Evidence map›Paper›PMID 42433502›Full record

ArticleEuropean journal of radiology open2026

Renal cortical T1 times at 1.5 T: exploratory reference estimates from a real-world cohort with preserved renal function.

L Lunzer, K Mascherbauer, C Kronberger, C Dona, C Nitsche, M Koschutnik, M Poledniczek, L Schmid, A Geppert, D Beitzke and 3 more

Abstract read
In one paragraph

Article in European journal of radiology open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

L LunzerMedical Department, Division of Cardiology, Medical University of Vienna, Austria.
K MascherbauerMedical Department, Division of Cardiology, Medical University of Vienna, Austria.
C KronbergerMedical Department, Division of Cardiology, Medical University of Vienna, Austria.
C DonaMedical Department, Division of Cardiology, Medical University of Vienna, Austria.
C NitscheMedical Department, Division of Cardiology, Medical University of Vienna, Austria.
M KoschutnikMedical Department, Division of Cardiology, Medical University of Vienna, Austria.
M PoledniczekMedical Department, Division of Cardiology, Medical University of Vienna, Austria.
L SchmidMedical Department, Division of Cardiology, Medical University of Vienna, Austria.
A GeppertMedical Department, Division of Cardiology and Intensive Care Medicine, Klinik Ottakring, Vienna, Austria.
D BeitzkeDivision of Cardiovascular and Interventional Radiology, Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
C LoeweDivision of Cardiovascular and Interventional Radiology, Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
C HengstenbergMedical Department, Division of Cardiology, Medical University of Vienna, Austria.
A KammerlanderMedical Department, Division of Cardiology, Medical University of Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Early detection of renal tissue alterations remains challenging, as laboratory markers often remain within the normal range until advanced stages of disease. T1 mapping offers a non-invasive approach to assess tissue composition, but data on typical renal cortical T1 times in real-world clinical populations at 1.5 T are limited. Aim: To define exploratory real-world reference estimates for renal cortical T1 times and to assess their association with demographic and laboratory parameters in individuals with preserved renal function. Methods: This retrospective study included patients undergoing clinical cardiac magnetic resonance (CMR) at 1.5 T in whom the kidneys were visible on native short-axis T1 maps. T1 times were derived from three manually placed regions of interest in the upper, middle, and lower renal cortex and averaged. Associations with sex, age, hemoglobin, and hematocrit were analysed. Results: In a cohort without relevant comorbidities (n = 65), mean renal cortical T1 times were 1054 ± 53 ms (95% CI 1040-1067). Renal cortical T1 times showed no significant difference between women and men (1068 ± 34 ms vs. 1046 ± 60 ms, p = 0.21). No significant differences were observed across age groups (p = 0.34). Renal cortical T1 times were not significantly associated with hemoglobin (r = -0.10, p = 0.45) or hematocrit (r = -0.08, p = 0.54). Conclusion: Renal cortical T1 times derived from routine CMR appear relatively stable across age and sex in individuals with preserved renal function. Opportunistic renal T1 assessment from routine CMR may provide additional, non-invasive information on renal tissue characteristics without extending scan time.

Indexed as

Cardiac magnetic resonancecardiorenal syndromechronic kidney diseasereference rangesrenal T1 times

Identifiers

PMID42433502
PMCPMC13351749

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.