Evidence map›Paper›PMID 41632754›Full record

Trial reportPLoS medicine2026

Mother and child health 4.5 years after gestational diabetes mellitus managed using tight or less tight targets for glycaemic control: Post-hoc follow-up study of the TARGET trial.

Lisa J Douglas, Greg D Gamble, Jane E Harding, Deborah Samuel, Carl L Eagleton, Jane M Alsweiler, Trecia A Wouldes, Benjamin Thompson, Christopher J D McKinlay, Caroline A Crowther

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in PLoS medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Lisa J DouglasLiggins Institute, University of Auckland, Auckland, New Zealand.ORCID https://orcid.org/0000-0003-4973-4948
Greg D GambleLiggins Institute, University of Auckland, Auckland, New Zealand.ORCID https://orcid.org/0000-0003-0412-3203
Jane E HardingLiggins Institute, University of Auckland, Auckland, New Zealand.ORCID https://orcid.org/0000-0003-2697-1422
Deborah SamuelLiggins Institute, University of Auckland, Auckland, New Zealand.ORCID https://orcid.org/0009-0008-2979-7419
Carl L EagletonLiggins Institute, University of Auckland, Auckland, New Zealand.
Jane M AlsweilerDepartment of Paediatrics: Child and Youth Health, University of Auckland, Auckland, New Zealand.ORCID https://orcid.org/0000-0002-0874-6654
Trecia A WouldesPsychological Medicine, University of Auckland, Auckland, New Zealand.ORCID https://orcid.org/0000-0002-6609-8464
Benjamin ThompsonLiggins Institute, University of Auckland, Auckland, New Zealand.ORCID https://orcid.org/0000-0002-3902-2712
Christopher J D McKinlayDepartment of Paediatrics: Child and Youth Health, University of Auckland, Auckland, New Zealand.
Caroline A CrowtherLiggins Institute, University of Auckland, Auckland, New Zealand.ORCID https://orcid.org/0000-0002-9079-4451

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOptimal glycaemic targets for women with gestational diabetes mellitus (GDM) are unclear. The aim of this study was to compare maternal and child health 4.5 years after women with GDM had been randomised to use tight or less tight targets for glycaemic control during their pregnancy. METHODS AND

findingsThe TARGET trial was a stepped-wedge, cluster-randomised trial conducted between May 29, 2015 and November 7, 2017 at 10 hospitals in New Zealand. All hospitals were initially allocated to use less tight glycaemic treatment targets (fasting plasma glucose (FPG) <5.5 mmol/L (<99 mg/dL), 1-hour <8.0 mmol/L (<144 mg/dL), 2 hour postprandial <7.0 mmol/L (<126 mg/dL)) for women with GDM and every 4 months two hospitals were randomised to use tighter targets (FPG ≤ 5.0 mmol/L (≤90 mg/dL), 1-hour ≤7.4 mmol/L (≤133 mg/dL), 2 hour postprandial ≤6.7 mmol/L) (≤121 mg/dL). Women with GDM, blinded to the targets in use, were eligible. The primary outcome was large for gestational age. This is a post-hoc follow-up study of the TARGET randomised trial, conducted from October 2020 to June 2022. We assessed 315/427 (74%) eligible mothers and 313/427 (73%) of their children. Primary outcomes were maternal glycated haemoglobin (HbA1c) and child body mass index (BMI) z-score. Secondary outcomes included maternal cardiometabolic risk, body size, and healthcare utilisation, and for the child, body size, vision, hearing, motor function, and behavioural outcomes. Data were collected from maternal and child health questionnaires, and their health records. Maternal HbA1c results were similar between tight and less tight glycaemic groups (40 mmol/mol standard deviation (SD) 12.6 versus 38 mmol/mol SD 8.8; adjusted mean difference (adjMD) 2.17 (95% confidence interval (CI) [-0.26, 4.60]; P = 0.080)). Child BMI z-scores were similar between groups (mean z-score 0.83 SD 1.72 versus 0.75 SD 1.48; adjMD 0.12 (95% CI [-0.24, 0.48]; P = 0.498)), although children in the tight glycaemic group were taller (107.8 cm SD 5.5 versus 106.0 cm SD 5.5; adjMD 1.83 (95% CI [0.58, 3.08]; P = 0.004)). Worse child outcomes were seen in the tight glycaemic group for coordination difficulties (31/109, 28.4% versus 21/118, 17.8%; adjusted relative risk (adjRR) 1.66 (95% CI [1.01, 2.73]; P = 0.044)), behaviour (likely on the autism spectrum 10/108, 9.3% versus 3/117, 2.6%; adjRR 3.67 (95% CI [1.02, 13.23]; P = 0.047)) and total difficulties scores from the strengths and difficulties questionnaire (mean score 8.4 SD 5.1 versus 6.8 SD 4.5; adjMD 1.75 (95% CI [0.51, 3.00]; P = 0.006)). The main limitation was the use of questionnaires rather than health professional assessments for some of the outcomes.

conclusionsTight compared to less tight glycaemic targets in women with GDM during pregnancy did not result in lower maternal HbA1c or lower child BMI z-scores 4.5 years later, and may be associated with adverse child motor and behavioural outcomes.

Indexed as

Blood GlucoseChild HealthDiabetes, GestationalGlycemic ControlHypoglycemic AgentsAdultChild, PreschoolFemaleFollow-Up StudiesGlycated HemoglobinHumansInfant, NewbornNew ZealandPregnancyTime FactorsBlood GlucoseGlycated HemoglobinHypoglycemic Agents

Identifiers

PMID41632754
PMCPMC12867249

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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.