uric acid has been researched along with ALDOB Deficiency in 16 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "In patients with hereditary fructose intolerance, fructose consumption is associated with acute hypoglycemia, renal tubular acidosis, and hyperuricemia." | 2.87 | Are heterozygous carriers for hereditary fructose intolerance predisposed to metabolic disturbances when exposed to fructose? ( Barbey, F; Bonafé, L; Braissant, O; Damjanovic, K; De Bandt, JP; Debray, FG; Mittaz-Crettol, L; Paquot, N; Rosset, R; Roux, C; Tappy, L; Tran, C, 2018) |
| "Hereditary fructose intolerance (HFI) is the most important disturbance in human fructose metabolism." | 2.36 | [Hereditary fructose intolerance (author's transl)]. ( Thanner, F, 1977) |
| "We conclude that in patients with hereditary fructose intolerance, clinically important chronic fructose intoxication can occur after infancy without causing symptoms of acute fructose intoxication and can be expressed as an apparently isolated, reversible retardation of somatic growth with a continuing disorder of adenine nucleotide metabolism, characterized in part by recurrently increased rates of degradation of adenine nucleotides." | 1.27 | Chronic fructose intoxication after infancy in children with hereditary fructose intolerance. A cause of growth retardation. ( Mock, DM; Morris, RC; Perman, JA; Thaler, M, 1983) |
| "31P-MRS could be used to diagnose fructose intolerance and to monitor the patients' compliance with a fructose-restricted diet." | 1.27 | Study of hereditary fructose intolerance by use of 31P magnetic resonance spectroscopy. ( Collins, JE; Herschkowitz, N; Leonard, JV; Oberhaensli, RD; Radda, GK; Rajagopalan, B; Schwarz, H; Taylor, DJ, 1987) |
| "In two patients with hereditary fructose intolerance (HFI) the peak blood uric acid levels were 12." | 1.25 | Fructose-induced hyperuricemia: observations in normal children and in patients with hereditary fructose intolerance and galactosemia. ( Kogut, MD; Ng, W; Nonnel, GN; Roe, TF, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 14 (87.50) | 18.7374 |
| 1990's | 1 (6.25) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (6.25) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Debray, FG | 1 |
| Damjanovic, K | 1 |
| Rosset, R | 1 |
| Mittaz-Crettol, L | 1 |
| Roux, C | 1 |
| Braissant, O | 1 |
| Barbey, F | 1 |
| Bonafé, L | 1 |
| De Bandt, JP | 1 |
| Tappy, L | 1 |
| Paquot, N | 1 |
| Tran, C | 1 |
| Halpern, MJ | 1 |
| Mock, DM | 1 |
| Perman, JA | 1 |
| Thaler, M | 1 |
| Morris, RC | 1 |
| Kawaguchi, Y | 1 |
| Shirasawa, K | 1 |
| Yotsumoto, S | 1 |
| Nagahara, S | 1 |
| Steinmann, B | 2 |
| Baerlocher, K | 1 |
| Gitzelmann, R | 2 |
| Van den Berghe, G | 1 |
| Lameire, N | 1 |
| Mussche, M | 1 |
| Baele, G | 1 |
| Kint, J | 1 |
| Ringoir, S | 1 |
| Thanner, F | 1 |
| Richardson, RM | 1 |
| Little, JA | 1 |
| Patten, RL | 1 |
| Goldstein, MB | 1 |
| Halperin, ML | 1 |
| Chodorowski, Z | 1 |
| Emmerson, BT | 1 |
| Ravenscroft, PJ | 1 |
| Kogut, MD | 1 |
| Roe, TF | 1 |
| Ng, W | 1 |
| Nonnel, GN | 1 |
| MacRae, AR | 1 |
| Macdonald, I | 1 |
| Sachs, M | 1 |
| Asskali, F | 1 |
| Encke, A | 1 |
| Förster, H | 1 |
| Oberhaensli, RD | 1 |
| Rajagopalan, B | 1 |
| Taylor, DJ | 1 |
| Radda, GK | 1 |
| Collins, JE | 1 |
| Leonard, JV | 1 |
| Schwarz, H | 1 |
| Herschkowitz, N | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Are Heterozygous Carriers for Hereditary Fructose Intolerance Predisposed to Metabolic Disturbances When Exposed to Fructose?[NCT02979106] | 18 participants (Actual) | Interventional | 2015-01-31 | Completed | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
3 reviews available for uric acid and ALDOB Deficiency
| Article | Year |
|---|---|
Metabolic effects of fructose in the liver.
