Statin in Combined With Xuezhikang Capsules Get More Lipid-Regulating Effective Than Statin Only: A Systematic Review and Meta-Analysis

Background: To compare the lipid-regulating effects and safety of statin combined with Xuezhikang capsules and statin used alone for hyperlipidemia. Methods: CNKI, Wanfang database, VIP Chinese Journals, PubMed, Embase, and Cochrane library were searched to comprehensively collect and screen RCTs of Xuezhikang combined with statin compared with statin used alone for lipid modifying treatment in hyperlipidemia patients from the database built as of July 2020, and the Cochrane 5.1.0 quality evaluation form was used to evaluate the quality of the included literature and The Cochrane 5.1.0 quality assessment form was used to evaluate the quality of the included literature and bias analysis, extract basic study information, primary and secondary outcome indicators, and meta-analysis of the outcome indicators was performed using RevMan 5.3. Results: A total of 14 studies with a total of 2042 patients were included, and the quality of the included studies was low to medium. rate: OR=3.63,95%CI[2.69,4.90],P<0.00001; the Conclusion: The combination of statin with Xuezhikang capsule has better effect on lipid regulation in patients with hyperlipidemia, and can effectively reduce the incidence of adverse events and has better safety. It is recommended that the treatment of Xuezhikang combined with statin can be used as a safer and more effective treatment for patients with hyperlipidemia. should regulation of and outcome indicator, and TG, HLDL and other lipoproteins should be secondary outcome indicators; (2) if safety is the study objective, the reporting of adverse effects should include liver, muscle and digestive system; (3) if TG is reported, whether to include dietary control should be considered.


Background
With the increasing standard of living of people, hyperlipidemia has become a common disease in modern society and has become a major risk factor for diseases such as atherosclerosis [1] . With childhood obesity becoming an epidemic in certain parts of the United States [2] , hyperlipidemia is either directly or indirectly affecting people's health. And the regulation and stabilization of lipid levels has become one of the health care behaviours in modern daily life [3] . Statins are the rst-line of lipid-modifying therapy [4] , but their intensive use can have borderline effects [5] , and the relationship between bene ts and risks and economic bene ts still needs to be studied [6][7][8] . Xuezhikang Capsules(Xuezhikang) represent a natural statin lipid-lowering drug, whose main ingredient is red yeast, re ned in a standard GMP process and containing 13 natural compound statins [9] and its toxicity is extremely low [10] . Compared with synthetic statins, Xuezhikang is not effective in the comprehensive regulation of blood lipids and reducing the incidence of adverse reactions, which not only can be used as a rst-line clinical drug [11] , but also can improve the bene ts [12] and reduce the risks of intensive statin use [13] . To further investigate the e cacy and adverse effects of statins combined with Xuezhikang in patients with hyperlipidemia, this study conducts a systematic review and meta-analysis of the relevant literature, with a view to provide evidencebased medicine for clinical application.

Registration Information
This systematic review and meta-analysis complies with the PRISMA Statement [14] and is registered in PROSPERO(No. CRD42020200277).

Subjects
Diagnostic criteria: "Guidelines for Clinical Research on New Chinese Medicines", "Guidelines for the Prevention and Treatment of Dyslipidemia in Chinese Adults", "Relevant Judgment Criteria Developed by the American Cholesterol Education Program Committee", "Practical Internal Medicine". Sex, age and comorbidities were not limited.

Intervention
The trial group was treated with Xuezhikang capsules combined with statins, and the control group was treated with the same type and dose of statins as the trial group.

Study Type
Randomized controlled trial(RCT), no matter whether to adopt blinded or allocation concealment, language was limited to Chinese or English.

Exclusion Criteria
For patients who have taken other drugs affecting lipid metabolism concurrently during treatment. Literature for which complete data are not available.

Literature Screening and Data Extraction
Two researchers(Chen and Feng) independently screened the literature according to the inclusion and exclusion criteria and crosschecked it, using a pre-designed data extraction form to extract information, including basic information about the study, study methods, observation of subjects, intervention and control measures, indicators, outcomes and occurrence of adverse effects. In case of disagreement, it was resolved in consultation with the third researcher (Li). If the information reported in the study was incomplete, further contact was made with the author to obtain it, and the study was excluded if relevant data were not eventually obtained.

Literature Evaluation
The Cochrane 5.1.0 Quality Assessor's Manual is used to screen and assess the quality of the literature. Judgements of bias (selection bias, implementation bias, measurement bias, follow-up bias, reporting bias and other biases) were made as "low risk/uncertain/high risk".

