Aging increases the risk of flap necrosis in murine models: A systematic review.

John P Garcia, Francisco R Avila, Ricardo A Torres-Guzman, Karla C Maita, Abdullah S Eldaly, Luiza Palmieri, Omar Emam, Claudia C Chini, Eduardo N Chini, Antonio J Forte
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引用次数: 0

Abstract

Background and aim: Although a natural phenomenon, aging is a degenerative condition that promotes cellular malfunction and subsequent organ and body dysfunction. According to the World Health Organization, the elderly are the fastest growing age group worldwide. A 2012 population report stated that 43.1 million adults of 65 years or older lived in the United States, which is expected to jump to 83.7 million in 2050, placing an additional burden on an already stretched health-care network. Elderly patients broadly impact our health-care system, as reported in a 2014 wound report. 8.2 million patients were diagnosed with at least one type of wound, with patients 75 years or older making up most of the diagnoses. Aging affects all stages of the wound healing cascade. Although wound healing is downregulated in the elderly, scarce information exists regarding the effects of aging and flap survival in this group. Therefore, this study aims to report the impact of age on the survival of flaps in murine models. We hypothesize that increased aged animals will have decreased flap survival.

Methods: A systematic review was performed on February 1, 2022, following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis. We searched for full-text articles written in English, consisting of experimental murine models that compared flap survival between aged and young animals, in the following databases: PubMed, Scopus, CINAHL, and Web of Science. The terms "mice" OR "rats" AND "surgical flaps" AND "aging" guided our search. Models affected by chronic diseases were excluded from the study.

Results: Out of the 208 articles found by our search, seven were included according to our inclusion and exclusion criteria. Five studies used rats as experimental models, while the remaining two used mice. Local flaps were done in five studies, and two performed free flaps, transferring them from young and aged animals to young controls. Five articles reported lower flap survival in elder groups when exposed to ischemic insults. Three papers reported a deficiency in angiogenesis, vasculogenesis, and vascular reactivity as plausible causes for lack of survival, with one author correlating and verifying their results in human subjects. Although one article reported a lack of statistical power, they perceived a trend similar to the previous studies. Finally, one article reported inconclusive and variable results.

Conclusion: Evidence suggests that a lack of angiogenic and vasculogenic response in conjunction with decreased vascular reactivity are responsible for the diminished survival of flaps in the elder. Therapeutic means to boost the angiogenic, vasculogenic, and vascular reactivity response to improve patient outcomes require further research to understand the time course and mechanisms of flap survival in the elderly.

Relevance for patients: All humans will feel the effects of aging one way or another. However, we can all agree that aging affects our basic biological processes, which negatively affects macroscopic appearance. One of the essential aspects downregulated in the elderly is their ability to respond to tissue injury and hypoxia, creating non-favorable circumstances for wound healing. Furthermore, to manage these non-healing wounds, flaps are raised to create a covering for these defects. However, age also impacts the ability of these flaps to survive, augmenting the problem and entering a vicious circle. To improve outcomes, we must focus our future research on understanding the basic principles of how aging affects the survival of flaps in elderly population.

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衰老增加小鼠模型皮瓣坏死的风险:一项系统综述。
背景与目的:虽然是一种自然现象,但衰老是一种退行性疾病,它会导致细胞功能障碍和随后的器官和身体功能障碍。根据世界卫生组织的数据,老年人是世界上人口增长最快的年龄组。2012年的一份人口报告指出,美国有4,310万65岁或以上的成年人,预计到2050年这一数字将跃升至8,370万,给本已捉襟襟肘的医疗保健网络带来额外负担。正如2014年伤口报告所报告的那样,老年患者对我们的医疗保健系统产生了广泛的影响。820万患者被诊断患有至少一种类型的伤口,其中75岁或以上的患者占大多数。衰老会影响伤口愈合的所有阶段。虽然伤口愈合在老年人中下调,但关于衰老和皮瓣存活对老年人的影响的信息很少。因此,本研究旨在报道年龄对小鼠模型皮瓣存活的影响。我们假设年龄的增加会降低皮瓣的存活率。方法:于2022年2月1日按照系统评价和meta分析的首选报告项目进行系统评价。我们在PubMed、Scopus、CINAHL和Web of Science等数据库中检索了用英文撰写的文章全文,包括比较老年和幼年动物皮瓣存活率的实验小鼠模型。“小鼠”或“大鼠”、“外科皮瓣”和“衰老”等术语指导了我们的搜索。受慢性疾病影响的模型被排除在研究之外。结果:在我们检索到的208篇文章中,有7篇根据我们的纳入和排除标准被纳入。五项研究以大鼠为实验模型,其余两项研究以小鼠为实验模型。在五项研究中进行了局部皮瓣,两项研究进行了自由皮瓣,将它们从年轻和年老的动物转移到年轻的对照组。五篇文章报道了老年组暴露于缺血性损伤时下皮瓣存活。三篇论文报道了血管生成、血管生成和血管反应性缺乏是缺乏存活率的合理原因,一位作者将其结果与人类受试者进行了关联和验证。尽管有一篇文章报道缺乏统计能力,但他们发现了与之前研究相似的趋势。最后,一篇文章报告了不确定和可变的结果。结论:有证据表明,血管生成和血管生成反应的缺乏以及血管反应性的降低是导致老年人皮瓣存活率降低的原因。提高血管生成、血管生成和血管反应性的治疗手段以改善患者预后,需要进一步研究以了解老年人皮瓣存活的时间过程和机制。与患者相关:所有人都会以这样或那样的方式感受到衰老的影响。然而,我们都同意衰老会影响我们的基本生物过程,从而对宏观外观产生负面影响。老年人下调的一个重要方面是他们对组织损伤和缺氧的反应能力,这为伤口愈合创造了不利的环境。此外,为了处理这些无法愈合的伤口,皮瓣被提起来为这些缺陷创造一个覆盖物。然而,年龄也会影响这些皮瓣的生存能力,从而加剧了问题并进入恶性循环。为了改善结果,我们必须将未来的研究重点放在了解衰老如何影响老年人皮瓣存活的基本原理上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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