Skowronek Anna Katarzyna, Jaskulak Marta, Zorena Katarzyna
Department of Immunobiology and Environment Microbiology, Medical University of Gdansk, 80-210 Gdansk, Poland.
Int J Mol Sci. 2024 Dec 26;26(1):90. doi: 10.3390/ijms26010090.
Obesity and its related diseases, such as type 2 diabetes (T2DM), cardiovascular disease (CVD), and metabolic fatty liver disease (MAFLD), require new diagnostic markers for earlier detection and intervention. The aim of this study is to demonstrate the potential of metabolomics as a tool for identifying biomarkers associated with obesity and its comorbidities in every age group. The presented systematic review makes an important contribution to the understanding of the potential of metabolomics in identifying biomarkers of obesity and its complications, especially considering the influence of branched-chain amino acids (BCAAs), amino acids (AAs) and adipokines on the development of T2DM, MAFLD, and CVD. The unique element of this study is the combination of research results from the last decade in different age groups and a wide demographic range. The review was based on the PubMed and Science Direct databases, and the inclusion criterion was English-language original studies conducted in humans between 2014 and 2024 and focusing on the influence of BCAAs, AAs or adipokines on the above-mentioned obesity complications. Based on the PRISMA protocol, a total of 21 papers were qualified for the review and then assigned to a specific disease entity. The collected data reveal that elevated levels of BCAAs and some AAs strongly correlate with insulin resistance, leading to T2DM, MAFLD, and CVD and often preceding conventional clinical markers. Valine and tyrosine emerge as potential markers of MAFLD progression, while BCAAs are primarily associated with insulin resistance in various demographic groups. Adipokines, although less studied, offer hope for elucidating the metabolic consequences of obesity. The review showed that in the case of CVDs, there is still a lack of studies in children and adolescents, who are increasingly affected by these diseases. Moreover, despite the knowledge that adipokines play an important role in the pathogenesis of obesity, there are no precise findings regarding the correlation between individual adipokines and T2DM, MAFLD, or CVD. In order to be able to introduce metabolites into the basic diagnostics of obesity-related diseases, it is necessary to develop panels of biochemical tests that will combine them with classical markers of selected diseases.
肥胖及其相关疾病,如2型糖尿病(T2DM)、心血管疾病(CVD)和代谢性脂肪性肝病(MAFLD),需要新的诊断标志物以便早期检测和干预。本研究的目的是证明代谢组学作为一种工具在识别各年龄组中与肥胖及其合并症相关的生物标志物方面的潜力。所呈现的系统评价对理解代谢组学在识别肥胖及其并发症的生物标志物方面的潜力做出了重要贡献,尤其是考虑到支链氨基酸(BCAAs)、氨基酸(AAs)和脂肪因子对T2DM、MAFLD和CVD发展的影响。本研究的独特之处在于结合了过去十年不同年龄组和广泛人口统计学范围的研究结果。该综述基于PubMed和ScienceDirect数据库,纳入标准是2014年至2024年期间在人类中进行的英文原创研究,且聚焦于BCAAs、AAs或脂肪因子对上述肥胖并发症的影响。根据PRISMA协议,共有21篇论文符合综述要求,然后被分配到特定的疾病实体。收集的数据表明,BCAAs和一些AAs水平升高与胰岛素抵抗密切相关,会导致T2DM、MAFLD和CVD,且往往先于传统临床标志物出现。缬氨酸和酪氨酸成为MAFLD进展的潜在标志物,而BCAAs在各人口统计学群体中主要与胰岛素抵抗相关。脂肪因子虽然研究较少,但为阐明肥胖的代谢后果带来了希望。该综述表明,在CVD方面,儿童和青少年中仍缺乏相关研究,而这些疾病对他们的影响日益增加。此外,尽管已知脂肪因子在肥胖发病机制中起重要作用,但关于个体脂肪因子与T2DM、MAFLD或CVD之间的相关性尚无确切研究结果。为了能够将代谢物引入肥胖相关疾病的基础诊断中,有必要开发生化检测组合,将它们与所选疾病的经典标志物相结合。