Evidence map›Paper›PMID 35448518›Full record

ArticleMetabolites2022

Evaluation of the Risk of

Tadakuni Monma, Junichi Iwamoto, Akira Honda, Hajime Ueda, Fumio Kakizaki, Shoichiro Yara, Teruo Miyazaki, Tadashi Ikegami

Open access · goldAbstract read
In one paragraph

Article in Metabolites, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 1 institution in 1 country.

Tadakuni MonmaDivision of Gastroenterology and Hepatology, Tokyo Medical University Ibaraki Medical Center, Ibaraki 300-0395, Japan.
Junichi IwamotoDivision of Gastroenterology and Hepatology, Tokyo Medical University Ibaraki Medical Center, Ibaraki 300-0395, Japan.ORCID 0000-0002-5238-3272
Akira HondaDivision of Gastroenterology and Hepatology, Tokyo Medical University Ibaraki Medical Center, Ibaraki 300-0395, Japan.ORCID 0000-0003-0902-8272
Hajime UedaDivision of Gastroenterology and Hepatology, Tokyo Medical University Ibaraki Medical Center, Ibaraki 300-0395, Japan.ORCID 0000-0003-3983-6393
Fumio KakizakiDivision of Gastroenterology and Hepatology, Tokyo Medical University Ibaraki Medical Center, Ibaraki 300-0395, Japan.ORCID 0000-0001-5582-3985
Shoichiro YaraDivision of Gastroenterology and Hepatology, Tokyo Medical University Ibaraki Medical Center, Ibaraki 300-0395, Japan.
Teruo MiyazakiJoint Research Center, Tokyo Medical University Ibaraki Medical Center, Ibaraki 300-0395, Japan.ORCID 0000-0001-9796-3011
Tadashi IkegamiDivision of Gastroenterology and Hepatology, Tokyo Medical University Ibaraki Medical Center, Ibaraki 300-0395, Japan.ORCID 0000-0002-9216-3186
Tokyo Medical University Ibaraki Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since intestinal secondary bile acids (BAs) prevent Clostridium difficile infection (CDI), the serum BA profile may be a convenient biomarker for CDI susceptibility in human subjects. To verify this hypothesis, we investigated blood samples from 71 patients of the Division of Gastroenterology and Hepatology at the time of admission (prior to antibiotic use and CDI onset). Twelve patients developed CDI during hospitalization, and the other 59 patients did not. The serum unconjugated deoxycholic acid (DCA)/[DCA + unconjugated cholic acid (CA)] ratio on admission was significantly lower in patients who developed CDI than in patients who did not develop CDI (p < 0.01) and in 46 healthy controls (p < 0.0001). Another unconjugated secondary BA ratio, 3β-hydroxy (3βOH)-BAs/(3βOH + 3αOH-BAs), was also significantly lower in patients who developed CDI than in healthy controls (p < 0.05) but was not significantly different between patients who developed and patients who did not develop CDI. A receiver operating characteristic (ROC) curve determined a cut-off point of DCA/(DCA + CA) < 0.349 that optimally discriminated on admission the high-risk patients who would develop CDI (sensitivity 91.7% and specificity 64.4%). In conclusion, a decreased serum DCA/(DCA + CA) ratio on admission strongly correlated with CDI onset during hospitalization in patients with gastrointestinal and hepatobiliary diseases. Serum BA composition could be a helpful biomarker for predicting susceptibility to CDI.

Indexed as

antibioticsbile acidsbiomarkerClostridium difficileHPLC-MS/MSproton pump inhibitors

Identifiers

PMID35448518
PMCPMC9032545
OpenAlexW4224295502

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.