| Literature DB >> 31408375 |
Guanlan Xu1,2, Lance A Thielen1, Junqin Chen1,2, Truman B Grayson1, Tiffany Grimes1,2, S Louis Bridges1,3, Hubert M Tse1,4, Blair Smith5, Rakesh Patel1,6, Peng Li7, Carmella Evans-Molina8, Fernando Ovalle1,2, Anath Shalev1,2.
Abstract
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.Entities:
Keywords: T1D; beta cell death; biomarker; miR-204
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Substances:
Year: 2019 PMID: 31408375 PMCID: PMC6842918 DOI: 10.1152/ajpendo.00122.2019
Source DB: PubMed Journal: Am J Physiol Endocrinol Metab ISSN: 0193-1849 Impact factor: 4.310