Computational Biomedicine Laboratory, Príncipe Felipe Research Center (CIPF), C/ Eduardo Primo Yúfera, 3, 46012, Valencia, Spain.
Carlos Simon Foundation-INCLIVA Instituto de Investigación Sanitaria, Valencia, Spain.
Biol Sex Differ. 2024 Jan 31;15(1):13. doi: 10.1186/s13293-024-00588-1.
The incidence of Alzheimer's disease (AD)-the most frequent cause of dementia-is expected to increase as life expectancies rise across the globe. While sex-based differences in AD have previously been described, there remain uncertainties regarding any association between sex and disease-associated molecular mechanisms. Studying sex-specific expression profiles of regulatory factors such as microRNAs (miRNAs) could contribute to more accurate disease diagnosis and treatment.
A systematic review identified six studies of microRNA expression in AD patients that incorporated information regarding the biological sex of samples in the Gene Expression Omnibus repository. A differential microRNA expression analysis was performed, considering disease status and patient sex. Subsequently, results were integrated within a meta-analysis methodology, with a functional enrichment of meta-analysis results establishing an association between altered miRNA expression and relevant Gene Ontology terms.
Meta-analyses of miRNA expression profiles in blood samples revealed the alteration of sixteen miRNAs in female and 22 miRNAs in male AD patients. We discovered nine miRNAs commonly overexpressed in both sexes, suggesting a shared miRNA dysregulation profile. Functional enrichment results based on miRNA profiles revealed sex-based differences in biological processes; most affected processes related to ubiquitination, regulation of different kinase activities, and apoptotic processes in males, but RNA splicing and translation in females. Meta-analyses of miRNA expression profiles in brain samples revealed the alteration of six miRNAs in female and four miRNAs in male AD patients. We observed a single underexpressed miRNA in female and male AD patients (hsa-miR-767-5p); however, the functional enrichment analysis for brain samples did not reveal any specifically affected biological process.
Sex-specific meta-analyses supported the detection of differentially expressed miRNAs in female and male AD patients, highlighting the relevance of sex-based information in biomedical data. Further studies on miRNA regulation in AD patients should meet the criteria for comparability and standardization of information.
随着全球预期寿命的延长,阿尔茨海默病(AD)——最常见的痴呆症病因——的发病率预计将会增加。尽管先前已经描述了 AD 中基于性别的差异,但对于性别与疾病相关分子机制之间的任何关联仍存在不确定性。研究调节因子(如 microRNA(miRNA))的性别特异性表达谱可能有助于更准确的疾病诊断和治疗。
系统综述确定了在 Gene Expression Omnibus 存储库中纳入样本生物学性别信息的六篇 AD 患者 miRNA 表达研究。对 miRNA 表达进行差异分析,同时考虑疾病状态和患者性别。随后,通过整合分析方法对结果进行整合,通过整合分析结果的功能富集,确定了 miRNA 表达改变与相关基因本体术语之间的关联。
对血液样本 miRNA 表达谱的荟萃分析显示,女性 AD 患者中有 16 种 miRNA 发生改变,男性 AD 患者中有 22 种 miRNA 发生改变。我们发现有 9 种 miRNA 在两性中均过度表达,表明存在共同的 miRNA 失调谱。基于 miRNA 谱的功能富集结果揭示了生物学过程中的性别差异;在男性中,受影响最大的过程与泛素化、不同激酶活性的调节以及凋亡过程有关,但在女性中与 RNA 剪接和翻译有关。对脑样本 miRNA 表达谱的荟萃分析显示,女性 AD 患者中有 6 种 miRNA 发生改变,男性 AD 患者中有 4 种 miRNA 发生改变。我们观察到女性和男性 AD 患者中均有一种 miRNA 表达下调(hsa-miR-767-5p);然而,脑样本的功能富集分析并未揭示任何受影响的特定生物学过程。
基于性别的荟萃分析支持在女性和男性 AD 患者中检测到差异表达的 miRNA,突出了生物医学数据中基于性别的信息的相关性。进一步研究 AD 患者的 miRNA 调节应符合可比性和信息标准化的标准。