BMC Gastroenterology | |
High prevalence of celiac disease among Saudi children with type 1 diabetes: a prospective cross-sectional study | |
Imad El Haj3  Ahmed Alenizi1  Musa Al-Zahrani1  Nimer Sulaiman1  Abdulrahman Al-Hussaini2  | |
[1] Children's Hospital, King Saud Medical City, Riyadh, Kingdom of Saudi Arabia;University of King Saud for Health Sciences, Division of Pediatric Gastroenterology, Hepatology & Nutrition, Children's Hospital, King Fahad Medical City, PO Box 59046, Riyadh, Postal code 11525, Kingdom of Saudi Arabia;Department of Pathology, King Saud Medical City, Riyadh, Kingdom of Saudi Arabia | |
关键词: Saudi Arabia; Ednomyseal antibody; Anti-tissue transglutaminase; Type 1 diabetes; Celiac disease; | |
Others : 858261 DOI : 10.1186/1471-230X-12-180 |
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received in 2012-06-27, accepted in 2012-12-19, 发布年份 2012 | |
【 摘 要 】
Background
There is lack of data on prevalence of celiac disease (CD) in children with type 1 diabetes (T1D) in Arabs in the Middle East. The present investigation aims to study the prevalence rate and clinical characteristics of CD among Saudi children with T1D using a combination of the most sensitive and specific screening serologic tests (anti- tissue transglutaminase antibodies IgA [anti-TTG] and ednomyseal antibodies [EMA]) and to determine the lower cut-off value of anti- anti-TTG level that best predicts CD in children with T1D.
Methods
Children with T1D following in diabetic clinic have been prospectively screened for presence of CD, over a two-year period (2008–2010), by doing anti-TTG, EMA, and total IgA. Children with positive anti-TTG titres (>50 U/ml) and/or EMA and children with persistently low positive anti-TTG titres (two readings 20–50 U/ml; within 6 months intervals) had upper endoscopy and 6 duodenal biopsies.
Results
One hundred and six children with T1D have been screened for CD: age ranged between 8 months to 15.5 years (62 females). Nineteen children had positive anti-TTG and/or EMA, however only 12 children had biopsy proven CD (11.3%). Five of 12 had gastrointestinal symptoms (42%). Children with T1D and CD had significantly lower serum iron than children with T1D alone (8.5 μgm/L Vs 12.5 μgm/L; P = 0.014). The sensitivity and specificity of anti-TTG were 91.6% and 93.6%, with a positive and negative predictive value of 64.7% and 98.8%, respectively. Receiver operated characteristics analysis for the best cut-off value of anti-TTG level for diagnosis of CD was 63 units (sensitivity 100% and specificity 98.8%).
Conclusion
CD is highly prevalent among Saudi children with T1D. Anti-TTG titres more than 3 times the upper limit of normal has very high sensitivity and specificity for diagnosis of CD in T1D children.
【 授权许可】
2012 Al-Hussaini et al.; licensee BioMed Central Ltd.
【 预 览 】
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【 参考文献 】
- [1]Tanure MG, Silva IN, Bahia M, Penna FJ: Prevalence of celiac disease in Brasilian children with type 1 diabetes mellitus. J Pediatr Gastroenterol Nutr 2006, 42:155-159.
- [2]Sakly W, Bienvenu F, Peretti N, Lachaux A, Morel S, Bouvier R, Nicolino M, Bienvenu J, Spiteri A, Fabien N: IgA anti-transglutaminase antibodies as a tool for screening atypical forms of coeliac disease in a French at-risk paediatric population. Eur J Gastroenterol Hepatol 2005, 17:235-239.
- [3]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 1996, 412(suppl):58-60.
- [4]Fraser-Reynolds KA, Butzner JD, Stephure DK, Trussell RA, Scott RB: Use of immunoglobulin A-antiendomysial antibody to screen for celiac disease in North American children with type 1 diabetes. Diabetes Care 1998, 21:1985-1989.
