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斑秃的家族聚集性。

Familial aggregation of alopecia areata.

作者信息

Blaumeiser Bettina, van der Goot Ineke, Fimmers Rolf, Hanneken Sandra, Ritzmann Sibylle, Seymons Katia, Betz Regina C, Ruzicka Thomas, Wienker Thomas F, De Weert Jozef, Lambert Julien, Kruse Roland, Nöthen Markus M

机构信息

Department of Medical Genetics, University Hospital of Antwerp, Antwerp, Belgium.

出版信息

J Am Acad Dermatol. 2006 Apr;54(4):627-32. doi: 10.1016/j.jaad.2005.12.007. Epub 2006 Jan 23.

Abstract

BACKGROUND

Familial aggregation of alopecia areata (AA) has been previously described, but systematic studies with information obtained directly from family members have yet to be undertaken.

OBJECTIVE

We sought to study the pattern of familial aggregation of AA by assessing the affection status of patients' relatives. The study included 206 index patients with a total of 1029 first-degree and 2625 second-degree relatives.

METHODS

First-degree relatives were directly interviewed, whereas information on second-degree relatives was obtained by interviewing the index patients and their first-degree relatives.

RESULTS

Estimated lifetime risks were 7.1% in siblings, 7.8% in parents, and 5.7% in offspring. The risk in second-degree relatives was slightly higher than the reported population risk. Age at onset in index patients and first-degree relatives was significantly correlated.

LIMITATIONS

Using patients drawn from specialized hair clinics may have produced results showing a higher proportion of early onset and severe cases.

CONCLUSION

The familial aggregation of AA supports the role of genetic factors in the development of the disease. In addition, our data indicate genetic factors might contribute to the age at onset of AA.

摘要

背景

斑秃(AA)的家族聚集现象此前已有描述,但尚未开展过直接从家庭成员获取信息的系统性研究。

目的

我们试图通过评估患者亲属的患病情况来研究AA的家族聚集模式。该研究纳入了206例索引患者,共有1029名一级亲属和2625名二级亲属。

方法

直接对一级亲属进行访谈,而关于二级亲属的信息则通过访谈索引患者及其一级亲属获得。

结果

兄弟姐妹的终生患病风险估计为7.1%,父母为7.8%,子女为5.7%。二级亲属的风险略高于所报道的人群风险。索引患者及其一级亲属的发病年龄显著相关。

局限性

使用从专业毛发诊所选取的患者可能导致结果显示早发型和重症病例的比例更高。

结论

AA的家族聚集支持遗传因素在该疾病发生中的作用。此外,我们的数据表明遗传因素可能影响AA的发病年龄。

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