Search tips
Search criteria 


Logo of scirepAboutEditorial BoardFor AuthorsScientific Reports
Sci Rep. 2017; 7: 17451.
Published online 2017 December 12. doi:  10.1038/s41598-017-16980-4
PMCID: PMC5727111

Sodium tanshinone IIA sulfate adjunct therapy reduces high-sensitivity C-reactive protein level in coronary artery disease patients: a randomized controlled trial


High-sensitivity C-reactive protein (hs-CRP) is independently associated with cardiovascular events in coronary artery disease (CAD) patients and reducing the hs-CRP level may further benefit this population. We conduct this parallel design, randomized-controlled trial to assess the effectiveness of adjunct sodium tanshinone IIA sulfate (STS) therapy on circulating inflammation markers in CAD patients. Unstable angina or non-ST-elevation myocardial infarction patients with increased hs-CRP level were randomly assigned to atorvastatin-based standard medical therapy or standard therapy plus STS injection (80 mg, once daily for 14 consecutive days). The primary outcome was hs-CRP level. After the 14-day treatment, the experimental group (n = 35) exhibited significantly lower levels of hs-CRP than the control group (n = 35) (1.72 vs 3.20 mg/L, p = 0.0191). Lower levels of interleukin-6, monocyte chemotactic protein-1 (MCP-1), and soluble CD40 ligand were also observed in the experimental group. Angina symptoms were also better controlled in the experimental group. At 30 days after treatment completion, MCP-1 levels remained lower in the experimental group than in the control group (313.88 vs 337.91 pg/mL, p = 0.0078). No serious adverse events occurred. Our study demonstrates that on the basis of standard medical therapy, STS further reduce elevated hs-CRP and other circulating inflammation markers in CAD patients. ( number: ChiCTR-TRC-12002361).


Cardiovascular disease is the worldwide leading cause of death, and coronary artery disease (CAD) is responsible for the greatest mortality. Inflammation plays an important role both in the development of atherosclerosis and in triggering cardiovascular events1. As a robust marker of systematic inflammation, high-sensitivity C-reactive protein (hs-CRP) has been closely studied25, and a meta-analysis showed that hs-CRP >3 mg/L is an independent risk factor for cardiovascular events6. Therefore, reducing the concentration of hs-CRP may further benefits patients with CAD. In fact, the mortality reduction and cardiovascular benefits of statins, a cornerstone of evidence-based standard medical therapy for CAD, may partly attribute to its anti-inflammation effect.

Indeed, the JUPITER trial found that, among non-hyperlipidemic patients with elevated hs-CRP, statin therapy reduced hs-CRP levels by 37%, and led to a significantly lower rate of major adverse cardiovascular events after 1.9 years compared to placebo7. Nevertheless, despite intensive statin therapy, 22.4% of patients with acute coronary syndrome suffer a serious cardiovascular or cerebrovascular event within two years of initiating treatment8, thus revealing the extent of residual cardiovascular risk, as well as the potential benefit of further dampening the inflammatory reaction of atherosclerosis.

Tanshinone IIA, one of the most pharmacologically active components extracted from Radix Salviae miltiorrhizae, has been identified as a promising natural cardioprotective agent9. Most noteworthy is the ability of tanshinone IIA to decrease the levels of multiple inflammatory factors associated with the progression of atherosclerosis, such as CRP, interleukin-6 (IL-6), tumor necrosis factor alpha (TNF-𝛼), vascular cell adhesion molecule-1 (VCAM-1), CD40, monocyte chemotactic protein-1 (MCP-1), and matrix metalloproteinase-9 (MMP-9)10,11. Because of the low oral bioavailability of tanshinone IIA12, intravenous sodium tanshinone IIA sulfate (STS) has been developed (Fig. 1), and is the most widely used clinical formulation of tanshinone IIA in China for patients with CAD.

Figure 1
The chemical structure of sodium tanshinone IIA sulfate.

In this trial, we hypothesized that the addition of STS to standard statin-containing medical therapy for patients with CAD will: 1) further reduce the levels of serum hs-CRP and other circulating inflammatory markers after 14 days of treatment; 2) show a sustained effect on inflammatory marker levels at 30 days after treatment completion; 3) improve angina symptoms; and 4) be a safe treatment, compared to standard medical therapy alone.


