Obesity, Diabetes and their Comorbidities: Prevention and Treatment

Lines of Research

01.Intestinal microflora, insulin resistance, and obesity.
02.Role of adipobiology in metabolic diseases.
03.Metabolic effect of bariatric surgery.
04.Environmental factors in the genesis of obesity and diabetes (brown adipose tissue and endocrine disruptors).
05.New celular and molecular mechanisms of inflammation in metabolic diseases: obesity, diabetes, and cancer
06.Genetic and epigenetic factors in the prevention, progression, and treatment of type 2 and gestational diabetes
07.PREDIMED PLUS Study.
08.Dietotherapeutic approach to obesity and cardiovascular disease: role of ketosis, intermittent fasting, physical exercise, and chronobiology.
09.Mitochondrial fitness in metabolic diseases.
10.Endocrine-metabolic complications of obesity
11.Obesity and brain aging.
12.Biomarker analysis of intervention response for weight loss.
13.Immunity in metabolic diseases.
14.Role of pregnancy and breastfeeding in the onset of metabolic diseases.

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AllerScreening

Point-of-care device base on KETs for diagnosis of food allergies

Financed by: European Comission

Programme: H2020-CALL FOR NANOTECHNOLOGIES, ADVANCED MATERIALS, BIOTECHNOLOGY AND PRODUCTION 2017 (2): H2020-NMBP-X-KET-2017

Rol in the project: Partner

Grant Agreement ID:  768641

Duration: October 2017 to March 2022

 

Contact: Torres Jaén, María José

Implementation centre: University Regional Hospital of Málaga

Research group of IBIMA involved: Allergic Diseases to Drugs and Allergens 

ABSTRACT

Food allergy is an immune-based disease that has become an important public health problem that affects children and adults and may be increasing in prevalence.In the US, food allergy affects 5% of children under the age of 5 years and 4% of teens and adults, and its prevalence appears to be on the increase. Globally, it is estimated that over 6% of the population, around 200 to 250 million people, suffer from some food allergies, affecting more than 17 million people only in Europe.

The main objective of this proposal is translating an optical diagnostic technology already proven in which the novel AllerScreening platform is based on, to the clinical routine, addressing a priority healthcare unmet need from the laboratory to the clinic. The unique features of AllerScreening will allow clinicians to early detect main food allergies (at least the 90% of European food allergies) through a simple test using a drop of sera, reducing the cost and technical requirements of the current clinical practice. This new and innovative cost-effective sensing system for the in vitro component diagnosis of food allergies will be feasible thanks to the multiplexed disposable BioKits and the optical Pont-of-Care (PoC) reader in which the novel AllerScreening platform is based on, allowing the adoption of a novel PoC diagnostic device specific for food allergies.

Partners

IUPITER

IUPITER

IntUitive Platform for monIToring and delivery of mEdical goods by dRones

Financed by: European Comission

Programme: DIH-HERO: CALL FOR HEALTHCARE ROBOTICS 2020

Grant Agreement ID:  CE-DIH-HERO-PI-ROBO-2020-01

Rol in the project: Partner

Duration: April 2021 to March 2022

 

Contact: García Gemar, Gracia María

Implementation Centre: Centro de Transfusiones, Tejidos y Células de Málaga

ABSTRACT

In the last few years, many examples of blood and medicine delivery drones have been

demonstrated worldwide, which mainly rely on aeronautical experience that is not common in the medical world. Speaking about drone delivery, attention should focus on the most important thing: the transported lifesaving good. Traditional boxes that monitor temperature are not usually in real time, and are not suitable for drone transportation because they are heavy and bulky.

This means that the biomedical characteristics of delivery are of primary importance. A Smart Capsule, equipped with artificial intelligence (AI), is the first system ever proposed to provide a fully autonomous drone delivery service for perishable and high-value medical products, integrating real-time quality monitoring and control. It consists in a smart casing that is able to guide any autonomous aerial vehicle attached to it, specifically designed for transporting blood, organs, tissues, test samples and drugs, among others. The system monitors the conditions of the product (e.g., temperature, agitation and humidity) and adjusts them when needed by exploiting, for instance, vibrations to maintain the required agitation, ensuring that goods are ready to be used as soon as they are delivered.

