Efficacy and tolerability of the hexanic extract of Serenoa repens compared to tamsulosin in moderate-severe LUTS-BPH patients.

dc.contributor.authorAlcaraz, Antonio
dc.contributor.authorRodríguez-Antolín, Alfredo
dc.contributor.authorCarballido-Rodríguez, Joaquín
dc.contributor.authorCastro-Díaz, David
dc.contributor.authorMedina-Polo, José
dc.contributor.authorFernández-Gómez, Jesús M
dc.contributor.authorFicarra, Vincenzo
dc.contributor.authorPalou, Joan
dc.contributor.authorPonce de León Roca, Javier
dc.contributor.authorAngulo, Javier C
dc.contributor.authorEsteban-Fuertes, Manuel
dc.contributor.authorCózar-Olmo, José M
dc.contributor.authorPérez-León, Noemí
dc.contributor.authorMolero-García, José M
dc.contributor.authorFernández-Pro Ledesma, Antonio
dc.contributor.authorBrenes-Bermúdez, Francisco J
dc.contributor.authorManasanch, José
dc.date.accessioned2025-01-07T14:17:58Z
dc.date.available2025-01-07T14:17:58Z
dc.date.issued2021-09-29
dc.description.abstractIn a subset analysis of data from a 6-month, multicenter, non-interventional study, we compared change in symptoms and quality of life (QoL), and treatment tolerability, in men with moderate to severe lower urinary tract symptoms associated with benign prostatic hyperplasia (LUTS/BPH) receiving tamsulosin (TAM, 0.4 mg/day) or the hexanic extract of Serenoa repens (HESr, 320 mg/day) as monotherapy. Symptoms and QoL were assessed using the IPSS and BII questionnaires, respectively. Patients in the treatment groups were matched using two statistical approaches (iterative and propensity score matching). Within the iterative matching approach, data was available from a total of 737 patients (353 TAM, 384 HESr). After 6 months, IPSS scores improved by a mean (SD) of 5.0 (4.3) points in the TAM group and 4.5 (4.7) points in the HESr group (p = 0.117, not significant). Improvements in QoL were equivalent in the two groups. TAM patients reported significantly more adverse effects than HESr patients (14.7% vs 2.1%; p 
dc.identifier.doi10.1038/s41598-021-98586-5
dc.identifier.essn2045-2322
dc.identifier.pmcPMC8481292
dc.identifier.pmid34588509
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC8481292/pdf
dc.identifier.unpaywallURLhttps://www.nature.com/articles/s41598-021-98586-5.pdf
dc.identifier.urihttps://hdl.handle.net/10668/26279
dc.issue.number1
dc.journal.titleScientific reports
dc.journal.titleabbreviationSci Rep
dc.language.isoen
dc.organizationSAS - Hospital Universitario Virgen de las Nieves
dc.page.number19401
dc.pubmedtypeComparative Study
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshLower Urinary Tract Symptoms
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshPhytotherapy
dc.subject.meshPlant Extracts
dc.subject.meshProstatic Hyperplasia
dc.subject.meshQuality of Life
dc.subject.meshSerenoa
dc.subject.meshTamsulosin
dc.subject.meshTreatment Outcome
dc.titleEfficacy and tolerability of the hexanic extract of Serenoa repens compared to tamsulosin in moderate-severe LUTS-BPH patients.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number11

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