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How Atorvastatin Affects the Gut Flora and Metabolomics?

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Xi'an Jiaotong University

Status

Unknown

Conditions

Atherosclerotic Cardiovascular Disease

Treatments

Drug: Atorvastatin 20 Mg Oral Tablet

Study type

Interventional

Funder types

Other

Identifiers

NCT04215237
XJTU1AF2018LSK-91

Details and patient eligibility

About

Recent studies suggest that gut microbiome, the microbial community in the intestine, may directly and indirectly influence the progression of atherosclerosis. The imbalance of gut microbiome may directly promote the formation of atherosclerotic plaques by promoting the inflammatory reaction and oxidative stress affecting vascular endothelial function and increasing platelet activity. Meanwhile, it can indirectly increase the risk of atherosclerosis by enhance insulin resistance, reducing the production of bile acids and raising serum LDL-C and angiotensin levels. As shown in these researches, gut microbiome, acting as a bridge between metabolism, energy and inflammatory responses, may play an important role in cardiovascular diseases, and we believe that the interaction between microbiome and host should be considered in the ASCVD study.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-80 years;
  • Statin indications such as lipid metabolism disorders, diabetes, elevated CRP, atherosclerosis; stratification according to ASCVD risk; indications for statin treatment
  • Not using statins and other lipid-lowering drugs for at least 6 months before enrollment;
  • Agree to receive research treatment plan;
  • Voluntarily sign the informed consent.

Exclusion criteria

  • People with active gastrointestinal bleeding or have a clear history of gastrointestinal ulcers or bleeding in the past 2 years;
  • Severe renal insufficiency (eGFR <30ml / min / 1.73m2);
  • Active hepatitis, liver cirrhosis, or ALT increase more than 3 times;
  • Those with severe hypertension (> 180 / 110mmHg) and currently have no control;
  • Hemoglobin <100g / L;
  • Platelet count <100 × 109 cells / L;
  • Suffering from a known serious progressive disease (such as a malignant tumor) or a disease that causes the patient to fail extremely, the estimated survival time is <12 months;
  • pregnant or intending to become pregnant;
  • Any situation that may interfere with the research process, such as dementia, paralysis, alcoholism, etc .;
  • Expected to undergo surgery within 1 year;
  • Patients participating in other ongoing clinical studies.

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Atorvastatin regulates intestinal flora
Other group
Treatment:
Drug: Atorvastatin 20 Mg Oral Tablet

Trial contacts and locations

1

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Central trial contact

Yue Wu, Professor; Xiang Hao

Data sourced from clinicaltrials.gov

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