Long-Term Pentoxifylline Therapy Is Associated with a Reduced Risk of Atherosclerotic Cardiovascular Disease by Inhibiting Oxidative Stress and Cell Apoptosis in Diabetic Kidney Disease Patients
2024

Long-Term Pentoxifylline Therapy and Cardiovascular Disease Risk in Diabetic Kidney Disease Patients

Sample size: 129764 publication 10 minutes Evidence: high

Author Information

Author(s): Wang Jie-Sian, Tsai Ping-Hsuan, Tseng Kuo-Feng, Lin Cheng-Li, Chen Fang-Yu, Chang Chiz-Tzung, Shen Ming-Yi

Primary Institution: China Medical University

Hypothesis

Does long-term pentoxifylline therapy reduce the risk of atherosclerotic cardiovascular disease in patients with diabetic kidney disease?

Conclusion

Long-term pentoxifylline therapy is associated with a 47% reduction in the risk of atherosclerotic cardiovascular disease in diabetic kidney disease patients.

Supporting Evidence

  • Long-term pentoxifylline users had a 47% lower cumulative incidence of ASCVD compared to short-term users.
  • Pentoxifylline treatment increased Klotho levels, which helps protect endothelial cells.
  • Short-term pentoxifylline users had a higher risk of ASCVD compared to non-users.

Takeaway

Taking a medicine called pentoxifylline for a long time can help people with kidney problems and diabetes avoid heart disease.

Methodology

This retrospective cohort study analyzed data from 129,764 diabetic kidney disease patients to compare the effects of long-term versus short-term pentoxifylline therapy on cardiovascular disease risk.

Potential Biases

Potential residual confounding due to indirect measures of lifestyle factors like BMI, alcohol intake, and smoking.

Limitations

The study lacked detailed lipid profile data and relied on claims data, which may not capture all relevant patient characteristics.

Participant Demographics

Patients with diabetic kidney disease, aged 20 and older, without pre-existing cardiovascular disease.

Statistical Information

P-Value

p<0.001

Confidence Interval

95% CI: 0.49–0.58

Statistical Significance

p<0.001

Digital Object Identifier (DOI)

10.3390/antiox13121471

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