25-羟维生素 D 与畸形精子风险之间的因果关系:双向孟德尔随机研究

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-04-21 DOI:10.1016/j.reprotox.2024.108597
Nannan Li , Ke Yang , Youjie Zeng , Si Cao , Liang Deng
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引用次数: 0

摘要

以往的研究表明,维生素 D 与畸形精子之间的关系存在矛盾。在此,我们通过双向孟德尔随机化(MR)分析评估了循环中25-羟维生素D(25OHD)水平与畸形精子风险之间的因果关系。25OHD与畸形精子症的全基因组关联研究汇总统计数据来自可公开访问的数据库。与 25OHD 相关的单核苷酸多态性(SNPs)和与精子异常相关的 SNPs 分别被用作正向 MR 分析和反向 MR 分析的工具变量(IVs)。反向方差加权法(IVW)是主要的MR方法,而加权中值法、MR-Egger法和最大似然法则是IVW的补充。此外,还有几项敏感性测试评估了磁共振分析的可靠性。前向 MR 分析显示,25OHD 水平升高可显著降低异常精子风险(几率比 [OR] = 0.75,95% 置信区间 [CI]:0.56-1.00,P<0.05):在排除与混杂因素相关的 SNPs 后(OR = 0.73,95 % CI:0.54-0.98,P = 3.83E-02)或仅利用位于 25OHD 相关基因附近的 SNPs 作为 IVs 后(OR = 0.58,95 % CI:0.41-0.81,P = 1.67E-03),该效应仍具有统计学意义。)反向 MR 分析表明,精子异常不会影响 25OHD 水平(P > 0.05)。敏感性测试表明,MR 分析不受异质性和水平多向性的影响。总之,本 MR 研究支持 25OHD 水平升高可降低畸形精子症的风险。因此,确保摄入充足的维生素 D 和保持 25OHD 水平稳定可能是优化生殖结果的有效策略。
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Causal association between 25-Hydroxyvitamin D and risk of abnormal spermatozoa: A bidirectional Mendelian randomization study

Previous studies indicated conflicting findings regarding the association between vitamin D and abnormal spermatozoa. Herein, we assessed the causal association between circulating 25-Hydroxyvitamin D (25OHD) levels and the risk of abnormal spermatozoa by utilizing bidirectional Mendelian randomization (MR) analysis. Genome-wide association study summary statistics for 25OHD and abnormal spermatozoa were obtained from publicly accessible databases. Single nucleotide polymorphisms (SNPs) associated with 25OHD and SNPs associated with abnormal spermatozoa were used as instrumental variables (IVs) for forward MR analysis and reverse MR analysis, respectively. Inverse variance weighted (IVW) was the main MR approach, while weighted median, MR-Egger, and maximum likelihood methods were employed to supplement IVW. In addition, several sensitivity tests assessed the reliability of MR analysis. Forward MR analysis showed that elevated 25OHD levels significantly reduced abnormal spermatozoa risk (odds ratio [OR] = 0.75, 95 % confidence interval [CI]: 0.56–1.00, P = 4.98E-02), and the effect remained statistically significant after excluding SNPs associated with confounders (OR = 0.73, 95 % CI: 0.54–0.98, P = 3.83E-02) or only utilizing SNPs located near 25OHD-associated genes only as IVs (OR = 0.58, 95 % CI: 0.41–0.81, P = 1.67E-03). Reverse MR analysis indicated abnormal spermatozoa not affecting 25OHD level (P > 0.05). Sensitivity tests showed that MR analyses were not affected by heterogeneity and horizontal polytropy. Overall, the present MR study supports that elevated 25OHD levels reduce the risk of abnormal spermatozoa. Therefore, ensuring adequate vitamin D intake and maintaining stable levels of 25OHD may be effective strategies to optimize reproductive outcomes.

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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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