Effects of RIPC on the Metabolomical Profile during Lower Limb Digital Subtraction Angiography: A Randomized Controlled Trial

Author:

Kuusik Karl12ORCID,Kasepalu Teele12,Zilmer Mihkel3,Eha Jaan12,Paapstel Kaido12,Kilk Kalle3ORCID,Rehema Aune3,Kals Jaak345ORCID

Affiliation:

1. Department of Cardiology, Institute of Clinical Medicine, University of Tartu, Puusepa 8, 50406 Tartu, Estonia

2. Heart Clinic, Tartu University Hospital, Puusepa 8, 50406 Tartu, Estonia

3. Department of Biochemistry, Institute of Biomedicine and Translational Medicine, University of Tartu, Puusepa 8, 50406 Tartu, Estonia

4. Department of Surgery, Institute of Clinical Medicine, University of Tartu, Puusepa 8, 50406 Tartu, Estonia

5. Department of Vascular Surgery, Surgery Clinic, Tartu University Hospital, Puusepa 8, 50406 Tartu, Estonia

Abstract

Remote ischemic preconditioning (RIPC) has demonstrated protective effects in patients with lower extremity arterial disease (LEAD) undergoing digital subtraction angiography (DSA) and/or percutaneous transluminal angioplasty (PTA). This study aimed to investigate the impact of RIPC on the metabolomical profile of LEAD patients undergoing these procedures and to elucidate its potential underlying mechanisms. A total of 100 LEAD patients were enrolled and randomly assigned to either the RIPC group (n = 46) or the sham group (n = 54). Blood samples were drawn before and 24 h after intervention. Targeted metabolomics analysis was performed using the AbsoluteIDQ p180 Kit, and changes in metabolite concentrations were compared between the groups. The RIPC group demonstrated significantly different dynamics in nine metabolites compared to the sham group, which generally showed a decrease in metabolite concentrations. The impacted metabolites included glutamate, taurine, the arginine-dimethyl-amide-to-arginine ratio, lysoPC a C24:0, lysoPC a C28:0, lysoPC a C26:1, PC aa C38:1, PC ae C30:2, and PC ae C44:3. RIPC exhibited a ‘stabilization’ effect, maintaining metabolite levels amidst ischemia-reperfusion injuries, suggesting its role in enhancing metabolic control. This may improve outcomes for LEAD patients. However, additional studies are needed to definitively establish causal relationships among these metabolic changes.

Funder

Estonian Research Council

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

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