Literature DB >> 2373552

A population study of renal function in sickle cell anemia.

A H Sklar1, H Campbell, R J Caruana, B O Lightfoot, J G Gaier, P Milner.   

Abstract

To define normal limits for serum creatinine levels, as well as to explore the relationship between age and the prevalence and severity of renal disease in patients with sickle cell anemia (SCA), we retrospectively analyzed renal function parameters in 368 patients followed in our SCA clinic. Dipstick proteinuria was present in 78 patients (20.6%). Chronic renal insufficiency (CRI) was present in 17 patients (4.6%) and showed a high degree of association with proteinuria and increased age. In patients with CRI, the severity of renal dysfunction was also age-related. In the 284 patients without proteinuria or CRI, mean serum creatinine levels were lower than predicted. We conclude that in patients with SCA, serum creatinine levels at the upper limit of normal should be regarded with suspicion, and that the prevalence and severity of proteinuria and CRI in SCA is high and increases with age.

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Year:  1990        PMID: 2373552

Source DB:  PubMed          Journal:  Int J Artif Organs        ISSN: 0391-3988            Impact factor:   1.595


  12 in total

1.  The renal papilla is a niche for adult kidney stem cells.

Authors:  Juan A Oliver; Omar Maarouf; Faisal H Cheema; Timothy P Martens; Qais Al-Awqati
Journal:  J Clin Invest       Date:  2004-09       Impact factor: 14.808

2.  Combination erythropoietin-hydroxyurea therapy in sickle cell disease: experience from the National Institutes of Health and a literature review.

Authors:  Jane A Little; Vicki R McGowan; Gregory J Kato; Kristine S Partovi; Jordan J Feld; Irina Maric; Sabrina Martyr; James G Taylor; Roberto F Machado; Theo Heller; Oswaldo Castro; Mark T Gladwin
Journal:  Haematologica       Date:  2006-08       Impact factor: 9.941

3.  Combined hydroxyurea and ETA receptor blockade reduces renal injury in the humanized sickle cell mouse.

Authors:  Crystal Taylor; Malgorzata Kasztan; Binli Tao; Jennifer S Pollock; David M Pollock
Journal:  Acta Physiol (Oxf)       Date:  2018-09-20       Impact factor: 6.311

4.  Levels of high-density lipoprotein cholesterol (HDL-C) among children with steady-state sickle cell disease.

Authors:  Magda O Seixas; Larissa C Rocha; Mauricio B Carvalho; Joelma F Menezes; Isa M Lyra; Valma M L Nascimento; Ricardo D Couto; Ájax M Atta; Mitermayer G Reis; Marilda S Goncalves
Journal:  Lipids Health Dis       Date:  2010-08-27       Impact factor: 3.876

Review 5.  Sickle cell disease and the kidney.

Authors:  Jon I Scheinman
Journal:  Nat Clin Pract Nephrol       Date:  2008-12-02

6.  Serum cystatin C levels in children with sickle cell disease.

Authors:  Ofelia Alvarez; Gaston Zilleruelo; Dale Wright; Brenda Montane; Gabriela Lopez-Mitnik
Journal:  Pediatr Nephrol       Date:  2006-02-21       Impact factor: 3.714

7.  Hematological profile of sickle cell disease in central India.

Authors:  A V Shrikhande; A A Dani; J R Tijare; A K Agrawal
Journal:  Indian J Hematol Blood Transfus       Date:  2008-03-19       Impact factor: 0.900

8.  Albuminuria correlates with hemolysis and NAG and KIM-1 in patients with sickle cell anemia.

Authors:  Dima Hamideh; Vimal Raj; Thomas Harrington; Hua Li; Emilio Margolles; Folasade Amole; Monica Garcia-Buitrago; Phillip Ruiz; Gaston Zilleruelo; Ofelia Alvarez
Journal:  Pediatr Nephrol       Date:  2014-06-03       Impact factor: 3.714

9.  Implementation of Indigenous Electronic Medical Record System to Facilitate Care of Sickle Cell Disease Patients in Chhattisgarh.

Authors:  Mona Choubey; Hrishikesh Mishra; Khushboo Soni; Pradeep Kumar Patra
Journal:  J Clin Diagn Res       Date:  2016-02-01

10.  Higher rates of hemolysis are not associated with albuminuria in Jamaicans with sickle cell disease.

Authors:  Monika R Asnani; Raphael A Fraser; Marvin E Reid
Journal:  PLoS One       Date:  2011-04-14       Impact factor: 3.240

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