Takaya Junji
Department of Pediatrics, Kawachi General Hospital, Higashi-Osaka, Osaka 578-0954, Japan.
AIMS Public Health. 2015 Dec 4;2(4):793-803. doi: 10.3934/publichealth.2015.4.793. eCollection 2015.
Magnesium deficiency during pregnancy as a result of insufficient or low intake of magnesium is common in developing and developed countries. Previous reports have shown that intracellular magnesium of cord blood platelets is lower among small for gestational age (SGA) groups than that of appropriate for gestational age (AGA) groups, suggesting that intrauterine magnesium deficiency may result in SGA. Additionally, the risk of adult-onset diseases such as insulin resistance syndrome is greater among children whose mothers were malnourished during pregnancy, and who consequently had a low birth weight. In a number of animal models, poor nutrition during pregnancy leads to offspring that exhibit pathophysiological changes similar to human diseases. The offspring of pregnant rats fed a magensium restricted diet have developed hypermethylation in the hepatic 11β-hydroxysteroid dehydrogenase-2 promoter. These findings indicate that maternal magnesium deficiencies during pregnancy influence regulation of non-imprinted genes by altering the epigenetic regulation of gene expression, thereby inducing different metabolic phenotypes. Magnesium deficiency during pregnancy may be responsible for not only maternal and fetal nutritional problems, but also lifelong consequences that affect the offspring throughout their life. Epidemiological, clinical, and basic research on the effects of magnesium deficiency now indicates underlying mechanisms, especially epigenetic processes.
由于镁摄入量不足或偏低,孕期镁缺乏在发展中国家和发达国家都很常见。先前的报告显示,小于胎龄儿(SGA)组脐带血血小板的细胞内镁含量低于适于胎龄儿(AGA)组,这表明宫内镁缺乏可能导致小于胎龄儿。此外,母亲在孕期营养不良、出生体重低的儿童患胰岛素抵抗综合征等成人期疾病的风险更高。在一些动物模型中,孕期营养不佳会导致后代出现与人类疾病相似的病理生理变化。喂食低镁饮食的怀孕大鼠的后代,其肝脏11β-羟基类固醇脱氢酶-2启动子发生了高甲基化。这些发现表明,孕期母体镁缺乏通过改变基因表达的表观遗传调控来影响非印记基因的调控,从而诱发不同的代谢表型。孕期镁缺乏可能不仅导致母婴营养问题,还会产生影响后代一生的长期后果。目前,关于镁缺乏影响的流行病学、临床和基础研究表明了其潜在机制,尤其是表观遗传过程。