Ivonne Suridjan

ORCID: 0000-0002-1803-9515
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About
Contact & Profiles
Research Areas
  • Alzheimer's disease research and treatments
  • Dementia and Cognitive Impairment Research
  • Tryptophan and brain disorders
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Functional Brain Connectivity Studies
  • Advanced Neuroimaging Techniques and Applications
  • Neurotransmitter Receptor Influence on Behavior
  • Schizophrenia research and treatment
  • Genetics, Aging, and Longevity in Model Organisms
  • Metabolomics and Mass Spectrometry Studies
  • Telomeres, Telomerase, and Senescence
  • Neuroscience and Neuropharmacology Research
  • Stress Responses and Cortisol
  • S100 Proteins and Annexins
  • Sleep and Wakefulness Research
  • Sleep and related disorders
  • Bioinformatics and Genomic Networks
  • Sphingolipid Metabolism and Signaling
  • Memory and Neural Mechanisms
  • Cancer-related cognitive impairment studies
  • Neurological Disease Mechanisms and Treatments
  • Neurological disorders and treatments
  • Medical Imaging Techniques and Applications
  • Diet and metabolism studies
  • Pharmacological Effects and Toxicity Studies

Roche (Switzerland)
2020-2023

Roche Pharma AG (Germany)
2021-2023

Hospital Del Mar
2021-2022

Centre for Genomic Regulation
2021-2022

Institute of Science and Technology
2022

Lundbeck (Denmark)
2021-2022

Institut de Biologia Evolutiva
2022

Universitat Pompeu Fabra
2021-2022

University College London
2021-2022

UK Dementia Research Institute
2021-2022

The neuroinflammatory hypothesis of major depressive disorder is supported by several main findings. First, in humans and animals, activation the immune system causes sickness behaviors that present during a episode (MDE), such as low mood, anhedonia, anorexia, weight loss. Second, peripheral markers inflammation are frequently reported disorder. Third, illnesses associated with high rates MDEs. However, fundamental limitation paucity evidence brain MDE. Translocator protein density measured...

10.1001/jamapsychiatry.2014.2427 article EN JAMA Psychiatry 2015-01-28

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

Parkinson disease is characterized by motor and nonmotor symptoms, reduced striatal dopamine signaling, loss of neurons in the substantia nigra. It now known that pathological process may begin decades before clinical diagnosis include a variety neuronal alterations addition to system.This study examined density all synapses with synaptic vesicle glycoprotein 2A (SV2A) subjects mild bilateral (n = 12) matched normal controls using vivo high-resolution positron emission tomographic imaging as...

10.1002/ana.25682 article EN cc-by-nc Annals of Neurology 2020-01-18

Neuroinflammation and abnormal immune responses have been implicated in schizophrenia (SCZ). Past studies using positron emission tomography (PET) that examined neuroinflammation patients with SCZ vivo the translocator protein 18kDa (TSPO) target were limited by insensitivity of first-generation imaging agent [(11)C]-PK11195, scanners used, small sample sizes studied. Present study uses a novel second-generation TSPO PET radioligand...

10.1093/schbul/sbu157 article EN Schizophrenia Bulletin 2014-11-09

[ 18 F]-FEPPA binds to the 18-kDa translocator protein (TSPO) and is used in positron emission tomography (PET) detect microglial activation. However, quantitative interpretations of PET signal with new generation TSPO radioligands are confounded by large interindividual variability binding affinity. This presents as a trimodal distribution, reflecting high-affinity binders (HABs), low-affinity binder (LAB), mixed-affinity (MABs). Here, we show that one polymorphism (rs6971) located exon 4...

10.1038/jcbfm.2012.46 article EN Journal of Cerebral Blood Flow & Metabolism 2012-04-04

Objective: Neuroinflammation and abnormal immune responses are increasingly implicated in the pathophysiology of schizophrenia. Previous positron emission tomography (PET) studies targeting translocator protein 18 kDa (TSPO) have been limited by high nonspecific binding first-generation radioligand, low-resolution scanners, small sample sizes, psychotic patients being on antipsychotics or not first episode their illness. The present study uses novel second-generation TSPO PET radioligand...

