Evidence map›Paper›PMID 39136015›Full record

ArticleFrontiers in immunology2024

Development and validation of a predictive model assessing the risk of sarcopenia in rheumatoid arthritis patients.

Yuan Qu, Lili Zhang, Yuan Liu, Yang Fu, Mengjie Wang, Chuanguo Liu, Xinyu Wang, Yakun Wan, Bing Xu, Qian Zhang and 2 more

Abstract readValidation Study
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
–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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Observational
  11. Article
  12. 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

12 authors.

Yuan Qu *First College of Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.
Lili Zhang *First College of Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.
Yuan Liu *First College of Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.
Yang FuSpinal and Spinal Cord Department, Shandong Wendeng Osteopathic Hospital, Weihai, China.
Mengjie WangFirst College of Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.
Chuanguo LiuExperimental Center, Shandong University of Traditional Chinese Medicine, Jinan, China.
Xinyu WangFirst College of Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.
Yakun WanRehabilitation College, Shandong University of Traditional Chinese Medicine, Jinan, China.
Bing XuDepartment of Rheumatology, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, China.
Qian ZhangScience and Technology Department, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, China.
Yancun LiCollege of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.
Ping JiangFirst College of Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sarcopenia is linked to an unfavorable prognosis in individuals with rheumatoid arthritis (RA). Early identification and treatment of sarcopenia are clinically significant. This study aimed to create and validate a nomogram for predicting sarcopenia risk in RA patients, providing clinicians with a reliable tool for the early identification of high-risk patients. Methods: Patients with RA diagnosed between August 2022 and January 2024 were included and randomized into training and validation sets in a 7:3 ratio. Least Absolute Shrinkage and Selection Operator (LASSO) regression analysis and multifactorial logistic regression analysis were used to screen the risk variables for RA-associated muscle loss and to create an RA sarcopenia risk score. The predictive performance and clinical utility of the risk model were evaluated by plotting the receiver operating characteristic curve and calculating the area under the curve (AUC), along with the calibration curve and clinical decision curve (DCA). Results: A total of 480 patients with RA were included in the study (90% female, with the largest number in the 45-59 age group, about 50%). In this study, four variables (body mass index, disease duration, hemoglobin, and grip strength) were included to construct a nomogram for predicting RA sarcopenia. The training and validation set AUCs were 0.915 (95% CI: 0.8795-0.9498) and 0.907 (95% CI: 0.8552-0.9597), respectively, proving that the predictive model was well discriminated. The calibration curve showed that the predicted values of the model were basically in line with the actual values, demonstrating good calibration. The DCA indicated that almost the entire range of patients with RA can benefit from this novel prediction model, suggesting good clinical utility. Conclusion: This study developed and validated a nomogram prediction model to predict the risk of sarcopenia in RA patients. The model can assist clinicians in enhancing their ability to screen for RA sarcopenia, assess patient prognosis, make early decisions, and improve the quality of life for RA patients.

Indexed as

Arthritis, RheumatoidNomogramsSarcopeniaAdultAgedFemaleHumansMaleMiddle AgedPrognosisReproducibility of ResultsRisk AssessmentRisk FactorsROC Curvediagnosisnomogramrheumatoid arthritisrisk predictionsarcopenia

Identifiers

PMID39136015
PMCPMC11317408

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.