The peptide, called HAEE (Ac-His-Ala-Glu-Glu-NH2), was originally designed by researchers from the startup Lifemission and the Russian Academy of Sciences to stop amyloid-beta plaques from forming by blocking zinc ions thought to act as biological 'glue'. In mouse tests, the peptide reduced plaque counts.
When the team developed a method to measure HAEE in human blood to prepare for clinical trials, they found the peptide in every sample from 150 healthy volunteers. Blood samples from people with Alzheimer's averaged roughly half the HAEE level of healthy controls, suggesting the molecule might be used as a disease biomarker.
"We discovered that the human blood contains an endogenous replica of this peptide, and that its concentration is sharply reduced in patients with a clinical diagnosis of Alzheimer's disease," the researchers wrote. "Our findings uncover a new molecule of the human body and suggest that endogenous HAEE deficiency plays a significant role in the pathogenesis of Alzheimer's disease."
The study has limitations. Alzheimer's diagnoses were based on clinical assessments alone, without brain imaging or biomarker tests, so some patients may have had other forms of dementia. Age varied between groups, and HAEE levels did not differ significantly by disease severity. The work was funded by Lifemission, which holds patents on HAEE as a blood test, and two of the study researchers are connected to the company.
The researchers say HAEE deficiency may result from reduced production or increased consumption during the disease. Further studies are needed to clarify the relationship and whether synthetic HAEE could be used as a drug.