Kvestad Ellen, Czajkowski Nikolai, Engdahl Bo, Hoffman Howard J, Tambs Kristian
Norwegian Institute of Public Health, Oslo, Norway.
Arch Otolaryngol Head Neck Surg. 2010 Feb;136(2):178-82. doi: 10.1001/archoto.2009.220.
To estimate the heritability of tinnitus.
Self-report questionnaire data collected from August 1, 1995, through June 30, 1997, from individuals in the Nord-Trøndelag Hearing Loss Study (an integrated part of the Nord-Trøndelag Health Study) were used. The study also included information on first-degree family relationships, and age-corrected polychoric correlations of relatives' tinnitus status were calculated. A structural equation model was fit to the data, and the relative contributions of genes and unique environmental effects were estimated. Models that included sex-specific effects were also tested.
Nord-Trøndelag County, Norway.
A population-based sample of 12 940 spouses, 27 607 parent-offspring, and 11 498 siblings was used. A total of 28 066 respondents were tested twice, yielding a test-retest correlation of 0.65 for the report of tinnitus.
Heritability of tinnitus.
Correlations for parent-offspring ranged from 0.01 to 0.07 for the various sex combinations, sibling correlation ranged from 0.06 to 0.14, and the spouse correlation was 0.04. This family correlation pattern implies an upper limit for heritability of 0.11 with no sex differences in the heritability estimates.
This is the first large population-based family study, to our knowledge, to report on the heritability of tinnitus. In contrast to previous speculations in the literature, this low heritability indicates that additive genetic effects explain only a small proportion of the variance of tinnitus in the population.
评估耳鸣的遗传度。
使用了从1995年8月1日至1997年6月30日从北特伦德拉格听力损失研究(北特伦德拉格健康研究的一个组成部分)中的个体收集的自我报告问卷数据。该研究还包括一级亲属关系信息,并计算了亲属耳鸣状态的年龄校正多系列相关系数。对数据拟合了结构方程模型,并估计了基因和独特环境效应的相对贡献。还测试了包括性别特异性效应的模型。
挪威北特伦德拉格郡。
使用了基于人群的样本,包括12940对配偶、27607对亲子和11498对兄弟姐妹。共有28066名受访者接受了两次测试,耳鸣报告的重测相关系数为0.65。
耳鸣的遗传度。
不同性别组合的亲子相关系数在0.01至0.07之间,兄弟姐妹相关系数在0.06至0.14之间,配偶相关系数为0.04。这种家族相关模式意味着遗传度上限为0.11,遗传度估计中无性别差异。
据我们所知,这是第一项基于大规模人群的家族研究,报告了耳鸣的遗传度。与文献中先前的推测相反,这种低遗传度表明加性基因效应仅解释了人群中耳鸣变异的一小部分。