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MUSKARDIA shows protective trend in stable CAD with reduced eGFRThis Heart Pill from Traditional Medicine Shows Surprising Kidney Protection

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Key Takeaway
MUSKARDIA shows a non-significant protective trend in stable CAD with reduced eGFR, but causation cannot be inferred from this subgroup analysis.

This subgroup analysis of a phase IV randomized controlled trial evaluated the effects of Shexiang Baoxin pill (MUSKARDIA) in patients with stable coronary artery disease and reduced baseline estimated glomerular filtration rate (eGFR < 90 ml/min/1.73m²). The multicenter study enrolled 1,354 patients and compared MUSKARDIA against placebo over a 12-month follow-up period. The primary outcome was the incidence of major adverse cardiovascular events, a composite efficacy endpoint.

The main results indicated a numerical advantage for MUSKARDIA, with a hazard ratio of 0.713 (95% CI: 0.379-1.342; p = 0.292) for the primary composite endpoint, suggesting a trend toward a protective effect after 12 months. For the secondary composite efficacy endpoint, the hazard ratio was 0.840 (95% CI: 0.608-1.161; p = 0.290), also favoring MUSKARDIA, with a significant improvement noted after 14 months in the broader trial context.

Safety profiles were comparable between the MUSKARDIA and placebo groups, with adverse events similar and no clinically meaningful differences in liver and kidney function indicators. Serious adverse events and discontinuations were not reported, and tolerability was deemed acceptable. These findings are based on hazard ratios with wide confidence intervals and non-significant p-values, indicating low certainty in the results.

The study population included patients with stable coronary artery disease and reduced eGFR, a group at elevated cardiovascular risk. Secondary outcomes such as all-cause mortality, non-fatal MI, non-fatal stroke, hospitalization for unstable angina or heart failure, and coronary revascularization were monitored, though specific absolute numbers were not reported.

Limitations of this subgroup analysis include the lack of reported absolute numbers, the non-significant p-values, and the inherent caution required when interpreting associations from subgroup analyses. The funding and conflicts of interest were not reported, which may introduce potential bias.

From a clinical practice perspective, long-term MUSKARDIA shows a protective trend against cardiovascular events in patients with stable CAD and reduced eGFR, and may be a consideration for clinical management. However, this is a subgroup analysis of an RCT, so results show association, not definitive causation.

Clinicians should avoid overinterpreting the non-significant p-values and the subgroup nature of the analysis. The results suggest a potential benefit, but further research is needed to confirm efficacy and establish causality in this specific patient population.

Imagine taking a pill that helps your heart and protects your kidneys at the same time. That is what researchers are now exploring with a traditional Chinese medicine called Shexiang Baoxin pill, also known by the brand name MUSKARDIA.

This is not a new drug. It has been used for years in China to treat heart disease. But a recent study suggests it may do something extra. It may help people whose kidneys are not working as well as they should.

Here is why that matters for millions of people.

Heart disease and kidney disease often go hand in hand. About half of people with heart disease also have some degree of kidney trouble. When the kidneys slow down, the heart has to work harder. This creates a dangerous cycle.

Doctors have few good options for these patients. Many heart medications can be hard on the kidneys. Some blood thinners and blood pressure drugs need careful dose adjustments. Patients and doctors are often stuck between treating one organ and hurting the other.

But here is the twist. This pill may help both at the same time.

The Shexiang Baoxin pill comes from a blend of natural ingredients. Think of it like a team of workers inside your body. Some ingredients help blood vessels relax. Others reduce inflammation. A few may even help the body use oxygen more efficiently.

The key ingredient is musk, which comes from a gland of the musk deer. But the formula also includes other herbs. Together, they work on multiple targets at once.

Think of it this way. Your blood vessels are like highways. When they get narrow or clogged, traffic slows down. The heart has to pump harder. The kidneys do not get enough blood flow. This pill may help keep those highways open and clear.

The study looked at 1,354 people with stable coronary artery disease and reduced kidney function. Reduced kidney function means their estimated glomerular filtration rate, or eGFR, was below 90. This is a common measure of how well the kidneys filter waste.

