Maternal and child gluten intake and association with type 1 diabetes: The Norwegian Mother and Child Cohort Study
Autoři:
Nicolai A. Lund-Blix aff001; German Tapia aff001; Karl Mårild aff001; Anne Lise Brantsaeter aff004; Pål R. Njølstad aff005; Geir Joner aff002; Torild Skrivarhaug aff002; Ketil Størdal aff001; Lars C. Stene aff001
Působiště autorů:
Department of Chronic Diseases and Ageing, Norwegian Institute of Public Health, Oslo, Norway
aff001; Department of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway
aff002; Department of Paediatrics, The Sahlgrenska Academy at University of Gothenburg and Queen Silvia Children’s Hospital, Gothenburg, Sweden
aff003; Department of Environmental Exposure and Epidemiology, Norwegian Institute of Public Health, Oslo, Norway
aff004; Department of Paediatric and Adolescent Medicine, Haukeland University Hospital, Bergen, Norway
aff005; KG Jebsen Center for Diabetes Research, Department of Clinical Science, University of Bergen, Bergen, Norway
aff006; Institute of Clinical Medicine, University of Oslo, Oslo, Norway
aff007; Department of Paediatrics, Østfold Hospital Trust, Grålum, Norway
aff008
Vyšlo v časopise:
Maternal and child gluten intake and association with type 1 diabetes: The Norwegian Mother and Child Cohort Study. PLoS Med 17(3): e32767. doi:10.1371/journal.pmed.1003032
Kategorie:
Research Article
doi:
https://doi.org/10.1371/journal.pmed.1003032
Souhrn
Background
The relationship between maternal gluten intake in pregnancy, offspring intake in childhood, and offspring risk of type 1 diabetes has not been examined jointly in any studies. Our aim was to study the relationship between maternal and child intake of gluten and risk of type 1 diabetes in children.
Methods and findings
We included 86,306 children in an observational nationwide cohort study, the Norwegian Mother and Child Cohort Study (MoBa), with recruitment from 1999 to 2008 and with follow-up time to April 15, 2018. We used registration of type 1 diabetes in the Norwegian childhood diabetes registry as the outcome. We used Cox proportional hazard regression to estimate hazard ratios (HRs) for the mother’s intake of gluten up to week 22 of pregnancy and offspring gluten intake when the child was 18 months old. The average time followed was 12.3 years (0.70–16.0). A total of 346 children (0.4%) children were diagnosed with type 1 diabetes, resulting in an incidence rate of 32.6/100,000 person-years. Mean gluten intake per day was 13.6 g for mothers and 8.8 g for children. There was no association between the mother’s intake of gluten in pregnancy and offspring type 1 diabetes, with an adjusted HR (aHR) of 1.02 (95% confidence interval [CI] 0.73–1.43, p = 0.91) for each 10-g-per-day increment. There was an association between offspring intake of gluten and a higher risk of type 1 diabetes, with an aHR of 1.46 (95% CI 1.06–2.01, p = 0.02) for each 10-g-per-day increment. Among the limitations are the likely imprecision in estimation of gluten intake and that we only had information regarding gluten intake at 2 time points in early life.
Conclusions
Our results show that, while the mother’s intake of gluten in pregnancy was not associated with type 1 diabetes, a higher intake of gluten by the child at an early age may give a higher risk of type 1 diabetes.
Klíčová slova:
Autoimmunity – Cohort studies – diabetes mellitus – Gluten – Child health – Norwegian people – Pregnancy – Questionnaires
Zdroje
1. Patterson CC, Harjutsalo V, Rosenbauer J, Neu A, Cinek O, Skrivarhaug T, et al. Trends and cyclical variation in the incidence of childhood type 1 diabetes in 26 European centres in the 25 year period 1989–2013: a multicentre prospective registration study. Diabetologia. 2018.
