Genome-Wide Association Analyses in Family Triads and Dyads Following Assisted Reproductive Technology

IF 1.7 4区 医学 Q3 GENETICS & HEREDITY
Siri N. Skodvin, Håkon K. Gjessing, Astanand Jugessur, Julia Romanowska, Alexandra Havdahl, Siri E. Håberg, Hans Ivar Hanevik, Robert Lyle, Rolv Terje Lie, Miriam Gjerdevik
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Abstract

Genetic selection occurs at different stages before a successful birth. The genetic makeup of a couple may influence the likelihood of needing assisted reproductive technology (ART) to achieve conception. However, frequent early fetal losses may also be perceived as reduced couple fertility and may thus be a contributing factor to the need for ART treatment. As ART procedures may enhance early fetal survival, genes that impact fetal viability may have a different allele distribution in ART offspring than expected under Mendelian transmission, as well as compared with the general population. With genetic data available from the Norwegian Mother, Father, and Child Cohort Study, we defined fetal survival as the study outcome and analyzed 1336 case-parent triads and dyads where the offspring were conceived by ART. Using log-linear models implemented in the R package Haplin, we conducted genome-wide scans to estimate fetal, maternal, and parent-of-origin effects and provided a detailed discussion on how these effects are estimated and interpreted. We detected fetal effects for single-nucleotide polymorphisms (SNPs) located in CXXC4-AS1, OPCML, and DYNLRB2-AS1. Since these effects were not observed in a limited follow-up analysis of non-ART triads, the identified effects are unlikely caused by genetic selection before fertilization.

辅助生殖技术后家庭三联体和双联体的全基因组关联分析
基因选择发生在成功分娩前的不同阶段。一对夫妇的基因组成可能会影响需要辅助生殖技术(ART)来实现受孕的可能性。然而,频繁的早期胎儿丢失也可能被视为夫妇生育能力下降,因此可能是需要抗逆转录病毒治疗的一个因素。由于抗逆转录病毒治疗可以提高早期胎儿存活率,影响胎儿生存能力的基因在抗逆转录病毒治疗后代中的等位基因分布可能与孟德尔传播下的预期不同,也可能与一般人群的等位基因分布不同。利用来自挪威母亲、父亲和儿童队列研究的遗传数据,我们将胎儿存活率定义为研究结果,并分析了1336例通过ART受孕的父母三胞胎和双胞胎。利用R软件包Haplin中实现的对数线性模型,我们进行了全基因组扫描,以估计胎儿、母亲和父母的起源效应,并就如何估计和解释这些效应提供了详细的讨论。我们检测了CXXC4-AS1、OPCML和DYNLRB2-AS1的单核苷酸多态性(snp)对胎儿的影响。由于在有限的非art三联体随访分析中没有观察到这些影响,因此所确定的影响不太可能是受精前的遗传选择引起的。
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来源期刊
Genetic Epidemiology
Genetic Epidemiology 医学-公共卫生、环境卫生与职业卫生
CiteScore
4.40
自引率
9.50%
发文量
49
审稿时长
6-12 weeks
期刊介绍: Genetic Epidemiology is a peer-reviewed journal for discussion of research on the genetic causes of the distribution of human traits in families and populations. Emphasis is placed on the relative contribution of genetic and environmental factors to human disease as revealed by genetic, epidemiological, and biologic investigations. Genetic Epidemiology primarily publishes papers in statistical genetics, a research field that is primarily concerned with development of statistical, bioinformatical, and computational models for analyzing genetic data. Incorporation of underlying biology and population genetics into conceptual models is favored. The Journal seeks original articles comprising either applied research or innovative statistical, mathematical, computational, or genomic methodologies that advance studies in genetic epidemiology. Other types of reports are encouraged, such as letters to the editor, topic reviews, and perspectives from other fields of research that will likely enrich the field of genetic epidemiology.
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