Evidence map›Paper›PMID 41133261›Full record

ArticleJournal of multidisciplinary healthcare2025

A Nomogram Combining Platelet to Lymphocyte Ratio (PLR) and Systemic Inflammatory Response Index (SIRI) to Predict Patients with

Jing-Wen Fang, Qiang She, Jian-Lei Xia, Yuan-Yuan Chen, Zhuo-Qi Liu, Yue Yu, Xin-Yu Fu, Xin Jiang, Yao-Yao Li, Min Zhang and 1 more

Abstract read
In one paragraph

Article in Journal of multidisciplinary healthcare, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Jing-Wen Fang *Department of Gastroenterology, The Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu Province, 225000, People's Republic of China.
Qiang She *Department of Gastroenterology, The Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu Province, 225000, People's Republic of China.ORCID 0000-0001-8861-2674
Jian-Lei XiaDepartment of Gastroenterology, The Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu Province, 225000, People's Republic of China.ORCID 0000-0003-4370-0667
Yuan-Yuan ChenDepartment of Gastroenterology, The Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu Province, 225000, People's Republic of China.
Zhuo-Qi LiuDepartment of Gastroenterology, The Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu Province, 225000, People's Republic of China.
Yue YuDepartment of Gastroenterology, The Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu Province, 225000, People's Republic of China.
Xin-Yu FuDepartment of Gastroenterology, The Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu Province, 225000, People's Republic of China.
Xin JiangDepartment of Gastroenterology, The Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu Province, 225000, People's Republic of China.
Yao-Yao LiDepartment of Gastroenterology, The Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu Province, 225000, People's Republic of China.
Min ZhangDepartment of Gastroenterology, The Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu Province, 225000, People's Republic of China.
Yan-Bing DingDepartment of Gastroenterology, The Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu Province, 225000, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Patients with Helicobacter pylori-positive gastric dysplasia are at a higher risk of progressing to gastric cancer (GC). Systemic inflammatory markers have been identified as predictors of poor prognosis in patients with GC. However, their role in gastric dysplasia remains elusive. The aim of this study is to evaluate the utility of systemic inflammatory markers as predictors in patients with Methods: This study included a total of 664 normal individuals and patients diagnosed with chronic gastritis from the Yangzhou screening cohort, as well as 135 patients with gastric dysplasia from the Affiliated Hospital of Yangzhou University, spanning the period from January 2017 to May 2024. The participants were randomly assigned to either a training group or a validation group in a ratio of 7:3. SPSS software was utilized to determine the optimal critical values for PLR and SIRI. Subsequently, univariate and multivariate regression analyses were conducted to assess the diagnostic utility of PLR and SIRI. A nomogram was developed to estimate the risk associated with gastric dysplasia. To evaluate model performance, receiver operating characteristic curves (ROC), calibration curves, decision curve analysis (DCA) and the Clinical Impact Curve (CIC) were generated. Results: Eight independent risk factors, including the PLR and SIRI, were identified with a significance level of Conclusion: PLR and SIRI are independent variables that influence the diagnosis of patients with gastric dysplasia. The nomogram model created using PLR and SIRI demonstrates a high predictive value for diagnosing individuals with gastric dysplasia.

Indexed as

gastric dysplasianomogramPLRSIRIsystemic inflammation markers

Identifiers

PMID41133261
PMCPMC12542855

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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.