NEWS

New Biomarkers Associated with Structural and Metabolic Changes in the Ventricles in Cardiovascular Disease Cases Identified

A multidisciplinary team made up of the Lipid and Cardiovascular Pathology Research Group led by Dr. Vicenta Llorente Cortés from the Sant Pau Research Institute, members of the Sant Pau Cardiology Service and physicists from the University of Toulouse have identified new biophysical and structural biomarkers for ventricular remodelling in patients with cardiovascular disease that open up a new way forward in diagnosis and more personalised treatments.

This multidisciplinary team of researchers from CIBER Cardiovascular Diseases (CIBERCV) has developed a translational porcine model of dilated cardiomyopathy in which they have identified new biomarkers of cardiac remodeling.

In this model, Dr. Llorente’s team has demonstrated the existence of metabolic and structural differences in cardiac remodeling between the two ventricles, in particular a greater degree of fibrosis in the right ventricle. On the other hand, they have observed that, in a normal heart, the left ventricle has less triglyceride accumulation than the right ventricle, probably due to greater energy expenditure, and this difference is lost in progression to dilated cardiomyopathy.

In addition, Vicenta Llorente indicates that the results obtained “point to the intramiocardiac lipid as a potential therapeutic target in the control of cardiac remodeling”. Currently, in line with this work, the CIBERCV team is carrying out a study on human myocardial samples with the aim of analysing the interest of the new biomarkers discovered in other cardiomyopathies and their relationship with molecular, lipidic and functional parameters.

Arrhythmias and sudden death, main clinical manifestation
Non-ischemic dilated cardiomyopathy (NICM) is characterized by dilation of the left ventricle and global systolic dysfunction with normal coronary arteries. Progressive heart failure, ventricular and supraventricular arrhythmias, thromboembolisms and sudden death are the main clinical manifestations. It is also the most common cause of heart failure leading to heart transplantation.

Ventricular remodeling that produces ventricular dilation and dysfunction has been extensively studied in vivo using non-invasive and post mortem techniques in human and animal studies for histopathology and biochemical analysis. At present, the current knowledge of the mechanisms involved in their genesis is still limited. As a result, treatments are reduced and have incomplete efficacy.

Reference article:
Identification of new biophysical markers for pathological ventricular remodelling in tachycardia-induced dilated cardiomyopathy. Benitez-Amaro, Samouillan, Jorge, Dandurand, Nasarre, de Gonzalo-Calvo, Bornachea, Amoros-Figueras, Lacabanne, Vilades, Leta, Carreras, Gallardo, Lerma, Cinca, Guerra, Llorente-Cortés.


Dr. Astrid Crespo, winner of the IV AstraZeneca Foundation Young Researchers Awards

Dr. Astrid Crespo, assistant of the Pneumology Service of the Hospital de Sant Pau and member of the Chronic Respiratory Diseases Group (GREC) of the Institut d’Investigació Biomédica (IIB-Sant Pau), linked to the CIBERES of the Asthma group, was the winner in the Asthma and Chronic Obstructive Pulmonary Disease (COPD) category of the IV AstraZeneca Foundation Young Researchers Awards. The award has been given for her research on neutrophilic asthma (AN), a serious disease that has no specific treatment.

Her research on neutrophilic asthma offers an opportunity to improve the knowledge of the physiopathological and cellular mechanisms involved in the AN in order to identify future therapeutic targets that allow the control of this disease until now without treatment. Dr. Crespo’s research, funded by the AstraZeneca Foundation, seeks to gain in-depth knowledge of the AN and to discover its clinical characteristics, its natural history and that of its subphenotypes, and to analyse the bronchial microbiological flora of these patients. In this way, a specific treatment for this disease could be developed.

The Young Researchers Awards promoted by the AstraZeneca Foundation, together with the Carlos III Health Institute, promote the scientific talent of researchers under the age of 40 in Spain.

