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家族性偏头痛集群的患病率:系统评价和荟萃分析。

Prevalence of familial cluster headache: a systematic review and meta-analysis.

机构信息

Department of Neuromuscular Disorders, UCL Institute of Neurology, DMN, Institute of Neurology, Queen Square, London, WC1N 3BG, UK.

Headache and Facial Pain Group, UCL Institute of Neurology, Queen Square and The National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.

出版信息

J Headache Pain. 2020 Apr 25;21(1):37. doi: 10.1186/s10194-020-01101-w.

Abstract

INTRODUCTION

The population rate of familial cluster headache (CH) has been reported to be as high as 20% however this varies considerably across studies. To obtain a true estimate of family history in CH, we conducted a systematic review and meta-analysis of previously published data.

METHODS

Our systematic review involved a search of electronic databases (Medline, EMBASE, PubMed, CINAHL) to identify and appraise studies of interest utilising the PRISMA (Preferred Reporting Items for Systematic Review and Meta-Analysis) guidelines. To further ameliorate the accuracy of our analysis we included an additional unpublished cohort of CH patients recruited at a tertiary referral centre for headache, who underwent detailed family history with diagnostic verification in relatives. Data was extracted and meta-analysis conducted to provide a true estimation of family history.

RESULTS

In total, we identified 7 studies which fulfilled our inclusion criteria. The estimated true prevalence of CH patients with a positive family history was 6.27% (95% CI:4.65-8.40%) with an overall I of 73%. Fitted models for gender subgroups showed higher estimates 9.26% (95% CI: 6.29-13.43%) in females. However the I for the female model was 58.42% and significant (p = 0.047).

CONCLUSION

Our findings estimate a rate of family history in CH to be approximately 6.27% (95% CI: 4.65-8.40%). While estimates were larger for female probands, we demonstrated high heterogeneity in this subgroup. These findings further support a genetic role in the aetiology of CH.

摘要

简介

家族性集群性头痛(CH)的人群发病率据报道高达 20%,但不同研究之间差异很大。为了准确估计 CH 的家族史,我们对以前发表的数据进行了系统回顾和荟萃分析。

方法

我们的系统回顾包括对电子数据库(Medline、EMBASE、PubMed、CINAHL)的搜索,以识别和评估使用 PRISMA(系统评价和荟萃分析的首选报告项目)指南的相关研究。为了进一步提高我们分析的准确性,我们还纳入了在头痛三级转诊中心招募的 CH 患者的未发表队列,这些患者接受了详细的家族史调查,并对亲属进行了诊断验证。提取数据并进行荟萃分析,以提供家族史的真实估计。

结果

总共确定了 7 项符合纳入标准的研究。有阳性家族史的 CH 患者的真实估计患病率为 6.27%(95%CI:4.65-8.40%),总体 I 为 73%。性别亚组的拟合模型显示,女性的估计值更高,为 9.26%(95%CI:6.29-13.43%)。然而,女性模型的 I 为 58.42%,且具有统计学意义(p=0.047)。

结论

我们的研究结果估计 CH 的家族史发生率约为 6.27%(95%CI:4.65-8.40%)。虽然女性患者的估计值较大,但我们在该亚组中发现了高度异质性。这些发现进一步支持 CH 的病因学中存在遗传作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d8/7183702/ba2fd2ce1c65/10194_2020_1101_Fig1_HTML.jpg

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