Evidence map›Paper›PMID 38825605›Full record

ArticleScientific reports2024

Constructing and validating a predictive nomogram for osteoporosis risk among Chinese single-center male population using the systemic immune-inflammation index.

Hang Zhuo, Zelin Zhou, Xingda Chen, Zefeng Song, Qi Shang, Hongwei Huang, Yun Xiao, Xiaowen Wang, Honglin Chen, Xianwei Yan and 8 more

Abstract readValidation Study
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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

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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

18 authors.

Hang Zhuo *The First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Zelin Zhou *The First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Xingda Chen *The First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Zefeng SongMedical Department, Dalian University of Technology, Dalian, 116024, China.
Qi ShangThe First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Hongwei HuangThe First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Yun XiaoThe Third Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, Guangdong, China.
Xiaowen WangThe First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Honglin ChenThe First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Xianwei YanThe First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Peng ZhangThe First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Yan GongThe First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Huiwen LiuThe First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Yu LiuThe First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Zixian WuThe First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
De LiangThe First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine, Guangzhou, 510405, China.
Hui RenThe Spine Surgery Department, Second Affiliated Hospital of Guangzhou Medical University, 250 Changgang East Road, Haizhu District, Guangzhou, 510260, Guangdong, China. renhuispine@163.com.
Xiaobing JiangThe Spine Surgery Department, Second Affiliated Hospital of Guangzhou Medical University, 250 Changgang East Road, Haizhu District, Guangzhou, 510260, Guangdong, China. spinedrjxb@sina.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoporosis (OP) is a bone metabolism disease that is associated with inflammatory pathological mechanism. Nonetheless, rare studies have investigated the diagnostic effectiveness of immune-inflammation index in the male population. Therefore, it is interesting to achieve early diagnosis of OP in male population based on the inflammatory makers from blood routine examination. We developed a prediction model based on a training dataset of 826 Chinese male patients through a retrospective study, and the data was collected from January 2022 to May 2023. All participants underwent the dual-energy X-ray absorptiometry (DXEA) and blood routine examination. Inflammatory markers such as systemic immune-inflammation index (SII) and platelet-to-lymphocyte ratio (PLR) was calculated and recorded. We utilized the least absolute shrinkage and selection operator (LASSO) regression model to optimize feature selection. Multivariable logistic regression analysis was applied to construct a predicting model incorporating the feature selected in the LASSO model. This predictive model was displayed as a nomogram. Receiver operating characteristic (ROC) curve, C-index, calibration curve, and clinical decision curve analysis (DCA) to evaluate model performance. Internal validation was test by the bootstrapping method. This study was approved by the Ethic Committee of the First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine (Ethic No. JY2023012) and conducted in accordance with the relevant guidelines and regulations. The predictive factors included in the prediction model were age, BMI, cardiovascular diseases, cerebrovascular diseases, neuropathy, thyroid diseases, fracture history, SII, PLR, C-reactive protein (CRP). The model displayed well discrimination with a C-index of 0.822 (95% confidence interval: 0.798-0.846) and good calibration. Internal validation showed a high C-index value of 0.805. Decision curve analysis (DCA) showed that when the threshold probability was between 3 and 76%, the nomogram had a good clinical value. This nomogram can effectively predict the incidence of OP in male population based on SII and PLR, which would help clinicians rapidly and conveniently diagnose OP with men in the future.

Indexed as

InflammationNomogramsOsteoporosisAbsorptiometry, PhotonAdultAgedBiomarkersChinaHumansMaleMiddle AgedRetrospective StudiesRisk AssessmentRisk FactorsROC CurveBiomarkersMaleNomogramOsteoporosisValidation

Identifiers

PMID38825605
PMCPMC11144694

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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.