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Benefits of dietary sodium restriction in the management of chronic kidney disease.
Curr Opin Nephrol Hypertens. 2009 Nov; 18(6):531-8.CO

Abstract

PURPOSE OF REVIEW

To evaluate the role of restricting dietary sodium intake in chronic kidney disease (CKD) and its complications.

RECENT FINDINGS

A consistent line of evidence shows that high dietary sodium intake is a determinant of therapy resistance to blockade of the renin-angiotensin-aldosterone system (RAAS). Addition of sodium restriction to RAAS blockade or to RAAS blockade combined with a diuretic permits a further reduction in urinary protein excretion of approximately 30%, which could be expected to reduce long-term renal risk by 25%.

SUMMARY

High sodium intake increases blood pressure and proteinuria, induces glomerular hyperfiltration and blunts the response to RAAS blockade. Although recommended in international guidelines, sodium restriction is not a spearhead in treating renal patients. Sodium status is only rarely mentioned in recent large intervention studies in CKD. Sodium intake in CKD is similar to that in the general population. Reduction of sodium intake to the target of 50-85 mmol/24 h in patients with CKD reduces blood pressure and proteinuria, the latter by approximately 30%, and should be actively pursued to improve outcome in CKD.

Authors+Show Affiliations

Department of Internal Medicine, Division of Nephrology, University Medical Center Groningen, Groningen, The Netherlands.No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Review

Language

eng

PubMed ID

19713840

Citation

Krikken, Jan A., et al. "Benefits of Dietary Sodium Restriction in the Management of Chronic Kidney Disease." Current Opinion in Nephrology and Hypertension, vol. 18, no. 6, 2009, pp. 531-8.
Krikken JA, Laverman GD, Navis G. Benefits of dietary sodium restriction in the management of chronic kidney disease. Curr Opin Nephrol Hypertens. 2009;18(6):531-8.
Krikken, J. A., Laverman, G. D., & Navis, G. (2009). Benefits of dietary sodium restriction in the management of chronic kidney disease. Current Opinion in Nephrology and Hypertension, 18(6), 531-8. https://doi.org/10.1097/MNH.0b013e3283312fc8
Krikken JA, Laverman GD, Navis G. Benefits of Dietary Sodium Restriction in the Management of Chronic Kidney Disease. Curr Opin Nephrol Hypertens. 2009;18(6):531-8. PubMed PMID: 19713840.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Benefits of dietary sodium restriction in the management of chronic kidney disease. AU - Krikken,Jan A, AU - Laverman,Gozewijn D, AU - Navis,Gerjan, PY - 2009/8/29/entrez PY - 2009/8/29/pubmed PY - 2009/12/25/medline SP - 531 EP - 8 JF - Current opinion in nephrology and hypertension JO - Curr Opin Nephrol Hypertens VL - 18 IS - 6 N2 - PURPOSE OF REVIEW: To evaluate the role of restricting dietary sodium intake in chronic kidney disease (CKD) and its complications. RECENT FINDINGS: A consistent line of evidence shows that high dietary sodium intake is a determinant of therapy resistance to blockade of the renin-angiotensin-aldosterone system (RAAS). Addition of sodium restriction to RAAS blockade or to RAAS blockade combined with a diuretic permits a further reduction in urinary protein excretion of approximately 30%, which could be expected to reduce long-term renal risk by 25%. SUMMARY: High sodium intake increases blood pressure and proteinuria, induces glomerular hyperfiltration and blunts the response to RAAS blockade. Although recommended in international guidelines, sodium restriction is not a spearhead in treating renal patients. Sodium status is only rarely mentioned in recent large intervention studies in CKD. Sodium intake in CKD is similar to that in the general population. Reduction of sodium intake to the target of 50-85 mmol/24 h in patients with CKD reduces blood pressure and proteinuria, the latter by approximately 30%, and should be actively pursued to improve outcome in CKD. SN - 1473-6543 UR - https://www.unboundmedicine.com/medline/citation/19713840/full_citation L2 - https://doi.org/10.1097/MNH.0b013e3283312fc8 DB - PRIME DP - Unbound Medicine ER -