Evidence map›Paper›PMID 41057689›Full record

Observational studyDiabetologia2025

Acute brain responses to hypoglycaemia and hyperglycaemia in adolescents with type 1 diabetes.

Michele A O'Connell, Richard Beare, Betty Messazos, Elisabeth A Northam, Myles Clarkson Fletcher, Marc L Seal, Fergus J Cameron

Abstract readObservational Study
In one paragraph

Observational study in Diabetologia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Review
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.

Michele A O'ConnellRoyal Children's Hospital Melbourne, Parkville, VIC, Australia. michele.oconnell@rch.org.au.ORCID http://orcid.org/0000-0003-4003-956X
Richard BeareMurdoch Children's Research Institute, Parkville, VIC, Australia.
Betty MessazosRoyal Children's Hospital Melbourne, Parkville, VIC, Australia.
Elisabeth A NorthamMurdoch Children's Research Institute, Parkville, VIC, Australia.
Myles Clarkson FletcherMurdoch Children's Research Institute, Parkville, VIC, Australia.
Marc L SealMurdoch Children's Research Institute, Parkville, VIC, Australia.
Fergus J CameronRoyal Children's Hospital Melbourne, Parkville, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aims/hypothesisThe physiological basis of the well-described neurocognitive decrements and structural brain changes in type 1 diabetes is unclear. We aimed to assess differences in cerebral blood flow (CBF) and neural activity before, during and after induced hypoglycaemia and hyperglycaemia in adolescents with type 1 diabetes.

methodsAn observational hyperinsulinaemic clamp and functional MRI study was conducted. Parallel study arms assessed participants during three consecutive glycaemic phases: baseline euglycaemia (5.0±0.5 mmol/l), either hypoglycaemia (2.6±0.5 mmol/l) or hyperglycaemia (18-20 mmol/l), and euglycaemic recovery (5.0±0.5 mmol/l). During each glycaemic phase, CBF/brain perfusion was measured with arterial spin labelling and brain neural activity was measured with fractional amplitude of low frequency fluctuations. Comparative analyses were based on the seven regional functional parcellation areas (networks) of the cerebral cortex. A Bayesian multi-level regression model was employed to test regional differences in CBF and brain neural activity between the various glycaemic conditions.

resultsTwenty adolescents with type 1 diabetes participated: ten in each of the hypoglycaemic and hyperglycaemic study arms. Relative to baseline, acute hypoglycaemia was associated with substantially reduced brain neural activity (six of seven functional networks); no significant differences in CBF were evident. By contrast, acute hyperglycaemia was associated with widespread increases in brain activity (five of seven functional networks) and decreased perfusion (six of seven functional networks). Hypoglycaemia and hyperglycaemia had symmetrically opposite effects on brain neural activity in the visual, ventral attention, dorsal attention, frontoparietal and default networks. Recovery from both hypoglycaemia and hyperglycaemia was associated with persistent alterations in both brain perfusion and neural activity, relative to baseline, despite >45 min of sustained euglycaemia. CONCLUSIONS/

interpretationAcross widespread areas of the brain, both brain perfusion and neural metabolic activity are altered by acute hypoglycaemia and hyperglycaemia in adolescents with type 1 diabetes. Recovery from glycaemic extremes is delayed. These findings offer important further insights into the acute cerebral responses to abnormal blood glucose levels.

Indexed as

BrainDiabetes Mellitus, Type 1HyperglycemiaHypoglycemiaAdolescentBlood GlucoseCerebrovascular CirculationChildFemaleGlucose Clamp TechniqueHumansMagnetic Resonance ImagingMaleBlood GlucoseBrainBrain metabolismCerebral blood flowFunctional MRIHyperglycaemiaHypoglycaemiaInsulin clampPaediatricsType 1 diabetes

Identifiers

PMID41057689
PMCPMC12594713

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Registered trials

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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.