期刊论文详细信息
BMC Pediatrics
Early infections are associated with increased risk for celiac disease: an incident case-referent study
Anneli Ivarsson1  Hans Stenlund1  Lars-Åke Persson4  Marie-Louise Hammarström2  Leif Gothefors3  Olle Hernell3  Anna Myléus1 
[1] Epidemiology and Global Health, Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden;Immunology, Department of Clinical Microbiology, Umeå University, Umeå, Sweden;Pediatrics, Department of Clinical Sciences, Umeå University, Umeå, Sweden;International Maternal and Child Health, Department of Women's and Children's Health, Uppsala University, Uppsala, Sweden
关键词: Infants and children;    Infections;    Gluten amount;    Epidemiology;    Celiac disease;   
Others  :  1170592
DOI  :  10.1186/1471-2431-12-194
 received in 2012-04-04, accepted in 2012-11-29,  发布年份 2012
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【 摘 要 】

Background

Celiac disease is defined as a ‘chronic small intestinal immune-mediated enteropathy precipitated by exposure to dietary gluten in genetically predisposed individuals’. Sweden has experienced an “epidemic” of celiac disease in children below two years of age. Celiac disease etiology is considered multifactorial; however, little is known regarding potential risk- or protecting factors. We present data on the possible association between early infectious episodes and celiac disease, including their possible contribution to the Swedish celiac disease epidemic.

Methods

A population-based incident case-referent study (475 cases, 950 referents) with exposure information obtained via a questionnaire (including family characteristics, infant feeding, and the child’s general health) was performed. Celiac disease cases were diagnosed before two years of age, fulfilling the diagnostic criteria of the European Society for Pediatric Gastroenterology, Hepatology and Nutrition. Referents were randomly selected from the national population register after fulfilling matching criteria. The final analyses included 954 children, 373 (79%) cases and 581 (61%) referents, with complete information on main variables of interest in a matched set of one case with one or two referents.

Results

Having three or more parental-reported infectious episodes, regardless of type of infection, during the first six months of life was associated with a significantly increased risk for later celiac disease, and this remained after adjusting for infant feeding and socioeconomic status (odds ratio [OR] 1.5; 95% confidence interval [CI], 1.1-2.0; P=0.014). The celiac disease risk increased synergistically if, in addition to having several infectious episodes, infants were introduced to dietary gluten in large amounts, compared to small or medium amounts, after breastfeeding was discontinued (OR 5.6; 95% CI, 3.1-10; P<0.001).

Conclusion

This study suggests that having repeated infectious episodes early in life increases the risk for later celiac disease. In addition, we found a synergistic effect between early infections and daily amount of gluten intake, more pronounced among infants for whom breastfeeding had been discontinued prior to gluten introduction. Regarding contribution to the Swedish celiac disease epidemic, which partly was attributed to concurrent changes in infant feeding, early infections probably made a minor contribution via the synergistic effect with gluten amount.

