Centre of Research and Development of Medical Diagnostic Laboratories (CMDL), Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.
Center for Innovation and Standard for Medical Technology and Physical Therapy (CISMaP), Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.
In Vivo. 2024 Mar-Apr;38(2):785-793. doi: 10.21873/invivo.13502.
BACKGROUND/AIM: Metabolic syndrome (MetS) stands as a significant risk for developing various severe health problems. Therefore, the discovery of biomarkers capable of predicting the progression of metabolic conditions is crucial for improving overall health outcomes. Recently, we reported that coiled-coil domain containing 25 (CCDC25) might be associated with key proteins involved in metabolic pathways, by bioinformatics analysis. Thus, we assumed that serum CCDC25 levels might have an association with MetS status.
In this study, based on the modified National Cholesterol Education Program-Adult Treatment Panel III (modified NCEP-ATP III) criteria, the participants who had three or more of abnormal criteria were defined as MetS, and those who had 1 or 2 abnormal criteria as pre-MetS groups; those who had no abnormal criteria were classified as the healthy control (HC) group. Serum CCDC25 levels were measured using the dot blot assay.
The results showed that serum CCDC25 levels of the MetS group (0.072±0.026 ng/μl) were significantly higher (p<0.001) than that of pre-MetS (0.031±0.011 ng/μl) or HC groups (0.018±0.007 ng/μl). We can discern a consistent trend indicating that serum CCDC25 level is well correlated with the number of abnormal criteria of MetS of each participant. Although serum CCDC25 levels correlated with the distribution of all 5 MetS criteria, the highest correlation was seen in serum CCDC25 levels and triglyceride (TG) levels, with r=0.563, followed by systolic blood pressure (SBP) levels (r=0.557) and high-density lipoprotein-cholesterol (HDL-C) levels (r=-0.545).
CCDC25 showed correlations with all MetS parameters, particularly with TG, SBP, and HDL-C. This prompts speculation that heightened CCDC25 levels may indicate the development and/or progression of those MetS-associated diseases.
背景/目的:代谢综合征(MetS)是多种严重健康问题发生的重要危险因素。因此,发现能够预测代谢状况进展的生物标志物对于改善整体健康结果至关重要。最近,我们通过生物信息学分析发现卷曲螺旋结构域蛋白 25(CCDC25)可能与代谢途径中的关键蛋白有关。因此,我们假设血清 CCDC25 水平可能与 MetS 状态有关。
在这项研究中,根据改良的国家胆固醇教育计划-成人治疗专家组 III (改良 NCEP-ATP III)标准,具有三个或更多异常标准的患者被定义为 MetS,具有 1 或 2 个异常标准的患者被定义为 MetS 前期组;没有异常标准的患者被归类为健康对照组(HC)。使用斑点印迹法测量血清 CCDC25 水平。
结果表明,MetS 组(0.072±0.026 ng/μl)的血清 CCDC25 水平显著高于 MetS 前期组(0.031±0.011 ng/μl)或 HC 组(0.018±0.007 ng/μl)(p<0.001)。我们可以看出一个一致的趋势,表明血清 CCDC25 水平与每位患者 MetS 异常标准的数量密切相关。尽管血清 CCDC25 水平与所有 5 个 MetS 标准的分布相关,但与甘油三酯(TG)水平的相关性最高,r=0.563,其次是收缩压(SBP)水平(r=0.557)和高密度脂蛋白胆固醇(HDL-C)水平(r=-0.545)。
CCDC25 与所有 MetS 参数相关,尤其是与 TG、SBP 和 HDL-C。这提示升高的 CCDC25 水平可能表明与 MetS 相关疾病的发生和/或进展。