Participant characteristics

Study participants were recruited from August 2012 to January 2014, and final follow-up was completed by February 2014. A flow diagram illustrating the study design is shown in Fig. 2. A total of 280 inpatients were assessed for eligibility, and finally, 72 eligible participants were enrolled. Among which, 36 participants were randomly assigned to receive standard statin-containing medical therapy with uniformly-dosed atorvastatin 20 mg daily (control statin group) and 36 to standard medical therapy plus 80 mg intravenous STS daily (experimental statin+STS group). Two patients were subsequently excluded because of mis-inclusion: 1 patient in the statin group withdrew to receive percutaneous coronary intervention (PCI) during hospitalization, and 1 patient in the statin+STS group developed pneumonia. Ultimately, 70 participants (35 in each group) completed the 14-day treatment. During the 30-day follow-up period, 3 participants, 2 in the statin+STS group and 1 in the statin group, were lost to follow up. Among them, one declined to participate in the follow-up since she has left Beijing, two were unreachable for data collection. Intention-to-treat analysis was performed, involving all 70 patients who were successfully randomized, and the last-observation-carried-forward (LOCF) imputation method was used to account for missing data.

Figure 2
Flow Diagram of Study Design. aTwo patients were excluded because of mis-inclusion: 1 patient in the control statin group elected to undergo percutaneous coronary intervention during hospitalization, and 1 patient in the experimental statin +STS group ...

Of our 70 enrolled patients, 63 (90%) presented with unstable angina, and 7 (10%) presented with non-ST-elevation myocardial infarction (NSTEMI). CAD diagnosis was documented by previous coronary angiography performed any time prior to enrollment in 57 patients (81.4%), and via prior or present history of myocardial infarction in 13 patients (18.6%). The baseline characteristics of the participants are shown in Table 1, and the two groups were comparable in demographics, presenting diagnosis, cardiovascular risk factors, number of diseased vessels, thrombolysis in myocardial infarction (TIMI) risk score, and blood lipid concentrations. The use of other cardiovascular medications comprising standard medical therapy for CAD, including aspirin, clopidogrel, beta-blockers, angiotensin-converting enzyme inhibitors (ACEI), angiotensin receptor blockers (ARB), calcium channel blockers (CCBs), and agents for diabetes mellitus, was also similar between the groups.

Table 1
Baseline Characteristics.

Primary endpoint

The levels of hs-CRP in the experimental statin + STS group and control statin group at baseline, immediately after 14 days of treatment, and at 30 days after completion of treatment are illustrated in Fig. 3. The data for comparisons in hs-CRP level between the statin + STS and statin groups are delineated in Table 2, while the data for comparisons within each group are presented in Table 3.

Figure 3
Comparison of hs-CRP level between groups at baseline, after 14-day treatment, and at 30 days after completion of treatment. *Statistically significant, p < 0.05. **Statistically significant, p < 0.01. hs-CRP, ...
Table 2
Comparison of hs-CRP between groups at baseline and after treatment.
Table 3
Comparison of hs-CRP, IL-6, MCP-1, sCD40L, MMP-9, sVCAM-1, TNF-α levels within each group at baseline and after treatment.

Baseline hs-CRP level was similar in the statin+STS and statin groups (5.35 vs 5.04 mg/L, respectively, p = 0.3894). After 14 days of treatment, however, hs-CRP level was significantly lower in the statin+STS group than in the statin group (1.72 vs 3.20 mg/L, p = 0.0191). Indeed, the magnitude of the absolute and relative reductions in hs-CRP level after 14 days of treatment were greater for the statin+STS group than for the statin group. Whereas a significant reduction in hs-CRP level was observed within the statin+STS group after 14 days of treatment compared to baseline (1.72 vs 5.35 mg/L, p < 0.01), the change in hs-CRP level within the statin group was not significant (3.20 mg/L after 14 days of treatment vs 5.04 mg/L at baseline, p = 0.26).

At 30 days after the completion of treatment, hs-CRP levels in the statin+STS and statin groups were not significantly different (1.80 vs 3.50 mg/L, respectively, p = 0.2408). The level of hs-CRP within the statin+STS group, however, remained significantly lower at 30 days after treatment completion than at baseline (1.80 vs 5.35 mg/L, p < 0.01). The level of hs-CRP within the statin group, too, was significantly lower at 30 days after treatment completion than at baseline (3.50 vs 5.04 mg/L, p = 0.03).

