Abstract | BACKGROUND/AIM: PATIENTS AND METHODS: RESULTS: DEA was well tolerated without hypoglycemia or adverse effects except transient diarrhea (n=1). DEA significantly reduced fasting glucose by 6.06 mg/dl (n=8) and insulin by 37.8% (n=8) in subjects with IR and/or A1c ≥5.6%. Furthermore, it improved cholesterol/HDL, LDL/HDL, and non- cholesterol HDL/HDL by 5.4, 6.5, and 6.6%, respectively in all subjects, and by 8.0, 9.8, and 9.8%, respectively in 9 subjects with A1c ≥5.6%. CONCLUSION: DEA efficacy correlates with the degree of IR. DEA holds promise as a novel treatment for the management of IR.
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Authors | Robert T Streeper, Christopher Louden, Elzbieta Izbicka |
Journal | In vivo (Athens, Greece)
(In Vivo)
2020 May-Jun
Vol. 34
Issue 3
Pg. 1173-1186
ISSN: 1791-7549 [Electronic] Greece |
PMID | 32354907
(Publication Type: Journal Article)
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Copyright | Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved. |
Chemical References |
- Biomarkers
- Blood Glucose
- Dicarboxylic Acids
- Esters
- Insulin
- azelaic acid
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Topics |
- Administration, Oral
- Biomarkers
- Blood Glucose
- Dicarboxylic Acids
(administration & dosage, chemistry)
- Esters
- Gas Chromatography-Mass Spectrometry
- Humans
- Insulin
(blood)
- Insulin Resistance
- Lipid Metabolism
- Male
- Overweight
(blood, drug therapy, etiology, metabolism)
- Sex Factors
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