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复发性妊娠丢失中 8.1 祖先单倍型的遗传。

Inheritance of the 8.1 ancestral haplotype in recurrent pregnancy loss.

机构信息

Recurrent Pregnancy Loss Unit, Fertility Clinic 4071, University Hospital Copenhagen Rigshospitalet, Blegdamsvej 9, Copenhagen Ø 2100, Denmark;

Department of Clinical Immunology, Aalborg University Hospital, North, Urbansgade 32, Aalborg 9000, Denmark;

出版信息

Evol Med Public Health. 2015 Dec 16;2015(1):325-31. doi: 10.1093/emph/eov031. Print 2015.

Abstract

BACKGROUND AND OBJECTIVES

The 8.1 ancestral haplotype (AH) (HLA-A1, C7, B8, C4AQ0, C4B1, DR3, DQ2) is a remarkably long and conserved haplotype in the human major histocompatibility complex. It has been associated with both beneficial and detrimental effects, consistent with antagonistic pleiotropy. It has also been proposed that the survival of long, conserved haplotypes may be due to gestational drive, i.e. selective miscarriage of fetuses who have not inherited the haplotype from a heterozygous mother. Recurrent pregnancy loss (RPL) is defined as three or more consecutive pregnancy losses. The objective was to test the gestational drive theory for the 8.1AH in women with RPL and their live born children.

METHODOLOGY

We investigated the inheritance of the 8.1AH from 82 heterozygous RPL women to 110 live born children. All participants were genotyped for HLA-A, -B and -DRB1 in DNA from EDTA-treated blood or buccal swaps. Inheritance was compared with a Mendelian inheritance of 50% using a two-sided exact binomial test.

RESULTS

We found that 55% of the live born children had inherited the 8.1AH, which was not significantly higher than the expected 50% (P = 0.29). Interestingly, we found a non-significant trend toward a higher inheritance of the 8.1AH in girls, 63%, P = 0.11 as opposed to boys, 50%, P = 1.00.

CONCLUSIONS AND IMPLICATIONS

We did not find that the 8.1AH was significantly more often inherited by live born children of 8.1AH heterozygous RPL women. However our data suggest that there may be a sex-specific effect which would be interesting to explore further, both in RPL and in a background population.

摘要

背景和目的

8.1 祖先单倍型(AH)(HLA-A1、C7、B8、C4AQ0、C4B1、DR3、DQ2)是人类主要组织相容性复合体中一个非常长且保守的单倍型。它与有益和有害的影响有关,与拮抗多效性一致。也有人提出,长而保守的单倍型的存活可能是由于妊娠驱动,即选择性流产未从杂合母亲那里继承单倍型的胎儿。复发性妊娠丢失(RPL)定义为连续三次或更多次妊娠丢失。目的是在有 RPL 的女性及其活产儿中测试 8.1AH 的妊娠驱动理论。

方法

我们调查了 82 位杂合 RPL 女性的 8.1AH 向 110 位活产儿的遗传情况。所有参与者均在 EDTA 处理的血液或口腔拭子 DNA 中进行 HLA-A、-B 和 -DRB1 基因分型。使用双侧精确二项式检验,将遗传与 50%的孟德尔遗传进行比较。

结果

我们发现,55%的活产儿继承了 8.1AH,这与预期的 50%没有显著差异(P=0.29)。有趣的是,我们发现 8.1AH 女性的遗传率呈非显著上升趋势,为 63%,P=0.11,而男性为 50%,P=1.00。

结论和意义

我们没有发现 8.1AH 在 8.1AH 杂合 RPL 女性的活产儿中更常被遗传。然而,我们的数据表明,可能存在性别特异性效应,这在 RPL 和背景人群中都值得进一步探讨。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff4d/4681376/0d03fc07891c/eov031f1p.jpg

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