- [5]Hansen D, Bennedbaek FN, Hansen LK, Høier-Madsen M, Hegedü LS, Jacobsen BB, Husby S: High prevalence of coeliac disease in Danish children with type I diabetes mellitus. Acta Paediatr 2001, 90:1238-1243.
- [6]Mankaï A, Ben Hamouda H, Amri F, Ghedira-Besbes L, Harbi A, TaharSfar M, SahloulEssoussi A, Jeddi M, Ghedira I: Screening by anti-endomysium antibodies for celiac disease in Tunisian children with type 1 diabetes mellitus. Gastroenterol Clin Biol 2007, 31:462-466.
- [7]Ashabani A, Abushofa U, Abusrewill S, Abdelazez M, Tucková L, Tlaskalová-Hogenová H: The prevalence of coeliac disease in Libyan children with type 1 diabetes mellitus. Diabetes Metab Res Rev 2003, 19:69-75.
- [8]Al-Ashwal A, Shabib S, Sakati N, Attia N: Prevalence and characterstics of celiac disease in type 1 diabetes mellitus in Saudi Arabia. Saudi Med J 2003, 24:1113-1115.
- [9]Rostom A, Dubé C, Cranney A, Saloojee N, Sy R, Garritty C, Sampson M, Zhang L, Yazdi F, Mamaladze V, Pan I, McNeil J, Moher D, Mack D, Patel D: Celiac disease. Evid Rep Technol Assess (Summ) 2004, 104:1-6.
- [10]Saadah OI, Al-Agha AE, Al Nahdi HM, Bokhary RY, Bin Talib YY, Al-Mughales JA, Al Bokhari SM: Prevalence of celiac disease in children with type 1 diabetes mellitus screened by anti-tissue transglutaminase antibody from Western Saudi Arabia. Saudi Med J 2012, 33:541-546.
- [11]Dahlbom I, Korponay-Szabo IR, Kovacs JB, Szalai Z, Maki M, Hansson T: Prediction ofclinical and mucosal severity of coeliac disease and dermatitis herpetiformis by quantification of IgA/IgG serum antibodies to tissue transglutaminase. J Pediatr Gastroenterol Nutr 2010, 50:140-146.
- [12]Hill PG, Holmes GK: Coeliac disease: a biopsy is not always necessary for diagnosis. Aliment Pharmacol Ther 2008, 27:572-577.
- [13]Vivas S, de Morales JG R, Riestra S, Arias L, Fuentes D, Alvarez N, Calleja S, Hernando M, Herrero B, Casqueiro J, Rodrigo L: Duodenal biopsy may be avoided when high transglutaminase antibody titers are present. World J Gastroenterol 2009, 15:4775-4780.
- [14]Bizzaro N, Tampoia M, Villalta D, Platzgummer S, Liguori M, Tozzoli R, Tonutti E: Low specificity of anti-tissue transglutaminase antibodies in patients with primary biliary cirrhosis. J Clin Lab Anal 2006, 20:184-189.
- [15]Villalta D, Bizzaro N, Tonutti E, Tozzoli R: IgG anti-transglutaminase autoantibodies in systemic lupus erythematosus and Sjogren syndrome. Clin Chem 2002, 48:1133.
- [16]Vecsei A, Arenz T, Heilig G, Arenz S, Bufler P, Koletzko S: Influence of age and geneticrisk on anti-tissue transglutaminase IgA titers. J Pediatr Gastroenterol Nutr 2009, 48:544-549.
- [17]Marsh MN: Gluten, major histocompatibility complex, and the small intestine. A molecular and immunobiologic approach to the spectrum of gluten sensitivity ('celiac sprue'). Gastroenterology 1992, 102:330-354.
- [18]Rostami K, Kerckhaert J, Tiemessen R, von Blomberg BM, Meijer JW, Mulder CJ: Sensitivity of antiendomysium and antigliadin antibodies in untreated celiac disease: disappointing in clinical practice. Am J Gastroenterol 1999, 94:888-894.