The Smart Capsule also leverages external temperature to reduce energy uptake from the drone, thus improving the drone’s battery life and flight range. The system replaces the need for specialized drivers and traditional road-bound transportation means, while guaranteeing compliance with all applicable safety regulations. A series of 16 experimental tests was performed to demonstrate the possibility of using the smart capsule to manage the flight and internal good delivery. Eighty-one missions were carried out for a total of 364 min of flight.

The Smart Capsule greatly improves emergency response and efficiency of healthcare systems by reducing delivery times by up to 80% and costs by at least 28%. The Smart Capsule and its enabling technology based on AI for drone deliveries are discussed in this paper. The aim of this work is to show the possibility of managing drone delivery with an AI-based device.

LEARN MORE ABOUT THE PROJECT

The video, recorded in Malaga, shows how The Smart Capsule is able to transport blood precisely thanks to AI technology.  

Placental injury and immune reaction transmitted to the neonates in cases of SARS-Cov2 infections during pregnancy

Placental injury and immune reaction transmitted to the neonates in cases of SARS-Cov2 infections during pregnancy

Financed by : FERRING Pharmaceuticals

Program : FERRING COVID-19 INVESTIGATIONAL GRANTS 2020

Grant Agreement ID:  FRI-PI-COVID-2020-02 

Role in the project:  Individual Participation in the project

Duration:  July 2020 to December 2022

 

Contact: González Mesa, Ernesto

Implementation Centre:  Hospital Regional Universitario de Málaga

Research group of IBIMA involved: Maternal-Fetal Medicine Research Group, Epigenetics, Women’s Diseases and Reproductive Health

FATZHEIMER

HIGH FAT DIET, MICROBIOTA AND NEUROINFLAMMATION IN THE PROGRESSION OF ALZHEIMER DISEASE

Financed by :Instituto de Salud Carlos III – ISCIII

Program : EU-LAC HEALTH JOINT CALL ON HEALTH RESEARCH AND INNOVATION 2017

Grant Agreement ID: AC17/00112

Role in the project: Coordinator

Duration: January 2018 to June 2022

 

Contact: Rodríguez de Fonseca, Fernando

Implementation Centre: University Regional Hospital of Málaga

Partners

SELF

SELF

Smart t-shirts for an Easier LiFe

Financed by: Instituto de Salud Carlos III – ISCIII

Programme: AAL- ACTIVE AND ASSISTED LIVING PROGRAMME 2019    

Grant Agreement ID: AC19 / 00062

Rol in the project: Partner

Duration:January 2020 to June 2022

 

Contact: García Alegría, José Javier

Implementation Centre: Costa del Sol Hospital

Research group of IBIMA involved: Chronic diseases and aging

 

ABSTRACT

The aim of the SELF project is to improve the quality of life (QoL) of older adults by assisting them with an innovative ICT-based SELF system (made by a comfortable smart t-shirt, dry polimer sensors, data management platform, a mobile APP and advanced communications devices) that allows the accurate monitoring of vital signs and of functional capacity providing in real time reliable information about the health status of the elderly using the system. The t-shirts have advanced sensors embedded and are capable to dynamically monitor ECG and respiratory frequency, in relation to users’ life context and real activity. This system is connected to a central unit which directly transmit data to an APP which provides an alarm signal if some standards are overcome: in this way, the smart t-shirt could be the enabling factor for the implementation of a service of “Health surveillance and monitoring”. 

The application of the SELF system is expected to favor the development of active lifestyles by improving the SELF-efficacy and perceived autonomy of older adults, while serving as a monitoring and measurement tool to acquire information on mobility and health status. The solution also differentiates from conventional wearables due to the capacity of higher integration into elderly’s daily routines. It favors wearing compliance without requiring a change of behavior. Moreover, it minimizes the risk of stigmatization due to the unobtrusiveness of the embedded solution and thus the overall technology acceptance. This project intends to insert a trend of innovation, of international relevance, in contextualizing the new proposed technology with respect to a new logic of health monitoring, less invasive, reliable and consistent with the instances of “active life” of subjects who have the need or aspiration of continuous monitoring. The methodological endeavor of test therefore intends to operationally validate and scale-up in 4 different European countries the importance of the proposed ICT-based solution. 

The service related to the use of the t-shirt will be developed in collaboration with the end-users, following a well-designed co-creation approach, in order to tailor the t-shirt on the basis of individual needs. The SELF system will respond at market and commercial level to the needs of two specific target consumer typologies: baby boomers and alert stage.