For more information click here


The Research Institute selected for funding under the Caixa Impulse programme

The project “Androgen receptor dimerization inhibitors as a new therapy against prostate cancer“, of the Saint Paul Research Institute and the Bosch i Gimpera Foundation (FBG) / UB Transfer Office, has been selected to receive a grant from the Caixa Impulse program.
See more
A project that seeks to develop new drugs for the treatment of prostate cancer (antiandrogens), with an innovative mechanism of action (MOA). For this project “we start from the dimeric androgen receptor (AR) structure, published last year (Nadal et al., Nature Communications 2017). From there, we have characterized by X-ray crystallography the union of small molecules capable of interfering with the dimerization of RA, and that therefore, are hits for the development of new antiandrogens “, Pablo Fuentes Prior, researcher of the group of Molecular Bases of Diseases at the Research Institute of Saint Paul. This project is co-lead by Dr. Eva Estébanez Perpiñá of IBUB (Institute of Biomedicine of the University of Barcelona).


Researchers from Sant Pau, UAB, CSIC and CIBER-BBN publish at EMBO Molecular Medicine

Researchers at the Biomedical Research Institute Sant Pau (IIB Sant Pau) of the Hospital de la Santa Creu i Sant Pau, together with researchers at the Universitat Autònoma de Barcelona (UAB), the Spanish Scientific Research Council (CSIC) and the Network for Biomedical Research in the Bioengineering, Biomaterials and Nanomedicine Network (CIBER-BBN), have published an article in one of the most prestigious international scientific journals in the field of Molecular Medicine, EMBO Molecular Medicine. This article demonstrates the efficacy of a nanopharmaceutical developed by this team that selectively eliminates metastatic stem cells in animal models of colon cancer.

The research team, led by Dr Ramon Mangues (IIB Sant Pau), Prof Antonio Villaverde (UAB) and Dr Esther Vázquez (UAB), all members of the CIBER-BBN, have demonstrated that the drug acts only on metastasis initiating cells, through the specific interaction between a peptide present in the protein nanoparticle that transports it and the cellular receptor CXCR4 that is overexpressed in tumour cells. This allows targeting only tumour cells, to block their dissemination at early cancer stages, by preventing the appearance of metastasis while avoiding the adverse effects associated with conventional chemotherapy.

The CXCR4 receptor is overexpressed in at least 20 different cancer types, including prostate, breast, ovary and others not as common as the pancreas. This means that the nanoparticle can achieve targeted drug delivery in different tumor types, therefore, being a highly versatile vehicle that could transport different highly potent therapeutic molecules.

Currently, no drug in the market is capable of selectively eliminating metastatic stem cells. Therefore, this new discovery could have a high clinical impact, after carrying out the required regulatory studies, before their application in humans. The Hospital de la Santa Creu i Sant Pau in Barcelona would be the first Centre in the world to evaluate this drug in humans, prior to its possible introduction in clinical therapy.

Nanoligent, a new spin-off to finance the nanoparticle

In June 2017, researchers from the IIB-Sant Pau, the Institute of Biotechnology and Biomedicine at the UAB and the CIBER-BBN, who sign the article now published in EMBO Molecular Medicine, created a spin-off, Nanoligent, with the goal of developing the first drug designed to eliminate metastatic cells that could enter the market.

This company, which has more than 10 years of studies behind, is directed by Dr. Manuel Rodríguez Mariscal, a professional with a long experience in the field of investment and the creation of biotechnology companies and aims to obtain founding for the realization of the project.


Sant Pau and CIBERCV describe a new technique for detecting scars after myocardial infarction by bioimpedance

Researchers from the Centro de Investigación Biomédica en Red de Enfermedades Cardiovascular (CIBERCV) of the Joan Cinca de San Pablo group have recently described a new technique to identify areas of scarring in patients with myocardial infarction by means of endocardium mapping of tissue electrical impedance.

In a preclinical study carried out in a porcine model of chronic myocardial infarction, it is evident that this procedure can allow recognition of the scar of the infarction and, theoretically, is not influenced by changes in the cardiac activation sequence. “Accurate identification of scar areas is essential for electrical ablation of arrhythmias in patients with myocardial infarction to provide optimal results,”says Dr. Cinca.

Currently, the identification of scar areas is based on a voltage mapping, i. e., analyzing the voltage of local electrocardiograms, so CIBERCV researchers have opened a new way, according to the head of the group. “Our study shows the mapping of the electrical impedance brought advantages over voltage mapping and, therefore, the simultaneous use of both procedures will allow a better detection of fibrosis zones and, in short, better results in patients undergoing ablation of ventricular arrhythmias,”Cinca says.