【 授权许可】

   
2012 Myleus et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Ludvigsson JF, Leffler DA, Bai JC, Biagi F, Fasano A, Green PH, Hadjivassiliou M, Kaukinen K, Kelly CP, Leonard JN, et al.: The Oslo definitions for coeliac disease and related terms. Gut 2013, 62(1):43-52.
  • [2]Green PH, Cellier C: Celiac disease. N Engl J Med 2007, 357(17):1731-1743.
  • [3]Lionetti E, Catassi C: New clues in celiac disease epidemiology, pathogenesis, clinical manifestations, and treatment. Int Rev Immunol 2011, 30(4):219-231.
  • [4]Dube C, Rostom A, Sy R, Cranney A, Saloojee N, Garritty C, Sampson M, Zhang L, Yazdi F, Mamaladze V, et al.: The prevalence of celiac disease in average-risk and at-risk Western European populations: a systematic review. Gastroenterology 2005, 128(4 Suppl 1):S57-67.
  • [5]Mustalahti K, Catassi C, Reunanen A, Fabiani E, Heier M, McMillan S, Murray L, Metzger MH, Gasparin M, Bravi E, et al.: The prevalence of celiac disease in Europe: results of a centralized, international mass screening project. Ann Med 2010, 42(8):587-595.
  • [6]Myleus A, Ivarsson A, Webb C, Danielsson L, Hernell O, Hogberg L, Karlsson E, Lagerqvist C, Norstrom F, Rosen A, et al.: Celiac disease revealed in 3% of Swedish 12-year-olds born during an epidemic. J Pediatr Gastroenterol Nutr 2009, 49(2):170-176.
  • [7]Ivarsson A, Persson LA, Nystrom L, Ascher H, Cavell B, Danielsson L, Dannaeus A, Lindberg T, Lindquist B, Stenhammar L, et al.: Epidemic of coeliac disease in Swedish children. Acta Paediatr 2000, 89(2):165-171.
  • [8]Olsson C, Hernell O, Hornell A, Lonnberg G, Ivarsson A: Difference in celiac disease risk between Swedish birth cohorts suggests an opportunity for primary prevention. Pediatrics 2008, 122(3):528-534.
  • [9]Ivarsson A, Hernell O, Stenlund H, Persson LA: Breast-feeding protects against celiac disease. Am J Clin Nutr 2002, 75(5):914-921.
  • [10]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.
  • [11]Ivarsson A, Hernell O, Nystrom L, Persson LA: Children born in the summer have increased risk for coeliac disease. J Epidemiol Community Health 2003, 57(1):36-39.
  • [12]Lewy H, Meirson H, Laron Z: Seasonality of birth month of children with celiac disease differs from that in the general population and between sexes and is linked to family history and environmental factors. J Pediatr Gastroenterol Nutr 2009, 48(2):181-185.
  • [13]Sandberg-Bennich S, Dahlquist G, Kallen B: Coeliac disease is associated with intrauterine growth and neonatal infections. Acta Paediatr 2002, 91(1):30-33.
  • [14]Stene LC, Honeyman MC, Hoffenberg EJ, Haas JE, Sokol RJ, Emery L, Taki I, Norris JM, Erlich HA, Eisenbarth GS, et al.: Rotavirus infection frequency and risk of celiac disease autoimmunity in early childhood: a longitudinal study. Am J Gastroenterol 2006, 101(10):2333-2340.
  • [15]Wingren CJ, Bjorck S, Lynch KF, Ohlsson H, Agardh D, Merlo J: Coeliac disease in children: a social epidemiological study in Sweden. Acta Paediatr 2011, 101(2):185-191.
  • [16]Olen O, Bihagen E, Rasmussen F, Ludvigsson JF: Socioeconomic position and education in patients with coeliac disease. Dig Liver Dis 2012, 44(6):471-476.
  • [17]Holm S, Andersson Y, Gothefors L, Lindberg T: Increased protein absorption after acute gastroenteritis in children. Acta Paediatr 1992, 81(8):585-588.
  • [18]Marild K, Stephansson O, Montgomery S, Murray JA, Ludvigsson JF: Pregnancy outcome and risk of celiac disease in offspring: a nationwide case–control study. Gastroenterology 2011, 142(1):39-45 e33.
  • [19]Welander A, Tjernberg AR, Montgomery SM, Ludvigsson J, Ludvigsson JF: Infectious disease and risk of later celiac disease in childhood. Pediatrics 2010, 125(3):e530-536.
  • [20]Statistics Swedenhttp://www.scb.se webcite.
  • [21]Swedish Socioeconomic Classification; Standard for Socioeconomic Index (SEI)http://www.scb.se/sei webcite.
  • [22]Ivarsson A: On the multifactorial etiology of celiac disease: An epidemiological approach to the Swedish epidemic. Umeå: Department of Clinical Sciences, Pediatrics. Umeå University; 2001. Dissertation]
  • [23]Ivarsson A: The Swedish epidemic of coeliac disease explored using an epidemiological approach–some lessons to be learnt. Best Pract Res Clin Gastroenterol 2005, 19(3):425-440.
