Cytogenetics and Genomics Research Unit, Department of Zoology, University of Calcutta, Kolkata, India.
Institute of Reproductive Medicine (IRM), Salt Lake City, Kolkata, India.
Am J Mens Health. 2024 Sep-Oct;18(5):15579883241279195. doi: 10.1177/15579883241279195.
The AZFc partial deletions of Y chromosome and lifestyle/epidemiological factors such as the use of smokeless chewing tobacco (SCT) exhibit intriguing variations in their association with male infertility across the population, ethnicity, and genetic background. Here, a pioneering attempt has been made to elucidate the interactions of such deletions with the habits of SCT consumption among the participating individuals, using their large epidemiological data. This screening program was conducted among Bengali-speaking men in West Bengal, India. We screened the prevalence and association of distinct partial deletions (gr/gr, b1/b3, and b2/b3) of the AZFc region using locus-specific sequence-tagged site (STS) markers among 728 case subjects and compared them with 264 ethnicity- and age-matched proven-fertile control men. The recorded epidemiological data of the study group and the outcome of partial deletion analysis were compiled to frame the plausible Gene × Epidemiological factor (G × E) interactions. The gr/gr deletion was reported to be significantly associated with azoospermic ( = .0015, odds ratio [OR] = 3.413) and oligozoospermic ( = .0382, OR = 3.012) case subgroups, and b1/b3 deletions were also detected among the infertile persons only. The G × E model revealed that men who carried microdeletions as well as were SCT users had an elevated risk of infertility ( = .002, OR = 6.38). The study highlights the fact that AZFc partial deletions and SCT, when co-occurred, synergistically increase the risk of infertility among men. This work helps to get more insight into the etiology of male infertility in the light of gene-environmental interaction.
Y 染色体的 AZFc 部分缺失和生活方式/流行病学因素,如使用无烟气化烟草(SCT),在人群、种族和遗传背景中与男性不育的相关性存在有趣的变化。在这里,我们首次尝试利用这些大型流行病学数据,阐明这些缺失与参与个体 SCT 消费习惯之间的相互作用。该筛查计划在印度西孟加拉邦讲孟加拉语的男性中进行。我们使用特定于基因座的序列标记位点(STS)标记,在 728 例病例和 264 例年龄和种族匹配的生育能力正常的对照男性中,筛查了 AZFc 区域的不同部分缺失(gr/gr、b1/b3 和 b2/b3)的流行率和相关性。研究组的记录流行病学数据和部分缺失分析的结果被汇编起来,以构建合理的基因与流行病学因素(G × E)相互作用。gr/gr 缺失与无精子症( = .0015,优势比 [OR] = 3.413)和少精子症( = .0382,OR = 3.012)病例亚组显著相关,并且仅在不育者中也检测到 b1/b3 缺失。G × E 模型显示,携带微缺失且使用 SCT 的男性患不育症的风险增加( = .002,OR = 6.38)。该研究强调了这样一个事实,即 AZFc 部分缺失和 SCT 同时发生时,会协同增加男性不育的风险。这项工作有助于深入了解男性不育症的病因,了解基因-环境相互作用。