Literature DB >> 11709806

Role of genetic variability in the renin-angiotensin system in diabetic and nondiabetic renal disease.

A Boonstra1, D de Zeeuw, P E de Jong, G Navis.   

Abstract

Studies on genetic variability in the renin-angiotensin system (RAS) provide intriguing data that support its possible relevance to renal pathophysiology. However, from the discrepancies between different studies it is clear that RAS polymorphisms do not provide simple markers for renal prognosis or therapy response. Rather than attempting to force a conclusion from the available discrepancies, we should attempt to develop strategies from the current state of knowledge to attack this complex issue from different angles. Unraveling their functional impact in renal pathophysiology can provide a framework for understanding that can guide further studies with the eventual purpose of improving the prognosis of renal patients. Clinical association studies should be large and prospective, to obtain the necessary robustness, with proper attention paid to the role of contextual factors. Moreover, studies elucidating the physiologic mechanisms of the genetic determinants of the disease phenotype are of prime importance. Such information is vital, not only to make sense of observed associations, but all the more so if one wants to apply the insights on the role of genetic factors into better strategies for disease intervention. Copyright 2001 by W.B. Saunders Company

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Year:  2001        PMID: 11709806     DOI: 10.1053/snep.2001.26804

Source DB:  PubMed          Journal:  Semin Nephrol        ISSN: 0270-9295            Impact factor:   5.299


  4 in total

1.  Rat Ace allele variation determines susceptibility to AngII-induced renal damage.

Authors:  Jelena Kamilic; Inge Hamming; A Titia Lely; Ron Korstanje; Ute Schulze; Wilfred J Poppinga; Anthony J Turner; Nicola E Clarke; Harry van Goor; Gerjan J Navis
Journal:  J Renin Angiotensin Aldosterone Syst       Date:  2011-07-25       Impact factor: 1.636

Review 2.  Progression of glomerular and tubular disease in pediatrics.

Authors:  Robert P Woroniecki; H William Schnaper
Journal:  Semin Nephrol       Date:  2009-07       Impact factor: 5.299

3.  Differential ACE expression among tissues in allele-specific Wistar rat lines.

Authors:  Jelena Kamilic; A Titia Lely; Harry van Goor; Hendrik Buikema; Hilde Tent; Gerjan J Navis; Ron Korstanje
Journal:  Mamm Genome       Date:  2009-03-03       Impact factor: 2.957

4.  Mechanisms of progression of chronic kidney disease.

Authors:  Agnes B Fogo
Journal:  Pediatr Nephrol       Date:  2007-07-24       Impact factor: 3.714

  4 in total

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