2. Atkinson MA, Eisenbarth GS, Michels AW. Type 1 diabetes. Lancet. 2014;383(9911):69–82. doi: 10.1016/S0140-6736(13)60591-7 23890997
3. Antvorskov JC, Josefsen K, Engkilde K, Funda DP, Buschard K. Dietary gluten and the development of type 1 diabetes. Diabetologia. 2014;57(9):1770–80. doi: 10.1007/s00125-014-3265-1 24871322
4. Norris JM, Barriga K, Klingensmith G, Hoffman M, Eisenbarth GS, Erlich HA, et al. Timing of initial cereal exposure in infancy and risk of islet autoimmunity. JAMA. 2003;290(13):1713–20. doi: 10.1001/jama.290.13.1713 14519705
5. 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(13):1721–8. doi: 10.1001/jama.290.13.1721 14519706
6. Frederiksen B, Kroehl M, Lamb MM, Seifert J, Barriga K, Eisenbarth GS, et al. Infant exposures and development of type 1 diabetes mellitus: The Diabetes Autoimmunity Study in the Young (DAISY). JAMA Pediatr. 2013;167(9):808–15. doi: 10.1001/jamapediatrics.2013.317 23836309
7. Lund-Blix NA, Stene LC, Rasmussen T, Torjesen PA, Andersen LF, Rønningen KS. Infant feeding in relation to islet autoimmunity and type 1 diabetes in genetically susceptible children: the MIDIA Study. Diabetes Care. 2015;38(2):257–63. doi: 10.2337/dc14-1130 25422170
8. Chmiel R, Beyerlein A, Knopff A, Hummel S, Ziegler AG, Winkler C. Early infant feeding and risk of developing islet autoimmunity and type 1 diabetes. Acta Diabetol. 2015;52(3):621–4. doi: 10.1007/s00592-014-0628-5 25038720
9. Hakola L, Takkinen HM, Niinistö S, Ahonen S, Nevalainen J, Veijola R, et al. Infant Feeding in Relation to the Risk of Advanced Islet Autoimmunity and Type 1 Diabetes in Children With Increased Genetic Susceptibility: A Cohort Study. Am J Epidemiol. 2018;187(1):34–44. doi: 10.1093/aje/kwx191 29309515
10. Uusitalo U, Lee HS, Andrén Aronsson C, Vehik K, Yang J, Hummel S, et al. Early Infant Diet and Islet Autoimmunity in the TEDDY Study. Diabetes Care. 2018;41(3):522–30. doi: 10.2337/dc17-1983 29343517
11. Lund-Blix NA, Dydensborg Sander S, Størdal K, Nybo Andersen AM, Rønningen KS, Joner G, et al. Infant Feeding and Risk of Type 1 Diabetes in Two Large Scandinavian Birth Cohorts. Diabetes Care. 2017;40(7):920–7. doi: 10.2337/dc17-0016 28487451
12. Lamb MM, Myers MA, Barriga K, Zimmet PZ, Rewers M, Norris JM. Maternal diet during pregnancy and islet autoimmunity in offspring. Pediatr Diabetes. 2008;9(2):135–41. doi: 10.1111/j.1399-5448.2007.00311.x 18221424
13. Virtanen SM, Uusitalo L, Kenward MG, Nevalainen J, Uusitalo U, Kronberg-Kippilä C, et al. Maternal food consumption during pregnancy and risk of advanced beta-cell autoimmunity in the offspring. Pediatr Diabetes. 2011;12(2):95–9. doi: 10.1111/j.1399-5448.2010.00668.x 21352426
14. Antvorskov JC, Halldorsson TI, Josefsen K, Svensson J, Granström C, Roep BO, et al. Association between maternal gluten intake and type 1 diabetes in offspring: national prospective cohort study in Denmark. BMJ. 2018;362:k3547. doi: 10.1136/bmj.k3547 30232082
15. Magnus P, Birke C, Vejrup K, Haugan A, Alsaker E, Daltveit AK, et al. Cohort Profile Update: The Norwegian Mother and Child Cohort Study (MoBa). Int J Epidemiol. 2016;45(2):382–8. doi: 10.1093/ije/dyw029 27063603
16. Brantsaeter AL, Haugen M, Alexander J, Meltzer HM. Validity of a new food frequency questionnaire for pregnant women in the Norwegian Mother and Child Cohort Study (MoBa). Matern Child Nutr. 2008;4(1):28–43. doi: 10.1111/j.1740-8709.2007.00103.x 18171405
17. Norwegian Food Safety Authority, University of Oslo, Norwegian Directorate of Health. Weights, measures and portion sizes for foods. Oslo: Norwegian Food Safety Authority, University of Oslo and Norwegian Directorate of Health; 2015.
