Effectiveness of alpha-lipoic acid in patients with neuropathic pain associated with type I and type II diabetes mellitus: A systematic review and meta-analysis

Author:

Orellana-Donoso Mathias12,López-Chaparro Michelle2,Barahona-Vásquez Marisol2,Santana-Machuca Andrés3,Bruna-Mejias Alejandro24,Nova-Baeza Pablo2,Valenzuela-Fuenzalida Juan José35ORCID

Affiliation:

1. Escuela de Medicina, Universidad Finis Terrae, Santiago, Chile Departamento de Morfología, Facultad de Medicina

2. Universidad Andres Bello, Santiago, Chile

3. Department of Morphology and Function, Faculty of Health Sciences, Universidad de Las Américas, Santiago, Chile

4. Departamento de Ciencias y Geografía, Facultad de Ciencias Naturales y Exactas, Universidad de Playa Ancha, Valparaíso, Chile

5. Departamento de Ciencias Química y Biológicas, Facultad de Ciencias de la Salud, Universidad Bernardo O’Higgins, Santiago, Chile.

Abstract

Background: This systematic review explores the most current evidence regarding the mechanisms of neuropathic pain in patients with different types of diabetes and how this pain affects different functional and structural components of the neuroanatomical pain pathways. The review also seeks to provide guidelines for the best approach and treatment for patients experiencing this type of pain. The objective is to determine the effectiveness of alpha-lipoic acid (ALA) in improving functional and symptomatic outcomes in patients with diabetes mellitus type I and type II. Objective: To determine the effectiveness of alpha-lipoic acid (ALA) in improving functional and symptomatic outcomes in patients with diabetes mellitus type I and type II. Methods: We systematically search MEDLINE (via PubMed), EMBASE, SCOPUS, the Cochrane Central Register of Controlled Trials, the Cumulative Index to Nursing and Allied Health Literature, and Web of Science databases. Results: The findings of this review show that different forms of ALA do not present statistically significant changes for any of the scales included, including total symptom score (standardized mean difference [SMD] = −3.59, confidence interval [CI] = −4.16 to −3.02, and P < .00001), neuropathy impairment score (SMD = −1.42, CI = −3.68 to 0.84, and P = .22), and neuropathy symptom checklist (SMD = −0.09, CI = −0.15 to −0.02, and P = .01). Conclusion: In comparison to the use of a placebo, the findings suggest that ALA does not exhibit significant differences in terms of pain reduction and different functional scales. Moreover, no specific dosages are identified to support the use of ALA for the reduction of neuropathic pain.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

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