Evidence map›Paper›PMID 39113878›Full record

ArticleAmerican journal of cancer research2024

Effects of N-acetylcysteine on hepatocellular carcinoma in chronic hepatitis C.

Gary Wong, Szu-Yuan Wu, Wan-Ming Chen, Po-Jung Hsu, Ta-Chun Chou, Ming-Feng Chiang, Ming-Shun Wu, Ming-Che Lee, Ruey-Shyang Soong

Abstract read
In one paragraph

Article in American journal of cancer research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

9 authors.

Gary WongDivision of General Surgery, Department of Surgery, Wan Fang Hospital, Taipei Medical University No. 111, Sec. 3, Xinglong Road, Wenshan District, Taipei 116, Taiwan.
Szu-Yuan WuGraduate Institute of Business Administration, College of Management, Fu Jen Catholic University New Taipei 242, Taiwan.
Wan-Ming ChenGraduate Institute of Business Administration, College of Management, Fu Jen Catholic University New Taipei 242, Taiwan.
Po-Jung HsuDivision of General Surgery, Department of Surgery, Wan Fang Hospital, Taipei Medical University No. 111, Sec. 3, Xinglong Road, Wenshan District, Taipei 116, Taiwan.
Ta-Chun ChouCenters for Regional Anesthesia and Pain Medicine, Taipei Municipal Wan Fang Hospital, Taipei Medical University Taipei 110, Taiwan.
Ming-Feng ChiangDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Lo-Hsu Medical Foundation, Lotung Poh-Ai Hospital Yilan 265, Taiwan.
Ming-Shun WuCollege of Medicine, Taipei Medical University No. 250 Wu-Hsing Street, Taipei 110, Taiwan.
Ming-Che LeeCollege of Medicine, Taipei Medical University No. 250 Wu-Hsing Street, Taipei 110, Taiwan.
Ruey-Shyang SoongDivision of General Surgery, Department of Surgery, Wan Fang Hospital, Taipei Medical University No. 111, Sec. 3, Xinglong Road, Wenshan District, Taipei 116, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatitis C virus (HCV) infection significantly contributes to global hepatocellular carcinoma (HCC) incidence. N-Acetylcysteine (NAC), known for its antioxidant properties, is a potential therapeutic agent. However, evidence on its efficacy in reducing HCC risk among HCV patients is limited. A retrospective cohort analysis using Taiwan's National Health Insurance Research Database (2008-2018) included ≥18-year-old HCV patients. NAC usage (≥28 cumulative defined daily doses [cDDDs]) was assessed for its association with HCC risk using Cox regression models and propensity score matching. The study comprised 269,647 HCV patients, with detailed NAC dosage characterization and hazard ratios (HRs) for HCC risk. Post-matching, NAC usage emerged as the significant predictor of reduced HCC risk (adjusted HR: 0.39, 95% CI: 0.37-0.41, P<0.0001). Dose-response analysis showed reduced HCC risk with increasing cDDDs of NAC (P<0.0001). Higher daily NAC dosage (≥1 DDD) was associated with significantly lower HCC risk (adjusted HR: 0.33, 95% CI: 0.31-0.36, P<0.0001). The study provides compelling evidence for NAC's potential in reducing HCC risk among HCV patients. Insights into dose-dependent effects and optimal daily intensity thresholds offer valuable directions for future therapeutic strategies and clinical trials targeting HCC burden in HCV-infected individuals.

Indexed as

chronic hepatitis Cdose-response relationshiphepatocellular carcinomaN-Acetylcysteinerisk reduction

Identifiers

PMID39113878
PMCPMC11301300

What Socratic holds

Textmetadata
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 Socratic graph.