Literature DB >> 28421299

Compared effects of calcium and sodium polystyrene sulfonate on mineral and bone metabolism and volume overload in pre-dialysis patients with hyperkalemia.

Yosuke Nakayama1, Kaoru Ueda1,2, Sho-Ichi Yamagishi3, Miki Sugiyama1, Chika Yoshida1, Yuka Kurokawa1, Nao Nakamura1, Tomofumi Moriyama1, Goh Kodama1, Tomohisa Minezaki1, Sakuya Ito1, Akiko Nagata1, Kensei Taguchi1, Junko Yano1, Yusuke Kaida1, Kazutaka Shibatomi2, Kei Fukami4.   

Abstract

BACKGROUND: Hyperkalemia is prevalent in end-stage renal disease patients, being involved in life-threatening arrhythmias. Although polystyrene sulfonate (PS) is commonly used for the treatment of hyperkalemia, direct comparison of effects between calcium and sodium PS (CPS and SPS) on mineral and bone metabolism has not yet been studied.
METHODS: In a randomized and crossover design, 20 pre-dialysis patients with hyperkalemia (>5 mmol/l) received either oral CPS or SPS therapy for 4 weeks.
RESULTS: After 4-week treatments, there was no significant difference of changes in serum potassium (K) from the baseline (ΔK) between the two groups. However, SPS significantly decreased serum calcium (Ca) and magnesium (Mg) and increased intact parathyroid hormone (iPTH) values, whereas CPS reduced iPTH. ΔiPTH was inversely correlated with ΔCa and ΔMg (r = -0.53 and r = -0.50, respectively). Furthermore, sodium (Na) and atrial natriuretic peptide (ANP) levels were significantly elevated in patients with SPS, but not with CPS, whereas ΔNa and ΔANP were significantly correlated with each other in all the patients. We also found that ΔNa and Δ(Na to chloride ratio) were positively correlated with ΔHCO3-. In artificial colon fluid, CPS increased Ca and decreased Na. Furthermore, SPS greatly reduced K, Mg, and NH3.
CONCLUSION: Compared with SPS, CPS may be safer for the treatment of hyperkalemia in pre-dialysis patients, because it did not induce hyperparathyroidism or volume overload.

Entities:  

Keywords:  Calcium; Chronic kidney disease; Hyperkalemia; Potassium; Secondary hyperparathyroidism; Sodium

Mesh:

Substances:

Year:  2017        PMID: 28421299     DOI: 10.1007/s10157-017-1412-y

Source DB:  PubMed          Journal:  Clin Exp Nephrol        ISSN: 1342-1751            Impact factor:   2.801


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