A pioneering study
This CIBERCV study is the first of its kind to analyze the ability to recognize areas of heart attack scar using a novel viewpoint based on the measurement of the electrical impedance catheter, a heart property that is influenced by the intrinsic structural characteristics of tissue. Previous investigations showed that this impedance is less in the scar of the infarction than in the normal myocardium, and this circumstance allows the recognition of the necrotic region.

Reference article:
Endocardial infarct scar recognition by myocardial electrical impedance is not influenced by changes in cardiac activation sequence. Amorós-Figueras G, Jorge E, Alonso-Martin C, Traver D, Ballesta M, Bragós R, Rosell-Ferrer J, Cinca J. Heart Rhythm. DOI: https://doi.org/10.1016/j.hrthm.2017.11.031


Sant Pau publishes in the Journal of the American College of Cardiology

Researchers at the Hospital Santa Creu i Sant Pau in Barcelona and Sant Joan de Reus, led by Francisco Blanco-Vaca and Juan Carlos Escolà-Gil, of the IIB Sant Pau and the CIBER of Diabetes and Associated Metabolic Diseases (CIBERDEM) have identified the Mechanisms for which lipoproteins that transport good cholesterol (HDL) lose their cardioprotective capacity in patients with family hypercholesterolemia.

The work, in collaboration with Finnish researchers, has been published in the Journal of the American College of Cardiology and shows that patients with familial hypercholesterolemia exhibit alterations in the activities of the main enzymes involved in the maturation of HDLs, which causes alterations in its composition and a reduction in its main cardioprotective function, its ability to prevent the accumulation of cholesterol in the macrophages of the arterial wall.

Lídia Cedó, the first signatory of the work, indicates that these findings “also found teenagers with family hypercholesterolemia, a very common disorder that affects more than 100,000 people in Spain, which affects the need for an early diagnosis that allows starting treatments Early men who reduce the risk of myocardial infarction in the future. ”

Family hypercholesterolemia is a disorder inherited mainly by mutations in the gene of the low density lipoprotein receptor and characterized by high levels of low density lipoprotein, which are often associated with low levels of HDL.

In the study, researchers Núria Plana and Lluís Masana from the Sant Joan de Reus University Hospital, CIBERDEM, José Luis Sanchez-Quesada from IIB Sant Pau (CIBERDEM), Miriam Lee-Rueckert and Petri Kovan from the Wihuri Research Institute and Matti Jauhiainen del Minerva Foundation Institute for Medical Research, all of them in Helsinki.

Reference item:

Altered HDL Remodeling and Functionality in Familial Hypercholesterolemia. Cedó L, Plana N, Metso J, Lee-Rueckert M, Sanchez-Quesada JL, Kovanen PT, Jauhiainen M, Masana L, Escolà-Gil JC, Blanc-Vaca F. DOI: 10.1016 / j.jacc.2017.11.035


New advances to combat type 1 diabetes

Researchers from the Lipids and Cardiovascular Pathology Group of the IIB Sant Pau, directed by Vicenta Llorente Cortés, have recently published an article in the journal Scientific Reports together with other researchers from the Endocrinology and Nutrition Service, from the Cardiac Imaging Unit at Hospital Sant Pau and from the Cardiovascular Biochemistry Group of the Institut de Recerca. The paper demonstrates the potential of the sLRP1 biomarker as a non-invasive indicator of epicardial fat in patients with type 1 diabetes.
The development of trials based on this protein could pave the way for new clinical tools for metabolic risk stratification in patients with type 1 diabetes.

“Soluble LRP1 is an independent biomarker of epicardial fat volumen in patients with type 1 diabetes mellitas”.


The Sant Pau Research Institute signs a collaboration agreement with the Universitat Pompeu Fabra

The Cardiac Imaging Unit of the Clinical and Translational Cardiology Research Group of the Institut de Recerca de l’ Hospital de la Santa Creu i Sant Pau has signed a collaboration agreement with the Department of Information and Communication Technologies of the UPF. The overall objective is to develop computational methods and tools for medical imaging analysis, specifically based on the radiological characteristics of cardiac magnetic resonance imaging.
Radiomics is a recent discipline in medical physics that focuses on the extraction of quantifiable characteristics from various types of medical images (computed tomography, magnetic resonance imaging, positron emission tomography). The use of numerical algorithms makes it possible to extract features that are not obvious to the naked eye, and that contribute to improve and complete the diagnosis of various pathologies.