Statistical Analysis
Meta-analysis was performed by using RevMan 5. 3 software. The odds ratio(OR) was measured using the MH algorithm for count data and the mean difference(MD) was measured using the IV algorithm for continuous variable data with 95% con dence intervals(CI). Heterogeneity between the results of each included study was tested by Q-test and I 2 -test. We will use Cochrane manual thresholds to explain I 2 -test [15] and Q-test [16] , random-effects model(RE) was used, and sources of heterogeneity were identi ed by subgroup method or single-study exclusion method to reduce heterogeneity. P<0.05 for the combined effect indicator indicates a statistically signi cant difference. When the number of included studies was ≥10, an inverted funnel plot analysis was performed to detect publication bias, using the effect indicators of the included studies as horizontal coordinates and the inverse of the log standard error(SE) as vertical coordinates. Descriptive analysis was used when data heterogeneity due to other reasons was clearly not possible to combine for analysis.

Basic Characteristics of the Included Studies
All the studies included 2042 patients, with 1022 in the trial group and 1020 in the control group. The statins involved included: atorvastatin, simvastatin, rosuvastatin and uvastatin, all of which are at moderate doses according to guidelines. Study duration ranged from 4 to 12 weeks. All studies were funded by grants, as detailed in Table 1(Additional le 1). once per night; bid: once in the morning and once in the evening.

Quality Evaluation of Included Studies and Risk of Bias Assessment
All studies were randomized. No sample size estimation or intentionality therapy analysis or blind method was performed. The methodological quality assessment of the included studies is described in detail in Table 2(Additional le 2). The risk of bias of the included studies is assessed in Figures 2.  Figure 3. The publication bias was analyzed on the row funnel plot with the effective rate. The shape of the funnel plot was consistent with the inverted funnel type with narrow upper and wide lower shape, but the loose lower part and the graph were all hollow dots, suggesting the existence of publication bias. More details are shown in

Adverse Event
8 studies [17,19,21,23,25,27,28,30] reported adverse events during and after the middle stage of the study, including bloating, nausea, vomiting and headache, with large heterogeneity between studies (P=0.001, I 2 =71%). 8 studies were subclassi ed according to whether the number of cases was greater than 100, then we nd out the heterogeneity was low in both subgroups(I 2 =0% in both).
With OR as effect value, combined effect size of RE model was used for analysis. The results of forest plot showed that adding Xuezhikang could signi cantly reduce the number of adverse events happening, as detailed in Figure 9.

