The Gut Microbiome and Personalized Mediterranean Diet Interventions for Cardiometabolic Disease Prevention
The Gut Microbiome and Personalized Mediterranean Diet Interventions for Cardiometabolic Disease Prevention
批准号:
10493258
负责人:
Dong Wang
金额:
$72.61万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-09-23 至 2026-06-30
关键词:
16S ribosomal RNA sequencingAddressAdherenceAutologousBiochemicalBiologicalBiological MarkersBody WeightBody Weight decreasedButyratesCardiometabolic DiseaseCardiovascular DiseasesCohort StudiesDataDevelopmentDietDietary InterventionDietary LeadEnzymesFecesFoodFoundationsGenetic TranscriptionHealthIndividualIndividual DifferencesInterventionIntervention StudiesIntervention TrialIsraelLeadLipidsMedicineMediterranean DietMemoryMetagenomicsMicrobeNatureNon-Insulin-Dependent Diabetes MellitusNutritional StudyObesityOutcomeParticipantPersonsPlasmaPopulationPreventionPrevotellaProductionPublishingRandomizedRandomized Controlled TrialsRecommendationReportingReproducibilityResearchResearch DesignResearch PriorityResolutionResourcesRoleShotgunsStrategic PlanningSubgroupTNF geneTaxonomyTechnologyTestingTimeTranslationsUnited States National Institutes of HealthVisceral fatVolatile Fatty Acidsauthoritybasebiobehaviorburden of illnesscardiometabolic riskcardiometabolismcost efficientdesigndietarydisorder preventiondisorder riskepidemiology studyexperiencefasting glucosefecal transplantationfollow-upgut microbiomegut microbiotaimprovedindividual variationinsightinter-individual variationintervention effectmetabolomicsmetatranscriptomicsmicrobialmicrobiome researchnovelpersonalized approachpost interventionprecision nutritionpreservationprospectiveprotective effectresponsetrimethyloxamine
中文摘要
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英文摘要
PROJECT SUMMARY
Many authorities recommend the Mediterranean diet (MedDiet) for the prevention of cardiometabolic disease.
These dietary recommendations are based on population averages and may not be best suited for a given
individual. Preliminary data from our group and others support that a specific dietary intervention may have highly
variable effects in different individuals due to the individual composition of the gut microbiome. Furthermore, we
recently reported that autologous fecal microbiota transplantation (aFMT) derived from the time of maximal
weight reduction enhanced the effects of MedDiet on maintaining cardiometabolic health in an RCT. This
background supports our central hypothesis that the gut microbiome can modify the effects of MedDiet on
cardiometabolic disease risk. However, no studies have utilized longitudinally collected data from RCTs to test
this hypothesis. Most diet-microbiome studies are limited by the use of 16S rRNA gene sequencing yielding only
very general taxonomic profiling, thus omitting strain-specific diet-related biochemical functions of microbes. To
gain more advanced mechanistic insights, combining shotgun metagenomics and metatranscriptomics and
metabolomics in an integrated framework presents a unique opportunity to probe both the composition and
functionality of gut microbial communities. This proposed project will leverage two long-term dietary RCTs, the
recently completed 18-month DIRECT-PLUS trial of 294 participants and the ongoing 3-year MIND trial of 604
participants, to examine whether individual gut microbial features modify the effects of MedDiet interventions on
cardiometabolic risk and body adiposity (Aim 1) and identify metabolites in feces and metabolites in plasma of
gut microbial origin that explain inter-individual differences in post-intervention changes in cardiometabolic risk
and adiposity (Aim 2) in the DIRECT-PLUS trial. Findings from Aims 1 and 2 will be tested for replication in the
MIND trial. In Aim 3, we will investigate long-lasting, post-intervention effects of combined MedDiet and aFMT,
and characterize gut microbial changes during and after the interventions in an RCT of 90 participants. Our
proposal addresses a major research priority, precision nutrition, emphasized in the 2020–2030 Strategic Plan
for NIH Nutrition Research and is directly responsive to PAR-19-377: “Omics-guided Biobehavioral Interventions
for Improved Health Outcomes: A Step Forward in Translation” as one of the first efforts to prospectively assess
the functional role of gut microbiome in explaining inter-individual heterogeneity in response to dietary
interventions. Built on existing biospecimen and data collected in two well-conducted long-term RCTs and state-
of-the-art multi'omics technologies, our proposal is a highly cost-efficient opportunity to generate translatable,
personalized dietary interventions grounded in reproducible biological mechanisms and contribute to the
paradigm shift towards precision nutrition for improved cardiometabolic health.
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