Potential Add-On Benefits of Dietary Intervention in the Treatment of Autosomal Dominant Polycystic Kidney Disease.
Erica RosatiGiulia CondelloChiara TacenteIlaria MarianiValeria TommoliniLuca CalvarusoPierluigi FulignatiGiuseppe GrandalianoFrancesco PescePublished in: Nutrients (2024)
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited cause of renal failure. The pathogenesis of the disease encompasses several pathways and metabolic alterations, including the hyperactivation of mTOR and suppression of AMPK signaling pathways, as well as mitochondrial dysfunction. This metabolic reprogramming makes epithelial cyst-lining cells highly dependent on glucose for energy and unable to oxidize fatty acids. Evidence suggests that high-carbohydrate diets may worsen the progression of ADPKD, providing the rationale for treating ADPKD patients with calorie restriction and, in particular, with ketogenic dietary interventions, already used for other purposes such as in overweight/obese patients or in the treatment of refractory epilepsy in children. Preclinical studies have demonstrated that calorie restriction may prevent and/or slow disease progression by inducing ketosis, particularly through increased beta-hydroxybutyrate (BHB) levels, which may modulate the metabolic signaling pathways altered in ADKPK. In these patients, although limited, ketogenic intervention studies have shown promising beneficial effects. However, larger and longer randomized controlled trials are needed to confirm their tolerability and safety in long-term maintenance and their additive role in the therapy of polycystic kidney disease.
Keyphrases
- polycystic kidney disease
- randomized controlled trial
- weight loss
- obese patients
- bariatric surgery
- signaling pathway
- induced apoptosis
- physical activity
- fatty acid
- ejection fraction
- gastric bypass
- roux en y gastric bypass
- young adults
- pi k akt
- type diabetes
- stem cells
- oxidative stress
- epithelial mesenchymal transition
- cell therapy
- blood pressure
- cell cycle arrest
- bone marrow
- study protocol
- climate change
- cell death
- adipose tissue
- body mass index
- open label
- patient reported outcomes
- blood glucose
- prognostic factors
- human health