Mechanisms of diabetic complications

Forbes, Josephine M. and Cooper, Mark E. (2013) Mechanisms of diabetic complications. Physiological Reviews, 93 1: 137-188. doi:10.1152/physrev.00045.2011

Attached Files (Some files may be inaccessible until you login with your UQ eSpace credentials)
Name Description MIMEType Size Downloads

Author Forbes, Josephine M.
Cooper, Mark E.
Title Mechanisms of diabetic complications
Journal name Physiological Reviews   Check publisher's open access policy
ISSN 0031-9333
Publication date 2013-01-01
Year available 2013
Sub-type Critical review of research, literature review, critical commentary
DOI 10.1152/physrev.00045.2011
Open Access Status Not yet assessed
Volume 93
Issue 1
Start page 137
End page 188
Total pages 52
Place of publication Bethesda, MD United States
Publisher American Physiological Society
Language eng
Abstract It is increasingly apparent that not only is a cure for the current worldwide diabetes epidemic required, but also for its major complications, affecting both small and large blood vessels. These complications occur in the majority of individuals with both type 1 and type 2 diabetes. Among the most prevalent microvascular complications are kidney disease, blindness, and amputations, with current therapies only slowing disease progression. Impaired kidney function, exhibited as a reduced glomerular filtration rate, is also a major risk factor for macrovascular complications, such as heart attacks and strokes. There have been a large number of new therapies tested in clinical trials for diabetic complications, with, in general, rather disappointing results. Indeed, it remains to be fully defined as to which pathways in diabetic complications are essentially protective rather than pathological, in terms of their effects on the underlying disease process. Furthermore, seemingly independent pathways are also showing significant interactions with each other to exacerbate pathology. Interestingly, some of these pathways may not only play key roles in complications but also in the development of diabetes per se. This review aims to comprehensively discuss the well validated, as well as putative mechanisms involved in the development of diabetic complications. In addition, new fields of research, which warrant targets of the future, will be highlighted.
Keyword Physiology
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Critical review of research, literature review, critical commentary
Collection: Mater Research Institute-UQ (MRI-UQ)
Version Filter Type
Citation counts: TR Web of Science Citation Count  Cited 479 times in Thomson Reuters Web of Science Article | Citations
Scopus Citation Count Cited 501 times in Scopus Article | Citations
Google Scholar Search Google Scholar
Created: Mon, 15 Dec 2014, 20:49:03 EST by System User on behalf of Mater Research Institute-UQ