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DLA Ⅱ类单体型与标准贵宾犬原发性肾上腺皮质功能减退症呈性别特异性相关。

DLA class II haplotypes show sex-specific associations with primary hypoadrenocorticism in Standard Poodle dogs.

机构信息

Department of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, MN, 55108, USA.

Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, MN, 55108, USA.

出版信息

Immunogenetics. 2019 May;71(5-6):373-382. doi: 10.1007/s00251-019-01113-0. Epub 2019 Apr 9.

Abstract

Addison's disease (AD) is a life-threatening endocrine disorder that occurs spontaneously in both humans and dogs. Associations between MHC class II genes and AD have been shown in several human studies. Our goal was to identify MHC class II associations with AD in a large population of Standard Poodles, a breed highly predisposed to AD. We sequenced exon 2 of the class II genes DLA-DRB1, DLA-DQA1, and DLA-DQB1 in 110 affected and 101 unaffected Standard Poodles and tested for association with AD. After correcting for population structure, two haplotypes were found to confer risk of developing AD in a sex-specific manner: DLA-DRB1015:01-DQA1006:01-DQB1023:01 in males (xp = 0.03, OR 2.1) and DLA-DRB1009:01-DQA1001:01-DQB1008:01:1 in females (xp = 0.02, OR 8.43). Sex-specific associations have been previously described in human populations, but this is the first report of this kind in dogs. Consistent with findings in other studies, we found the DLA-DQA1006:01 allele (xp = 0.04) to be associated with AD in males independent of haplotype. In females, the haplotype DLA-DRB1009:01-DQA1001:01-DQB1008:01:1 confers a very high risk for developing AD, although its frequency was rare (9 of 124 females) in our study population. Further studies are warranted to validate the findings of this exploratory dataset and to assess the usefulness of this haplotype as a risk marker for AD in female Standard Poodles. Our results highlight the importance of evaluating MHC class II disease associations in large populations, and accounting for both biological sex and population structure.

摘要

艾迪生氏病(Addison's disease,AD)是一种危及生命的内分泌紊乱疾病,在人类和犬类中均可自发发生。几项人类研究表明,MHC Ⅱ类基因与 AD 之间存在关联。我们的目标是在大型标准贵宾犬群体中鉴定与 AD 相关的 MHC Ⅱ类基因,该品种极易患 AD。我们对 110 只患病和 101 只未患病的标准贵宾犬的 MHC Ⅱ类基因 DLA-DRB1、DLA-DQA1 和 DLA-DQB1 的外显子 2 进行了测序,并检测了其与 AD 的相关性。在对群体结构进行校正后,发现两种单倍型以性别特异性的方式赋予了患 AD 的风险:雄性中的 DLA-DRB1015:01-DQA1006:01-DQB1023:01(xp=0.03,OR 2.1)和雌性中的 DLA-DRB1009:01-DQA1001:01-DQB1008:01:1(xp=0.02,OR 8.43)。这种性别特异性的关联在人类群体中已有先前的描述,但这是首次在犬类中报告。与其他研究的发现一致,我们发现 DLA-DQA1006:01 等位基因(xp=0.04)在雄性中与 AD 相关,而与单倍型无关。在雌性中,DLA-DRB1009:01-DQA1001:01-DQB1008:01:1 单倍型赋予了极高的 AD 发病风险,尽管在我们的研究人群中其频率很低(124 只雌性中 9 只)。需要进一步的研究来验证这个探索性数据集的发现,并评估这种单倍型作为雌性标准贵宾犬 AD 的风险标记的有用性。我们的结果强调了在大群体中评估 MHC Ⅱ类疾病关联以及考虑生物性别和群体结构的重要性。

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