18. Norwegian Food Composition Database 2018 [Internet]. Norwegian Food Safety Authority. Available from: www.matvaretabellen.no. [1 December 2018].
19. Lebwohl B, Cao Y, Zong G, Hu FB, Green PHR, Neugut AI, et al. Long term gluten consumption in adults without celiac disease and risk of coronary heart disease: prospective cohort study. BMJ. 2017;357:j1892. doi: 10.1136/bmj.j1892 28465308
20. Kasarda DD. Can an increase in celiac disease be attributed to an increase in the gluten content of wheat as a consequence of wheat breeding? J Agric Food Chem. 2013;61(6):1155–9. doi: 10.1021/jf305122s 23311690
21. van Overbeek FM, Uil-Dieterman IG, Mol IW, Köhler-Brands L, Heymans HS, Mulder CJ. The daily gluten intake in relatives of patients with coeliac disease compared with that of the general Dutch population. Eur J Gastroenterol Hepatol. 1997;9(11):1097–9. doi: 10.1097/00042737-199711000-00013 9431901
22. Gellrich C, Schieberle P, Weiser H. Biochemical characterization and quantification of the storage protein (secalin) types in rye flour. Cereal Chem. 2003(80):102–9.
23. Ellis HJ, Freedman AR, Ciclitira PJ. Detection and estimation of the barley prolamin content of beer and malt to assess their suitability for patients with coeliac disease. Clin Chim Acta. 1990;189(2):123–30. doi: 10.1016/0009-8981(90)90082-4 2204500
24. Skrivarhaug T, Stene LC, Drivvoll AK, Strøm H, Joner G. Incidence of type 1 diabetes in Norway among children aged 0–14 years between 1989 and 2012: has the incidence stopped rising? Results from the Norwegian Childhood Diabetes Registry. Diabetologia. 2014;57(1):57–62. doi: 10.1007/s00125-013-3090-y 24149838
25. Mårild K, Kahrs CR, Tapia G, Stene LC, Størdal K. Infections and risk of celiac disease in childhood: a prospective nationwide cohort study. Am J Gastroenterol. 2015;110(10):1475–84. doi: 10.1038/ajg.2015.287 26346866
26. Størdal K, Haugen M, Brantsæter AL, Lundin KE, Stene LC. Association between maternal iron supplementation during pregnancy and risk of celiac disease in children. Clin Gastroenterol Hepatol. 2014;12(4):624–31.e1-2. doi: 10.1016/j.cgh.2013.09.061 24112997
27. Cummings P. Missing data and multiple imputation. JAMA Pediatr. 2013;167(7):656–61. doi: 10.1001/jamapediatrics.2013.1329 23699969
28. Hakola L, Miettinen ME, Syrjälä E, Åkerlund M, Takkinen HM, Korhonen TE, et al. Association of Cereal, Gluten, and Dietary Fiber Intake With Islet Autoimmunity and Type 1 Diabetes. JAMA Pediatr. 2019.
