Evidence map›Paper›PMID 42827731›Full record

ArticleFrontiers in endocrinology2026

Reward-related functioning across diabetes subtypes: associations with glycaemic control.

Ayse Kurtulmuş, Fatma Büşra Parlakkaya Yıldız, Emek Esra Sahinbaş, Merve Özyıldırım, Pınar Ertunç, Zülal Çelik, Mümtaz Takır

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Article in Frontiers in endocrinology, 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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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Ayse KurtulmuşDepartment of Psychiatry, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Türkiye.
Fatma Büşra Parlakkaya YıldızDepartment of Psychiatry, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Türkiye.
Emek Esra SahinbaşDepartment of Psychiatry, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Türkiye.
Merve ÖzyıldırımDepartment of Psychiatry, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Türkiye.
Pınar ErtunçDepartment of Psychiatry, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Türkiye.
Zülal ÇelikDepartment of Psychiatry, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Türkiye.
Mümtaz TakırDepartment of Endocrinology, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Insulin signaling has been implicated in reward processing and motivational regulation through its modulatory effects on mesolimbic pathways. However, reward-related behavioral functioning across different diabetes subtypes and insulin-related metabolic states remains poorly understood. This study aimed to compare motivational and reward-related behavioral measures among individuals with type 1 diabetes mellitus (T1DM), type 2 diabetes mellitus (T2DM), prediabetes, and healthy controls, and to investigate their associations with diabetes self-management and glycaemic control. Methods: This cross-sectional study included 44 individuals with T1DM, 43 with T2DM, 28 with prediabetes, and 46 healthy controls. Participants completed measures assessing behavioral inhibition/activation (BIS/BAS), anhedonia, delay discounting, depressive symptoms, and diabetes self-management. Group differences were examined using analyses of covariance controlling for age, sex, education level, and depressive symptoms. Correlation and hierarchical regression analyses were conducted to evaluate associations with diabetes self-management and HbA1c levels. Results: Significant group differences were observed for BIS and BAS Reward Responsiveness scores after false discovery rate correction (p = .004). Conclusions: Altered reward responsiveness and behavioral inhibition may be particularly associated with T1DM rather than T2DM or prediabetes. Reward-related behavioral functioning also showed a modest association with glycaemic control, with BAS Drive demonstrating the most consistent individual association with HbA1c. These findings highlight the potential clinical relevance of motivational and reward-related processes in diabetes and suggest that considering these behavioural dimensions may help inform more individualized approaches to diabetes management and glycaemic control.

Indexed as

Diabetes Mellitus, Type 1Diabetes Mellitus, Type 2Glycemic ControlPrediabetic StateRewardAdultAnhedoniaBlood GlucoseCase-Control StudiesCross-Sectional StudiesDelay DiscountingDepressionFemaleGlycated HemoglobinHumansMaleBlood GlucoseGlycated Hemoglobinhemoglobin A1c protein, humananhedoniabehavioral inhibitiondelay discountingdiabetesHbA1c

Identifiers

PMID42827731
PMCPMC13630698

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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.