C57BL/6小鼠溃疡性皮炎危险因素及治疗的系统文献综述。

Comparative medicine Pub Date : 2015-12-01
Jennifer L Sargent, Nathan J Koewler, Helen E Diggs
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引用次数: 0

摘要

C57BL/6小鼠的溃疡性皮炎(UD)尚不清楚,治疗也具有挑战性。我们试图评估关于UD的常见危险因素和报道的UD治疗的证据。用“溃疡性皮炎”和“C57BL/6”检索3个电子数据库。筛选所得的347篇文章,以确定根据性别、季节、饮食或年龄比较野生型C57BL/6小鼠自发性UD风险的出版物,以及根据所使用的干预措施比较愈合程度或病变消退率的出版物。采用已发表的评价方法学质量的标准对文章进行评价,包括研究设计、每个研究组的动物数量、病例定义、诊断方法、随机化、入组标准、排除标准和结果。搜索确定了11篇符合纳入标准的危险因素的出版物,没有一篇关于UD治疗的出版物符合所有标准。放宽危险因素和治疗结果报告的纳入标准,包括野生型C57BL/6小鼠和具有B6背景的基因工程小鼠,产生了12篇关于危险因素的出版物和3篇关于治疗的出版物。饮食因素,特别是热量限制,似乎影响UD的风险。雌性与UD风险较高的关系并不一致,在回顾的研究中,UD最常见于13至24个月大的小鼠。在评估UD治疗的3篇出版物中,只有1篇纳入了未治疗组或替代治疗对照组。需要进一步的研究来探索UD的流行病学方面并比较治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systematic Literature Review of Risk Factors and Treatments for Ulcerative Dermatitis in C57BL/6 Mice.

Ulcerative dermatitis (UD) in C57BL/6 mice is poorly understood and challenging to treat. We sought to evaluate the evidence regarding commonly cited risk factors for UD and reported UD treatments. The terms 'ulcerative dermatitis' and 'C57BL/6' were used to search 3 electronic databases. The resulting 347 articles were screened to identify publications that compared the risk of spontaneous UD in wild-type C57BL/6 mice according to sex, season, diet, or age and those that compared the degree of healing or rate of lesion resolution according to the intervention used. Articles were evaluated by using published criteria for assessing methodologic quality, including study design, number of animals per study group, case definition, method of diagnosis, randomization, enrollment criteria, exclusion criteria, and outcomes. The search identified 11 publications on risk factors that met the inclusion criteria, and no publication on UD treatment met all of the criteria. Relaxing the inclusion criteria for reporting of risk factors and treatment outcomes to include both wild-type C57BL/6 mice and genetically engineered mice on a B6 background yielded 12 publications on risk factors and 3 publications on treatment. Dietary factors, particularly caloric restriction, appear to influence UD risk. Female sex was inconsistently associated with a higher risk of UD, which most often occurred in 13- to 24-mo-old mice in the studies that were reviewed. Only 1 of the 3 publications that evaluated UD treatments included an untreated group or alternative therapy control. Further research is needed to explore epidemiologic aspects of UD and to compare treatment options.

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