Systemic Cytokine Expression in Diabetes Is Associated with Prolonged Gastrointestinal Transit Times and Cardinal Gastroparesis Symptoms
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Systemic Cytokine Expression in Diabetes Is Associated with Prolonged Gastrointestinal Transit Times and Cardinal Gastroparesis Symptoms. / Okdahl, Tina; Wegeberg, Anne-Marie; Jensen, Anne Birthe Helweg; Jensen, Sarah Thorius; Andersen, Helene Riis Pontoppidan; Storling, Joachim; Brock, Birgitte; Brock, Christina.
In: Biomedicines, Vol. 11, No. 4, 1027, 2023.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Systemic Cytokine Expression in Diabetes Is Associated with Prolonged Gastrointestinal Transit Times and Cardinal Gastroparesis Symptoms
AU - Okdahl, Tina
AU - Wegeberg, Anne-Marie
AU - Jensen, Anne Birthe Helweg
AU - Jensen, Sarah Thorius
AU - Andersen, Helene Riis Pontoppidan
AU - Storling, Joachim
AU - Brock, Birgitte
AU - Brock, Christina
PY - 2023
Y1 - 2023
N2 - Gastroenteropathy is a common complication in diabetes associated with damages to the enteric nervous system. Systemic low-grade inflammation facilitates neurotoxicity, and associations with peripheral and autonomic neuropathy have been reported. However, less is known of associations with gastroenteropathy. To explore the area cross-sectionally, we included individuals with diabetes (type 1: 56, type 2: 100) and 21 healthy controls. Serum levels of interleukin (IL)-6, IL-8, IL-10, tumour necrosis factor (TNF)-alpha, and interferon (IFN)-gamma were measured by multiplex technology. Segmental gastrointestinal transit times were assessed by wireless motility capsule investigations. Symptoms of gastroparesis were rated on Gastroparesis Cardinal Symptom Index questionnaires. Compared to healthy, levels of TNF-alpha were decreased in type 1 diabetes and increased in type 2 diabetes, while colonic transit time was increased (all p < 0.05). In diabetes, associations between IL-8 and prolonged gastric emptying (odds ratio (OR) 1.07, p = 0.027) and between IL-10 and prolonged colonic transit (OR 29.99, p = 0.013) were seen. Inverse correlations between IL-6 and nausea/vomiting (rho = -0.19, p = 0.026) and bloating (rho = -0.29; p < 0.001) were found. These findings indicate a plausible interaction between inflammation and the enteric nervous system in diabetes, which raises the question of whether anti-inflammatory strategies could be applied in management of diabetic gastroenteropathy.
AB - Gastroenteropathy is a common complication in diabetes associated with damages to the enteric nervous system. Systemic low-grade inflammation facilitates neurotoxicity, and associations with peripheral and autonomic neuropathy have been reported. However, less is known of associations with gastroenteropathy. To explore the area cross-sectionally, we included individuals with diabetes (type 1: 56, type 2: 100) and 21 healthy controls. Serum levels of interleukin (IL)-6, IL-8, IL-10, tumour necrosis factor (TNF)-alpha, and interferon (IFN)-gamma were measured by multiplex technology. Segmental gastrointestinal transit times were assessed by wireless motility capsule investigations. Symptoms of gastroparesis were rated on Gastroparesis Cardinal Symptom Index questionnaires. Compared to healthy, levels of TNF-alpha were decreased in type 1 diabetes and increased in type 2 diabetes, while colonic transit time was increased (all p < 0.05). In diabetes, associations between IL-8 and prolonged gastric emptying (odds ratio (OR) 1.07, p = 0.027) and between IL-10 and prolonged colonic transit (OR 29.99, p = 0.013) were seen. Inverse correlations between IL-6 and nausea/vomiting (rho = -0.19, p = 0.026) and bloating (rho = -0.29; p < 0.001) were found. These findings indicate a plausible interaction between inflammation and the enteric nervous system in diabetes, which raises the question of whether anti-inflammatory strategies could be applied in management of diabetic gastroenteropathy.
KW - enteric nervous system
KW - diabetes
KW - gastroenteropathy
KW - inflammation
KW - cytokine
KW - wireless motility capsule
KW - TNF-ALPHA
KW - MOTILITY
KW - TYPE-1
KW - INTERLEUKIN-6
KW - NEUROPATHY
KW - INFLAMMATION
KW - MECHANISMS
KW - MODEL
KW - IL-6
U2 - 10.3390/biomedicines11041027
DO - 10.3390/biomedicines11041027
M3 - Journal article
C2 - 37189645
VL - 11
JO - Biomedicines
JF - Biomedicines
SN - 2227-9059
IS - 4
M1 - 1027
ER -
ID: 347975059