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遗传性凝血障碍似乎可预防炎症性肠病。

Inherited disorders of coagulation appear to protect against inflammatory bowel disease.

作者信息

Thompson N P, Wakefield A J, Pounder R E

机构信息

University Department of Medicine, Royal Free Hospital School of Medicine, London, England.

出版信息

Gastroenterology. 1995 Apr;108(4):1011-5. doi: 10.1016/0016-5085(95)90197-3.

Abstract

BACKGROUND/AIMS: Crohn's disease and ulcerative colitis seem to be rarely associated with inherited diseases of coagulation. Histological and hematologic studies suggest that thrombotic mesenteric microvascular occlusion is involved in the pathogenesis of inflammatory bowel disease. The aim of this study was to perform a national survey to determine the prevalence of inflammatory bowel disease among patients with inherited disorders of coagulation.

METHODS

Using a postal and telephone questionnaire survey sent to directors of all 129 hemophilia centers in the United Kingdom, the number of patients with inflammatory bowel disease and either hemophilia or von Willebrand's disease was determined. The expected number of cases of inflammatory bowel disease in this population was estimated using published data.

RESULTS

Of 6433 patients with hemophilia and 3129 patients with von Willebrand's disease, 4 cases of Crohn's disease were reported compared with expected 11.97-16.58 cases (standardized morbidity ratio, 0.33-0.24; 95% confidence interval, 0.90-0.01; P < 0.05). Ulcerative colitis also occurred significantly less frequently than expected: 9 observed cases in comparison with expected 19.43-31.35 cases (standardized morbidity ratio, 0.46-0.29; 95% confidence interval, 0.91-0.01; P < 0.025).

CONCLUSIONS

This epidemiological study provides further evidence that thrombosis and vascular occlusion may be important in the pathogenesis of inflammatory bowel disease.

摘要

背景/目的:克罗恩病和溃疡性结肠炎似乎很少与遗传性凝血疾病相关。组织学和血液学研究表明,血栓性肠系膜微血管闭塞参与了炎症性肠病的发病机制。本研究的目的是进行一项全国性调查,以确定遗传性凝血障碍患者中炎症性肠病的患病率。

方法

通过向英国所有129个血友病中心的主任发送邮政和电话问卷调查,确定患有炎症性肠病以及血友病或血管性血友病的患者数量。使用已发表的数据估计该人群中炎症性肠病的预期病例数。

结果

在6433例血友病患者和3129例血管性血友病患者中,报告了4例克罗恩病,而预期为11.97 - 16.58例(标准化发病率,0.33 - 0.24;95%置信区间,0.90 - 0.01;P < 0.05)。溃疡性结肠炎的发生频率也显著低于预期:观察到9例,而预期为19.43 - 31.35例(标准化发病率,0.46 - 0.29;95%置信区间,0.91 - 0.01;P < 0.025)。

结论

这项流行病学研究提供了进一步的证据,表明血栓形成和血管闭塞可能在炎症性肠病的发病机制中起重要作用。

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