Anti-islet cell antibodies in a sample of Egyptian females with gestational diabetes and its relation to development of type 1 diabetes mellitus

2017 ◽  
Author(s):  
Amer Hanan M ◽  
elbaky Rania S Abd ◽  
Merhan S Nasr ◽  
Laila M Hendawy ◽  
Mohamed O Taha ◽  
...  
2018 ◽  
Vol 14 (4) ◽  
pp. 389-394 ◽  
Author(s):  
Hanan M. Amer ◽  
Rania S. Abd El Baky ◽  
Merhan S. Nasr ◽  
Laila M. Hendawy ◽  
Wessam A. Ibrahim ◽  
...  

2005 ◽  
Vol 14 (2-3) ◽  
pp. 77-84 ◽  
Author(s):  
Milene C. Geiger ◽  
Jacqueline V. Ferreira ◽  
Muhammad M. Hafiz ◽  
Tatiana Froud ◽  
David A. Baidal ◽  
...  

This study evaluated the Medtronic MiniMed Continuous Glucose Monitoring System (CGMS) in patients with type 1 diabetes mellitus who underwent successful islet cell transplantation (ICT). The results are compared to standardized self-monitoring (SMBG) of hyperglycemia and mean amplitude of glycemic excursions (MAGE). We studied 19 patients (mean age 40.0 ± 6.7 years) in three groups: six patients post-ICT, seven patients awaiting ICT, and six normal volunteers (controls). Continuous glucose monitoring post-ICT showed remarkable glucose stability compared with patients awaiting ICT. The CGMS group showed modestly higher glucoses (mean 111.5 mg/dl) compared with controls (88 mg/dl). Postprandial glucoses in ICT recipients rarely exceeded 180 mg/dl and were similar to controls. There was no difference in asymptomatic hypoglycemia between control and post-ICT groups. However, a higher incidence of hypoglycemia was observed in patients awaiting ICT. HbA1c and MAGE pre- and post-ICT were 8.3 ± 0.9% and 6 ± 0.3% (p < 0.001) and 109 ± 34 and 41 ± 11 (p < 0.001), respectively. No complications were associated with CGMS. This study suggests ICT significantly improves metabolic control and rate of hypoglycemia when compared with controls and patients awaiting ICT. Similar improvement in metabolic control was observed with SMBG, HbA1c, and MAGE. Although CGMS was not demonstrated to be a superior tool for routine assessment in ICT, it is very helpful in special clinical situations.


2005 ◽  
Vol 80 (12) ◽  
pp. 1718-1728 ◽  
Author(s):  
Muhammad M. Hafiz ◽  
Raquel N. Faradji ◽  
Tatiana Froud ◽  
Antonello Pileggi ◽  
David A. Baidal ◽  
...  

2018 ◽  
Vol 15 (6) ◽  
pp. 528-540 ◽  
Author(s):  
Azlina A Razak ◽  
Lopa Leach ◽  
Vera Ralevic

Background: There is clinical and experimental evidence for altered adenosine signalling in the fetoplacental circulation in pregnancies complicated by diabetes, leading to adenosine accumulation in the placenta. However, the consequence for fetoplacental vasocontractility is unclear. This study examined contractility to adenosine of chorionic vessels from type 1 diabetes mellitus, gestational diabetes mellitus and normal pregnancies. Methods: Chorionic arteries and veins were isolated from human placenta from normal, gestational diabetes mellitus and type 1 diabetes mellitus pregnancies. Isometric tension recording measured responses to adenosine and the thromboxane A2 analogue U46619 (thromboxane A2 mediates fetoplacental vasoconstriction to adenosine). Adenosine and thromboxane prostanoid receptor protein expression was determined by immunoblotting. Results: Adenosine elicited contractions in chorionic arteries and veins which were impaired in both gestational diabetes mellitus and type 1 diabetes mellitus. Contractions to potassium chloride were unchanged. Adenosine A2A and A2B receptor protein levels were not different in gestational diabetes mellitus and normal pregnancies. Contractions to U46619 were unaltered in gestational diabetes mellitus arteries and increased in type 1 diabetes mellitus arteries. Overnight storage of vessels restored contractility to adenosine in gestational diabetes mellitus arteries and normalized contraction to U46619 in type 1 diabetes mellitus arteries. Conclusion: These data are consistent with the concept of aberrant adenosine signalling in diabetes; they show for the first time that this involves impaired adenosine contractility of the fetoplacental vasculature.


2011 ◽  
Vol 37 (1) ◽  
pp. 47-51 ◽  
Author(s):  
H. Wucher ◽  
J. Lepercq ◽  
C. Carette ◽  
C. Colas ◽  
D. Dubois-Laforgue ◽  
...  

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