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观察者间分歧对克罗恩病表型-基因型关联的影响。

Impact of interobserver disagreement on phenotype-genotype associations in Crohn's disease.

作者信息

Oefferlbauer-Ernst Anna, Miehsler Wolfgang, Eckmüllner Otto, Travis Simon, Waldhoer Thomas, Dejaco Clemens, Gangl Alfred, Vogelsang Harald, Reinisch Walter

机构信息

Department of Internal Medicine IV, Division of Gastroenterology and Hepatology, Medical University of Vienna, Vienna, Austria.

出版信息

Inflamm Bowel Dis. 2007 Feb;13(2):156-63. doi: 10.1002/ibd.20016.

Abstract

BACKGROUND

Nonvalidated definitions of disease-related parameters in inflammatory bowel disease cause variations in diagnosis and disease classification. We determined interobserver agreement on applications of definitions of the Vienna Classification variables and computed the potential influence of misclassification on genotype/phenotype associations.

METHODS

Ten records of patients with Crohn's disease (CD) were independently evaluated by 19 observers using a standardized inflammatory bowel disease documentation system, which included the Vienna Classification. Interobserver agreement (IOA) was calculated as a percentage of the observers' agreement with a predetermined reference observer and by Cohen's kappa. Randomized reclassifications were then computed with 10,000 simulation runs using the IOA results and published NOD2/CARD15 gene status. A chi-square independence test was calculated for each simulation run.

RESULTS

IOA for location and behavior was 70% (K = 0.57) and 95% (K = 0.91), respectively. IOA for location subgroups ranged from 48% to 88% and for behavior from 91% to 97%. By including the results of histopathology into the evaluation of location, the overall IOA increased significantly, to 80% (P = 0.019). Assuming a true genotype/phenotype association, the proportion of studies with nonsignificant findings (P > 0.05) because of the observed misclassification of location ranged from 13.3% to 63.8% and of behavior from 0.2% to 22.2%, depending on a study sample size of 500 or 150 patients respectively.

CONCLUSIONS

We concluded that there is appreciable interobserver disagreement on the location of CD according to the original Vienna Classification that may obscure true genotype/phenotype associations. Definitions of disease parameters have to be validated before being used as the bases for classifications.

摘要

背景

炎症性肠病中疾病相关参数的未经验证的定义导致诊断和疾病分类存在差异。我们确定了观察者间对维也纳分类变量定义应用的一致性,并计算了错误分类对基因型/表型关联的潜在影响。

方法

19名观察者使用包括维也纳分类在内的标准化炎症性肠病记录系统,对10例克罗恩病(CD)患者的记录进行独立评估。观察者间一致性(IOA)以观察者与预先确定的参考观察者的一致率百分比以及科恩kappa系数来计算。然后使用IOA结果和已发表的NOD2/CARD15基因状态,通过10000次模拟运行计算随机重新分类。对每次模拟运行计算卡方独立性检验。

结果

部位和行为的IOA分别为70%(K = 0.57)和95%(K = 0.91)。部位亚组的IOA范围为48%至88%,行为的IOA范围为91%至97%。将组织病理学结果纳入部位评估后,总体IOA显著提高至80%(P = 0.019)。假设存在真正的基因型/表型关联,由于观察到的部位错误分类导致无显著结果(P > 0.05)的研究比例,根据研究样本量分别为500例或150例患者,范围为13.3%至63.8%,行为的错误分类导致的比例为0.2%至22.2%。

结论

我们得出结论,根据原始维也纳分类,观察者间对CD部位存在明显分歧,这可能掩盖真正的基因型/表型关联。疾病参数的定义在用作分类基础之前必须经过验证。

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