Evidence map›Paper›PMID 42310581›Full record

ArticleBMC nephrology2026

Fracture risk prediction using bone mineral density and biochemical markers of bone and mineral metabolism in dialysis and non-dialysis CKD patients.

Jin Woo Choi, Ji Eun Kim

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Article in BMC nephrology, 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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5 · Who and what money

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2 authors.

Jin Woo ChoiDepartment of Internal Medicine, Korea University Guro Hospital, Seoul, Republic of Korea.ORCID http://orcid.org/0009-0000-4251-9351
Ji Eun KimDepartment of Internal Medicine, Korea University Guro Hospital, Seoul, Republic of Korea. beeswaxag@korea.ac.kr.ORCID http://orcid.org/0000-0003-3094-2229

Funding

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6 · The paper itself

Abstract

backgroundBone mineral density (BMD) is a recognized predictor of fracture risk in the general population, but its utility in chronic kidney disease (CKD) remains uncertain. This study evaluated BMD and biochemical markers of bone and mineral metabolism (BMMs)-parathyroid hormone (PTH) and bone-specific alkaline phosphatase (bone ALP)-as fracture predictors in CKD patients, both with and without dialysis.

methodsWe retrospectively analyzed 918 adult patients with CKD who underwent BMD and BMM assessments between 2010 and 2024. Patients were stratified by dialysis status (RRT: n = 514; non-RRT: n = 404); non-RRT patients who initiated RRT during follow-up were censored at the date of RRT initiation. Cox proportional hazards models (Firth correction) and Fine-Gray competing-risk models were applied, with adjustment for age, sex, BMI, and diabetes mellitus. Time-dependent receiver operating characteristic (ROC) curves were used to compare predictive performance for 5-year fracture risk.

resultsOver a median follow-up of 1,694 days (IQR 751-2,314), 83 fracture events occurred. Fracture risk did not significantly differ across tertiles of PTH or bone ALP in either group. In contrast, BMD was significantly associated with fracture risk in both groups: patients with osteoporosis (T-score ≤ - 2.5) had directionally elevated fracture risk in both groups, although the extremely wide confidence intervals around the categorical hazard ratios preclude precise interpretation of effect magnitude. More stable estimates from Fine-Gray competing-risk models showed that each one-unit increase in BMD T-score was associated with an approximately 45% lower fracture risk in both groups (RRT: SHR 0.54, 95% CI 0.38-0.75; non-RRT: SHR 0.57, 95% CI 0.41-0.79). Time-dependent ROC analysis confirmed BMD significantly outperformed BMMs for 5-year fracture risk prediction, with AUCs of 0.712 (RRT) and 0.658 (non-RRT).

conclusionBMD was strongly associated with fracture risk in CKD patients, regardless of dialysis status, and significantly outperformed BMMs in predicting fracture risk. In contrast, BMMs were not associated with fracture risk. These results support the role of BMD assessment in fracture risk evaluation across the full spectrum of CKD.

Indexed as

Alkaline PhosphataseBone and BonesBone DensityFractures, BoneRenal DialysisRenal Insufficiency, ChronicAgedBiomarkersFemaleHumansMaleMiddle AgedParathyroid HormoneRetrospective StudiesRisk AssessmentRisk FactorsAlkaline PhosphataseBiomarkersParathyroid HormoneBone ALPBone mineral densityChronic kidney disease-mineral bone disorderDialysisFracture riskParathyroid hormone

Identifiers

PMID42310581
PMCPMC13523207

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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.