Laila Abdullah

ORCID: 0000-0003-0258-8146
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About
Contact & Profiles
Research Areas
  • Alzheimer's disease research and treatments
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • Dementia and Cognitive Impairment Research
  • Mitochondrial Function and Pathology
  • Metabolomics and Mass Spectrometry Studies
  • Traumatic Brain Injury and Neurovascular Disturbances
  • Neuroinflammation and Neurodegeneration Mechanisms
  • S100 Proteins and Annexins
  • Traumatic Brain Injury Research
  • Immunotoxicology and immune responses
  • Fatty Acid Research and Health
  • Computational Drug Discovery Methods
  • Diet and metabolism studies
  • Nuclear Receptors and Signaling
  • Health, psychology, and well-being
  • Metabolism and Genetic Disorders
  • Alcoholism and Thiamine Deficiency
  • Eicosanoids and Hypertension Pharmacology
  • Cholinesterase and Neurodegenerative Diseases
  • Peroxisome Proliferator-Activated Receptors
  • Neuropeptides and Animal Physiology
  • Protease and Inhibitor Mechanisms
  • MicroRNA in disease regulation
  • Medicinal Plants and Neuroprotection
  • Neurological Disease Mechanisms and Treatments

Roskamp Institute
2015-2024

James A. Haley Veterans' Hospital
2015-2024

Radboud University Nijmegen
2024

Radboud University Medical Center
2024

University of Leicester
2024

Trinity College Dublin
2024

University of Copenhagen
2024

St. Vincent's University Hospital
2024

The Open University
2011-2023

Kuwait Petroleum Corporation (Kuwait)
2023

John A. Bowden N. Alan Heckert Candice Z. Ulmer Christina M. Jones Jeremy P. Koelmel and 89 more Laila Abdullah Linda Ahonen Yazen Alnouti Aaron M. Armando John M. Asara Takeshi Bamba John R. Barr Jonas Bergquist Christoph H. Borchers Joost Brandsma Susanne B. Breitkopf Tomáš Čajka Amaury Cazenave‐Gassiot Antonio Checa Michelle Cinel Romain A. Colas Serge Cremers Edward A. Dennis James Evans Alexander Fauland Oliver Fiehn Michael S. Gardner Timothy J. Garrett Katherine Gotlinger Jun Han Yingying Huang Aveline Huipeng Neo Tuulia Hyötyläinen Yoshihiro Izumi Hongfeng Jiang Houli Jiang Jiang Jiang Maureen Kachman Reiko Kiyonami Kristaps Klavins Christian Klose Harald Köfeler Johan Kolmert Therese Koal Grielof Koster Zsuzsanna Kuklenyik Irwin J. Kurland Michael Leadley Karen Lin Krishna Rao Maddipati Danielle McDougall Peter J. Meikle Natalie A. Mellett Cian Monnin M. Arthur Moseley Renu Nandakumar Matej Orešič R. E. Patterson David A. Peake Jason S. Pierce Martin Post Anthony D. Postle Rebecca S. Pugh Yunping Qiu Oswald Quehenberger Parsram Ramrup Jon C. Rees Barbara Rembiesa Dénis Reynaud Mary R. Roth Susanne Sales Kai Schuhmann Michal L. Schwartzman Charles N. Serhan Andrej Shevchenko Stephen E. Somerville Lisa St. John‐Williams Michał A. Surma Hiroaki Takeda Rhishikesh Thakare J. Will Thompson Federico Torta Alexander Triebl Martin Trötzmüller S. J. Kumari A. Ubhayasekera Dajana Vuckovic Jacquelyn M. Weir Ruth Welti Markus R. Wenk Craig E. Wheelock Libin Yao Min Yuan Xueqing Zhao Sen-Lin Zhou

As the lipidomics field continues to advance, self-evaluation within community is critical. Here, we performed an interlaboratory comparison exercise for using Standard Reference Material (SRM) 1950-Metabolites in Frozen Human Plasma, a commercially available reference material. The study comprised 31 diverse laboratories, with each laboratory different workflow. A total of 1,527 unique lipids were measured across all laboratories and consensus location estimates associated uncertainties...

10.1194/jlr.m079012 article EN cc-by Journal of Lipid Research 2017-10-07

<b><i></i></b><i>APOE</i> has been demonstrated to influence traumatic brain injury (TBI) outcome. The relationship between <i>APOE</i> genotype and memory following TBI was examined in 110 participants the Defense Veterans' Head Injury Program. Memory performance worse those who had an ε4 allele (n = 30) than did not 80), whereas groups differ on demographic or variables measures of executive functioning. These data support a specific role for APOE protein outcome TBI, suggest...

10.1212/wnl.58.7.1115 article EN Neurology 2002-04-09

Early stages of many neurodegenerative diseases, such as Alzheimer's disease, vascular and frontotemporal dementia, Parkinson's are frequently associated with Mild Cognitive Impairment (MCI). A minimally invasive screening test for early detection MCI may be used to select optimal patient groups in clinical trials, monitor disease progression response treatment, better plan care. Here, we examined the feasibility using pairs brain-enriched plasma microRNA (miRNA), at least one which is...

10.18632/aging.100486 article EN cc-by Aging 2012-09-19

A minimally invasive test for early detection and monitoring of Alzheimer's other neurodegenerative diseases is a highly unmet need drug development planning patient care. Mild Cognitive Impairment (MCI) syndrome characteristic stages many diseases. Recently, we have identified two sets circulating brain-enriched miRNAs, the miR-132 family (miR-128, miR-132, miR-874) normalized per miR-491-5p miR-134 (miR-134, miR-323-3p, miR-382) miR-370, capable differentiating MCI from age-matched control...

