Evidence map›Paper›PMID 42039941›Full record

ArticleHealth care science2026

Refining Osteoarthritis Risk Prediction: Average Sagittal Abdominal Diameter Complements and Enhances Body Mass Index With Sex-Specific Insights From National Health and Nutrition Examination Survey.

Yuwei Zhang, Xiaoshuai Wang, Hu Zhu, Haowei Chen, Zhaohua Zhu, Liangbin Zhou, Michael Tim Yun Ong, Dongquan Shi, Xin Zhang, David J Hunter and 3 more

Abstract read
In one paragraph

Article in Health care science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Yuwei ZhangDepartment of Biomedical Engineering The Chinese University of Hong Kong Hong Kong China.ORCID https://orcid.org/0000-0003-2909-3397
Xiaoshuai WangDepartment of Biomedical Engineering The Chinese University of Hong Kong Hong Kong China.ORCID https://orcid.org/0000-0002-3895-1384
Hu ZhuDepartment of Computing The Hong Kong Polytechnic University Hong Kong China.ORCID https://orcid.org/0000-0003-3848-0110
Haowei ChenClinical Research Centre Zhujiang Hospital, Southern Medical University Guangzhou China.ORCID https://orcid.org/0000-0003-1466-5348
Zhaohua ZhuClinical Research Centre Zhujiang Hospital, Southern Medical University Guangzhou China.ORCID https://orcid.org/0000-0003-3913-2564
Liangbin ZhouDepartment of Biomedical Engineering The Chinese University of Hong Kong Hong Kong China.ORCID https://orcid.org/0000-0003-4153-4984
Michael Tim Yun OngDepartment of Orthopaedics and Traumatology Prince of Wales Hospital Hong Kong China.ORCID https://orcid.org/0000-0002-4460-9286
Dongquan ShiDepartment of Orthopedic Surgery Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School Nanjing China.ORCID https://orcid.org/0000-0002-4769-7816
Xin ZhangBeijing Key Laboratory of Sports Injuries Peking University Third Hospital Beijing China.ORCID https://orcid.org/0009-0000-6975-4730
David J HunterFaculty of Medicine and Health The University of Sydney Sydney Australia.ORCID https://orcid.org/0000-0003-3197-752X
Changhai DingClinical Research Centre Zhujiang Hospital, Southern Medical University Guangzhou China.ORCID https://orcid.org/0000-0002-9479-730X
Rocky S TuanDepartment of Biomedical Engineering The Chinese University of Hong Kong Hong Kong China.ORCID https://orcid.org/0000-0001-6067-6705
Zhong Alan LiDepartment of Biomedical Engineering The Chinese University of Hong Kong Hong Kong China.ORCID https://orcid.org/0000-0002-6009-629X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Osteoarthritis (OA), the most prevalent joint disease and a leading cause of disability globally, has its disease burden inadequately captured by body mass index (BMI). As the sole quantified risk factor in current Global Burden of Disease estimates, BMI accounted for only 20% of OA burden. A critical limitation of BMI is its inability to distinguish fat distribution patterns, particularly abdominal adiposity, which is increasingly recognized as a key driver of metabolic and musculoskeletal pathologies. Herein, we hypothesize that anthropometric indicators reflecting central adiposity, such as average sagittal abdominal diameter (ASAD), may outperform BMI in predicting OA risk, especially when considering sex and age differences. Methods: This cross-sectional study analyzed 27,791 National Health and Nutrition Examination Survey participants (1999-2023) with complete OA diagnosis, anthropometric, and metabolic data. Participants were stratified by sex and age (40-year cutoff). Multivariable logistic regression, adjusted for confounders, estimated predictor-OA associations via standardized odds ratios (sORs), and these associations were evaluated by the area under the receiver operating characteristic curve (AUROC). Data were split into training (70%) and validation (30%) sets, with DeLong's test comparing different predictors against BMI. Results: In the overall population, ASAD showed a stronger association with OA (sOR = 1.483) than BMI (sOR = 1.436), with comparable validation AUROC (ASAD: 0.857; BMI: 0.854). Sex-stratified analysis revealed that BMI was the optimal predictor for males (sOR = 1.466; validation AUROC = 0.844), while ASAD outperformed BMI in females (sOR = 1.486 vs. 1.450; validation AUROC = 0.865 vs. 0.863). Further age stratification revealed that in males under 40, both BMI (sOR = 1.261; validation AUROC = 0.750) and ASAD (sOR = 1.194; validation AUROC = 0.889) were the strongest predictors, and that ASAD (sOR = 1.490; validation AUROC = 0.769) and BMI (sOR = 1.482; validation AUROC = 0.736) remained strong for males aged 40 and above. In age-stratified analyses of females, ASAD showed the strongest consistent association with OA risk, both in participants under 40 (sOR = 1.472; validation AUROC = 0.801) and those aged 40 and above (sOR = 1.421; validation AUROC = 0.764). Conclusions: ASAD emerges as a superior predictor for females and a competitive population-level complement to BMI. BMI remains an optimal OA predictor for males. Within the National Health and Nutrition Examination Survey framework, these findings underscore the necessity of integrating abdominal adiposity metrics, particularly ASAD, into OA risk assessment to improve sex-specific prevention strategies.

Indexed as

anthropometric predictoraverage sagittal abdominal diameterbody mass indexNHANESosteoarthritissex differences

Identifiers

PMID42039941
PMCPMC13109838

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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.