Evidence map›Paper›PMID 38528272›Full record

ArticleJournal of cancer research and clinical oncology2024

Alteration of serum bile acid profiles of HBV-related hepatocellular carcinoma identified by LC-MS/MS.

Sijia Dai, Jingfei Zhu, Xuqiong Chen, Liming Zheng, Xiaoping Li, Longgen Liu

Open access · goldAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Sijia Dai *Changzhou Clinical Medical College, Nanjing Medical University, 300 Lanling Road, Changzhou City, 213001, Jiangsu, China.
Jingfei Zhu *Clinical Lab, Changzhou Third People's Hospital, Changzhou Medical Center, Nanjing Medical University, Changzhou, 213001, China.
Xuqiong ChenChangzhou Clinical Medical College, Nanjing Medical University, 300 Lanling Road, Changzhou City, 213001, Jiangsu, China.
Liming ZhengClinical Lab, Changzhou Third People's Hospital, Changzhou Medical Center, Nanjing Medical University, Changzhou, 213001, China.
Xiaoping LiClinical Lab, Changzhou Third People's Hospital, Changzhou Medical Center, Nanjing Medical University, Changzhou, 213001, China. 3406966332@qq.com.
Longgen LiuChangzhou Clinical Medical College, Nanjing Medical University, 300 Lanling Road, Changzhou City, 213001, Jiangsu, China. ssewllg@163.com.ORCID http://orcid.org/0000-0001-8652-2499
Changzhou No.2 People's Hospital · CNChangzhou Third People's Hospital · CNNanjing Medical University · CN

Funding

Major Projects of Changzhou Health Commission ZD202119
6 · The paper itself

Abstract

backgroundHepatocellular carcinoma closely related to metabolic disorders is a common and aggressive liver malignancy. The dysregulation of bile acid homeostasis has emerged as a key factor for the development and progression of HCC. We aimed to investigate the relationship between bile acids and HCC diagnosis and progression.

methodsA total of 744 HBV-related patients (including 396 HCC patients and 348 patients with chronic liver diseases) were enrolled in the current study. The baseline characteristics of patients were collected from electronic medical records, and the levels of bile acid profiles were determined by LC-MS/MS. Propensity score matching analysis was conducted to reduce the effect of selection bias, and receiver operating characteristic analysis was performed to evaluate the clinical application values of bile acid.

resultsSignificant differences were observed for most characteristics between the HCC group and the CLD group before PSM analysis. Patients with HCC were older and fatter (p < 0.05). After adjusting with a 1:1 ratio for age, gender and BMI, 42 HCC patients and 42 non-HCC patients were matched in 2 groups, respectively. The total bile acid level in HCC patients was lower than that in patients with chronic liver diseases before and after PSM analysis (p < 0.05). However, patients with HCC had significantly higher levels of DCA, LCA, and GLCA and lower levels of TCDCA, GUDCA, and TUDCA (p < 0.05, respectively). Besides, the TCDCA, TUDCA, GLCA, and GUDCA were significantly correlated with tumor procession. Moreover, the BAs profiles had a superior predictive ability for predicting the development of HCC even in patients with low serum AFP levels.

conclusionPatients with HCC had significantly lower levels of total bile acid, but higher levels of secondary bile acids (DCA, LCA, and GLCA). The levels of primary bile acid (TCDCA) were closely related to tumor size and stage, which indicated that the bile acids were involved in the HCC procession and had important clinical application values.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsTaurochenodeoxycholic AcidBile Acids and SaltsChromatography, LiquidHepatitis B virusHumansLiquid Chromatography-Mass SpectrometryTandem Mass SpectrometryBile Acids and SaltsTaurochenodeoxycholic AcidursodoxicoltaurineBile acidsHepatitis B virusHepatocellular carcinomaLiquid chromatography–mass spectrometry

Identifiers

PMID38528272
PMCPMC10963458
OpenAlexW4393142263

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LicenceCC BY
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Registered trials

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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.