Literature DB >> 12957883

Urinary saturation and risk factors for calcium oxalate stone disease based on spot and 24-hour urine specimens.

Yoshihide Ogawa1, Hiroyuki Yonou, Sanehiro Hokama, Masami Oda, Makoto Morozumi, Kimio Sugaya.   

Abstract

In 222 random spot urine specimens, the calcium concentration and calcium oxalate saturation [DG(CaOx)] were significantly higher among stone formers than among non-stone formers, while the citrate and creatinine-corrected citrate concentrations were lower. In 188 24-hour urine specimens, magnesium excretion was lower among stone formers than non-stone formers, while the creatinine-corrected calcium concentration and DG(CaOx) were higher. Among stone formers, there was no gender difference in the urinary concentrations of calcium, oxalate, citrate, magnesium, and DG(CaOx), but the creatinine-corrected calcium, citrate, and magnesium concentrations were higher in women, as well as 24-hour citrate excretion. The levels of calcium and oxalate have a major influence on DG(CaOx), while citrate and magnesium levels have a minor influence. DG(CaOx) was correlated with calcium and oxalate excretion, as well as with the creatinine-corrected calcium and oxalate concentrations. Approximately 5% of 24-hour urine specimens showed critical supersaturation, 80% showed metastable supersaturation, and 15% were unsaturated. Hypercalciuria or hyperoxaluria was fairly common (30% and 40%) in critically supersaturated urine, while it was less common (22.4% and 8.6%) in metastably supersaturated urine and was not detected in unsaturated urine. Hypocitraturia and/or hypomagnesiuria was more common (63.8-80%) at any saturation. The urinary calcium, oxalate, and citrate concentrations, as well as the creatinine-corrected calcium, oxalate, citrate, and magnesium concentrations and DG(CaOx), showed a significant correlation between 57 paired early morning spot urine and 24-hour urine specimens. The creatinine-corrected calcium and citrate concentrations of the early morning urine specimens were significantly correlated with the levels of calcium and citrate excretion in the paired 24-hour urine specimens. In conclusion, no parameter other than urinary saturation gives more than a vague indication of the risk of lithogenesis, so DG(CaOx) in either early morning urine or 24-hour urine specimens appears to be the best predictor of stone risk. Finally, the creatinine-corrected calcium and citrate concentrations in early morning urine can be used as a substitute for measuring 24-hour excretion.

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Year:  2003        PMID: 12957883     DOI: 10.2741/1139

Source DB:  PubMed          Journal:  Front Biosci        ISSN: 1093-4715


  14 in total

1.  A proposed method for approximate estimates of the ion-activity products of calcium oxalate and calcium phosphate in spot-urine samples or in urine samples collected during less well defined periods of time.

Authors:  Hans-Göran Tiselius
Journal:  Urolithiasis       Date:  2013-02-06       Impact factor: 3.436

Review 2.  Fasting and postprandial spot urine calcium-to-creatinine ratios do not detect hypercalciuria.

Authors:  A N Jones; M M Shafer; N S Keuler; E M Crone; K E Hansen
Journal:  Osteoporos Int       Date:  2011-02-24       Impact factor: 4.507

3.  Stress-stones-stress-recurrent stones: a self-propagating cycle? Difficulties in solving this dichotomy.

Authors:  Montserrat Arzoz-Fabregas; Josep Roca-Antonio; Luis Ibarz-Servio; Dalielah Jappie-Mahomed; Allen Rodgers
Journal:  Urolithiasis       Date:  2017-03-21       Impact factor: 3.436

4.  Gastrointestinal oxalic acid absorption in calcium-treated rats.

Authors:  Makoto Morozumi; Rayhan Zubair Hossain; Ken-ichi Yamakawa; Sanehiro Hokama; Saori Nishijima; Yoshinori Oshiro; Atsushi Uchida; Kimio Sugaya; Yoshihide Ogawa
Journal:  Urol Res       Date:  2006-01-28

5.  Fasting versus 24-h urine pH in the evaluation of nephrolithiasis.

Authors:  Giovanna Capolongo; Khashayar Sakhaee; Charles Y C Pak; Naim M Maalouf
Journal:  Urol Res       Date:  2011-02-19

6.  Temporary risk identification in urolithiasis.

Authors:  Y M Fazil Marickar; Abiya Salim
Journal:  Urol Res       Date:  2009-10-15

7.  Assessment of crystallization risk formulas in pediatric calcium stone-formers.

Authors:  Przemysław Sikora; Małgorzata Zajaczkowska; Bernd Hoppe
Journal:  Pediatr Nephrol       Date:  2009-03-31       Impact factor: 3.714

8.  Absence of the sulfate transporter SAT-1 has no impact on oxalate handling by mouse intestine and does not cause hyperoxaluria or hyperoxalemia.

Authors:  Jonathan M Whittamore; Christine E Stephens; Marguerite Hatch
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2018-11-01       Impact factor: 4.052

9.  Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications.

Authors:  J Warner; M Epstein; A Sweet; D Singh; J Burgess; S Stranks; P Hill; D Perry-Keene; D Learoyd; B Robinson; P Birdsey; E Mackenzie; B T Teh; J B Prins; J Cardinal
Journal:  J Med Genet       Date:  2004-03       Impact factor: 6.318

10.  Oxalate synthesis from hydroxypyruvate in vitamin-B6-deficient rats.

Authors:  Yaovalak Teerajetgul; Rayhan Zubair Hossain; Kenichi Yamakawa; Makoto Morozumi; Kimio Sugaya; Yoshihide Ogawa
Journal:  Urol Res       Date:  2007-06-13
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