Evidence map›Paper›PMID 36385445›Full record

ReviewJournal of internal medicine2023

The complexity of kidney disease and diagnosing it - cystatin C, selective glomerular hypofiltration syndromes and proteome regulation.

Linnea Malmgren, Carl Öberg, Emil den Bakker, Felicia Leion, Joanna Siódmiak, Anna Åkesson, Veronica Lindström, Erik Herou, Alain Dardashti, Liana Xhakollari and 28 more

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of internal medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
10.8field-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.

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

43 citing papers in PubMed, 80 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

38 authors at 16 institutions in 11 countries.

Linnea MalmgrenDepartment of Clinical Sciences Malmö, Clinical and Molecular Osteoporosis Research Unit, Lund University, Malmö, Sweden.ORCID 0000-0003-3296-7083
Carl ÖbergDepartment of Clinical Sciences Lund, Division of Nephrology, Skåne University Hospital, Lund University, Lund, Sweden.ORCID 0000-0002-2471-6914
Emil den BakkerDepartment of Pediatrics, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Felicia LeionDepartment of Clinical Chemistry, Skåne University Hospital, Lund University, Lund, Sweden.
Joanna SiódmiakDepartment of Laboratory Medicine, Faculty of Pharmacy, Ludwik Rydygier Collegium Medicum (Nicolaus Copernicus University in Torun), Bydgoszcz, Poland.ORCID 0000-0002-7374-9122
Anna ÅkessonDivision of Occupational and Environmental Medicine, Lund University, Lund, Sweden.ORCID 0000-0003-0204-7446
Veronica LindströmDepartment of Clinical Chemistry, Skåne University Hospital, Lund University, Lund, Sweden.ORCID 0000-0002-7213-0264
Erik HerouDepartment of Cardiothoracic Surgery, Skåne University Hospital, Lund University, Lund, Sweden.ORCID 0000-0002-8071-0381
Alain DardashtiDepartment of Cardiothoracic Surgery, Skåne University Hospital, Lund University, Lund, Sweden.
Liana XhakollariDepartment of Clinical Sciences, Lund University, Malmö, Sweden.
Gabriel GrubbDepartment of Radiology, Skåne University Hospital, Lund, Sweden.
Helena StrevensDepartment of Clinical Sciences Lund, Department of Obstetrics and Gynaecology, Lund University, Lund, Sweden.
Magnus AbrahamsonDepartment of Clinical Chemistry, Skåne University Hospital, Lund University, Lund, Sweden.ORCID 0000-0001-7793-4571
Johanna Helmersson-KarlqvistDepartment of Medical Sciences, Clinical Chemistry, Uppsala University Hospital, Uppsala, Sweden.ORCID 0000-0002-6095-9163
Martin MagnussonDepartment of Clinical Sciences, Lund University, Malmö, Sweden.ORCID 0000-0002-8049-2142
Jonas BjörkDivision of Occupational and Environmental Medicine, Lund University, Lund, Sweden.ORCID 0000-0003-1883-2000
Ulf NymanDepartment of Translational Medicine, Division of Medical Radiology, University of Lund, Malmö, Sweden.ORCID 0000-0003-2542-5067
Johan ÄrnlövDepartment of Neurobiology, Care Sciences and Society (NVS), Family Medicine and Primary Care Unit, Karolinska Institute, Huddinge, Sweden.ORCID 0000-0002-6933-4637
Peter RidefeltDepartment of Medical Sciences, Clinical Chemistry, Uppsala University Hospital, Uppsala, Sweden.
Torbjörn ÅkerfeldtDepartment of Medical Sciences, Clinical Chemistry, Uppsala University Hospital, Uppsala, Sweden.
Magnus HanssonDepartment of Clinical Chemistry, Karolinska University Hospital, Huddinge, Sweden.
Anna SjöströmDepartment of Clinical Chemistry, Karolinska University Hospital, Huddinge, Sweden.ORCID 0000-0001-6766-2234
Johan MårtenssonDepartment of Physiology and Pharmacology, Section of Anaesthesia and Intensive Care, Karolinska Institute, Stockholm, Sweden.ORCID 0000-0001-8739-7896
Yoshihisa ItohClinical Laboratory, Eiju General Hospital, Life Extension Research Institute, Tokyo, Japan.
David GrubbDepartment of Cardiothoracic Surgery, Skåne University Hospital, Lund University, Lund, Sweden.
Olav TenstadDepartment of Biomedicine, University of Bergen, Bergen, Norway.ORCID 0000-0001-5833-2620
Lars-Olov HanssonDepartment of Clinical Chemistry, Karolinska University Hospital, Huddinge, Sweden.
