Evidence map›Paper›PMID 41563361›Full record

ArticleJournal of the American Society of Nephrology : JASN2026

Bone Mineral Density and the Risk of Fracture According to eGFR in Postmenopausal Women.

Minsang Kim, Kyungdo Han, Jin Kyung Kwon, Jae-Ik Oh, Jinsun Lee, Jung Hun Koh, Min Woo Kang, Jeong Min Cho, Semin Cho, Seong Geun Kim and 8 more

Abstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Cassandra's Cortex: The False Reassurance of a Normal T Score in CKD.Journal of the American Society of Nephrology : JASN · 2026
    Article
  2. 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

18 authors.

Minsang KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0002-7209-198
Kyungdo HanDepartment of Statistics and Actuarial Science, Soongsil University, Seoul, Republic of Korea.ORCID 0000-0002-6096-1263
Jin Kyung KwonDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0009-0000-3986-0639
Jae-Ik OhDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0009-0001-7497-1067
Jinsun LeeDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0009-0006-9086-1075
Jung Hun KohDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0001-7373-5487
Min Woo KangDepartment of Internal Medicine, Korea University Guro Hospital, Seoul, Republic of Korea.ORCID 0000-0002-9411-3481
Jeong Min ChoDepartment of Internal Medicine, Chung-Ang University Gwangmyeong Hospital, Gwangmyeong, Republic of Korea.ORCID 0000-0001-7643-994
Semin ChoDepartment of Internal Medicine, Chung-Ang University Gwangmyeong Hospital, Gwangmyeong, Republic of Korea.ORCID 0000-0002-6060-9032
Seong Geun KimDepartment of Internal Medicine, Inje University Sanggye Paik Hospital, Seoul, Republic of Korea.ORCID 0000-0002-8831-9838
Sehyun JungDepartment of Internal Medicine, Gyeongsang National University Hospital, Jinju, Republic of Korea.ORCID 0000-0002-2510-8822
Hyuk HuhDepartment of Internal Medicine, Hallym University Kangnam Sacred Heart Hospital, Seoul, Republic of Korea.
Soojin LeeDepartment of Internal Medicine, Uijeongbu Eulji University Medical Center, Uijeongbu, Republic of Korea.ORCID 0000-0001-5633-3961
Eunjeong KangDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0002-2191-2784
Yaerim KimDepartment of Internal Medicine, Keimyung University School of Medicine, Daegu, Republic of Korea.ORCID 0000-0003-1596-1528
Kwon Wook JooDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0001-9941-7858
Dong Ki KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0002-5195-7852
Sehoon ParkDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.ORCID 0000-0002-4221-2453

Funding

College of Medicine, Seoul National University 800-20190571Ministry of Health and Welfare, Republic of Korea RS-2024-00403375National Research Foundation of Korea RS-2024-00345867
6 · The paper itself

Abstract

key pointsLower bone mineral density was associated with a higher risk of fracture, irrespective of eGFR. At a similar bone mineral density, the fracture risk was higher with lower eGFR, more prominently for hip fractures than for vertebral fractures. The higher risk of fracture associated with lower eGFR was more pronounced in individuals with poor static balance.

backgroundAlthough both lower bone mineral density (BMD) and impaired kidney function are well-established risk factors for fracture, large-scale studies evaluating their effects and interaction on fracture, particularly site-specific fractures including vertebra and hip, are still limited.

methodsThe main study population included female participants aged 66 years who underwent BMD assessment through dual-energy x-ray absorptiometry through the Korean National Screening Program between 2010 and 2016. BMD was categorized as normal, osteopenia, and osteoporosis on the basis of T -score. Kidney function was classified as eGFR ≥60, 45-59, and <45 ml/min per 1.73 m 2 . Primary outcome was any fracture, including vertebral, hip, and other fractures, defined using International Classification of Diseases, Tenth Revision codes. Subgroup analysis was performed by physical performance, including the single-leg stance test.

resultsAmong 551,548 participants included in the main study population, 80,514 developed any fracture over a median follow-up of 8.2 (interquartile range, 6.7-10.0) years. The prevalence of osteoporosis was 36%, and those with lower BMD showed higher eGFR and lower body mass index. Lower BMD was associated with a higher risk of any fracture, irrespective of eGFR, with nonsignificant interaction ( P for interaction = 0.54). Among participants with normal BMD, those with eGFR <45 ml/min per 1.73 m 2 showed a greater risk of hip fracture than those with normal eGFR (adjusted hazard ratio, 2.44 [1.88-3.18]), whereas vertebral fracture risks were similar across different eGFR categories at a given BMD status. Furthermore, a higher fracture risk with lower eGFR was more pronounced in women with poor static balance assessed by the single-leg stance test than in those with normal static balance.

conclusionsIn postmenopausal women, lower BMD was associated with a higher fracture risk, irrespective of eGFR. However, at any given BMD, lower eGFR was associated with a greater risk for hip fracture, but not for vertebral fracture.

Indexed as

Bone DensityFractures, BoneGlomerular Filtration RateOsteoporosis, PostmenopausalOsteoporotic FracturesPostmenopauseAbsorptiometry, PhotonAgedFemaleHip FracturesHumansRisk FactorsSpinal Fracturesbones, stones, and mineral metabolismCKDcohort studiesGFRhealth status

Identifiers

PMID41563361
PMCPMC13143439

What OpenQuestion holds

Textmetadata
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.