Discussion
Blood lipids are the general term for cholesterol, triglycerides, and lipids in serum. Hyperlipidemia refers to plasma lipoprotein disorders. It is a metabolic disease, and its direct damage to the body is not obvious, and it generally does not have speci c clinical discomfort symptoms [31] . Cholesterol is the total amount of cholesterol contained in various lipoproteins in the blood. It exists in the human body mainly in the form of free cholesterol and cholesteryl esters, and its level is related to the patient's age, gender, dietary habits and genetic factors, but its metabolic changes are relatively slow [32] and is less valuable than LDL for risk assessment [33] and prediction [34] of atherosclerotic cardiovascular disease. Triglycerides are formed when the three hydroxyl groups in the glycerol molecule are esteri ed by fatty acids and, similar to cholesterol, their levels are in uenced by both genetics and the environment.
However, unlike cholesterol, the metabolism of triglycerides is more in uenced by diet and time, and triglyceride measurements may vary considerably within a short period of time in the same individual with dietary changes [35] . There was a study [36] suggested that elevated triglycerides are likely to have atherogenic effects by affecting the structure of lipoproteins, and that mild to moderate elevations in serum triglyceride levels may increase the risk of coronary heart disease in patients. LDL is the lipid core that makes up the atherosclerotic plaque and is also the initial and maintaining element of the chronic in ammatory response that is the pathological manifestation of atherosclerosis, so an increase in LDL is a major risk factor for the occurrence and development of atherosclerosis [37] . HDL is responsible for reverse cholesterol transport -transporting cholesterol from peripheral tissues to the liver for circulation or excretion in the form of bile acids, reducing cholesterol deposition in the vascular wall and acting as an antiatherosclerotic agent [38] .
Dyslipidemia, characterized by elevated LDL and cholesterol, is a noteworthy risk factor for atherosclerotic cardiovascular diseases(ASCVD). Other types of dyslipidemia, such as increased TG and decreased HDLC, are also associated with the development of ASCVD [39] . The ultimate treatment goal for dyslipidemia is to effectively reduce the risk of developing ASCVD [34] . In the 2016-edition of the Chinese Guidelines for the Prevention and Treatment of Dyslipidemia [40] , it is recommended that patients with dyslipidemia need to be assessed for residual risk of ASCVD. LDL and cholesterol levels can be independent predictors of the risk of ASCVD in individuals or groups of patients. Cholesterol accounts for 50% of LDL, and although the two levels are generally parallel, cholesterol is susceptible to HDL [41] , and LDL plays a central role in the development of ASCVD. So lowering LDL levels is the main target of intervention in the treatment of dyslipidemia in clinical practice.
Although there is no clear evidence to support that lower lipid levels are associated with a lower risk of ASCVD, nor is there evidence of a speci c lipid threshold for ASCVD risk reduction, current medication guidelines in most countries, mainly in China, support the setting of lipid-lowering targets rather than minimizing lipid levels [42] . Apart from considerations of improving patient compliance and facilitating physician assessment of lipid-lowering e cacy, the main reasons are that lipid modulation is a long-term treatment and intensive use has a borderline effect -a signi cant increase in adverse drug reactions [43] , a doubling of the patient's nancial burden, a small but modest increase in lipid-lowering bene t, and no reduction in all-cause mortality [44] .
Statins are clinically preferred and are Class I Recommendations and Class A Evidence in a variety of cardiovascular guidelines, including lovastatin, simvastatin, pravastatin, uvastatin, atorvastatin, resuprastatin and pitavastatin. As inhibitors of HMG-COA reductase, statins inhibit cholesterol synthesis of the rate-limiting enzyme HMG-CoA reductase, reduce cholesterol synthesis and subsequently cells are upregulated to indicate LDL receptors, and accelerate serum LDL catabolism, while inhibiting very low-density lipoprotein synthesis, thereby regulating blood lipids to reduce coronary heart disease mortality [45] . A number of studies [46][47][48][49]  natural lipid-regulating drug. Its main ingredient is monascus -which has been used for centuries in China as a food colouring and avour enhancer [50] . It is re ned through a modern GMP-standard process by adding special monascus to rice fermentation. It has a mechanism similar to that of statins, with 13 natural statin complexes as the main ingredients [51] . It is unique in reducing the risk of adverse reactions associated with the use of a single statin [52] . A number of RCTs [53][54][55][56][57][58][59][60] have demonstrated that Xuezhikang can lower cholesterol and LDL levels, reduce the incidence of adverse events, reduce the risk of cardiovascular events and recurrence, and signi cantly reduce coronary heart disease mortality and all-cause mortality. It is also inexpensive compared to synthetic statins. The 14 RCTs included in this study were low to moderate quality studies with obvious limitations, including: 1. All studies did not specify sample size estimates, which may affect test validity; 2. Although all included studies indicated that cases were randomly assigned to two groups, only eight studies clearly indicated the randomization method they used, while the remaining studies did not mention the speci c randomization method and allocation concealment method, which is subject to unknowable selectivity bias. The remaining studies did not mention the speci c randomization method and allocation concealment method, resulting in unknowable selectivity bias; 3. All cases did not mention whether they were blinded, either blinding of investigators and subjects or blinded evaluation of study outcomes, resulting in unknowable implementation bias and measurement bias; 4. Funnel plots of e ciency rates were found to be consistent with an inverted funnel shape with a narrow top and a wide bottom, but the lower part of the graph was lax and there are all hollow dots in the graphs, suggesting that there are insu cient large sample studies, low sample quality and publication bias; 5. Only 8 studies fully reported adverse events during the study period and follow-up, resulting in follow-up bias, Moreover, none of the three major systemic adverse reactions of statins -liver, muscle and digestive system -have been tracked and reported, which is not highly targeted; 6. In the study design, the effective rate of all studies took the proportion of cholesterol In Conclusion, the information extracted from the 14 RCTs included in this study was systematically evaluated and the results showed that Xuezhikang combined with statins had better and more stable modulation of cholesterol, triglyceride and LDL levels than statins used alone in terms of regulation of lipids in patients with hyperlipidemia, and there is a lower incidence rate of adverse events. The RCTs included in this study were of low to moderate quality and more high quality RCTs with large samples are needed to provide more reliable evidence.

Figure 1
Flow diagram of the study selection process   The funnel plot for all observation studies in the meta-analysis.
Page 16/20   Comparison of HDLC between statin in combination with Xuezhikang and statin only in 13 studies which were divided into 4 subgroup according to different statins.

Figure 9
Adverse event of 8 studies in which statins combined with Xuezhikang were compared with statin alone were divided into 2 subgroups based on whether the patients included were more than 100.