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Consumption of differently processed milk products in infancy and early childhood and the risk of islet autoimmunity

Jaakko Peltonen; Riitta Veijola; Mikael Knip; Jorma Toppari; Mari Åkerlund; Hanna-Mari Takkinen; Tuuli E. Korhonen; Sari Niinistö; Suvi M. Virtanen; Tapani Alatossava; Suvi Ahonen; Jorma Ilonen; Essi Syrjälä; Jaakko Nevalainen; Katariina Koivusaari

Consumption of differently processed milk products in infancy and early childhood and the risk of islet autoimmunity

Jaakko Peltonen
Riitta Veijola
Mikael Knip
Jorma Toppari
Mari Åkerlund
Hanna-Mari Takkinen
Tuuli E. Korhonen
Sari Niinistö
Suvi M. Virtanen
Tapani Alatossava
Suvi Ahonen
Jorma Ilonen
Essi Syrjälä
Jaakko Nevalainen
Katariina Koivusaari
Katso/Avaa
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CAMBRIDGE UNIV PRESS
doi:10.1017/S0007114520000744
URI
https://www.cambridge.org/core/journals/british-journal-of-nutrition/article/consumption-of-differently-processed-milk-products-in-infancy-and-early-childhood-and-the-risk-of-islet-autoimmunity/1BBA575807D1ABA8B93A8F9197995729/share/f1ea36795a193090a03a5fd0bfefb72373624a80
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2022021519282
Tiivistelmä
Several prospective studies have shown an association between cows' milk consumption and the risk of islet autoimmunity and/or type 1 diabetes. We wanted to study whether processing of milk plays a role. A population-based birth cohort of 6081 children with HLA-DQB1-conferred risk to type 1 diabetes was followed until the age of 15 years. We included 5545 children in the analyses. Food records were completed at the ages of 3 and 6 months and 1, 2, 3, 4 and 6 years, and diabetes-associated autoantibodies were measured at 3-12-month intervals. For milk products in the food composition database, we used conventional and processing-based classifications. We analysed the data using a joint model for longitudinal and time-to-event data. By the age of 6 years, islet autoimmunity developed in 246 children. Consumption of all cows' milk products together (energy-adjusted hazard ratio 1·06; 95 % CI 1·02, 1·11; P = 0·003), non-fermented milk products (1·06; 95 % CI 1·01, 1·10; P = 0·011) and fermented milk products (1·35; 95 % CI 1·10, 1·67; P = 0·005) was associated with an increased risk of islet autoimmunity. The early milk consumption was not associated with the risk beyond 6 years. We observed no clear differences based on milk homogenisation and heat treatment. Our results are consistent with the previous studies, which indicate that high milk consumption may cause islet autoimmunity in children at increased genetic risk. The study did not identify any specific type of milk processing that would clearly stand out as a sole risk factor apart from other milk products.
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