TY - JOUR
T1 - Dietary fatty acid intake in childhood and the risk of islet autoimmunity and type 1 diabetes
T2 - The DIPP birth cohort study
AU - Hakola, Leena
AU - Vuorinen, Anna Leena
AU - Takkinen, Hanna Mari
AU - Niinistö, Sari
AU - Ahonen, Suvi
AU - Rautanen, Jenna
AU - Peltonen, Essi J.
AU - Nevalainen, Jaakko
AU - Ilonen, Jorma
AU - Toppari, Jorma
AU - Veijola, Riitta
AU - Knip, Mikael
AU - Virtanen, Suvi M.
N1 - Funding Information:
The study has been supported by: Academy of Finland (Grants 63672, 68292, 79685, 79686, 80846, 114666, 126813, 129492, 139391, 201988, 210632, 250114, 276475, 308066, 339922), Emil Aaltonen Foundation, Ella and Georg Ehrnrooth Foundation, European Foundation for the Study of Diabetes, Finnish Diabetes Association, Finnish Diabetes Research Foundation, Juho Vainio Foundation, JDRF (Grants 4-1998-274, 4-1999-731, 4-2001-435, 1-SRA-2016-342-M-R, 1-SRA-2019-732-M-B, and 3-SRA-2020-955-S-B), competitive state research financing of the expert responsibility area of Tampere University Hospital (Grants 9E082, 9F089, 9G087, 9H092, 9J147, 9K149, 9L042, 9L117, 9M036, 9M114, 9N086, 9P057, 9R055, 9S074, 9T072, 9U065, 9V072, 9X062, 9AA084), Oulu University Hospital research funds, Turku University Hospital governmental grants, the European Union (Grant BMH4-CT98-3314), the Novo Nordisk Foundation, and the Sigrid Juselius Foundation.
Publisher Copyright:
© 2022, The Author(s).
PY - 2023/3
Y1 - 2023/3
N2 - Purpose: The aim was to study the associations between dietary intake of fatty acids in childhood and the risk of islet autoimmunity and type 1 diabetes (T1D). Methods: The prospective Finnish Type 1 Diabetes Prediction and Prevention (DIPP) Study included children with genetic susceptibility to T1D born between 1996 and 2004. Participants were followed up every 3 to 12 months up to 6 years for diet, islet autoantibodies, and T1D. Dietary intake of several fatty acids at the age of 3 months to 6 years was assessed 1–8 times per participant with a 3-day food record. Joint models adjusted for energy intake, sex, HLA genotype and familial diabetes were used to investigate the associations of longitudinal intake of fatty acids and the development of islet autoimmunity and T1D. Results: During the 6-year follow-up, 247 (4.4%) children of 5626 developed islet autoimmunity and 94 (1.7%) children of 5674 developed T1D. Higher intake of monounsaturated fatty acids (HR 0.63; 95% CI 0.47, 0.82), arachidonic acid (0.69; 0.50, 0.94), total n-3 fatty acids (0.64; 0.48, 0.84), and long-chain n-3 fatty acids (0.14; 0.04, 0.43), was associated with a decreased risk of islet autoimmunity with and without energy adjustment. Higher intake of total fat (0.73; 0.53, 0.98), and saturated fatty acids (0.55; 0.33, 0.90) was associated with a decreased risk of T1D only when energy adjusted. Conclusion: Intake of several fatty acids was associated with a decreased risk of islet autoimmunity or T1D among high-risk children. Our findings support the idea that dietary factors, including n-3 fatty acids, may play a role in the disease process of T1D.
AB - Purpose: The aim was to study the associations between dietary intake of fatty acids in childhood and the risk of islet autoimmunity and type 1 diabetes (T1D). Methods: The prospective Finnish Type 1 Diabetes Prediction and Prevention (DIPP) Study included children with genetic susceptibility to T1D born between 1996 and 2004. Participants were followed up every 3 to 12 months up to 6 years for diet, islet autoantibodies, and T1D. Dietary intake of several fatty acids at the age of 3 months to 6 years was assessed 1–8 times per participant with a 3-day food record. Joint models adjusted for energy intake, sex, HLA genotype and familial diabetes were used to investigate the associations of longitudinal intake of fatty acids and the development of islet autoimmunity and T1D. Results: During the 6-year follow-up, 247 (4.4%) children of 5626 developed islet autoimmunity and 94 (1.7%) children of 5674 developed T1D. Higher intake of monounsaturated fatty acids (HR 0.63; 95% CI 0.47, 0.82), arachidonic acid (0.69; 0.50, 0.94), total n-3 fatty acids (0.64; 0.48, 0.84), and long-chain n-3 fatty acids (0.14; 0.04, 0.43), was associated with a decreased risk of islet autoimmunity with and without energy adjustment. Higher intake of total fat (0.73; 0.53, 0.98), and saturated fatty acids (0.55; 0.33, 0.90) was associated with a decreased risk of T1D only when energy adjusted. Conclusion: Intake of several fatty acids was associated with a decreased risk of islet autoimmunity or T1D among high-risk children. Our findings support the idea that dietary factors, including n-3 fatty acids, may play a role in the disease process of T1D.
KW - Autoimmune diseases
KW - Children Dietary intake
KW - Cohort study
KW - Diabetes mellitus, Type 1
KW - Fatty acids
KW - Autoimmunity
KW - Autoantibodies
KW - Fatty Acids
KW - Prospective Studies
KW - Humans
KW - Infant
KW - Diabetes Mellitus, Type 1
KW - Islets of Langerhans
KW - Child
KW - Fatty Acids, Omega-3
KW - Cohort Studies
UR - http://www.scopus.com/inward/record.url?scp=85141052087&partnerID=8YFLogxK
U2 - 10.1007/s00394-022-03035-2
DO - 10.1007/s00394-022-03035-2
M3 - Article
C2 - 36284022
AN - SCOPUS:85141052087
SN - 1436-6207
VL - 62
SP - 847
EP - 856
JO - European Journal of Nutrition
JF - European Journal of Nutrition
IS - 2
ER -