Guanxinning for Residual Inflammation of Stable Coronary Artery Disease: A Pilot Randomized Controlled Trial

被引:0
作者
Chen, Tielong [1 ]
Zheng, Jianwu
Bao, Cheng
Wang, Yu
Wang, Shiwang
Liang, Lu
Zhang, Li
Zhang, Hui
Ji, Chaoxia
Wang, Jian
Zhang, Xudong
Zhu, Guangli
Zhu, Houyong [1 ]
机构
[1] Zhejiang Chinese Med Univ, Hangzhou TCM Hosp, Dept Cardiol, 453 Stadium Rd, Hangzhou 310007, Zhejiang, Peoples R China
关键词
Guanxinning; stable coronary artery disease; risk of residual inflammation; secondary prevention; CHOLESTEROL; THERAPY;
D O I
10.2147/JIR.S490896
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Despite statins and other medications central to atherosclerotic cardiovascular disease (ASCVD) secondary prevention, stable coronary artery disease (SCAD) patients remain at significant cardiovascular risk, partly due to residual inflammation risk (RIR). This study aims to assess if adding Guanxinning to standard ASCVD therapy further mitigates RIR in SCAD patients. Methods: In a prospective, randomized, single-blind endpoint design, 50 patients with SCAD who received ASCVD standardized treatment strategy were randomly assigned to either take Guanxinning tablets (4 tablets, thrice daily) or no Guanxinning tablets and were followed up for an average of 12 weeks. The primary outcomes were changes in inflammation-related indicators, including interleukin-2 (IL-2), IL-4, IL-6, tumor necrosis factor-alpha (TNF-alpha), and high sensitivity C-reactive protein (hs-CRP). Results: Compared with the control group, the intervention group showed significantly greater decreases in the levels of IL-2, IL-6, TNF-alpha, and hs-CRP (all P < 0.05). However, there was no significant difference in the IL-4 level between the two groups (P > 0.05). Compared with the control group, there were also significant improvements in endothelial function-related indicators (vascular endothelial growth factor (VEGF), nitric oxide (NO), and peroxisome proliferator-activated receptor-gamma (PPAR-gamma)), blood lipid profile (total cholesterol (Tch), low-density lipoprotein cholesterol (LDL-C)), and chest pain related scores (angina and Traditional Chinese medicine syndrome scores) in the intervention group (all P<0.05). There was no significant difference in the triglyceride (TG) and carotid intima-media thickness between the two groups (P<0.05). Compared to the control group, there was no significant difference in the white blood cell line, liver and kidney function, anemia, and bleeding in the intervention group (all P<0.05). Conclusion: The addition of Guanxinning tablets (4 tablets, thrice daily) to the standard treatment strategy for ASCVD was associated with a reduction in the RIR in patients with SCAD and demonstrated good safety. Plain Language Summary: In the quest for a heart-healthy life, even with statins at our side, some folks with stable heart troubles still face a sneaky foe: lingering inflammation. Our study explored whether adding Guanxinning, a traditional Chinese medicine, to the standard treatment might help. Over 12 weeks, patients who took Guanxinning along with their usual heart meds showed promising signs of reduced inflammation and improved heart health markers. These preliminary positive signs hint at the potential benefits of Guanxinning, which, however, need further studies to confirm. Fortunately, it appears to be safe to use Guanxinning alongside conventional treatments for now. As we delve deeper into the mysteries of heart health, every promising discovery brings us one step closer to developing better therapeutic strategies.
引用
收藏
页码:8047 / 8060
页数:14
相关论文
共 37 条
  • [1] A Comprehensive Review on Therapeutic Applications of Ferulic Acid and its Novel Analogues: A Brief Literature
    Babbar, Ritchu
    Dhiman, Sonia
    Grover, Rupanshi
    Kaur, Arashmeet
    Arora, Sandeep
    [J]. MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2021, 21 (12) : 1578 - 1593
  • [2] Inflammation and its resolution in atherosclerosis: mediators and therapeutic opportunities
    Back, Magnus
    Yurdagul, Arif, Jr.
    Tabas, Ira
    Oorni, Katariina
    Kovanen, Petri T.
    [J]. NATURE REVIEWS CARDIOLOGY, 2019, 16 (07) : 389 - 406
  • [3] Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170 000 participants in 26 randomised trials
    Baigent, C.
    Blackwell, L.
    Emberson, J.
    Holland, L. E.
    Reith, C.
    Bhala, N.
    Peto, R.
    Barnes, E. H.
    Keech, A.
    Simes, J.
    Collins, R.
    [J]. LANCET, 2010, 376 (9753) : 1670 - 1681
  • [4] Tackling inflammation in atherosclerosis: Are we there yet and what lies beyond?
    Bhattacharya, Purbasha
    Kanagasooriyan, Ragulan
    Subramanian, Manikandan
    [J]. CURRENT OPINION IN PHARMACOLOGY, 2022, 66
  • [5] JCL roundtable: Lipids and inflammation in atherosclerosis
    Bornfeldt, Karin E.
    Linton, MacRae F.
    Fisher, Edward A.
    Guyton, John R.
    [J]. JOURNAL OF CLINICAL LIPIDOLOGY, 2021, 15 (01) : 3 - 17
  • [6] Cai L, 2019, Chin Pat Med, V41, P933
  • [7] Relationship Between Systemic Immune-Inflammation Index (SII) and the Severity of Stable Coronary Artery Disease
    Candemir, Mustafa
    Kiziltunc, Emrullah
    Nurkoc, Serdar
    Sahinarslan, Asife
    [J]. ANGIOLOGY, 2021, 72 (06) : 575 - 581
  • [8] Ezetimibe Added to Statin Therapy after Acute Coronary Syndromes
    Cannon, Christopher P.
    Blazing, Michael A.
    Giugliano, Robert P.
    McCagg, Amy
    White, Jennifer A.
    Theroux, Pierre
    Darius, Harald
    Lewis, Basil S.
    Ophuis, Ton Oude
    Jukema, J. Wouter
    De Ferrari, Gaetano M.
    Ruzyllo, Witold
    De Lucca, Paul
    Im, KyungAh
    Bohula, Erin A.
    Reist, Craig
    Wiviott, Stephen D.
    Tershakovec, Andrew M.
    Musliner, Thomas A.
    Braunwald, Eugene
    Califf, Robert M.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (25) : 2387 - 2397
  • [9] Cardiovascular effects of Danshen
    Cheng, Tsung O.
    [J]. INTERNATIONAL JOURNAL OF CARDIOLOGY, 2007, 121 (01) : 9 - 22
  • [10] Chinese Expert Group of Intravascular Ultrasound Imaging in Coronary Artery Disease, 2018, Zhonghua Xin Xue Guan Bing Za Zhi, V46, P344, DOI 10.3760/cma.j.issn.0253-3758.2018.05.005