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Effects of low-dose niacin on dyslipidemia and serum phosphorus in patients with chronic kidney disease

BACKGROUND: Niacin supplementation improves dyslipidemia and lowers serum phosphorus levels in patients with chronic kidney disease (CKD). We evaluated whether low-dose niacin supplementation can improve dyslipidemia, lower serum phosphorus levels, and be administered with a low frequency of adverse...

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Autores principales: Jin Kang, Hyo, Kim, Do Kyong, Mi Lee, Su, Han Kim, Kyung, Hee Han, Seung, Hyun Kim, Ki, Eun Kim, Seong, Ki Son, Young, An, Won Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716108/
https://www.ncbi.nlm.nih.gov/pubmed/26889433
http://dx.doi.org/10.1016/j.krcp.2012.12.001
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author Jin Kang, Hyo
Kim, Do Kyong
Mi Lee, Su
Han Kim, Kyung
Hee Han, Seung
Hyun Kim, Ki
Eun Kim, Seong
Ki Son, Young
An, Won Suk
author_facet Jin Kang, Hyo
Kim, Do Kyong
Mi Lee, Su
Han Kim, Kyung
Hee Han, Seung
Hyun Kim, Ki
Eun Kim, Seong
Ki Son, Young
An, Won Suk
author_sort Jin Kang, Hyo
collection PubMed
description BACKGROUND: Niacin supplementation improves dyslipidemia and lowers serum phosphorus levels in patients with chronic kidney disease (CKD). We evaluated whether low-dose niacin supplementation can improve dyslipidemia, lower serum phosphorus levels, and be administered with a low frequency of adverse effects in patients with CKD. METHODS: We retrospectively analyzed the clinical records of patients with CKD who had taken niacin from January 2009 to June 2011. We excluded patients with CKD stage 1 and 5. We then enrolled 31 patients with CKD who had taken niacin at a fixed dose of 500 mg/day for 6 months. We also randomly selected 30 patients with CKD who had been taking statin for 9 months as a control group. RESULTS: Among the 34 patients with CKD who were prescribed niacin, five (14%) complained of adverse effects, and three (8%) discontinued niacin. The proportion of patients in the niacin group who had been taking a statin or omega-3 fatty acids was 67.7% and 48.8%, respectively. In the niacin group, high-density lipoprotein cholesterol level was significantly increased and triglyceride level was significantly decreased at 12 and 24 weeks compared with baseline levels (P<0.05). In the niacin group, phosphorous level (P<0.05) was significantly decreased, and glomerular filtration rate (GFR) was significantly increased (P<0.05) at 24 weeks compared with baseline values. CONCLUSION: Low-dose niacin had a low frequency of adverse effects and also improved dyslipidemia, lowered serum phosphorus level, and increased GFR in patients with CKD. Further studies are needed to evaluate the long-term effects of low-dose niacin for renal progression of CKD.
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spelling pubmed-47161082016-02-17 Effects of low-dose niacin on dyslipidemia and serum phosphorus in patients with chronic kidney disease Jin Kang, Hyo Kim, Do Kyong Mi Lee, Su Han Kim, Kyung Hee Han, Seung Hyun Kim, Ki Eun Kim, Seong Ki Son, Young An, Won Suk Kidney Res Clin Pract Original Article BACKGROUND: Niacin supplementation improves dyslipidemia and lowers serum phosphorus levels in patients with chronic kidney disease (CKD). We evaluated whether low-dose niacin supplementation can improve dyslipidemia, lower serum phosphorus levels, and be administered with a low frequency of adverse effects in patients with CKD. METHODS: We retrospectively analyzed the clinical records of patients with CKD who had taken niacin from January 2009 to June 2011. We excluded patients with CKD stage 1 and 5. We then enrolled 31 patients with CKD who had taken niacin at a fixed dose of 500 mg/day for 6 months. We also randomly selected 30 patients with CKD who had been taking statin for 9 months as a control group. RESULTS: Among the 34 patients with CKD who were prescribed niacin, five (14%) complained of adverse effects, and three (8%) discontinued niacin. The proportion of patients in the niacin group who had been taking a statin or omega-3 fatty acids was 67.7% and 48.8%, respectively. In the niacin group, high-density lipoprotein cholesterol level was significantly increased and triglyceride level was significantly decreased at 12 and 24 weeks compared with baseline levels (P<0.05). In the niacin group, phosphorous level (P<0.05) was significantly decreased, and glomerular filtration rate (GFR) was significantly increased (P<0.05) at 24 weeks compared with baseline values. CONCLUSION: Low-dose niacin had a low frequency of adverse effects and also improved dyslipidemia, lowered serum phosphorus level, and increased GFR in patients with CKD. Further studies are needed to evaluate the long-term effects of low-dose niacin for renal progression of CKD. Elsevier 2013-03 2012-12-31 /pmc/articles/PMC4716108/ /pubmed/26889433 http://dx.doi.org/10.1016/j.krcp.2012.12.001 Text en © 2013. The Korean Society of Nephrology. Published by Elsevier. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Jin Kang, Hyo
Kim, Do Kyong
Mi Lee, Su
Han Kim, Kyung
Hee Han, Seung
Hyun Kim, Ki
Eun Kim, Seong
Ki Son, Young
An, Won Suk
Effects of low-dose niacin on dyslipidemia and serum phosphorus in patients with chronic kidney disease
title Effects of low-dose niacin on dyslipidemia and serum phosphorus in patients with chronic kidney disease
title_full Effects of low-dose niacin on dyslipidemia and serum phosphorus in patients with chronic kidney disease
title_fullStr Effects of low-dose niacin on dyslipidemia and serum phosphorus in patients with chronic kidney disease
title_full_unstemmed Effects of low-dose niacin on dyslipidemia and serum phosphorus in patients with chronic kidney disease
title_short Effects of low-dose niacin on dyslipidemia and serum phosphorus in patients with chronic kidney disease
title_sort effects of low-dose niacin on dyslipidemia and serum phosphorus in patients with chronic kidney disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716108/
https://www.ncbi.nlm.nih.gov/pubmed/26889433
http://dx.doi.org/10.1016/j.krcp.2012.12.001
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