%0 Journal Article
%T Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase
%A Amanda J Heslegrave
%A Ritika R Kapoor
%A Simon Eaton
%A Bernadette Chadefaux
%A Teoman Ackay
%A Enver Simsek
%A Sarah E Flanagan
%A Sian Ellard
%A Khalid Hussain
%J Orphanet Journal of Rare Diseases
%D 2012
%I BioMed Central
%R 10.1186/1750-1172-7-25
%X An oral leucine tolerance test was conducted in controls and nine patients with HADH mutations. Basal GDH activity and the effect of GTP were determined in lymphoblast homogenates from 4 patients and 3 controls. Immunoprecipitation was conducted in patient and control lymphoblasts to investigate protein interactions.Patients demonstrated severe HH (glucose range 1.7¨C3.2£żmmol/l; insulin range 4.8-63.8£żmU/l) in response to the oral leucine load, this HH was not observed in control patients subjected to the same leucine load. Basal GDH activity and half maximal inhibitory concentration of GTP was similar in patients and controls. HADH protein could be co-immunoprecipitated with GDH protein in control samples but not in patient samples.We conclude that GDH and HADH have a direct protein-protein interaction, which is lost in patients with HADH mutations causing leucine induced HH. This is not associated with loss of inhibitory effect of GTP on GDH (as in patients with GLUD1 mutations).
%K Hyperinsulinism
%K Hypoglycaemia
%K Leucine tolerance
%U http://www.ojrd.com/content/7/1/25/abstract