Topics: Alcohols; AMP Deaminase; Animals; Child; Fructose; Fructose Intolerance; Fructosephosphates; Glucago | 1978 |
[Hereditary fructose intolerance (author's transl)].
Topics: Carbohydrate Metabolism, Inborn Errors; Fructose; Fructose Intolerance; Fructose-Bisphosphate Aldola | 1977 |
[Selected phsiopathological and clinical aspects of purine metabolism].
Topics: Alkalosis, Respiratory; Diabetes Mellitus; Diuresis; Female; Fructose Intolerance; Glomerular Filtra | 1976 |
1 trial available for uric acid and ALDOB Deficiency
| Article | Year |
|---|---|
Are heterozygous carriers for hereditary fructose intolerance predisposed to metabolic disturbances when exposed to fructose?
Topics: Adult; Carbohydrate Metabolism; Creatinine; Female; Fructose; Fructose Intolerance; Heterozygote; Hu | 2018 |
12 other studies available for uric acid and ALDOB Deficiency
| Article | Year |
|---|---|
Carbohydrate sensitivity, triglycerides and uric acid.
Topics: Carbohydrate Metabolism, Inborn Errors; Fructose Intolerance; Humans; Triglycerides; Uric Acid | 1984 |
Chronic fructose intoxication after infancy in children with hereditary fructose intolerance. A cause of growth retardation.
Topics: Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Chronic Disease; Fructose; Fructose Intole | 1983 |
Type III glycogenosis with deposition of urate and amyloid.
Topics: Adult; Amyloid; Fructose Intolerance; Glycogen Storage Disease; Glycogen Storage Disease Type IV; Go | 1980 |
[Hereditary disorders of fructose metabolism. Loading tests with fructose, sorbitol and dihydroxyacetone].
Topics: Bicarbonates; Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Depression, Chemical; Dihydroxy | 1975 |
[Fructose and sorbitol in infusion solutions are not always harmless].
Topics: Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Female; Fructose; Fructose Intolerance; Fruct | 1976 |
Hereditary fructose intolerance: a difficult diagnosis in the adult.
Topics: Acidosis, Renal Tubular; Adult; Age Factors; Bicarbonates; Carbohydrate Metabolism, Inborn Errors; C | 1978 |
Pathogenesis of acidosis in hereditary fructose intolerance.
Topics: Acid-Base Imbalance; Acidosis, Renal Tubular; Adolescent; Bicarbonates; Blood Glucose; Carbohydrate | 1979 |
Abnormal renal urate homeostasis in systemic disorders.
Topics: Alcoholism; Diabetes Mellitus; Female; Fructose Intolerance; Glomerular Filtration Rate; Glycogen St | 1975 |
Fructose-induced hyperuricemia: observations in normal children and in patients with hereditary fructose intolerance and galactosemia.
Topics: Adult; Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Fruct | 1975 |
A comparison of the effects of an oral fructose load in hypertriglyceridaemic and normolipidaemic men.
Topics: Adult; Carbohydrate Metabolism, Inborn Errors; Fructose; Fructose Intolerance; Humans; Hyperlipidemi | 1975 |
[Metabolic changes in patients with hereditary fructose intolerance. A contribution to the topic of fructose administration for parenteral feeding].
Topics: Adult; Ammonia; Blood Glucose; Female; Fructose; Fructose Intolerance; Glutamine; Humans; Lactates; | 1991 |
Study of hereditary fructose intolerance by use of 31P magnetic resonance spectroscopy.
Topics: Carbohydrate Metabolism, Inborn Errors; Female; Fructose; Fructose Intolerance; Fructose-Bisphosphat | 1987 |