Evidence map›Paper›PMID 33810868›Full record

Trial reportAmerican journal of kidney diseases : the official journal of the National Kidney Foundation2021

Effect of Bicarbonate on Net Acid Excretion, Blood Pressure, and Metabolism in Patients With and Without CKD: The Acid Base Compensation in CKD Study.

Crystal C Tyson, Alison Luciano, Jennifer L Modliszewski, David L Corcoran, James R Bain, Michael Muehlbauer, Olga Ilkayeva, Shirin Pourafshar, Jenifer Allen, Cassandra Bowman and 6 more

Registry-linked trialOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in American journal of kidney diseases : the official journal of the National Kidney Foundation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02427594 (Acid-Base Compensation in Chronic Kidney Disease), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 12% 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.

NCT02427594 phase1completednot on this map

Acid-Base Compensation in Chronic Kidney Disease: Measurement and Physiologic Impact

TypeinterventionalSponsorDuke UniversityRan2015 to 2017Enrolled14ConditionsChronic Kidney DiseaseArmsSodium bicarbonate, Controlled diet
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
  2. Urine tricarboxylic acid cycle signatures of early-stage diabetic kidney disease.Metabolomics : Official journal of the Metabolomic Society · 2021
    Trial
  3. Trial
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. A Urine pH-Ammonium Acid/Base Score and CKD Progression.Journal of the American Society of Nephrology : JASN · 2024
    Article
  10. Article
  11. Diversity of plant DNA in stool is linked to dietary quality, age, and household income.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Review
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 1 country.

Crystal C TysonDepartment of Medicine, Duke University School of Medicine, Durham, NC.
Alison LucianoCenter for the Study of Aging and Human Development, Duke University School of Medicine, Durham, NC.
Jennifer L ModliszewskiCenter for Genomic and Computational Biology, Duke University School of Medicine, Durham, NC; Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC.
David L CorcoranCenter for Genomic and Computational Biology, Duke University School of Medicine, Durham, NC; Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC.
James R BainDepartment of Medicine, Duke University School of Medicine, Durham, NC; Center for the Study of Aging and Human Development, Duke University School of Medicine, Durham, NC; Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, NC.
Michael MuehlbauerDuke Molecular Physiology Institute, Duke University School of Medicine, Durham, NC.
Olga IlkayevaDuke Molecular Physiology Institute, Duke University School of Medicine, Durham, NC.
Shirin PourafsharDepartment of Medicine, University of Virginia School of Medicine, Charlottesville, VA.
Jenifer AllenDepartment of Medicine, Duke University School of Medicine, Durham, NC.
Cassandra BowmanDepartment of Medicine, Duke University School of Medicine, Durham, NC.
Joseph GungDepartment of Medicine, Duke University School of Medicine, Durham, NC.
John R AsplinLitholink Corp, Laboratory Corporation of America Holdings, Chicago, IL.
Jane PendergastDepartment of Medicine, Duke University School of Medicine, Durham, NC; Center for the Study of Aging and Human Development, Duke University School of Medicine, Durham, NC; Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC.
Laura P SvetkeyDepartment of Medicine, Duke University School of Medicine, Durham, NC; Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, NC.
Pao-Hwa LinDepartment of Medicine, Duke University School of Medicine, Durham, NC; Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, NC.
Julia J SciallaDepartment of Medicine, University of Virginia School of Medicine, Charlottesville, VA. Electronic address: jscialla@virginia.edu.
Duke University · USUniversity of Virginia · USLabCorp (United States) · US

Funding

Resource Core 3 - Metabolomics CoreP30AG028716 · NIA · DUKE UNIVERSITY · PI Sarah B. Peskoe · 2006 to 2026
$24.6M
Renal Genomics CoreP30DK096493 · NIDDK · DUKE UNIVERSITY · PI PATEL, UPTAL D · 2012 to 2016
$5.9M
Facility and Web-based Approaches to Lifestyle Change in Resistant HypertensionR01HL122836 · NHLBI · DUKE UNIVERSITY · PI BLUMENTHAL, JAMES A, SHERWOOD, ANDREW · 2015 to 2019
$4.2M
Dietary Acid Load, Subclinical Acidosis and Outcomes in Chronic Kidney DiseaseK23DK095949 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI SCIALLA, JULIA J · 2012 to 2016
$839k
NHLBI NIH HHS R01 HL122836NIA NIH HHS P30 AG028716NIDDK NIH HHS K23 DK095949NIDDK NIH HHS P30 DK096493
6 · The paper itself

Abstract

RATIONALE &

objectivePatients with CKD are at elevated risk of metabolic acidosis due to impaired net acid excretion (NAE). Identifying early markers of acidosis may guide prevention in chronic kidney disease (CKD). This study compared NAE in participants with and without CKD, as well as the NAE, blood pressure (BP), and metabolomic response to bicarbonate supplementation. STUDY

designRandomized order, cross-over study with controlled feeding. SETTING &

participantsParticipants consisted of 8 patients with CKD (estimated glomerular filtration rate 30-59mL/min/1.73m

interventionParticipants were fed a fixed-acid-load diet with bicarbonate supplementation (7 days) and with sodium chloride control (7 days) in a randomized order, cross-over fashion. OUTCOMES: Urine NAE, 24-hour ambulatory BP, and 24-hour urine and plasma metabolomic profiles were measured after each period.

resultsDuring the control period, mean NAE was 28.3±10.2 mEq/d overall without differences across groups (P=0.5). Urine pH, ammonium, and citrate were significantly lower in CKD than in non-CKD (P<0.05 for each). Bicarbonate supplementation reduced NAE and urine ammonium in the CKD group, increased urine pH in both groups (but more in patients with CKD than in those without), and increased; urine citrate in the CKD group (P< 0.2 for interaction for each). Metabolomic analysis revealed several urine organic anions were increased with bicarbonate in CKD, including 3-indoleacetate, citrate/isocitrate, and glutarate. BP was not significantly changed. LIMITATIONS: Small sample size and short feeding duration.

conclusionsCompared to patients without CKD, those with CKD had lower acid excretion in the form of ammonium but also lower base excretion such as citrate and other organic anions, a potential compensation to preserve acid-base homeostasis. In CKD, acid excretion decreased further, but base excretion (eg, citrate) increased in response to alkali. Urine citrate should be evaluated as an early and responsive marker of impaired acid-base homeostasis.

fundingNational Institute of Diabetes and Digestive and Kidney Diseases and the Duke O'Brien Center for Kidney Research.

trial registrationRegistered at ClinicalTrials.gov with study number NCT02427594.

Indexed as

Acid-Base EquilibriumBlood PressureDietAgedBicarbonatesCross-Over StudiesFemaleHumansMaleMiddle AgedRenal Insufficiency, ChronicBicarbonatesacid-base homeostasisalkalibicarbonatebicarbonate supplementationchronic kidney diseaseCKDcross-over trialdiethuman feeding studyhypertensionmetabolic acidosisNAEnet acid excretionsubclinical acidosis

Identifiers

PMID33810868
PMCPMC9254549
OpenAlexW3145397586

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.