Blood-based signatures in type 1 diabetes. Diabetologia 2016 Mar;59(3):414-25
Date
12/25/2015Pubmed ID
26699650Pubmed Central ID
PMC4744128DOI
10.1007/s00125-015-3843-xScopus ID
2-s2.0-84957427317 (requires institutional sign-in at Scopus site) 41 CitationsAbstract
Type 1 diabetes mellitus is one of the most common chronic diseases in childhood. It develops through autoimmune destruction of the pancreatic beta cells and results in lifelong dependence on exogenous insulin. The pathogenesis of type 1 diabetes involves a complex interplay of genetic and environmental factors and has historically been attributed to aberrant adaptive immunity; however, there is increasing evidence for a role of innate inflammation. Over the past decade new methodologies for the analysis of nucleic acid and protein signals have been applied to type 1 diabetes. These studies are providing a new understanding of type 1 diabetes pathogenesis and have the potential to inform the development of new biomarkers for predicting diabetes onset and monitoring therapeutic interventions. In this review we will focus on blood-based signatures in type 1 diabetes, with special attention to both direct transcriptomic analyses of whole blood and immunocyte subsets, as well as plasma/serum-induced transcriptional signatures. Attention will also be given to proteomics, microRNA assays and markers of beta cell death. We will also discuss the results of blood-based profiling in type 1 diabetes within the context of the genetic and environmental factors implicated in the natural history of autoimmune diabetes.
Author List
Cabrera SM, Chen YG, Hagopian WA, Hessner MJAuthors
Susanne M. Cabrera MD Associate Professor in the Pediatrics department at Medical College of WisconsinYi-Guang Chen PhD Professor in the Pediatrics department at Medical College of Wisconsin
Martin J. Hessner PhD Professor in the Pediatrics department at Medical College of Wisconsin
MESH terms used to index this publication - Major topics in bold
BiomarkersDiabetes Mellitus, Type 1
Humans
Immunity, Innate