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Towards Clinical Application of Neurotrophic Factors to the Auditory Nerve; Assessment of Safety and Efficacy by a Systematic Review of Neurotrophic Treatments in Humans

机译:神经营养因子在听神经中的临床应用通过系统评价人类的神经营养疗法评估安全性和有效性

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Animal studies have evidenced protection of the auditory nerve by exogenous neurotrophic factors. In order to assess clinical applicability of neurotrophic treatment of the auditory nerve, the safety and efficacy of neurotrophic therapies in various human disorders were systematically reviewed. Outcomes of our literature search included disorder, neurotrophic factor, administration route, therapeutic outcome, and adverse event. From 2103 articles retrieved, 20 randomized controlled trials including 3974 patients were selected. Amyotrophic lateral sclerosis (53%) was the most frequently reported indication for neurotrophic therapy followed by diabetic polyneuropathy (28%). Ciliary neurotrophic factor (50%), nerve growth factor (24%) and insulin-like growth factor (21%) were most often used. Injection site reaction was a frequently occurring adverse event (61%) followed by asthenia (24%) and gastrointestinal disturbances (20%). Eighteen out of 20 trials deemed neurotrophic therapy to be safe, and six out of 17 studies concluded the neurotrophic therapy to be effective. Positive outcomes were generally small or contradicted by other studies. Most non-neurodegenerative diseases treated by targeted deliveries of neurotrophic factors were considered safe and effective. Hence, since local delivery to the cochlea is feasible, translation from animal studies to human trials in treating auditory nerve degeneration seems promising.
机译:动物研究证明外源性神经营养因子对听觉神经有保护作用。为了评估听神经神经营养治疗的临床适用性,系统评价了神经营养治疗在各种人类疾病中的安全性和有效性。我们文献检索的结果包括疾病,神经营养因子,给药途径,治疗结果和不良事件。从检索到的2103篇文章中,选择了20项包括3974例患者的随机对照试验。肌萎缩性侧索硬化症(53%)是神经营养疗法最常见的适应症,其次是糖尿病性多神经病(28%)。睫状神经营养因子(50%),神经生长因子(24%)和胰岛素样生长因子(21%)最常用。注射部位反应是经常发生的不良事件(61%),其次是乏力(24%)和胃肠道不适(20%)。 20项试验中有18项认为神经营养疗法是安全的,而17项研究中有6项认为神经营养疗法是有效的。阳性结果通常很小或与其他研究相矛盾。通过定向递送神经营养因子治疗的大多数非神经退行性疾病被认为是安全有效的。因此,由于局部递送至耳蜗是可行的,因此从动物研究到人体试验的治疗听神经变性的翻译似乎是有希望的。

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