10.1176/appi.ajp.2016.16020171 article EN American Journal of Psychiatry 2016-09-09

Abstract Introduction Further evidence is needed to support the use of plasma amyloid β (Aβ) biomarkers as Alzheimer's disease prescreening tools. This study evaluated clinical performance and robustness Aβ 42 /Aβ 40 for positivity prescreening. Methods Data were collected from 333 BioFINDER 121 Disease Neuroimaging Initiative participants. Risk predictive values versus percentile actionability , simulations modeled impact potential uncertainties biases. Amyloid PET was brain amyloidosis...

10.1002/alz.12801 article EN cc-by-nc Alzheimer s & Dementia 2022-09-23

Abstract Introduction The effect of random error on the performance blood‐based biomarkers for Alzheimer's disease (AD) must be determined before clinical implementation. Methods We measured test‐retest variability plasma amyloid beta (Aβ)42/Aβ40, neurofilament light (NfL), glial fibrillary acidic protein (GFAP), and phosphorylated tau (p‐tau)217 simulated effects this biomarker when predicting either cerebrospinal fluid (CSF) Aβ status or conversion to AD dementia in 399 non‐demented...

10.1002/alz.12706 article EN cc-by-nc Alzheimer s & Dementia 2022-06-14

Abstract INTRODUCTION A hallmark of Alzheimer's disease (AD) is the aggregation proteins (amyloid beta [A] and hyperphosphorylated tau [T]) in brain, making cerebrospinal fluid (CSF) particular interest. METHODS We conducted a CSF proteome‐wide analysis among participants varying AT pathology ( n = 137 participants; 915 proteins) with nine biomarkers neurodegeneration neuroinflammation. RESULTS identified 61 significantly associated category P < 5.46 × 10 −5 ) 636 significant...

10.1002/alz.13130 article EN cc-by-nc-nd Alzheimer s & Dementia 2023-05-22

Abstract Age-related disease may be mediated by low levels of chronic inflammation (“inflammaging”). Recent work suggests that gut microbes can contribute to via degradation the intestinal barrier. While aging and age-related diseases including Alzheimer’s (AD) are linked altered microbiome composition higher microbial components in systemic circulation, role remains unclear. To investigate whether greater is associated with advanced age AD pathology, we assessed fecal samples from older...

10.1038/s41598-023-45929-z article EN cc-by Scientific Reports 2023-11-14

Abstract Study Objectives Fast frequency sleep spindles are reduced in aging and Alzheimer’s disease (AD), but the mechanisms functional relevance of these deficits remain unclear. The study objective was to identify AD biomarkers associated with fast spindle cognitively unimpaired older adults at risk for AD. Methods Fifty-eight unimpaired, β-amyloid-negative, (mean ± SD; 61.4 6.3 years, 38 female) enriched parental history (77.6%) apolipoprotein E (APOE) ε4 positivity (25.9%) completed...

10.1093/sleep/zsac135 article EN SLEEP 2022-06-07
Pontus Erickson Joel Simrén Wagner S. Brum Gilda E. Ennis Gwendlyn Kollmorgen and 95 more Ivonne Suridjan Rebecca Langhough Erin M. Jonaitis Carol A. Van Hulle Tobey J. Betthauser Cynthia M. Carlsson Sanjay Asthana Nicholas J. Ashton Sterling C. Johnson Leslie M. Shaw Kaj Blennow Ulf Andréasson Barbara B. Bendlin Henrik Zetterberg Michael W. Weiner Paul Aisen Ronald C. Petersen Clifford R. Jack William J. Jagust John Q. Trojanowki Arthur W. Toga Laurel Beckett Robert C. Green Andrew J. Saykin John C. Morris Leslie M. Shaw Enchi Liu Tom Montine Ronald G. Thomas Michael Donohue Sarah Walter Devon Gessert Tamie Sather Gus Jiminez Danielle Harvey Matt A. Bernstein Nick C. Fox Paul M. Thompson Norbert Schuff Charles DeCarli Bret Borowski Jeff Gunter Matthew L. Senjem Prashanthi Vemuri David Jones Kejal Kantarci Chad Ward Robert A. Koeppe Norm Foster Eric M. Reiman Kewei Chen Chester A. Mathis Susan Landau Nigel J. Cairns Erin Householder Lisa Taylor Reinwald Virginia Lee Magdalena Korecka Michal Figurski Karen Crawford Scott Neu Tatiana Foroud Steven G. Potkin Li Shen Kelley Faber Sungeun Kim Kwangsik Nho Zaven Kachaturian Richard Frank Peter J. Snyder Susan Molchan Jeffrey Kaye Joseph F. Quinn Betty Lind Raina Carter Sara Dolen Lon S. Schneider Sonia Pawluczyk Mauricio Beccera Liberty Teodoro Bryan M. Spann James Brewer Helen Vanderswag Adam Fleisher Judith L. Heidebrink Joanne Lord Sara S. Mason Colleen S. Albers David S. Knopman Kris Johnson Rachelle S. Doody Javier Villanueva Meyer Munir Chowdhury Susan Rountree Mimi Dang

