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Series GSE50866 Query DataSets for GSE50866
Status Public on Jul 30, 2014
Title Identification of Novel Auto-antibodies in Type 1 Diabetic Patients using a High-density Protein Microarray
Organism Homo sapiens
Experiment type Protein profiling by protein array
Summary Type 1 diabetes mellitus (T1DM) results from immune mediated destruction of pancreatic beta cells. However, clinical and immunologic phenotypes of T1DM are variable. Several auto-antibodies including GADA, IA-2A, and ZnT8A, were identified in T1DM, but the prevalence of these auto-antibodies varied for a broad spectrum of T1DM. Here, we systemically profiled auto-antibodies from serum samples of 16 T1DM, 16 type 2 diabetes (T2DM) patients, and 27 healthy controls with normal glucose tolerance (NGT) using protein microarrays containing 9,480 proteins. Among 9,480 different proteins on the array, we identified novel auto-antibody candidates (EEF1A1-AAb and UBE2L3-AAb) by M-test coupled with PLS-DA. These auto-antibodies were highly present in T1DM than controls and detected in 40% of T1DM without GADA. Furthermore, these auto-antibodies might help to differentiate subtype of T1DM when combined with GADA. These novel auto-antibodies provide new diagnostic information of T1DM, as well as new insights into the pathogenesis of T1DM.
 
Overall design Auto-antibodies from serum samples were profiled using a high-density, fluorescence-based protein microarray containing duplicate spots of 9,480 human proteins derived from the Ultimate ORF collection
The cohort of patients and controls consisted of 16 T1DM, 16 T2DM patients, and 27 healthy controls with NGT. This cohort was used to screen candidate auto-antibodies using protein microarrays (ProtoArray platform version 5.0, Invitrogen Corp., Carlsbad, CA). Serum samples were drawn from T1DM patients who have 1) fasting C-peptide level <0.3 nmol/L or serum C-peptide <0.6 nmol/L after glucagon loading, 2) initiation of insulin treatment within six months after diagnosis, and 3) duration of diabetes ≤12 months. Mean age of T1DM in the first cohort was 42 ± 16 years. The control serum samples were obtained from T2DM patients who were treated only with oral anti-diabetic drug at least 5 years and from NGTs who had no history of diabetes, no first-degree relatives with diabetes, a fasting plasma glucose concentration of <6.1 mmol/l, and a HbA1c value of <5.8%.
 
Contributor(s) Koo B, Chae S, Kim KM, Hwang D, Yi EC, Park K
Citation(s) 24947363
Submission date Sep 13, 2013
Last update date Jul 30, 2014
Contact name Sehyun Chae
E-mail(s) implish@postech.ac.kr
Organization name POSTECH
Department Department of Interdisciplinary Bioscience and Bioengineering(I-BIO)
Lab Lab of SYSTEMS BIOLOGY and MEDICINE
Street address San 31, Hyoja-Dong, Nam-Gu
City Pohang, Gyungbuk
ZIP/Postal code 790-784
Country South Korea
 
Platforms (1)
GPL13669 Invitrogen ProtoArray v5.0
Samples (59)
GSM1231310 NGT_1
GSM1231311 NGT_2
GSM1231312 NGT_3
Relations
BioProject PRJNA219232

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE50866_RAW.tar 69.0 Mb (http)(custom) TAR (of GPR)
GSE50866_average_non_normalized_output.txt.gz 932.7 Kb (ftp)(http) TXT
Processed data included within Sample table

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