In addition, the reduction of the experimental group was more significant than that of the control group (2.99 vs 1.54 mg/L, P = 0.0485) after 14-day treatment, so as the percent change (71.75% vs 30%, P = 0.0114) (Table 2).

Secondary endpoints

Other circulating inflammatory marker levels

The levels of IL-6, MCP-1, soluble CD40 ligand (sCD40L), MMP-9, soluble VCAM-1 (sVCAM-1), and TNF-α in the experimental statin + STS group and control statin group at baseline, immediately after 14 days of treatment, and at 30 days after completion of treatment are illustrated in Fig. 4. The data for comparisons within each group are presented in Table 3.

Figure 4
Comparison of IL-6, MCP-1, sCD40L, MMP-9, sVCAM-1, and TNF-𝛼 levels between groups at baseline, after 14-day treatment, and at 30 days after completion of treatment. *Statistically significant, p < 0.05. **Statistically ...

For all the inflammatory markers above, baseline levels were similar between the 2 groups. After 14 days of treatment, the level of IL-6 in the statin + STS group was significantly less than that in the statin group (7.76 vs 9.55 pg/mL, p = 0.0096), and the same was true of MCP-1 (301.65 vs 327.24 pg/mL, p = 0.0014) and sCD40L (728.80 vs 848.90 pg/mL, p = 0.0361). In addition, within both groups, all of the inflammatory markers were significantly decreased after 14 days of treatment compared to baseline.

At 30 days after the completion of treatment, the level of MCP-1 in the statin + STS group remained significantly less than that in the statin group (313.88 vs 337.91 pg/mL, respectively, p = 0.0078). Whereas levels of all the other inflammatory markers were similar between the 2 groups. Within the statin + STS group, the levels of all the inflammatory markers except sVCAM-1 remained significantly lower at 30 days after treatment completion than at baseline, and within the statin group, the same was true for all the inflammatory markers except sCD40L and sVCAM-1.

No significant differences in the levels of MMP-9, sVCAM-1, and TNF-α were observed between the 2 groups after 14 days of treatment, or at 30 days after the completion of treatment.


Total angina scores for the experimental statin + STS group and control statin group at each time point are presented in Table 4. The median total angina score (no angina = 0 points, maximum = 24 points) was similar at baseline between the statin+STS and statin groups (10 vs 12 points, respectively, p = 0.105). Median total angina score for the statin+STS group was significantly lower compared to that of the statin group both immediately after 14 days of treatment (0 vs 6 points, respectively, p < 0.01) and at 30 days after the completion of treatment (2 vs 8 points, p < 0.01).

Table 4
Comparison of angina score between groups at baseline and after treatment.


No significant adverse side effects (e.g. bleeding events, abnormal liver or kidney function tests) or major adverse cardiovascular events (e.g. myocardial infarction, stroke, urgent coronary revascularization, death) were observed during the whole study period in all 72 participants. Two participants in the statin + STS group complained of mild dizziness (n = 1) or headache (n = 1) with initiation of treatment, which all fully disappeared the next day without special intervention. At 30 days after the completion of treatment, the survival in both groups was 100%.


Recent research has established a fundamental role for inflammation in atherosclerosis and CAD. Among the various systemic inflammatory markers, hs-CRP has the greatest predictive value for atherosclerotic plaque stability and acute cardiovascular events5. In the JUPITER trial, de novo initiation of rosuvastatin 20 mg daily reduced the incidence of major adverse cardiovascular events in apparently healthy persons without hyperlipidemia but with elevated hs-CRP level7, thus suggesting the potential of hs-CRP to be a therapeutic target. A meta-analysis including 22 trials indicated that hs-CRP >3 mg/L was independently associated with risk of incident CAD events6, while hs-CRP >15 mg/L may be more suggestive of infection. Therefore, hs-CRP was adopted as the primary outcome measure in this trial, but only patients with confirmed CAD and with elevated hs-CRP level between 3 mg/L and 15 mg/L were enrolled. Our results showed that 14 days of adjunctive STS therapy was more effective in reducing elevated hs-CRP level than standard medical therapy alone.

