1984
DOI: 10.1203/00006450-198404000-00011
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The 2-Deoxyglucose Test as a Supplement to Fasting for Detection of Childhood Hypoglycemia

Abstract: Summaryhvvodycemic, it is inevitably difficult and not without risk.The acute response to simulated hypoglycemia induced by 2-deoxyglucose (2DG) was compared with the prolonged fasting test as a possible screening test for detection of childhood hypoglycemia. Ten children, ages 2-9 yr, without a documented history of hypoglycemia were classified retrospectively as reference subjects. While fasting, their plasma glucose decreased to an average of 50 mg/dl (range, 30-74) between 28-36 h. After infusion of 2DG, … Show more

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Cited by 14 publications
(9 citation statements)
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“…MS is a chronic disease, and we recognize the limitation of the 2DG being translated for MS treatment due to poor drug-like characteristics including rapid metabolism and short half-life ( 57 ). To enhance its drug-like property, new analogs of 2DG are being tested ( 58 ).…”
Section: Discussionmentioning
confidence: 99%
“…MS is a chronic disease, and we recognize the limitation of the 2DG being translated for MS treatment due to poor drug-like characteristics including rapid metabolism and short half-life ( 57 ). To enhance its drug-like property, new analogs of 2DG are being tested ( 58 ).…”
Section: Discussionmentioning
confidence: 99%
“…Despite the numerous preclinical and clinical studies, the use of 2-DG in anticancer therapy is still limited. Its rapid metabolism and short half-life (according to Hansen et al, after infusion of 50 mg/kg 2-DG, its plasma half-life was only 48 min) [ 13 ], making 2-DG a rather poor drug candidate. Moreover, 2-DG has to be used at a relatively high concentration (5 mmol/L) to compete with blood glucose.…”
Section: Discussionmentioning
confidence: 99%
“…The main obstacle to an efficient therapy with 2-DG is its rapid metabolism and short half-life (according to Hansen et al, after infusion of 50 mg/kg 2-DG, its plasma half-life was only 48 min.) [ 13 ]. Moreover, 2-DG has to be used at relatively high concentrations (≥5 mmol/L) to compete with blood glucose [ 14 ].…”
Section: Introductionmentioning
confidence: 99%
“…Bevacizumab -GBM [112] 5 -Fluorouracil -pancreatic cancer [73] Trastuzumab -breast cancer [113] Ferulic acid with irradiation -non-small cell lung carcinoma [114] Radiotherapy -breast cancer [ Despite the numerous preclinical and clinical studies cited above, the use of 2-DG in cancer treatment is still limited. Its rapid metabolism and short half-life (according to Hansen et al, after infusion of 50 mg/kg 2-DG, its plasma half-life was only 48 min [117]) make 2-DG a rather poor drug candidate. Moreover, 2-DG has to be used at relatively high concentrations (≥5 mmol/L) in order to compete with blood glucose [118].…”
Section: Combined Therapy With 2-dg Cancer Type Referencesmentioning
confidence: 99%