Department of Environmental Health Sciences, School of Public Health and Health Sciences, University of Massachusetts Amherst, 173A Goessmann, 686 North Pleasant Street, Amherst, MA 01003, USA.
Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, 3127 Scott Hall, 540 East Canfield, Detroit, MI 48201, USA.
Hum Reprod. 2017 Nov 1;32(11):2159-2169. doi: 10.1093/humrep/dex283.
Are preconception phthalate and phthalate replacements associated with sperm differentially methylated regions (DMRs) among men undergoing IVF?
Ten phthalate metabolites were associated with 131 sperm DMRs that were enriched in genes related to growth and development, cell movement and cytoskeleton structure.
Several phthalate compounds and their metabolites are known endocrine disrupting compounds and are pervasive environmental contaminants. Rodent studies report that prenatal phthalate exposures induce sperm DMRs, but the influence of preconception phthalate exposure on sperm DNA methylation in humans is unknown.
STUDY DESIGN, SIZE, DURATION: An exploratory cross-sectional study with 48 male participants from the Sperm Environmental Epigenetics and Development Study (SEEDS).
PARTICIPANTS/MATERIALS, SETTING, METHODS: The first 48 couples provided a spot urine sample on the same day as semen sample procurement. Sperm DNA methylation was assessed with the HumanMethylation 450 K array. Seventeen urinary phthalate and 1,2-Cyclohexane dicarboxylic acid diisononyl ester (DINCH) metabolite concentrations were measured from spot urine samples. The A-clust algorithm was employed to identify co-regulated regions. DMRs associated with urinary metabolite concentrations were identified via linear models, corrected for false discovery rate (FDR).
Adjusting for age, BMI, and current smoking, 131 DMRs were associated with at least one urinary metabolite. Most sperm DMRs were associated with anti-androgenic metabolites, including mono(2-ethylhexyl) phthalate (MEHP, n = 83), mono(2-ethyl-5-oxohexyl) phthalate (MEOHP, n = 16), mono-n-butyl phthalate (MBP, n = 22) and cyclohexane-1,2-dicarboxylic acid-monocarboxy isooctyl (MCOCH, n = 7). The DMRs were enriched in lincRNAs as well as in regions near coding regions. Functional analyses of DMRs revealed enrichment of genes related to growth and development as well as cellular function and maintenance. Finally, 13% of sperm DMRs were inversely associated with high quality blastocyst-stage embryos after IVF.
LIMITATIONS, REASONS FOR CAUTION: Our modest sample size only included 48 males and additional larger studies are necessary to confirm our observed results. Non-differential misclassification of exposure is also a concern given the single spot urine collection.
To our knowledge, this is the first study to report that preconception urinary phthalate metabolite concentrations are associated with sperm DNA methylation in humans. These results suggest that paternal adult environmental conditions may influence epigenetic reprogramming during spermatogenesis, and in turn, influence early-life development.
STUDY FUNDING/COMPETING INTEREST(S): This work was supported by grant K22-ES023085 from the National Institute of Environmental Health Sciences. The authors declare no competing interests.
在接受试管婴儿治疗的男性中,孕前邻苯二甲酸酯和邻苯二甲酸酯替代品与精子差异甲基化区域(DMRs)有关吗?
十种邻苯二甲酸代谢物与 131 个精子 DMR 相关,这些 DMR 富集在与生长和发育、细胞运动和细胞骨架结构相关的基因中。
几种邻苯二甲酸化合物及其代谢物是已知的内分泌干扰化合物,也是普遍存在的环境污染物。啮齿动物研究报告称,产前邻苯二甲酸暴露会导致精子 DMR,但孕前邻苯二甲酸暴露对人类精子 DNA 甲基化的影响尚不清楚。
研究设计、大小和持续时间:这是一项探索性的横断面研究,共有 48 名来自精子环境表观遗传学和发育研究(SEEDS)的男性参与者。
参与者/材料、设置、方法:前 48 对夫妇在采集精液样本的同一天提供了一份尿液样本。通过 HumanMethylation 450 K 阵列评估精子 DNA 甲基化。从尿液样本中测量了 17 种尿邻苯二甲酸和 1,2-环己烷二羧酸二异壬酯(DINCH)代谢物浓度。采用 A-clust 算法识别共同调节区域。通过线性模型识别与尿代谢物浓度相关的 DMR,并通过错误发现率(FDR)进行校正。
调整年龄、BMI 和当前吸烟状况后,有 131 个 DMR 与至少一种尿代谢物相关。大多数精子 DMR 与抗雄激素代谢物有关,包括单(2-乙基己基)邻苯二甲酸酯(MEHP,n=83)、单(2-乙基-5-氧代己基)邻苯二甲酸酯(MEOHP,n=16)、单正丁基邻苯二甲酸酯(MBP,n=22)和环己烷-1,2-二羧酸单甲酯异辛基(MCOCH,n=7)。DMRs 在 lincRNAs 以及靠近编码区域的区域中富集。DMRs 的功能分析显示,与生长和发育以及细胞功能和维持相关的基因富集。最后,在接受试管婴儿治疗后,13%的精子 DMR 与高质量的囊胚阶段胚胎呈负相关。
局限性、谨慎的原因:我们的样本量较小,仅包括 48 名男性,需要更大规模的研究来证实我们的观察结果。鉴于单次尿液采集,非差异的暴露错误分类也是一个问题。
据我们所知,这是第一项报告孕前尿邻苯二甲酸代谢物浓度与人类精子 DNA 甲基化有关的研究。这些结果表明,父亲的成年环境条件可能会影响精子发生过程中的表观遗传重编程,并进而影响生命早期的发育。
研究资金/利益冲突:本工作得到美国国立环境卫生科学研究所 K22-ES023085 基金的支持。作者没有利益冲突。