Literature DB >> 15533729

Characteristics of hypertension in young adults with autosomal dominant polycystic kidney disease compared with the general U.S. population.

Catherine L Kelleher1, Kim K McFann, Ann M Johnson, Robert W Schrier.   

Abstract

BACKGROUND: Patients with autosomal dominant polycystic kidney disease (ADPKD) often develop hypertension before any abnormalities in renal function are detected clinically. Therefore, standard screening (serum creatinine and urinalysis) of young individuals with unexplained hypertension to exclude renal parenchymal disease would rarely detect ADPKD.
METHODS: Data from 516 subjects with ADPKD (217 male and 299 female), aged newbornto 55 years with a normal serum creatinine and no proteinuria based on urine dipstick, studied between 1985 and 2000, were compared with data from similar subjects from the National Health and Nutrition Examination Survey (NHANES) III (1988-1994) and NHANES IV (1999-2000) data, by gender.
RESULTS: There was a highly significant occurrence of hypertension in young patients with ADPKD when compared to patients aged 20 to 34 years in the U.S. population. The hypertension in patients with ADPKD occurred in the absence of abnormal renal function or abnormal urinalysis.
CONCLUSIONS: These data indicate that renal ultrasound screening of young hypertensive individuals (aged 20 to 34 years) should be considered when searching for causes of secondary hypertension. Identifying affected ADPKD individuals early in their disease will permit aggressive blood pressure treatment and early inhibition of the renin-angiotensin-aldosterone system, which has been shown to reverse left ventricular hypertrophy, an important cardiovascular risk factor. In the present era of renal replacement therapy, cardiovascular complications are the main cause of death in patients with ADPKD.

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Year:  2004        PMID: 15533729     DOI: 10.1016/j.amjhyper.2004.06.020

Source DB:  PubMed          Journal:  Am J Hypertens        ISSN: 0895-7061            Impact factor:   2.689


  29 in total

1.  Hypertension in Autosomal Dominant Polycystic Kidney Disease: A Clinical and Basic Science Perspective.

Authors:  Shobha Ratnam; Surya M Nauli
Journal:  Int J Nephrol Urol       Date:  2010

2.  Primary cilia regulates the directional migration and barrier integrity of endothelial cells through the modulation of hsp27 dependent actin cytoskeletal organization.

Authors:  Thomas J Jones; Ravi K Adapala; Werner J Geldenhuys; Chris Bursley; Wissam A AbouAlaiwi; Surya M Nauli; Charles K Thodeti
Journal:  J Cell Physiol       Date:  2012-01       Impact factor: 6.384

Review 3.  Diagnosis and management of childhood polycystic kidney disease.

Authors:  William E Sweeney; Ellis D Avner
Journal:  Pediatr Nephrol       Date:  2010-10-29       Impact factor: 3.714

4.  Improved prognosis in patients with autosomal dominant polycystic kidney disease in Denmark.

Authors:  Bjarne Orskov; Vibeke Rømming Sørensen; Bo Feldt-Rasmussen; Svend Strandgaard
Journal:  Clin J Am Soc Nephrol       Date:  2010-07-29       Impact factor: 8.237

5.  L-type calcium channel modulates cystic kidney phenotype.

Authors:  Xingjian Jin; Brian S Muntean; Munaf S Aal-Aaboda; Qiming Duan; Jing Zhou; Surya M Nauli
Journal:  Biochim Biophys Acta       Date:  2014-06-09

6.  Similar renal outcomes in children with ADPKD diagnosed by screening or presenting with symptoms.

Authors:  Djalila Mekahli; Adrian S Woolf; Detlef Bockenhauer
Journal:  Pediatr Nephrol       Date:  2010-08-05       Impact factor: 3.714

7.  Polycystic kidneys have decreased vascular density: a micro-CT study.

Authors:  Rende Xu; Federico Franchi; Brent Miller; John A Crane; Karen M Peterson; Peter J Psaltis; Peter C Harris; Lilach O Lerman; Martin Rodriguez-Porcel
Journal:  Microcirculation       Date:  2013-02       Impact factor: 2.628

Review 8.  Autosomal dominant polycystic kidney disease and transplantation.

Authors:  Mariusz Niemczyk; Stanisław Niemczyk; Leszek Paczek
Journal:  Ann Transplant       Date:  2009 Oct-Dec       Impact factor: 1.530

9.  Endothelial cilia are fluid shear sensors that regulate calcium signaling and nitric oxide production through polycystin-1.

Authors:  Surya M Nauli; Yoshifumi Kawanabe; John J Kaminski; William J Pearce; Donald E Ingber; Jing Zhou
Journal:  Circulation       Date:  2008-02-19       Impact factor: 29.690

Review 10.  From bone abnormalities to mineral metabolism dysregulation in autosomal dominant polycystic kidney disease.

Authors:  Djalila Mekahli; Justine Bacchetta
Journal:  Pediatr Nephrol       Date:  2013-01-24       Impact factor: 3.714

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