Microbiome and Cardiovascular Disease in CKD

Anna Jovanovich1,2, Tamara Isakova3, Jason Stubbs4

  • 1Renal Section, Veterans Affairs Eastern Colorado Health Care System, Denver, Colorado.

Insights

Chronic kidney disease (CKD) patients face high cardiovascular mortality due to gut microbiome changes. Intestinal dysbiosis in CKD contributes to inflammation and atherosclerosis, increasing cardiovascular risk.

Area of Science:

  • Microbiology
  • Nephrology
  • Cardiology

Background:

  • Patients with chronic kidney disease (CKD) experience significantly higher rates of cardiovascular mortality compared to the general population.
  • Unique, non-traditional risk factors associated with declining kidney function are increasingly implicated in this disparity.
  • Alterations in the intestinal microbiome, known as intestinal dysbiosis, are emerging as a critical factor in CKD pathophysiology.

Purpose of the Study:

  • To review the role of the gut microbiome in promoting cardiovascular disease (CVD) in CKD patients.
  • To explore how intestinal dysbiosis and associated mechanisms contribute to atherosclerosis and adverse cardiovascular outcomes.
  • To discuss potential interventions targeting the microbiome for CVD prevention in CKD.

Main Methods:

  • This is a narrative review synthesizing current scientific literature.
  • Focuses on microbiome-mediated pathways linking CKD to CVD.
  • Includes analysis of new data on intestinal barrier dysfunction, bacterial translocation, and endotoxemia.

Main Results:

  • CKD is associated with intestinal dysbiosis, altering gut micro-organism composition and function.
  • Dysbiosis byproducts are linked to vascular calcification, atherosclerosis, and poor cardiovascular outcomes in CKD.
  • Defective intestinal barrier function in CKD may exacerbate the impact of pathogenic bacteria, increasing systemic inflammation.

Conclusions:

  • Intestinal dysbiosis, impaired gut barrier function, and reduced kidney clearance of bacterial products collectively promote CVD in CKD.
  • Bacterial translocation and endotoxemia resulting from barrier dysfunction drive systemic inflammation.
  • Accumulation of dietary-derived bacterial byproducts stimulates atheromatous changes in arteries, contributing to CVD.

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