A project of the Biochemistry Service, chosen by the Spanish Society of Laboratory Medicine

Dr. Álvaro García Osuna, assistant of the Biochemistry Service, is the principal investigator of the project “High sensitivity troponin: New horizons in habitual clinical practice” presented jointly with the Cardiology and Emergency Services of Sant Pau, and financed by the Enrique Concustell Fellowship.

The project will be developed in the context of an agreement with Singulex Inc. (Alameda, CA, USA) and aims to evaluate the information provided by the determination of ultrasensitive troponin I (in comparison to that currently used: ultrasensitive troponin T) in the diagnosis and follow-up of patients with acute coronary syndrome.


CCL20 chemokines, new biomarker for abdominal aortic aneurysm detection

Researchers from the Centre de Recerca en Xarxa de Malalties Cardiovasculars (CIBERCV) of José Martínez González’s group at the IIB Sant Pau have shown that CCL20 protein levels are increased in patients with abdominal aortic aneurysms compared to healthy controls and, more importantly, respect atherosclerotic patients who are not aneurysmal. The study, led by Mercedes Camacho, investigates the expression of CCL20 and assesses its possible role as a biomarker to aid in the prognosis of patients with abdominal aortic aneurysm.

In this way, it is demonstrated that CCL20 and its CCR6 receptor are increased in aneurysm and that their circulating levels are higher in patients with this aneurysm than in healthy individuals and patients with non-aneurysmal arteriosclerotic disease. “This is undoubtedly a unique feature that is not seen when other cytokines are analyzed that are also found to be increased in abdominal aortic aneurysm and, therefore, CCL20 is particularly relevant in these patients,”Mercedes Camacho says. In addition, plasma levels of CCL20 predict with high sensitivity the presence of aneurysm.

Autoimmunity is known to play a role, not fully clarified, in the pathology of abdominal aortic aneurysm. CCL20 chemokines are involved in the development of autoimmune diseases, although their potential contribution to the development and progression of abdominal aneurysm is unknown.

This work shows an association of the CCL20 and its possible role as a biomarker of the disease, which opens new avenues of research, as the author of the CIBERCV study acknowledges.

“It is essential to find new specific biomarkers for early detection of disease and stratification of risk. In addition, the identification of new biomarkers could help to discover new pathways involved in the pathophysiology of AAA and thus discover new therapeutic targets for pharmacological intervention of the disease,”says Dr. Camacho.

An asymptomatic pathology
Abdominal aortic aneurysm, prevalent in elderly people in industrialized countries, is a pathology that consists of a localized and permanent dilation of the aorta, usually in its infrarenal portion. It is a disease that is mostly asymptomatically, so the diagnosis occurs in many cases casually and currently there is no drug treatment capable of limiting the progression of the aneurysm or preventing its rupture.

Link to reference article
Circulating CCL20 as a New Biomarker of Abdominal AorticAneurysm.
B. Soto, T. Gallastegi-Mossos, C. Rodríguez, J. Martínez-González, J.-R. Escudero, L. Vila & M. Camacho.
SciRep. 2017 Dec 11;7(1):17331. doi: 10.1038/s41598-017-17594-6.


The mechanisms by which the enzyme hepatic lipase produces obesity are identified

A study by researchers from the Institut d’Investigació Biomèdica de Sant Pau (IIB Sant Pau) and the CIBER of Diabetes and Associated Metabolic Diseases (CIBERDEM) demonstrates the key role of the liver lipase enzyme in the accumulation of liver lipids and the development of adiposity.

The work has been published in the prestigious scientific journal Plos One.

Researchers from the CIBER of Diabetes and associated Metabolic Diseases (CIBERDEM) and the Institut d’Investigació Biomèdica de Sant Pau (IIB Sant Pau), have identified the mechanisms by which the enzyme hepatic lipase, associated with the presence of metabolic alterations, obesity and the development of hepatic steatosis (fatty liver), causes accumulation of hepatic lipids and the development of adiposity.

