Benefits of Taurisolo in Diabetic Patients with Peripheral Artery Disease

Author:

Amato Bruno1ORCID,Novellino Ettore2ORCID,Morlando Davide1,Vanoli Camilla3,Vanoli Emilio4,Ferrara Fulvio5ORCID,Difruscolo Rossana6,Goffredo Vito Maria7,Compagna Rita8,Tenore Gian Carlo9ORCID,Stornaiuolo Mariano9ORCID,Fordellone Mario10ORCID,Caradonna Eugenio5

Affiliation:

1. Department of Public Health, Università degli Studi di Napoli Federico II, 80138 Naples, Italy

2. Chimica Farmaceutica e Tossicologica, Università Cattolica del Sacro Cuore, 20123 Rome, Italy

3. Clinical Psychology, Antioch University Los Angeles, Culver City, CA 90230, USA

4. School of Nursing, University of Pavia, 27100 Pavia, Italy

5. Centro Diagnostico Italiano, Department of Clinical Laboratory, 20100 Milan, Italy

6. Biotecnologie Mediche e Farmaceutiche, Università degli Studi di Bari, 70126 Bari, Italy

7. Department of Interdisciplinary Medicine, Università degli Studi di Bari, 70124 Bari, Italy

8. Vascular Surgery Unit AORN Ospedale dei Colli, 80131 Naples, Italy

9. Department of Pharmacy, Università degli Studi di Napoli Federico II, 80138 Naples, Italy

10. Unità di Statistica Medica, Dipartimento di Salute Mentale e Fisica e Medicina Preventiva, Università degli Studi della Campania ‘Luigi Vanvitelli’, 81020 Napoli, Italy

Abstract

Trimethyl-N-oxide (TMAO) has been linked to peripheral artery disease (PAD). TaurisoloⓇ is a natural, balanced phytocomplex containing resveratrol, quercetin, catechins, procianidins, gallic acid, and caffeic acid. Numerous studies have shown that TaurisoloⓇ reduces the damage of TMAO and exerts a protective effect on endothelial cells (ECs). The aim of this randomized, double-blind, single-center study was to evaluate the effects of TaurisoloⓇ on claudication in patients with PAD (Rutheford grade I, category II, Fontaine Classification: Stage IIA, American Medical Association Whole Person Impairment Classification: Class 0—WPI 0%) in two parallel groups of 31 patients. The primary outcomes were an increase in the pain-free walking distance and the ankle/brachial pressure index at the beginning and at the end of the treatment with Taurisolo. The secondary endpoint was the serum TMAO changes. The claudication distance improved by 14.1% in the Taurisolo group and by 2.0% in the placebo group, while the maximal distance increased by 15.8% and 0.6% only, respectively (both p < 0.05). The TMAO plasma levels decreased from 3.97 ± 2.13 micromole/L to 0.87 ± 0.48 (p < 0.0001) in the treated group. All these changes were highly significant both in univariate mixed models as well as in the adjusted model. Ultimately, TaurisoloⓇ might be an effective intervention to ameliorate intermittent claudication.

Publisher

MDPI AG

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