Evidence map›Paper›PMID 29057963›Full record

ArticleScientific reports2017

Impact of analytical and biological variations on classification of diabetes using fasting plasma glucose, oral glucose tolerance test and HbA1c.

Jia Hui Chai, Stefan Ma, Derick Heng, Joanne Yoong, Wei-Yen Lim, Sue-Anne Toh, Tze Ping Loh

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Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

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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

7 authors.

Jia Hui ChaiSaw Swee Hock School of Public Health, National University of Singapore, Singapore, Singapore.
Stefan MaEpidemiology & Disease Control Division, Ministry of Health, Singapore, Singapore.
Derick HengPublic Health Group, Ministry of Health, Singapore, Singapore.
Joanne YoongSaw Swee Hock School of Public Health, National University of Singapore, Singapore, Singapore.ORCID 0000-0002-0162-9885
Wei-Yen LimResearch and Development Office, Agency for Integrated Care, Singapore, Singapore.
Sue-Anne TohDepartment of Medicine, National University Hospital, Singapore, Singapore.
Tze Ping LohDepartment Laboratory Medicine, National University Hospital, Singapore, Singapore. tploh@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Historically, diabetes is diagnosed by measuring fasting (FPG) and two-hour post oral glucose load (OGTT) plasma concentration and interpreting it against recommended clinical thresholds of the patient. More recently, glycated haemoglobin A1c (HbA1c) has been included as a diagnostic criterion. Within-individual biological variation (CVi), analytical variation (CVa) and analytical bias of a test can impact on the accuracy and reproducibility of the classification of a disease. A test with large biological and analytical variation increases the likelihood of erroneous classification of the underlying disease state of a patient. Through numerical simulations based on the laboratory results generated from a large population health survey, we examined the impact of CVi, CVa and bias on the classification of diabetes using fasting plasma glucose (FPG), oral glucose tolerance test (OGTT) and HbA1c. From the results of the simulations, HbA1c has comparable performance to FPG and is better than OGTT in classifying subjects with diabetes, particularly when laboratory methods with smaller CVa are used. The use of the average of the results of the repeat laboratory tests has the effect of ameliorating the combined (analytical and biological) variation. The averaged result improves the consistency of the disease classification.

Indexed as

Blood GlucoseGlucose Tolerance TestAdolescentAdultAgedBiological Variation, IndividualComputer SimulationCross-Sectional StudiesDiabetes MellitusDiagnostic ErrorsFastingFemaleGlycated HemoglobinHumansMaleMiddle AgedBlood GlucoseGlycated Hemoglobin

Identifiers

PMID29057963
PMCPMC5651837

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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.