Evidence map›Paper›PMID 26936907›Full record

ArticleBMJ open2016

Proteomic prediction and Renin angiotensin aldosterone system Inhibition prevention Of early diabetic nephRopathy in TYpe 2 diabetic patients with normoalbuminuria (PRIORITY): essential study design and rationale of a randomised clinical multicentre trial.

Morten Lindhardt, Frederik Persson, Gemma Currie, Claudia Pontillo, Joachim Beige, Christian Delles, Heiko von der Leyen, Harald Mischak, Gerjan Navis, Marina Noutsou and 5 more

Registry-linked trialOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02040441 (Proteomic Prediction and Renin Angiotensin Aldosterone System Inhibition Prevention Of Early Diabetic nephRopathy In TYpe 2 Diabetic Patients With Normoalbuminuria), which is not on this map. Cited by 54 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 2 pooled it
17.2field-weighted citation impact, top 1% 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.

NCT02040441 phase2 / phase3completednot on this map

Proteomic Prediction and Renin Angiotensin Aldosterone System Inhibition Prevention Of Early Diabetic nephRopathy In TYpe 2 Diabetic Patients With Normoalbuminuria

TypeinterventionalSponsorPeter RossingRan2014 to 2018Enrolled1,777ConditionsDiabetic Nephropathy, Diabetic RetinopathyArmsSpironolactone, Placebo, Standard care
3 · Its place in the literature

Who cites it

54 citing papers in PubMed, 2 syntheses or guidelines pooled it, 122 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. A Five-Plasma Protein-Based Algorithm for Predicting Incident CKD in Type 2 Diabetes.Journal of the American Society of Nephrology : JASN · 2026
    Article
  5. Review
  6. Review
  7. Article
  8. CKD Urine Metabolomics: Modern Concepts and Approaches.Pathophysiology : the official journal of the International Society for Pathophysiology · 2023
    Review
  9. Novel biomarkers for diabetic kidney disease.Kidney research and clinical practice · 2022
    Article
  10. Precision Nephrology in Patients with Diabetes and Chronic Kidney Disease.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Is there a role for proteomics in diabetic renal disease?Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2020
    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

15 authors at 11 institutions in 8 countries.

Morten LindhardtSteno Diabetes Center, Gentofte, Denmark.
Frederik PerssonSteno Diabetes Center, Gentofte, Denmark.ORCID http://orcid.org/0000-0001-6242-6638
Gemma CurrieInstitute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
Claudia PontilloMosaiques Diagnostics, Hannover, Germany.
Joachim BeigeKlinikum St. Georg, Nephrology and KfH Renal Unit, Leipzig, Germany Martin-Luther-University Halle, Wittenberg, Germany.
Christian DellesInstitute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
Heiko von der LeyenHannover Clinical Trial Center, Hannover, Germany.
Harald MischakMosaiques Diagnostics, Hannover, Germany.
Gerjan NavisDivision of Nephrology, Department of Internal Medicine, University Medical Center Groningen, Groningen, The Netherlands.
Marina NoutsouDiabetes Center, Geniko Nosokomeio Athinas Ippokrateio, Athens, Greece.
Alberto OrtizInstituto de Investigacion Sanitaria de la Fundacion Jimenez D¡az (IIS-FJD UAM), Madrid, Spain.
Piero Luigi RuggenentiIstituto di Richerche Farmacologiche Mario Negri, Bergamo, Italy.
Ivan Rychlik2nd Department of Medicine, 3rd Faculty of Medicine, Universita Karlova v Praze, Prague, Czech Republic.
Goce SpasovskiDepartment of Nephrology, Cyril and Methodius University in Skopje, Skopje, Former Yugoslav Republic of Macedonia.
Peter RossingSteno Diabetes Center, Gentofte, Denmark The Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark.
Mosaiques Diagnostics and Therapeutics (Germany) · DESteno Diabetes Centers · DKUniversity of Glasgow · GBHannover Clinical Trial Center (Germany) · DEHospital Universitario Fundación Jiménez Díaz · ESKlinikum St. Georg · DEMario Negri Institute for Pharmacological Research · ITPrague University of Economics and Business · CZSs. Cyril and Methodius University in Skopje · MKUniversity Medical Center Groningen · NLUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDiabetes mellitus affects 9% of the European population and accounts for 15% of healthcare expenditure, in particular, due to excess costs related to complications. Clinical trials aiming for earlier prevention of diabetic nephropathy by renin angiotensin system blocking treatment in normoalbumuric patients have given mixed results. This might reflect that the large fraction of normoalbuminuric patients are not at risk of progression, thereby reducing power in previous studies. A specific risk classifier based on urinary proteomics (chronic kidney disease (CKD)273) has been shown to identify normoalbuminuric diabetic patients who later progressed to overt kidney disease, and may hold the potential for selection of high-risk patients for early intervention. Combining the ability of CKD273 to identify patients at highest risk of progression with prescription of preventive aldosterone blockade only to this high-risk population will increase power. We aim to confirm performance of CKD273 in a prospective multicentre clinical trial and test the ability of spironolactone to delay progression of early diabetic nephropathy. METHODS AND ANALYSIS: Investigator-initiated, prospective multicentre clinical trial, with randomised double-masked placebo-controlled intervention and a prospective observational study. We aim to include 3280 type 2 diabetic participants with normoalbuminuria. The CKD273 classifier will be assessed in all participants. Participants with high-risk pattern are randomised to treatment with spironolactone 25 mg once daily, or placebo, whereas, those with low-risk pattern will be observed without intervention other than standard of care. Treatment or observational period is 3 years.The primary endpoint is development of confirmed microalbuminuria in 2 of 3 first morning voids urine samples. ETHICS AND DISSEMINATION: The study will be conducted under International Conference on Harmonisation - Good clinical practice (ICH-GCP) requirements, ethical principles of Declaration of Helsinki and national laws. This first new biomarker-directed intervention trial aiming at primary prevention of diabetic nephropathy may pave the way for personalised medicine approaches in treatment of diabetes complications. TRIAL REGISTRATION NUMBER: NCT02040441; Pre-results.

Indexed as

BiomarkersDiabetes Mellitus, Type 2Diabetic NephropathiesProteomicsRenin-Angiotensin SystemResearch DesignAdolescentAdultAgedDisease ProgressionDouble-Blind MethodEuropeFemaleHumansMaleMiddle AgedBiomarkers

Identifiers

PMID26936907
PMCPMC4785328
OpenAlexW2289876298

What OpenQuestion holds

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Registered trials

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.