TY - JOUR
T1 - Altered dietary salt intake for people with chronic kidney disease (Review)
AU - McMahon, Emma J.
AU - Campbell, Katrina L.
AU - Bauer, Judith D.
AU - Mudge, David W.
AU - Kelly, Jaimon T.
N1 - Funding Information:
Funding: Baxter Healthcare Corporation and Kidney Foundation of Canada, Manitoba Branch
Funding Information:
Funding: AbbVie (Chicago, IL) funded the study medication (paricalcitol and placebo) Quote: “This trial was supported by a consortium grant from the Dutch Kidney Foundation (NIGRAM Consortium grant CP10.11).H.J.L.H. is supported by a grant from The Netherlands Organization for Scientific Research (Veni and Vidi grants). M.H.d.B. is supported by personal grants from the Dutch Kidney Foundation (grant no. KJPB.08.07) and the Netherlands Organization for Scientific Research (Veni grant). The funding source had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; or preparation, review, or approval of the manuscript.”
Funding Information:
Quote:“Dr Krediet was supported by the innovation grant IP-11.40 of the Dutch Kidney Foundation.”
Funding Information:
Funding: The study has been supported by Cassella Riedel, Frankfurt, Germany, and by the E Klockner StiQung, Duisburg, Germany. Unclear of role of funding bodies
Funding Information:
Funding: supported by Merck Sharp & Dohme (grant MSGP NETH-15-01) Additional data: provided by authors
Funding Information:
Quote: "One patient had missing data for urinary measures (sample not collected, n = 1), and two for fluid measurement (presence of a pacemaker contraindicating measurement [n = 1]; data loss [n = 1])." Study was pre-registered online and the pre-specified outcomes were reported. Data for all outcomes available for inclusion in review "To test for ... variation due to treatment order ... analysis of covariance was conducted" No relationship found significant difference. Data analysed for carry over effect Major confounding factors measured (potassium intake, energy intake, protein intake, body weight, medication changes) and assessed for potential impact on outcomes. Medication changes may have affected outcomes, although likely to underestimate effect size Funding by hospital trust and not-for-profit organisation. Funding: research grants from the Princess Alexandra Hospital Private Practice Trust Fund and Kidney Health Australia. Study foods provided by Freedom Foods, Norco, Real Foods, Carman’s Fine Foods, Sanitarium Health & Wellbeing Company, Rosella, and Diego’s
Funding Information:
Funding: study supported by Novartis; declaration of non-involvement by funder Quote: "Funding: Unrestricted grant from Novartis. No role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; and preparation, review, or approval of the manuscript"
Funding Information:
We would like to acknowledge the Cochrane Kidney and Transplant for providing administrative and support for the conduct of this review, and Brydee Johnston and Rabia Khalid for providing support with data extraction. We would also like to acknowledge the ongoing support from Menzies School of Health Research, University of Queensland, the Princess Alexandra Hospital and the Queensland Government. Emma McMahon is currently supported by a cofunded NHMRC/Australian Heart Foundation Early Career Fellowship (100085) and previously received support from the Australian Government through an Australian Postgraduate Award scholarship. The information and opinions contained in this paper are solely the responsibility of the authors and do not necessarily reflect the views or policy of NHMRC, Australian Heart Foundation, Menzies School of Health Research, University of Queensland, Griffith University, the Princess Alexandra Hospital and the Queensland Government.
Funding Information:
We would like to acknowledge the Cochrane Kidney and Transplant for providing administrative and support for the conduct of this review, and Brydee Johnston and Rabia Khalid for providing support with data extraction. We would also like to acknowledge the ongoing support from Menzies School of Health Research, University of Queensland, the Princess Alexandra Hospital and the Queensland Government. Emma McMahon is currently supported by a cofunded NHMRC/Australian Heart Foundation Early Career Fellowship (100085) and previously received support from the Australian Government through an Australian Postgraduate Award scholarship. The information and opinions contained in this paper are solely the responsibility of the authors and do not necessarily reflect the views or policy of NHMRC, Australian Heart Foundation, Menzies School of Health Research, University of Queensland, Griffith University, the Princess Alexandra Hospital and the Queensland Government. The authors are grateful to the following peer reviewers for their time and comments: Ronald L. Koretz, M.D. Emeritus Professor of Clinical Medicine, David Geffen-UCLA School of Medicine, Los Angeles, California, USA; Retired Chief, Division of Gastroenterology, Olive View-UCLA Medical Center, Sylmar, California, USA; Colin H Jones, Consultant Physician and Nephrologist, York Teaching Hospital NHS Foundation Trust.
