Does pregabalin offer potential as a first-line therapy for generalized anxiety disorder? A meta-analysis of efficacy, safety, and cost-effectiveness


Por: Cardoner, N, Gutiérrez-Rojas, L, Saiz, P, Lahera, G, alvarez-Mon, MA, Ortega, PA, Pérez-Páramo, M

Publicada: 7 feb 2025
Resumen:
Introduction: Generalized Anxiety Disorder (GAD) is a mental health condition with a recent increase in prevalence. GAD is often underdiagnosed, leading to negative consequences for individuals, healthcare systems, and society. The economic burden and impaired quality of life associated with GAD underscores the need for effective treatment. Pregabalin has shown promise in reducing anxiety symptoms; however, further research is needed to evaluate its efficacy and compare it with other treatment options. This study aimed to assess the efficacy, safety, and optimal pregabalin dosage for the treatment of GAD. Methods: This meta-analysis followed PRISMA guidelines. Pregabalin-treated patients comprised the intervention group, whereas the comparator group received benzodiazepines, SSRIs, SNRIs, or placebo. Efficacy and safety were evaluated using various scales and adverse events (AEs). Randomized clinical trials were included in the study. Four major databases were used for this study. Outcome measures included the Hamilton Anxiety Rating Scale (HAM-A), Clinical Global Impression Improvement Scale (CGI-I), discontinuation rates, costs, and quality-adjusted life-years (QALYs). Meta-analyses were conducted using Review Manager 5.4 software, employing odds ratios (ORs) and mean differences (MDs) with 95% confidence intervals (CIs). Subgroup and sensitivity analyses were performed based on follow-up and dosage. Results: Fourteen studies involving 4,822 patients were analyzed. Pregabalin demonstrated superior efficacy in reducing HAM-A global scores at 2 weeks (MD -1.23, 95% CI -1.79 to -0.66), 4 weeks (MD -1.12, 95% CI -1.60 to -0.63), 8 weeks (MD -2.50, 95% CI -4.21 to -0.79), 12 weeks (MD 0.99, 95% CI 0.35-1.63), and 6 months to 1 year (MD -3.31, 95% CI -4.30 to -2.31). Pregabalin also showed a higher response rate to HAM-A (OR 1.51, 95% CI 1.31 1.75). CGI-I scores favored pregabalin (MD -0.25, 95% CI -0.38 to -0.12), with a higher response rate (OR 1.33, 95% CI 1.15-1.55). The discontinuation rates were lower with pregabalin (OR 0.80, 95% CI 0.70, 0.91). Adverse events favored pregabalin over SSRIs/SNRIs and benzodiazepines at different doses. Pregabalin was associated with higher cost-effectiveness (MD 0.02, 95% CI 0.01, 0.03). Conclusion: Pregabalin is an effective and well-tolerated treatment for generalized anxiety disorder, showing superior efficacy and safety compared with first-line medications.

Filiaciones:
Cardoner, N:
 Hosp Santa Creu & Sant Pau, Dept Paediat, Barcelona, Spain

 Hosp Santa Creu & Sant Pau, Inst Invest Biomed St Pau IIB St Pau, Barcelona 08025, Spain

 Inst Salud Carlos III, Ctr Invest Biomed Red Salud Mental CIBERSAM, Madrid, Spain

 Univ Autonoma Barcelona, Sch Med Bellaterra, Dept Psychiat & Forens Med, Barcelona, Spain

Gutiérrez-Rojas, L:
 Univ Granada, Dept Psychiat, Granada, Spain

 Univ Granada, Inst Neurosci, CTS Res Grp 549, Granada, Spain

Saiz, P:
 Univ Oviedo, Dept Psychiat, Oviedo, Spain

 Inst Salud Carlos III, CIBER Salud Mental, Madrid, Spain

 Inst Invest Sanitaria Principado Asturias ISPA, Oviedo, Spain

 Inst Univ Neurociencias Principado Asturias INEURO, Oviedo, Spain

 Serv Salud Principado Asturias SESPA Oviedo, Oviedo, Spain

Lahera, G:
 Inst Salud Carlos III, CIBER Salud Mental, Madrid, Spain

 Univ Alcala, Dept Psychiat, Madrid, Spain

 Principe Asturias Univ Hosp, Oviedo, Spain

 Inst Invest Sanitaria Ramon & Cajal IRyCIS, Madrid, Spain

alvarez-Mon, MA:
 Hosp Univ Infanta Leonor, Dept Psychiat & Mental Hlth, Madrid, Spain

 Univ Alcala, Dept Med & Med Specialties, Alcala De Henares, Spain

 Ramon & Cajal Inst Sanitary Res IRYCIS, Madrid, Spain

 Inst Salud Carlos III, CIBER Salud Mental, Madrid, Spain

Ortega, PA:
 Inst Salud Carlos III, CIBER Salud Mental, Madrid, Spain

 Hosp Bellvitge Princeps Espanya, Dept Psychiat, Barcelona, Spain

 Bellvitge Biomed Res Inst IDIBELL, Barcelona, Spain

 Univ Barcelona, Dept Clin Sci, Barcelona, Spain

Pérez-Páramo, M:
 Viatris, Med Dept, Madrid, Spain
ISSN: 16639812





Frontiers in Pharmacology
Editorial
FRONTIERS MEDIA SA, AVENUE DU TRIBUNAL FEDERAL 34, LAUSANNE, CH-1015, SWITZERLAND, Suiza
Tipo de documento: Article
Volumen: 16 Número:
Páginas:
WOS Id: 001427869800001
ID de PubMed: 39989902
imagen Green Submitted, gold

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