Evidence map›Paper›PMID 30288572›Full record

ArticleDiabetologia2019

Serum kidney injury molecule 1 and β

Marco Colombo, Helen C Looker, Bassam Farran, Sibylle Hess, Leif Groop, Colin N A Palmer, Mary Julia Brosnan, R Neil Dalton, Max Wong, Charles Turner and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Diabetologia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Novel biomarkers for diabetic kidney disease.Kidney research and clinical practice · 2022
    Article
  19. Review
  20. Associations of Plasma Biomarkers of Inflammation, Fibrosis, and Kidney Tubular Injury With Progression of Diabetic Kidney Disease: A Cohort Study.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2022
    Article
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

19 authors at 10 institutions in 4 countries.

Marco ColomboUsher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK.
Helen C LookerPopulation Health Sciences, University of Dundee, Dundee, UK.
Bassam FarranMRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road South, Edinburgh, EH4 2XU, UK.
Sibylle HessSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Leif GroopLund University Diabetes Centre, Lund University, Malmö, Sweden.
Colin N A PalmerNinewells Hospital and Medical School, University of Dundee, Dundee, UK.
Mary Julia BrosnanPfizer Inc, Cambridge, MA, USA.
R Neil DaltonEvelina London Children's Hospital, Guy's & St Thomas NHS Foundation Trust, London, UK.
Max WongEvelina London Children's Hospital, Guy's & St Thomas NHS Foundation Trust, London, UK.
Charles TurnerEvelina London Children's Hospital, Guy's & St Thomas NHS Foundation Trust, London, UK.
Emma AhlqvistLund University Diabetes Centre, Lund University, Malmö, Sweden.
David DungerDepartment of Paediatrics, Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge, Cambridge, UK.
Felix AgakovPharmatics Limited, Edinburgh, UK.
Paul DurringtonDivision of Cardiovascular Sciences, University of Manchester, Manchester, UK.
Shona LivingstonePopulation Health Sciences, University of Dundee, Dundee, UK.
John BetteridgeDepartment of Endocrinology and Diabetes, University College London Hospitals, London, UK.
Paul M McKeigueUsher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK.
Helen M ColhounMRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road South, Edinburgh, EH4 2XU, UK. helen.colhoun@igmm.ed.ac.uk.
SUMMIT Investigators
University of Dundee · GBLund University · SEGuy's and St Thomas' NHS Foundation Trust · GBWestern General Hospital · GBNHS Fife · GBPfizer (United States) · USRoyal London Hospital · GBUniversity of Cambridge · GBUniversity of Edinburgh · GBUniversity of Manchester · GB

Funding

Chief Scientist Office ETM/47Department of Health
6 · The paper itself

Abstract

aims/hypothesisAs part of the Surrogate Markers for Micro- and Macrovascular Hard Endpoints for Innovative Diabetes Tools (SUMMIT) programme we previously reported that large panels of biomarkers derived from three analytical platforms maximised prediction of progression of renal decline in type 2 diabetes. Here, we hypothesised that smaller (n ≤ 5), platform-specific combinations of biomarkers selected from these larger panels might achieve similar prediction performance when tested in three additional type 2 diabetes cohorts.

methodsWe used 657 serum samples, held under differing storage conditions, from the Scania Diabetes Registry (SDR) and Genetics of Diabetes Audit and Research Tayside (GoDARTS), and a further 183 nested case-control sample set from the Collaborative Atorvastatin in Diabetes Study (CARDS). We analysed 42 biomarkers measured on the SDR and GoDARTS samples by a variety of methods including standard ELISA, multiplexed ELISA (Luminex) and mass spectrometry. The subset of 21 Luminex biomarkers was also measured on the CARDS samples. We used the event definition of loss of >20% of baseline eGFR during follow-up from a baseline eGFR of 30-75 ml min

resultsTwelve biomarkers showed significant association with eGFR decline adjusted for covariates in one or more of the sample sets when evaluated singly. Kidney injury molecule 1 (KIM-1) and β CONCLUSIONS/

interpretationSerum KIM-1 and B2M independently improve prediction of renal decline from an eGFR of 30-75 ml min

Indexed as

Agedbeta 2-MicroglobulinBiomarkersDiabetes Mellitus, Type 2Diabetic NephropathiesDisease ProgressionEnzyme-Linked Immunosorbent AssayFemaleGlomerular Filtration RateHepatitis A Virus Cellular Receptor 1HumansKidneyMaleMass SpectrometryMiddle AgedOdds Ratiobeta 2-MicroglobulinBiomarkersHAVCR1 protein, humanHepatitis A Virus Cellular Receptor 1Clinical scienceEpidemiologyNephropathyProteomics/metabolomics

Identifiers

PMID30288572
PMCPMC6290680
OpenAlexW2895638174

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.