Association between gene expression levels of GDF9 and BMP15 and clinicopathological factors in the prognosis of female infertility in northeast Indian populations

IF 0.8 Q4 GENETICS & HEREDITY Meta Gene Pub Date : 2021-12-01 DOI:10.1016/j.mgene.2021.100964
Sumita Dutta Gupta , Bishal Dhar , Sharbadeb Kundu , Nabarun Das , Arun Paul Choudhury , Monica Deb , Abhijit Das , Amrita Das , Nayanika Das , Biswadeep Choudhury , Alex C. Varghese , Kushal Kumar Kar , Yashmin Choudhury , Sankar Kumar Ghosh
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Abstract

Female Infertility is a serious health issue, and genetic factors plays crucial role in female infertility. To explore the molecular mechanism involved in female infertility, we had investigated demographic, clinicopathological factors and gene expression profile of BMP15 and GDF9 in primary and secondary female infertility patients. Present study comprised of 469 primary and 210 secondary infertile females, and 419 fertile females (controls). The expression level of GDF9 and BMP15 genes was studied using quantitative real-time PCR and multifactor dimensionality reduction tool (MDR) was used to detect high-risk interaction. Finding revealed that there was down-regulation of the BMP15 and GDF9 gene in both primary and secondary infertile women in comparison to fertile women. A significant difference in the expression level of GDF9 gene among the study subjects for the various levels of TSH and RBS (p < 0.01) indicating that the level of gene expression was influenced by few hormonal factors. The best risk factor model predicted for female infertility was the five-factors model of TSH, LH, LH/FSH ratio, Hb, MCV with 100% CVC and maximum TBA = 0.921 and p < 0.01. Thus, down-regulation of GDF9 and BMP15 gene and interaction of clinicopathological factors significantly persuade female infertility, and these findings might be useful as possible biomarker for the estimation of primary and secondary female infertility.

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印度东北部人群中GDF9和BMP15基因表达水平与女性不孕症预后的临床病理因素的关系
女性不孕症是严重的健康问题,遗传因素在女性不孕症中起着至关重要的作用。为了探讨女性不孕症的分子机制,我们研究了原发性和继发性女性不孕症患者的人口统计学、临床病理因素和BMP15和GDF9的基因表达谱。本研究包括469只原发不育雌性和210只继发不育雌性,以及419只可育雌性(对照)。采用实时荧光定量PCR检测GDF9和BMP15基因的表达水平,采用多因素降维工具(MDR)检测高危相互作用。研究结果显示,与有生育能力的女性相比,原发性和继发性不孕女性的BMP15和GDF9基因均下调。不同TSH和RBS水平的受试者中GDF9基因表达水平有显著差异(p <0.01),表明基因表达水平受激素因素影响较少。预测女性不孕症的最佳危险因素模型为TSH、LH、LH/FSH比值、Hb、MCV (CVC 100%, TBA最大值= 0.921,p <0.01. 因此,GDF9和BMP15基因的下调以及临床病理因素的相互作用对女性不孕症具有重要的指导作用,这些发现可能作为估计女性原发性和继发性不孕症的生物标志物。
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来源期刊
Meta Gene
Meta Gene Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
1.10
自引率
0.00%
发文量
20
期刊介绍: Meta Gene publishes meta-analysis, polymorphism and population study papers that are relevant to both human and non-human species. Examples include but are not limited to: (Relevant to human specimens): 1Meta-Analysis Papers - statistical reviews of the published literature of human genetic variation (typically linked to medical conditionals and/or congenital diseases) 2Genome Wide Association Studies (GWAS) - examination of large patient cohorts to identify common genetic factors that influence health and disease 3Human Genetics Papers - original studies describing new data on genetic variation in smaller patient populations 4Genetic Case Reports - short communications describing novel and in formative genetic mutations or chromosomal aberrations (e.g., probands) in very small demographic groups (e.g., family or unique ethnic group). (Relevant to non-human specimens): 1Small Genome Papers - Analysis of genetic variation in organelle genomes (e.g., mitochondrial DNA) 2Microbiota Papers - Analysis of microbiological variation through analysis of DNA sequencing in different biological environments 3Ecological Diversity Papers - Geographical distribution of genetic diversity of zoological or botanical species.
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