  • [24]Ivarsson A, Myleus A, Wall S: Towards preventing celiac disease - An epidemiological approach. In Frontiers in celiac disease Pediatr Adolesc Med. 12th edition. Edited by Fasano A, Troncone R, Branski D. Basel: Krager; 2008:198-209.
  • [25]Ivarsson A, Persson LA, Hernell O: Primary prevention of coeliac disease by favourable infant feeding practices. In: Primary prevention of coeliac disease - The utopia of the new millenium. In Perspectives on coeliac disease. Edited by Catassi C, Fasano A, Corazza GR. Pisa: AIC Press; 2003:43-60.
  • [26]Troncone R, Ivarsson A, Szajewska H, Mearin ML: Review article: future research on coeliac disease - a position report from the European multistakeholder platform on coeliac disease (CDEUSSA). Aliment Pharmacol Ther 2008, 27(11):1030-1043.
  • [27]Hernell O, Forsberg G, Hammarstrom ML, Hammarstrom S, Ivarsson A: Celiac disease: Effect of weaning on disease risk. In Feeding during late infancy and early childhood: impact on health. Nestlé Nutrition Workshop Series, Pediatric Program. 56th edition. Edited by Hernell O, Schmitz J. Denges: Les Presses de la Venoge; 2005:27-38.
  • [28]Roberts SE, Williams JG, Meddings D, Davidson R, Goldacre MJ: Perinatal risk factors and coeliac disease in children and young adults: a record linkage study. Aliment Pharmacol Ther 2009, 29(2):222-231.
  • [29]Kondrashova A, Mustalahti K, Kaukinen K, Viskari H, Volodicheva V, Haapala AM, Ilonen J, Knip M, Maki M, Hyoty H: Lower economic status and inferior hygienic environment may protect against celiac disease. Ann Med 2008, 40(3):223-231.
  • [30]Van Damme P, Giaquinto C, Huet F, Gothefors L, Maxwell M, Van der Wielen M: Multicenter prospective study of the burden of rotavirus acute gastroenteritis in Europe, 2004–2005: the REVEAL study. J Infect Dis 2007, 195(Suppl 1):S4-S16.
  • [31]Marild K, Fredlund H, Ludvigsson JF: Increased risk of hospital admission for influenza in patients with celiac disease: a nationwide cohort study in Sweden. Am J Gastroenterol 2010, 105(11):2465-2473.
  • [32]Decker E, Engelmann G, Findeisen A, Gerner P, Laass M, Ney D, Posovszky C, Hoy L, Hornef MW: Cesarean delivery is associated with celiac disease but not inflammatory bowel disease in children. Pediatrics 2010, 125(6):e1433-1440.
  • [33]Sanz Y, De Pama G, Laparra M: Unraveling the ties between celiac disease and intestinal microbiota. Int Rev Immunol 2011, 30(4):207-218.
  • [34]Sanchez E, Laparra JM, Sanz Y: Discerning the Role of Bacteroides fragilis in Celiac Disease Pathogenesis. Appl Environ Microbiol 2012, 78(18):6507-6515.
  • [35]Sanchez E, Ribes-Koninckx C, Calabuig M, Sanz Y: Intestinal Staphylococcus spp. and virulent features associated with coeliac disease. J Clin Pathol 2012, 65(9):830-834.
  • [36]Tjellstrom B, Stenhammar L, Hogberg L, Falth-Magnusson K, Magnusson KE, Midtvedt T, Sundqvist T, Norin E: Gut microflora associated characteristics in children with celiac disease. Am J Gastroenterol 2005, 100(12):2784-2788.
  • [37]Verhasselt V: Oral tolerance in neonates: from basics to potential prevention of allergic disease. Mucosal Immunol 2010, 3(4):326-333.
  • [38]Willing BP, Gill N, Finlay BB: The role of the immune system in regulating the microbiota. Gut Microbes 2011, 1(4):213-223.
  • [39]Willing BP, Russell SL, Finlay BB: Shifting the balance: antibiotic effects on host-microbiota mutualism. Nat Rev Microbiol 2011, 9(4):233-243.
  • [40]Myleus A, Stenlund H, Hernell O, Gothefors L, Hammarstrom ML, Persson LA, Ivarsson A: Early vaccinations are not risk factors for celiac disease. Pediatrics 2012, 130(1):e63-70.
  • [41]Forsberg G, Fahlgren A, Horstedt P, Hammarstrom S, Hernell O, Hammarstrom ML: Presence of bacteria and innate immunity of intestinal epithelium in childhood celiac disease. Am J Gastroenterol 2004, 99(5):894-904.
  • [42]Ou G, Hedberg M, Horstedt P, Baranov V, Forsberg G, Drobni M, Sandstrom O, Wai SN, Johansson I, Hammarstrom ML, et al.: Proximal small intestinal microbiota and identification of rod-shaped bacteria associated with childhood celiac disease. Am J Gastroenterol 2009, 104(12):3058-3067.
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