Robinson Research Institute, The University of Adelaide, Adelaide, SA, 5005, Australia.
Freemasons Centre for Male Health and Wellbeing, The University of Adelaide, Adelaide, SA, 5005, Australia.
J Assist Reprod Genet. 2024 Apr;41(4):1097-1109. doi: 10.1007/s10815-024-03030-y. Epub 2024 Jan 31.
Semen parameters are subjected to within-individual variability over time. The driving factors for this variability are likely multi-factorial, with healthier lifestyle associated with better semen quality. The extent in which variations in individual's lifestyle contributes to within-individual semen variability is unknown.
A total of 116 repeat semen samples from 29 men aged 19-37 over 6 months were collected. Basic semen analysis as per 5th WHO manual and extended semen parameters (sperm DNA fragmentation, redox potential and lipid peroxidation, sperm binding to hyaluronan and hyperactive motility) were assessed. An additional 39 lifestyle/biological factors (weight, blood pressure, etc.) were collected at each sample including validated health questionnaires SF36 Health Status, Australian Recommend Food Score, and International Physical Activity Questionnaire.
Only 10 out of the 39 lifestyle factors varied within men across samples including age (P = 0.0024), systolic blood pressure (P = 0.0080), social functioning (P = 0.0340), energy (P = 0.0069), non-alcoholic caffeinated beverages (P = 0.0010), and nutrition (P < 0.0001). The only semen parameter that varied between collections was sperm morphology (coefficient of variation 23.8 (6.1-72.0), P < 0.05). We only observed weak (r < 0.3) to moderate (r > 0.3- < 0.6) correlations between lifestyle factors, including body mass index, waist circumference, nutrition, exercise, blood pressure and semen parameters including sperm count, progressive motility, and sperm DNA fragmentation (P < 0.05).
In healthy men from the general population, semen quality and associated lifestyle factors do not significantly vary over 6 months, indicating that one semen sample is likely sufficient for determining male fertility in this population.
精液参数随时间在个体内发生变化。这种可变性的驱动因素可能是多因素的,与更健康的生活方式相关的更好的精液质量。个体生活方式的变化在多大程度上导致个体内精液变异性尚不清楚。
共收集了 29 名年龄在 19-37 岁的男性在 6 个月内的 116 次重复精液样本。按照第 5 版世卫组织手册进行基本精液分析,并评估了扩展的精液参数(精子 DNA 碎片化、氧化还原电位和脂质过氧化、精子与透明质酸的结合以及超活跃运动)。在每个样本中还收集了 39 个生活方式/生物学因素(体重、血压等),包括经过验证的健康问卷 SF36 健康状况、澳大利亚推荐食品评分和国际体力活动问卷。
在男性中,只有 10 个生活方式因素在样本之间发生了变化,包括年龄(P=0.0024)、收缩压(P=0.0080)、社会功能(P=0.0340)、能量(P=0.0069)、不含酒精的含咖啡因饮料(P=0.0010)和营养(P<0.0001)。唯一在采集之间发生变化的精液参数是精子形态(变异系数 23.8(6.1-72.0),P<0.05)。我们仅观察到生活方式因素之间存在弱(r<0.3)到中度(r>0.3-<0.6)相关性,包括体重指数、腰围、营养、运动、血压和精液参数,包括精子计数、前向运动精子和精子 DNA 碎片化(P<0.05)。
在来自普通人群的健康男性中,精液质量和相关生活方式因素在 6 个月内没有显著变化,这表明在该人群中,一次精液样本可能足以确定男性生育能力。