uric acid has been researched along with Glucosephosphate Dehydrogenase Deficiency in 13 studies
Uric Acid: An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN.
uric acid : An oxopurine that is the final oxidation product of purine metabolism.
6-hydroxy-1H-purine-2,8(7H,9H)-dione : A tautomer of uric acid having oxo groups at C-2 and C-8 and a hydroxy group at C-6.
7,9-dihydro-1H-purine-2,6,8(3H)-trione : An oxopurine in which the purine ring is substituted by oxo groups at positions 2, 6, and 8.
Glucosephosphate Dehydrogenase Deficiency: A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Bilirubin and Hb were unchanged." | 2.78 | Α-lipoic acid supplementation up-regulates antioxidant capacity in adults with G6PD deficiency. ( Deli, CK; Fatouros, IG; Georgakouli, K; Jamurtas, AZ; Kouretas, D; Koutedakis, Y; Zalavras, A, 2013) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (61.54) | 18.7374 |
| 1990's | 2 (15.38) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (15.38) | 24.3611 |
| 2020's | 1 (7.69) | 2.80 |
| Authors | Studies |
|---|---|
| Ganapathi, M | 1 |
| Campbell, P | 1 |
| Ofori, K | 1 |
| Aggarwal, V | 1 |
| Francis, RO | 1 |
| Kratz, A | 1 |
| Jung, S | 1 |
| Sayad, K | 1 |
| Staitieh, BS | 1 |
| Georgakouli, K | 1 |
| Deli, CK | 1 |
| Zalavras, A | 1 |
| Fatouros, IG | 1 |
| Kouretas, D | 1 |
| Koutedakis, Y | 1 |
| Jamurtas, AZ | 1 |
| BROMBACHER, PJ | 1 |
| VANCREVELD, S | 1 |
| DAMME, JP | 1 |
| HUIJING, F | 1 |
| PLOEM, JE | 1 |
| Jakovcic, S | 1 |
| Sorensen, LB | 1 |
| Greene, HL | 1 |
| al-Ali, AK | 1 |
| Ahmed, MA | 1 |
| Qaw, FS | 1 |
| al-Fadel Saleh, M | 1 |
| al-Bashir, A | 1 |
| Corbucci, GG | 1 |
| Dancis, J | 1 |
| Yip, LC | 1 |
| Cox, RP | 1 |
| Piomelli, S | 1 |
| Balis, ME | 1 |
| Buchanan, KD | 1 |
| Watts, RW | 1 |
| Kelley, WN | 1 |
| Rosenbloom, FM | 1 |
| Seegmiller, JE | 1 |
| Howell, RR | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Effects of Alpha Lipoic Acid Supplementation in G6PD Deficient Individuals After Acute Exercise[NCT02937363] | 10 participants (Actual) | Interventional | 2016-12-31 | Completed | |||
| The Association Between Oxidative Stress and Carbohydrate Metabolism Disorders in G6PD Deficient Individuals[NCT05571748] | 40 participants (Anticipated) | Interventional | 2023-02-28 | Not yet recruiting | |||
| Effects of N-acetyl Cystein (NAC) Supplementation in G6PD Deficient Individuals After Acute Exercise[NCT02937376] | Early Phase 1 | 12 participants (Anticipated) | Interventional | 2023-02-01 | Not yet recruiting | ||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
3 reviews available for uric acid and Glucosephosphate Dehydrogenase Deficiency
| Article | Year |
|---|---|
Glycogen storage disease.
Topics: Blood Glucose; Glucosephosphate Dehydrogenase Deficiency; Glycogen; Glycogen Storage Disease; Glycog | 1982 |
Diabetes mellitus and gout.
Topics: Benzothiadiazines; Blood Glucose; Carbohydrate Metabolism; Diabetes Complications; Diabetes Mellitus | 1972 |
Molecular variation in relation to purine metabolism.
Topics: Amidophosphoribosyltransferase; Chemical Phenomena; Chemistry; Glucosephosphate Dehydrogenase Defici | 1974 |
2 trials available for uric acid and Glucosephosphate Dehydrogenase Deficiency
| Article | Year |
|---|---|
Α-lipoic acid supplementation up-regulates antioxidant capacity in adults with G6PD deficiency.
Topics: Adult; Antioxidants; Bilirubin; Catalase; Dietary Supplements; Glucosephosphate Dehydrogenase Defici | 2013 |
Α-lipoic acid supplementation up-regulates antioxidant capacity in adults with G6PD deficiency.
