Maternal coffee consumption and biomarkers of reproductive health in young, adult sons: a cohort study

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-08-17 DOI:10.1016/j.reprotox.2024.108689
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Abstract

It has been proposed that poor semen quality may have its origins from fetal programming due to environmental factors. We investigated whether maternal coffee consumption during early pregnancy was associated with biomarkers of reproductive health in adult sons in the Fetal Programming of Semen Quality (FEPOS) cohort. In 2017–2019, 1058 young men provided a semen and blood sample and self-measured their testis volume. Daily maternal coffee consumption was reported by the mothers around gestational week 17. We estimated relative percentage differences with 95 % confidence intervals (CI) for semen quality measures, testis volume, and reproductive hormone levels according to maternal coffee consumption during pregnancy. Maternal coffee consumption (yes/no (reference)) was associated with lower semen volume (-7.0 % (95 % CI:-12.9;-0.7)), lower proportion of morphologically normal spermatozoa (-8.3 % (95 % CI:-16.5;0.8)), higher proportion of non-progressive and immotile spermatozoa (4.3 % (95 % CI:-1.5;10.3)), and lower testis volume (-4.8 % (95 % CI:-9.0;-0.4)). No indication of a dose-response association or threshold effects was observed in the categorized and continuous analyses. No associations with reproductive hormone levels were observed in any of the analyses. Overall, the study does not provide obvious indications that maternal coffee consumption in early pregnancy deteriorates male offspring fecundity. While some minor changes were observed, most estimates were small with confidence intervals overlapping the null. Future studies, preferably with greater exposure contrast, are warranted before a conclusion can be drawn as to whether maternal coffee consumption during pregnancy constitutes a risk for reproductive health in adult sons.

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母亲饮用咖啡与年轻成年儿子生殖健康的生物标志物:一项队列研究。
有人认为,精液质量差可能源于环境因素导致的胎儿编程。我们在精液质量胎儿编程(FEPOS)队列中调查了母亲在怀孕早期饮用咖啡是否与成年儿子的生殖健康生物标志物有关。2017-2019年,1058名年轻男性提供了精液和血液样本,并自我测量了他们的睾丸体积。母亲在孕 17 周左右报告了每天的母体咖啡饮用量。我们估算了精液质量指标、睾丸体积和生殖激素水平的相对百分比差异及 95% 的置信区间 (CI),这些差异与母亲在孕期饮用咖啡的情况有关。孕妇饮用咖啡(是/否(参考值))与精液量较低(-7.0% (95% CI:-12.9;-0.7))、形态正常精子比例较低(-8.3% (95% CI:-16.5;-0.8))、非渐进和不运动精子比例较高(4.3% (95% CI:-1.5;10.3))以及睾丸体积较小(-4.8% (95% CI:-9.0;-0.4))。在分类分析和连续分析中未观察到剂量反应关联或阈值效应的迹象。在所有分析中均未观察到与生殖激素水平的关联。总体而言,这项研究没有提供明显的迹象表明母体在孕早期饮用咖啡会降低雄性后代的生育能力。虽然观察到了一些微小的变化,但大多数估计值较小,置信区间与空值重叠。在就母亲在怀孕期间饮用咖啡是否会对成年儿子的生殖健康构成风险得出结论之前,还需要进行更多的研究,最好是具有更大的暴露对比度的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Reproductive toxicology
Reproductive toxicology 生物-毒理学
CiteScore
6.50
自引率
3.00%
发文量
131
审稿时长
45 days
期刊介绍: Drawing from a large number of disciplines, Reproductive Toxicology publishes timely, original research on the influence of chemical and physical agents on reproduction. Written by and for obstetricians, pediatricians, embryologists, teratologists, geneticists, toxicologists, andrologists, and others interested in detecting potential reproductive hazards, the journal is a forum for communication among researchers and practitioners. Articles focus on the application of in vitro, animal and clinical research to the practice of clinical medicine. All aspects of reproduction are within the scope of Reproductive Toxicology, including the formation and maturation of male and female gametes, sexual function, the events surrounding the fusion of gametes and the development of the fertilized ovum, nourishment and transport of the conceptus within the genital tract, implantation, embryogenesis, intrauterine growth, placentation and placental function, parturition, lactation and neonatal survival. Adverse reproductive effects in males will be considered as significant as adverse effects occurring in females. To provide a balanced presentation of approaches, equal emphasis will be given to clinical and animal or in vitro work. Typical end points that will be studied by contributors include infertility, sexual dysfunction, spontaneous abortion, malformations, abnormal histogenesis, stillbirth, intrauterine growth retardation, prematurity, behavioral abnormalities, and perinatal mortality.
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