Partners

EUROPEAN RESEARCH COUNCIL

CONVOCATORIAS DEL CONSEJO EUROPEO DE INVESTIGACIÓN (EUROPEAN RESEARCH COUNCIL)

El Consejo Europeo de Investigación (ERC, European Research Council) proporciona financiación atractiva para apoyar proyectos de investigadores excelentes que supongan un avance significativo en la frontera del conocimiento. Deben ser investigaciones novedosas y ambiciosas en cualquier campo de investigación.

Las subvenciones del ERC se conceden mediante convocatorias abiertas a proyectos dirigidos por investigadores tanto en fase de iniciación como ya consolidados que trabajen en Europa o se trasladen aquí, con independencia de su origen, basándose en la excelencia científica como único criterio de selección. La finalidad es premiar las mejores ideas y conservar, reconocer y dar visibilidad a las mejores mentes de Europa, así como atraer talento del exterior.

Existen tres esquemas de financiación individuales (Starting, Consolidator y Advanced Grants), un esquema de financiación colaborativa (Synergy Grant) y un esquema para explorar el potencial de comercialización o social de los resultados obtenidos en el seno de proyectos ERC ya financiados (Proof of Concept).

1. ERC Starting Grant

Convocatoria destinada a apoyar investigadores principales excelentes en la fase de su carrera en la que inician su propio grupo/línea de investigación independiente. El investigador principal debe estar en posesión de un título de doctor, con antigüedad de entre 2 y 7 años antes del 1 de enero de 2025, y cuya actividad investigadora esté en la frontera del conocimiento, demostrando la ambición y viabilidad de su proyectos de investigación dentro de cualquier área temática. El Investigador deberá demostrar su potencial de independencia investigadora, con al menos una publicación importante como autor principal o sin la participación de su supervisor de tesis.

  • Duración: 5 años
  • Dotación: 1,5M€ + 1M€ adicional
  • Deadline: 15 de Octubre de 2024
  • Más información

2. ERC Consolidator Grant

Estas ayudas están dirigidas a investigadores principales de cualquier nacionalidad, que hayan obtenido el doctorado entre 7 y 12 años antes al 1 de enero de 2025, y con carrera destacable que se encuentren consolidando su grupo de investigación y puedan acreditar su independencia investigadora. Los Investigadores Principales deberán demostrar el carácter innovador, la ambición y la viabilidad de su propuesta de investigación.

  • Duración: 5 años
  • Dotación: 2M€ + 1M€ adicional
  • Deadline:  14 de enero de 2025
  • Más información

    3. ERC Advanced Grant

    Convocatoria para apoyar a investigadores excelentes en la fase de su carrera en la que ya son líderes de investigación consolidados con un historial reconocido de logros en investigación. Estos investigadores principales deben demostrar el carácter innovador, la ambición y la viabilidad de su propuesta de investigación.

    • Duración: 5 años
    • Dotación: 2,5M€ + 1M€ adicional
    • Deadline:  29 agosto de 2024 
    • Más información

        4. ERC Synergy Grant

        Convocatorias dirigidas a proyectos de investigación ambiciosos que requieren la colaboración de un grupo de dos a cuatro investigadores principales, aportando diferentes habilidades y recursos para abordar problemas científicos desafiantes. Las propuestas pueden ser en cualquier campo de investigación, y los proyectos deben demostrar que no pueden llevarse de manera individual.

        • Duración: 6 años
        • Dotación: 10 M€
        • Deadline: 6 de Noviembre de 2024 
        • Más información

              5. ERC Proof of Concept

              Ayuda dirigida a investigadores principales que cuenten con un proyecto financiado por ERC en desarrollo o finalizado en el último año. El objetivo de la ayuda es verificar el potencial innovador de ideas y resultados derivados de dichos proyectos.

