Safety of 12-Months Administration of Ashwagandha ( Withania somnifera ) Standardized Root Extract in Healthy Adults: A Prospective, Observational Study
Salve J, Kale S, Prajapati BL, Sparavigna A, Savant M, Ademola J, Langade D
Phytotherapy research : PTR · 10 citas
Cómo se estudió
- Diseño
- Estudio de cohortes (indexado por PubMed)
- Estudiado en
- Personas
- Resultado principal
- Marcadores de salud y funcionamiento
Quién lo pagó
- Financiación
- Financiación independiente
Según la declaración de financiación del texto completo.
Publicación
- Publicado
- 2025-10-08 · Phytother Res · vol. 40 · número 8 · págs. 4802–4812
- Editorial
- Wiley
- Citado
- 6 citas · más que el 97% de estudios similares · 6.8× el promedio de su campo
- Impacto
- Entre el 10 % más citado de su campo
- Referencias
- 56 trabajos
- Acceso
- Acceso abierto (revista híbrida) · CC-BY-NC-ND
- Áreas de investigación
- Phytochemicals and Medicinal Plants · Complementary and Alternative Medicine Studies
- Palabras clave
- Observational study, Adverse effect, Alanine aminotransferase, Oral administration, Clinical trial, Quality of life (healthcare), Alanine transaminase, Phytotherapy
- MeSH
- humans, withania, plant roots, hydrocortisone, alanine transaminase, aspartate aminotransferases, plant extracts, prospective studies, quality of life, adolescent, adult, aged, middle aged, female, male, young adult
7 autores
- Jaising Salve
- Sanjeev Kale🇮🇳D.Y. Patil University
- Banwari Lal Prajapati
- Adele Sparavigna🇮🇹Bioengineering Technology and Systems (Italy)
- Mark Savant🇺🇸San Francisco Art Institute
- John Ademola🇺🇸San Francisco Art Institute
- Deepak Langade🇮🇳 · autor de correspondenciaD.Y. Patil University
Resumen
El texto original del estudio, en el idioma en que se publicó.
Ashwagandha, an adaptogen, is an important herb of Ayurveda used as a Rasayana for its various health benefits. This prospective, multi-center, observational clinical study evaluates the safety (clinical and laboratory) of a standardized Ashwagandha Root Extract (ARE) on long-term administration over 12 months. Male and female adults (N = 191) aged between 18 and 65 years were included in the study. Clinical assessments were done at baseline, followed by monthly for 12 months, whereas laboratory and other study assessments were done at baseline, 6 and 12 months. The primary outcome was the clinical adverse events reported by the patients, whereas secondary outcomes were Clinical Global Impression-Improvement scale (CGI-I), health-related Short Form-12 Quality of Life (SF-12 QoL), and laboratory estimations of serum for cortisol, hepatic, renal, and thyroid function. ARE administration for 12 months reported 18 mild adverse events, which were resolved without intervention. The study reported no clinical significant changes in serum alanine transaminases (baseline: 31.31 ± 9.28 IU/L, end of study: 33.68 ± 6.80 IU/L), aspartate transaminases (baseline: 30.61 ± 7.18 IU/L, end of study: 29.02 ± 4.63 IU/L). Serum cortisol levels decreased significantly (p < 0.001), while lipid profile and plasma glucose levels remained unaffected. Serum testosterone (free and total) significantly increased (p < 0.05). SF-12 scores demonstrated significant improvements at 12 months (p < 0.001), indicating enhanced health-related quality of life. CGI assessment indicated overall improvement in 68.7% of patients, particularly notable in those aged ≥ 50 years. This study validates the long-term safety of ARE use over 12 months. Trial Registration: ClinicalTrials.gov identifier: CTRI/2022/10/046180; NCT06244147.
Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial (CC BY-NC-ND).
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