Study protocol: long-term effect of the New Nordic Renal Diet on phosphorus and lipid homeostasis in patients with chronic kidney disease, stages 3 and 4: a randomised controlled trial

Nikita Misella Hansen, Marianne Rix, Anne-Lise Kamper, Bo Feldt-Rasmussen, Christina Christoffersen, Arne Astrup, Louise Salomo, Nikita Misella Hansen, Marianne Rix, Anne-Lise Kamper, Bo Feldt-Rasmussen, Christina Christoffersen, Arne Astrup, Louise Salomo

Abstract

Introduction: Chronic kidney disease (CKD) causes severe disturbances in phosphate metabolism. New Nordic Renal Diet (NNRD) is a new dietary concept designed by the present research group that aims to offer patients with moderate CKD a whole food approach with a markedly reduction in dietary phosphorus intake, corresponding to 850 mg/day. The present protocol describes a randomised controlled trial aiming to test the long-term effects of dietary intervention with NNRD versus a non-restricted habitual diet on important parameters of phosphorus and lipid homeostasis.

Methods and analysis: This trial will be executed at the Department of Nephrology, Rigshospitalet, University of Copenhagen, Denmark. Sixty patients aged >18 years with CKD stages 3 and 4 (estimated glomerular filtration rate between 15 and 45 mL/min) will be recruited and randomly assigned to the intervention or control group. The other inclusion criterion includes a medically stable condition for at least 2 months prior to the start of the study. Exclusion criteria are treatment with phosphate binders, metabolic disorders that require specific dietary regulation, pregnancy and breast feeding, any types of food allergies or those who are vegans. The observation period is 26 weeks including seven study visits at the outpatient clinic combined with a weekly telephone consultation in both groups. A follow-up visit 3 months after study completion finalises the intervention. The primary outcome is the difference in the change in 24-hour urine phosphorus excretion from baseline to week 26 between the two study groups. Secondary outcomes include changes in phosphate-related and lipid metabolism-related blood and urine biochemistry, blood pressure and body composition. Moreover, we wish to explore adherence to the diet as well as quality of life.

Ethics and dissemination: The study has been approved by the Scientific Ethical Committee of the Capital Region of Denmark and the Danish Data Protection Agency. The results of the studies will be presented at national and international scientific meetings, and publications will be submitted to peer-reviewed journals.

Trial registration number: ClinicalTrials.gov (wwwclinicaltrialsgov) Registry (NCT04579315).

Protocol version: The protocol, version 2, has been approved by the Ethical Committee Denmark on 18 September 2020. The protocol has also been approved by Data Protection Regulation and Data Protection Law on 15 September 2020. This study protocol is in accordance with the Standard Protocol Items: Recommendations for International Trials.

Keywords: chronic renal failure; hypertension; lipid disorders; nephrology; nutrition & dietetics.

Conflict of interest statement

Competing interests: None declared.

© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

References

    1. Chen J, Budoff MJ, Reilly MP, et al. . Coronary artery calcification and risk of cardiovascular disease and death among patients with chronic kidney disease. JAMA Cardiol 2017;2:635–43. 10.1001/jamacardio.2017.0363
    1. Mikolasevic I, Žutelija M, Mavrinac V, et al. . Dyslipidemia in patients with chronic kidney disease: etiology and management. Int J Nephrol Renovasc Dis 2017;10:35–45. 10.2147/IJNRD.S101808
    1. Wahl P, Wolf M. Fgf23 in chronic kidney disease. Adv Exp Med Biol 2012;728:107–25. 10.1007/978-1-4614-0887-1_8
    1. Isakova T, Wahl P, Vargas GS, et al. . Fibroblast growth factor 23 is elevated before parathyroid hormone and phosphate in chronic kidney disease. Kidney Int 2011;79:1370–8. 10.1038/ki.2011.47
    1. Kuro-O M. The FGF23 and klotho system beyond mineral metabolism. Clin Exp Nephrol 2017;21:64–9. 10.1007/s10157-016-1357-6
    1. Salomo L, Kamper A-L, Poulsen GM, et al. . Habitual dietary phosphorus intake and urinary excretion in chronic kidney disease patients: a 3-day observational study. Eur J Clin Nutr 2017;71:798–800. 10.1038/ejcn.2016.247
    1. Institute of Medicine (US), Standing Committee on the Scientific Evaluation of Dietary Reference Intakes . Dietary reference intakes for calcium, phosphorus, magnesium, vitamin D, and fluorideDietary reference intakes for calcium, phosphorus, magnesium, vitamin D, and fluoride. Washington, DC: National Academies Press (US), 1997.
    1. Salomo L, Poulsen SK, Rix M, et al. . The new Nordic diet: phosphorus content and absorption. Eur J Nutr 2016;55:991–6. 10.1007/s00394-015-0913-2
    1. Salomo L, Rix M, Kamper A-L, et al. . Short-Term effect of the new Nordic renal diet on phosphorus homoeostasis in chronic kidney disease stages 3 and 4. Nephrol Dial Transplant 2019;34:1691–9. 10.1093/ndt/gfy366
    1. Poulsen SK, Due A, Jordy AB, et al. . Health effect of the new Nordic diet in adults with increased waist circumference: a 6-mo randomized controlled trial. Am J Clin Nutr 2014;99:35–45. 10.3945/ajcn.113.069393
    1. Scialla JJ, Lin P-H. Revamping the ‘renal’ diet: using foods to control phosphorus physiology. Nephrology Dialysis Transplantation 2019;34:1619–22. 10.1093/ndt/gfz019
    1. Mensink RP, Zock PL, Kester ADM, et al. . Effects of dietary fatty acids and carbohydrates on the ratio of serum total to HDL cholesterol and on serum lipids and apolipoproteins: a meta-analysis of 60 controlled trials. Am J Clin Nutr 2003;77:1146–55. 10.1093/ajcn/77.5.1146
    1. de Lorgeril M, Renaud S, Mamelle N, et al. . Mediterranean alpha-linolenic acid-rich diet in secondary prevention of coronary heart disease. Lancet 1994;343:1454–9. 10.1016/S0140-6736(94)92580-1
    1. Fitó M, Guxens M, Corella D, et al. . Effect of a traditional Mediterranean diet on lipoprotein oxidation: a randomized controlled trial. Arch Intern Med 2007;167:1195–203. 10.1001/archinte.167.11.1195
    1. Scheen AJ. Cardiovascular effects of new oral glucose-lowering agents: DPP-4 and SGLT-2 inhibitors. Circ Res 2018;122:1439–59. 10.1161/CIRCRESAHA.117.311588
    1. Mente A, Dehghan M, Rangarajan S, et al. . Association of dietary nutrients with blood lipids and blood pressure in 18 countries: a cross-sectional analysis from the pure study. Lancet Diabetes Endocrinol 2017;5:774–87. 10.1016/S2213-8587(17)30283-8
    1. Herdman M, Gudex C, Lloyd A, et al. . Development and preliminary testing of the new five-level version of EQ-5D (EQ-5D-5L). Qual Life Res 2011;20:1727–36. 10.1007/s11136-011-9903-x
    1. van Hout B, Janssen MF, Feng Y-S, et al. . Interim scoring for the EQ-5D-5L: mapping the EQ-5D-5L to EQ-5D-3L value sets. Value Health 2012;15:708–15. 10.1016/j.jval.2012.02.008
    1. Sakuma M, Morimoto Y, Suzuki Y, et al. . Availability of 24-h urine collection method on dietary phosphorus intake estimation. J Clin Biochem Nutr 2017;60:125–9. 10.3164/jcbn.16-50
    1. Kaneko I, Tatsumi S, Segawa H, et al. . Control of phosphate balance by the kidney and intestine. Clin Exp Nephrol 2017;21:21–6. 10.1007/s10157-016-1359-4
    1. Slatopolsky E, Robson AM, Elkan I, et al. . Control of phosphate excretion in uremic man. J Clin Invest 1968;47:1865–74. 10.1172/JCI105877
    1. Farrow EG, White KE. Recent advances in renal phosphate handling. Nat Rev Nephrol 2010;6:207–17. 10.1038/nrneph.2010.17

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