- [19]Boudras G, Hachdef W, Benbouadbellah M, Belkadi M, Benmansour FZ, Touchami M: Prevalence of celiac disease in diabetic children and their first degree relatives in west Algeria—screening with serological markers. Acta Pediatr 1996, 412:58-60.
- [20]Wasertreguer S, Litwin N, Mora M: Enfermedad celı’aca asociada com diabetes mellitus insulinodependiente. Arch Arg Pediatr 1996, 94:10-13.
- [21]Amin R, Murphy N, Edge J, Ahmed ML, Acerini CL, Dunger DB: A longitudinal study of the effects of a gluten-free diet on glycemic control and weight gain in subjects with Type 1 diabetes and celiac disease. Diabetes Care 2002, 25:1117-1122.
- [22]Kaspers S, Kordonouri O, Schober E, Krause U, Schimmel U, Hauffa BP, Holl RW: Anthropometric parameters, metabolic control and thyroid autoimmunity in 127 biopsy-positive children and adolescents with Type 1 diabetes and celiac disease compared to 18,470 diabetic subjects without celiac disease. A multicenter survey. Diabetologia 2003, 44(Suppl):A232-A233.
- [23]Birgit R, Zdenek S, Edith S, Thomas W, Tadej B, Nina B, Kalman K, Jan L, Catarina L, Laszlo M, Roetloef J, Magdalena P, Gyula S: Screening Detected Celiac Disease in Children with Type 1 Diabetes Mellitus: Effect on the Clinical Course (A Case Control Study). J Pediatr Gastroenterol Nutr 2005, 41:317-321.
- [24]Buysschaert M, Tomasi JP, Hermans MP: Prospective screening for biopsy proven coeliac disease, autoimmunity and malabsorption markers in Belgian subjects with Type 1 diabetes. Diabet Med 2005, 22:889-892.
- [25]Fallahi GH, Ahmadian JH, Rabbani A, Yousefnezhad A, Reaei N: Screening for celiac disease in diabetic children from Iran. Ind Pediatr 2010, 47:268-270.
- [26]Shahbazkhani B, Faezi T, Akbari MR, Mohamadnejad M, Sotoudeh M, Rajab A, Tahaghoghi S, Malekzadeh R: Coeliac disease in Iranian type I diabetic patients. Dig Liver Dis 2004, 36:191-194.
- [27]Araújo J, da Silva GA, de Melo FM: Serum prevalence of celiac disease in children and adolescents with type 1 diabetes mellitus. J Pediatr (Rio J) 2006, 82:210-214.
- [28]Agrawal RP, Rathore A, Joshi A, Changal H, Kochar DK: Prevalence of celiac disease in type 1 diabetes mellitus in North West Rajasthan. India Diabet Res Clin Pract 2008, 79:e15-e16.
- [29]Holmes GKT: Coeliac disease and type 1 diabetes mellitus: the case for screening. Diabet Med 2001, 18:169-177.
- [30]Koletzko S, Burgin-Wolff A, Koletzko B, Knapp M, Burger W, Griineklee D, Herz G, Ruch W, Thon A, Wendel U, Zuppinger K: Prevalence of coeliac disease in diabetic children and adolescents. A multicenter study. Eur J Pediatr 1988, 148:113-117.
- [31]Crone J, Rami B, Huber W, Granditsch G, Schober E: Prevalence of Celiac Disease and Follow-up of EMA in Children and Adolescents with Type 1 Diabetes Mellitus. J Pediatr Gastroenterol Nutr 2003, 37:67-71.
- [32]Husby S, Koletzko S, Korponay-Szabó IR, Mearin ML, Phillips A, Shamir R, Troncone R, Giersiepen K, Branski D, Catassi C, Lelgeman M, Mäki M, Ribes-Koninckx C, Ventura A, Zimmer KP, ESPGHAN Working Group on Coeliac Disease Diagnosis; ESPGHAN Gastroenterology Committee: European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease. J Pediatr Gastroenterol Nutr 2012, 54:136-160.