Bramhall Michael, Flórez-Vargas Oscar, Stevens Robert, Brass Andy, Cruickshank Sheena
*Bio-Health Informatics Group, School of Computer Science, University of Manchester, Manchester, United Kingdom; and †Manchester Immunology Group, Faculty of Life Science, University of Manchester, Manchester, United Kingdom.
Inflamm Bowel Dis. 2015 Jun;21(6):1248-59. doi: 10.1097/MIB.0000000000000369.
Current understanding of the onset of inflammatory bowel diseases relies heavily on data derived from animal models of colitis. However, the omission of information concerning the method used makes the interpretation of studies difficult or impossible. We assessed the current quality of methods reporting in 4 animal models of colitis that are used to inform clinical research into inflammatory bowel disease: dextran sulfate sodium, interleukin-10, CD45RB T cell transfer, and 2,4,6-trinitrobenzene sulfonic acid (TNBS).
We performed a systematic review based on PRISMA guidelines, using a PubMed search (2000-2014) to obtain publications that used a microarray to describe gene expression in colitic tissue. Methods reporting quality was scored against a checklist of essential and desirable criteria.
Fifty-eight articles were identified and included in this review (29 dextran sulfate sodium, 15 interleukin-10, 5 T cell transfer, and 16 TNBS; some articles use more than 1 colitis model). A mean of 81.7% (SD = ±7.038) of criteria were reported across all models. Only 1 of the 58 articles reported all essential criteria on our checklist. Animal age, gender, housing conditions, and mortality/morbidity were all poorly reported.
Failure to include all essential criteria is a cause for concern; this failure can have large impact on the quality and replicability of published colitis experiments. We recommend adoption of our checklist as a requirement for publication to improve the quality, comparability, and standardization of colitis studies and will make interpretation and translation of data to human disease more reliable.
目前对炎症性肠病发病机制的理解在很大程度上依赖于结肠炎动物模型的数据。然而,由于缺少关于所使用方法的信息,使得对研究的解读变得困难甚至无法进行。我们评估了用于为炎症性肠病临床研究提供信息的4种结肠炎动物模型(葡聚糖硫酸钠、白细胞介素-10、CD45RB T细胞转移和2,4,6-三硝基苯磺酸(TNBS))中方法报告的当前质量。
我们根据PRISMA指南进行了系统评价,使用PubMed搜索(2000 - 2014年)来获取使用微阵列描述结肠炎组织中基因表达的出版物。方法报告质量根据基本和理想标准清单进行评分。
共识别并纳入了58篇文章进行本综述(29篇关于葡聚糖硫酸钠,15篇关于白细胞介素-10,5篇关于T细胞转移,16篇关于TNBS;一些文章使用了不止一种结肠炎模型)。所有模型报告的标准平均为81.7%(标准差 = ±7.038)。58篇文章中只有1篇报告了我们清单上的所有基本标准。动物年龄、性别、饲养条件以及死亡率/发病率的报告都很差。
未纳入所有基本标准令人担忧;这种情况可能对已发表的结肠炎实验的质量和可重复性产生重大影响。我们建议采用我们的清单作为发表要求,以提高结肠炎研究的质量、可比性和标准化,并使数据向人类疾病的解读和转化更加可靠。