Inflammatory bowel disease. An epidemiological and genetic study.

U Monsén
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Abstract

The epidemiology of ulcerative colitis (UC) in Stockholm County over a 25-year period, 1955-1979, was investigated. There were 1,274 cases--681 males and 593 females. The proportion of patients with proctitis, left-sided, and total extent of disease remained constant over the study period, as did the time interval between onset of symptoms and definite diagnosis. The incidence increased over the first 20 years followed by a plateau and was 4.3 per 10(5) inhabitants at the end of the study period. The peak incidence in relation to age increased, but remained in the 3rd and 4th decade throughout the study period. In a population-based study of UC the overall prevalence of extracolonic diagnoses was 21%. Seventy percent of patients with extracolonic diagnoses had extensive colitis whereas among the patients without extracolonic diagnoses only 28% had extensive colitis (p less than 0.001). The extracolonic diagnoses were classified into two major groups, activity-related and autoimmune, the former is related to the extent and activity of UC and responds to both medical and surgical treatment, whereas the latter is unaffected by medical and surgical treatment for UC. A total of 364 diagnoses were distributed among 271 UC patients. The prevalence of extracolonic diagnoses was higher in familial UC (p less than 0.05), but was distributed as UC in general mostly with activity-related diagnoses. The familial occurrence of inflammatory bowel disease (IBD) was investigated among 963 patients with UC. There was a general prevalence of 7.9% for familial IBD. In 80% one relative was affected, in most cases this was a first degree relative with UC. Sibship was the most common relationship. No concordance for UC was found among three pairs of monozygotic twins. The prevalence of UC in first degree relatives of index patients was 15 times higher than in non-relatives. The age at onset was significantly lower among patients with a family history for UC; they also had a higher prevalence of total colitis. The prevalence of Crohn's disease (CD) in first degree relatives of index patients with UC was almost 3.5 times higher than in non-relatives. Complex segregation analysis of 124 families with UC where two or more individuals were affected points to a rare additive major gene with a low penetrance as the cause of the disease with. About 20% of the affected were heterozygotes for the gene. There was no evidence for multifactorial inheritance. The prevalence of IBD was found to be 13.4% in a population-based study on patients with CD.(ABSTRACT TRUNCATED AT 400 WORDS)

炎症性肠病。流行病学和遗传学研究。
研究了1955-1979年25年间斯德哥尔摩县溃疡性结肠炎(UC)的流行病学。共有1274例,其中男性681例,女性593例。在研究期间,直肠炎、左侧直肠炎患者的比例和疾病的总范围保持不变,症状发作和明确诊断之间的时间间隔也保持不变。发病率在前20年上升,随后进入平稳期,在研究期结束时为每10(5)名居民4.3例。与年龄相关的发病率高峰增加,但在整个研究期间仍保持在第3和第4个十年。在一项以人群为基础的UC研究中,结肠外诊断的总体患病率为21%。70%的经结肠外诊断的患者有广泛结肠炎,而未经结肠外诊断的患者只有28%有广泛结肠炎(p < 0.001)。结肠外诊断分为活动相关和自身免疫性两大类,前者与UC的程度和活动有关,对药物和手术治疗均有反应,而后者不受UC的药物和手术治疗的影响。271例UC患者共364例诊断。家族性UC的结肠外诊出率较高(p < 0.05),但总体上分布为UC,多与活动相关的诊断。对963例UC患者进行家族性炎症性肠病(IBD)的调查。家族性IBD的总体患病率为7.9%。在80%的情况下,有一位亲属受到影响,在大多数情况下,这是患有UC的一级亲属。姐妹关系是最常见的关系。在三对同卵双胞胎中未发现UC的一致性。指数患者一级亲属的UC患病率是非亲属的15倍。有UC家族史的患者发病年龄明显较低;他们也有更高的全结肠炎患病率。指数UC患者的一级亲属中克罗恩病(CD)的患病率几乎是非亲属的3.5倍。对124个两个或两个以上个体受影响的UC家族的复杂分离分析表明,一个罕见的外显率低的加性主基因是导致该疾病的原因。大约20%的患者是该基因的杂合子。没有多因子遗传的证据。在一项针对CD患者的人群研究中,发现IBD的患病率为13.4%。
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