Evidence map›Paper›PMID 38174155›Full record

ArticleJournal of the Endocrine Society2023

Exploration of Metabolomic Markers Associated With Declining Kidney Function in People With Type 2 Diabetes Mellitus.

Justina Krasauskaite, Bryan Conway, Christopher Weir, Zhe Huang, Jackie Price

Open access · goldAbstract read
In one paragraph

Article in Journal of the Endocrine Society, 2023. 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
0.6field-weighted citation impact, top 27% of its field
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, 3 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Justina KrasauskaiteUsher Institute, University of Edinburgh, EH8 9AG, Edinburgh, UK.ORCID https://orcid.org/0000-0002-9583-3480
Bryan ConwayCentre for Cardiovascular Science, The Queen's Medical Research Institute, Edinburgh BioQuarter, University of Edinburgh, EH16 4TJ, Edinburgh, UK.
Christopher WeirUsher Institute, University of Edinburgh, EH8 9AG, Edinburgh, UK.ORCID https://orcid.org/0000-0002-6494-4903
Zhe HuangUsher Institute, University of Edinburgh, EH8 9AG, Edinburgh, UK.ORCID https://orcid.org/0000-0002-4441-0015
Jackie PriceUsher Institute, University of Edinburgh, EH8 9AG, Edinburgh, UK.ORCID https://orcid.org/0000-0003-3251-3970
University of Edinburgh · GBThe Queen's Medical Research Institute · GB

Funding

Medical Research Council G0500877
6 · The paper itself

Abstract

Background: Metabolomics, the study of small molecules in biological systems, can provide valuable insights into kidney dysfunction in people with type 2 diabetes mellitus (T2DM), but prospective studies are scarce. We investigated the association between metabolites and kidney function decline in people with T2DM. Methods: The Edinburgh Type 2 Diabetes Study, a population-based cohort of 1066 men and women aged 60 to 75 years with T2DM. We measured 149 serum metabolites at baseline and investigated individual associations with baseline estimated glomerular filtration rate (eGFR), incident chronic kidney disease [CKD; eGFR <60 mL/min/(1.73 m) Results: At baseline, mean eGFR was 77.5 mL/min/(1.73 m) Conclusion: Our study revealed widespread changes within the metabolomic profile of CKD, particularly in lipoproteins and their lipid compounds. We identified a smaller number of individual metabolites that are specifically associated with kidney function decline. Replication studies are needed to confirm the longitudinal findings and explore if metabolic signals at baseline can predict kidney decline.

Indexed as

chronic kidney diseasemetabolomicstype 2 diabetes

Identifiers

PMID38174155
PMCPMC10763986
OpenAlexW4390098639

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.