Davidsen Line, Lebech Cichosz Simon, Knoph Cecilie Siggaard, Larsen Isabelle Myriam, Stæhr Peter Bisgaard, Vestergaard Peter, Jensen Morten Hasselstrøm, Hartmann Bolette, Holst Jens Juul, Drewes Asbjørn Mohr, Juel Caroline Trunk-Black, Knop Filip Krag, Olesen Søren Schou
Department of Gastroenterology and Hepatology, Centre for Pancreatic Diseases & Mech-Sense, Aalborg University Hospital, Aalborg, Denmark.
Clinical Institute, Aalborg University, Aalborg, Denmark.
Diabet Med. 2025 Aug;42(8):e70080. doi: 10.1111/dme.70080. Epub 2025 May 31.
Diabetes in patients with chronic pancreatitis is a heterogeneous condition with some patients presenting with pre-existing diabetes and others developing diabetes after pancreatitis onset. We aimed to characterise beta and alpha cell function in these patients and examine differences between those with and without pre-existing diabetes.
We included 26 patients with chronic pancreatitis and insulin-treated diabetes, divided into two subgroups: 13 with pre-pancreatitis diabetes (having type 2 diabetes before their chronic pancreatitis diagnosis) and 13 with post-pancreatitis diabetes. Patients underwent comprehensive clinical characterisation, including an arginine stimulation test to measure fasting and stimulated levels of C-peptide and glucagon. Additionally, they were monitored with continuous glucose monitoring over 20 days.
Patients with chronic pancreatitis and diabetes exhibited reduced fasting and stimulated C-peptide and glucagon responses to arginine, though responses varied considerably among individuals. Post-pancreatitis diabetes patients had lower glucagon responses than those with pre-pancreatitis diabetes (mean difference -19.3 pmol/L, 95% confidence interval (CI) -35.6 to -3.0). However, C-peptide levels were similar between the groups. Pre-pancreatitis diabetes patients spent more time in level 2 hyperglycaemia compared to post-pancreatitis patients (12.9% vs. 6.7%, p = 0.02). In contrast, post-pancreatitis diabetes patients had more time in both level 1 and level 2 hypoglycaemia (p = 0.03 and p = 0.05, respectively). A low glucagon response was correlated with time spent in hypoglycaemia (Rho = -0.54, p < 0.01).
Diabetes in chronic pancreatitis is a heterogeneous entity. The presence of type 2 diabetes prior to chronic pancreatitis is associated with a reduced risk of alpha cell dysfunction and hypoglycaemia.
慢性胰腺炎患者的糖尿病情况具有异质性,部分患者在胰腺炎发病前就已患有糖尿病,而另一些患者则在胰腺炎发病后才患上糖尿病。我们旨在描述这些患者的β细胞和α细胞功能,并研究有或无胰腺炎发病前糖尿病患者之间的差异。
我们纳入了26例接受胰岛素治疗的慢性胰腺炎合并糖尿病患者,分为两个亚组:13例患有胰腺炎前糖尿病(在慢性胰腺炎诊断前患有2型糖尿病)和13例患有胰腺炎后糖尿病。患者接受了全面的临床特征分析,包括精氨酸刺激试验,以测量空腹和刺激状态下的C肽和胰高血糖素水平。此外,他们还进行了20天的连续血糖监测。
慢性胰腺炎合并糖尿病患者对精氨酸的空腹和刺激状态下的C肽和胰高血糖素反应均降低,尽管个体之间的反应差异很大。胰腺炎后糖尿病患者的胰高血糖素反应低于胰腺炎前糖尿病患者(平均差异-19.3 pmol/L,95%置信区间(CI)-35.6至-3.0)。然而,两组之间的C肽水平相似。与胰腺炎后患者相比,胰腺炎前糖尿病患者处于2级高血糖状态的时间更长(12.9%对6.7%,p = 0.02)。相比之下,胰腺炎后糖尿病患者处于1级和2级低血糖状态的时间更多(分别为p = 0.03和p = 0.05)。低胰高血糖素反应与低血糖状态下的时间相关(Rho = -0.54,p < 0.01)。
慢性胰腺炎中的糖尿病是一种异质性疾病。慢性胰腺炎之前存在2型糖尿病与α细胞功能障碍和低血糖风险降低有关。