In addition to affecting hs-CRP, adjunctive STS therapy also reduced the levels of IL-6, MCP-1, and sCD40L further than did standard medical therapy alone. IL-6 is a potent pro-inflammatory cytokine that coordinates the release of CRP during the acute-phase response, and may have autocrine, paracrine, and endocrine mechanisms that all contribute to CAD pathogenesis13. Furthermore, MCP-1 plays an important role in atherosclerosis as a key chemokine regulating the migration and infiltration of mononuclear cells and macrophages14, and CD40-mediated signaling has been implicated in the process of plaque destabilization15. The upregulation of IL-6, MCP-1, and CD40L in the setting of CAD has each been associated with worse clinical outcomes1619, and as such, these important inflammatory factors represent additional targets for future anti-inflammatory CAD therapy. However, our study did not show a significant effect of adjunctive STS on levels of TNF-α, MMP-9, and sVCAM-1, which differs from the results of previous experimental studies10. Nevertheless, STS represents a promising adjunctive therapy for mitigating residual cardiovascular risk secondary to inflammation in CAD patients. Indeed, Robertson et al. recently conducted a large-scale screening of anti-inflammatory compounds using zebrafish as an animal model, and identified tanshinone IIA as one of the most potent anti-inflammatory agents among thousands of compounds screened20.

Since STS is an intravenous preparation not suitable for long-term application, we investigated whether adjunctive STS therapy might yield sustained anti-inflammatory effects after discontinuation of treatment. Our results showed that the significant reduction in MCP-1 level following administration of integrative statin-STS therapy compared to standard medical therapy alone persisted to 30 days after the treatment was completed. Although there was no statistically significant difference in hs-CRP reduction between the groups at 30 days after the completion of treatment, we nevertheless observed a clear trend toward lower hs-CRP levels in the statin-STS group as compared to the control group. This negative result might be due to the small sample size of this preliminary trial. Larger clinical trials with longer duration of follow-up are necessary to clarify whether there is a sustained, long-term effect of adjunctive STS on hs-CRP, and whether this promising anti-inflammatory effect might be translatable into clinical benefits.

In addition to anti-inflammatory effects, STS also possesses both anti-platelet and anticoagulant properties21,22. Considering the potential for drug interactions between STS and the various anti-thrombotic agents commonly used in conventional CAD treatment, increased hemorrhagic events associated with adjunctive STS therapy may be an issue of concern in clinical practice. In this short-term, small-sized clinical trial, we did not observe any bleeding events or any other serious adverse events associated with adjunctive STS therapy. Our results suggest that the addition of STS to standard medical therapy for CAD might not increase the risk of bleeding events or hepatorenal side effects, although the full safety profile of this integrative therapy should be further assessed in future larger scale clinical trials.

Some limitations of this trial should be noted. First, the sample size was small, and thus the study may not have sufficient power to detect statistical differences between the 2 groups for each serum inflammatory marker. Second, the open-label design of our study introduces the potential for patients, physicians, or researchers to be influenced by their knowledge of a patient’s treatment allocation. Nevertheless, blinded end-point assessment by outcome adjudicators, laboratory blood technicians, and data analysts minimized the potential biases. Third, the short 30-day follow-up period after the completion of treatment limits our ability to resolve the long-term effects of STS on serum inflammatory markers, and also hinders our ability to determine the potential benefit of STS in preventing recurrent cardiovascular events.

In conclusion, we demonstrate in this trial that an 80 mg intravenous dose of STS administered daily for 14 days, as an adjunct to standard medical therapy with uniformly-dosed atorvastatin, further reduced the levels of circulating inflammatory markers including hs-CRP, IL-6, MCP-1, and sCD40L in CAD patients compared to standard medical therapy alone. The apparent additive effect of STS in reducing the level of MCP-1 even persisted to 30 days after the completion of treatment. Our study also demonstrated a considerable improvement in angina symptoms, including the frequency and severity of angina pectoris, as compared with standard medical therapy alone. Given that no previous high-quality study has examined the effect of STS on hs-CRP and other inflammatory markers in CAD patients, our findings shed light on the benefit and safety of an integrative statin + STS regimen for CAD patients with enhanced inflammatory reaction, thereby offering potential implications for clinical practice. Whether the additional reduction of inflammatory factors in CAD patients will ultimately reduce future cardiovascular events and yield long-term prognostic benefit will be the focus of future clinical trials.



The study protocol (2012XL022-2) was approved by the ethics review board of Xiyuan Hospital, China Academy of Chinese Medical Sciences (CACMS), and is available23. The study is registered at ( number: ChiCTR-TRC-12002361, registered on 07/22/2012). All aspects of our study were conducted with adherence to the current version of the Declaration of Helsinki, the guidelines established by the International Conference on Harmonization of Good Clinical Practice, and the laws of China. All participants signed informed consent forms before enrollment.

