WP 6.2Spoke 06

Reduce malnutrition: strategies in a sustainable framework

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Highlights

Research projects
Outputs
WP 6.2 developed sustainable and multidimensional strategies to prevent and counteract malnutrition, recognising that nutritional vulnerability arises from the interaction between diet, environment and individual biological characteristics. The work aimed to design adaptable prevention models tailored to different population groups, supported by a comprehensive chain of scientific evidence.

An initial phase focused on building a solid methodological foundation. Nutritional guidelines were collected, analysed and harmonised, and multidimensional questionnaires were developed to integrate dietary habits, lifestyle, socioeconomic status, pharmacological treatments and psychological well-being. This approach reduced fragmentation and ensured coherent nutritional pathways for vulnerable groups, including individuals with non-communicable diseases and metabolic frailties.

A significant research line investigated plant-based raw materials such as sorghum, rice and lentils to evaluate their potential role in preventing inflammation-related and metabolic forms of malnutrition. Experimental studies demonstrated favourable effects on lipid metabolism and oxidative stress, supporting the identification of promising functional ingredients. Standardised protocols were adopted to assess compound stability and bioavailability, and experimental models were developed to validate biological effects in vitro and in vivo.

Advanced analytical techniques, including omics approaches integrated with artificial intelligence tools, strengthened the experimental pipeline. AI-based models enabled accurate prediction of antioxidant activity in plant extracts, accelerating the selection of the most promising bioactive compounds.

In parallel, WP 6.2 developed digital applications designed to facilitate monitoring of nutritional status and lifestyle behaviours in adults, older individuals and children. These tools, interoperable with wearable devices, support continuous data collection and contribute to personalised and sustainable dietary strategies.

The legacy of WP 6.2 is a complete and transferable pipeline connecting the study of food matrices to biological validation and digital monitoring tools, providing a structured framework for sustainable nutrition research and future public health applications.

Task and deliverables

Task 6.2.1.

Identification of sustainable tailored multidimensional approach including nutritional strategies aimed at reducing malnutrition in target specific populations by exploiting the interactions between environment, food, genotype and phenotype: a) analysis of the positive and negative interactions between lifestyle, socioeconomic status, clinical condition, psychological distress, medical treatment and diet for the implementation of sustainable dietary patterns; b) malnutrition biomarker validation; c) draft of sustainable nutritional protocols (in connection with Spoke 1 and 4).

Task 6.2.2.

Development and application of in vitro, in vivo and in silico experimental models for the understanding of the mechanism of action in counteracting malnutrition of new sustainable bioactive molecules from different matrices (in connection with Spoke 2, 3 and 4).

Task 6.2.3.

Design of a friendly end user personalised web responsive application for remote promoting and monitoring of sustainable target specific dietary patterns. The responsiveness features of the application will be made available on different devices (e.g., PC, smartphone)

Milestones

M6.2.1.1.

List of nutrition protocols and existing biomarkers for specific target groups with malnutrition that would benefit improvement (M12)

M6.2.2.1.

List of new sustainable bioactive molecules proven to directly impact nutritional status in specific target groups with malnutrition (M18)

M6.2.3.1.

Identification and computerization of existing Clinical Practice Guidelines addressing malnutrition (M8)

M6.2.3.2.

Development of an engine for assessing dietary regimens based on their observed efficacy on the target patients (M18).