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

IF 2.7 Q3 ENDOCRINOLOGY & METABOLISM
Sondre Meling, Erling Tjora, Heike Eichele, Rasmus B. Nedergaard, Filip K. Knop, Niels Ejskjaer, Siri Carlsen, Pål R. Njølstad, Christina Brock, Eirik Søfteland
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Abstract

Objective

The 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 Methods

For 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).

Results

Sixty-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.

Conclusions

Rectal 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 Published

Some 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.

Abstract Image

直肠敏感性与胃肠道介导的葡萄糖处理相关,但与肠促胰岛素效应无关。
目的:2型糖尿病中肠促胰岛素作用减弱的机制尚不清楚,但迷走神经传导受损已被提出。我们的目的是研究肠促胰岛素效应与自主神经病变、血糖异常程度和糖尿病病程之间的关系。设计和方法:在一项横断面研究中,我们纳入了长期2型糖尿病患者、近期发病患者、未经治疗的糖尿病患者和年龄、性别和体重指数相匹配的非糖尿病对照组。自主神经功能通过心血管反射试验、心率变异性和sudommotor功能进行评估。采用快速直肠球囊扩张法检测肠内内脏传入神经。通过口服葡萄糖耐量试验和静脉异糖血糖输注来计算肠促胰岛素效应和胃肠道介导的葡萄糖处置(GIGD)。结果:65名参与者被招募。与对照组(3.0±0.9 kPa)相比,糖尿病患者的直肠早期感觉低(长期为3.7±1.1 kPa,早期为4.0±1.3 kPa), p = 0.005。直肠早期感觉的低敏感性与肠促胰岛素效应无关(rho = -0.204, p = .106),但与GIGD相关(rho -0.341, p = .005)。肠促胰岛素效应和GIGD与所有血糖值、HbA1c和糖尿病病程相关。结论:直肠低敏感性在长期和早期2型糖尿病中都被发现,并且与肠促胰岛素效应无关,但与GIGD有关,这意味着内脏神经病变与胃肠道葡萄糖处理之间存在潜在联系。肠促胰岛素效应和GIGD均与血糖异常程度和糖尿病持续时间有关。先前发表:一些数据先前已发表,并作为美国糖尿病协会第83届科学会议的海报:Meling等人;1658-P:直肠低敏感性,肠自主神经功能障碍的潜在标志,与2型糖尿病患者胃肠道介导的葡萄糖处理显著相关。2023年6月20日;72(增刊1):1658-P。https://doi.org/10.2337/db23 - 1658 p。
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来源期刊
Endocrinology, Diabetes and Metabolism
Endocrinology, Diabetes and Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
5.00
自引率
0.00%
发文量
66
审稿时长
6 weeks
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