{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Oluwagbemigun K"],"funding":["Bundesministerium für Bildung und Forschung","Ministry of Science and Research of North Rhine Westphalia","Science Foundation Ireland"],"pagination":["647-656"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7948843"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["113(3)"],"pubmed_abstract":["<h4>Background</h4>Gut microbiota composition as influenced by long-term diet may be associated with the risk of adult chronic diseases. Thus, establishing the relation of long-term diet, particularly starting from early life, with adult microbiota composition would be an important research advance.<h4>Objective</h4>We aimed to investigate the association of long-term intake of energy, carbohydrate, fiber, protein, and fat from infancy to late adolescence with microbiota composition in adulthood.<h4>Methods</h4>Within the prospective DOrtmund Nutritional and Anthropometric Longitudinally Designed (DONALD) Study, we sampled stool 1 or 2 times within 1 y from 128 adults (median age: 29 y). Microbiota composition was profiled by 16S ribosomal RNA sequencing. Annual dietary records from age 1 to 18 y were retrieved. We estimated trajectories of energy, energy-adjusted carbohydrate, fiber, protein, and fat intake with multilevel models, producing predicted intake at age 1 y and rates of change in intake. A multivariate, zero-inflated, logistic-normal model was used to model the association between intake trajectories and the composition of 158 genera in single-sampled individuals. Associations found in this model were confirmed in double-sampled individuals using a zero-inflated Beta regression model.<h4>Results</h4>Adjusting for covariates and temporal differences in microbiota composition, long-term carbohydrate intake was associated with 3 genera. Specifically, carbohydrate intake at age 1 y was negatively associated with Phascolarctobacterium [coefficient = -4.31; false discovery rate (FDR)-adjusted P = 0.006] and positively associated with Dialister (coefficient = 3.06; FDR-adjusted P = 0.003), and the rate of change in carbohydrate intake was positively associated with Desulfovibrio (coefficient = 13.16; FDR-adjusted P = 0.00039). Energy and other macronutrients were not associated with any genus.<h4>Conclusions</h4>This work links long-term carbohydrate intake to microbiota composition. Considering the associations of high carbohydrate intake and microbiota composition with some diseases, these findings could inform the development of gut microbiota-targeted dietary recommendations for disease prevention."],"journal":["The American journal of clinical nutrition"],"pubmed_title":["Long-term dietary intake from infancy to late adolescence is associated with gut microbiota composition in young adulthood."],"pmcid":["PMC7948843"],"funding_grant_id":["01EA1809A","16/ERA-HDHL/3362"],"pubmed_authors":["Lyons K","Cryan J","Nothlings U","Clarke G","Oluwagbemigun K","Alexy U","Stanton C","Berding K","Schmid M","O'Donovan AN"],"additional_accession":[]},"is_claimable":false,"name":"Long-term dietary intake from infancy to late adolescence is associated with gut microbiota composition in young adulthood.","description":"<h4>Background</h4>Gut microbiota composition as influenced by long-term diet may be associated with the risk of adult chronic diseases. Thus, establishing the relation of long-term diet, particularly starting from early life, with adult microbiota composition would be an important research advance.<h4>Objective</h4>We aimed to investigate the association of long-term intake of energy, carbohydrate, fiber, protein, and fat from infancy to late adolescence with microbiota composition in adulthood.<h4>Methods</h4>Within the prospective DOrtmund Nutritional and Anthropometric Longitudinally Designed (DONALD) Study, we sampled stool 1 or 2 times within 1 y from 128 adults (median age: 29 y). Microbiota composition was profiled by 16S ribosomal RNA sequencing. Annual dietary records from age 1 to 18 y were retrieved. We estimated trajectories of energy, energy-adjusted carbohydrate, fiber, protein, and fat intake with multilevel models, producing predicted intake at age 1 y and rates of change in intake. A multivariate, zero-inflated, logistic-normal model was used to model the association between intake trajectories and the composition of 158 genera in single-sampled individuals. Associations found in this model were confirmed in double-sampled individuals using a zero-inflated Beta regression model.<h4>Results</h4>Adjusting for covariates and temporal differences in microbiota composition, long-term carbohydrate intake was associated with 3 genera. Specifically, carbohydrate intake at age 1 y was negatively associated with Phascolarctobacterium [coefficient = -4.31; false discovery rate (FDR)-adjusted P = 0.006] and positively associated with Dialister (coefficient = 3.06; FDR-adjusted P = 0.003), and the rate of change in carbohydrate intake was positively associated with Desulfovibrio (coefficient = 13.16; FDR-adjusted P = 0.00039). Energy and other macronutrients were not associated with any genus.<h4>Conclusions</h4>This work links long-term carbohydrate intake to microbiota composition. Considering the associations of high carbohydrate intake and microbiota composition with some diseases, these findings could inform the development of gut microbiota-targeted dietary recommendations for disease prevention.","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021 Mar","modification":"2025-04-26T11:54:10.587Z","creation":"2025-04-06T13:47:25.747Z"},"accession":"S-EPMC7948843","cross_references":{"pubmed":["33471048"],"doi":["10.1093/ajcn/nqaa340"]}}