              • Duración: 18 meses
              • Dotación: 150.000€
              • Deadline: 18 de Septiembre de 2024
              • Más información

              6. Calendario de Convocatorias ERC Programa de trabajo 2025

              Work Programme
              Open Call
              Closure Call
              Total Budget
              Budget per proposal

              Starting Grant

              2025

              10/07/2024

              15/10/2024

              751 M

              1,5 M + 1 M adicional

              Consolidator Grant

              2025

              26/09/2024

              14/01/2025

              719 M

              2 M + 1 M adicional

              Advanced Grant

              2025

              22/05/2025

              29/08/2024

              683 M

              2,5M€ + 1M€ adicional

              Synergy Grant

              2025

              11/07/2024

              06/11/2024

              500 M

              10M€ + 4M€ adicional

              Proof of Concept

              2025

              13/11/2024

              13/03/ &  18/09/2024

              30 M

              150.000

              7. Documentación clave

              8. FORMACIÓN

              COMBACTE‐CARE

              Combatting Bacterial Resistance in Europe – Carbapenem Resistance

              Financed by: European Comission

              Programme:  6 Call INICIATIVA DE MEDICAMENTOS INNOVADORES (IMI) 2012

              Grant Agreement ID:  668596

              Rol in the project: Partner

              Duration: March 2015 to February 2020

               

              Contact: Colmenero Castillo, Juan de Dios

              Implementation Centre: Hospital Regional Universitario de Málaga

              Research group of IBIMA involved: Group for the study of infectious diseases

               

              ABSTRACT

              “Multi-drug resistant Gram-negative bacteria (MDR-GNB): the ultimate challenge!
              Antibiotic resistance is a global public health concern recently elevated to the top three threats identified by the WHO, and subject of numerous national and international government activities. Although focused strategies have beneficially influenced infection rates due to methicillin resistant Staphylococcus aureus (MRSA), infections due to MDR-GNB are rapidly increasing. In a very recent report the Centers for Disease Control and Prevention concluded that Carbapenem-Resistant Enterobacteriaceae (CRE) represent an immediate public health threat that requires urgent and aggressive action (CDC: Antibiotic Resistance Threats in the United States 2013).

              The epidemiology of MDR-GNB, and especially of CRE, is characterized by large heterogeneity in genotypes (with >20 reported resistance genes, such as NDM, KPC, VIM, OXA-48) and even larger heterogeneity of phenotypes, seriously hampering rapid detection of resistant types when using routine susceptibility testing. Treatment of infections caused by CRE relies on combinations of “older” antibiotics, lacking a strong evidence base of effectiveness and safety. New treatments for these infections are, therefore, urgently needed.

              The COMBACTE-CARE consortium is building on the recently funded Topic 1a/b/c consortium: COMBACTE, and contains three networks: CLIN-Net, LAB-Net and STAT-Net. To fulfil the specific objectives of Topic 5 the consortium has focussed on capacity building in clinical sites in some of the new member states in south-eastern Europe, where infection rates with MDR-GNB are expected to be high. Together with high-quality study sites in countries with endemic levels of MDR-GNB (such as Israel and Greece) CLIN-Net and LAB-Net will maximize capacity to provide a highly efficient resource for the conduct of the proposed studies on ATM-AVI. Furthermore, the consortium brings in four of the most prominent MDR-GNB diagnostic research groups in Europe, able to address the diagnostic challenges for the epidemiological and clinical studies, and a highly successful – and already operational – cohort for biomarker identification in critically ill patients. Furthermore, the participation of the PENTA network offers the unique opportunity to efficiently include neonates and children in the observational studies.

              The COMBACTE-CARE consortium brings together 20 academic partners (10 also partner in COMBACTE) and two CROs that build upon prior EU Commission investments which present unique expertise and capabilities to the overall project partnership.

              For all these reasons, APC2 (aligned with the COMBACTE infrastructure) will (1) increase the efficiency of antibiotic R&D through analysing observational clinical and microbiological data sets and making recommendations for the development of novel antibiotic agents for MDR GNB; will (2) provide new knowledge on the clinical management and outcomes of patients (neonates/children and adults) with serious hospitalised infections and will validate this knowledge for clinical outcomes for patients in areas of emerging and endemic antibiotic resistance; will (3) support the sustainability of ND4BB supported investigator and laboratory networks (COMBACTE); will (4) conduct prospective clinical trials with novel trial designs to deliver safety, pharmacology, and proof of efficacy data for novel agents directed towards treatment of infections due to MDR pathogens, prevention or sequelae of infections due to priority pathogens; will (5) validate novel bacterial identification and follow-up diagnostics or clinical endpoints with the aim of reducing the size and cost of clinical trials; and will (6) provide new knowledge on biomarkers predicting poor outcome in patients with serious healthcare-associated infections.”

