Neurogenesis occurs in an important part of the brain called the hippocampus which is involved in learning and memory.
While Alzheimer’s disease affects the formation of new brain cells in the hippocampus during the early stages of the disease, previous studies have only been able to study neurogenesis in its later stages through autopsies.
To understand the early changes, researchers collected blood samples over several years from 56 individuals with Mild Cognitive Impairment (MCI), a condition where someone will begin to experience a worsening of their memory or cognitive ability.
Of the 56 participants in the study, 36 went on to receive a diagnosis of Alzheimer’s disease.
“In our study, we treated brain cells with blood taken from people with MCI, exploring how those cells changed in response to blood as Alzheimer’s disease progressed,” said Aleksandra Maruszak, one of the study’s joint first authors from King’s College London.
In studying how blood affected the brain cells, the researchers made several key discoveries.
The blood samples collected from participants over the years who subsequently deteriorated and developed Alzheimer’s disease promoted a decrease in cell growth and division and an increase in apoptotic cell death — the process by which cells are programmed to die.
However, the researchers noted that these samples also increased the conversion of immature brain cells to hippocampal neurons.
While the underlying reasons for the increased neurogenesis remain unclear, the researchers theorise that it may be an early compensating mechanism for the neurodegeneration or loss of brain cells experienced by those developing Alzheimer’s disease.
“Previous studies have shown that blood from young mice can have a rejuvenating effect on the cognition of older mice by improving hippocampal neurogenesis,” said Professor Sandrine Thuret, the study’s lead author from King’s College London.
“This gave us the idea of modeling the process of neurogenesis in a dish using human brain cells and human blood,” Thuret said.
The researchers aimed to use this model to understand the process of neurogenesis and to use changes in this process to predict Alzheimer’s disease.
They found the first evidence in humans that the body’s circulatory system can have an effect on the brain’s ability to form new cells.
When the researchers used only the blood samples collected furthest away from when the participants were diagnosed with Alzheimer’s disease, they found that the changes in neurogenesis occurred 3.5 years prior to a clinical diagnosis.
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“Our findings are extremely important, potentially allowing us to predict onset of Alzheimer’s early in a non-invasive fashion,” said Edina Silajdzic, the study’s joint first author said.
“This could complement other blood-based biomarkers that reflect the classical signs of the disease, such as the accumulation of amyloid and tau (the flagship proteins of Alzheimer’s disease),” Silajdzic added.
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