Literature DB >> 29208626

The Effect of Extended Release Niacin on Markers of Mineral Metabolism in CKD.

Rakesh Malhotra1,2, Ronit Katz3, Andrew Hoofnagle4, Andrew Bostom5, Dena E Rifkin1,6,7, Ruth Mcbride8, Jeffrey Probstfield9, Geoffrey Block10, Joachim H Ix11,6,7.   

Abstract

BACKGROUND AND OBJECTIVES: Niacin downregulates intestinal sodium-dependent phosphate transporter 2b expression and reduces intestinal phosphate transport. Short-term studies have suggested that niacin lowers serum phosphate concentrations in patients with CKD and ESRD. However, the long-term effects of niacin on serum phosphate and other mineral markers are unknown. DESIGN, SETTING, PARTICIPANTS, &amp; MEASUREMENTS: The Atherothrombosis Intervention in Metabolic Syndrome with Low HDL/High Triglycerides: Impact on Global Health Trial was a randomized, double-blind, placebo-controlled trial testing extended release niacin in persons with prevalent cardiovascular disease. We examined the effect of randomized treatment with niacin (1500 or 2000 mg) or placebo on temporal changes in markers of mineral metabolism in 352 participants with eGFR<60 ml/min per 1.73 m2 over 3 years. Changes in each marker were compared over time between the niacin and placebo arms using linear mixed effects models.
RESULTS: Randomization to niacin led to 0.08 mg/dl lower plasma phosphate concentrations per year of treatment compared with placebo (P<0.01) and 0.25 mg/dl lower mean phosphate 3 years after baseline (3.32 versus 3.57 mg/dl; P=0.03). In contrast, randomization to niacin was not associated with statistically significant changes in plasma intact fibroblast growth factor 23, parathyroid hormone, calcium, or vitamin D metabolites over 3 years.
CONCLUSIONS: The use of niacin over 3 years lowered serum phosphorous concentrations but did not affect other markers of mineral metabolism in participants with CKD.
Copyright © 2018 by the American Society of Nephrology.

Entities:  

Keywords:  Cardiovascular Diseases; Double-Blind Method; Fibroblast Growth Factors; Global Health; Humans; Kidney Failure, Chronic; Metabolic Syndrome X; Minerals; Niacin; Phosphate Transport Proteins; Phosphates; Phosphorus; Random Allocation; Renal Insufficiency, Chronic; Sodium; Triglycerides; Vitamin D; calcium; chronic kidney disease; fibroblast growth factor 23; glomerular filtration rate; hyperphosphatemia; mineral metabolism; parathyroid hormone

Mesh:

Substances:

Year:  2017        PMID: 29208626      PMCID: PMC5753310          DOI: 10.2215/CJN.05440517

Source DB:  PubMed          Journal:  Clin J Am Soc Nephrol        ISSN: 1555-9041            Impact factor:   8.237


  35 in total

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Journal:  J Am Soc Nephrol       Date:  2017-01-12       Impact factor: 10.121

Review 2.  Phosphate toxicity and vascular mineralization.

Authors:  Mohammed S Razzaque
Journal:  Contrib Nephrol       Date:  2013-05-03       Impact factor: 1.580

Review 3.  Regulation and function of the FGF23/klotho endocrine pathways.

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4.  Relation of sex and estrogen therapy to serum fibroblast growth factor 23, serum phosphorus, and urine phosphorus: the Heart and Soul Study.

Authors:  Joachim H Ix; Michel Chonchol; Gail A Laughlin; Michael G Shlipak; Mary A Whooley
Journal:  Am J Kidney Dis       Date:  2011-08-19       Impact factor: 8.860

5.  Niacin in patients with low HDL cholesterol levels receiving intensive statin therapy.

Authors:  William E Boden; Jeffrey L Probstfield; Todd Anderson; Bernard R Chaitman; Patrice Desvignes-Nickens; Kent Koprowicz; Ruth McBride; Koon Teo; William Weintraub
Journal:  N Engl J Med       Date:  2011-11-15       Impact factor: 91.245

6.  Fibroblast growth factor 23 and Inflammation in CKD.

Authors:  Jair Munoz Mendoza; Tamara Isakova; Ana C Ricardo; Huiliang Xie; Sankar D Navaneethan; Amanda H Anderson; Lydia A Bazzano; Dawei Xie; Matthias Kretzler; Lisa Nessel; L Lee Hamm; Lavinia Negrea; Mary B Leonard; Dominic Raj; Myles Wolf
Journal:  Clin J Am Soc Nephrol       Date:  2012-05-03       Impact factor: 8.237

7.  Phosphate regulation of vascular smooth muscle cell calcification.

Authors:  S Jono; M D McKee; C E Murry; A Shioi; Y Nishizawa; K Mori; H Morii; C M Giachelli
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Journal:  N Engl J Med       Date:  2012-07-05       Impact factor: 91.245

9.  Iron and fibroblast growth factor 23 in X-linked hypophosphatemia.

Authors:  Erik A Imel; Amie K Gray; Leah R Padgett; Michael J Econs
Journal:  Bone       Date:  2013-12-08       Impact factor: 4.398

10.  Efficacy and safety of nicotinamide in haemodialysis patients: the NICOREN study.

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2.  Lowering Expectations with Niacin Treatment for CKD-MBD.

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3.  Molecular Control of Phosphorus Homeostasis and Precision Treatment of Hypophosphatemic Disorders.

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Journal:  Curr Mol Biol Rep       Date:  2019-02-09

Review 4.  Concepts and Controversies: Lipid Management in Patients with Chronic Kidney Disease.

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Review 6.  Targeting Gastrointestinal Transport Proteins to Control Hyperphosphatemia in Chronic Kidney Disease.

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7.  NaPi-IIb Inhibition for Hyperphosphatemia in CKD Hemodialysis Patients.

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Review 8.  Sodium phosphate cotransporter 2a inhibitors: potential therapeutic uses.

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9.  Investigation of nicotinamide as more than an anti-phosphorus drug in chronic hemodialysis patients: a single-center, double-blind, randomized, placebo-controlled trial.

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10.  Nicotinamide and acute kidney injury.

Authors:  Miguel Fontecha-Barriuso; Ana M Lopez-Diaz; Sol Carriazo; Alberto Ortiz; Ana Belen Sanz
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