The influence of low‐carbohydrate diets on the metabolic response to androgen‐deprivation therapy in prostate cancer. Issue 10 (5th May 2021)

• Record Type: Journal Article
• Authors: Chi, Jen‐Tsan; Lin, Pao‐Hwa; Tolstikov, Vladimir; Oyekunle, Taofik; Galvan, Gloria C.; Ramirez‐Torres, Adela; Chen, Emily Y.; Bussberg, Valerie; Chi, Bo; Greenwood, Bennett; Sarangarajan, Rangaprasad; Narain, Niven R.; Kiebish, Michael A.; Freedland, Stephen J.
• Is Part Of: Prostate. Volume 81:Issue 10(2021)
• Page Start: 618
• Page End: 628
• Publication Date: 2021-05-05
• Subjects: 3‐formyl indole -- 3‐hydroxybutyric acid -- ADT -- androgen sulfate -- indole‐3‐carboxaldehyde -- ketogenesis -- low carbohydrate diet -- metabolomics -- prostate cancer; Prostate -- Diseases -- Periodicals; 616
• DOI: 10.1002/pros.24136
• Languages: English
• ISSNs: 0270-4137

Abstract

Abstract: Background: Prostate cancer (PC) is the second most lethal cancer for men. For metastatic PC, standard first‐line treatment is androgen deprivation therapy (ADT). While effective, ADT has many metabolic side effects. Previously, we found in serum metabolome analysis that ADT reduced androsterone sulfate, 3‐hydroxybutyric acid, acyl‐carnitines but increased serum glucose. Since ADT reduced ketogenesis, we speculate that low‐carbohydrate diets (LCD) may reverse many ADT‐induced metabolic abnormalities in animals and humans. Methods: In a multicenter trial of patients with PC initiating ADT randomized to no diet change (control) or LCD, we previously showed that LCD intervention led to significant weight loss, reduced fat mass, improved insulin resistance, and lipid profiles. To determine whether and how LCD affects ADT‐induced metabolic changes, we analyzed serum metabolites after 3‐, and 6‐months of ADT on LCD versus control. Results: We found androsterone sulfate was most consistently reduced by ADT and was slightly further reduced in the LCD arm. Contrastingly, LCD intervention increased 3‐hydroxybutyric acid and various acyl‐carnitines, counteracting their reduction during ADT. LCD also reversed the ADT‐reduced lactic acid, alanine, and S‐adenosyl methionine (SAM), elevating glycolysis metabolites and alanine. While the degree of androsterone reduction by ADT was strongly correlated with glucose and indole‐3‐carboxaldehyde, LCD disrupted such correlations. Conclusions: Together, LCD intervention significantly reversed many ADT‐induced metabolic changes while slightly enhancing androgen reduction. Future research is needed to confirm these findings and determine whether LCD can mitigate ADT‐linked comorbidities and possibly delaying disease progression by further lowering androgens.