Evidence map›Paper›PMID 19373503›Full record

ArticleLipids2009

Bile acids conjugation in human bile is not random: new insights from (1)H-NMR spectroscopy at 800 MHz.

G A Nagana Gowda, Narasimhamurthy Shanaiah, Amanda Cooper, Mary Maluccio, Daniel Raftery

Abstract read
In one paragraph

Article in Lipids, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Bile Processing Protocol for Improved Proteomic Analysis.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  5. Functional, Diagnostic and Therapeutic Aspects of Bile.Clinical and experimental gastroenterology · 2022
    Article
  6. Precision Oncology via NMR-Based Metabolomics: A Review on Breast Cancer.International journal of molecular sciences · 2021
    Review
  7. Article
  8. Article
  9. Article
  10. Metabolic rearrangements in primary liver cancers: cause and consequences.Nature reviews. Gastroenterology & hepatology · 2019
    Review
  11. Sodium Taurocholate StimulatesFrontiers in cellular and infection microbiology · 2019
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
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

5 authors at 3 institutions in 1 country.

G A Nagana GowdaDepartment of Chemistry, Purdue University, West Lafayette, IN 47907, USA. ngowda@purdue.edu
Narasimhamurthy Shanaiah
Amanda Cooper
Mary Maluccio
Daniel Raftery
Purdue University West Lafayette · USIndiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

TOOLS FOR DIFFERENTIAL METABOLOMICS (RMI)R21DK070290 · NIDDK · PURDUE UNIVERSITY WEST LAFAYETTE · PI REGNIER, FRED E · 2004 to 2005
$1.0M
NIDDK NIH HHS R21 DK070290
6 · The paper itself

Abstract

Bile acids constitute a group of structurally closely related molecules and represent the most abundant constituents of human bile. Investigations of bile acids have garnered increased interest owing to their recently discovered additional biological functions including their role as signaling molecules that govern glucose, fat and energy metabolism. Recent NMR methodological developments have enabled single-step analysis of several highly abundant and common glycine- and taurine- conjugated bile acids, such as glycocholic acid, glycodeoxycholic acid, glycochenodeoxycholic acid, taurocholic acid, taurodeoxycholic acid, and taurochenodeoxycholic acid. Investigation of these conjugated bile acids in human bile employing high field (800 MHz) (1)H-NMR spectroscopy reveals that the ratios between two glycine-conjugated bile acids and their taurine counterparts correlate positively (R2 = 0.83-0.97; p = 0.001 x 10(-2)-0.006 x 10(-7)) as do the ratios between a glycine-conjugated bile acid and its taurine counterpart (R2 = 0.92-0.95; p = 0.004 x 10(-3)-0.002 x 10(-10)). Using such correlations, concentration of individual bile acids in each sample could be predicted in good agreement with the experimentally determined values. These insights into the pattern of bile acid conjugation in human bile between glycine and taurine promise useful clues to the mechanism of bile acids' biosynthesis, conjugation and enterohepatic circulation, and may improve our understanding of the role of individual conjugated bile acids in health and disease.

Indexed as

BileBile Acids and SaltsFemaleGlycineHumansMagnetic Resonance SpectroscopyMaleMiddle AgedProtonsReference StandardsReproducibility of ResultsTaurineBile Acids and SaltsGlycineProtonsTaurine

Identifiers

PMID19373503
PMCPMC5459358
OpenAlexW1964504097

What OpenQuestion holds

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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.