The team of researchers, led by doctors Juan Carlos Escolà-Gil and Francisco Blanco-Vaca (IIB Sant Pau /CIBERDEM), used a transgenic mouse model that expressed human liver lipase in the liver. They demonstrated that enzyme expression promotes in vivo liver lipogenesis through the induction of a transcription factor (Srebf1) that controls the expression of major genes involved in fatty acid biosynthesis.

Lídia Cedó, researcher at CIBERDEM at the IIB Sant Pau and first signatory of the work, explains that “this study has been able to demonstrate the key role of liver lipase in the regulation of liver metabolism of lipids and fatty tissue accumulation “.

The researchers also found that the expression of this enzyme increased the ability of fat tissue cells to hydrolyze triglycerides by another enzyme (lipoprotein lipase) and the accumulation of fatty acids.

Vicenta Llorente-Cortes, researcher at the CIBERCV/CSIC-ICCC and Juan Carlos Laguna and Nuria Roglans from the Faculty of Pharmacy of the University of Barcelona, among others, have also participated in the study, published in Plos One.

Reference article:

Cedó L, Santos D, Roglans N, Julve J, Pallarès V, Rivas-Urbina A, et al. (2017) Human hepatic lipase overexpression in mice induces hepatic steatosis and obesity through promoting hepatic lipogenesis and white adipose tissue lipolysis and fatty acid uptake. PLoS ONE 12(12):e0189834.



San Pablo publishes Translational Research, The Journal of Laboratory and Clinical Medicine

Dr. José Julve, from the IIB Sant Pau and Dr. Francisco Blanco Vaca, director of the Biochemistry Service of Sant Pau and PI of the Grupo de Bases metabólicos del riesgo cardiovascular del IIB, is the main author of an article published in Translational Research, The Journal of Laboratory and Clinical Medicine.

The article demonstrates an important alteration in fecal cholesterol excretion in a model of rodents of the Muridae family of diabetes and extreme obesity, due to an alteration of signaling that regulates this excretion and is controlled by an adjustable transcriptional factor for binders called LXR alpha that controls the entero-hepatic cholesterol transporters ABCG5/G8.

Although this finding corresponds to a specific animal model, bariatric surgery of patients with morbid obesity improved the liver expression of alpha LXR and ABCG5/G8 suggesting that these alterations in cholesterol traffic, which are known to favor the development of cardiovascular diseases, are observed in patients with morbid obesity and diabetes.

You can view the article in pdf in the attached file.


A race for IIB research

On Sunday 19 November will take place in Les Franqueses del Vallès the 6th. edition of the race “Los 10 kilómetros de Les Franqueses” with the collaboration of the Town Hall of this locality and the endorsement of the Catalan Athletics Federation. The collection of all the editions of the career is destined to the Clinical Research Group in Oncology of the IIB, led by Dr. Agustín Barnadas, specifically in the field of kidney cancer research, for which Dr. Pablo Maroto is responsible.

Registration: www.xipgroc.cat
More information: www.els10delesfranqueses.cat

We encourage you to participate in this race of solidarity with Research.


Sant Pau wins three of the La Marató de TV3 fellowships

The Board of Trustees of the La Marató de TV3 Foundation has granted 694,987.51 euros to Sant Pau. Three projects out of the five applied for have been chosen to receive one of the 37 grants awarded by La Marató 2016 in projects focused on finding tangible advances in the prevention, treatment and rehabilitation of motor, sensory and cognitive disabilities that cause stroke and traumatic injuries to the spine and brain.

The three Sant Pau projects that have been financed by La Marató 2016 are the following:

Dra. Raquel Delgado Mederos
Cerebrovascular Diseases Unit, Neurology Service of Sant Pau.
Coordinated project “Stroke, stroke unit, rehabilitation, optics, diffuse correlation spectroscopy, cerebral blood flow, brain self-regulation.“, 298.000,00 €.

Dra. Elena Jiménez Xarrié
Sant Pau Research Institute
Lipoprotein biomarkers to determine the inflammation of carotid plaque in ischaemic stroke.“, 197.575,00 €.

Dr. Gerard Urrutia Cuchí
Epidemiology Service of Sant Pau
Effectiveness of a core stability exercise program on dynamic balance in seating, trunk control and functional rehabilitation in patients with subacute stroke: randomized clinical trial.“, 199.412,51 €.

