Evidence map›Paper›PMID 40198816›Full record

ArticleThe Journal of clinical endocrinology and metabolism2025

Association Between Visit-to-Visit Glucose Variability and Brain Morphology and Cognitive Function in Type 2 Diabetes.

Weiye Lu, Die Shen, Shijun Qiu

Abstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

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

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

  1. Pooled it
  2. 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.

Weiye LuFirst Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou 510000, China.ORCID 0009-0002-6073-2281
Die ShenFirst Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou 510000, China.
Shijun QiuDepartment of Radiology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou 510000, China.ORCID 0000-0002-6739-4265

Funding

the National Natural Science Foundation of China 82330058the National Natural Science Foundation of China T2341014
6 · The paper itself

Abstract

objectiveTo investigate the effect of varying visit-to-visit glucose variability (GV) on brain morphometry and cognitive performance in patients with type 2 diabetes mellitus (T2DM).

methodsThis was a retrospective cohort study in which we recruited 426 participants (173 T2DM patients and 253 healthy controls) who underwent cognitive assessment and structural magnetic resonance imaging. In patients with T2DM, visit-to-visit GV was calculated using the SD of glycated hemoglobin (HbA1c) during the follow-up period. Multiple linear regression models were used to analyze the associations between different levels of GV and brain morphometry as well as cognitive function after adjusting for mean HbA1c levels and other traditional risk factors.

resultsHigher GV is associated with poorer global cognitive performance and executive function. After full multivariate adjustment, higher GV is linked to cortical thinning in the left superior parietal cortex, right postcentral gyrus, and insula, as well as a reduction in total gray matter volume. In contrast, no association was observed between GV and cortical volume or surface area.

conclusionOur findings indicate that higher visit-to-visit GV is associated with reduced cortical thickness, total gray matter volume atrophy, and poorer cognitive performance in patients with T2DM, and these associations are independent of mean HbA1c levels.

Indexed as

Blood GlucoseBrainCognitionDiabetes Mellitus, Type 2AgedCase-Control StudiesFemaleFollow-Up StudiesGlycated HemoglobinHumansMagnetic Resonance ImagingMaleMiddle AgedRetrospective StudiesBlood GlucoseGlycated Hemoglobinhemoglobin A1c protein, humanbrain morphometrycognitive functionglucose variabilitytype 2 diabetes mellitus

Identifiers

PMID40198816
PMCPMC12623016

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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.