母体咖啡因摄入与胎儿端粒长度的种族差异。

International Journal of MCH and AIDS Pub Date : 2020-01-01 Epub Date: 2019-12-30 DOI:10.21106/ijma.290
Isabel Griffin, Boubakari Ibrahimou, Natasha Navejar, Anjali Aggarwal, Kristopher Myers, Daniel Mauck, Korede K Yusuf, Usman J Wudil, Muktar H Aliyu, Hamisu M Salihu
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引用次数: 1

摘要

背景和目的:确定端粒长度缩短的危险因素,特别是在胎儿发育期间,对全球范围内孕妇的咖啡因摄入量建议具有重要意义。本研究的目的是评估咖啡因摄入量与胎儿端粒长度之间的关系,以及在不考虑母体咖啡因摄入状况的情况下端粒长度的种族/民族差异。方法:采用食物频率问卷(FFQ)测量咖啡因摄入量。以数据均值117.3 mg为截止值,比较三种基于咖啡因水平二元分类变量的广义线性模型(GLM);世界卫生组织(世卫组织)建议300毫克;而美国妇产科学会(ACOG)的建议摄入量为200毫克。然后评估咖啡因摄入量与端粒长度(端粒与单拷贝[T/S]比率)之间的关系。结果:在57对母胎中,77.2%的人报告咖啡因低于200 mg (ACOG), 89.5%的人报告咖啡因低于300 mg (WHO)。WHO和ACOG模型均发现,咖啡因摄入量与端粒长度延长显著正相关(结论和全球健康影响:咖啡因摄入量、母亲年龄和种族可能与胎儿端粒长度的改变有关)。这表明孕期摄入咖啡因可能对胎儿发育有长期影响。本研究中发现的端粒长度的种族/民族差异需要更大规模的研究来进一步证实这些关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Maternal Caffeine Consumption and Racial Disparities in Fetal Telomere Length.

Maternal Caffeine Consumption and Racial Disparities in Fetal Telomere Length.

Maternal Caffeine Consumption and Racial Disparities in Fetal Telomere Length.

Background and objectives: The identification of risk factors for shorter telomere length, especially during fetal development, would be important towards caffeine consumption recommendations for pregnant women on a global scale. The purpose of this study was to evaluate the association between caffeine intake and fetal telomere length as well as racial/ethnic differences in telomere length regardless of maternal caffeine consumption status.

Methods: Caffeine intake was measured using a food frequency questionnaire (FFQ). Three generalized linear models (GLM) were compared based on binary categorical variables of caffeine levels using data mean value of 117.3 mg as cut-off; the World Health Organization (WHO) recommendations of 300 mg; and the American College of Obstetricians and Gynecologists (ACOG) recommendations of 200 mg. The association between caffeine consumption and telomere length (telomere to single-copy [T/S] ratio) was then assessed.

Results: Among 57 maternal-fetal dyads, 77.2% reported less than 200 mg of caffeine (ACOG) and 89.5% less than 300 mg (WHO). Both WHO and ACOG models found that caffeine intake was significantly and positively associated with longer telomere length (p<0.05); and sodium (p<0.05). Other" race (p<0.001) and "white" race (p<0.001) were also significantly and positively associated with longer telomere length in the same models. Increasing maternal age shortened telomere length significantly in all models (p<0.001).

Conclusion and global health implications: Caffeine intake, maternal age, and race may be associated with alterations in fetal telomere length. This indicates that caffeine consumption during pregnancy may have long-term implications for fetal development. The racial/ethnic differences in telomere length found in this study warrant larger studies to further confirm these associations.

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