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Impact of Potassium Citrate vs Citric Acid on Urinary Stone Risk in Calcium Phosphate Stone Formers

医学 柠檬酸 磷酸盐 泌尿系统 内科学 生物化学 冶金 化学 材料科学
作者
Steeve Doizi,John Poindexter,Margaret S. Pearle,Francisco J. Blanco,Orson W. Moe,Khashayar Sakhaee,Naim M. Maalouf
出处
期刊:The Journal of Urology [Lippincott Williams & Wilkins]
卷期号:200 (6): 1278-1284 被引量:26
标识
DOI:10.1016/j.juro.2018.07.039
摘要

No AccessJournal of UrologyAdult Urology1 Dec 2018Impact of Potassium Citrate vs Citric Acid on Urinary Stone Risk in Calcium Phosphate Stone Formers Steeve Doizi, John R. Poindexter, Margaret S. Pearle, Francisco Blanco, Orson W. Moe, Khashayar Sakhaee, and Naim M. Maalouf Steeve DoiziSteeve Doizi Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas Current address: Sorbonne Université, GRC n°20, Groupe de Recherche Clinique sur la Lithiase Urinaire, Hôpital Tenon, F-75020 Paris, France. More articles by this author , John R. PoindexterJohn R. Poindexter Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas More articles by this author , Margaret S. PearleMargaret S. Pearle Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas Department of Urology, University of Texas Southwestern Medical Center, Dallas, Texas More articles by this author , Francisco BlancoFrancisco Blanco Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas More articles by this author , Orson W. MoeOrson W. Moe Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas Department of Physiology, University of Texas Southwestern Medical Center, Dallas, Texas Division of Nephrology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas More articles by this author , Khashayar SakhaeeKhashayar Sakhaee Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas Division of Mineral Metabolism, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas More articles by this author , and Naim M. MaaloufNaim M. Maalouf Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas Division of Mineral Metabolism, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas More articles by this author View All Author Informationhttps://doi.org/10.1016/j.juro.2018.07.039AboutFull TextPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract Purpose: To our knowledge no medication has been shown to be effective for preventing recurrent calcium phosphate urinary stones. Potassium citrate may protect against calcium phosphate stones by enhancing urine citrate excretion and lowering urine calcium but it raises urine pH, which increases calcium phosphate saturation and may negate the beneficial effects. Citric acid can potentially raise urine citrate but not pH and, thus, it may be a useful countermeasure against calcium phosphate stones. We assessed whether these 2 agents could significantly alter urine composition and reduce calcium phosphate saturation. Materials and Methods: In a crossover metabolic study 13 recurrent calcium phosphate stone formers without hypercalciuria were evaluated at the end of 3, 1-week study phases during which they consumed a fixed metabolic diet and received assigned study medications, including citric acid 30 mEq twice daily, potassium citrate 20 mEq twice daily or matching placebo. We collected 24-hour urine specimens to perform urine chemistry studies and calculate calcium phosphate saturation indexes. Results: Urine parameters did not significantly differ between the citric acid and placebo phases. Potassium citrate significantly increased urine pH, potassium and citrate compared to citric acid and placebo (p <0.01) with a trend toward lower urine calcium (p = 0.062). Brushite saturation was increased by potassium citrate when calculated by the relative supersaturation ratio but not by the saturation index. Conclusions: Citric acid at a dose of 60 mEq per day did not significantly alter urine composition in calcium phosphate stone formers. The long-term impact of potassium citrate on calcium phosphate stone recurrence needs to be studied further. References 1 : Composition and morphology of phosphate stones and their relation with etiology. Urol Res2010; 38: 459. Google Scholar 2 : Conversion of calcium oxalate to calcium phosphate with recurrent stone episodes. J Urol2003; 169: 2026. Link, Google Scholar 3 : Clinical implications of abundant calcium phosphate in routinely analyzed kidney stones. Kidney Int2004; 66: 777. Google Scholar 4 : Profile of the brushite stone former. 