Serum glutathione peroxidase-3 concentration at diagnosis as a biomarker for assessing disease activity and damage of antineutrophil cytoplasmic antibody-associated vasculitis at diagnosis.

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in Molecular Biosciences Pub Date : 2025-02-07 eCollection Date: 2025-01-01 DOI:10.3389/fmolb.2025.1549454
Jihye Chung, Jang Woo Ha, Yong-Beom Park, Sang-Won Lee
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Abstract

Background: In this study, we investigated whether serum glutathione peroxidase-1 (GPX-3) concentration at diagnosis could be used to assess vasculitis activity and damage at diagnosis in immunosuppressive drug-naïve patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV).

Methods: We included 71 immunosuppressive drug-naïve patients newly diagnosed with AAV. Medical records were retrospectively reviewed and serum GPX-3 concentration was measured using serum samples collected and stored at diagnosis. The degree of vascular activity and extent of damage were assessed using the Birmingham vasculitis activity score (BVAS) and vasculitis damage index (VDI), respectively. Poor outcomes including all-cause mortality, end-stage kidney disease, and cerebrovascular and cardiovascular diseases were also investigated.

Results: The median age of the study subjects was 63.0 years, 26 and 45 patients were males and females, respectively. The median GPX-3 concentration was measured as 82.8 ng/mL. Serum GPX-3 concentration at diagnosis was inversely correlated with BVAS (r = -0.280), VDI (r = -0.263), and C-reactive protein (r = -0.261) at diagnosis, whereas, it was positively correlated with haemoglobin (r = 0.255), and serum albumin (r = 0.240) at diagnosis, respectively. However, serum GPX-3 concentration at diagnosis was not significantly associated with poor outcomes during follow-up in patients with AAV.

Conclusion: In this study, we demonstrated for the first time that serum GPX-3 concentration at diagnosis correlates with vasculitis activity and damage at diagnosis in patients with AAV, suggesting a possible role of serum GPX-3 as a complementary biomarker for assessing AAV activity in real clinical practice.

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诊断时血清谷胱甘肽过氧化物酶-3浓度作为评估疾病活动性和抗中性粒细胞细胞质抗体相关血管炎诊断时损害的生物标志物。
背景:在本研究中,我们研究了抗中性粒细胞细胞质抗体(ANCA)相关血管炎(AAV)免疫抑制drug-naïve患者诊断时血清谷胱甘肽过氧化物酶-1 (gx -3)浓度是否可用于评估诊断时血管炎活性和损害。方法:纳入71例新诊断为AAV的免疫抑制drug-naïve患者。回顾性回顾医疗记录,并使用诊断时收集和保存的血清样本测量血清GPX-3浓度。血管活动程度和损伤程度分别采用伯明翰血管炎活动评分(BVAS)和血管炎损伤指数(VDI)进行评估。不良结局包括全因死亡率、终末期肾病、脑血管和心血管疾病也进行了调查。结果:研究对象年龄中位数为63.0岁,男性26例,女性45例。GPX-3中位浓度为82.8 ng/mL。诊断时血清GPX-3浓度与诊断时BVAS (r = -0.280)、VDI (r = -0.263)、c反应蛋白(r = -0.261)呈负相关,与诊断时血红蛋白(r = 0.255)、血清白蛋白(r = 0.240)呈正相关。然而,诊断时血清GPX-3浓度与AAV患者随访期间的不良预后无显著相关。结论:在本研究中,我们首次证明了诊断时血清GPX-3浓度与AAV患者诊断时血管炎活性和损害相关,提示血清GPX-3可能在实际临床实践中作为评估AAV活性的补充生物标志物。
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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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