Page last updated: 2024-10-20

uric acid and Anemia, Cooley's

uric acid has been researched along with Anemia, Cooley's in 14 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.

Research Excerpts

ExcerptRelevanceReference
" Mild adverse events were reported in 48 (9%) patients and serious adverse events, including cerebral vascular accident and portal vein thrombosis were reported in two patients each."3.30Long-term clinical efficacy and safety of thalidomide in patients with transfusion-dependent β-thalassemia: results from Thal-Thalido study. ( Ali, M; Ali, Z; Ismail, M; Khan, MTM; Rani, GF; Rehman, IU, 2023)
"The majority of patients with thalassemia major were males."1.46Kidney Function in Patients With Different Variants of Beta-Thalassemia. ( Ansari, S; Nickavar, A; Qmarsi, A; Zarei, E, 2017)
"Although all types of beta thalassemia patients should be closely monitored to prevent further decrease in renal functions, the patients with TI should be considered to have a higher risk of glomerular and tubular deterioration as well as TM."1.42Glomerular and tubular functions in children with different forms of beta thalassemia. ( Akdağ, B; Aral, YZ; Aybek, H; Balcı, YI; Uzun, E; Yüksel, S, 2015)
"However, patients with elevated phosphaturia, elevated uricuria and/or abnormal levels of calcaemia show a significant decline in eGFR over time, suggesting that tubular damage acquired in childhood caused by either TM or its treatment may eventually result in abnormal eGFR."1.38Renal function in patients with β-thalassaemia major: a long-term follow-up study. ( Carta, MP; Corrias, C; Lai, ME; Ponticelli, C; Spiga, A; Vacquer, S, 2012)
"Persons with beta-thalassemia minor usually are symptomless."1.32Renal tubular dysfunction in beta-thalassemia minor. ( Bulucu, F; Cetin, T; Kocar, IH; Kurt, I; Musabak, U; Oguz, Y; Oktenli, C; Ozgurtas, T; Sanisoglu, SY; Yenicesu, M; Yildiz, O, 2003)
"A study on thalassemia intermedia and major patients in Jakarta was initiated to obtain a comprehensive picture of metabolic dysregulation, iron overload, oxidative stress, and cell damage."1.32Iron status and oxidative stress in beta-thalassemia patients in Jakarta. ( Adhiyanto, C; Dillon, HS; Freisleben, HJ; Handayani, S; Hidayat, J; Kurniati, V; Kusnandar, S; Laksmitawati, DR; Munthe, BG; Ramelan, W; Soegianto, RR; Udyaningsih-Freisleben, SK; Wirawan, R, 2003)
"In patients with beta-thalassemia major, the most important cause of mortality and morbidity is organ failure due to deposits of iron."1.31Renal function in pediatric patients with beta-thalassemia major. ( Aldudak, B; Anarat, A; Anarat, R; Dikmen, N; Gali, E; Karabay Bayazit, A; Kilinç, Y; Noyan, A; Ozel, A; Sasmaz, I, 2000)

Research

Studies (14)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (7.14)18.2507
2000's3 (21.43)29.6817
2010's8 (57.14)24.3611
2020's2 (14.29)2.80

Authors

AuthorsStudies
Ali, Z1
Ismail, M1
Rehman, IU1
Rani, GF1
Ali, M1
Khan, MTM1
Ricchi, P1
Meloni, A2
Pistoia, L2
Spasiano, A2
Rita Gamberini, M1
Maggio, A1
Gerardi, C2
Messina, G1
Campisi, S1
Allò, M1
Renne, S1
Righi, R2
Midiri, M1
Positano, V2
Filosa, A2
Pepe, A2
Vassalle, C1
Gamberini, MR1
Zuccarelli, A1
Casini, T1
Missere, M1
Ndreu, R1
Chaloemwong, J1
Tantiworawit, A1
Rattanathammethee, T1
Chai-Adisaksopha, C1
Rattarittamrong, E1
Norasetthada, L1
Charoenkwan, P1
Louthrenoo, W1
Dasgupta, S1
Dasgupta, A1
Mukhopadhayay, T1
Bhattacharya, S1
Swaika, B1
Banarjee, U1
Chakrabarty, P1
Uzun, E1
Balcı, YI1
Yüksel, S1
Aral, YZ1
Aybek, H1
Akdağ, B1
Nickavar, A1
Qmarsi, A1
Ansari, S1
Zarei, E1
Sadeghi-Bojd, S1
Hashemi, M1
Naderi, M1
Shikhani, S1
Ahmadzadeh, A1
Jalali, A1
Assar, S1
Khalilian, H1
Zandian, K1
Pedram, M1
Lai, ME1
Spiga, A1
Vacquer, S1
Carta, MP1
Corrias, C1
Ponticelli, C1
Cetin, T1
Oktenli, C1
Ozgurtas, T1
Yenicesu, M1
Sanisoglu, SY1
Oguz, Y1
Yildiz, O1
Kurt, I1
Musabak, U1
Bulucu, F1
Kocar, IH1
Laksmitawati, DR1
Handayani, S1
Udyaningsih-Freisleben, SK1
Kurniati, V1
Adhiyanto, C1
Hidayat, J1
Kusnandar, S1
Dillon, HS1
Munthe, BG1
Wirawan, R1
Soegianto, RR1
Ramelan, W1
Freisleben, HJ1
De Luca, C1
Grandinetti, M1
Maggio, F1
Lamba, M1
Passi, S1
Aldudak, B1
Karabay Bayazit, A1
Noyan, A1
Ozel, A1
Anarat, A1
Sasmaz, I1
Kilinç, Y1
Gali, E1
Anarat, R1
Dikmen, N1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Cystatin C and Beta 2 Microglobulin as Biochemical Markers for Early Detection of Renal Impairment in Children With Beta Thalassemia[NCT03881917]150 participants (Anticipated)Observational2019-11-01Not yet recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trials