Trial design and settings

This trial was a parallel-group, prospective randomized open-label blinded-endpoint (PROBE) study conducted in China. The eligible participants were randomized 1:1 into either the control group (standard medical therapy for CAD with uniformly-dosed atorvastatin) or the experimental group (control regimen plus 80 mg intravenous dose of STS daily). Because atorvastatin reduces hs-CRP to a greater extent than other statins24, and is more popular in clinical practice, we treated participants with uniformly-dosed atorvastatin instead of simvastatin, as originally proposed in our published study protocol.


Hospitalized patients with unstable angina or non-ST-elevation myocardial infarction between 35 and 75 years of age were eligible if they were on statin therapies for at least 1 month, had increased hs-CRP level (between 3 mg/L and 15 mg/L) at enrollment, and with documented CAD (with at least 1 coronary artery stenosis ≥50% confirmed by previous coronary angiography, or with a documented history of myocardial infarction [coronary angiography not required]). The diagnosis of CAD was based on the standardized criteria established in “Nomenclature and criteria for diagnosis of ischemic heart disease,” a joint report published by the International Society and Federation of Cardiology and the World Health Organization25, and the ESC Guidelines for the management of acute coronary syndromes in patients presenting without persistent ST-segment elevation26.

Exclusion criteria included severe heart failure (ejection fraction <35%), reduced platelet count or other bleeding diatheses, cancer, sexually transmitted diseases, tuberculosis, rheumatoid arthritis or other autoimmune diseases, infection, fever, trauma, burn injury, surgery within one month prior to recruitment, or any history of serious pulmonary, hepatic, renal, neurological, psychiatric, or hematological diseases. Additional exclusion criteria included active use of any antibiotics or any traditional Chinese medicine with the function of clearing heat and removing toxins (e.g. Honeysuckle, Forsythiae Fructus, Taraxacum, Rheum officinale, Polygonum cuspidatum). Patients participating in other clinical trials were also excluded. Finally, patients must not have previously (within one month) undergone or currently be planning to undergo PCI or coronary artery bypass grafting, considering their effect on inflammatory factors.

Recruitment, intervention, and data collection took place at the inpatient department of Xiyuan Hospital, CACMS, and China-Japan Friendship Hospital in Beijing, China. Subjects were recruited from August 2012 to January 2014, and follow-up was completed by February 2014.


Each patient in the control group received 20 mg atorvastatin orally once per evening, in addition to any other oral or intravenous medications (e.g. beta-blockers, ACEI/ARB, CCB, aspirin, clopidogrel, nitrates) deemed appropriate for a standard treatment of the patient’s individual condition. Doses of ACEI/ARB or beta-blockers were titrated gradually to target levels whenever possible. These standard medications were prescribed by physicians who were not associated with the trial. Additionally, patients in the experiment group received intravenous STS (80 mg, once daily for 14 consecutive days, 10 mg per ampoule, Jiangsu Carefree Pharmaceutical Co., Ltd., national drug approval number: H31022558), diluted with 250 mL 0.9% sodium chloride solution.

All study participants received treatment as indicated above for 14 consecutive days. After 14 days, patients in both groups continued to receive guideline-based standard medical therapy for CAD.

Outcome measures

Serum hs-CRP level was the primary outcome. Secondary outcomes included 1) the levels of other inflammatory mediators, including IL-6, TNF-𝛼, VCAM-1, sCD40L, MCP-1, and MMP-9, as measured by enzyme-linked immunosorbent assay; 2) the extent of improvement in angina symptoms; and 3) treatment safety.

The extent of improvement in angina symptoms was evaluated by a scoring system (Supplementary Table S1) based on the frequency, duration, and intensity of angina episodes, as well as the dose of nitroglycerin utilized, according to “Cardiovascular Drug Clinical Research Guiding Principles” by the Ministry of Health, People’s Republic of China, 1998. The total angina score ranges from a minimum 0 points (no angina) to a maximum 24 points, and higher score indicates more severe angina symptoms.

