Evidence mapPaperPMID 39225105Full record

Trial reportInternal medicine journal2024

Vitamin D status and intermediate vascular and bone outcomes in chronic kidney disease: a secondary post hoc analysis of IMPROVE-CKD.

Wing-Chi G Yeung, Nigel D Toussaint, Nicole Lioufas, Carmel M Hawley, Elaine M Pascoe, Grahame J Elder, Andrea Valks, Sunil V Badve

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Internal medicine journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Correlation between hyperuricemia and coronary artery calcification.The Journal of international medical research · 2026
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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.

Wing-Chi G YeungDepartment of Nephrology, Wollongong Hospital, Wollongong, New South Wales, Australia.ORCID 0000-0002-3387-3743
Nigel D ToussaintDepartment of Nephrology, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.ORCID 0000-0002-2853-5096
Nicole LioufasDepartment of Nephrology, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.
Carmel M HawleyTranslational Research Institute, Brisbane, Queensland, Australia.
Elaine M PascoeCentre for Health Services Research, The University of Queensland, Brisbane, Queensland, Australia.
Grahame J ElderSchool of Medicine, University of Notre Dame, Sydney, New South Wales, Australia.
Andrea ValksAustralasian Kidney Trials Network, The University of Queensland, Brisbane, Queensland, Australia.
Sunil V BadveRenal and Metabolic Division, The George Institute for Global Health, Sydney, New South Wales, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsCardiovascular disease is the leading cause of death in patients with chronic kidney disease (CKD) and has been associated with abnormalities of mineral metabolism and vascular calcification. Vitamin D influences parathyroid hormone values and calcium and phosphate metabolism, and may play a role in vascular function and bone health. We aimed to test our hypothesis that vitamin D deficiency is associated with arterial stiffness, aortic calcification and lower bone mineral density (BMD) in patients with CKD.

methodsA cross-sectional analysis was performed using baseline data from the IMpact of Phosphate Reduction On Vascular Endpoints in CKD (IMPROVE-CKD) study cohort. Clinical and laboratory parameters were compared between those with and without vitamin D deficiency, defined as 25-hydroxyvitamin D (25(OH)D) <50 nmol/L. Univariable and multivariable linear regression analyses were performed to assess associations between serum 25(OH)D levels and pulse wave velocity (PWV), augmentation index (AIx), abdominal aortic calcification (measured by the Agatston score) and lumbar spine BMD.

resultsBaseline 25(OHD) values were available in 208 out of 278 IMPROVE-CKD study participants, with a mean value of 70.1 ± 30.7 nmol/L. Of these, 57 (27%) patients had vitamin D deficiency. Those with 25(OH)D deficiency were more likely to have diabetes (56% vs 38%), cardiovascular disease (54% vs 36%) and lower serum calcium (2.29 ± 0.13 vs 2.34 ± 0.13 mmol/L). On univariable and multivariable regression analyses, baseline 25(OH)D values were not associated with PWV, the AIx, Agatston score or BMD.

conclusionBaseline 25(OH)D levels were not associated with intermediate markers of vascular function and BMD in patients with CKD stages 3b and 4.

Indexed as

Bone DensityRenal Insufficiency, ChronicVascular CalcificationVascular StiffnessVitamin DVitamin D DeficiencyAgedCross-Sectional StudiesFemaleHumansMaleMiddle AgedPulse Wave Analysis25-hydroxyvitamin DVitamin Darterial stiffnessbone mineral densityCKD‐MBDvascular calcificationvitamin D

Identifiers

PMID39225105
PMCPMC11610653

What Socratic holds

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Registered trials

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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 Socratic graph.