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1型神经纤维瘤病患儿使用他汀类药物:随机对照试验的系统评价

Statins in Children with Neurofibromatosis Type 1: A Systematic Review of Randomized Controlled Trials.

作者信息

Agouridis Aris P, Palli Nikoletta, Karagiorga Vasiliki-Eirini, Konsoula Afroditi, Markaki Lamprini, Spernovasilis Nikolaos, Tsioutis Constantinos

机构信息

School of Medicine, European University Cyprus, 2404 Nicosia, Cyprus.

Department of Internal Medicine, German Oncology Center, 4108 Limassol, Cyprus.

出版信息

Children (Basel). 2023 Sep 15;10(9):1556. doi: 10.3390/children10091556.

Abstract

BACKGROUND

Statins, apart from their plasma-cholesterol-lowering ability, exert several pleiotropic effects, making them a potential treatment for other diseases. Animal studies have showed that statins, through the inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase, can affect the Ras/MAPK pathway, thus providing impetus to examine the efficacy of statins in the pediatric population with neurofibromatosis type 1 (NF1). We aimed to systematically address all relevant evidence of statin treatment in children with NF1.

METHODS

We searched PubMed and Cochrane Library resources up to 2 June 2023 for randomized controlled trials (RCTs) written in English and evaluating statins versus placebo in children with NF1 (PROSPERO registration number: CRD42023439424).

RESULTS

Seven RCTs were suitable to be included in this qualitative synthesis, with a total participation of 336 children with NF1. The duration of the studies ranged from 12 to 52 weeks. The mean age of the pediatric population was 10.9 years old. Three studies investigated the role of simvastatin, while four studies examined lovastatin. According to our analysis, neither simvastatin nor lovastatin improved cognitive function, full-scale intelligence, school performance, attention problems, or internalizing behavioral problems when compared with placebo in children with NF1. Statins were well tolerated in all included RCTs.

CONCLUSION

Although safe, current evidence demonstrates that statins exert no beneficial effect in cognitive function and behavioral problems in children with NF1.

摘要

背景

他汀类药物除了具有降低血浆胆固醇的能力外,还具有多种多效性作用,使其成为治疗其他疾病的潜在药物。动物研究表明,他汀类药物通过抑制3-羟基-3-甲基戊二酰辅酶A还原酶,可影响Ras/丝裂原活化蛋白激酶(MAPK)途径,从而促使人们研究他汀类药物在1型神经纤维瘤病(NF1)儿童患者中的疗效。我们旨在系统地梳理有关他汀类药物治疗NF1儿童的所有相关证据。

方法

我们检索了截至2023年6月2日的PubMed和Cochrane图书馆资源,以查找用英文撰写的、评估他汀类药物与安慰剂治疗NF1儿童的随机对照试验(RCT)(国际前瞻性系统评价注册库注册号:CRD42023439424)。

结果

七项RCT适合纳入本定性综合分析,共有336名NF1儿童参与。研究持续时间为12至52周。儿科人群的平均年龄为10.9岁。三项研究调查了辛伐他汀的作用,四项研究考察了洛伐他汀。根据我们的分析,与安慰剂相比,辛伐他汀和洛伐他汀均未改善NF1儿童的认知功能、全量表智力、学业成绩、注意力问题或内化行为问题。在所有纳入的RCT中,他汀类药物耐受性良好。

结论

尽管他汀类药物安全,但目前的证据表明,它们对NF1儿童的认知功能和行为问题没有有益影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7907/10528298/2f7f87fd9282/children-10-01556-g001.jpg

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