Evidence map›Paper›PMID 28801122›Full record

Trial reportAmerican journal of kidney diseases : the official journal of the National Kidney Foundation2018

Deoxycholic Acid, a Metabolite of Circulating Bile Acids, and Coronary Artery Vascular Calcification in CKD.

Anna Jovanovich, Tamara Isakova, Geoffrey Block, Jason Stubbs, Gerard Smits, Michel Chonchol, Makoto Miyazaki

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in American journal of kidney diseases : the official journal of the National Kidney Foundation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 3 pooled it
4.9field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 3 syntheses or guidelines pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Prebiotic Administration to Chronic Kidney Disease Patients Modifies Their Fecal Microbiome and Host Metabolism.Journal of renal nutrition : the official journal of the Council on Renal Nutrition of the National Kidney Foundation · 2026
    Trial
  5. Trial
  6. Article
  7. Links between bone fractures and the gut microbiota.Nature reviews. Endocrinology · 2026
    Review
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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

7 authors at 6 institutions in 1 country.

Anna JovanovichRenal Section, Denver VA Medical Center, Denver, CO; Division of Renal Diseases and Hypertension, University of Colorado Denver Anschutz Medical Campus, Aurora, CO. Electronic address: anna.jovanovich@ucdenver.edu.
Tamara IsakovaDivision of Nephrology and Hypertension, Department of Medicine and Center for Translational Metabolism and Health, Institute for Public Health and Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
Geoffrey BlockDenver Nephrology, Denver, CO.
Jason StubbsKidney Institute, University of Kansas Medical Center, Kansas City, KS.
Gerard SmitsDivision of Renal Diseases and Hypertension, University of Colorado Denver Anschutz Medical Campus, Aurora, CO.
Michel ChoncholDivision of Renal Diseases and Hypertension, University of Colorado Denver Anschutz Medical Campus, Aurora, CO.
Makoto MiyazakiDivision of Renal Diseases and Hypertension, University of Colorado Denver Anschutz Medical Campus, Aurora, CO.
University of Colorado Denver · USColorado Kidney Care · USDenver VA Medical Center · USNorthwestern University · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Kansas Medical Center · US

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Edward L Melanson · 1995 to 2026
$32.6M
The role of MLKL in the regulation of vascular calcification in CKDR01HL132318 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MIYAZAKI, MAKOTO · 2016 to 2025
$3.8M
Impact of phosphate and FGF23 reduction on intermediate end points in CKDR01DK102438 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ISAKOVA, TAMARA · 2014 to 2018
$3.0M
Novel Diagnostics and Therapeutic Targets for Calcification in CKDR01DK110087 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ISAKOVA, TAMARA · 2016 to 2020
$2.3M
FGF-23 and clinical outcomes in ADPKD patientsR01DK094796 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI CHONCHOL, MICHEL BENJAMIN, GITOMER, BERENICE YOLANDE · 2012 to 2016
$2.3M
Molecular Pathogenesis of Chronic Kidney Disease-Dependent Vascular CalcificationR01DK096030 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI MIYAZAKI, MAKOTO · 2013 to 2017
$2.2M
The contributory role of microbial metabolite in the pathogenesis of CKD-dependent vascular calcificationR01HL133545 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MIYAZAKI, MAKOTO · 2018 to 2021
$1.9M
Pilot Studies Targeting Mineral Metabolism in CKDU01DK099930 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ISAKOVA, TAMARA · 2013 to 2018
$1.8M
The Role of Stearate in The Regulation of Vascular Calcification in Chronic Kidney DiseaseR01HL117062 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MIYAZAKI, MAKOTO · 2013 to 2016
$1.5M
Phosphate Lowering to Treat Vascular Dysfunction in Chronic Kidney DiseaseIK2CX001030 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI JOVANOVICH, ANNA · 2014 to 2020
–
CSRD VA IK2 CX001030NHLBI NIH HHS R01 HL117062NHLBI NIH HHS R01 HL132318NHLBI NIH HHS R01 HL133545NIDDK NIH HHS P30 DK048520NIDDK NIH HHS R01 DK094796NIDDK NIH HHS R01 DK096030NIDDK NIH HHS R01 DK102438NIDDK NIH HHS R01 DK110087NIDDK NIH HHS U01 DK099930
6 · The paper itself

Abstract

backgroundVascular calcification is common among patients with chronic kidney disease (CKD), and it is associated with all-cause and cardiovascular disease mortality. Deoxycholic acid, a metabolite of circulating bile acids, is elevated in CKD and induces vascular mineralization and osteogenic differentiation in animal models. STUDY

designCohort analysis of clinical trial participants. SETTING &

participants112 patients with moderate to severe CKD (estimated glomerular filtration rate, 20-45mL/min/1.73m PREDICTOR: Serum deoxycholic acid concentration. OUTCOMES: Baseline coronary artery calcification (CAC) volume score and bone mineral density (BMD) and change in CAC volume score and BMD after 9 months. MEASUREMENTS: Deoxycholic acid was assayed in stored baseline serum samples using liquid chromatography-tandem mass spectrometry, CAC was measured using a GE-Imitron C150 scanner, and BMD was determined using computed tomographic scans of the abdomen with calibrated phantom of known density.

resultsHigher serum deoxycholic acid concentrations were significantly correlated with greater baseline CAC volume and lower baseline BMD. After adjusting for demographics, coexisting illness, body mass index, estimated glomerular filtration rate, and concentrations of circulating markers of mineral metabolism, including serum calcium, phosphorus, vitamin D, parathyroid hormone, and fibroblast growth factor 23, a serum deoxycholic acid concentration > 58ng/mL (the median) was positively associated with baseline CAC volume (β=0.71; 95% CI, 0.26-1.16; P=0.003) and negatively associated with baseline BMD (β = -20.3; 95% CI, -1.5 to -39.1; P=0.04). Serum deoxycholic acid concentration > 58ng/mL was not significantly associated with change in CAC volume score after 9 months (β=0.06; 95% CI, -0.09 to 0.21; P=0.4). The analysis for the relationship between baseline deoxycholic acid concentrations and change in BMD after 9 months was not statistically significant, but was underpowered. LIMITATIONS: The use of nonfasting serum samples is a limitation because deoxycholic acid concentrations may vary based on time of day and dietary intake. Few trial participants with complete data to evaluate the change in CAC volume score (n=75) and BMD (n=59). No data for changes in deoxycholic acid concentrations over time.

conclusionsAmong patients with moderate to severe CKD, higher serum deoxycholic acid concentrations were independently associated with greater baseline CAC volume score and lower baseline BMD.

Indexed as

Coronary Artery DiseaseCoronary VesselsRenal Insufficiency, ChronicVascular CalcificationAgedBile Acids and SaltsBiomarkersBone DensityChelating AgentsChromatography, LiquidCorrelation of DataDeoxycholic AcidFemaleHumansMaleMiddle AgedBile Acids and SaltsBiomarkersChelating AgentsDeoxycholic AcidPhosphorusbiomarkerbone mineral density (BMD)cardiovascular diseasechronic kidney disease (CKD)circulating bile acidcoronary artery calcification (CAC)deoxycholic acid (DCA)mineral metabolismVascular calcification

Identifiers

PMID28801122
PMCPMC5742074
OpenAlexW2745302715

What OpenQuestion holds

Textmetadata
LicenceTDM
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.