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ABSTRACT: Introduction
Preclinical studies demonstrate the potential of amylin in the diagnosis of Alzheimer's disease (AD). We aimed to lay the foundation for repurposing the amylin analog and a diabetes drug, pramlintide, for AD in humans.Methods
We administered a single subcutaneous injection of 60 μg of pramlintide to nondiabetic subjects under fasting conditions.Results
None of the participants developed hypoglycemia after the injection of pramlintide. The pramlintide challenge induced a significant surge of amyloid-β peptide and a decrease in total tau in the plasma of AD subjects but not in control participants. The pramlintide injection provoked an increase in interleukin 1 receptor antagonist and a decrease in retinol-binding protein 4, which separates AD subjects from control subjects.Discussion
Pramlintide use appeared to be safe in the absence of diabetes. The biomarker changes as a result of the pramlintide challenge, which distinguished AD from control subjects and mild cognitive impairment.
SUBMITTER: Zhu H
PROVIDER: S-EPMC5424531 | biostudies-literature |
REPOSITORIES: biostudies-literature