko DL, Blom-Hoffman J, Kelly CP: Factors that influence adherence to a gluten-free diet in adults with celiac disease. Dig Dis Sci 2008;53:1573–1581.
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