Evidence map›Paper›PMID 39706674›Full record

ArticleBMJ open diabetes research & care2024

Beta-cell, but not autonomic nervous system, function is related to MAFLD in early stages of glucose intolerance.

Rumyana Dimova, Nevena Chakarova, Mina Serdarova, Cvetelina Marinova, Dimitar Popov, Stefano Del Prato, Tsvetalina Tankova

Abstract read
In one paragraph

Article in BMJ open diabetes research & care, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

7 authors.

Rumyana DimovaDepartment of Endocrinology, Medical University-Sofia, Sofia, Bulgaria dr.roumyana.dimova@gmail.com.ORCID 0000-0003-2838-4344
Nevena ChakarovaDepartment of Endocrinology, Medical University-Sofia, Sofia, Bulgaria.
Mina SerdarovaDepartment of Endocrinology, Medical University-Sofia, Sofia, Bulgaria.
Cvetelina MarinovaDepartment of Gastroenterology, Medical University-Sofia, Sofia, Bulgaria.
Dimitar PopovDepartment of Gastroenterology, Medical University-Sofia, Sofia, Bulgaria.
Stefano Del PratoClinical & Experimental Medicine, University of Pisa, Pisa, Italy.ORCID 0000-0002-5388-0270
Tsvetalina TankovaDepartment of Endocrinology, Medical University-Sofia, Sofia, Bulgaria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPrevious studies have suggested an association between beta-cell and autonomic function and metabolic-associated fatty liver disease (MAFLD). We explored the association between controlled attenuated parameter (CAP) and insulin secretion and action, as well as sympathetic and parasympathetic activity in normal (NGT) and impaired (IGT) glucose tolerance. RESEARCH DESIGN AND

methodsTwenty-five NGT (age 44.8±9.6 years; body mass index (BMI) 32.3±6.9 kg/m

resultsA CAP >233 dB/m was found in 72% of subjects with NGT and 67% of subjects with IGT. Subjects with MAFLD, irrespective of glucose tolerance, had higher BMI and waist circumference, lower insulin secretion and action, and lower parasympathetic activity. On a matrix analysis, after adjustment for age and BMI, CAP was positively related to systolic blood pressure (SBP); insulin action was negatively related to parasympathetic activity. Regression analysis showed that AUC-insulin MMTT remained independently related to MAFLD: OR 24.4 (95% CI 2.17 to 274.77; p=0.010). A "cut-off" value of 15,620 uIU/mL

conclusionsOur results do not support a role for parasympathetic activity in MAFLD. Rather, they show that stimulated hyperinsulinemia may be associated with greater risk of MAFLD irrespective of glucose tolerance in a high-risk population without diabetes.

Indexed as

Autonomic Nervous SystemBlood GlucoseGlucose IntoleranceGlucose Tolerance TestInsulin ResistanceInsulin-Secreting CellsAdultBiomarkersBody Mass IndexFemaleFollow-Up StudiesHumansInsulinInsulin SecretionMaleMiddle AgedBiomarkersBlood GlucoseInsulinAutonomic FunctionHyperinsulinemiaImpaired Glucose Tolerance

Identifiers

PMID39706674
PMCPMC11667428

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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.