Evidence map›Paper›PMID 31101664›Full record

ArticleJournal of the American Society of Nephrology : JASN2019

Chlorthalidone Is Superior to Potassium Citrate in Reducing Calcium Phosphate Stones and Increasing Bone Quality in Hypercalciuric Stone-Forming Rats.

Nancy S Krieger, John R Asplin, Ignacio Granja, Felix M Ramos, Courtney Flotteron, Luojing Chen, Tong Tong Wu, Marc D Grynpas, David A Bushinsky

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Kidney Stone Prevention.Advances in nutrition (Bethesda, Md.) · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. ChlorthalidoneAnnals of translational medicine · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Nancy S KriegerDivision of Nephrology, Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, New York; Nancy_Krieger@URMC.Rochester.edu.
John R AsplinLitholink Corporation, Laboratory Corporation of America Holdings, Chicago, Illinois.
Ignacio GranjaLitholink Corporation, Laboratory Corporation of America Holdings, Chicago, Illinois.
Felix M RamosDivision of Nephrology, Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, New York.
Courtney FlotteronDivision of Nephrology, Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, New York.
Luojing ChenDivision of Nephrology, Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, New York.
Tong Tong WuDepartment of Biostatistics and Computational Biology, University of Rochester School of Medicine, Rochester, New York; and.
Marc D GrynpasLunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.
David A BushinskyDivision of Nephrology, Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, New York.
University of Rochester · USLink Foundation · USMount Sinai Hospital · CA

Funding

Hypercalciuria and Bone Quality in the Genetic Hypercalciuric Stone-Forming RatsR01DK075462 · NIDDK · UNIVERSITY OF ROCHESTER · PI BUSHINSKY, DAVID A · 2008 to 2019
$3.8M
NIDDK NIH HHS R01 DK075462
6 · The paper itself

Abstract

backgroundThe pathophysiology of genetic hypercalciuric stone-forming rats parallels that of human idiopathic hypercalciuria. In this model, all animals form calcium phosphate stones. We previously found that chlorthalidone, but not potassium citrate, decreased stone formation in these rats.

methodsTo test whether chlorthalidone and potassium citrate combined would reduce calcium phosphate stone formation more than either medication alone, four groups of rats were fed a fixed amount of a normal calcium and phosphorus diet, supplemented with potassium chloride (as control), potassium citrate, chlorthalidone (with potassium chloride to equalize potassium intake), or potassium citrate plus chlorthalidone. We measured urine every 6 weeks and assessed stone formation and bone quality at 18 weeks.

resultsPotassium citrate reduced urine calcium compared with controls, chlorthalidone reduced it further, and potassium citrate plus chlorthalidone reduced it even more. Chlorthalidone increased urine citrate and potassium citrate increased it even more; the combination did not increase it further. Potassium citrate, alone or with chlorthalidone, increased urine calcium phosphate supersaturation, but chlorthalidone did not. All control rats formed stones. Potassium citrate did not alter stone formation. No stones formed with chlorthalidone, and rats given potassium citrate plus chlorthalidone had some stones but fewer than controls. Rats given chlorthalidone with or without potassium citrate had higher bone mineral density and better mechanical properties than controls, whereas those given potassium citrate did not.

conclusionsIn genetic hypercalciuric stone-forming rats, chlorthalidone is superior to potassium citrate alone or combined with chlorthalidone in reducing calcium phosphate stone formation and improving bone quality.

Indexed as

AnimalsBone DensityCalcium PhosphatesChlorthalidoneHypercalciuriaKidney CalculiMaleOxalatesPotassium CitrateRatscalcium phosphateCalcium PhosphatesChlorthalidoneOxalatesPotassium Citratecalciumhypercalciuriakidney stones

Identifiers

PMID31101664
PMCPMC6622425
OpenAlexW2946478947

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.