10.18632/aging.100624 article EN cc-by Aging 2013-12-22

Exposure to repetitive mild traumatic brain injury (mTBI) is a risk factor for chronic encephalopathy, which characterized by patchy deposition of hyperphosphorylated tau aggregates in neurons and astrocytes at the depths cortical sulci. We developed an mTBI paradigm explore effects concussive-type over several months mice with human genetic background (hTau). Two injuries were induced hTau weekly period 3 or 4 compared those noninjured sham animals. Behavioral vivo measures detailed...

10.1093/jnen/nlw035 article EN Journal of Neuropathology & Experimental Neurology 2016-05-31

Mounting evidence suggests that cholesterol may contribute to the pathogenesis of Alzheimer disease (AD). We examined whether might be present in senile plaques, a hallmark neuropathological feature AD. employed 2 different fluorometric-staining techniques (filipin staining and an enzymatic technique) for determination brains postmortem confirmed AD patients nondemented, age-matched histopathologically normal controls. patient showed abnormal accumulation congophilic/birefringent dense cores...

10.1093/jnen/60.8.778 article EN Journal of Neuropathology & Experimental Neurology 2001-08-01

Phospholipid (PL) abnormalities are observed in the cerebrospinal fluid of patients with traumatic brain injury (TBI), suggesting their role TBI pathology. Therefore, PL levels were examined a mouse model that received 1.8 mm deep controlled cortical impact or craniectomy only (control). The rotarod and Barnes maze acquisition probe tests performed within 2 wk after injury, another test 3 mo postinjury. Liquid chromatography/mass spectrometry analyses on lipid extracts from several regions...

10.1096/fj.14-258228 article EN The FASEB Journal 2014-09-10

Gulf War illness ( GWI ) is a currently untreatable multi‐symptom disorder experienced by 1990–1991 Persian GW veterans. The characteristic hallmarks of include cognitive dysfunction, tremors, migraine, and psychological disturbances such as depression anxiety. Meta‐analyses epidemiological studies have consistently linked these symptomatic profiles to the combined exposure agents organophosphate‐based pyrethroid‐based pesticides (e.g. chlorpyrifos CPF permethrin PER respectively)...

10.1111/neup.12061 article EN Neuropathology 2013-09-30

Gulf War Illness (GWI) is a chronic multisymptom illness with central nervous system component such as memory deficits, neurological, and musculoskeletal problems. There are ample data that demonstrate exposure to (GW) agents, pyridostigmine bromide (PB) pesticides permethrin (PER), were key contributors the etiology of GWI post deployment Persian GW. In current study, we examined consequences acute (10 days) PB PER in C57BL6 mice. Learning tests performed at 18 days 5 months post-exposure....

10.1371/journal.pone.0119579 article EN cc-by PLoS ONE 2015-03-18

Abstract Background Matrix metallopeptidase 9 (MMP9) has been implicated in a variety of neurological disorders, including Alzheimer’s disease (AD), where MMP9 levels are elevated the brain and cerebrovasculature. Previously our group demonstrated apolipoprotein E4 (apoE4) was less efficient regulating activity than other apoE isoforms, that inhibition facilitated beta-amyloid (Aβ) elimination across blood–brain barrier (BBB) Methods In current studies, we evaluated impact modulation on Aβ...

10.1186/s12868-021-00643-2 article EN cc-by BMC Neuroscience 2021-05-25

In the military population, there is high comorbidity between mild traumatic brain injury (mTBI) and post-traumatic stress disorder (PTSD) due to inherent risk of psychological trauma associated with combat. These disorders present long-term neurological dysfunction remain difficult diagnose their overlapping clinical presentation. Therefore, we performed cross-sectional analysis blood samples from demographically matched soldiers (total, n = 120) mTBI, PTSD, mTBI+PTSD those who were...

10.1089/neu.2015.4061 article EN Journal of Neurotrauma 2015-12-30

This study was designed to explore the influence of apolipoprotein E (APOE) on blood phospholipids (PL) in predicting preclinical Alzheimer's disease (AD).Lipidomic analyses were also performed from an AD mouse model expressing human APOE isoforms (EFAD) and five mutations 195 cognitively normal participants, 23 who converted mild cognitive impairment (MCI)/AD within 3 years.APOE ε4-carriers converting MCI/AD had high arachidonic acid (AA)/docosahexaenoic (DHA) ratios PL compared ε4 non-ε4...

10.18632/aging.101203 article EN cc-by Aging 2017-03-23

Repetitive mild traumatic brain injury (rmTBI) is a major epigenetic risk factor for Alzheimer’s disease (AD). The precise nature of how rmTBI leads to or precipitates AD pathology currently unknown. Numerous neurological conditions have shown an important role dysfunctional phospholipid metabolism as driving the pathogenesis neurodegenerative diseases. However, in and remains elusive. We hypothesized that detailed characterization would reveal profiles response TBI overlap with...

10.3389/fnins.2019.00103 article EN cc-by Frontiers in Neuroscience 2019-02-19

Abstract Background Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex illness which disproportionally affects females. This associated with immune and metabolic perturbations that may be influenced by lipid metabolism. We therefore hypothesized plasma lipids from ME/CFS patients will provide unique biomarker signature of disturbances in immune, inflammation processes ME/CFS. Methods Lipidomic analyses were performed on cohort 50 controls (50% males similar age...

10.1186/s12967-021-03035-6 article EN cc-by Journal of Translational Medicine 2021-08-28
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