Funding Information:
• Funding: Renal Research Institute and grant from the National Center for Research Resources (NCRR) • Additional data: requested • Trial registration: https://clinicaltrials.gov/ct2/show/record/NCT00974636
Funding Information:
Quote: "this study was funded by a PhD fellowship grant from the trustees of Barts and The London Charitable Foundation. The analysis, interpretation of data, generation of the manuscript and decision to submit for publication were carried out independently of the funding body"
Publisher Copyright:
Copyright © 2021 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
PY - 2021/6/24
Y1 - 2021/6/24
N2 - Background: Evidence indicates that reducing dietary salt may reduce the incidence of heart disease and delay decline in kidney function in people with chronic kidney disease (CKD). This is an update of a review first published in 2015. Objectives: To evaluate the benefits and harms of altering dietary salt for adults with CKD. Search methods: We searched the Cochrane Kidney and Transplant Register of Studies up to 6 October 2020 through contact with the Information Specialist using search terms relevant to this review. Studies in the Register are identified through searches of CENTRAL, MEDLINE, and EMBASE, conference proceedings, the International Clinical Trials Register (ICTRP) Search Portal and ClinicalTrials.gov. Selection criteria: Randomised controlled trials comparing two or more levels of salt intake in adults with any stage of CKD. Data collection and analysis: Two authors independently assessed studies for eligibility, conducted risk of bias evaluation and evaluated confidence in the evidence using GRADE. Results were summarised using random effects models as risk ratios (RR) for dichotomous outcomes or mean differences (MD) for continuous outcomes, with 95% confidence intervals (CI). Main results: We included 21 studies (1197 randomised participants), 12 in the earlier stages of CKD (779 randomised participants), seven in dialysis (363 randomised participants) and two in post-transplant (55 randomised participants). Selection bias was low in seven studies, high in one and unclear in 13. Performance and detection biases were low in four studies, high in two, and unclear in 15. Attrition and reporting biases were low in 10 studies, high in three and unclear in eight. Because duration of the included studies was too short (1 to 36 weeks) to test the effect of salt restriction on endpoints such as death, cardiovascular events or CKD progression, changes in salt intake on blood pressure and other secondary risk factors were examined. Reducing salt by mean -73.51 mmol/day (95% CI -92.76 to -54.27), equivalent to 4.2 g or 1690 mg sodium/day, reduced systolic/diastolic blood pressure by -6.91/-3.91 mm Hg (95% CI -8.82 to -4.99/-4.80 to -3.02; 19 studies, 1405 participants; high certainty evidence). Albuminuria was reduced by 36% (95% CI 26 to 44) in six studies, five of which were carried out in people in the earlier stages of CKD (MD -0.44, 95% CI -0.58 to -0.30; 501 participants; high certainty evidence). The evidence is very uncertain about the effect of lower salt intake on weight, as the weight change observed (-1.32 kg, 95% CI -1.94 to -0.70; 12 studies, 759 participants) may have been due to fluid volume, lean tissue, or body fat. Lower salt intake may reduce extracellular fluid volume in the earlier stages of CKD (-0.87 L, 95% CI -1.17 to -0.58; 3 studies; 187 participants; low certainty evidence). The evidence is very uncertain about the effect of lower salt intake on reduction in antihypertensive dose (RR 2.45, 95% CI 0.98 to 6.08; 8 studies; 754 participants). Lower salt intake may lead to symptomatic hypotension (RR 6.70, 95% CI 2.40 to 18.69; 6 studies; 678 participants; moderate certainty evidence). Data were sparse for other types of adverse events. Authors' conclusions: We found high certainty evidence that salt reduction reduced blood pressure in people with CKD, and albuminuria in people with earlier stage CKD in the short-term. If such reductions could be maintained long-term, this effect may translate to clinically significant reductions in CKD progression and cardiovascular events. Research into the long-term effects of sodium-restricted diet for people with CKD is warranted.
