Evidence map›Paper›PMID 40181326›Full record

ArticleBMC public health2025

Developing and validating a nomogram prediction model for osteoporosis risk in the UK biobank: a national prospective cohort.

Xinning Tong, Shuangnan Cui, Huiyong Shen, Xiaoxin Iris Yao

Abstract readValidation Study
In one paragraph

Article in BMC public health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Association of frailty trajectories with osteoporosis and hip fracture in an older female population.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2026
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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

4 authors.

Xinning TongDepartment of Orthopaedics, The Eighth Affiliated Hospital, Sun Yat-Sen University, 3025 Shennan Road, Shenzhen, 518033, China.
Shuangnan CuiDepartment of Orthopaedics, The Eighth Affiliated Hospital, Sun Yat-Sen University, 3025 Shennan Road, Shenzhen, 518033, China.
Huiyong ShenDepartment of Orthopaedics, The Eighth Affiliated Hospital, Sun Yat-Sen University, 3025 Shennan Road, Shenzhen, 518033, China.
Xiaoxin Iris YaoDepartment of Orthopaedics, The Eighth Affiliated Hospital, Sun Yat-Sen University, 3025 Shennan Road, Shenzhen, 518033, China. yaoxx8@mail.sysu.edu.cn.

Funding

Basic and Applied Basic Research Foundation of Guangdong Province 2023A1515110720Guangdong Provincial Clinical Research Center for Orthopedic Diseases 2023B110001National Natural Science Foundation of China 82103909Natural Science Foundation of Guangdong Province, China 2021A1515220132Outstanding Medical Innovation Talent Program of The Eighth Affiliated Hospital of Sun Yat-sen University YXYXCXRC202101Shenzhen Science and Technology Innovation Program JCYJ20220530144403007
6 · The paper itself

Abstract

backgroundOsteoporosis is a prevalent bone disease that increases frailty. Developing a nomogram prediction model to predict osteoporosis risk at multiple time points using bone mineral densities, behavioral habits, and clinical risk factors would be essential to identify individual risk and guide prevention.

methodsThe study population from the UK Biobank was followed from 2014 to December 31st, 2022. The study outcome was identified as the first occurrence of osteoporosis in the UK Biobank during the follow-up period. After rebalancing with the synthetic minority over-sampling technique, a nomogram prediction model was developed using a LASSO Cox regression. Model discrimination between different risk levels was visualised with Kaplan-Meier curves, and model performance was evaluated with integrated c-index, time-dependent AUC, calibration curves and decision curve analysis (DCA).

resultsThe model identified several risk factors for osteoporosis, including higher age, underweight, and various clinical risk factors (such as menopause, lower hand grip strength, lower bone mineral density, fracture history within 5 years, and a history of chronic disease including hypercholesterolemia, cardiovascular disease, bone disease, arthritis, and cancer). Kaplan-Meier curves showed that risk levels predicted by the nomogram model were significantly distinct. The c-indexes were 0.844 and 0.823 for training and validation datasets, respectively. Time-dependent AUC, calibration curves and DCA indicated good discrimination, model fit and clinical utility, respectively.

conclusionsThe nomogram model could properly quantify the five-year risk of osteoporosis and identify high-risk individuals. This might effectively reduce the burden of osteoporosis on the population.

Indexed as

NomogramsOsteoporosisAdultAgedBiological Specimen BanksBone DensityFemaleHumansMaleMiddle AgedProspective StudiesRisk AssessmentRisk FactorsUK BiobankUnited KingdomDisease preventionNomogram prediction modelOsteoporosisRisk identification

Identifiers

PMID40181326
PMCPMC11970002

What Socratic holds

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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 Socratic graph.