2 trials available for uric acid and Anemia, Cooley's

ArticleYear
Long-term clinical efficacy and safety of thalidomide in patients with transfusion-dependent β-thalassemia: results from Thal-Thalido study.
    Scientific reports, 2023, 08-21, Volume: 13, Issue:1

    Topics: beta-Thalassemia; Ferritins; Humans; Hydroxyurea; Thalidomide; Treatment Outcome; Uric Acid

2023
Hyperuricemia, urine uric excretion, and associated complications in thalassemia patients.
    Annals of hematology, 2019, Volume: 98, Issue:5

    Topics: Adolescent; Adult; Arthritis, Gouty; beta-Thalassemia; Cross-Sectional Studies; Female; Glomerular F

2019

Other Studies

12 other studies available for uric acid and Anemia, Cooley's

ArticleYear
Longitudinal follow-up of patients with thalassaemia intermedia who started transfusion therapy in adulthood: a cohort study.
    British journal of haematology, 2020, Volume: 191, Issue:1

    Topics: Adolescent; Adult; Aged; beta-Thalassemia; Bilirubin; Blood Platelets; Blood Transfusion; Bone Disea

2020
Relationship between uric acid levels and cardiometabolic findings in a large cohort of β-thalassemia major patients.
    Biomarkers in medicine, 2018, Volume: 12, Issue:4

    Topics: Adult; beta-Thalassemia; Cohort Studies; Female; Ferritins; Humans; Iron; Liver; Magnetic Resonance

2018
Serum uric acid: an early indicator of oxidative stress in beta thalassemia population.
    Mymensingh medical journal : MMJ, 2013, Volume: 22, Issue:3

    Topics: Adolescent; Adult; Bangladesh; beta-Thalassemia; Case-Control Studies; Female; Ferritins; Humans; Ir

2013
Glomerular and tubular functions in children with different forms of beta thalassemia.
    Renal failure, 2015, Volume: 37, Issue:9

    Topics: Adolescent; alpha-Macroglobulins; beta 2-Microglobulin; beta-Thalassemia; Case-Control Studies; Chil

2015
Kidney Function in Patients With Different Variants of Beta-Thalassemia.
    Iranian journal of kidney diseases, 2017, Volume: 11, Issue:2

    Topics: Adolescent; Adult; beta-Thalassemia; Child; Creatinine; Cross-Sectional Studies; Female; Glomerular

2017
Kidney function tests in children with beta-thalassemia minor in Zahedan, southeast of Iran.
    Iranian journal of kidney diseases, 2011, Volume: 5, Issue:3

    Topics: Adolescent; beta 2-Microglobulin; beta-Thalassemia; Biomarkers; Child; Child, Preschool; Creatinine;

2011
Renal tubular dysfunction in pediatric patients with beta-thalassemia major.
    Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia, 2011, Volume: 22, Issue:3

    Topics: Acetylglucosaminidase; Adolescent; beta-Thalassemia; Child; Cross-Sectional Studies; Female; Ferriti

2011
Renal function in patients with β-thalassaemia major: a long-term follow-up study.
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2012, Volume: 27, Issue:9

    Topics: Adult; beta-Thalassemia; Calcium; Female; Follow-Up Studies; Glomerular Filtration Rate; Humans; Hyp

2012
Renal tubular dysfunction in beta-thalassemia minor.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 2003, Volume: 42, Issue:6

    Topics: Adult; beta 2-Microglobulin; beta-Thalassemia; Bone Diseases, Metabolic; Female; Hemoglobins; Humans

2003
Iron status and oxidative stress in beta-thalassemia patients in Jakarta.
    BioFactors (Oxford, England), 2003, Volume: 19, Issue:1-2

    Topics: Adolescent; Adult; Antioxidants; beta-Thalassemia; Bilirubin; Blood Proteins; Child; Hemoglobins; Hu

2003
Blood antioxidant status and urinary levels of catecholamine metabolites in beta-thalassemia.
    Free radical research, 1999, Volume: 30, Issue:6

    Topics: Adolescent; Adult; Antioxidants; beta-Thalassemia; Bilirubin; Carotenoids; Catecholamines; Child; Fa

1999
Renal function in pediatric patients with beta-thalassemia major.
    Pediatric nephrology (Berlin, Germany), 2000, Volume: 15, Issue:1-2

    Topics: Acetylglucosaminidase; Adolescent; Adult; beta-Thalassemia; Blood Urea Nitrogen; Child; Child, Presc

2000