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基于人群的加拿大队列中多发性硬化症的亲代传播

Parental transmission of MS in a population-based Canadian cohort.

作者信息

Herrera B M, Ramagopalan S V, Orton S, Chao M J, Yee I M, Sadovnick A D, Ebers G C

机构信息

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

出版信息

Neurology. 2007 Sep 18;69(12):1208-12. doi: 10.1212/01.wnl.0000268486.40851.d6. Epub 2007 Jun 27.

Abstract

OBJECTIVE

Genetic and environmental factors have important roles in multiple sclerosis (MS) susceptibility. The precise nature of these factors and mode of inheritance remains unknown. A female predominance is universally found. Recently, offspring of affected fathers were reported to be more likely to have MS than those of affected mothers. This was attributed to the Carter effect, which is seen in polygenic disorders. The Carter effect predicts that affected parents of the sex lesser affected by a disease/trait are more genetically loaded for risk alleles and thus transmit these more often to their offspring. This hypothesis was tested in a population-based Canadian MS cohort.

METHODS

Using the longitudinal Canadian database, we identified 3,088 nuclear families with one affected parent and a total of 8,401 offspring, of which 798 had MS. Transmission to daughters and sons from affected mothers and fathers was compared.

RESULTS

There was equal transmission of MS from affected fathers vs affected mothers (9.41% vs 9.76%). Stratifying by gender of affected parent there were no differences in the female:male sex ratio of affected (2.46% vs 2.41%, p = 0.88) or unaffected offspring (0.91% vs 0.95%, p = 0.46).

CONCLUSIONS

We observed equal disease transmission to offspring from affected mothers and affected fathers, no difference in the female:male sex ratio of affected offspring, and previously no difference in sibling recurrence risk by gender of parent affected. These findings show no evidence for the Carter effect and do not support the hypothesis of polygenic inheritance of multiple sclerosis susceptibility by parent.

摘要

目的

遗传和环境因素在多发性硬化症(MS)易感性中起重要作用。这些因素的确切性质和遗传模式尚不清楚。普遍发现女性患者居多。最近有报道称,患病父亲的后代比患病母亲的后代更易患MS。这被归因于卡特效应,该效应在多基因疾病中可见。卡特效应预测,受疾病/性状影响较小的性别的患病父母携带更多风险等位基因,因此更常将这些基因传递给后代。在一个基于人群的加拿大MS队列中对这一假设进行了检验。

方法

利用加拿大纵向数据库,我们识别出3088个有一位患病父母的核心家庭,共有8401名后代,其中798人患有MS。比较了患病母亲和患病父亲向女儿和儿子的疾病传递情况。

结果

患病父亲与患病母亲的MS传递率相同(9.41%对9.76%)。按患病父母的性别分层,患病后代的女性:男性性别比例(2.46%对2.41%,p = 0.88)或未患病后代的女性:男性性别比例(0.91%对0.95%,p = 0.46)均无差异。

结论

我们观察到患病母亲和患病父亲向后代的疾病传递率相同,患病后代的女性:男性性别比例无差异,且之前按患病父母性别分类的同胞复发风险也无差异。这些发现没有证据支持卡特效应,也不支持父母对多发性硬化症易感性的多基因遗传假说。

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