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Efficacy and Safety of Da-Chai-Hu-Tang in Lipid Profiles in High-Risk, Statin-Treated Patients with Residual HyperTG: A 12-Week, Randomized, Active-Control, Open Clinical Study.
Lee, Young-Shin; Lee, Jung-Myung; Chung, Hyemoon; Woo, Jong-Shin; Lee, Byung-Cheol; Kim, Weon.
Affiliation
  • Lee YS; Department of Internal Medicine, Division of Cardiology, Kyung Hee University Hospital, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Korea.
  • Lee JM; Department of Internal Medicine, Division of Cardiology, Kyung Hee University Hospital, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Korea.
  • Chung H; Department of Internal Medicine, Division of Cardiology, Kyung Hee University Hospital, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Korea.
  • Woo JS; Department of Internal Medicine, Division of Cardiology, Kyung Hee University Hospital, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Korea.
  • Lee BC; Department of Clinical Korean Medicine, Graduate School, Kyung Hee University, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Korea.
  • Kim W; Department of Internal Medicine, Division of Cardiology, Kyung Hee University Hospital, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Korea.
Life (Basel) ; 12(3)2022 Mar 11.
Article in En | MEDLINE | ID: mdl-35330160
ABSTRACT
Da-Chai-Hu-Tang (DCHT) is a herbal extract that has been shown to reduce serum triglyceride (TG) levels in animal experiments as well as small clinical trials. This study aimed to evaluate the efficacy and safety of DCHT in high-risk, statin-treated patients with residual hypertriglyceridemia (hyperTG). This was a 12-week, randomized, active-controlled, open-label, single-center trial. Of these patients, 42 had high cardiovascular risks whose LDL cholesterol levels were controlled by statin treatment; however, with TG levels of 200 to 500 mg/dL they were randomly assigned 11 to the OMEGA3 or DCHT group. The primary endpoint was defined as the percentage change in TG at 12 weeks, and changes in other lipid profiles and endothelial cell function were included as secondary endpoints. Safety analyses were also conducted. In the OMEGA3 group, the average TG level decreased from 294.5 ± 72.0 to 210.0 ± 107.8 mg/dL (p = 0.004), and in the DCHT group, from 288.7 ± 59.1 to 227.5 ± 98.1 mg/dL (p = 0.001). The percentage change in TG was -27.6 ± 33.6 and -22.4 ± 24.1 (p = 0.58), respectively, and there was no significant difference between the two groups. There were no severe adverse events in either group. In high-risk, statin-treated patients with residual hyperTG, the administration of OMEGA3 or DCHT for 12 weeks resulted in a significant reduction in TG, and the effect of DCHT was not inferior to that of OMEGA3.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Etiology_studies / Risk_factors_studies Language: En Journal: Life (Basel) Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Etiology_studies / Risk_factors_studies Language: En Journal: Life (Basel) Year: 2022 Document type: Article