New gene editor enables greater precision
Peer-Reviewed Publication
Updates every hour. Last Updated: 26-Jun-2025 21:10 ET (27-Jun-2025 01:10 GMT/UTC)
An often-ignored type of cell in the brain plays a dynamic and surprisingly complex role in our ability to process information, according to new research from Oregon Health & Science University.
A new USC-led study, published in Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, has uncovered a significant link between type 2 diabetes mellitus and cortical thickness in older adults from various populations. The study highlights the potential impact of diabetes on brain structure and the importance of managing blood sugar levels to protect brain health in older age. The researchers utilized advanced neuroimaging techniques to analyze cortical thickness and hippocampal volume in participants from the Health and Aging Brain Study-Health Disparities (HABS-HD) cohort. The study’s diverse sample, comprising Hispanic, non-Hispanic Black, and non-Hispanic white adults, provides critical insights into how diabetes affects brain health across different populations. The team found poor glycemic control may be a key driver of the observed association between T2DM and cortical thinning. The researchers found that the association between T2DM and cortical thinning remained strong even after accounting for socioeconomic factors and common comorbidities such as hypertension, dyslipidemia, and obesity. Hispanic participants showed the strongest associations, while no significant effects were observed among non-Hispanic Black adults. Given the rising prevalence of diabetes, particularly among minority populations, these results underscore the urgent need for targeted interventions to improve diabetes management and mitigate its neurological consequences.
USC researchers have developed a blood test that can identify early signs of Alzheimer’s disease by measuring proteins linked to the condition. The new test, known as Penta-Plex Alzheimer’s Disease Capture Sandwich Immunoassay (5ADCSI), detects five biomarkers simultaneously, which is more than existing blood tests and runs on equipment commonly used in many laboratories. In proof-of-concept study published in the Journal of Alzheimer’s Disease, the researchers selected a series of biomarkers known to build up in Alzheimer’s disease: two types of amyloid (Aβ40 and Aβ42), phosphorylated tau, neurofilament light chain (NfL) and glial fibrillary acidic protein (GFAP). They developed a custom test to detect the presence of those biomarkers in a blood sample using the xMAP® technology. This method uses tiny color-coded beads coated with antibodies that bind to specific biomarkers. When a blood sample is added, the biomarkers in the sample bind to the beads. Powerful imaging sensors then detect the colors emitted from the beads in order to measure the biomarkers. Once the test was built, researchers used it to measure Alzheimer’s-associated biomarkers in 63 blood samples across three groups: 11 patients with Alzheimer’s disease, 17 patients with mild cognitive impairment (a precursor of Alzheimer’s) and 35 healthy participants. The 5ADCSI test detected the highest levels of the biomarkers in patients with Alzheimer’s disease, followed by those with mild cognitive impairment. Researchers then used the same test to measure biomarkers in cerebrospinal fluid (CSF), which typically contains higher levels of Alzheimer’s-associated proteins but is harder and more expensive to collect. They found moderate to strong correlations between blood and CSF results, suggesting the blood test is sensitive enough for early detection of the proteins.