The role of m6A methylation in prenatal maternal psychological distress and birth outcome

被引:0
|
作者
Li, Jing [1 ]
Gao, Xueyun [1 ]
Wang, Shan [1 ]
Yao, Dan [1 ]
Shao, Shuya [1 ]
Wu, Haoyue [1 ]
Xu, Meina [1 ]
Yi, Qiqi [1 ]
Xie, Longshan [2 ]
Zhu, Zhongliang [3 ]
Song, Dongli [4 ,5 ]
Li, Hui [1 ,6 ]
机构
[1] XVan Jiaotong Univ, Dept Neonatol, Affiliated Hosp 1, 277 West Yanta Rd, Xian 710061, Shaanxi, Peoples R China
[2] First Peoples Hosp Foshan, Dept Funct Neurosci, North 81 Lingnan Ave, Foshan 528000, Guangdong, Peoples R China
[3] Northwestern Univ, Maternal & Infant Hlth Res Inst, Med Coll, Key Lab Resource Biol & Biotechnol Western China, 229 Taibai North Rd, Xian 710069, Shaanxi, Peoples R China
[4] Santa Clara Valley Med Ctr, Dept Pediat, Div Neonatol, 751 South Bascom Ave, San Jose, CA 95128 USA
[5] Stanford Univ, Dept Pediat, Div Neonatal & Dev Med, Sch Med, 725 Welch Rd 2 West, Palo Alto, CA 94304 USA
[6] Xi An Jiao Tong Univ, Dept Neonatol, Affiliated Childrens Hosp, Xian 710002, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Prenatal maternal psychological distress; N6-methyladenosine (m6A) methylation; Birth weight; Gestational age; MESSENGER-RNA METHYLATION; PERINATAL DEPRESSION; PREGNANCY PREVALENCE; RISK-FACTORS; STRESS; ANXIETY; DEMETHYLASE; EXPRESSION; ALKBH5;
D O I
10.1016/j.jad.2023.05.098
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Prenatal maternal psychological distress (PMPD) is a known risk factor for adverse birth outcomes. N6-methyladenosine RNA (m6A) methylation is crucial in moderating RNA biology. This study aimed to evaluate the relationships between PMPD, birth outcomes, and placental m6A methylation.Methods: This was a prospective cohort study. PMPD exposure was assessed by questionnaires about prenatal stress, depression, and anxiety. Placental m6A methylation was measured using a colorimetric assay. The re-lationships between PMPD, m6A methylation, gestational age (GA), and birth weight (BW) were analyzed using structural equation models (SEMs). Maternal weight gain during pregnancy and infant sex were included as covariables. Results: The study included 209 mother-infant dyads. In an adjusted SEM, PMPD was associated with BW (B = -26.034; 95 % CI:-47.123,-4.868) and GA (B = - 0.603; 95 % CI:-1.102,-0.154). M6A methylation was associated with PMPD (B = 0.055; 95 % CI: 0.040,0.073) and BW (B = - 305.799; 95 % CI:-520.164,-86.460) but not GA. The effect of PMPD on BW was partially mediated by m6A methylation (B =-16.817; 95 % CI: -31.348,-4.638) and GA (B = - 12.280; 95 % CI:-23.612,-3.079). Maternal weight gain was associated with BW (B = 5.113; 95 % CI: 0.229,10.438). Limitations: The study sample size was small, and the specific mechanism of m6A methylation on birth outcomes needs to be further explored. Conclusions: In this study, PMPD exposure negatively affected BW and GA. Placental m6A methylation was associated with PMPD and BW and partially mediated the effect of PMPD on BW. Our findings highlight the importance of perinatal psychological evaluation and intervention.
引用
收藏
页码:52 / 59
页数:8
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