Ma Dongsheng, Xi Jianhong
Department of Reproductive Medicine, The People's Hospital Bozhou, Bozhou, China.
Department of Urology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Front Cell Dev Biol. 2025 May 2;13:1586069. doi: 10.3389/fcell.2025.1586069. eCollection 2025.
To investigate the correlation between Metabolic syndrome (Mets) and Sperm DNA fragmentation index (DFI) in men of reproductive age, and to summarise the Mets and metabolic component health management model in men.
The Male Reproductive Health Follow-up Database in Bozhou City, Anhui Province, China (2020-2024) included in the study 1,008 outpatient cases of men with reproductive age,in which normal sperm DFI was the Control group (n = 858) and abnormal DFI was the Observation group (n = 150), and the general data, metabolic endocrine related indicators, and indicators related to fertility assessment were analysed in both groups, and fertility and metabolic indicators were followed up. Spearman rank correlation coefficient was used for correlation analysis, segmented package for threshold analysis, Bootstrap sampling method and Bayesian method for mediation effect test analysis. Univariate-multivariate logistic regression analyses were performed to build a predictive model using R Programming Language (4.42), and to plot the Nomogram, Calibration Curve, Decision Curve Analysis (DCA) Curve, and Clinical impact curve (CIC) to assess the consistency between the predicted probability of the model and the actual occurrence probability, as well as to evaluate the practicality and applicability in clinical decision-making.
Intergroup comparison between the observation and control groups in this study showed no statistical difference between the two groups in terms of baseline information and fertility assessment ( > 0.05). However, there was statistical difference between the two groups in MetS and metabolic scores ( < 0.001). One-way ANOVA showed a statistically significant difference between DFI and MetS scores ( = 0.021), and two-way comparisons showed a statistically significant difference between the groups with 0-4 points ( < 0.05). There was a moderate-strength positive correlation between metabolic score and DFI by Spearman's correlation analysis (r = 0.475, < 0.001). Overall, DFI and MetS were positively associated [OR (95%CI):1.09 (1.07-1.11)] when DFI< 32.26 [OR (95%CI): 1.15 (1.12-1.19)]. In the overall analysis, the association between MetS and adverse maternity outcomes was statistically significant (OR = 1.50, 95% CI: 1.01-2.22, = 0.045). In the sperm DFI subgroup, the association of MetS with adverse maternity outcomes was significant in both DFI ≤15 and DFI >30 (15: OR = 2.51, 95%CI: 1.01-6.22, = 0.047; >30:OR = 2.94, 95%CI: 1.19-7.22, = 0.019), and subgroup analyses of age showed significant association between MetS and adverse maternity outcomes in age >30 years (OR = 1.94, 95% CI: 1.13-3.33, = 0.016). The results of the mediated analysis pathway showed that obesity and hyperlipidaemia lead to sperm DFI abnormalities, which indirectly contribute to adverse maternity outcomes, but it has not been proven that sperm DFI abnormalities contribute to the occurrence of adverse maternity outcomes. The results of multifactorial logistic regression analysis showed that varicocele (OR = 1.975), obesity (OR = 2.296), hyperlipidaemia (OR = 2.422), and Low-HDL (OR = 3.654) were the independent risk factors for abnormal sperm DFI. And effective interventions for the group with abnormal sperm DFI could significantly reduce sperm DFI values and metabolic scores ( < 0.001). The predictive model has been validated to show positive predictive efficacy and clinical benefit.
MetS may lead to abnormal sperm DNA fragmentation indices, which in turn suggests that abnormal sperm DFI due to MetS may be a risk factor for male infertility and spousal adverse maternity, and that effective interventions to reduce sperm DFI values and metabolic scores are necessary and urgent. This study is part of the China Anhui Regional Male Fertility Survey Phase I (2020-2024).
探讨育龄男性代谢综合征(Mets)与精子DNA碎片化指数(DFI)之间的相关性,并总结男性Mets及代谢组分健康管理模式。
纳入中国安徽省亳州市男性生殖健康随访数据库(2020 - 2024年)中的1008例育龄男性门诊病例,其中精子DFI正常者为对照组(n = 858),DFI异常者为观察组(n = 150),分析两组的一般资料、代谢内分泌相关指标及生育评估相关指标,并对生育和代谢指标进行随访。采用Spearman等级相关系数进行相关性分析,分段包进行阈值分析,采用Bootstrap抽样法和贝叶斯方法进行中介效应检验分析。使用R编程语言(4.42)进行单因素 - 多因素逻辑回归分析以建立预测模型,并绘制列线图、校准曲线、决策曲线分析(DCA)曲线和临床影响曲线(CIC),以评估模型预测概率与实际发生概率之间的一致性,以及评估其在临床决策中的实用性和适用性。
本研究观察组与对照组的组间比较显示,两组在基线信息和生育评估方面无统计学差异(> 0.05)。然而,两组在Mets和代谢评分方面存在统计学差异(< 0.001)。单因素方差分析显示DFI与Mets评分之间存在统计学差异(= 0.021),两组间0 - 4分的双向比较显示存在统计学差异(< 0.05)。Spearman相关性分析显示代谢评分与DFI之间存在中等强度正相关(r = 0.475,< 0.001)。总体而言,当DFI < 32.26时,DFI与Mets呈正相关[OR(95%CI):1.09(1.07 - 1.11)];当DFI≥32.26时[OR(95%CI):1.15(1.12 - 1.19)]。在总体分析中,Mets与不良妊娠结局之间的关联具有统计学意义(OR = 1.50,95%CI:1.01 - 2.22,= 0.045)。在精子DFI亚组中,Mets与不良妊娠结局在DFI≤15和DFI > 30时均有显著关联(DFI≤15:OR = 2.51,95%CI:1.01 - 6.22,= 0.047;DFI > 30:OR = 2.94,95%CI:1.19 - 7.22,= 0.019),年龄亚组分析显示年龄> 30岁时Mets与不良妊娠结局之间存在显著关联(OR = 1.94,95%CI:1.13 - 3.33,= 0.016)。中介分析路径结果显示,肥胖和高脂血症导致精子DFI异常,间接导致不良妊娠结局,但尚未证实精子DFI异常导致不良妊娠结局的发生。多因素逻辑回归分析结果显示,精索静脉曲张(OR = 1.975)、肥胖(OR = 2.296)、高脂血症(OR = 2.422)和低高密度脂蛋白(OR = 3.654)是精子DFI异常的独立危险因素。对精子DFI异常组进行有效干预可显著降低精子DFI值和代谢评分(< 0.001)。预测模型经验证显示具有阳性预测效能和临床效益。
Mets可能导致精子DNA碎片化指数异常,这反过来表明Mets导致的精子DFI异常可能是男性不育和配偶不良妊娠的危险因素,并且采取有效干预措施降低精子DFI值和代谢评分是必要且紧迫的。本研究是中国安徽地区男性生育力调查第一阶段(2020 - 2024年)的一部分。