Armatussolikha Herna Rizkia, Winarni Tri Indah, Maharani Nani, Dewantiningrum Julian, Muniroh Muflihatul
Magister Program of Biomedical Science, Faculty of Medicine Universitas Diponegoro, Semarang 50275, Indonesia.
Department of Anatomy, Faculty of Medicine, Universitas Diponegoro, Semarang, Central Java 50275, Indonesia; Center for Biomedical Research (CEBIOR), Faculty of Medicine, Universitas Diponegoro, Semarang, Central Java 50275, Indonesia.
Reprod Toxicol. 2024 Apr;125:108574. doi: 10.1016/j.reprotox.2024.108574. Epub 2024 Mar 8.
The GSTT1 and GSTM1 genes have a role in mercury metabolism and excretion, as well as blood pressure response, impacting birth outcomes. The present study assesses whether GSTT1 and GSTM1 deletion variants and maternal hair Hg concentration are associated with blood pressure and birth outcomes among the Indonesian coastal pregnant mother population. A cross-sectional study was conducted on 139 pregnant women in the Jepara coastal area of Central Java, Indonesia. Maternal characteristics during pregnancy, including blood pressure and birth outcomes, were collected. GSTT1 and GSTM1 gene variants were detected using polymerase chain reaction (PCR). Hair Hg levels were measured using the reducing-vaporization mercury analyzer. The mean maternal hair Hg concentration was 0.727±0.558 μg/g. GSTT1 genotype homozygous deletion was found in 41.7% of subjects, while no GSTM1 deletion was found. No statistically significant difference was found between deletion and non-deletion groups for hair Hg. GSTT1 deletion genotype shows protection but is inconclusive toward diastolic hypertension (p=0.048, OR 0.285, CI 0.077-1.052) and insignificant with birth outcomes (all p>0.05). High hair Hg concentration and positive history of cardiovascular diseases increase the risk of systolic and diastolic hypertension during pregnancy with OR 6.871 (CI 95% 1.445-32.660) and 8.518 (CI 95% 2.126-34.125), respectively, while not in birth outcomes. Maternal Hg exposure and history of cardiovascular diseases are independent risk factors for pregnant hypertension, whereas the GSTT1 homozygous deletion genotype has no role in diastolic hypertension and birth outcomes among the Indonesian coastal pregnant mother population.
GSTT1和GSTM1基因在汞代谢和排泄以及血压反应中发挥作用,进而影响出生结局。本研究评估GSTT1和GSTM1缺失变异体以及孕妇头发汞浓度是否与印度尼西亚沿海孕妇群体的血压和出生结局相关。对印度尼西亚中爪哇省杰帕拉沿海地区的139名孕妇进行了一项横断面研究。收集了孕期的孕妇特征,包括血压和出生结局。使用聚合酶链反应(PCR)检测GSTT1和GSTM1基因变异体。使用还原汽化汞分析仪测量头发汞水平。孕妇头发汞平均浓度为0.727±0.558μg/g。41.7%的受试者中发现GSTT1基因型纯合缺失,而未发现GSTM1缺失。在头发汞方面,缺失组和非缺失组之间未发现统计学显著差异。GSTT1缺失基因型显示出对舒张期高血压有保护作用,但结果不明确(p = 0.048,OR 0.285,CI 0.077 - 1.052),且与出生结局无关(所有p>0.05)。高头发汞浓度和心血管疾病阳性史分别使孕期收缩期和舒张期高血压风险增加,OR分别为6.871(CI 95% 1.445 - 32.660)和8.518(CI 95% 2.126 - 34.125),而与出生结局无关。孕妇汞暴露和心血管疾病史是妊娠高血压的独立危险因素,而GSTT1纯合缺失基因型在印度尼西亚沿海孕妇群体的舒张期高血压和出生结局中不起作用。