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全基因组关联研究与常见和持续的宫颈高危型人乳头瘤病毒(HPV)感染。

Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection.

机构信息

Department of Epidemiology and Public Health, University of Maryland School of Medicine, 660 West Redwood Street, Howard Hall, Room 119, Baltimore, MD, 21201, USA.

University of Maryland Greenebaum Comprehensive Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA.

出版信息

BMC Med Genet. 2020 Nov 23;21(1):231. doi: 10.1186/s12881-020-01156-1.

Abstract

BACKGROUND

Genetic factors may influence the susceptibility to high-risk (hr) human papillomavirus (HPV) infection and persistence. We conducted the first genome-wide association study (GWAS) to identify variants associated with cervical hrHPV infection and persistence.

METHODS

Participants were 517 Nigerian women evaluated at baseline and 6 months follow-up visits for HPV. HPV was characterized using SPF/LiPA. hrHPV infection was positive if at least one carcinogenic HPV genotype was detected in a sample provided at the baseline visit and persistent if at least one carcinogenic HPV genotype was detected in each of the samples provided at the baseline and follow-up visits. Genotyping was done using the Illumina Multi-Ethnic Genotyping Array (MEGA) and imputation was done using the African Genome Resources Haplotype Reference Panel. Association analysis was done for hrHPV infection (125 cases/392 controls) and for persistent hrHPV infection (51 cases/355 controls) under additive genetic models adjusted for age, HIV status and the first principal component (PC) of the genotypes.

RESULTS

The mean (±SD) age of the study participants was 38 (±8) years, 48% were HIV negative, 24% were hrHPV positive and 10% had persistent hrHPV infections. No single variant reached genome-wide significance (p < 5 X 10). The top three variants associated with hrHPV infections were intronic variants clustered in KLF12 (all OR: 7.06, p = 1.43 × 10). The top variants associated with cervical hrHPV persistence were in DAP (OR: 6.86, p = 7.15 × 10), NR5A2 (OR: 3.65, p = 2.03 × 10) and MIR365-2 (OR: 7.71, p = 2.63 × 10) gene regions.

CONCLUSIONS

This exploratory GWAS yielded suggestive candidate risk loci for cervical hrHPV infection and persistence. The identified loci have biological annotation and functional data supporting their role in hrHPV infection and persistence. Given our limited sample size, larger discovery and replication studies are warranted to further characterize the reported associations.

摘要

背景

遗传因素可能会影响高危(hr)人乳头瘤病毒(HPV)感染和持续感染的易感性。我们进行了首次全基因组关联研究(GWAS),以鉴定与宫颈 hrHPV 感染和持续感染相关的变异。

方法

517 名尼日利亚女性参加了本研究,在基线和 6 个月的随访时进行 HPV 检测。HPV 采用 SPF/LiPA 进行特征分析。基线时检测到至少一种致癌 HPV 基因型则为阳性 HPV 感染,如果在基线和随访时的每个样本中均检测到至少一种致癌 HPV 基因型则为持续 HPV 感染。基因分型采用 Illumina 多族裔基因分型阵列(MEGA)进行,使用非洲基因组资源单体型参考面板进行单倍型推断。采用加性遗传模型,调整年龄、HIV 状态和基因型的第一主成分(PC),对 hrHPV 感染(125 例/392 例对照)和持续 hrHPV 感染(51 例/355 例对照)进行关联分析。

结果

研究参与者的平均(±SD)年龄为 38(±8)岁,48%为 HIV 阴性,24%为 hrHPV 阳性,10%为持续 hrHPV 感染。没有单个变异达到全基因组显著水平(p < 5 X 10)。与 hrHPV 感染相关的前三个变异是位于 KLF12 中的内含子变异簇(所有 OR:7.06,p = 1.43×10)。与宫颈 hrHPV 持续感染相关的前三个变异是位于 DAP(OR:6.86,p = 7.15×10)、NR5A2(OR:3.65,p = 2.03×10)和 MIR365-2(OR:7.71,p = 2.63×10)基因区域。

结论

这项探索性 GWAS 产生了宫颈 hrHPV 感染和持续感染的候选风险基因座的提示性结果。鉴定出的基因座具有生物学注释和功能数据,支持它们在 hrHPV 感染和持续感染中的作用。鉴于我们的样本量有限,需要进行更大的发现和复制研究,以进一步描述报告的关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b3/7682060/78601432ab19/12881_2020_1156_Fig1_HTML.jpg

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