Circulating miR-122-5p, miR-151a-3p, miR-126-5p and miR-21-5p as potential predictive biomarkers for Metabolic Dysfunction-Associated Steatotic Liver Disease assessment.

IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of physiology and biochemistry Pub Date : 2024-08-14 DOI:10.1007/s13105-024-01037-8
Ana Luz Tobaruela-Resola, Fermín I Milagro, Mariana Elorz, Alberto Benito-Boillos, José I Herrero, Paola Mogna-Peláez, Josep A Tur, J Alfredo Martínez, Itziar Abete, M Ángeles Zulet
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Abstract

Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) is a worldwide leading cause of liver-related associated morbidities and mortality. Currently, there is a lack of reliable non-invasive biomarkers for an accurate of MASLD. Hence, this study aimed to evidence the functional role of miRNAs as potential biomarkers for MASLD assessment. Data from 55 participants with steatosis (MASLD group) and 45 without steatosis (control group) from the Fatty Liver in Obesity (FLiO) Study (NCT03183193) were analyzed. Anthropometrics and body composition, biochemical and inflammatory markers, lifestyle factors and liver status were evaluated. Circulating miRNA levels were measured by RT-PCR. Circulating levels of miR-122-5p, miR-151a-3p, miR-126-5p and miR-21-5p were significantly increased in the MASLD group. These miRNAs were significantly associated with steatosis, liver stiffness and hepatic fat content. Logistic regression analyses revealed that miR-151a-3p or miR-21-5p in combination with leptin showed a significant diagnostic accuracy for liver stiffness obtaining an area under the curve (AUC) of 0.76 as well as miR-151a-3p in combination with glucose for hepatic fat content an AUC of 0.81. The best predictor value for steatosis was obtained by combining miR-126-5p with leptin, presenting an AUC of 0.95. Circulating miRNAs could be used as a non-invasive biomarkers for evaluating steatosis, liver stiffness and hepatic fat content, which are crucial in determining MASLD. CLINICAL TRIAL REGISTRATION: • Trial registration number: NCT03183193 ( www.clinicaltrials.gov ). • Date of registration: 12/06/2017.

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循环 miR-122-5p、miR-151a-3p、miR-126-5p 和 miR-21-5p 作为代谢功能障碍相关性脂肪肝评估的潜在预测性生物标记物。
代谢功能障碍相关性脂肪性肝病(MASLD)是导致肝脏相关疾病和死亡的全球主要原因。目前,还缺乏可靠的非侵入性生物标志物来准确判断 MASLD。因此,本研究旨在证明 miRNAs 作为潜在生物标志物在 MASLD 评估中的功能作用。研究分析了肥胖症脂肪肝(FLiO)研究(NCT03183193)中 55 名脂肪肝患者(MASLD 组)和 45 名无脂肪肝患者(对照组)的数据。对人体测量和身体成分、生化和炎症指标、生活方式因素和肝脏状况进行了评估。循环 miRNA 水平通过 RT-PCR 进行了测定。MASLD组的循环miR-122-5p、miR-151a-3p、miR-126-5p和miR-21-5p水平显著升高。这些 miRNA 与脂肪变性、肝硬度和肝脏脂肪含量明显相关。逻辑回归分析表明,miR-151a-3p 或 miR-21-5p 与瘦素结合对肝僵化有明显的诊断准确性,曲线下面积(AUC)为 0.76;miR-151a-3p 与葡萄糖结合对肝脏脂肪含量有明显的诊断准确性,曲线下面积(AUC)为 0.81。将 miR-126-5p 与瘦素结合使用可获得脂肪变性的最佳预测值,其 AUC 为 0.95。循环 miRNA 可用作评估脂肪变性、肝脏硬度和肝脏脂肪含量的非侵入性生物标记物,这些因素对确定 MASLD 至关重要。临床试验注册:- 试验注册号NCT03183193 ( www.clinicaltrials.gov ).- 注册日期:12/06/2017.
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来源期刊
Journal of physiology and biochemistry
Journal of physiology and biochemistry 生物-生化与分子生物学
CiteScore
6.60
自引率
0.00%
发文量
86
审稿时长
6-12 weeks
期刊介绍: The Journal of Physiology and Biochemistry publishes original research articles and reviews describing relevant new observations on molecular, biochemical and cellular mechanisms involved in human physiology. All areas of the physiology are covered. Special emphasis is placed on the integration of those levels in the whole-organism. The Journal of Physiology and Biochemistry also welcomes articles on molecular nutrition and metabolism studies, and works related to the genomic or proteomic bases of the physiological functions. Descriptive manuscripts about physiological/biochemical processes or clinical manuscripts will not be considered. The journal will not accept manuscripts testing effects of animal or plant extracts.
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