              Partners

              iGame

              Multi-dimensional Intervention Support Architecture for Gamified eHealth and mHealth Products

              Financed by : European Union

              Program : H2020-EU.1.3.3. – Stimulating innovation by means of cross-fertilization of knowledge (H2020-MSCA-RISE-2018)

              Grant Agreement ID: 823871 

              Role in the project: Partner

              Duration: January 2019 to June 2024

               

              Contact: Mayoral Cleries, Fermín

              Implementation Center: Regional University Hospital of Malaga

              Research group of IBIMA involved: Basic, Clinical and Epidemiological Research in Mental Health

              ABSTRACT

              This project investigates evidence based gamification techniques for eHealth and mHealth and develops a multi-dimensional intervention support architecture/platform in order to improve the efficacy of gamified eHealth products (web-based health tools and health apps). The project will develop advanced game production techniques with ready-to-use toolkits to accelerate the innovation process for eHealth and mHealth products. This will help digital industry (games, IoT and ICT) to innovate new products and services with science and technology underpinnings.

              It addresses fundamental issues of gamification for eHealth interventions including its development process and evaluation methods for measuring its efficacy. The outcomes of the project, manifested as gamification Toolkits, an integrated ICT Platform, and clinical assessment Methodologies as whole as a framework, will greatly accelerate the pace and scale of eHealth innovation by transforming and increasing its quality and efficiency through advanced technology tools, frameworks and methodologies. By using gamified physical activity engagement as a clinical intervention case study, the proposed framework will be evaluated and tested within patients in primary care settings, who are identified as physical inactive and at risk for their conditions due to sedentary behaviours. However, the gamification framework remains flexible and portable to other contexts of digital health interventions.

                • The project presents two key innovation components:
                  An innovative collaborative R&D programme in collaboration with industry, focus on delivering solutions to address challenges in the development process of gamified eHealth products i.e. productivity and efficacy.
                • A strong and sustainable model of collaboration with digital industry and other relevant stakeholders fully integrated to develop the innovation capacity in SMEs in eHealth products, specifically gamified eHealth products and services

              Partners

              CONECT4CHILDREN

              COllaborative Network for European Clinical Trials For Children

              Financed by: European Union

              Programme: IMI2: CALL 10-INNOVATIVE MEDICINES INITIATIVE 2017

              Grant Agreement ID:  777389

              Rol in the project: Partner

              Duration: May 2018 to May 2024

               

              Contact: Urda Cardona, Antonio Luis

              Implementation Centre: Hospital Regional Universitario de Málaga

              Research group of IBIMA involved: Multidisciplinary Pediatric Research Group

              ABSTRACT

              “Paediatric medicines development is embedded in the European policy, legislation and in the work of the pharmaceutical industry but currently the potential of this effort is not realised.

              The conect4children (c4c) project will address the critical problems with the design, implementation and operational conduct of paediatric clinical trials, for example the fragmented and redundant efforts between sponsors, sites and countries.
              This project will generate a sustainable infrastructure that optimises the delivery of clinical trials in children through: a) a single point of contact for all sponsors, sites and investigators; b) efficient implementation of trials adopting consistent approaches, aligned quality standards and coordination of sites at national and international level; c) collaboration with specialist networks; d) high quality input to study design and preparation through rigorous strategic and operational feasibility assessment and e) the promotion of innovative methodologies.

              The project will be managed according to IMI2 best practice with a dedicated communications effort. The clinical trials infrastructure will be setup, implemented and tested by implementing 3-4 industry and at least 1 non-industry proof-of-viability studies. Expert advice groups will promote innovative methodologies and engagement with regulators. The business model for a sustainable infrastructure will be based on the European landscape of paediatric networks and available trial sites, the evaluation of services needs of sponsors of all kinds, and will be informed by the proof-of-viability studies. Supporting activities will include: data management (data about the trials and the network, including performance metrics for network management and promotion; handling trial data for non-industry sponsors; support for common data dictionaries); education and training.
              The voices of children, young people and their families will be central to the network.”

