Background: The early detection of neurologic damage at the microscopic level when the disease is subclinical would facilitate intervention preventing progression or potentially reversing the condition. The early determination of drug efficacy could shorten the length of drug studies, thereby reducing research costs. The eye is the only place in the body where an artery, vein, and nerve can be directly visualized The nerve fiber layer of the retina is an outgrowth of the brain.
Method: Dynamic Light Scattering (DLS) Spectroscopy measures the thermal random movement (Brownian Motion) of particles by analyzing the temporal fluctuations of scattered light. A proof-of-concept instrument for making retinal measurements provides optical power well below the maximal permissible exposure recommended by the ANSI Z136.1 standard. Scattered light is analyzed by a digital autocorrelator with an extended delay option for baseline determination. The testing duration is 5 seconds. DLS measurements were made from the macular area of 4 patients diagnosed with mild cognitive impairment and 4 age-matched controls with no history of neurologic disease. Both groups of patients had normal retinal examinations, including normal Optical Coherence Tomography, (OCT).
Result: Figure 1 Screenshot - 62-year-old female recently with mild cognitive impairment, subsequently diagnosed with Alzheimer's disease 1 year after DLS testing. Figure 2 Screenshot - Age-matched control CONCLUSION: The 4 patients with mild cognitive impairment were subsequently diagnosed with Alzheimer's disease approximately 1 year after the abnormal DLS measurement. The differences between the patients subsequently diagnosed with Alzheimer's disease, compared to the normal age-matched controls, was consistent across the tested patients. Alzheimer's measurements begin above 0.6 g 2(t)-1 and exhibit flattening of the initial line as opposed to the curve seen in non-Alzheimer's patients. The development of an early, noninvasive, quantitative test to diagnose Alzheimer's disease will lead to breakthroughs in drug development and hopefully, to the successful treatment of patients before dementia is irreversible.
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http://dx.doi.org/10.1002/alz.083932 | DOI Listing |
Mol Neurodegener
January 2025
Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO, USA.
TREM2 is a signaling receptor expressed on microglia that has emerged as an important drug target for Alzheimer's disease and other neurodegenerative diseases. While a number of TREM2 ligands have been identified, little is known regarding the structural details of how they engage. To better understand this, we created a protein library of 28 different TREM2 variants that could be used to map interactions with various ligands using biolayer interferometry.
View Article and Find Full Text PDFFluids Barriers CNS
January 2025
Sanders-Brown Center on Aging, College of Medicine, University of Kentucky, 760 Press Ave, 124 HKRB, Lexington, KY, 40536-0679, USA.
Background: Blood-brain barrier dysfunction is one characteristic of Alzheimer's disease (AD) and is recognized as both a cause and consequence of the pathological cascade leading to cognitive decline. The goal of this study was to assess markers for barrier dysfunction in postmortem tissue samples from research participants who were either cognitively normal individuals (CNI) or diagnosed with AD at the time of autopsy and determine to what extent these markers are associated with AD neuropathologic changes (ADNC) and cognitive impairment.
Methods: We used postmortem brain tissue and plasma samples from 19 participants: 9 CNI and 10 AD dementia patients who had come to autopsy from the University of Kentucky AD Research Center (UK-ADRC) community-based cohort; all cases with dementia had confirmed severe ADNC.
Alzheimers Res Ther
January 2025
Laboratory for Clinical Neuroscience, Center for Biomedical Technology, Universidad Politécnica de Madrid, IdISSC, Crta M40, km38, Madrid, 28223, Spain.
Background: Dementia patients commonly present multiple neuropathologies, worsening cognitive function, yet structural neuroimaging signatures of dementia have not been positioned in the context of combined pathology. In this study, we implemented an MRI voxel-based approach to explore combined and independent effects of dementia pathologies on grey and white matter structural changes.
Methods: In 91 amnestic dementia patients with post-mortem brain donation, grey matter density and white matter hyperintensity (WMH) burdens were obtained from pre-mortem MRI and analyzed in relation to Alzheimer's, vascular, Lewy body, TDP-43, and hippocampal sclerosis (HS) pathologies.
Commun Biol
January 2025
Department of Neurodegenerative Diseases, Beckman Research Institute of City of Hope, 1500 E. Duarte Rd, Duarte, CA, 91010, USA.
Brain organoid models have greatly facilitated our understanding of human brain development and disease. However, key brain cell types, such as microglia, are lacking in most brain organoid models. Because microglia have been shown to play important roles in brain development and pathologies, attempts have been made to add microglia to brain organoids through co-culture.
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