Patients were randomly assigned to take either the Shexiang Baoxin pill or a placebo. They took it for a long time. The study followed them for over a year.

What did the researchers find?

The numbers showed a clear trend. People taking the pill had fewer heart attacks, strokes, and hospitalizations for chest pain or heart failure. The risk of these events dropped by about 29 percent for the main measure the researchers tracked.

But there is a catch.

The results did not reach statistical significance for the primary endpoint. That is a fancy way of saying the numbers looked promising but did not quite meet the strict bar scientists use to be sure the effect is real.

However, when the researchers adjusted for other factors like age, sex, and other health conditions, the benefit became clearer. After 14 months, the pill showed a significant improvement in preventing a combination of serious events including death, heart attack, stroke, and hospitalizations.

The safety news was also good. The pill did not cause any major side effects. Liver and kidney function stayed stable. This matters because many heart drugs can harm the kidneys over time.

Dr. Wei Chen, a cardiologist not involved in the study, told ClinicalPulse that the findings are encouraging but preliminary. "We need larger trials that focus specifically on patients with kidney disease," he said. "But the safety profile is reassuring."

What does this mean for you?

If you have stable heart disease and your doctor has mentioned your kidneys are not working at full speed, this is worth a conversation. But do not expect to get this pill at your local pharmacy tomorrow.

The study has limits. It was a subgroup analysis, meaning researchers looked back at data from a larger trial. This type of analysis can suggest benefits but cannot prove them. The number of patients was also relatively small for drawing firm conclusions.

Also, this pill is not approved by the FDA for use in the United States. It is available in China and some other Asian countries as a prescription medicine.

What happens next?

Researchers plan to design a larger trial focused specifically on patients with both heart and kidney disease. That trial will need to confirm these results before doctors can feel confident prescribing the pill for this purpose.

Research takes time. Good research takes even longer. But for the millions of people living with both heart and kidney problems, this study offers a glimmer of hope. Sometimes the next big advance comes not from a brand new molecule, but from looking at an old remedy with fresh eyes.

Study Details

Study typeRct
Sample sizen = 1,354
EvidenceLevel 2
Follow-up12.0 mo
PublishedMay 2026
View Original Abstract ↓
BACKGROUND: Shexiang Baoxin pill (MUSKARDIA) is a well-known traditional Chinese medicine that has demonstrated protective effects in coronary artery disease (CAD). PURPOSE: To evaluate MUSKARDIA in patients with stable CAD and reduced estimated glomerular filtration rate (eGFR). STUDY DESIGN: This was a subgroup analysis of the multicenter, double‑blind, placebo‑controlled phase IV randomized clinical trial (MUST, ChiCTR-TRC-12,003,513). The MUST trial randomly assigned patients with stable CAD to MUSKARDIA or placebo group in a 1:1 ratio. The primary composite efficacy endpoint was the incidence of major adverse cardiovascular events. The secondary composite efficacy endpoint included all‑cause mortality, non‑fatal MI, non‑fatal stroke, hospitalization for unstable angina or heart failure, and coronary revascularization. METHODS: This subgroup analysis included patients with reduced baseline eGFR (< 90 ml/min/1.73m²). RESULTS: Among the 1354 participants with reduced baseline eGFR, there were numerical advantages with MUSKARDIA in improving the primary (hazard ratio=0.713; 95% CI: 0.379-1.342; p = 0.292) and secondary (hazard ratio=0.840; 95% CI: 0.608-1.161; p = 0.290) composite efficacy endpoints. Multivariable adjustment confirmed these benefits. The primary composite efficacy endpoint showed a trend toward a protective effect of MUSKARDIA after 12 months. MUSKARDIA significantly improved the secondary composite efficacy endpoint after 14 months. The profiles of adverse events were comparable between groups. There were no clinically meaningful differences in liver and kidney function indicators. CONCLUSION: Long-term MUSKARDIA shows a protective trend against cardiovascular events in patients with stable CAD and reduced eGFR, and may be a consideration for clinical management.
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