José Luís Molinuevo

ORCID: 0000-0003-0485-6001
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About
Contact & Profiles
Research Areas
  • Dementia and Cognitive Impairment Research
  • Alzheimer's disease research and treatments
  • Functional Brain Connectivity Studies
  • Health, Environment, Cognitive Aging
  • Advanced Neuroimaging Techniques and Applications
  • Neurological Disease Mechanisms and Treatments
  • Parkinson's Disease Mechanisms and Treatments
  • Health Systems, Economic Evaluations, Quality of Life
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Bioinformatics and Genomic Networks
  • Cholinesterase and Neurodegenerative Diseases
  • Neurological disorders and treatments
  • Memory and Neural Mechanisms
  • Genetics, Aging, and Longevity in Model Organisms
  • Neurological diseases and metabolism
  • Diet and metabolism studies
  • Blood Pressure and Hypertension Studies
  • Neurobiology of Language and Bilingualism
  • Cancer-related cognitive impairment studies
  • Sleep and Wakefulness Research
  • Nutritional Studies and Diet
  • Neuroscience and Neuropharmacology Research
  • Medical Imaging Techniques and Applications
  • Genetic Associations and Epidemiology
  • Sleep and related disorders

Pasqual Maragall Foundation
2016-2025

Barcelonaβeta Brain Research Center
2016-2025

Lundbeck (Spain)
2025

Lundbeck (Denmark)
2021-2024

Forschungszentrum Jülich
2024

University Hospital Cologne
2024

University of Cologne
2022-2024

University of Brescia
2024

Centro de Investigación Biomédica en Red de Fragilidad y Envejecimiento Saludable
2017-2023

Consorci Institut D'Investigacions Biomediques August Pi I Sunyer
2014-2023

Abstract The National Institute on Aging and the Alzheimer's Association convened three separate work groups in 2011 single 2012 2018 to create recommendations for diagnosis characterization of disease (AD). present document updates research framework response several recent developments. Defining diseases biologically, rather than based syndromic presentation, has long been standard many areas medicine (e.g., oncology), is becoming a unifying concept common all neurodegenerative diseases,...

10.1002/alz.13859 article EN cc-by-nc-nd Alzheimer s & Dementia 2024-06-27

Abstract Introduction Subjective cognitive decline (SCD) manifesting before clinical impairment could serve as a target population for early intervention trials in Alzheimer's disease (AD). A working group, the Cognitive Decline Initiative (SCD‐I), published SCD research criteria context of preclinical AD. To successfully apply them, number issues regarding assessment and implementation needed to be addressed. Methods Members SCD‐I met identify agree on topics relevant operationalization...

10.1016/j.jalz.2016.09.012 article EN Alzheimer s & Dementia 2016-11-05

Objective To estimate the risk for developing a defined neurodegenerative syndrome in large cohort of idiopathic REM sleep behavior disorder (IRBD) patients with long follow-up. Methods Using Kaplan-Meier method, we estimated disease-free survival rate from syndromes all consecutive IRBD diagnosed and followed-up our tertiary referal center between November 1991 July 2013. Results The comprises 174 median age at diagnosis 69 years follow-up four years. time was 33.1% five years, 75.7% ten...

10.1371/journal.pone.0089741 article EN cc-by PLoS ONE 2014-02-26

TREM2 is an innate immune receptor expressed on the surface of microglia. Loss-of-function mutations are associated with increased risk Alzheimer's disease (AD). a type-1 protein ectodomain that proteolytically cleaved and released into extracellular space as soluble variant (sTREM2), which can be measured in cerebrospinal fluid (CSF). In this cross-sectional multicenter study, we investigated whether CSF levels sTREM2 changed during clinical course AD, cognitively normal individuals...

10.15252/emmm.201506123 article EN cc-by EMBO Molecular Medicine 2016-03-03

Background The cerebrospinal fluid (CSF) biomarkers amyloid β (Aβ)‐42, total‐tau (T‐tau), and phosphorylated‐tau (P‐tau) demonstrate good diagnostic accuracy for Alzheimer's disease (AD). However, there are large variations in biomarker measurements between studies, within laboratories. Association has initiated a global quality control program to estimate monitor variability of measurements, quantify batch‐to‐batch assay variations, identify sources variability. In this article, we present...