              Partners

                  • FONDAZIONE PENTA – FOR THE TREATMENT AND CARE OF CHILDREN WITH HIV ANDRELATED DISEASES – ONLUS (Coordinator)
                  • THE UNIVERSITY OF LIVERPOOL
                  • OSPEDALE PEDIATRICO BAMBINO GESU
                  • EURORDIS – EUROPEAN ORGANISATION FOR RARE DISEASES ASSOCIATION
                  • EUROPEAN CYSTIC FIBROSIS SOCIETY
                  • STICHTING KATHOLIEKE UNIVERSITEIT
                  • SWISS CLINICAL TRIAL ORGANISATION
                  • Associação para Investigação e Desenvolvimento da Faculdade de Medicina
                  • ISTITUTO GIANNINA GASLINI
                  • UNIVERSITY COLLEGE LONDON
                  • SIOP EUROPE ASBL
                  • TARTU ULIKOOL
                  • OKIDS GMBH
                  • UNIVERSITY OF
                  • NEWCASTLE UPON TYNE
                  • UNIVERSITEIT GENT
                  • UNIVERSITATSKLINIKUM HEIDELBER
                  • ARISTOTELIO PANEPISTIMIO THESSALONIKIS
                  • INSTYTUT POMNIK CENTRUM ZDROWIA DZIECKA
                  • HELSE BERGEN HF*HAUKELAND UNIVERSITY HOSPITAL
                  • ECNP RESEARCH AND SCHOLARSHIP STICHTING
                  • ROBERT BOSCH GESELLSCHAFT FUR MEDIZINISCHE FORSCHUNG MBH
                  • UNIVERSITY COLLEGE CORK – NATIONAL UNIVERSITY OF IRELAND, CORK
                  • KAROLINSKA INSTITUTET
                  • FUNDACIO SANT JOAN DE DEU,
                  • SERVIZO GALEGO DE SAUDE,
                  • GYERMEKGYOGYASZATI KLINIKAI VIZSGALOI HALOZAT,
                  • FONDAZIONE PER LA RICERCA FARMACOLOGICA GIANNI BENZI ONLUS,
                  • ECRIN EUROPEAN CLINICAL RESEARCH INFRASTRUCTURE NETWORK,
                  • HELSINGIN JA UUDENMAAN SAIRAANHOITOPIIRIN KUNTAYHTYMÄ,
                  • INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE,
                  • HELIOS DR. HORST SCHMIDT KLINIKEN WIESBADEN GMBH (participation ended),
                  • ARSENAL.IT – CENTRO VENETO RICERCAE INNOVAZIONE PER LA SANITA DIGITALE,
                  • UNIVERZITA KARLOVA,
                  • JANSSEN PHARMACEUTICA NV,
                  • BAYER AKTIENGESELLSCHAFT,
                  • SANOFI-AVENTIS RECHERCHE & DEVELOPPEMENT,
                  • Eli Lilly and Company Limited,
                  • UCB BIOPHARMA SRL,
                  • NOVARTIS PHARMA AG,
                  • INSTITUT DE RECHERCHES INTERNATIONALES SERVIER IRIS,
                  • GLAXOSMITHKLINE RESEARCH AND DEVELOPMENT LTD.,
                  • PFIZER LIMITED, 43. F. HOFFMANN-LA ROCHE AG,
                  • AZIENDA SANITARIA UNIVERSITARIA FRIULI CENTRALE,
                  • UNIVERSITA DEGLI STUDI DI CAGLIARI,
                  • SERVICIO MADRILENO DE SALUD,
                  • RETE ITALIANA PER LE SPERIMENTAZIONI CLINICHE IN PEDIATRIA

              Increased ultra-processed food consumption is associated with worsening of cardiometabolic risk factors in adults with metabolic syndrome: Longitudinal analysis from a randomized trial. – ATHEROSCLEROSIS

              González-Palacios, S; Oncina-Cánovas, A; García-de-la-Hera, M; Martínez-González, MA; Salas-Salvadó, J; Corella, D; Schröder, H; Martínez, JA; Alonso-Gómez, AM; Wärnberg, J; Romaguera, D; López-Miranda, J; Estruch, R; Tinahones, FJ; Lapetra, J; Serra-Majem, JL; Cano-Ibañez, N; Tur, JA; Martín-Sánchez, V; Pintó, X; Delgado-Rodríguez, M; Matía-Martín, P; Vidal, J; Vázquer, C; Daimiel, L; Ros, E; Bes-Rastrollo, M; Atzeni, A; Sorli, J; Zomeño, MD; Peña-Orihuela, PJ; Compañ-Gabucio, LM; Barón-López, FJ; Zulet, MA; Konieczna, J; Casas, RM; Garrido-Garrido, EM; Tojal-Sierra, L; Gomez-Perez, AM; Ruiz-Canela, M; Palau, A; Saiz, C; Pérez-Vega, KA; Garcia-Rios, A; Torres-Collado, L; Basterra-Gortari, J; Garcidueñas-Fimbres, TE; Malcampo, M; Vioque, J – 2023 – 10.1016/j.atherosclerosis.2023.05.022

