The Gut Microbiome and Symptom Burden After Kidney Transplantation: An Overview and Research Opportunities.
Mark B LockwoodChoa SungSuzanne A AlvernazJohn R LeeJennifer L ChinMehdi NayebpourBeatriz Peñalver BernabéLisa M Tussing-HumphreysHongjin LiMario SpaggiariAlessandro MartininoChang G ParkGeorge E ChlipalaArdith Z DoorenbosStefan J GreenPublished in: Biological research for nursing (2024)
Many kidney transplant recipients continue to experience high symptom burden despite restoration of kidney function. High symptom burden is a significant driver of quality of life. In the post-transplant setting, high symptom burden has been linked to negative outcomes including medication non-adherence, allograft rejection, graft loss, and even mortality. Symbiotic bacteria (microbiota) in the human gastrointestinal tract critically interact with the immune, endocrine, and neurological systems to maintain homeostasis of the host. The gut microbiome has been proposed as an underlying mechanism mediating symptoms in several chronic medical conditions including irritable bowel syndrome, chronic fatigue syndrome, fibromyalgia, and psychoneurological disorders via the gut-brain-microbiota axis, a bidirectional signaling pathway between the enteric and central nervous system. Post-transplant exposure to antibiotics, antivirals, and immunosuppressant medications results in significant alterations in gut microbiota community composition and function, which in turn alter these commensal microorganisms' protective effects. This overview will discuss the current state of the science on the effects of the gut microbiome on symptom burden in kidney transplantation and future directions to guide this field of study.
Keyphrases
- kidney transplantation
- healthcare
- signaling pathway
- risk factors
- irritable bowel syndrome
- patient reported
- endothelial cells
- public health
- sleep quality
- cardiovascular disease
- physical activity
- case report
- cell proliferation
- epithelial mesenchymal transition
- oxidative stress
- living cells
- sensitive detection
- skeletal muscle
- endoplasmic reticulum stress
- cerebral ischemia
- fluorescent probe
- cerebrospinal fluid
- pluripotent stem cells