4.6 Article

Serum miR-204 is an early biomarker of type 1 diabetes-associated pancreatic beta-cell loss

Journal

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpendo.00122.2019

Keywords

beta cell death; biomarker; miR-204; T1D

Funding

  1. NIH [R01-DK-093954, UC4-DK-104166, R01-DK-078752, U01-DK-120379]
  2. JDRF [2-SRA-2018-493-A-B, 3-SRA-2014-302-M-R]
  3. Diabetes Research Center (NIH) [P30-DK-079626]
  4. Veterans Affairs Merit Award [I01-BX-001733]

Ask authors/readers for more resources

Pancreatic beta-cell death is a major factor in the pathogenesis of type 1 diabetes (T1D). but straightforward methods to measure beta-cell loss in humans are lacking, underlining the need for novel biomarkers. Using studies in INS-1 cells, human islets, diabetic mice, and serum samples of subjects with T1D at different stages, we have identified serum miR-204 as an early biomarker of T1D-associated beta-cell loss in humans. MiR-204 is a highly enriched microRNA in human beta-cells, and we found that it is released from dying beta-cells and detectable in human serum. We further discovered that serum miR-204 was elevated in children and adults with T1D and in autoantibody-positive at-risk subjects but not in type 2 diabetes or other autoimmune diseases and was inversely correlated with remaining beta-cell function in recent-onset T1D. Thus, serum miR-204 may provide a much needed novel approach to assess early T1D-associated human beta-cell loss even before onset of overt disease.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available