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SYSTEMATIC REVIEW article

Front. Pharmacol.

Sec. Ethnopharmacology

Volume 16 - 2025 | doi: 10.3389/fphar.2025.1520039

This article is part of the Research Topic Herbal Medicine for the Treatment of Chronic Metabolic Diseases, Volume II View all 15 articles

Efficacy and safety of Tanshinone capsule in Acne vulgaris:a systematic review and meta-analysis

Provisionally accepted
Yutong Deng Yutong Deng 1*Ruli Feng Ruli Feng 1Bo Hu Bo Hu 2Xuewen Ren Xuewen Ren 3Fengchuan Zhang Fengchuan Zhang 2Huishang Feng Huishang Feng 4Xuewan Wang Xuewan Wang 1Yatong Li Yatong Li 1Tangyunni Liu Tangyunni Liu 1Lingling Cai Lingling Cai 2*Yuanwen Li Yuanwen Li 2*
  • 1 Beijing University of Chinese Medicine, Beijing, China
  • 2 Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, Beijing, China
  • 3 Shanxi Traditional Chinese Medical Hospital, Taiyuan, Shanxi Province, China
  • 4 Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, Beijing Municipality, China

The final, formatted version of the article will be published soon.

    Objectives: To evaluate the efficacy and safety of Tanshinone capsule as a complementary therapy in managing of Acne Vulgaris.A systematic search of six databases was conducted to identify relevant randomized controlled trials (RCTs) from each database for nearly 20 years (from Jan 1, 2004, to June 1, 2024). The Cochrane Handbook was used to evaluate the risk of bias. Meta-analysis was performed using Review Manager 5.4.1, and publication bias was assessed the Stata SE 12.0 software. GRADEpro was used to assess the quality of the evidence.Results: A total of 2,969 participants from 28 studies were included. We found that Tanshinone capsules can reduce acne recurrence rates [ risk ratio (RR) 0.44, 95% confidence interval (CI): 0.34 to 0.57, p < 0.00001]; downregulate levels of necrosis factor-alpha (TNF-α) [ mean difference (MD) 0.44, -10.18, 95% CI: -13.57 to -8.04, p

    Keywords: Tanshinone capsule, Acne Vulgaris, Meta-analysis, Systematic review, randomized controlled trial 1.Introduction

    Received: 30 Oct 2024; Accepted: 10 Mar 2025.

    Copyright: © 2025 Deng, Feng, Hu, Ren, Zhang, Feng, Wang, Li, Liu, Cai and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence:
    Yutong Deng, Beijing University of Chinese Medicine, Beijing, China
    Lingling Cai, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, Beijing, China
    Yuanwen Li, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, Beijing, China

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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