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[Antiastenic effect of sequential levocarnitine and acetylcarnitine therapy in patients with cardiovascular diseases]
1Volgograd State Medical University, Volgograd, Russia.
Insights
Sequential therapy with levocarnitine (LC) and acetylcarnitine (ALC) effectively reduced asthenic syndrome (AS) in patients with cardiovascular disease. This treatment also demonstrated endothelium-protective effects, improving patient outcomes.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Neurology
Context:
- Asthenic syndrome (AS) is a common complication in patients with arterial hypertension and/or coronary heart disease (CHD).
- Fatigue significantly impacts quality of life and treatment adherence in cardiovascular patients.
- Limited therapeutic options exist for managing asthenia in this population.
Purpose:
- To evaluate the antiasthenic efficacy of a sequential therapy combining levocarnitine (LC) and acetylcarnitine (ALC).
- To assess the impact of this sequential therapy on asthenic syndrome (AS) in patients with arterial hypertension and/or coronary heart disease (CHD).
- To investigate the endothelium-protective effects of LC and ALC in this patient group.
Summary:
- An open comparative study involved 120 patients with arterial hypertension and/or CHD experiencing AS.
- Group 1 received 10 days of intravenous LC followed by 2 months of oral ALC, alongside basic therapy.
- Group 2 received only basic therapy. Asthenia was assessed using the MFI-20 and VAS-A scales.
- Group 1 showed a statistically significant reduction in AS manifestations compared to baseline and Group 2.
- LC and ALC demonstrated endothelium-protective effects.
Impact:
- Sequential LC and ALC therapy significantly reduces asthenic syndrome severity in comorbid cardiovascular patients.
- The established endotheliotropic properties support the use of LC and ALC in personalized cardiovascular disease management.
- This therapeutic approach offers a novel strategy to improve the quality of life for patients with cardiovascular diseases and asthenia.
Objective:
Evaluation of the antiasthenic effect of sequential therapy with levocarnitine (LC) and acetylcarnitine (ALC) in patients with arterial hypertension and/or ischemic heart disease (CHD) with asthenic syndrome (AS).
Material And Methods:
An open comparative study included 120 patients aged 54-67 years in patients with arterial hypertension and/or coronary artery disease with AS. Patients of group1 (n=60), in addition to basic therapy for the underlying disease, received LC (Elcar solution for intravenous and intramuscular injection of 100 mg/ml, the company PIQ-PHARMA) intravenously for 10 days at a dose of 1000 mg/day, followed by a transition to oral administration of ALC (Carnicetine, the company PIQ-PHARMA) 500 mg (2 capsules) 2 times a day for 2 months. Group2 patients (n=60) received only basic therapy for major diseases. The duration of observation was 70 days. The severity of AS was assessed using the MFI-20 questionnaire (MultidiMensional Fatigue Inventory) and the visual analog scale VAS-A (Visual Analog Scale Measuring fatigue).
Results:
In patients of group1, a statistically significant decrease in various manifestations of AS was noted. The differences were significant both in comparison with the baseline level and in comparison with the 2nd group. The endothelium-protective effect of LC and ALC has been established.
Conclusion:
The results obtained indicate that in such comorbid patients, the use of LC and ALC reduces the severity of AS manifestations, and the established endotheliotropic properties of the drugs allow them to be recommended as part of the complex personalized therapy of patients with cardiovascular diseases.
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