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前庭性偏头痛患病率研究与家族聚集性的系统评价

Systematic Review of Prevalence Studies and Familial Aggregation in Vestibular Migraine.

作者信息

Paz-Tamayo Ana, Perez-Carpena Patricia, Lopez-Escamez Jose A

机构信息

Division of Otolaryngology, Department of Surgery, Universidad de Granada, Granada, Spain.

Department of Otolaryngology, Instituto de Investigación Biosanitaria ibs.GRANADA, Hospital Universitario San Cecilio, Granada, Spain.

出版信息

Front Genet. 2020 Aug 31;11:954. doi: 10.3389/fgene.2020.00954. eCollection 2020.

Abstract

Vestibular migraine (VM) is complex disorder consisting of episodes of migraine and vertigo with an estimated prevalence of 1-3%. As migraine, it is considered that VM has genetic predisposition; however, evidence to support a genetic contribution has not been critically appraised. The aim of this systematic review is to assess available evidence in scientific publications to determine the role of inheritance in VM. After performing the quality assessment of the retrieved records, 31 studies were included (24 epidemiological reports and 7 genetic association studies in families or case-control in candidate genes). We gathered data about prevalence of VM in different populations and in families, and also about the genetic findings reported. In addition, other variables were considered to assess the heritability of VM, such as the ancestry, the age of onset or the familial history of vertigo and migraine. The estimated prevalence of VM was different between black (3.13%), white (2.64%) and Asian (1.07%) ethnicities. The reported prevalence of VM in migraine patients is higher in European countries (21%) than in Asian countries (10%). Moreover, the prevalence of the migraine-vertigo association in families is 4-10 times higher than the prevalence reported in the general population (sibling recurrence risk ratio λ = 4.31-10.42). We also found that the age of onset is lower in patients with simultaneous onset of symptoms and in those who have familial history for migraine and/or vertigo, suggesting anticipation. Although some genetic studies have reported few allelic variants associated to MV, replication studies are needed to validate these results. The available evidence to support heritability in VM is limited. Variability in prevalence depending on ethnicity and geographic location suggests a combined genetic and environmental contribution to VM. However, the familial aggregation observed in VM support genetic and shared familial environmental effects that remarks the necessity of twins and adoptees-based epidemiological studies to estimate its heritability.

摘要

前庭性偏头痛(VM)是一种复杂的疾病,由偏头痛和眩晕发作组成,估计患病率为1%-3%。与偏头痛一样,人们认为VM有遗传易感性;然而,支持遗传因素的证据尚未得到严格评估。本系统评价的目的是评估科学出版物中的现有证据,以确定遗传因素在VM中的作用。在对检索到的记录进行质量评估后,纳入了31项研究(24份流行病学报告和7项关于家族或候选基因病例对照的遗传关联研究)。我们收集了不同人群和家族中VM患病率的数据,以及所报道的遗传研究结果。此外,还考虑了其他变量来评估VM的遗传度,如血统、发病年龄或眩晕和偏头痛的家族史。VM的估计患病率在黑人(3.13%)、白人(2.64%)和亚洲人(1.07%)种族之间有所不同。欧洲国家偏头痛患者中VM的报告患病率(21%)高于亚洲国家(10%)。此外,家族中偏头痛-眩晕关联的患病率比普通人群中报告的患病率高4-10倍(同胞复发风险比λ=4.31-10.42)。我们还发现,症状同时出现的患者以及有偏头痛和/或眩晕家族史的患者发病年龄较低,提示有遗传早现现象。尽管一些基因研究报告了少数与MV相关的等位基因变异,但仍需要重复研究来验证这些结果。支持VM遗传度的现有证据有限。患病率因种族和地理位置而异,这表明遗传和环境因素共同作用于VM。然而,VM中观察到的家族聚集现象支持遗传和共同的家族环境效应,这表明有必要进行基于双胞胎和领养者的流行病学研究来估计其遗传度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/668a/7489493/a594e8ccae5d/fgene-11-00954-g0001.jpg

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