29. Lund-Blix NA, Dong F, Mårild K, Barón AE, Seifert J, Waugh KC, et al. Gluten Intake and Risk of Islet Autoimmunity and Progression to Type 1 Diabetes in Children at Increased Risk of the Disease: The Diabetes Autoimmunity Study in the Young (DAISY). Diabetes Care. 2019;42(5):789–96. doi: 10.2337/dc18-2315 30796108
30. Andrén Aronsson C, Lee HS, Hård Af Segerstad EM, Uusitalo U, Yang J, Koletzko S, et al. Association of Gluten Intake During the First 5 Years of Life With Incidence of Celiac Disease Autoimmunity and Celiac Disease Among Children at Increased Risk. JAMA. 2019;322(6):514–23. doi: 10.1001/jama.2019.10329 31408136
31. Mårild K, Dong F, Lund-Blix NA, Seifert J, Barón AE, Waugh KC, et al. Gluten Intake and Risk of Celiac Disease: Long-Term Follow-up of an At-Risk Birth Cohort. Am J Gastroenterol. 2019;114(8):1307–14. doi: 10.14309/ajg.0000000000000255 31082869
32. Lund-Blix NA, Mårild K, Tapia G, Norris JM, Stene LC, Størdal K. Gluten Intake in Early Childhood and Risk of Celiac Disease in Childhood. Am J Gastroenterol. 2019;114(8):1299–306. doi: 10.14309/ajg.0000000000000331 31343439
33. Reynolds AN, Mann J. Re: Association between maternal gluten intake and type 1 diabetes in offspring: national prospective cohort study in Denmark. BMJ [Internet]. 2018. Available from: https://www.bmj.com/content/362/bmj.k3547/rr-0. [1 December 2018].
34. Magnus MC, Olsen SF, Granström C, Joner G, Skrivarhaug T, Svensson J, et al. Infant Growth and Risk of Childhood-Onset Type 1 Diabetes in Children From 2 Scandinavian Birth Cohorts. JAMA Pediatr. 2015;169(12):e153759. doi: 10.1001/jamapediatrics.2015.3759 26642117
35. Virtanen SM. Dietary factors in the development of type 1 diabetes. Pediatr Diabetes. 2016;17 Suppl 22:49–55.
36. Crespo-Escobar P, Mearin ML, Hervás D, Auricchio R, Castillejo G, Gyimesi J, et al. The role of gluten consumption at an early age in celiac disease development: a further analysis of the prospective PreventCD cohort study. Am J Clin Nutr. 2017;105(4):890–6. doi: 10.3945/ajcn.116.144352 28228423
37. Vriezinga SL, Auricchio R, Bravi E, Castillejo G, Chmielewska A, Crespo Escobar P, et al. Randomized feeding intervention in infants at high risk for celiac disease. N Engl J Med. 2014;371(14):1304–15. doi: 10.1056/NEJMoa1404172 25271603
38. Aronsson CA, Lee HS, Koletzko S, Uusitalo U, Yang J, Virtanen SM, et al. Effects of Gluten Intake on Risk of Celiac Disease: A Case-Control Study on a Swedish Birth Cohort. Clin Gastroenterol Hepatol. 2015.
39. Hoppe C, Trolle E, Gondolf UH, Husby S. Gluten intake in 6-36-month-old Danish infants and children based on a national survey. J Nutr Sci. 2013;2:e7. doi: 10.1017/jns.2013.1 25191593
40. Nilsen RM, Vollset SE, Gjessing HK, Skjærven R, Melve KK, Schreuder P, et al. Self-selection and bias in a large prospective pregnancy cohort in Norway. Paediatr Perinat Epidemiol. 2009;23(6):597–608. doi: 10.1111/j.1365-3016.2009.01062.x 19840297
41. Bosi E, Molteni L, Radaelli MG, Folini L, Fermo I, Bazzigaluppi E, et al. Increased intestinal permeability precedes clinical onset of type 1 diabetes. Diabetologia. 2006;49(12):2824–7. doi: 10.1007/s00125-006-0465-3 17028899
42. Stewart CJ, Ajami NJ, O'Brien JL, Hutchinson DS, Smith DP, Wong MC, et al. Temporal development of the gut microbiome in early childhood from the TEDDY study. Nature. 2018;562(7728):583–8. doi: 10.1038/s41586-018-0617-x 30356187
43. Krischer JP, Lynch KF, Schatz DA, Ilonen J, Lernmark Å, Hagopian WA, et al. The 6 year incidence of diabetes-associated autoantibodies in genetically at-risk children: the TEDDY study. Diabetologia. 2015;58(5):980–7. doi: 10.1007/s00125-015-3514-y 25660258
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