Diabetes

  0012-1797

  1939-327X

  Mỹ

Cơ quản chủ quản:  American Diabetes Association Inc. , AMER DIABETES ASSOC

Lĩnh vực:
Endocrinology, Diabetes and MetabolismInternal Medicine

Các bài báo tiêu biểu

Autoantibodies to protein tyrosine phosphatase-like proteins in type I diabetes. Overlapping specificities to phogrin and ICA512/IA-2
Tập 45 Số 10 - Trang 1344-1349 - 1996
E. Kawasaki, George S. Eisenbarth, C. Wasmeier, J. C. Hutton
HLA heterogeneity of insulin-dependent diabetes mellitus at diagnosis. The Pittsburgh IDDM study
Tập 34 Số 12 - Trang 1247-1252 - 1985
Mark S. Eberhardt, D. K. Wagener, T. J. Orchard, R. E. LaPorte, D. E. Cavender, B. S. Rabin, R. W. Atchison, L. H. Kuller, Allan Drash, D. J. Becker
Value of antibodies to islet protein tyrosine phosphatase-like molecule in predicting type 1 diabetes
Tập 46 Số 8 - Trang 1270-1275 - 1997
Mohammed I. Hawa, Rachel Rowe, Michael S. Lan, Abner Louis Notkins, P. Pozzilli, M. R. Christie, R. D. G. Leslie
Antibodies to islet 37k antigen, but not to glutamate decarboxylase, discriminate rapid progression to IDDM in endocrine autoimmunity
Tập 43 Số 10 - Trang 1254-1259 - 1994
M. R. Christie, Salvatore Genovese, David D. Cassidy, Emanuele Bosi, Thomas J. Brown, Meizan Lai, Ezio Bonifacio, G. F. Bottazzo
Prediction of IDDM in the general population: strategies based on combinations of autoantibody markers
Tập 46 Số 11 - Trang 1701-1710 - 1997
P. J. Bingley, Ezio Bonifacio, Alistair J.K. Williams, S. Genovese, G. F. Bottazzo, Elaine Gale
Diabetes Antibody Standardization Program: First Assay Proficiency Evaluation
Tập 52 Số 5 - Trang 1128-1136 - 2003
Polly J. Bingley, Ezio Bonifacio, Patricia W. Mueller
The aims of the first proficiency evaluation of the Diabetes Antibody Standardization Program (DASP) were to assess general implementation of assay methods and to evaluate the new World Health Organization (WHO) reference reagent for autoantibodies to GAD and IA-2. Forty-six laboratories in 13 countries received coded sera from 50 patients with newly diagnosed type 1 diabetes and 50 blood donor control subjects, together with the WHO reference reagent and diluent serum. Results were analyzed using receiver operator characteristic (ROC) curves. Sensitivity was adjusted to 90% specificity in workshop controls. The median adjusted sensitivity for GADA (45 laboratories) was 84% (range 62–96%), for IA-2A (43 laboratories) was 58% (50–74%), and for insulin autoantibody (IAA; 23 laboratories) was 36% (13–66%). ROC curve analysis showed all GADA and IA-2A assays, and 18/23 IAA assays found significant differences between patients and control subjects. There was good concordance between laboratories in ranking of samples by GADA and IA-2A levels or if results were expressed in relation to the WHO reference reagent. Assays that achieved the highest sensitivity for IAA were also concordant in ranking samples, but overall concordance for IAA was poor. Differences in assay protocols between laboratories must be addressed so that all centers and kit manufacturers can perform to the same high standard.
Antibodies to glutamic acid decarboxylase reveal latent autoimmune diabetes mellitus in adults with a non-insulin-dependent onset of disease
Tập 42 Số 2 - Trang 359-362 - 1993
Jaakko Tuomilehto, Leif Groop, Paul Zimmet, Merrill J. Rowley, W. Knowles, Ian R. Mackay
Prediction of type I diabetes in first-degree relatives using a combination of insulin, GAD, and ICA512bdc/IA-2 autoantibodies
Tập 45 Số 7 - Trang 926-933 - 1996
C. F. Verge, R. Gianani, Eiji Kawasaki, L. Yu, M. Pietropaolo, R. A. Jackson, H. Peter Chase, George S. Eisenbarth
Increased glycogen synthase kinase-3 activity in diabetes- and obesity-prone C57BL/6J mice.
Tập 48 Số 8 - Trang 1662-1666 - 1999
Hagit Eldar-Finkelman, S A Schreyer, Michi M. Shinohara, Renee Leboeuf, E G Krebs
Although the precise mechanisms contributing to insulin resistance and type 2 diabetes are unknown, it is believed that defects in downstream components of the insulin signaling pathway may be involved. In this work, we hypothesize that a serine/threonine kinase, glycogen synthase kinase-3 (GSK-3), may be pertinent in this regard. To test this hypothesis, we examined GSK-3 activity in two inbred mouse strains known to be susceptible (C57BL/6J) or resistant (A/J) to diet-induced obesity and diabetes. Examination of GSK-3 in fat, liver, and muscle tissues of C57BL/6J mice revealed that GSK-3 activity increased twofold in the epididymal fat tissue and remained unchanged in muscle and liver of mice fed a high-fat diet, compared with their low-fat diet-fed counterparts. In contrast, GSK-3 activity did not change in the epididymal fat tissue of A/J mice, regardless of the type of diet they were fed. In addition, both basal and diet-induced GSK-3 activity was higher (2.3- and 3.2-fold, respectively) in the adipose tissue of C57BL/6J mice compared with that in A/J mice. Taken together, our studies suggest an unsuspected link between increased GSK-3 activity and development of insulin resistance and type 2 diabetes in fat tissue of C57BL/6J mice, and implicate GSK-3 as a potential factor contributing to susceptibility of C57BL/6J mice to diet-induced diabetes.