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全基因组关联研究常见单核苷酸多态性和罕见拷贝数变异在神经性厌食症中的作用。

A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.

机构信息

Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.

出版信息

Mol Psychiatry. 2011 Sep;16(9):949-59. doi: 10.1038/mp.2010.107. Epub 2010 Nov 16.

Abstract

Anorexia nervosa (AN) is a mental illness with high mortality that most commonly afflicts adolescent female individuals. Clinical symptoms include chronic food refusal, weight loss and body image distortions. We carried out a genome-wide association study on 1033 AN cases and 3733 pediatric control subjects, all of whom were of European ancestry and were genotyped on the Illumina HumanHap610 platform (Illumina, San Diego, CA, USA). We confirmed that common single-nucleotide polymorphisms (SNPs) within OPRD1 (rs533123, P=0.0015) confer risk for AN, and obtained suggestive evidence that common SNPs near HTR1D (rs7532266, P=0.04) confer risk for restricting-type AN specifically. However, no SNPs reached genome-wide significance in our data, whereas top association signals were detected near ZNF804B, CSRP2BP, NTNG1, AKAP6 and CDH9. In parallel, we performed genome-wide analysis on copy number variations (CNVs) using the signal intensity data from the SNP arrays. We did not find evidence that AN cases have more CNVs than control subjects, nor do they have over-representation of rare or large CNVs. However, we identified several regions with rare CNVs that were only observed in AN cases, including a recurrent 13q12 deletion (1.5 Mb) disrupting SCAS in two cases, and CNVs disrupting the CNTN6/CNTN4 region in several AN cases. In conclusion, our study suggests that both common SNPs and rare CNVs may confer genetic risk to AN. These results point to intriguing genes that await further validation in independent cohorts for confirmatory roles in AN.

摘要

神经性厌食症(AN)是一种死亡率较高的精神疾病,主要影响青少年女性。临床症状包括慢性拒食、体重减轻和身体形象扭曲。我们对 1033 例 AN 病例和 3733 名儿科对照进行了全基因组关联研究,所有研究对象均为欧洲血统,在 Illumina HumanHap610 平台(Illumina,圣地亚哥,CA,美国)上进行基因分型。我们证实了 OPRD1 内常见的单核苷酸多态性(SNPs)(rs533123,P=0.0015)可增加 AN 的风险,并且有证据表明 HTR1D 附近的常见 SNPs(rs7532266,P=0.04)可特别增加限制型 AN 的风险。然而,在我们的数据中,没有 SNPs 达到全基因组显著水平,而在 ZNF804B、CSRP2BP、NTNG1、AKAP6 和 CDH9 附近检测到最高的关联信号。同时,我们使用 SNP 阵列的信号强度数据对拷贝数变异(CNVs)进行了全基因组分析。我们没有发现 AN 病例比对照有更多的 CNVs 的证据,也没有发现罕见或大的 CNVs 的过度表达。然而,我们确定了几个仅在 AN 病例中观察到的罕见 CNV 区域,包括在两个病例中破坏 SCAS 的 13q12 缺失(1.5 Mb)和破坏几个 AN 病例中 CNTN6/CNTN4 区域的 CNV。总之,我们的研究表明,常见的 SNPs 和罕见的 CNVs 都可能为 AN 提供遗传风险。这些结果表明,一些有待进一步在独立队列中验证的基因在 AN 中可能具有确认作用。

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