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Background <p>Tricuspid regurgitation (TR) is associated with adverse clinical outcomes, yet the underlying right atrial (RA) molecular remodeling remains poorly understood. We aimed to define TR-associated RA remodeling using metabolomic and lipidomic profiling of human RA tissue.</p> Methods <p>RA appendage tissue was obtained intraoperatively from 24 adults undergoing cardiac surgery (11 with ≥severe TR; 13 controls). Gas chromatography mass spectrometry (GC-MS) was used for targeted small-molecule metabolomics, and liquid chromatography quadrupole time of flight mass spectrometry (LC-qTOF-MS) for untargeted lipidomics. Mann Whitney U testing, principal component analysis (PCA), partial least squares discriminant analysis (PLS-DA), and variable importance in projection (VIP) scoring were used to identify discriminatory multi-omics patterns between groups.</p> Results <p>Patients with TR demonstrated a distinct metabolic phenotype characterized by reduced glycolysis-related intermediates (glucose-6-phosphate, β-alanine, α-glucosamine-1-phosphate; all <i>p</i> &lt; 0.05) and metabolites consistent with oxidative stress and amino acid catabolism markers (6-hydroxycaproic acid, porphine, phosphoric acid; all <i>p</i> &lt; 0.05). Lipidomic analysis revealed broad phospholipid remodeling and signals consistent with mitochondrial-associated alterations, including a decreased phosphatidylcholine/phosphatidylethanolamine (PC/PE) ratio and reductions in selected diacylglycerol and ceramide species. PCA and PLS-DA demonstrated clear group separation with consistent VIP signals, indicating consistent multi-omics discrimination.</p> Conclusions <p>TR is associated with coordinated metabolic and lipidomic reprogramming in the RA, a pattern compatible with, though not direct evidence of, mitochondrial stress, impaired bioenergetics, and membrane destabilization. These findings support a model in which RA remodeling is tightly linked to TR pathophysiology, highlighting candidate molecular features for future validation. Multi-omics biomarkers may enhance risk stratification, inform the timing of intervention, and guide the development of future point-of-care molecular diagnostics.</p> Graphical Abstract <p></p> <p>Severe tricuspid regurgitation leads to chronic right atrial volume and pressure overload, resulting in progressive right atrial remodeling. Tissue-based metabolomic and lipidomic analyses demonstrate a coordinated pattern of metabolic and lipid alterations, including reduced glycolytic intermediates, altered amino acid metabolism, and disrupted phospholipid and cardiolipin homeostasis, that is compatible with, but does not directly demonstrate, impaired mitochondrial energy metabolism. These molecular alterations are associated with adverse structural and functional consequences, including right atrial enlargement, increased right ventricular end-diastolic dimensions, reduced tricuspid annular plane systolic excursion, and right ventricle–pulmonary artery uncoupling. Collectively, these findings support the concept of an active, biologically driven right atrial cardiomyopathy that may contribute to heterogeneous postoperative recovery and inform future biomarker guided risk stratification and surgical timing.</p>

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Multi-omics analysis of human right atrial tissue ıdentifies molecular signatures of remodeling in tricuspid regurgitation

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年7月27日

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  • Melih Alma,
  • Ahmet Aydın,
  • Aysima Sezer,
  • Sevilay Erdoğan Kablan,
  • İpek Baysal,
  • Emirhan Nemutlu,
  • Samiye Yabanoğlu Çiftçi,
  • Mustafa Yılmaz

摘要

Background

Tricuspid regurgitation (TR) is associated with adverse clinical outcomes, yet the underlying right atrial (RA) molecular remodeling remains poorly understood. We aimed to define TR-associated RA remodeling using metabolomic and lipidomic profiling of human RA tissue.

Methods

RA appendage tissue was obtained intraoperatively from 24 adults undergoing cardiac surgery (11 with ≥severe TR; 13 controls). Gas chromatography mass spectrometry (GC-MS) was used for targeted small-molecule metabolomics, and liquid chromatography quadrupole time of flight mass spectrometry (LC-qTOF-MS) for untargeted lipidomics. Mann Whitney U testing, principal component analysis (PCA), partial least squares discriminant analysis (PLS-DA), and variable importance in projection (VIP) scoring were used to identify discriminatory multi-omics patterns between groups.

Results

Patients with TR demonstrated a distinct metabolic phenotype characterized by reduced glycolysis-related intermediates (glucose-6-phosphate, β-alanine, α-glucosamine-1-phosphate; all p < 0.05) and metabolites consistent with oxidative stress and amino acid catabolism markers (6-hydroxycaproic acid, porphine, phosphoric acid; all p < 0.05). Lipidomic analysis revealed broad phospholipid remodeling and signals consistent with mitochondrial-associated alterations, including a decreased phosphatidylcholine/phosphatidylethanolamine (PC/PE) ratio and reductions in selected diacylglycerol and ceramide species. PCA and PLS-DA demonstrated clear group separation with consistent VIP signals, indicating consistent multi-omics discrimination.

Conclusions

TR is associated with coordinated metabolic and lipidomic reprogramming in the RA, a pattern compatible with, though not direct evidence of, mitochondrial stress, impaired bioenergetics, and membrane destabilization. These findings support a model in which RA remodeling is tightly linked to TR pathophysiology, highlighting candidate molecular features for future validation. Multi-omics biomarkers may enhance risk stratification, inform the timing of intervention, and guide the development of future point-of-care molecular diagnostics.

Graphical Abstract

Severe tricuspid regurgitation leads to chronic right atrial volume and pressure overload, resulting in progressive right atrial remodeling. Tissue-based metabolomic and lipidomic analyses demonstrate a coordinated pattern of metabolic and lipid alterations, including reduced glycolytic intermediates, altered amino acid metabolism, and disrupted phospholipid and cardiolipin homeostasis, that is compatible with, but does not directly demonstrate, impaired mitochondrial energy metabolism. These molecular alterations are associated with adverse structural and functional consequences, including right atrial enlargement, increased right ventricular end-diastolic dimensions, reduced tricuspid annular plane systolic excursion, and right ventricle–pulmonary artery uncoupling. Collectively, these findings support the concept of an active, biologically driven right atrial cardiomyopathy that may contribute to heterogeneous postoperative recovery and inform future biomarker guided risk stratification and surgical timing.