AB - Background: Evidence indicates that reducing dietary salt may reduce the incidence of heart disease and delay decline in kidney function in people with chronic kidney disease (CKD). This is an update of a review first published in 2015. Objectives: To evaluate the benefits and harms of altering dietary salt for adults with CKD. Search methods: We searched the Cochrane Kidney and Transplant Register of Studies up to 6 October 2020 through contact with the Information Specialist using search terms relevant to this review. Studies in the Register are identified through searches of CENTRAL, MEDLINE, and EMBASE, conference proceedings, the International Clinical Trials Register (ICTRP) Search Portal and ClinicalTrials.gov. Selection criteria: Randomised controlled trials comparing two or more levels of salt intake in adults with any stage of CKD. Data collection and analysis: Two authors independently assessed studies for eligibility, conducted risk of bias evaluation and evaluated confidence in the evidence using GRADE. Results were summarised using random effects models as risk ratios (RR) for dichotomous outcomes or mean differences (MD) for continuous outcomes, with 95% confidence intervals (CI). Main results: We included 21 studies (1197 randomised participants), 12 in the earlier stages of CKD (779 randomised participants), seven in dialysis (363 randomised participants) and two in post-transplant (55 randomised participants). Selection bias was low in seven studies, high in one and unclear in 13. Performance and detection biases were low in four studies, high in two, and unclear in 15. Attrition and reporting biases were low in 10 studies, high in three and unclear in eight. Because duration of the included studies was too short (1 to 36 weeks) to test the effect of salt restriction on endpoints such as death, cardiovascular events or CKD progression, changes in salt intake on blood pressure and other secondary risk factors were examined. Reducing salt by mean -73.51 mmol/day (95% CI -92.76 to -54.27), equivalent to 4.2 g or 1690 mg sodium/day, reduced systolic/diastolic blood pressure by -6.91/-3.91 mm Hg (95% CI -8.82 to -4.99/-4.80 to -3.02; 19 studies, 1405 participants; high certainty evidence). Albuminuria was reduced by 36% (95% CI 26 to 44) in six studies, five of which were carried out in people in the earlier stages of CKD (MD -0.44, 95% CI -0.58 to -0.30; 501 participants; high certainty evidence). The evidence is very uncertain about the effect of lower salt intake on weight, as the weight change observed (-1.32 kg, 95% CI -1.94 to -0.70; 12 studies, 759 participants) may have been due to fluid volume, lean tissue, or body fat. Lower salt intake may reduce extracellular fluid volume in the earlier stages of CKD (-0.87 L, 95% CI -1.17 to -0.58; 3 studies; 187 participants; low certainty evidence). The evidence is very uncertain about the effect of lower salt intake on reduction in antihypertensive dose (RR 2.45, 95% CI 0.98 to 6.08; 8 studies; 754 participants). Lower salt intake may lead to symptomatic hypotension (RR 6.70, 95% CI 2.40 to 18.69; 6 studies; 678 participants; moderate certainty evidence). Data were sparse for other types of adverse events. Authors' conclusions: We found high certainty evidence that salt reduction reduced blood pressure in people with CKD, and albuminuria in people with earlier stage CKD in the short-term. If such reductions could be maintained long-term, this effect may translate to clinically significant reductions in CKD progression and cardiovascular events. Research into the long-term effects of sodium-restricted diet for people with CKD is warranted.
UR - https://www.scopus.com/pages/publications/85108727132
U2 - 10.1002/14651858.CD010070.pub3
DO - 10.1002/14651858.CD010070.pub3
M3 - Review Article
C2 - 34164803
AN - SCOPUS:85108727132
SN - 1469-493X
VL - 2021
JO - Cochrane Database of Systematic Reviews
JF - Cochrane Database of Systematic Reviews
IS - 6
M1 - CD010070
ER -