              Organoleptic evaluation of a diabetes-specific oral nutritional supplement with extra virgin olive oil in patients at nutritional risk and type 2 diabetes mellitus: Double-blind, randomized, crossover and multicenter clinical trial (DIACARE)]. – NUTRICION HOSPITALARIA

              Vegas Aguilar, Isabel Maria; Porca Fernandez, Cristina; Casanas Quintana, Tamara; Calleja Fernandez, Alicia; Tejera Perez, Cristina; Tinahones Madueno, Francisco Jose; Bellido Guerrero, Diego; Garcia Almeida, Jose Manuel – 2023 – 10.20960/nh.04569

              Comprehensive approach to people with type 2 diabetes. Diabetes Knowledge Area of the Spanish Society of Endocrinology and Nutrition. – ENDOCRINOLOGIA DIABETES Y NUTRICION

              Reyes-García, R; Moreno-Pérez, O; Bellido, V; Botana-López, M; Rodríguez-Hervada, AD; Fernández-García, D; Fernández-García, JC; Gargallo-Fernández, M; González-Clemente, JM; Jódar-Gimeno, E; Casares, MLDL; López-Fernández, J; Martínez, A; Mezquita-Raya, P; Rozas-Moreno, P; Tejera-Pérez, C; Martín, JS – 2023 – 10.1016/j.endien.2023.03.002

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              Members

              • Researcher in Charge
                Será Investigador de este nivel los Investigadores Responsable que lideren un grupo de investigación del Instituto y sus Co-IR. Esta categoría puede incluir investigadores muy excepcionales en su disciplina.

              Francisco José Tinahones Madueño

              • Co-investigator in Charge
                Será Investigador de este nivel los Investigadores Responsable que lideren un grupo de investigación del Instituto y sus Co-IR. Esta categoría puede incluir investigadores muy excepcionales en su disciplina.

              Manuel Macías González

              Isabel Moreno Indias

              • Senior Investigator
                Serán aquellos que tengan una actividad investigadora de al menos 5 años en la etapa posdoctoral. Estos investigadores estarán adscritos a un Grupo de Investigación liderado por un Investigador Responsable. Las funciones serán las que le tenga asignadas su IR.
                Pueden liderar una línea de investigación de alguno de los grupos de investigación del Instituto, con financiación competitiva propia, y con potencial para llegar a convertirse responsable de un grupo de investigación.

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              • Collaborating Healthcare Researcher
                Será Investigador Asistencial Colaborador el Investigador que no reúne la consideración de Investigador Posdoctoral. Estarán adscritos a un Grupo de Investigación liderado por un IR. Las funciones serán las que le tenga asignada su IR.

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              • Postdoctoral and/or junior researchers
                Esta etapa posdoctoral estará restringida a Investigadores del Instituto que tengan el título doctor y no contemplados en los perfiles posteriores. Durante su etapa posdoctoral pueden llegar a liderar proyectos de I+D+i como Investigadores Principales, aunque aún no hayan establecido un nivel significativo de independencia. Además, pueden tener actividades de docencia y/o asistencial más allá de su trabajo de investigación.

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              • Predoctoral and/or Training Researchers

                Los investigadores predoctorales y/o en formación serán aquellos investigadores que realizan investigaciones bajo supervisión en una línea de investigación orientada a la resolución de problemas de salud. Incluye aquellos investigadores que están cursando un doctorado (incluyendo a los contratados Río Hortega)

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              • Technical staff

                Los investigadores predoctorales y/o en formación serán aquellos investigadores que realizan investigaciones bajo supervisión en una línea de investigación orientada a la resolución de problemas de salud. Incluye aquellos investigadores que están cursando un doctorado (incluyendo a los contratados Río Hortega)

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