Evidence map›Paper›PMID 26140920›Full record

ArticleBMC nephrology2015

Validation of two prediction models of undiagnosed chronic kidney disease in mixed-ancestry South Africans.

Amelie Mogueo, Justin B Echouffo-Tcheugui, Tandi E Matsha, Rajiv T Erasmus, Andre P Kengne

Open access · goldAbstract readValidation Study
In one paragraph

Article in BMC nephrology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 3 pooled it
0.8field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 3 syntheses or guidelines pooled it, 16 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 4 institutions in 3 countries.

Amelie MogueoNon-Communicable Diseases Research Unit, South African Medical Research Council, Cape Town, South Africa. amely.mogueo@yahoo.fr.
Justin B Echouffo-TcheuguiHubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA, USA. echouffotcheugui@yahoo.com.
Tandi E MatshaFaculty of Health and Wellness Science, Cape Peninsula University of Technology, Cape Town, South Africa. tandimatsha@gmail.com.
Rajiv T ErasmusDivision of Chemical Pathology, Faculty of Health Sciences, National Health Laboratory Service (NHLS) and University of Stellenbosch, Cape Town, South Africa. erasmusrajiv@gmail.com.
Andre P KengneNon-Communicable Diseases Research Unit, South African Medical Research Council, Cape Town, South Africa. apkengne@yahoo.com.
Cape Peninsula University of Technology · ZACatholic University of Central Africa · CMEmory University · USGroote Schuur Hospital · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic kidney disease (CKD) is a global challenge. Risk models to predict prevalent undiagnosed CKD have been published. However, none was developed or validated in an African population. We validated the Korean and Thai CKD prediction model in mixed-ancestry South Africans.

methodsDiscrimination and calibration were assessed overall and by major subgroups. CKD was defined as 'estimated glomerular filtration rate (eGFR) <60 ml/min/1.73 m(2)' or 'any nephropathy'. eGFR was based on the 4-variable Modification of Diet in Renal Disease (MDRD) formula.

resultsIn all 902 participants (mean age 55 years) included, 259 (28.7 %) had prevalent undiagnosed CKD. C-statistics were 0.76 (95 % CI: 0.73-0.79) for 'eGFR <60 ml/min/1.73 m(2)' and 0.81 (0.78-0.84) for 'any nephropathy' for the Korean model; corresponding values for the Thai model were 0.80 (0.77-0.83) and 0.77 (0.74-0.81). Discrimination was better in men, older and normal weight individuals. The model underestimated CKD risk by 10 % to 13 % for the Thai and 9 % to 93 % for the Korean model. Intercept adjustment significantly improved the calibration with an expected/observed risk of 'eGFR <60 ml/min/1.73 m(2)' and 'any nephropathy' respectively of 0.98 (0.87-1.10) and 0.97 (0.86-1.09) for the Thai model; but resulted in an underestimation by 24 % with the Korean model. Results were broadly similar for CKD derived from the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula.

conclusionAsian prevalent CKD risk models had acceptable performances in mixed-ancestry South Africans. This highlights the potential importance of using existing models for risk CKD screening in developing countries.

Indexed as

Decision Support TechniquesGlomerular Filtration RateAdultAgedBlack PeopleFemaleHumansKidney DiseasesMaleMiddle AgedPrevalenceRenal Insufficiency, ChronicRisk AssessmentSouth AfricaWhite People

Identifiers

PMID26140920
PMCPMC4491228
OpenAlexW1606951415

What OpenQuestion holds

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LicenceCC BY
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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.