Summary: Researchers have discovered that a person’s “bioenergetic age,” reflecting how efficiently cells produce energy, strongly predicts Alzheimer’s risk and progression. High blood levels of molecules called acylcarnitines, markers of aging metabolism, were linked to faster cognitive decline and greater Alzheimer’s symptoms.
However, lifestyle choices like plant-based diets and regular exercise can effectively lower these molecules, reducing bioenergetic age and potentially delaying Alzheimer’s onset. This bioenergetic approach could help identify individuals at risk earlier and provide personalized strategies to maintain brain health without relying solely on medication.
Key Facts:
- Bioenergetic Clock: High acylcarnitine levels indicate an older bioenergetic age, significantly linked to Alzheimer’s risk.
- Lifestyle Benefits: Healthy living, including diet and exercise, can lower bioenergetic age, potentially offering protective benefits similar to Alzheimer’s medications.
- Personalized Prevention: About 30% of study participants with genetic risks but favorable bioenergetic profiles may especially benefit from lifestyle interventions.
Source: Weill Cornell University
A person’s “bioenergetic age”—or how youthfully their cells generate energy—might be a key indicator of whether they’re at risk of developing Alzheimer’s disease, new research from Weill Cornell Medicine shows.
The study, published Feb. 24 in Nature Communications, suggests healthy living can turn back the bioenergetic clock for some people, helping them fend off Alzheimer’s as effectively as a new drug called lecanemab.
“That’s quite big because it means some people can lower their risk without the uncertain side effects of current treatments,” said senior author Dr. Jan Krumsiek, associate professor of physiology and biophysics and computational genomics in the Institute for Computational Biomedicine at Weill Cornell Medicine. The study’s first author, Dr. Matthias Arnold, is head of the computational neurobiology team at Helmholtz Munich.
The new findings bring us a step closer to solving a long-standing puzzle. One of the early warning signs of Alzheimer’s is that brain cells start losing their ability to produce and use energy efficiently, such as metabolizing glucose (sugar). But some people don’t show disease symptoms for years.
This delay between abnormalities in energy pathways and the onset of symptomatic disease suggests there is a “bioenergetic capacity” that provides a buffer for these individuals. Their bodies and brains are better at keeping energy levels up even when problems start.
“In these cases, people can be unusually healthy when we look at their cognition,” said Dr. Krumsiek, who is also a member of the Englander Institute for Precision Medicine. “They make it to old age without the kind of declines that usually creep in.”
But could the researchers identify individuals with this beneficial higher bioenergetic capacity and help those without it?
A New Tool to Predict Risk of Alzheimer’s
Dr. Krumsiek and his colleagues turned to a group of molecules called acylcarnitines, which are associated with declining cognition and breaking down or metabolizing fats and proteins for energy.
To test if high acylcarnitine levels in the blood could predict who’s at risk of developing Alzheimer’s, the researchers used data from a large-scale study called the Alzheimer’s Disease Neuroimaging Initiative.
“It was fascinating,” Dr. Krumsiek said.
“Dividing research participants into groups based on their specific acylcarnitine levels highlighted people with more severe Alzheimer’s disease and others with fewer symptoms.”
This led the researchers to define a bioenergetic clock based on acylcarnitines—how old a person’s metabolism acts, compared to actual age. Higher bioenergetic age is linked to higher acylcarnitine levels, worsened Alzheimer’s pathology, cognitive decline and brain atrophy.
The researchers also quantified cognitive decline using a common test called the mini-mental state examination, on which a score below 24 out of 30 points indicates impairment.
They found that people with low acylcarnitine levels to begin with declined more slowly, losing about 0.5 points less per year than people with high acylcarnitine levels. The benefit is on par with the Alzheimer’s drug lecanemab.
To some degree, a person’s bioenergetic clock ticks forward at a rate determined by their genetics, but having a healthy lifestyle—for example, eating a plant-based diet and exercising —can help keep acylcarnitine levels low, which means a younger bioenergetic age, Dr. Krumsiek explained.
They went on to identify a subgroup of participants, about 30% of the Alzheimer’s Disease Neuroimaging Initiative, with older bioenergetic age but favorable genetic background.
These individuals may benefit more from early lifestyle interventions designed to decrease their bioenergetic age and potentially delay or prevent the onset of Alzheimer’s.
Next Steps
Moving forward, Dr. Krumsiek hopes to home in on the lifestyle interventions most effective for lowering bioenergetic age. For example, eating a low-carb diet may help maintain metabolic health, but just how low would carbohydrate consumption have to be for a person to see benefits?
The study also points to an inexpensive, rapid test that could determine a person’s acylcarnitine levels.
“It’s fortunate that these blood tests—originally developed to identify metabolic and mitochondrial disorders in newborns—can also help assess a person’s bioenergetic age,” Dr. Krumsiek said.
“If we can repurpose this technology for older adults, that could provide a way to start personalized treatment earlier.”
About this bioenergetic age and Alzheimer’s disease research news
Author: Barbara Prempeh
Source: Weill Cornell University
Contact: Barbara Prempeh – Weill Cornell University
Image: The image is credited to Neuroscience News
Original Research: Open access.
“Individual bioenergetic capacity as a potential source of resilience to Alzheimer’s disease” by Jan Krumsiek et al. Nature Communications
Abstract
Individual bioenergetic capacity as a potential source of resilience to Alzheimer’s disease
Impaired glucose uptake in the brain is an early presymptomatic manifestation of Alzheimer’s disease (AD), with symptom-free periods of varying duration that likely reflect individual differences in metabolic resilience.
We propose a systemic “bioenergetic capacity”, the individual ability to maintain energy homeostasis under pathological conditions.
Using fasting serum acylcarnitine profiles from the AD Neuroimaging Initiative as a blood-based readout for this capacity, we identified subgroups with distinct clinical and biomarker presentations of AD.
Our data suggests that improving beta-oxidation efficiency can decelerate bioenergetic aging and disease progression.
The estimated treatment effects of targeting the bioenergetic capacity were comparable to those of recently approved anti-amyloid therapies, particularly in individuals with specific mitochondrial genotypes linked to succinylcarnitine metabolism.
Taken together, our findings provide evidence that therapeutically enhancing bioenergetic health may reduce the risk of symptomatic AD.
Furthermore, monitoring the bioenergetic capacity via blood acylcarnitine measurements can be achieved using existing clinical assays.