Rectal sensitivity correlated with gastrointestinal‐mediated glucose disposal, but not the incretin effect

Author:

Meling Sondre12ORCID,Tjora Erling23ORCID,Eichele Heike45ORCID,Nedergaard Rasmus B.6ORCID,Knop Filip K.78910ORCID,Ejskjaer Niels111213ORCID,Carlsen Siri1ORCID,Njølstad Pål R.2314ORCID,Brock Christina61112ORCID,Søfteland Eirik215ORCID

Affiliation:

1. Department of Medicine Stavanger University Hospital Stavanger Norway

2. Department of Clinical Science University of Bergen Bergen Norway

3. Children and Youth Clinic Haukeland University Hospital Bergen Norway

4. Department of Biological and Medical Psychology, Faculty of Psychology University of Bergen Bergen Norway

5. Regional resource Centre for Autism, ADHD and Tourette Syndrome Western Norway, Division of Psychiatry Haukeland University Hospital Bergen Norway

6. Mech‐Sense, Department of Gastroenterology and Hepatology Aalborg University Hospital Aalborg Denmark

7. Center for Clinical Metabolic Research Copenhagen University Hospital—Herlev and Gentofte Copenhagen Denmark

8. Department of Clinical Medicine, Faculty of Health and Medical Sciences University of Copenhagen Copenhagen Denmark

9. Steno Diabetes Center Copenhagen Gentofte Denmark

10. Novo Nordisk Foundation Center for Basic Metabolic Research University of Copenhagen Copenhagen Denmark

11. Department of Clinical Medicine, Faculty of Medicine Aalborg University Hospital Aalborg Denmark

12. Steno Diabetes Center North Denmark Aalborg University Hospital Aalborg Denmark

13. Department of Endocrinology Aalborg University Hospital Aalborg Denmark

14. Mohn Center for Diabetes Precision Medicine, Department of Clinical Science University of Bergen Bergen Norway

15. Department of Medicine Haukeland University Hospital Bergen Norway

Abstract

AbstractObjectiveThe mechanisms behind the diminished incretin effect in type 2 diabetes are uncertain, but impaired vagal transmission has been suggested. We aimed to investigate the association between the incretin effect and autonomic neuropathy, and the degree of dysglycaemia and duration of diabetes.Design and MethodsFor a cross‐sectional study, we included participants with either longstanding type 2 diabetes, recent onset, untreated diabetes and controls without diabetes matched for age, sex and body mass index. Autonomic nerve function was assessed with cardiovascular reflex tests, heart rate variability and sudomotor function. Visceral afferent nerves in the gut were tested performing rapid rectal balloon distention. An oral glucose tolerance test and an intravenous isoglycaemic glucose infusion were performed to calculate the incretin effect and gastrointestinal‐mediated glucose disposal (GIGD).ResultsSixty‐five participants were recruited. Participants with diabetes had rectal hyposensitivity for earliest sensation (3.7 ± 1.1 kPa in longstanding, 4.0 ± 1.3 in early), compared to controls (3.0 ± 0.9 kPa), p = .005. Rectal hyposensitivity for earliest sensation was not associated with the incretin effect (rho = −0.204, p = .106), but an association was found with GIGD (rho −0.341, p = .005). Incretin effect and GIGD were correlated with all glucose values, HbA1c and duration of diabetes.ConclusionsRectal hyposensitivity was uncovered in both longstanding and early type 2 diabetes, and was not associated with the incretin effect, but with GIGD, implying a potential link between visceral neuropathy and gastrointestinal handling of glucose. Both the incretin effect and GIGD were associated with the degree of dysglycaemia and the duration of diabetes.Previously PublishedSome of the data have previously been published and presented as a poster on the American Diabetes Association 83rd Scientific Sessions: Meling et al; 1658‐P: Rectal Hyposensitivity, a Potential Marker of Enteric Autonomic Nerve Dysfunction, Is Significantly Associated with Gastrointestinally Mediated Glucose Disposal in Persons with Type 2 Diabetes. Diabetes 20 June 2023; 72 (Supplement_1): 1658–P. https://doi.org/10.2337/db23‐1658‐P.

Funder

Helse Vest

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism

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