Topics: Adult; Antioxidants; Bilirubin; Catalase; Dietary Supplements; Glucosephosphate Dehydrogenase Defici | 2013 |
Α-lipoic acid supplementation up-regulates antioxidant capacity in adults with G6PD deficiency.
Topics: Adult; Antioxidants; Bilirubin; Catalase; Dietary Supplements; Glucosephosphate Dehydrogenase Defici | 2013 |
Α-lipoic acid supplementation up-regulates antioxidant capacity in adults with G6PD deficiency.
Topics: Adult; Antioxidants; Bilirubin; Catalase; Dietary Supplements; Glucosephosphate Dehydrogenase Defici | 2013 |
Α-lipoic acid supplementation up-regulates antioxidant capacity in adults with G6PD deficiency.
Topics: Adult; Antioxidants; Bilirubin; Catalase; Dietary Supplements; Glucosephosphate Dehydrogenase Defici | 2013 |
Α-lipoic acid supplementation up-regulates antioxidant capacity in adults with G6PD deficiency.
Topics: Adult; Antioxidants; Bilirubin; Catalase; Dietary Supplements; Glucosephosphate Dehydrogenase Defici | 2013 |
Α-lipoic acid supplementation up-regulates antioxidant capacity in adults with G6PD deficiency.
Topics: Adult; Antioxidants; Bilirubin; Catalase; Dietary Supplements; Glucosephosphate Dehydrogenase Defici | 2013 |
Α-lipoic acid supplementation up-regulates antioxidant capacity in adults with G6PD deficiency.
Topics: Adult; Antioxidants; Bilirubin; Catalase; Dietary Supplements; Glucosephosphate Dehydrogenase Defici | 2013 |
Α-lipoic acid supplementation up-regulates antioxidant capacity in adults with G6PD deficiency.
Topics: Adult; Antioxidants; Bilirubin; Catalase; Dietary Supplements; Glucosephosphate Dehydrogenase Defici | 2013 |
The role of reduced glutathione during the course of acute haemolysis in glucose-6-phosphate dehydrogenase deficient patients: clinical and pharmacodynamic aspects.
Topics: Adolescent; Adult; Alanine Transaminase; Aspartate Aminotransferases; Cell Hypoxia; Double-Blind Met | 1990 |
8 other studies available for uric acid and Glucosephosphate Dehydrogenase Deficiency
| Article | Year |
|---|---|
Impact of pre-emptive rapid testing for glucose-6-phosphate dehydrogenase deficiency prior to rasburicase administration at a tertiary care centre: A retrospective study.
Topics: Female; Glucosephosphate Dehydrogenase Deficiency; Hemolysis; Humans; Retrospective Studies; Tertiar | 2022 |
Low Hemoglobin Saturation in the Setting of Hyperuricemia.
Topics: Aged; Female; Glucosephosphate Dehydrogenase Deficiency; Gout Suppressants; Hemoglobins; Humans; Hyp | 2019 |
A REPORT OF TWO ADULT PATIENTS WITH GLYCOGEN STORAGE DISEASE.
Topics: Acetone; Adult; Blood Glucose; Carbohydrate Metabolism; Child; Epinephrine; Galactose; Glucagon; Glu | 1964 |
Studies of uric acid metabolism in glycogen storage disease associated with gouty arthritis.
Topics: Adolescent; Allopurinol; Body Height; Body Weight; Carbon Isotopes; Enzyme Therapy; Glucosephosphate | 1967 |
Uric acid, creatinine and urea in normal, glucose-6-phosphate dehydrogenase-deficient and Hb SS Saudi subjects.
Topics: Anemia, Sickle Cell; Creatinine; Glucosephosphate Dehydrogenase Deficiency; Humans; Saudi Arabia; Si | 1995 |
Vitamin C toxicity.
Topics: Ascorbic Acid; Burns; Dose-Response Relationship, Drug; Erythrocytes; Female; Glucosephosphate Dehyd | 1976 |
Disparate enzyme activity in erythocytes and leukocytes. A variant of hypoxanthine phosphoribosyl-transferase deficiency with an unstable enzyme.
Topics: Adolescent; Carbon Isotopes; Diphosphates; Epilepsy, Tonic-Clonic; Erythrocytes; Genotype; Glucoseph | 1973 |
Excessive production of uric acid in type I glycogen storage disease.
Topics: Adolescent; Carbon Isotopes; Female; Glucosephosphate Dehydrogenase Deficiency; Glucosyltransferases | 1968 |