Literature DB >> 36224286

Nephrons, podocytes and chronic kidney disease: Strategic antihypertensive therapy for renoprotection.

Kotaro Haruhara1, Go Kanzaki1, Nobuo Tsuboi2.   

Abstract

Chronic kidney disease (CKD) is one of the strongest risk factors for hypertension, and hypertension can exacerbate the progression of CKD. Thus, the management of CKD and antihypertensive therapy are inextricably linked. Research over the past decades has shown that the human kidney is more diverse than initially thought. Subjects with low nephron endowment are at increased risk of developing CKD and hypertension, which is consistent with the theory of the developmental origins of health and disease. Combined with other lifetime risks of CKD, hypertension may lead to a vicious cycle consisting of podocyte injury, glomerulosclerosis and further loss of nephrons. Of note, recent studies have shown that the number of nephrons correlates well with the number of podocytes, suggesting that these two components are intrinsically linked and may influence each other. Both nephrons and podocytes have no or very limited regenerative capacity and are destined to decrease throughout life. Therefore, one of the best strategies to slow the progression of CKD is to maintain the "numbers" of these essential components necessary to preserve renal function. To this end, both the achievement of an optimal blood pressure and a maximum reduction in urinary protein excretion are essential. Lifestyle modifications and antihypertensive drug therapy must be carefully individualized to address the potential diversity of the kidneys.
© 2022. The Author(s).

Entities:  

Keywords:  Chronic kidney disease; Hypertension; Nephron; Podocyte; Salt handling

Year:  2022        PMID: 36224286     DOI: 10.1038/s41440-022-01061-5

Source DB:  PubMed          Journal:  Hypertens Res        ISSN: 0916-9636            Impact factor:   5.528


  87 in total

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Journal:  Kidney Int       Date:  2001-02       Impact factor: 10.612

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Journal:  Curr Opin Nephrol Hypertens       Date:  2011-01       Impact factor: 2.894

Review 3.  Adult hypertension and kidney disease: the role of fetal programming.

Authors:  Kambiz Zandi-Nejad; Valerie A Luyckx; Barry M Brenner
Journal:  Hypertension       Date:  2006-01-16       Impact factor: 10.190

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Journal:  BMJ       Date:  1989-03-04

Review 5.  Proteinuria should be used as a surrogate in CKD.

Authors:  Paolo Cravedi; Piero Ruggenenti; Giuseppe Remuzzi
Journal:  Nat Rev Nephrol       Date:  2012-03-06       Impact factor: 28.314

6.  Estimating total nephron number in the adult kidney using the physical disector/fractionator combination.

Authors:  Luise A Cullen-McEwen; Rebecca N Douglas-Denton; John F Bertram
Journal:  Methods Mol Biol       Date:  2012

Review 7.  Mechanisms of progression and regression of renal lesions of chronic nephropathies and diabetes.

Authors:  Giuseppe Remuzzi; Ariela Benigni; Andrea Remuzzi
Journal:  J Clin Invest       Date:  2006-02       Impact factor: 14.808

Review 8.  The clinical importance of nephron mass.

Authors:  Valerie A Luyckx; Barry M Brenner
Journal:  J Am Soc Nephrol       Date:  2010-02-11       Impact factor: 10.121

9.  Nephron number in patients with primary hypertension.

Authors:  Gunhild Keller; Gisela Zimmer; Gerhard Mall; Eberhard Ritz; Kerstin Amann
Journal:  N Engl J Med       Date:  2003-01-09       Impact factor: 91.245

Review 10.  Effect of fetal and child health on kidney development and long-term risk of hypertension and kidney disease.

Authors:  Valerie A Luyckx; John F Bertram; Barry M Brenner; Caroline Fall; Wendy E Hoy; Susan E Ozanne; Bjorn E Vikse
Journal:  Lancet       Date:  2013-05-31       Impact factor: 79.321

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