Literature DB >> 32060930

Titrating a modified ketogenic diet for patients with McArdle disease: A pilot study.

Nicoline Løkken1, Kit K Hansen2, Jesper H Storgaard1, Mette C Ørngreen1, Ros Quinlivan2, John Vissing1.   

Abstract

Glycogen storage disease type V (GSDV) is a rare inborn error of carbohydrate metabolism. Patients present with exercise intolerance due to blocked glycogen breakdown in skeletal muscle. Introducing alternative fuel substrates, such as ketone bodies (KBs), could potentially alleviate muscle symptoms. This pilot study investigates which of three different modified ketogenic diet regimes is optimal for GSDV-patients to follow in a future large-scale study. Participants were randomised to follow one of three diet regimes for 3 weeks (#1: 65%/15%/20%; #2: 75%/15%/10%, or #3: 80%/15%/5%, fat/protein/carbohydrate). The primary outcome was exercise tolerance assessed by heart rate (HR) changes during constant load cycling. Secondary outcomes included levels of ketosis, and changes in perceived exertion and indirect calorimetry measures during exercise. Ten GSDV-patients were included. Eight completed the study. The other two were excluded. Diet #3 showed the highest average KB level (1.1 mmol/L) vs #2 (0.5 mmol/L) and #1 (0.3 mmol/L). Five patients reported subjective symptom relief, all of whom were on diets #2 and #3. All diet regimes seemed to improve fatty acid oxidation rates and exercise capacity as indicated by a small decrease in HR and perceived exertion. The results of this open-label pilot study show that diets #2 and #3 induce ketosis and improve symptoms and exercise capacity in GSDV-patients. Diet #2 had the highest acceptability score and was superior or equal to diet #3 in all other parameters, except level of ketosis. Based on this, we suggest testing diet #2 in a large-scale, placebo-controlled study in GSDV.
© 2020 SSIEM.

Entities:  

Keywords:  GSDV; McArdle disease; glycogen storage disease type V; ketogenic diet; ketone bodies; modified ketogenic diet

Year:  2020        PMID: 32060930     DOI: 10.1002/jimd.12223

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  2 in total

1.  A new phenotype of aldolase a deficiency in a 14 year-old boy with epilepsy and rhabdomyolysis - case report.

Authors:  Lucia Santoro; Dorina Pjetraj; Virtut Velmishi; Carmen Campana; Carlo Catassi; Carlo Dionisi-Vici; Arianna Maiorana
Journal:  Ital J Pediatr       Date:  2022-03-04       Impact factor: 2.638

2.  No effect of oral ketone ester supplementation on exercise capacity in patients with McArdle disease and healthy controls: A randomized placebo-controlled cross-over study.

Authors:  Nicoline Løkken; Jesper H Storgaard; Karoline L Revsbech; Nicol C Voermans; Gerrit Van Hall; John Vissing; Mette C Ørngreen
Journal:  J Inherit Metab Dis       Date:  2022-02-20       Impact factor: 4.750

  2 in total

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