Isleifur OlafssonDepartment of Clinical Biochemistry, Landspitali - National University Hospital of Iceland, Reykjavik, Iceland.ORCID 0000-0002-3921-5805
Araceli Jarquin CamposFaculty of Medical Sciences, Private University in the Principality of Liechtenstein, Triesen, Liechtenstein.ORCID 0000-0002-0438-4748
Martin RischCentral Laboratory, Cantonal Hospital Graubünden, Chur, Switzerland.ORCID 0000-0003-4587-5639
Lorenz RischFaculty of Medical Sciences, Private University in the Principality of Liechtenstein, Triesen, Liechtenstein.ORCID 0000-0003-2692-6699
Anders LarssonDepartment of Medical Sciences, Clinical Chemistry, Uppsala University Hospital, Uppsala, Sweden.ORCID 0000-0003-3161-0402
Gunnar NordinEqualis AB, Uppsala, Sweden.ORCID 0000-0002-5175-8351
Hans PottelDepartment of Public Health and Primary Care, Katholieke Universiteit Leuven Campus Kulak Kortrijk, Kortrijk, Belgium.ORCID 0000-0003-0074-8919
Anders ChristenssonDepartment of Nephrology, Skåne University Hospital, Lund University, Malmö, Sweden.ORCID 0000-0002-7328-8418
Henrik BjurstenDepartment of Cardiothoracic Surgery, Skåne University Hospital, Lund University, Lund, Sweden.ORCID 0000-0001-5428-7455
Arend BökenkampDepartment of Pediatric Nephrology, Emma Children's Hospital, Amsterdam University Medical Centers, Amsterdam, The Netherlands.ORCID 0000-0002-3492-2252
Anders GrubbDepartment of Clinical Chemistry, Skåne University Hospital, Lund University, Lund, Sweden.ORCID 0000-0002-0125-3662
Lund University · SEUppsala University Hospital · SEKarolinska University Hospital · SEAmsterdam University Medical Centers · NLDalarna University · SEEiju General Hospital · JPEmma Kinderziekenhuis · NLKantonsspital Graubünden · CHKarolinska Institutet · SEKatholieke Hogeschool Vives · BENational University Hospital of Iceland · ISNicolaus Copernicus University · PLPrivate University in the Principality of Liechtenstein · LISkåne University Hospital · SEUniversity of Bergen · NOUniversity of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estimation of kidney function is often part of daily clinical practice, mostly done by using the endogenous glomerular filtration rate (GFR)-markers creatinine or cystatin C. A recommendation to use both markers in parallel in 2010 has resulted in new knowledge concerning the pathophysiology of kidney disorders by the identification of a new set of kidney disorders, selective glomerular hypofiltration syndromes. These syndromes, connected to strong increases in mortality and morbidity, are characterized by a selective reduction in the glomerular filtration of 5-30 kDa molecules, such as cystatin C, compared to the filtration of small molecules <1 kDa dominating the glomerular filtrate, for example water, urea and creatinine. At least two types of such disorders, shrunken or elongated pore syndrome, are possible according to the pore model for glomerular filtration. Selective glomerular hypofiltration syndromes are prevalent in investigated populations, and patients with these syndromes often display normal measured GFR or creatinine-based GFR-estimates. The syndromes are characterized by proteomic changes promoting the development of atherosclerosis, indicating antibodies and specific receptor-blocking substances as possible new treatment modalities. Presently, the KDIGO guidelines for diagnosing kidney disorders do not recommend cystatin C as a general marker of kidney function and will therefore not allow the identification of a considerable number of patients with selective glomerular hypofiltration syndromes. Furthermore, as cystatin C is uninfluenced by muscle mass, diet or variations in tubular secretion and cystatin C-based GFR-estimation equations do not require controversial race or sex terms, it is obvious that cystatin C should be a part of future KDIGO guidelines.

Indexed as

Cystatin CKidney DiseasesBiomarkersCreatinineGlomerular Filtration RateHumansProteomeProteomicsBiomarkersCreatinineCystatin CProteomekidney diseaseproteomics

Identifiers

PMID36385445
PMCPMC10107454
OpenAlexW4309176374

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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 OpenQuestion graph.