Center for Clinical Research and Prevention, Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark; Department of Epidemiology Research, Statens Serum Institut, Copenhagen S, Denmark.
Center for Clinical Research and Prevention, Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark.
Clin Gastroenterol Hepatol. 2020 Apr;18(4):881-888.e1. doi: 10.1016/j.cgh.2019.07.052. Epub 2019 Aug 5.
BACKGROUND & AIMS: The intestine regulates glucose homeostasis, but it is not clear whether chronic intestinal inflammation affects risk for type 2 diabetes. We investigated the long-term risk of type 2 diabetes in patients with inflammatory bowel diseases (IBD) in a nationwide cohort study in Denmark.
In a nationwide population-based cohort of 6,028,844 persons in Denmark, we compared data from individuals with a diagnosis of IBD (Crohn's disease [CD] or ulcerative colitis UC]) with data from individuals from the general population from 1977 through 2014. Persons with type 2 diabetes were identified in the National Patient Register. Risk is presented as standardized incidence ratios (SIR) with 95% CIs.
During 736,072 person-years of follow-up, 3436 patients with IBD developed type 2 diabetes vs 2224 expected (SIR, 1.54; 95% CI, 1.49-1.60). The risk was significantly increased in patients with UC (SIR, 1.54; 95% CI, 1.48-1.60), in patients with CD (SIR, 1.57; 95% CI, 1.47-1.67), in women (SIR, 1.51; 95% CI, 1.44-1.59), and in men (SIR, 1.57; 95% CI, 1.50-1.65). The risk was highest the first year after a diagnosis of IBD (SIR, 4.48; 95% CI, 4.16-4.83), but remained increased for 20 or more years following the diagnosis (SIR, 1.26; 95% CI, 1.16-1.38). The increased risk could not be accounted for by frequency of health care contacts or corticosteroid exposure. Patients who received a diagnosis of IBD from 2003 through 2014 (SIR, 1.79; 95% CI, 1.67-1.91) had a significantly higher risk of type 2 diabetes than patients who received a diagnosis of IBD from 1977 through 1988 (SIR, 1.47; 95% CI, 1.39-1.56) or 1989 through 2002 (SIR, 1.48; 95% CI, 1.41-1.56) (P < .001).
In a population-based cohort study, we found an increased risk of type 2 diabetes in patients with UC or CD, with highest risk estimates from 2003 through 2014, compared with earlier years. Studies are needed to determine the effects of IBD treatment on risk of type 2 diabetes.
肠道调节葡萄糖稳态,但尚不清楚慢性肠道炎症是否会增加 2 型糖尿病的风险。我们在丹麦的全国队列研究中调查了炎症性肠病(IBD)患者发生 2 型糖尿病的长期风险。
在丹麦的一个全国性基于人群的队列中,我们比较了 6028844 名个体的 IBD(克罗恩病[CD]或溃疡性结肠炎 UC])数据与 1977 年至 2014 年一般人群数据。2 型糖尿病患者在国家患者登记处中确定。风险以标准化发病率比(SIR)和 95%CI 表示。
在 736072 人年的随访期间,3436 名 IBD 患者发生 2 型糖尿病,而预期为 2224 例(SIR,1.54;95%CI,1.49-1.60)。UC(SIR,1.54;95%CI,1.48-1.60)、CD(SIR,1.57;95%CI,1.47-1.67)、女性(SIR,1.51;95%CI,1.44-1.59)和男性(SIR,1.57;95%CI,1.50-1.65)患者的风险明显增加。IBD 诊断后第一年的风险最高(SIR,4.48;95%CI,4.16-4.83),但在诊断后 20 年或更长时间仍持续增加(SIR,1.26;95%CI,1.16-1.38)。增加的风险不能用医疗保健接触频率或皮质类固醇暴露来解释。2003 年至 2014 年接受 IBD 诊断的患者(SIR,1.79;95%CI,1.67-1.91)与 1977 年至 1988 年(SIR,1.47;95%CI,1.39-1.56)或 1989 年至 2002 年(SIR,1.48;95%CI,1.41-1.56)接受 IBD 诊断的患者相比,2 型糖尿病的风险显著增加(P<.001)。
在一项基于人群的队列研究中,我们发现 UC 或 CD 患者发生 2 型糖尿病的风险增加,与早年相比,2003 年至 2014 年的风险估计值最高。需要研究 IBD 治疗对 2 型糖尿病风险的影响。