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Google Scholar 16 : The effects of citrate and urinary macromolecules on the aggregation of hydroxyapatite crystals in solutions with a composition similar to that in the distal tubule. Urol Res1998; 26: 89. Google Scholar 17 : A woman with recurrent calcium phosphate kidney stones. Clin J Am Soc Nephrol2012; 7: 1172. Google Scholar 18 : Therapeutic action of citrate in urolithiasis explained by chemical speciation: increase in pH is the determinant factor. Nephrol Dial Transplant2006; 21: 361. Google Scholar 19 : Comparison of semi-empirical and computer derived methods for estimating urinary saturation of brushite. J Urol2009; 181: 1423. Link, Google Scholar 20 : Citraturic response to oral citric acid load. J Urol1992; 147: 975. Link, Google Scholar 21 : Comparison between lemonade and potassium citrate and impact on urine pH and 24-hour urine parameters in patients with kidney stone formation. Urology2007; 69: 1013. Google Scholar 22 : JESS, a joint expert speciation system—I. Raison d'être. Talanta1991; 38: 1409. Google Scholar 23 : Inhibitors of crystal growth of hydroxyapatite: a constant composition approach. J Urol1985; 134: 1255. Link, Google Scholar 24 : New methods of assessing crystal growth and saturation of brushite in whole urine: effect of pH, calcium and citrate. J Urol2008; 180: 1532. Link, Google Scholar 25 : Nucleation and growth of brushite and calcium oxalate in urine of stone-formers. Metabolism1976; 25: 665. Crossref, Medline, Google Scholar 26 : Long-term treatment with potassium citrate and renal stones in medullary sponge kidney. Clin J Am Soc Nephrol2010; 5: 1663. Google Scholar 27 : Effect of potassium citrate on calcium phosphate stones in a model of hypercalciuria. J Am Soc Nephrol2015; 26: 3001. Google Scholar 28 : Comparative value of orange juice versus lemonade in reducing stone-forming risk. Clin J Am Soc Nephrol2006; 1: 1269. 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Google Scholar © 2018 by American Urological Association Education and Research, Inc.FiguresReferencesRelatedDetailsCited byWong D, Elson L, Nottingham C and Desai A (2022) Pharmaceutical versus Over-the-Counter Potassium Citrate: A Benchtop ComparisonUrology Practice, VOL. 9, NO. 3, (205-211), Online publication date: 1-May-2022.Assimos D (2020) Re: Urinary Lithogenic Risk Profile in ADPKD Patients Treated with TolvaptanJournal of Urology, VOL. 204, NO. 5, (1090-1091), Online publication date: 1-Nov-2020.Assimos D (2019) Re: Chlorthalidone is Superior to Potassium Citrate in Reducing Calcium Phosphate Stones and Increasing Bone Quality in Hypercalciuric Stone-Forming RatsJournal of Urology, VOL. 203, NO. 1, (26-26), Online publication date: 1-Jan-2020.Assimos D (2019) Re: The Impact of Potassium Citrate Therapy in the Natural Course of Medullary Sponge Kidney with Associated NephrolithiasisJournal of Urology, VOL. 202, NO. 6, (1091-1092), Online publication date: 1-Dec-2019.Assimos D (2019) Re: Hydroxycitrate: A Potential New Therapy for Calcium UrolithiasisJournal of Urology, VOL. 202, NO. 3, (454-455), Online publication date: 1-Sep-2019. Volume 200Issue 6December 2018Page: 1278-1284Supplementary Materials Advertisement Copyright & Permissions© 2018 by American Urological Association Education and Research, Inc.Keywordscalcium phosphatesurolithiasisurinary tractcitric acidpotassium citrateMetricsAuthor Information Steeve Doizi Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas Current address: Sorbonne Université, GRC n°20, Groupe de Recherche Clinique sur la Lithiase Urinaire, Hôpital Tenon, F-75020 Paris, France. More articles by this author John R. Poindexter Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas More articles by this author Margaret S. Pearle Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas Department of Urology, University of Texas Southwestern Medical Center, Dallas, Texas More articles by this author Francisco Blanco Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas More articles by this author Orson W. Moe Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas Department of Physiology, University of Texas Southwestern Medical Center, Dallas, Texas Division of Nephrology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas More articles by this author Khashayar Sakhaee Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas Division of Mineral Metabolism, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas More articles by this author Naim M. Maalouf Charles and Jane Pak Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas Division of Mineral Metabolism, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas More articles by this author Expand All Advertisement PDF downloadLoading ...

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