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Biomarkers, Proteoforms, and Mass Spectrometry–Based Assays for Diabetes Clinical Research

  • Lorenz A. Nierves
  • , Tai Tu Lin
  • , Annie Moradian
  • , Qingqing Shen
  • , Salvatore Sechi
  • , Michael J. MacCoss
  • , Jun Qu
  • , Jennifer E. van Eyk
  • , Andrew N. Hoofnagle
  • , Wei Jun Qian
  • Pacific Northwest National Laboratory
  • Cedars-Sinai Medical Center
  • SUNY Buffalo
  • National Institutes of Health
  • University of Washington

Research output: Contribution to journalReview articlepeer-review

6 Scopus citations

Abstract

The prevalence of diabetes, particularly type 2 diabetes, has reached epidemic proportions globally. The number of patients with type 1 diabetes (T1D) is also increasing rapidly. Despite advancements in understanding the pathogenesis of diabetes, the lack of circulating pancreatic biomarkers and reliable clinical-grade assays remains a major gap in diabetes research, often hindering the ability to adequately assess disease progression and therapeutic responses. This mini-review discusses emerging pancreatic biomarkers, with an emphasis on T1D, the limitations of current immunoassays, and the expanding role of mass spectrometry–based assays. Highlights include the recent work within the NIDDK-funded “Targeted Mass Spectrometry Assays for Diabetes and Obesity Research (TaMADOR)” consortium, which aims to develop robust, quantitative, and transferable assays for translational research. The review also emphasizes the importance of proteoform-specific assays for monitoring pancreatic function, including prohormone processing during disease progression or in responses to therapy.

Original languageEnglish
Pages (from-to)1514-1523
Number of pages10
JournalJournal of Clinical Endocrinology and Metabolism
Volume110
Issue number6
DOIs
StatePublished - Jun 1 2025

Keywords

  • TaMADOR
  • glucagon
  • pancreatic dysfunction
  • post-translational modification
  • proinsulin
  • type 1 diabetes

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