NEUVAS
Fundació Institut Mar d’Investigacions Mèdiques (IMIM) / Hospital del Mar. Barcelona
The Neurovascular Research Group (NEUVAS) is a multidisciplinary team based at the Clinical Neurology department at Hospital del Mar that has been working for years in the field of cerebrovascular pathology (Coordinator: Dr. Jaume Roquer).
Located in the Barcelona Biomedical Research Park (PRBB) of the Hospital del Mar Medical Research Institute (IMIM), the group is part of the Research in Inflammatory and Cardiovascular Disorders Programme (RICAD). The team has participated in the HERACLES research network on essential hypertension (Red de Análisis de Canales iónicos de la musculatura Lisa arterial y su Explotación terapéutica Sistemática) since 2006 as the NEUVAS node. This research agenda of ion channel analysis in arterial smooth muscle is now the HERACLES Programme within the Cardiovascular Research Network (RIC).
The NEUVAS location at PRBB and connection to the Hospital del Mar clinical neurology services gives the group the benefit of combining theoretical, epidemiological and technical perspectives on biomedical research with applications and daily practice in the healthcare environment.
BASICMAR (BASe de datos de ICtus del hospital del MAR) is the main matrix or register supporting most of the NEUVAS research lines. This prospective database of all acute stroke events attended since 2005 at IMIM-Hospital del Mar (Barcelona, Spain) includes both first and recurrent strokes, with no exclusion criteria related to age, sex, or race.
This register is associated with the biological samples collection (BIOBASICMAR) and neuroimaging archives (RADIOBASICMAR).
1. Clinical Markers and Research (clinNEUVAS): Study of cerebrovascular disease and its clinical and epidemiological risk factors, as well as markers of stroke recurrence and evolution. There are 5 internal research lines:
a. Epidemiology and clinical evolution (Dr. Ángel Ois)
b. Biomarkers (Dra. Elisa Cuadrado-Godia): Study of plasma and serum markers in patients with acute stroke in the acute phase. The objective of this line of research is to identify markers that are useful both in the etiological diagnosis of stroke and in calculating the risk of recurrence or poor prognosis. Diverse laboratory techniques are used, including ELISA, western blot and flow cytometry.
c. Nutrition and lípids (REHANIM) (Dra. Ana Rodríguez-Campello)
d. Neurosonology (Dra. Elisa Cuadrado-Godia): Study of arterial morphology and functionality in patients with cerebrovascular disease. The objective of this line of research is to analyze the etiopathogenic and prognostic role of endothelial cerebral function in patients with different subtypes of cerebrovascular pathology. Among the tests used is intima-media thickness measurement and the analysis of cerebral vasorreactivity using CO2 testing.
e. Neuroimaging (Dra. Eva Giralt-Steinhauer): Software treatments of radiologic images (e.g., CAT, brain MRI) to measure infarction, hematoma and leukoaraiosis volumes. The application of a validated and rigorous methodology results in precise, reliable phenotypic data with high information value for the study of cerebrovascular diseases.
2. Research in Cerebrovascular Genetics (genNEUVAS): This group develops, participates and collaborates in studies designed to clarify the genetic bases of cerebrovascular pathology. It investigates the genetic and clinical-genetic risk of disease, as well as genetic involvement in the clinical status and development of patients. Our group has a clear commitment to collaboration, exemplified by our coordination and co-leadership of the “Spanish Consortium on the Genetics of Stroke (Genestroke)” and membership in the “International Stroke Genetics Consortium (ISGC)”, participating in various international projects.
a. Genome Wide Association Studies (Dr. Jordi Jiménez-Conde)
Technical advances in massive genotyping in recent years have led to platforms that permit genotyping of between 50,000 and 2.7 million SNPs per individual. This has permitted the development of the studies called Genome Wide Association (GWA), which represent an important advance in the genetic study of complex diseases, such as stroke. In genetics, we are carrying out our own studies as well as coordinated GWA projects in the field of cerebrovascular pathology.
b. Genetic and clinical-genetic scores (Dr. Jordi Jiménez-Conde)
In complex diseases, multiple common genetic variants (SNPs) tend to be associated with a phenotype and the strength of the association for each one tends to be low. Therefore, to integrate the information and the predictive capacity of the SNPs associated with a phenotype it is necessary to design appropriate strategies and statistical tools. This is why we work on the design of genetic scores and clinical-genetic and genetic networks that help to explain a mechanism of action or can offer practical applications of the discoveries.
c. Epigenetics (Dra. Carolina Soriano)
Ischemic stroke is a heterogeneous disease for which a genetic component is suggested because the epigenetic component is unknown. Epigenetic mechanisms such as DNA methylation regulate the structure of the chromatin and gene expression. DNA methylation has been associated with cardiovascular diseases and the hypomethylation of DNA with increased risk of ischemic heart disease/ictus. Analysis of DNA methylation could provide new information about the disease, prognosis and the effect of vascular risk factors.
d. Sequencing (Dra. Carolina Soriano/ Marina Mola)
i. Exome Sequencing studies.
Exome sequencing is an efficient strategy to selectively sequence codifying whole-genome regions for a single individual. Exons (approximately 1% of the human genome) are functionally important DNA sequences that represent the regions in genes that are translated into proteins.
We use this technique to compare stroke cases with favorable and unfavorable 3-month prognosis after cerebrovascular ischemic accident.
Utilizamos esta técnica para comparar casos de ictus con pronóstico favorable y desfavorable a los tres meses después del accidente cerebrovascular isquémico.
ii. Sequencing of candidate genes
Target genes that are likely associated or involved in a particular disease, condition or alteration cerebrovascular are specifically sequenced. The objective is to establish associations between the genetic variations of the genes of interest and phenotypes or symptoms of cerebrovascular disease. The selection of candidate genes is based on a priori knowledge of the functional or biological impact of these genes on the clinical condition or disease under study.