GAD antibodies in classification of Asian type 2 diabetes

Diabetes Care ◽  
1999 ◽  
Vol 22 (6) ◽  
pp. 1011-1012 ◽  
Author(s):  
M. Fukui ◽  
N. Nakamura ◽  
M. Kondo
Diabetes Care ◽  
2014 ◽  
Vol 38 (1) ◽  
pp. 16-21 ◽  
Author(s):  
Lingjiao Liu ◽  
Xia Li ◽  
Yufei Xiang ◽  
Gan Huang ◽  
Jian Lin ◽  
...  

Author(s):  
Ramalingaswamy Cheruku ◽  
Damodar Reddy Edla ◽  
Venkatanareshbabu Kuppili
Keyword(s):  

Author(s):  
Ramalingaswamy Cheruku ◽  
Damodar Reddy Edla ◽  
Venkatanareshbabu Kuppili
Keyword(s):  

Author(s):  
Ramalingaswamy Cheruku ◽  
Damodar Reddy Edla ◽  
Venkatanareshbabu Kuppili

2019 ◽  
Author(s):  
Sandra Reitmeier ◽  
Silke Kießling ◽  
Thomas Clavel ◽  
Markus List ◽  
Eduardo L. Almeida ◽  
...  

SummaryTo combat the epidemic increase in Type-2-Diabetes (T2D), risk factors need to be identified. Diet, lifestyle and the gut microbiome are among the most important factors affecting metabolic health. We demonstrate in 1,976 subjects of a prospective population cohort that specific gut microbiota members show diurnal oscillations in their relative abundance and we identified 13 taxa with disrupted rhythmicity in T2D. Prediction models based on this signature classified T2D with an area under the curve of 73%. BMI as microbiota-independent risk marker further improved diagnostic classification of T2D. The validity of this arrhythmic risk signature to predict T2D was confirmed in 699 KORA subjects five years after initial sampling. Shotgun metagenomic analysis linked 26 pathways associated with xenobiotic, amino acid, fatty acid, and taurine metabolism to the diurnal oscillation of gut bacteria. In summary, we determined a cohort-specific risk pattern of arrhythmic taxa which significantly contributes to the classification and prediction of T2D, highlighting the importance of circadian rhythmicity of the microbiome in targeting metabolic human diseases.


2018 ◽  
Vol 6 (1) ◽  
pp. e000604 ◽  
Author(s):  
Erin S LeBlanc ◽  
Ning X Smith ◽  
Gregory A Nichols ◽  
Michael J Allison ◽  
Gregory N Clarke

ObjectiveTo determine the possible association between insomnia and risk of type 2 diabetes mellitus (T2DM) in the naturalistic clinical setting.Research design and methodsWe conducted a retrospective cohort study to examine the risk of developing T2DM among patients with pre-diabetes with and without insomnia. Participants with pre-diabetes (identified by a physician or via two laboratory tests) between January 1, 2007 and December 31, 2015 and without sleep apnea were followed until December 31, 2016. Patients were determined to have T2DM when two of the following occurred within a 2-year window: physician-entered outpatient T2DM diagnosis (International Classification of Diseases [ICD]-9 250.00; ICD-10 E11), dispensing of an antihyperglycemia agent, and hemoglobin A1c (A1c) >6.5% (48 mmol/mol) or fasting plasma glucose (FPG) >125 mg/dL. One hospital inpatient stay with an associated T2DM diagnosis was also sufficient for classification of T2DM.ResultsOur cohort consisted of 81 233 persons with pre-diabetes, 24 146 (29.7%) of whom had insomnia at some point during the 4.3-year average observation period. After adjustment for traditional risk factors, those with insomnia were 28% more likely to develop T2DM than those without insomnia (HR 1.28; 95% CI 1.24 to 1.33). The estimate was essentially unchanged after adjusting for baseline A1c level (HR 1.32; 95% CI 1.25 to 1.40) or FPG (HR 1.28; 95% CI 1.23 to 1.33).ConclusionsInsomnia imparts an increased risk of T2DM comparable with that conferred by traditional risk factors (eg, overweight, non-white race, cardiovascular risk factors). This association could have clinical importance because it suggests a new potentially modifiable risk factor that could be targeted to prevent diabetes.


Diabetes Care ◽  
2005 ◽  
Vol 28 (7) ◽  
pp. 1798-1800 ◽  
Author(s):  
A. M. Wagner ◽  
A. Perez ◽  
J. L. Sanchez-Quesada ◽  
J. Ordonez-Llanos

2006 ◽  
Vol 23 (8) ◽  
pp. 834-838 ◽  
Author(s):  
H. A. J. Castleden ◽  
B. Shields ◽  
P. J. Bingley ◽  
A. J. K. Williams ◽  
M. Sampson ◽  
...  

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