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. J Urol2010; 184: 1367. Link, Google Scholar 5 : Biochemical and physicochemical presentations of patients with brushite stones. J Urol2004; 171: 1046. Link, Google Scholar 6 : Spontaneous precipitation of brushite in urine: evidence that brushite is the nidus of renal stones originating as calcium phosphate. Proc Natl Acad Sci U S A1971; 68: 1456. Google Scholar 7 : Pathophysiology-based treatment of idiopathic calcium kidney stones. Clin J Am Soc Nephrol2011; 6: 2083. Google Scholar 8 : Long-term treatment of calcium nephrolithiasis with potassium citrate. J Urol1985; 134: 11. Link, Google Scholar 9 : Prevention of recurrent calcium stone formation with potassium citrate therapy in patients with distal renal tubular acidosis. J Urol1985; 134: 20. Link, Google Scholar 10 : Successful management of uric acid nephrolithiasis with potassium citrate. Kidney Int1986; 30: 422. Crossref, Medline, Google Scholar 11 : Randomized double-blind study of potassium citrate in idiopathic hypocitraturic calcium nephrolithiasis. J Urol1993; 150: 1761. Link, Google Scholar 12 : Long-term effects of potassium citrate therapy on the formation of new stones in groups of recurrent stone formers with hypocitraturia. Br J Urol1996; 78: 10. Google Scholar 13 : Effect of potassium citrate therapy on stone recurrence and residual fragments after shockwave lithotripsy in lower caliceal calcium oxalate urolithiasis: a randomized controlled trial. J Endourol2002; 16: 149. Google Scholar 14 : Contrasting effects of potassium citrate and sodium citrate therapies on urinary chemistries and crystallization of stone-forming salts. Kidney Int1983; 24: 348. Crossref, Medline, Google Scholar 15 : The effects of citrate on hydroxyapatite induced calcium oxalate crystallization and on the formation of calcium phosphate crystals. Urol Res1989; 17: 167. 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. Google Scholar 29 : Saturation-inhibition index as a measure of the risk of calcium oxalate stone formation in the urinary tract. N Engl J Med1976; 294: 249. 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 ...

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
量子星尘发布了新的文献求助10
刚刚
1秒前
犹豫战斗机完成签到,获得积分10
1秒前
风趣采白完成签到,获得积分10
1秒前
脑洞疼应助xxw采纳,获得10
2秒前
脱壳金蝉完成签到,获得积分10
2秒前
3秒前
大力水手完成签到,获得积分10
3秒前
4秒前
6秒前
科研通AI2S应助now采纳,获得10
6秒前
len完成签到,获得积分10
6秒前
1111完成签到,获得积分10
7秒前
努力向前看完成签到,获得积分10
8秒前
量子星尘发布了新的文献求助10
9秒前
wt完成签到,获得积分10
10秒前
赵赵赵发布了新的文献求助10
11秒前
11秒前
木木水完成签到,获得积分10
11秒前
阿刚完成签到,获得积分10
11秒前
kryptonite完成签到 ,获得积分10
12秒前
EH完成签到,获得积分10
12秒前
13秒前
李健完成签到 ,获得积分10
13秒前
呆萌幻竹完成签到 ,获得积分10
15秒前
冰销雪释完成签到,获得积分10
15秒前
xxw发布了新的文献求助10
16秒前
TS完成签到,获得积分10
16秒前
聚乙二醇完成签到 ,获得积分10
16秒前
量子星尘发布了新的文献求助10
17秒前
Ava应助喜悦香萱采纳,获得10
17秒前
17秒前
123完成签到,获得积分10
19秒前
20秒前
exosome发布了新的文献求助10
20秒前
www完成签到,获得积分10
21秒前
研友_VZG7GZ应助xh采纳,获得10
22秒前
Yvan完成签到,获得积分10
22秒前
雨辰完成签到,获得积分10
23秒前
冰淇淋啦啦啦完成签到,获得积分10
23秒前
高分求助中
Production Logging: Theoretical and Interpretive Elements 2700
Neuromuscular and Electrodiagnostic Medicine Board Review 1000
Statistical Methods for the Social Sciences, Global Edition, 6th edition 600
こんなに痛いのにどうして「なんでもない」と医者にいわれてしまうのでしょうか 510
Walter Gilbert: Selected Works 500
An Annotated Checklist of Dinosaur Species by Continent 500
岡本唐貴自伝的回想画集 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3661181
求助须知:如何正确求助?哪些是违规求助? 3222298
关于积分的说明 9744486
捐赠科研通 2931912
什么是DOI,文献DOI怎么找? 1605300
邀请新用户注册赠送积分活动 757805
科研通“疑难数据库(出版商)”最低求助积分说明 734569