Predictors of Ketoacidosis and Severe Hypoglycemia in Type I Diabetes

2002 ◽  
Vol 8 (1) ◽  
pp. 3-4
Author(s):  
C. Foster ◽  
S. L. Bratton
Diabetes Care ◽  
1995 ◽  
Vol 18 (12) ◽  
pp. 1621-1622 ◽  
Author(s):  
N. Sakane ◽  
T. Yoshida ◽  
K. Yoshioka ◽  
T. Umekawa ◽  
M. Kondo

2009 ◽  
Vol 29 (11) ◽  
pp. 1790-1795
Author(s):  
Lise Grimmeshave Bie-Olsen ◽  
Ulrik Pedersen-Bjergaard ◽  
Troels Wesenberg Kjær ◽  
Markus Nowak Lonsdale ◽  
Ian Law ◽  
...  

The risk of severe hypoglycemia in patients with type I diabetes and high basal activity in the renin–angiotensin system (RAS) is significantly higher than in patients with low basal RAS activity. In healthy men, we tested the hypothesis that differences in spontaneous RAS activity are associated with differences in cerebral activity responses during mild hypoglycemia. A total of 10 healthy men with high and 10 with low spontaneous RAS activity were selected. An H215O-PET (H215O-positron emission tomography) study was conducted with a series of six scans, i.e., two during normoglycemia, two during hypoglycemia, and two after hypoglycemia. The mean plasma glucose concentration was similar in both the groups (i.e., 2.1 mmol/L (s.d.: 0.4) in the low RAS group and 2.2 mmol/L (s.d.: 0.4) in the high RAS group ( P=0.47)). The high RAS group has lower cerebral activity in the frontal area and a higher cerebral activity in the entorhinal area that expanded to include the parahippocampal gyrus after hypoglycemia. Our findings suggest that the high RAS group to a lesser extent than the low RAS group activates areas involving executive function that may explain the correlation between high basal RAS activity and risk of severe hypoglycemia in type I diabetes.


Author(s):  
T. A. Stewart ◽  
D. Liggitt ◽  
S. Pitts ◽  
L. Martin ◽  
M. Siegel ◽  
...  

Insulin-dependant (Type I) diabetes mellitus (IDDM) is a metabolic disorder resulting from the lack of endogenous insulin secretion. The disease is thought to result from the autoimmune mediated destruction of the insulin producing ß cells within the islets of Langerhans. The disease process is probably triggered by environmental agents, e.g. virus or chemical toxins on a background of genetic susceptibility associated with particular alleles within the major histocompatiblity complex (MHC). The relation between IDDM and the MHC locus has been reinforced by the demonstration of both class I and class II MHC proteins on the surface of ß cells from newly diagnosed patients as well as mounting evidence that IDDM has an autoimmune pathogenesis. In 1984, a series of observations were used to advance a hypothesis, in which it was suggested that aberrant expression of class II MHC molecules, perhaps induced by gamma-interferon (IFN γ) could present self antigens and initiate an autoimmune disease. We have tested some aspects of this model and demonstrated that expression of IFN γ by pancreatic ß cells can initiate an inflammatory destruction of both the islets and pancreas and does lead to IDDM.


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