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

被引:21
|
作者
O'Connor, Emer [1 ,2 ,3 ]
Simpson, Benjamin S. [4 ]
Houlden, Henry [1 ]
Vandrovcova, Jana [1 ]
Matharu, Manjit [2 ,3 ]
机构
[1] UCL Inst Neurol, Inst Neurol, Dept Neuromuscular Disorders, DMN, Queen Sq, London WC1N 3BG, England
[2] UCL Inst Neurol, Headache & Facial Pain Grp, Queen Sq, London, England
[3] Natl Hosp Neurol & Neurosurg, Queen Sq, London, England
[4] UCL, UCL Div Surg & Intervent Sci, London, England
来源
JOURNAL OF HEADACHE AND PAIN | 2020年 / 21卷 / 01期
基金
英国惠康基金;
关键词
Cluster headache; Trigeminal autonomic cephalalgia; Headache; Genetics; Gene; Systematic review; Meta-analysis; Family history; Heritability; Heredity; Inheritance; G1246A POLYMORPHISM; ASSOCIATION; GENE; MIGRAINE;
D O I
10.1186/s10194-020-01101-w
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
IntroductionThe 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.MethodsOur 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 To further ameliorate the accuracy of our analysis we included an additional unpublished cohort of CH patients recruited at a tertiary referral centre for headache, who underwent detailed family history with diagnostic verification in relatives.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.ResultsIn 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-2 of 73%. Fitted models for gender subgroups showed higher estimates 9.26% (95% CI: 6.29-13.43%) in females. However the I-2 for the female model was 58.42% and significant (p=0.047).ConclusionOur 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.
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页数:10
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