10.1016/j.jalz.2011.05.2243 article EN Alzheimer s & Dementia 2011-07-01

Glial fibrillary acidic protein (GFAP) is a marker of reactive astrogliosis that increases in the cerebrospinal fluid (CSF) and blood individuals with Alzheimer disease (AD). However, it not known whether there are differences GFAP levels across entire AD continuum its performance similar to CSF GFAP.To evaluate plasma throughout continuum, from preclinical dementia, compared GFAP.This observational, cross-sectional study collected data July 29, 2014, January 31, 2020, 3 centers. The...

10.1001/jamaneurol.2021.3671 article EN cc-by JAMA Neurology 2021-10-20
Niklas Mattsson Ulf Andréasson Staffan Persson María C. Carrillo Steven Collins and 95 more Sonia Chalbot Neal E. Cutler Diane Dufour‐Rainfray Anne M. Fagan Niels H. H. Heegaard Ging‐Yuek Robin Hsiung Bradley T. Hyman Khalid Iqbal D. Richard Lachno Alberto Lleó Piotr Lewczuk José Luís Molinuevo Piero Parchi Axel Regeniter Robert A. Rissman Hanna Rosenmann Giuseppe Sancesario Johannes Schröder Leslie M. Shaw Charlotte E. Teunissen John Q. Trojanowski Hugo Vanderstichele Manu Vandijck Marcel M. Verbeek Henrik Zetterberg Kaj Blennow Stephan A. Käser Aladro José A. Rojo Marilyn Albert Daniel Alcolea Ulf Andréasson Anna Antonell Hiroyuki Arai Silvana Archetti Eva Lagberg Arkblad Inês Baldeiras Aleš Bartoš Dev Batish Aurélie Bedel Danièle Bentué‐Ferrer Flora Berisha Sergio Bernardini Marinus A. Blankenstein Kaj Blennow Olivier Bousiges Michael C. Camuso Maria Carrillo Tiziana Casoli Sebastiano Cavallaro Sonia Chalbot Steven Collins Odete Cruz e Silva Neal E. Cutler I. Cuvelier Odile Delaroche Diane Dufour‐Rainfray Roy B. Dyer Sebastiaan Engelborghs Anne M. Fagan Anne Fogli Orestes Vicente Forlenza Nick C. Fox Giovanni B. Frisoni Daniela Galimberti Elisabetta Galloni Silvana Maria Gritti Karen H. Gylys Harald Hampel Sabine Haustein Theresa Heath Niels H. H. Heegaard Michael T. Heneka Sanna‐Kaisa Herukka David M. Holtzman Ging‐Yuek Robin Hsiung Christian Humpel Bradley T. Hyman Takeshi Iwatsubo Khalid Iqbal Claude Jardel Mathias Jucker Elisabeth Kapaki Stephan A. Käser Daniel Kidd Péter Klivényi Ryozo Kuwano D. Richard Lachno Foudil Lamari Jean Laplanche Jordan Laser Sylvian Lehmann Piotr Lewczuk Qiao‐Xin Li Alberto Lleó Walter Maetzler

Abstract Background The cerebrospinal fluid (CSF) biomarkers amyloid beta 1–42, total tau, and phosphorylated tau are used increasingly for Alzheimer's disease (AD) research patient management. However, there large variations in biomarker measurements among within laboratories. Methods Data from the first nine rounds of Association quality control program was to define extent sources analytical variability. In each round, three CSF samples prepared at Clinical Neurochemistry Laboratory...

10.1016/j.jalz.2013.01.010 article EN Alzheimer s & Dementia 2013-05-01

Abstract Reducing the risk of dementia can halt worldwide increase affected people. The multifactorial and heterogeneous nature late‐onset dementia, including Alzheimer's disease (AD), indicates a potential impact multidomain lifestyle interventions on reduction. positive results landmark Finnish Geriatric Intervention Study to Prevent Cognitive Impairment Disability (FINGER) support such an approach. World‐Wide FINGERS (WW‐FINGERS), launched in 2017 over 25 countries, is first global...

10.1002/alz.12123 article EN Alzheimer s & Dementia 2020-07-01
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