Evidence map›Paper›PMID 42387458›Full record

ArticleBMC nephrology2026

Fracture risk assessment in early-stage autosomal dominant polycystic kidney disease: a cross-sectional study using FRAX

Helena Kamieniecka, Per Magnusson, Mathias Haarhaus, Magdalena Dzitkowska-Zabielska, Izabella Kuźmiuk-Glembin, Alicja Dębska-Ślizień, Djalila Mekahli, Magdalena Jankowska

Abstract read
In one paragraph

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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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

The trial behind it

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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.

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4 · The record

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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

8 authors.

Helena KamienieckaFaculty of Medicine, Medical University of Gdańsk, Gdańsk, Poland.ORCID http://orcid.org/0009-0003-3216-5969
Per MagnussonDepartment of Clinical Chemistry, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.ORCID http://orcid.org/0000-0002-2123-7838
Mathias HaarhausDivision of Renal Medicine, Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0001-8274-6356
Magdalena Dzitkowska-ZabielskaFaculty of Physical Education, Gdansk University of Physical Education and Sport, Gdańsk, Poland.ORCID http://orcid.org/0000-0002-7375-9814
Izabella Kuźmiuk-GlembinDepartment of Nephrology, Transplantology and Internal Medicine, Medical University of Gdańsk, M. Sklodowskiej-Curie 3a, Gdańsk, 80-210, Poland.ORCID http://orcid.org/0000-0002-0625-148X
Alicja Dębska-ŚlizieńDepartment of Nephrology, Transplantology and Internal Medicine, Medical University of Gdańsk, M. Sklodowskiej-Curie 3a, Gdańsk, 80-210, Poland.ORCID http://orcid.org/0000-0001-8210-8063
Djalila MekahliPKD Research Group, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0003-0954-6088
Magdalena JankowskaDepartment of Nephrology, Transplantology and Internal Medicine, Medical University of Gdańsk, M. Sklodowskiej-Curie 3a, Gdańsk, 80-210, Poland. magdalena.jankowska@gumed.edu.pl.ORCID http://orcid.org/0000-0002-2432-6350

Funding

National Science Centre, Kraków, Poland No. 2018/30/M/NZ5/00480Research Foundation Flanders (FWO) G0C8920N, G060623N
6 · The paper itself

Abstract

backgroundCompared with individuals with other chronic kidney disease (CKD), individuals with autosomal dominant polycystic kidney disease (ADPKD) may face increased fracture risk. This study provides the first clinical evaluation of fracture risk prediction in early-stage ADPKD using the FRAX

methodsIn this cross-sectional study, adult ADPKD patients with preserved kidney function were screened for fracture risk. Due to age eligibility criteria and data availability, fracture risk estimates could be calculated in 67 individuals using QFracture

resultsAll evaluated calculators were broadly in agreement at the group level, and the median fracture risk values for major osteoporotic and hip fractures remained consistently low. In our cohort, QFracture

conclusionsThis is the first study to explore the use of online fracture risk calculators in an early-stage ADPKD population. Although fracture risk calculators offer a practical and cost-effective approach for estimating fracture risk, their use in ADPKD requires cautious interpretation. Our findings indicate that age significantly influences the predicted risk, whereas neither the eGFR nor HtTKV, despite their relevance to kidney disease progression, were associated with any of the evaluated models. Future research should aim to refine fracture risk models by incorporating disease-specific variables and validating them in larger, prospective ADPKD cohorts.

Indexed as

Fractures, BonePolycystic Kidney, Autosomal DominantAbsorptiometry, PhotonAdultBone DensityCross-Sectional StudiesFemaleHumansMaleMiddle AgedRisk AssessmentAutosomal dominant polycystic kidney disease (ADPKD)Bone mineral density (BMD)Chronic kidney disease (CKD)Fracture risk assessmentFRAX®QFracture®

Identifiers

PMID42387458
PMCPMC13595751

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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.