Evidence map›Paper›PMID 41042780›Full record

ArticlePloS one2025

Within-individual variation of HbA1c measurements in primary care: A retrospective cohort study.

Alex Gough, Tom Marshall, Alice Sitch

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Yonder: Social prescribing, asking about drug allergies, commercial primary care pricing, and HbA1c variability.The British journal of general practice : the journal of the Royal College of General Practitioners · 2026
    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

3 authors.

Alex GoughDepartment of Applied Health Sciences, University of Birmingham, Edgbaston Campus, Birmingham, West Midlands, United kingdom.ORCID https://orcid.org/0000-0001-6954-7408
Tom MarshallDepartment of Applied Health Sciences, University of Birmingham, Edgbaston Campus, Birmingham, West Midlands, United kingdom.
Alice SitchDepartment of Applied Health Sciences, University of Birmingham, Edgbaston Campus, Birmingham, West Midlands, United kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHbA1c is a marker for diabetes mellitus that reflects average glucose concentrations over the previous eight to twelve weeks. It is used to aid in the diagnosis and management of diabetes. Variation in within-individual measured HbA1c may affect its clinical utility but estimates of this are based on limited data that is often not generalisable to real-world settings.

methodsA retrospective cohort study was performed using data on HbA1c results and sociodemographic, lifestyle and comorbidity covariates extracted from the IQVIA Medical Research Database (IMRD) database using the DEXTER tool. A minimum of four measurements in the same individual was the only inclusion criterion. Within-individual measured variation was calculated as a coefficient of variation (CV) using a linear regression random effects model for the whole population and various subgroups.

results587,023 participants were included in this study, making it the largest study of variation of HbA1c to date. The overall measured within-individual coefficient of variation (CVT) was 0.20 (95%CI 0.20 to 0.20). This is around three times higher than reported in a previous systematic review. CVT increased with patient mean HbA1c level. STRENGTHS AND LIMITATIONS: The large number of participants and the real-world nature of the results are important strengths of this study. Weaknesses included the problem of accounting for confounding by indication.

conclusionsEstimated within-individual variation in this analysis of real-world data is very high and is higher than previously reported. Variation increases with patient mean HbA1c, that is with more severe disease status. This has important implications for the diagnosis, monitoring and clinical decision-making for diabetes.

Indexed as

Diabetes MellitusGlycated HemoglobinPrimary Health CareAdultAgedBiomarkersFemaleHumansMaleMiddle AgedRetrospective StudiesBiomarkersGlycated Hemoglobinhemoglobin A1c protein, human

Identifiers

PMID41042780
PMCPMC12494249

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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.