Evidence map›Paper›PMID 40077644›Full record

ArticleNutrients2025

Assessment of Vitamin D Metabolism Disorders in Hemodialysis Patients.

Maksymilian Hryciuk, Zbigniew Heleniak, Sylwia Małgorzewicz, Konrad Kowalski, Jędrzej Antosiewicz, Anna Koelmer, Michał Żmijewski, Alicja Dębska-Ślizień

Abstract read
In one paragraph

Article in Nutrients, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

8 authors.

Maksymilian HryciukDepartment of Nephrology, Medical University of Gdańsk, Dębinki 7 Street, 80-211 Gdańsk, Poland.ORCID 0009-0001-7937-3859
Zbigniew HeleniakDepartment of Nephrology, Medical University of Gdańsk, Dębinki 7 Street, 80-211 Gdańsk, Poland.ORCID 0000-0002-3284-0149
Sylwia MałgorzewiczDepartment of Nephrology, Medical University of Gdańsk, Dębinki 7 Street, 80-211 Gdańsk, Poland.ORCID 0000-0001-8773-9649
Konrad KowalskiDepartment of Bioenergetics and Exercise Physiology, Medical University of Gdańsk, Dębinki 1 Street, 80-211 Gdańsk, Poland.
Jędrzej AntosiewiczDepartment of Bioenergetics and Exercise Physiology, Medical University of Gdańsk, Dębinki 1 Street, 80-211 Gdańsk, Poland.
Anna KoelmerCentre of Biostatistics and Bioinformatics Analysis, Medical University of Gdańsk, 1a Dębinki, 80-211 Gdańsk, Poland.
Michał ŻmijewskiDepartment of Histology, Medical University of Gdańsk, Dębinki 1 Street, 80-211 Gdańsk, Poland.ORCID 0000-0003-2206-3531
Alicja Dębska-ŚlizieńDepartment of Nephrology, Medical University of Gdańsk, Dębinki 7 Street, 80-211 Gdańsk, Poland.ORCID 0000-0001-8210-8063

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with end-stage chronic diseases, especially those undergoing hemodialysis (HD), often experience mineral bone disease (MBD), leading to hypocalcemia, hyperphosphatemia, and elevated parathyroid hormone (PTH). Vitamin D deficiency and metabolism disorders are also common, resulting from impaired conversion of 25(OH)D3 to its active form, 1,25(OH)2D3, and reduced inactivation to 24,25(OH)2D3. This study aimed to assess the levels of 25(OH)D2, 25(OH)D3, 24,25(OH)2D3, 3-epi-25(OH)D3, and the vitamin D metabolism ratio (VMR) in patients with maintenance HD.

methodsA cross-sectional study was conducted on 66 HD patients (22-90 years, average 61.3 ± 16.4), with a control group of 206 adults without chronic kidney disease (CKD), both without cholecalciferol supplementation.

resultsthe HD patients had significantly lower 25(OH)D3 levels (15 ng/mL vs. 22 ng/mL) and higher deficiency rates (69% vs. 39%) compared to the controls. However, both groups showed similarly low levels of optimal vitamin D3. The HD patients had lower 24,25(OH)D3 levels (0.1 vs. 2.1 ng/mL) and a lower VMR (0.9% vs. 9%). 3-epi-25(OH)D3 levels and its ratio to 25(OH)D3 were significantly lower in the HD group. Alphacalcidol supplementation raised 1,25(OH)2D3 levels (30.4 vs. 16.2 pg/mL) without affecting other vitamin D metabolites. The HD patients had higher levels of 25(OH)D2 compared to the controls (0.61 vs. 0.31 ng/mL).

conclusionsVitamin D3 reserves are lower, and both functional deficiency and impaired catabolism of vitamin D3 are present in HD patients compared to the general population. The VMR index is the most sensitive parameter for vitamin D3 deficiency assessment, highlighting the importance of measuring 24,25(OH)D3. Alphacalcidol supplementation increases 1,25(OH)2D3 levels without affecting other vitamin D metabolites. 25(OH)D2 is the only metabolite that was higher in HD patients than the controls.

Indexed as

Kidney Failure, ChronicRenal DialysisVitamin DVitamin D DeficiencyAdultAgedAged, 80 and overCross-Sectional StudiesFemaleHumansMaleMiddle AgedYoung AdultVitamin D1,25(OH)2D324,25(OH)2D325(OH)D225(OH)D33-epi-25(OH)D3alphacalcidiolchronic kidney diseasehemodialysisvitamin Dvitamin D metabolite ratio

Identifiers

PMID40077644
PMCPMC11901569

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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.