Assessment of Cardiorenal Involvement in Systemic Sclerosis Patients.

IF 4.8 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Biomolecules Pub Date : 2025-09-09 DOI:10.3390/biom15091297
Chiara Pellicano, Giancarlo D'Ippolito, Annalisa Villa, Ottavio Martellucci, Umberto Basile, Valeria Carnazzo, Valerio Basile, Edoardo Rosato, Mariapaola Marino, Antonietta Gigante
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Abstract

Systemic sclerosis (SSc) is an autoimmune disease associated with a high burden of morbidity and mortality due to organ complications. Pulmonary arterial hypertension (PAH) and cardiac involvement, characterized by chronic right ventricular (RV) pressure overload with consequent RV dysfunction and ultimately right heart failure (HF), are among these. A common comorbidity in SSc is chronic kidney disease (CKD). CKD is often present at the time of PAH diagnosis or a decline in renal function may occur during the course of the disease. CKD is strongly and independently associated with mortality in patients with PAH and HF. The cardiovascular and renal systems are closely interconnected, and disruption of this balance may result in cardiorenal syndrome (CRS). Type 2 CRS refers to CKD as a consequence of chronic HF. In clinical practice, non-specific markers such as troponin, B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP), and serum creatinine aid in CRS diagnosis. More specific biomarkers, including cystatin C (CysC), neutrophil gelatinase-associated lipocalin (NGAL), galectin-3, and soluble urokinase plasminogen activator receptor (suPAR), have shown value for diagnosis and prognosis in CRS. This study aimed to evaluate comprehensively heart/kidney damage markers related to CRS in SSc patients compared with healthy controls (HC) and to examine their association with renal and cardiac ultrasound parameters. SSc patients showed significantly higher CRS markers than HC (p < 0.001). SSc patients with clinically diagnosed CRS had significantly elevated galectin-3, suPAR, sNGAL, and uNGAL levels (p < 0.05) than SSc patients without CRS. Positive correlations were found between renal resistive index (RRI) and NT-proBNP (r = 0.335, p < 0.05), and between RRI and suPAR (r = 0.331, p < 0.05). NT-proBNP, suPAR, galectin-3, sNGAL, and uNGAL emerge as promising biomarkers for the early detection of cardiac and renal involvement in SSc patients.

系统性硬化症患者心肾受累的评估。
系统性硬化症(SSc)是一种由器官并发症引起的高发病率和高死亡率的自身免疫性疾病。其中包括肺动脉高压(PAH)和心脏受累,其特征是慢性右心室(RV)压力过载,导致右心室功能障碍,最终导致右心衰(HF)。慢性肾病(CKD)是SSc常见的合并症。慢性肾病常在PAH诊断时出现,或者在病程中可能出现肾功能下降。CKD与PAH和HF患者的死亡率密切相关。心血管和肾脏系统紧密相连,这种平衡的破坏可能导致心肾综合征(CRS)。2型CRS是指慢性心衰引起的CKD。在临床实践中,肌钙蛋白、b型利钠肽(BNP)、n端前BNP (NT-proBNP)、血清肌酐等非特异性标志物有助于诊断CRS。包括胱抑素C (CysC)、中性粒细胞明胶酶相关脂钙素(NGAL)、半乳糖凝集素-3和可溶性尿激酶纤溶酶原激活物受体(suPAR)在内的更多特异性生物标志物已显示出对CRS的诊断和预后的价值。本研究旨在全面评估SSc患者与健康对照组(HC)相比与CRS相关的心脏/肾脏损伤标志物,并研究它们与肾脏和心脏超声参数的关系。SSc患者的CRS指标明显高于HC (p < 0.001)。SSc临床诊断为CRS的患者galectin-3、suPAR、sNGAL、uNGAL水平明显高于无CRS的SSc患者(p < 0.05)。肾阻力指数(RRI)与NT-proBNP呈正相关(r = 0.335, p < 0.05),与suPAR呈正相关(r = 0.331, p < 0.05)。NT-proBNP、suPAR、半乳糖凝集素-3、sNGAL和uNGAL被认为是早期检测SSc患者心脏和肾脏受累的有希望的生物标志物。
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来源期刊
Biomolecules
Biomolecules Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.40
自引率
3.60%
发文量
1640
审稿时长
18.28 days
期刊介绍: Biomolecules (ISSN 2218-273X) is an international, peer-reviewed open access journal focusing on biogenic substances and their biological functions, structures, interactions with other molecules, and their microenvironment as well as biological systems. Biomolecules publishes reviews, regular research papers and short communications.  Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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