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Cardiac biomarkers are enzymes, proteins, and hormones released into the blood when cardiac cells are injured. They are powerful tools for triaging.
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Biomarkers.

Barbara Mroczko1, Agnieszka Kulczynska-Przybik1, Daria Krawczuk1

  • 1Department of Neurodegeneration Diagnostics, Medical University of Bialystok, Bialystok, Poland.

Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|December 26, 2025
PubMed
Summary
This summary is machine-generated.

Kallikrein 5 (KLK5) levels are elevated in Alzheimer's disease (AD) patients' cerebrospinal fluid and correlate with amyloid pathology. KLK5 may serve as an additional biomarker for AD diagnosis alongside Aβ and tau proteins.

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Area of Science:

  • Neuroscience
  • Biochemistry
  • Molecular Biology

Background:

  • Alzheimer's disease (AD) presents a significant global health challenge, necessitating a deeper understanding of its molecular pathogenesis.
  • Kallikrein-related peptidases (KLKs), a family of serine proteases, are emerging as potential biomarkers and therapeutic targets for AD.
  • While KLK6 and KLK8 have been studied, information regarding KLK5's role in AD pathogenesis remains limited.

Purpose of the Study:

  • To investigate the levels of KLK5 in the cerebrospinal fluid (CSF) of AD patients.
  • To explore the association between KLK5 concentrations and established AD biomarkers.

Main Methods:

  • Cerebrospinal fluid (CSF) samples were collected from AD patients and cognitively normal individuals.
  • Concentrations of KLK5, amyloid beta 1-42 (Aß-42), amyloid beta 1-40, Tau, and pTau181 were measured using multiplexing and enzyme-linked immunosorbent assays.

Main Results:

  • CSF KLK5 concentrations were significantly higher in AD patients compared to controls.
  • In AD patients, KLK5 levels showed a significant correlation with the CSF amyloid beta ratio.

Conclusions:

  • Kallikrein 5 (KLK5) may play a role in Alzheimer's disease pathogenesis, particularly in relation to amyloid pathology.
  • KLKs, including KLK5, could potentially serve as supplementary biomarkers for AD when used in conjunction with established markers like amyloid beta and tau proteins.