The funds raised in the 2016 edition of La Marató, which amount to 11.3 million euros, will boost awareness and research on stroke and traumatic spinal cord injuries. The 70 award-winning teams will work over the next three years to gain more and more quality of life for people who have had a stroke or traumatic injury to the spine or brain. Of the total number of works, 17 are unitary and 20 are coordinated between two or more research institutions.

With these new 37 projects, La Marató has already added 794 in its 25 years of history, which have brought important results in the health of citizens and notable advances in knowledge, prevention, prognosis and treatment of multiple diseases.


Sant Pau publishes in the European Journal of Vascular and Endovascular Surgery

The Joint Service of Angiology, Vascular and Endovascular Surgery of Sant Pau – Dos de Maig has published an original article in the European Journal of Vascular and Endovascular Surgery describing the application of software originally developed in the fields of engineering and architecture for the calculation of strength of materials. This software is based on finite element analysis.
The application of this technology in patients with abdominal aortic aneurysms could help in assessing the risk of rupture and open a new avenue in deciding which patients and when they should have surgery.
This study is a joint work of the Joint Service of Angiology, Vascular and Endovascular Surgery of Sant Pau – Dos de Maig, IIB Sant Pau, UAB and CIBER of cardiovascular diseases.
More information (pdf artícle)


Neurology Service Publishes in Nature Genetics

The Memory Unit of the Neurology Service of Sant Pau has recently published an article in the scientific journal Nature Genetics about a study on Alzheimer’s disease. The article “Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer’s disease”can be found in the attached document.


Dr. Kulisevsky becomes Vice Dean of Graduate School of Medicine

Dr. Jaume Kulisevsky, scientific director of the “Institut de Recerca de Sant Pau”; director of the Parkinson’s and Movement Disorders Unit, of the Neurology Service of Sant Pau and Adjunct Professor of Neurology and Speech Therapy in the Department of Medicine, is the new postgraduate vice-dean at the Faculty of Medicine, Autonomous University of Barcelona. Dr. Kulisevsky will also be co-ordinator of the Master’s Commission and a member of the Academic Council of the Graduate School on behalf of the Faculty of Medicine.


Dr. Nadal participates in the conference of Spetses del karolinska Institutet

Dr. Marta Navidad from the group of Molecular Bases of Diseases, from the “Institut de Recerca de Sant Pau”, received a scholarship to participate in the conference “Advanced Lecture Course ALC17-01 Nuclear Receptors and epigenomic Mechanisms in Human Disease and Aging”. The meeting, organised by the Karolinska Institutet in Stockholm, took place from 27 August to 1 September in Spetses, Greece.


Gene therapy is feasible in stem cells from patients with Fanconi’s anemia

A team of scientific and clinical researchers from the Spanish Network of Research on Anemia of Fanconi, coordinated by the Division of Innovative Therapies of CIEMAT, demonstrates for the first time that gene therapy in stem cells of patients with Fanconi’s Anemia is feasible. Dr. Surrallés, director of the Genetics Service of Sant Pau, has participated in this finding, which has been published in the most prestigious journal of Hematology: BLOOD.

In their article, the researchers show that the gene correction procedure based on their own technology allows us to correct the pathology of the stem cells in these patients’ bone marrow.

The demonstration is based on a protocol for the genetic correction of hematopoietic stem cells in patients. After their mobilization in the patients’ blood, stem cells were corrected with clinically used viral vectors, and a very small part of them were transplanted to immunodeficient mice, in which human blood cells can be generated.

In this way, scientists have shown for the first time that through a gene therapy procedure, stem cells from patients with Fanconi’s anemia can generate disease-free human blood cells in transplanted mice.

These findings are a major boost that reinforces the researchers’ hypothesis that gene therapy will be a new way to effectively treat patients with Fanconi’s anemia. It is also of particular interest to the expectations of a clinical trial of gene therapy for these patients, which is currently underway in Spain and will soon be opened in other European countries.

This finding has been published in the most prestigious journal of Hematology: BLOOD

The news has also been highlighted by the weekly “Cell Therapy News”  on August 21 as Top Story by this newspaper.


This website uses cookies to improve the browsing experience and perform analytical tasks. If you continue browsing, we understand that you agree our cookies policy. More information