Importance Knowledge is lacking on the prevalence and prognosis of individuals with a β-amyloid–negative, tau-positive (A−T+) cerebrospinal fluid (CSF) biomarker profile. Objective To estimate CSF A−T+ profile investigate its clinical implications. Design, Setting, Participants This was retrospective cohort study cross-sectional multicenter University Gothenburg (UGOT) (November 2019-January 2021), longitudinal Alzheimer Disease Neuroimaging Initiative (ADNI) (individuals mild cognitive...

10.1001/jamaneurol.2023.2338 article EN cc-by JAMA Neurology 2023-07-31

An unmet need exists for reliable plasma biomarkers of amyloid pathology, in the clinical laboratory setting, to streamline diagnosis Alzheimer's disease (AD). For routine use, a biomarker must provide robust and results under pre-analytical sample handling conditions. We investigated impact different procedures on levels seven development potential use AD. Using (1) fresh (never frozen) (2) previously frozen plasma, we evaluated effects (A) storage time temperature, (B) freeze/thaw (F/T)...

10.1111/jnc.15757 article EN cc-by Journal of Neurochemistry 2023-01-10

Migration is a major risk factor for schizophrenia but the neurochemical processes involved are unknown. One candidate mechanism through elevations in striatal dopamine synthesis and release. The objective of this research was to determine whether function elevated immigrants compared nonimmigrants relationship with psychosis. Two complementary case-control studies vivo (stress-induced release capacity) were performed Canada United Kingdom. Canadian study included 25 immigrant 31 nonmigrant...

10.1093/schbul/sbw181 article EN cc-by Schizophrenia Bulletin 2016-12-20

Glial activation is one of the earliest mechanisms to be altered in Alzheimer's disease (AD). fibrillary acidic protein (GFAP) relates reactive astrogliosis and can measured both cerebrospinal fluid (CSF) blood. Plasma GFAP has been suggested become earlier AD than its CSF counterpart. Although astrocytes consume approximately half glucose-derived energy brain, relationship between cerebral glucose metabolism poorly understood. Here, we aimed investigate association fluorodeoxyglucose...

10.1007/s00259-022-05897-4 article EN cc-by European Journal of Nuclear Medicine and Molecular Imaging 2022-07-18

Abstract Telomere length (TL) is associated with biological aging, consequently influencing the risk of age-related diseases such as Alzheimer’s disease (AD). We aimed to evaluate potential causal role TL in AD endophenotypes (i.e . , cognitive performance, N = 2233; brain age and AD-related signatures, 1134; cerebrospinal fluid biomarkers (CSF) neurodegeneration, 304) through a Mendelian randomization (MR) analysis. Our analysis was conducted context ALFA (ALzheimer FAmilies) study,...

10.1186/s13195-022-01101-9 article EN cc-by Alzheimer s Research & Therapy 2022-11-07

Higher grey matter volumes/cortical thickness and fluorodeoxyglucose uptake have been consistently found in cognitively unimpaired individuals with abnormal Alzheimer's disease biomarkers compared those normal biomarkers. It has hypothesized that such transient increases may be associated neuroinflammatory mechanisms triggered response to early pathology. Here, we evaluated, the earliest stages of continuum, associations between volume CSF several pathophysiological known altered preclinical...

10.1093/braincomms/fcac134 article EN cc-by Brain Communications 2022-05-02

<h3>Background and Objectives</h3> To determine whether CSF synaptic biomarkers are altered in the early preclinical stage of Alzheimer continuum associated with disease (AD) risk factors, primary pathology, neurodegeneration markers. <h3>Methods</h3> This cross-sectional study was performed Alzheimer9s Families (ALFA+) cohort, comprising middle-aged cognitively unimpaired participants. neurogranin growth-associated protein-43 (GAP-43) were measured immunoassays, synaptosomal-associated...

10.1212/wnl.0000000000012853 article EN cc-by-nc-nd Neurology 2021-09-23
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