Interplay between elevated RAB5B gene expression and insulin resistance among women with PCOS-insights from a case-control study.

IF 3.7 3区 医学 Q2 Medicine Endocrine Pub Date : 2024-12-27 DOI:10.1007/s12020-024-04137-z
Khurshid Ahmad Padder, Mohmad Aadil Yousuf, Nusrat Jahan, Syed Douhath Yousuf, Mohd Ashraf Ganie
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Abstract

Background: Polycystic ovary syndrome (PCOS) represents a multifaceted endocrine, reproductive, and metabolic disorder characterized by hyperandrogenism and hyperinsulinemia-induced insulin resistance (IR). Recent studies reported that the etiology of PCOS is likely correlated with genes involved in steriodogenesis, IR and glucose metabolism. Among the candidate genes in insulin signaling pathways, RAB5B, a small GTPase involved in vesicle trafficking, significantly impacts cellular pathways in ovarian follicular cells, leading to clinical and endocrine changes among women with PCOS. Additionally, RAB5B is crucial for insulin-mediated glucose uptake and is involved in PI3K, AKT, and MAPK/ERK pathways, affecting LHCGR-stimulated steroidogenesis. Despite extensive research, the precise molecular mechanisms underlying RAB5B mediated IR in PCOS remained elusive.

Objective: The study aimed to explore the potential link between RAB5B gene expression and IR among women with PCOS.

Methodology: A total of age matched 270 subjects were enrolled in this study including 135 PCOS women and 135 apparently healthy controls. These study participants were subjected to detailed medical history, clinical and physical examination. All subjects were further evaluated for biochemical, hormonal and RAB5B gene expression estimation. Expression levels of RAB5B gene were analyzed using gene-specific primers and the SYBR® Green PCR Kit (Qiagen, Germany) and their qPCR reaction mix, according to the manufacturer's guidelines. Student t-test and ANOVA were used to evaluate the differences in the means of various parameters.

Results: The HOMA-IR (2.28 ± 1.4 vs. 1.36 ± 0.73) was significantly elevated among women with PCOS than controls (p < 0.05). We also found that the QUICKI (0.35 ± 0.04 vs. 0.37 ± 0.04), MATSUDA (12.59 ± 4.71 vs. 15.47 ± 4.33) and FGIR (11.56 ± 7.06 vs. 14.32 ± 8.66) were higher in controls than women with PCOS (p < 0.05). We also observed that women with PCOS had elevated levels of RAB5B mRNA levels when compared with apparently healthy controls. Bivariate correlation analysis among HOMA-IR stratified PCOS and control subjects revealed strong negative correlation between IR+ PCOS and IR- PCOS (r = -0.61, P < 0.05) and IR- control (r = -0.37, p < 0.05) subjects respectively.

Conclusion: Our study demonstrated that there is potential link between RAB5B gene expression and IR specifically in the context of IR indices among women with PCOS.

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来自病例对照研究的RAB5B基因表达升高与多囊卵巢综合征女性胰岛素抵抗之间的相互作用
背景:多囊卵巢综合征(PCOS)是一种多方面的内分泌、生殖和代谢紊乱,以高雄激素和高胰岛素诱导的胰岛素抵抗(IR)为特征。最近的研究报道多囊卵巢综合征的病因可能与甾体生成、IR和葡萄糖代谢相关的基因有关。在胰岛素信号通路的候选基因中,参与囊泡运输的小GTPase RAB5B显著影响卵巢滤泡细胞的细胞通路,导致PCOS女性的临床和内分泌变化。此外,RAB5B对胰岛素介导的葡萄糖摄取至关重要,并参与PI3K、AKT和MAPK/ERK通路,影响lhcgr刺激的类固醇生成。尽管有广泛的研究,RAB5B介导的IR在PCOS中的确切分子机制仍然难以捉摸。目的:探讨多囊卵巢综合征(PCOS)患者RAB5B基因表达与IR之间的潜在联系。方法:本研究共纳入年龄匹配的270名受试者,其中135名PCOS女性和135名表面健康对照。这些研究参与者接受了详细的病史、临床和体格检查。所有受试者进一步进行生化、激素和RAB5B基因表达评估。使用基因特异性引物和SYBR®Green PCR Kit (Qiagen, Germany)及其qPCR反应组合,根据制造商指南分析RAB5B基因的表达水平。采用学生t检验和方差分析来评价各参数均值的差异。结果:PCOS女性的HOMA-IR(2.28±1.4比1.36±0.73)明显高于对照组(p + PCOS和IR- PCOS) (r = -0.61, p -对照(r = -0.37, p)。结论:本研究表明,在PCOS女性IR指标的背景下,RAB5B基因表达与IR之间存在潜在的联系。
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来源期刊
Endocrine
Endocrine 医学-内分泌学与代谢
CiteScore
6.40
自引率
5.40%
发文量
0
期刊介绍: Well-established as a major journal in today’s rapidly advancing experimental and clinical research areas, Endocrine publishes original articles devoted to basic (including molecular, cellular and physiological studies), translational and clinical research in all the different fields of endocrinology and metabolism. Articles will be accepted based on peer-reviews, priority, and editorial decision. Invited reviews, mini-reviews and viewpoints on relevant pathophysiological and clinical topics, as well as Editorials on articles appearing in the Journal, are published. Unsolicited Editorials will be evaluated by the editorial team. Outcomes of scientific meetings, as well as guidelines and position statements, may be submitted. The Journal also considers special feature articles in the field of endocrine genetics and epigenetics, as well as articles devoted to novel methods and techniques in endocrinology. Endocrine covers controversial, clinical endocrine issues. Meta-analyses on endocrine and metabolic topics are also accepted. Descriptions of single clinical cases and/or small patients studies are not published unless of exceptional interest. However, reports of novel imaging studies and endocrine side effects in single patients may be considered. Research letters and letters to the editor related or unrelated to recently published articles can be submitted. Endocrine covers leading topics in endocrinology such as neuroendocrinology, pituitary and hypothalamic peptides, thyroid physiological and clinical aspects, bone and mineral metabolism and osteoporosis, obesity, lipid and energy metabolism and food intake control, insulin, Type 1 and Type 2 diabetes, hormones of male and female reproduction, adrenal diseases pediatric and geriatric endocrinology, endocrine hypertension and endocrine oncology.
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