EGOITZ ASTIGARRAGA

Dr. EGOITZ ASTIGARRAGA

IMG PHARMA BIOTECH
orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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MLMiguel de la Fuente López
Miguel de la Fuente López
LLLaura Lombardero
Laura Lombardero
AGAlfonso Gomez Gonzalez
Alfonso Gomez Gonzalez
CSCristina Solari
Cristina Solari
IAIñigo Angulo-Barturen
Iñigo Angulo-Barturen
GBGabriel Barreda-Gómez
Gabriel Barreda-Gómez
In recent years, enzymes have risen as promising therapeutic tools for different pathologies, from metabolic deficiencies, such as fibrosis conditions, ocular pathologies or joint problems, to cancer or cardiovascular diseases. Treatments based on the catalytic activity of enzymes are able to convert a wide range of target molecules to restore the correct physiological metabolism. These treatments present several advantages compared to established therapeutic approaches thanks to their affinity and specificity properties. However, enzymes present some challenges, such as short in vivo half-life, lack of targeted action and, in particular, patient immune system reaction against the enzyme. For this reason, it is important to monitor serum immune response during treatment. This can be achieved by conventional techniques (ELISA) but also by new promising tools such as microarrays. These assays have gained popularity due to their high-throughput analysis capacity, their simplicity, and their potential to monitor the immune response of patients during enzyme therapies. In this growing field, research is still ongoing to solve current health problems such as COVID-19. Currently, promising therapeutic alternatives using the angiotensin-converting enzyme 2 (ACE2) are being studied to treat COVID-19.

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EDEguzkine Diez-Martin
Eguzkine Diez-Martin
LSLeidi Hernandez Suarez
Leidi Hernandez Suarez
CMCarmen Muñoz-Villafranca
Carmen Muñoz-Villafranca
Leire Martin-SoutoLeire Martin-Souto
Leire Martin-Souto
EAEGOITZ ASTIGARRAGA
EGOITZ ASTIGARRAGA
GBGabriel Barreda-Gómez
Gabriel Barreda-Gómez
In inflammatory bowel diseases (IBDs), such as Crohn’s disease (CD) and ulcerative colitis (UC), the immune system relentlessly attacks intestinal cells, causing recurrent tissue damage over the lifetime of patients. The etiology of IBD is complex and multifactorial, involving environmental, microbiota, genetic, and immunological factors that alter the molecular basis of the organism. Among these, the microbiota and immune cells play pivotal roles; the microbiota generates antigens recognized by immune cells and antibodies, while autoantibodies target and attack the intestinal membrane, exacerbating inflammation and tissue damage. Given the altered molecular framework, the analysis of multiple molecular biomarkers in patients proves exceedingly valuable for diagnosing and prognosing IBD, including markers like C reactive protein and fecal calprotectin. Upon detection and classification of patients, specific treatments are administered, ranging from conventional drugs to new biological therapies, such as antibodies to neutralize inflammatory molecules like tumor necrosis factor (TNF) and integrin. This review delves into the molecular basis and targets, biomarkers, treatment options, monitoring techniques, and, ultimately, current challenges in IBD management.

29 October 2008 in Analytical Chemistry
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EAEGOITZ ASTIGARRAGA
EGOITZ ASTIGARRAGA
GBGabriel Barreda-Gómez
Gabriel Barreda-Gómez
LLLaura Lombardero
Laura Lombardero
OFOlatz Fresnedo
Olatz Fresnedo
FCFernando Castaño
Fernando Castaño
JFJose A. Fernandez
Jose A. Fernandez

26 March 2011 in Analytical and Bioanalytical Chemistry
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AVANTONIO VELOSO
ANTONIO VELOSO
RFRoberto Fernandez
Roberto Fernandez
EAEGOITZ ASTIGARRAGA
EGOITZ ASTIGARRAGA
GBGabriel Barreda-Gómez
Gabriel Barreda-Gómez
IMIván Manuel
Iván Manuel
JFJose A. Fernandez
Jose A. Fernandez

1 February 2010 in Journal of Molecular Biology
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MLMaría Lucas
María Lucas
JEJosé Antonio Encinar
José Antonio Encinar
EAEGOITZ ASTIGARRAGA
EGOITZ ASTIGARRAGA
IOIker Oyenarte
Iker Oyenarte
IGInmaculada Gómez García
Inmaculada Gómez García
LMLuis Alfonso Martínez-Cruz
Luis Alfonso Martínez-Cruz

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CFCeltia Domínguez Fernández
Celtia Domínguez Fernández
JOJune Egiguren Ortiz
June Egiguren Ortiz
JRJone Razquin
Jone Razquin
MGMargarita Gómez-Galán
Margarita Gómez-Galán
LHLaura De Las Heras-García
Laura De Las Heras-García
GBGabriel Barreda-Gómez
Gabriel Barreda-Gómez
Neurodegenerative disorders are characterised by progressive neuron loss in specific brain areas. The most common are Alzheimer’s disease and Parkinson’s disease; in both cases, diagnosis is based on clinical tests with limited capability to discriminate between similar neurodegenerative disorders and detect the early stages of the disease. It is common that by the time a patient is diagnosed with the disease, the level of neurodegeneration is already severe. Thus, it is critical to find new diagnostic methods that allow earlier and more accurate disease detection. This study reviews the methods available for the clinical diagnosis of neurodegenerative diseases and potentially interesting new technologies. Neuroimaging techniques are the most widely used in clinical practice, and new techniques such as magnetic resonance imaging (MRI) and positron emission tomography (PET) have significantly improved the diagnosis quality. Identifying biomarkers in peripheral samples such as blood or cerebrospinal fluid is a major focus of the current research on neurodegenerative diseases. The discovery of good markers could allow preventive screening to identify early or asymptomatic stages of the neurodegenerative process. These methods, in combination with artificial intelligence, could contribute to the generation of predictive models that will help clinicians in the early diagnosis, stratification, and prognostic assessment of patients, leading to improvements in patient treatment and quality of life.