Mini brains from patients test Alzheimer’s drug responses

Researchers at Johns Hopkins Medicine created lab-grown brain organoids from cells of people with Alzheimer’s disease to study how they respond to the antidepressant escitalopram oxalate.

The organoids, made from blood cells reprogrammed into stem cells, replicated key molecular features of the disease. Some showed increased proteins linked to serotonin signaling after treatment, while others displayed little change.

Vasiliki Machairaki, the study leader, said the models could help identify patient subgroups likely to benefit from certain drugs. The work also examined extracellular vesicles released by the organoids as potential biomarkers for diagnosis and disease staging.

The study, funded in part by the National Institutes of Health, appeared in Alzheimer’s & Dementia. It involved hundreds of organoids from patients and healthy controls, focusing on the hindbrain region.

Machairaki plans further development of the models to include immune cells and vascular structures for greater realism.

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Microscopic illustration of protective microglia clearing amyloid plaques in an Alzheimer's brain model due to the OLE molecule
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Study identifies OLE molecule that shifts microglia into a more protective state in Alzheimer’s models

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Researchers in Spain and Switzerland report that an experimental molecule called OLE helped restore protective behavior in the brain’s immune cells in animal models of Alzheimer’s disease, reducing amyloid-related pathology and improving performance on memory and movement tests.

Researchers at the Indiana University School of Medicine have identified the enzyme IDOL as a potential new target for treating Alzheimer's disease. Laboratory studies showed that removing the enzyme from neurons reduced amyloid plaques and improved brain cell communication.

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Researchers at the University of Cambridge have developed miniature lab-grown models of the human brain and spinal cord that show damaged nerve fibers can regain the ability to regrow under certain conditions.

A study of 440 participants from the Women’s Interagency HIV Study found that accelerated epigenetic aging in monocytes—an immune cell type—tracked more closely with emotional and cognitive depression symptoms such as hopelessness and loss of pleasure than with physical symptoms like fatigue. The work, published in The Journals of Gerontology: Series A, adds evidence that cell-type-specific aging measures could contribute to future biological tools to complement symptom-based depression screening, though researchers say more validation is needed before clinical use.

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A widely studied anti-aging treatment triggered significant brain damage in mice, according to new research from the University of Connecticut. The drug combination dasatinib plus quercetin caused myelin loss and changes resembling those seen in multiple sclerosis. The findings raise questions about its use in longevity studies and off-label therapies.

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