Burisch Johan
Department of Gastroenterology, Herlev University Hospital, Herlev Ringvej 75, 2730 Herlev, Denmark.
Dan Med J. 2014 Jan;61(1):B4778.
Inflammatory bowel diseases (IBD), consisting of Crohn's disease (CD) and ulcerative colitis (UC), are chronic immune mediated diseases of unknown aetiology. Traditionally, the highest occurrence of both UC and CD is found in North America and Europe, including Scandinavia and the United Kingdom, while the diseases remain rare in Eastern Europe. Until recently, few population-based cohort data were available on the epidemiology of IBD in Eastern Europe. However, recent studies from Hungary and Croatia have reported steep increases in IBD incidence that means they are now comparable with Western European countries. The reasons for these changes remain unknown but could include an increasing awareness of the diseases, better access to diagnostic procedures, methodological bias in previous studies from Eastern Europe, or real differences in environmental factors, lifestyle and genetic susceptibility. The aim of this thesis was to create a prospective European population-based inception cohort of incident IBD patients in order to investigate whether an East-West gradient in the incidence of IBD exists in Europe. Furthermore, we investigated possible differences throughout Europe during the first year subsequent to diagnosis in terms of clinical presentation, disease outcome, treatment choices, frequency of environmental risk factors, as well as patient-reported health-related quality of life (HRQoL) and quality of care (QoC). Finally, we assessed resource utilization during the initial year of disease in both geographic regions. A total number of 31 centres from 14 Western and 8 Eastern European countries covering a total background population of approximately 10.1 million participated in this study. During the inclusion period from 1 January to 31 December 2010 a total number of 1,515 patients aged 15 years or older were included in the cohort. Annual incidence rates were twice as high in Western Europe (CD: 6.3/100,000; UC: 9.8/100,000) compared to Eastern Europe (CD: 3.3/100,000; UC: 4.6/100,000), thus confirming a gradient in IBD incidence. The incidence gradient could not be explained by marked differences in environmental factors prior to IBD diagnosis. In fact, Eastern European patients had higher frequencies of dietary risk factors than Western European patients, while the remaining risk factors occurred just as frequently. Furthermore, the availability of diagnostic tools and the diagnostic strategy did not differ, and in fact was better in Eastern Europe in terms of the use of colonoscopies and diagnostic delay. In terms of socio-economic characteristics as well as clinical presentation at diagnosis Eastern and Western European IBD patients did not differ significantly. However, regarding treatment choices during the initial year of disease the use of biological therapy was significantly higher in Western Europe for both CD and UC, while Eastern European centres used 5-ASA more often in CD and UC. In both regions patients were treated earlier and more frequently with immunomodulators compared to previous cohorts. But despite these differences in treatment, disease course - including hospitalisation and surgery rates during the first year of disease - were similar in both regions and the majority of patients were in clinical remission at follow-up. Finally, generic and disease-specific HRQoL improved in all IBD patients and at twelve months follow-up the majority of patients had a good disease-specific HRQoL score. Differences in how, and from whom, patients received disease-specific education and information were noted between the geographic regions; for instance IBD specialist nurses were not used in Eastern European IBD centres. Expenses for the cohort during the initial year of disease exceeded four million Euros with most money spent on diagnostics and surgery. Biological therapy accounted for one fourth costs in Western European CD patients. Long-term follow-up of the EpiCom cohort is needed in order to assess whether the earlier and more frequent treatment with immunomodulators and biologicals observed in this study will change the natural disease course and phenotypes over time or merely postpone outcomes such as surgery. Furthermore, the question of if and how differences in treatment choices between Eastern and Western Europe impact on the disease course requires long-term follow-up.
炎症性肠病(IBD)包括克罗恩病(CD)和溃疡性结肠炎(UC),是病因不明的慢性免疫介导疾病。传统上,UC和CD在北美和欧洲,包括斯堪的纳维亚和英国发病率最高,而在东欧这些疾病仍然罕见。直到最近,东欧关于IBD流行病学的基于人群的队列数据很少。然而,匈牙利和克罗地亚最近的研究报告称IBD发病率急剧上升,这意味着它们现在与西欧国家相当。这些变化的原因尚不清楚,但可能包括对疾病的认识增加、诊断程序的可及性提高、东欧以前研究中的方法学偏差,或环境因素、生活方式和遗传易感性的实际差异。本论文的目的是建立一个基于欧洲人群的前瞻性新发IBD患者队列,以调查欧洲IBD发病率是否存在东西方梯度。此外,我们调查了欧洲各地在诊断后的第一年,在临床表现、疾病结局、治疗选择、环境危险因素频率,以及患者报告的健康相关生活质量(HRQoL)和护理质量(QoC)方面可能存在的差异。最后,我们评估了两个地理区域疾病初始年的资源利用情况。来自14个西欧国家和8个东欧国家的31个中心参与了本研究,总背景人口约为1010万。在2010年1月1日至12月31日的纳入期内,队列中纳入了1515名15岁及以上的患者。西欧的年发病率(CD:6.3/10万;UC:9.8/10万)是东欧(CD:3.3/10万;UC:4.6/10万)的两倍,从而证实了IBD发病率的梯度。IBD诊断前环境因素的显著差异无法解释发病率梯度。事实上,东欧患者饮食危险因素的频率高于西欧患者,而其他危险因素的发生频率相同。此外,诊断工具的可用性和诊断策略没有差异,实际上东欧在结肠镜检查的使用和诊断延迟方面更好。在社会经济特征以及诊断时的临床表现方面,东欧和西欧的IBD患者没有显著差异。然而,在疾病初始年的治疗选择方面,西欧CD和UC患者使用生物疗法的比例显著更高,而东欧中心在CD和UC中更常使用5-氨基水杨酸(5-ASA)。与以前的队列相比,两个地区的患者免疫调节剂治疗更早且更频繁。但尽管治疗存在这些差异,两个地区的疾病进程——包括疾病第一年的住院率和手术率——相似,大多数患者在随访时处于临床缓解状态。最后,所有IBD患者的一般和疾病特异性HRQoL均有所改善,在12个月随访时,大多数患者的疾病特异性HRQoL评分良好。地理区域之间在患者接受疾病特异性教育和信息的方式及来源方面存在差异;例如,东欧IBD中心未使用IBD专科护士。该队列在疾病初始年的费用超过400万欧元,大部分资金用于诊断和手术。生物疗法占西欧CD患者费用的四分之一。需要对EpiCom队列进行长期随访,以评估本研究中观察到的免疫调节剂和生物制剂的更早、更频繁治疗是否会随时间改变疾病自然进程和表型,或者仅仅推迟手术等结局。此外,东欧和西欧治疗选择的差异是否以及如何影响疾病进程的问题需要长期随访。