To assess treatment safety, patients were asked to report any side effects or changes in feelings that they had noticed. In addition, the results of routine blood, urine, and stool tests, liver and kidney function tests, coagulation tests, and electrocardiogram tests were also considered in the evaluation of safety. Finally, adverse events including death, adverse cardiovascular events (myocardial infarction, stroke, etc.) were closely monitored and recorded by the clinical researchers during the whole study period.

All outcomes were measured at baseline, immediately after completion of the 14-day treatment, and at 30 days after completion of treatment. No changes to the designated trial outcomes were made after the study commenced.

Sample size estimation

Because the data needed to perform an a priori sample size calculation for this pilot study was not available, we adopted the sample size of a comparable trial which involved 60 subjects randomized into two groups of 30 each27. For our study, planned to recruit 72 patients, assuming conservatively that 20% of the participants would be lost to follow-up. No interim analyses were undertaken.

Randomization and blinding

A member of the Institute of Clinical Pharmacology (ICP) of Xiyuan Hospital who was independent of the study used SAS 9.3 software (SAS Institute, Cary, NC, USA) to perform a permuted-block randomization, generating a sequence of 72 random numbers. To maintain concealment, the group assignments were relayed by another member of the ICP using a central randomization strategy. Once a patient met all the criteria for enrollment in the trial, the group assignment was delivered by telephone to the clinical researchers. Given that the color of the STS solution is unique and challenging to emulate, unblinding was permitted at the physician and patient levels only after baseline data was collected. In order to minimize biases as much as possible, all other potential sources of information that may reveal treatment allocation to the patients were judiciously guarded. Additionally, the details of treatment allocation were not disclosed to any patient until the study had concluded, and all study participants were discouraged from discussing with one another their involvement in the trial. Finally, the clinical researchers strictly abided by the study’s random design and interacted with the patients in each group with as few differences as possible. Blinding was maintained at the level of outcome assessment. The individuals performing laboratory blood analyses, data management, and statistical analysis were independent of the clinical component of the study, and were not provided with any information that may reveal treatment allocation details.

Statistical analysis

Statistical analyses were performed with SAS9.3 software (SPSS, Inc., Chicago, IL, USA). Categorical data were reported as counts with the percentage of the total and continuous data as a mean with standard deviation, or as a median with 95% confidence interval (CI) or interquartile range (IQR). The χ2 test or Fisher’s exact test was used for comparisons of categorical data. Because serum levels of hs-CRP, IL-6, TNF𝛼, VCAM-1, sCD40L, MCP-1, and MMP-9 were measurement data, an independent Student’s t-test was used for the analysis of intergroup differences when the date meet the normal distribution; Wilcoxon rank-sum test was used when the distribution of levels of the data was non-normality. In addition, comparison of inflammatory markers levels within the group be conducted by paired t-test or paired Wilcoxon rank-sum test. Wilcoxon rank-sum test was used to the analysis of intergroup differences of total angina scores because the distribution of levels of the data was non-normality. All tests were two tailed and a statistical probability of <0.05 was considered significant.

Electronic supplementary material


The authors are grateful to Profs. Feng-Qin Xu, Wen-Xin Tong, Jin Zhang, Li Xin, Wen-Ying Zeng (Cadre Department of Xiyuan Hospital); Profs. Zheng-Tang Liu, Jie-Hong Yang, Lan-Feng Zhang (Geriatric Department of Xiyuan Hospital); Profs. Guo-Ju Dong, Pei-Li Wang, Wen-Hui Duan, Zhu-Ye Gao, Jian-Peng Du, Da-Wu Zhang (Cardiovascular Diseases Center of Xiyuan Hospital); and Profs. Chun-Yan Li, Xiao-Yan Lu, Huan Gu, Ming-Jing Shao (Integrative Cardiology Department of China-Japan Friendship Hospital) for supporting the enrollment of participants. The authors thank Mei-Li Yu and Ying-Nan Yu for the collection of clinical data; Zhuo Chen, Fang-Yuan Che, An-Lu Wang for their participation in data input; and Lei Zhang, Zhuo Chen, Jing Luo for ELISA testing; Jin-Gen Li and Xue-Zhong Zhou (Beijing Jiaotong University) for statistical analysis of consulting. The authors would also like to thank Yang Zhao and Yan Dong from the ICP of Xiyuan Hospital for their contributions in creating the database, maintaining quality control, and participating in data analysis. This work was supported by the Jiangsu Carefree Pharmaceutical Co., Ltd, and “the Fundamental Research Funds for the Central Public Welfare Research Institutes” [grant number ZZ0708102].

