Department of Informative Genetics, Environment and Genome Research Center, Tohoku University Graduate School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai, 980-8575, Japan.
Kyono ART Clinic, 1-1-1, Honcho, Aoba-ku, Sendai, 980-0014, Japan.
Clin Epigenetics. 2019 Feb 7;11(1):21. doi: 10.1186/s13148-019-0623-3.
Human-assisted reproductive technologies (ART) are a widely accepted treatment for infertile couples. At the same time, many studies have suggested the correlation between ART and increased incidences of normally rare imprinting disorders such as Beckwith-Wiedemann syndrome (BWS), Angelman syndrome (AS), Prader-Willi syndrome (PWS), and Silver-Russell syndrome (SRS). Major methylation dynamics take place during cell development and the preimplantation stages of embryonic development. ART may prevent the proper erasure, establishment, and maintenance of DNA methylation. However, the causes and ART risk factors for these disorders are not well understood.
A nationwide epidemiological study in Japan in 2015 in which 2777 pediatrics departments were contacted and a total of 931 patients with imprinting disorders including 117 BWS, 227 AS, 520 PWS, and 67 SRS patients, were recruited. We found 4.46- and 8.91-fold increased frequencies of BWS and SRS associated with ART, respectively. Most of these patients were conceived via in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI), and showed aberrant imprinted DNA methylation. We also found that ART-conceived SRS (ART-SRS) patients had incomplete and more widespread DNA methylation variations than spontaneously conceived SRS patients, especially in sperm-specific methylated regions using reduced representation bisulfite sequencing to compare DNA methylomes. In addition, we found that the ART patients with one of three imprinting disorders, PWS, AS, and SRS, displayed additional minor phenotypes and lack of the phenotypes. The frequency of ART-conceived Prader-Willi syndrome (ART-PWS) was 3.44-fold higher than anticipated. When maternal age was 37 years or less, the rate of DNA methylation errors in ART-PWS patients was significantly increased compared with spontaneously conceived PWS patients.
We reconfirmed the association between ART and imprinting disorders. In addition, we found unique methylation patterns in ART-SRS patients, therefore, concluded that the imprinting disorders related to ART might tend to take place just after fertilization at a time when the epigenome is most vulnerable and might be affected by the techniques of manipulation used for IVF or ICSI and the culture medium of the fertilized egg.
人类辅助生殖技术(ART)是治疗不孕夫妇的一种广泛接受的方法。与此同时,许多研究表明,ART 与正常罕见印迹疾病的发生率增加有关,如 Beckwith-Wiedemann 综合征(BWS)、Angelman 综合征(AS)、Prader-Willi 综合征(PWS)和 Silver-Russell 综合征(SRS)。主要的甲基化动力学发生在细胞发育和胚胎发育的着床前阶段。ART 可能会阻止 DNA 甲基化的正确清除、建立和维持。然而,这些疾病的原因和 ART 风险因素尚不清楚。
2015 年,日本进行了一项全国性的流行病学研究,共联系了 2777 个儿科部门,共招募了 931 名印迹疾病患者,包括 117 名 BWS、227 名 AS、520 名 PWS 和 67 名 SRS 患者。我们发现 BWS 和 SRS 与 ART 相关的频率分别增加了 4.46 倍和 8.91 倍。这些患者大多通过体外受精(IVF)和胞浆内精子注射(ICSI)受孕,并表现出异常的印迹 DNA 甲基化。我们还发现,与自然受孕的 SRS 患者相比,ART 受孕的 SRS(ART-SRS)患者的 DNA 甲基化变异更不完整且更广泛,尤其是在使用简化重亚硫酸盐测序比较 DNA 甲基组时,精子特异性甲基化区域。此外,我们发现,三种印迹疾病之一的 ART 患者,即 PWS、AS 和 SRS,表现出额外的次要表型和缺乏表型。ART 受孕的 Prader-Willi 综合征(ART-PWS)的频率是预期的 3.44 倍。当母亲年龄为 37 岁或以下时,ART-PWS 患者的 DNA 甲基化错误率明显高于自然受孕的 PWS 患者。
我们再次证实了 ART 与印迹疾病之间的关联。此外,我们在 ART-SRS 患者中发现了独特的甲基化模式,因此得出结论,与 ART 相关的印迹疾病可能倾向于在胚胎发生时发生,此时表观基因组最脆弱,并且可能受到用于 IVF 或 ICSI 的操作技术和受精卵的培养基的影响。