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Tripterygium glycosides for safely controlling disease activity in systemic lupus erythematosus: a systematic review with meta-analysis and trial sequential analysis.
Chen, Yifan; Wang, Liuding; Li, Nannan; Zhou, Caiyun.
Afiliación
  • Chen Y; Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
  • Wang L; Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
  • Li N; Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
  • Zhou C; Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Front Pharmacol ; 14: 1207385, 2023.
Article en En | MEDLINE | ID: mdl-37601046
ABSTRACT

Background:

Tripterygium glycosides have been used to treat systemic lupus erythematosus (SLE) for a long time, showing the effects of immune regulation. We aimed to evaluate the benefits and risks of Tripterygium Glycosides Tablets (TGT) for patients with SLE.

Methods:

We searched electronic databases and clinical trial registries for relevant randomized controlled trials (RCTs). We identified eligible RCTs and assessed risk of bias. We conducted a meta-analysis to estimate the pooled effects. The Trial Sequential Analysis (TSA) 0.9.5.10 software was used to verify the reliability of the results.

Results:

Eight RCTs encompassing 538 patients with SLE were included. TGT combined with conventional treatments (CTs) was superior to CTs alone in reducing lupus activity (MD = -1.66, 95% CI = -2.07 to -1.26, p < 0.00001, low-certainty evidence) and improving overall response rate (ORR) (RR = 1.21, 95% CI = 1.11 to 1.32, p < 0.0001, moderate-certainty evidence). The robustness of the results was confirmed by TSA. Regarding safety, there was no statistical difference in the overall incidence of adverse reactions between the two groups.

Conclusion:

In patients with SLE, TGT might safely reduce disease activity. However, further high-quality studies are needed to firmly establish the clinical efficacy of TGT. Systematic Review Registration https//www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022300474; Identifier CRD42022300474.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Systematic_reviews Idioma: En Revista: Front Pharmacol Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Systematic_reviews Idioma: En Revista: Front Pharmacol Año: 2023 Tipo del documento: Article País de afiliación: China