Author Contributions

Author Contributions

Siming Li and Yang Jiao conducted the study. Qinghua Shang, Hanjay Wang, and Hao Xu designed the study. Fang Lu analyzed the data. Li Huang provided essential materials. Jiangang Liu guided ELISA testing. Siming Li wrote the manuscript and Hanjay Wang revised it. Keji Chen, Hao Xu, and Fang Lu critically reviewed the manuscript for important intellectual content. All authors read and approved the final manuscript.


Competing Interests

This trial received financial support from the Jiangsu Carefree Pharmaceutical Co., Ltd. The company was not involved in developing the study design, collecting or interpreting the data, writing the paper, or publishing the results related to this trial. All of the authors declare that they have no conflict of interest.


Siming Li and Yang Jiao contributed equally to this work.

Electronic supplementary material

Supplementary information accompanies this paper at 10.1038/s41598-017-16980-4.

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.


1. Pepys MB, Hirschfield GM. C-reactive protein: a critical update. J. Clin. Invest. 2003;111:1805–1812. doi: 10.1172/JCI200318921. [PMC free article] [PubMed] [Cross Ref]
2. Ridker PM. High-sensitivity C-reactive protein: potential adjunct for global risk assessment in the primary prevention of cardiovascular disease. Circulation. 2001;103:1813–1818. doi: 10.1161/01.CIR.103.13.1813. [PubMed] [Cross Ref]
3. Ridker PM, Hennekens CH, Buring JE, Rifai N. C-reactive protein and other markers of inflammation in the prediction of cardiovascular disease in women. N. Engl. J. Med. 2000;342:836–843. doi: 10.1056/NEJM200003233421202. [PubMed] [Cross Ref]
4. Danesh J, et al. Low grade inflammation and coronary heart disease: prospective study and updated meta-analyses. BMJ. 2000;321:199–204. doi: 10.1136/bmj.321.7255.199. [PMC free article] [PubMed] [Cross Ref]
5. Koenig W. High-sensitivity C-reactive protein and atherosclerotic disease: from improved risk prediction to risk-guided therapy. Int. J. Cardiol. 2013;168:5126–5134. doi: 10.1016/j.ijcard.2013.07.113. [PubMed] [Cross Ref]
6. Buckley DI, Fu R, Freeman M, Rogers K, Helfand M. C-reactive protein as a risk factor for coronary heart disease: a systematic review and meta-analyses for the U.S. Preventive Services Task Force. Ann. Intern. Med. 2009;151:483–495. doi: 10.7326/0003-4819-151-7-200910060-00009. [PubMed] [Cross Ref]
7. Ridker PM, et al. Rosuvastatin to prevent vascular events in men and women with elevated C-reactive protein. N. Engl. J. Med. 2008;359:2195–2207. doi: 10.1056/NEJMoa0807646. [PubMed] [Cross Ref]
8. Cannon CP, et al. Intensive versus moderate lipid lowering with statins after acute coronary syndromes. N. Engl. J. Med. 2004;350:1495–1504. doi: 10.1056/NEJMoa040583. [PubMed] [Cross Ref]
9. Shang Q. H., Xu H. & Huang L. Tanshinone IIA: a promising natural cardioprotective agent. Evid. Based Complement. Alternat. Med. 716459, 10.1155/2012/716459 (2012). [PMC free article] [PubMed]
10. Gao S, et al. Cardiovascular actions and therapeutic potential of tanshinone IIA. Atherosclerosis. 2012;220:3–10. doi: 10.1016/j.atherosclerosis.2011.06.041. [PubMed] [Cross Ref]
11. Wang QL, Deng XJ, Li XQ, Chen XT. Effect of sodium tanshinone injection on CRP and D-dimer level in patients with unstable angina. J. N. Chin. Med. 2007;39:16–17.
12. Yu XY, et al. Role of P-glycoprotein in the intestinal absorption of tanshinone IIA, a major active ingredient in the root of Salvia miltiorrhiza Bunge. Curr. Drug Metab. 2007;8:325–40. doi: 10.2174/138920007780655450. [PubMed] [Cross Ref]
13. Yudkin JS, Kumari M, Humphries SE, Mohamed-Ali V. Inflammation, obesity, stress and coronary heart disease: is interleukin-6 the link? Atherosclerosis. 2000;148:209–214. doi: 10.1016/S0021-9150(99)00463-3. [PubMed] [Cross Ref]
