Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

A sensitive and specific ELISA for plasma pentosidine.

Y Izuhara1, T Miyata, Y Ueda

  • 1Molecular and Cellular Nephrology, Institute of Medical Sciences and Department of Medicine, Tokai University School of Medicine, Isehara, Kanagawa, Japan.

Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association
|April 8, 1999
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Validation of the ^{10}Be Ground-State Molecular Structure Using ^{10}Be(p,pα)^{6}He Triple Differential Reaction Cross-Section Measurements.

Physical review letters·2023
Same author

N=16 Magicity Revealed at the Proton Drip Line through the Study of ^{35}Ca.

Physical review letters·2023
Same author

Multiple Mechanisms in Proton-Induced Nucleon Removal at ∼100  MeV/Nucleon.

Physical review letters·2023
Same author

Study of the N=32 and N=34 Shell Gap for Ti and V by the First High-Precision Multireflection Time-of-Flight Mass Measurements at BigRIPS-SLOWRI.

Physical review letters·2023
Same author

Structure of ^{36}Ca under the Coulomb Magnifying Glass.

Physical review letters·2022
Same author

High-power laser experiment forming a supercritical collisionless shock in a magnetized uniform plasma at rest.

Physical review. E·2022

A new enzyme-linked immunosorbent assay (ELISA) accurately measures plasma pentosidine, a marker linked to dialysis complications. This method is faster and more convenient than current assays for assessing carbonyl stress in kidney failure patients.

Area of Science:

  • Biochemistry
  • Clinical Chemistry
  • Nephrology

Background:

  • Advanced glycation end products (AGEs) arise from non-enzymatic glycation and oxidation.
  • Pentosidine, a specific AGE, is implicated in complications of chronic kidney disease (CKD) and dialysis, including amyloidosis and atherosclerosis.

Purpose of the Study:

  • To develop and validate a sensitive and specific competitive enzyme-linked immunosorbent assay (ELISA) for quantifying plasma pentosidine.
  • To compare the performance of the developed ELISA with the established high-performance liquid chromatography (HPLC) method.

Main Methods:

  • A competitive ELISA was established for plasma pentosidine detection.
  • The ELISA was applied to plasma samples from hemodialysis (HD) and continuous ambulatory peritoneal dialysis (CAPD) patients.

Related Experiment Videos

  • Results from ELISA were compared with those obtained from HPLC analysis.
  • Main Results:

    • Plasma pentosidine levels measured by ELISA strongly correlated with HPLC assay results in both diabetic and non-diabetic dialysis patients.
    • Both methods showed significantly elevated plasma pentosidine levels (over 8-fold) in HD and CAPD patients compared to healthy individuals and non-uraemic diabetic patients.
    • The presence or absence of diabetes did not significantly alter the elevated pentosidine levels in dialysis patients.

    Conclusions:

    • The developed competitive ELISA offers a rapid, convenient, and reliable method for determining plasma pentosidine.
    • This assay is valuable for assessing carbonyl stress in uraemic patients.
    • The findings highlight elevated pentosidine levels as a common feature in patients undergoing long-term dialysis.