14. Namiki M, et al. Local overexpression of monocyte chemoattractant protein-1 at vessel wall induces infiltration of macrophages and formation of atherosclerotic lesion: synergism with hypercholesterolemia. Arterioscler. Thromb. Vasc. Biol. 2002;122:115–120. doi: 10.1161/hq0102.102278. [PubMed] [Cross Ref]
15. Schonbeck U, et al. Regulation of matrix metalloproteinase expression in human vascular smooth muscle cells by T lymphocytes: a role for CD40 signaling in plaque rupture? Circ. Res. 1997;81:448–454. doi: 10.1161/01.RES.81.3.448. [PubMed] [Cross Ref]
16. Biasucci LM, et al. Elevated levels of interleukin-6 in unstable angina. Circulation. 1996;94:874–877. doi: 10.1161/01.CIR.94.5.874. [PubMed] [Cross Ref]
17. de Lemos JA, et al. Association between plasma levels of monocyte chemoattractant protein-1 and long-term clinical outcomes in patients with acute coronary syndromes. Circulation. 2003;107:690–695. doi: 10.1161/01.CIR.0000049742.68848.99. [PubMed] [Cross Ref]
18. Pamukcu B, Lip GY, Snezhitskiy V, Shantsila E. The CD40-CD40L system in cardiovascular disease. Ann. Med. 2011;43:331–340. doi: 10.3109/07853890.2010.546362. [PubMed] [Cross Ref]
19. Zakynthinos E, Pappa N. Inflammatory biomarkers in coronary artery disease. J. Cardiol. 2009;53:317–333. doi: 10.1016/j.jjcc.2008.12.007. [PubMed] [Cross Ref]
20. Robertson AL, et al. A zebrafish compound screen reveals modulation of neutrophil reverse migration as an anti-inflammatory mechanism. Sci. Transl. Med. 2014;6:225ra29. doi: 10.1126/scitranslmed.3007672. [PMC free article] [PubMed] [Cross Ref]
21. Li XJ, et al. Effects of tanshinone IIa on cytokines and platelets in immune vasculitis and its mechanism. J. Exp. Hematol. 2009;17:188–192. [PubMed]
22. Li CZ, Yang SC, Zhao FD. Effects of tanshinone II-A sulfonate on thrombus formation, platelet and blood coagulation in rats and mice. Acta Pharmacol. Sin. 1984;5:39–42. [PubMed]
23. Shang, Q. H., Wang, H., Li, S. M. & Xu, H. The effect of sodium tanshinone IIA sulfate and simvastatin on elevated serum levels of inflammatory markers in patients with coronary heart disease: a study protocol for a randomized controlled trial. Evid. Based Complement. Alternat. Med. 756519, 10.1155/2013/756519 (2013). [PMC free article] [PubMed]
24. Chen H, et al. Clinical study of unstable angina patients undergoing percutaneous coronary intervention treated with Chinese medicine for activating blood circulation and detoxification. Chin. J. Integr. Med. Cardio/Cerebrovasc. Dis. 2009;7:1135–1137.
25. Schaefer EJ, et al. Effects of atorvastatin versus other statins on fasting and postprandial C-reactive protein and lipoprotein-associated phospholipase A2 in patients with coronary heart disease versus control subjects. Am. J. Cardiol. 2005;95:1025–1032. doi: 10.1016/j.amjcard.2005.01.023. [PubMed] [Cross Ref]
26. Hamm, C. W. et al. ESC guidelines for the management of acute coronary syndromes in patients presenting without persistent ST-segment elevation: the Task Force for the management of acute coronary syndromes (ACS) in patients presenting without persistent ST-segment elevation of the European Society of Cardiology (ESC). Eur. Heart J.32, 2999–3054 (2011). [PubMed]
27. Hamm CW, et al. ESC guidelines for the management of acute coronary syndromes in patients presenting without persistent ST-segment elevation: the Task Force for the management of acute coronary syndromes (ACS) in patients presenting without persistent ST-segment elevation of the European Society of Cardiology (ESC) Eur. Heart J. 2011;32:2999–3054. doi: 10.1093/eurheartj/ehr236. [PubMed] [Cross Ref]

Articles from Scientific Reports are provided here courtesy of Nature Publishing Group