Mitochondrial ß-oxidation disorders : from screening to diagnosis, fasting metabolism and optimized treatment
Author: Olsson, David
Date: 2024-09-27
Location: Rolf Luft Auditorium, Karolinska University Hospital, Solna
Time: 09.00
Department: Inst för kvinnors och barns hälsa / Dept of Women's and Children's Health
View/ Open:
Thesis (2.699Mb)
Abstract
Mitochondrial beta-oxidation disorders are a group of recessive diseases characterized by fasting intolerance and symptoms ranging from intermittent myalgia and rhabdomyolysis to cardiomyopathy and severe hypoketotic hypoglycemia. The studies in this thesis have focused on some of the unresolved issues regarding the pathogenesis of these disorders and how to best care for patients: phenotype prediction (study I), mitochondrial function (study II) and fasting metabolism (study III and IV).
In study I, the phenotype, biochemical data and clinical outcome of 22 Swedish pediatric patients with VLCADD were related to newborn screening data and VLCAD residual enzyme activity. Patients had a wide phenotypic spectrum, varying from asymptomatic to severely affected cases. The identified correlation between newborn screening results, residual enzyme activity analysis, and clinical outcome could significantly aid in treatment decisions and disease severity prediction.
In study II, mitochondrial respiration and glycolysis in peripheral blood mononuclear cells (PBMCs) from 21 patients with VLCADD, MCADD or CUD were determined using an XFe flux analyzer. PMBCs were suitable for analysis within a 6-hour sampling window, and VLCADD and MCADD cells consistently showed lower mitochondrial respiration rates than CUD cells.
Study III investigated fasting metabolism during a 9-hour night fast in 12 children with VLCADD or MCADD using subcutaneous microdialysis. The VLCADD group showed an earlier fasting-induced initiation of lipolysis compared to the MCADD group, and all patients maintained euglycemia during the fast. Patients with VLCADD with lower residual enzyme activity had an earlier initiation of lipolysis than those with higher enzyme activity.
Study IV investigated the fasting and postprandial hormonal and incretin response after a 4-hour daytime fast and after the intake of a standardized meal in 15 children with LCHADD, VLCADD or MCADD compared to 12 age-matched healthy controls. All participants showed a normal glycemic response, and most fasting hormone fluctuations were similar to those observed in controls. Findings of possible increased risk for insulin resistance in patients with LCHADD and a blunted postprandial incretin response in patients compared to controls warrant further investigation.
In study I, the phenotype, biochemical data and clinical outcome of 22 Swedish pediatric patients with VLCADD were related to newborn screening data and VLCAD residual enzyme activity. Patients had a wide phenotypic spectrum, varying from asymptomatic to severely affected cases. The identified correlation between newborn screening results, residual enzyme activity analysis, and clinical outcome could significantly aid in treatment decisions and disease severity prediction.
In study II, mitochondrial respiration and glycolysis in peripheral blood mononuclear cells (PBMCs) from 21 patients with VLCADD, MCADD or CUD were determined using an XFe flux analyzer. PMBCs were suitable for analysis within a 6-hour sampling window, and VLCADD and MCADD cells consistently showed lower mitochondrial respiration rates than CUD cells.
Study III investigated fasting metabolism during a 9-hour night fast in 12 children with VLCADD or MCADD using subcutaneous microdialysis. The VLCADD group showed an earlier fasting-induced initiation of lipolysis compared to the MCADD group, and all patients maintained euglycemia during the fast. Patients with VLCADD with lower residual enzyme activity had an earlier initiation of lipolysis than those with higher enzyme activity.
Study IV investigated the fasting and postprandial hormonal and incretin response after a 4-hour daytime fast and after the intake of a standardized meal in 15 children with LCHADD, VLCADD or MCADD compared to 12 age-matched healthy controls. All participants showed a normal glycemic response, and most fasting hormone fluctuations were similar to those observed in controls. Findings of possible increased risk for insulin resistance in patients with LCHADD and a blunted postprandial incretin response in patients compared to controls warrant further investigation.
List of papers:
I. Olsson, D., M. Barbaro, C. Haglind, M. Halldin, S. Lajic, S. Tucci, R. H. Zetterström and A. Nordenström (2022). Very long-chain acyl-CoA dehydrogenase deficiency in a Swedish cohort: Clinical symptoms, newborn screening, enzyme activity, and genetics. JIMD Rep. 63(2): 181-190.
Fulltext (DOI)
Pubmed
II. Stenlid, R., D. Olsson, J. Cen, H. Manell, C. Haglind, A. I. Chowdhury, P. Bergsten, A. Nordenström and M. Halldin (2022). Altered mitochondrial metabolism in peripheral blood cells from patients with inborn errors of β-oxidation. Clin Transl Sci. 15(1): 182-194.
Fulltext (DOI)
Pubmed
View record in Web of Science®
III. Olsson, D., C. Haglind, M. Halldin, S. Lajic and A. Nordenström. Assessment of fasting metabolism with microdialysis indicates earlier lipolysis in children with VLCADD compared to MCADD. [Submitted]
IV. Olsson, D., M. Halldin, C. Haglind, T. Gustafsson, S. Lajic and A. Nordenström. Hormonal responses to a short daytime fast in children with beta-oxidation disorders. [Manuscript]
I. Olsson, D., M. Barbaro, C. Haglind, M. Halldin, S. Lajic, S. Tucci, R. H. Zetterström and A. Nordenström (2022). Very long-chain acyl-CoA dehydrogenase deficiency in a Swedish cohort: Clinical symptoms, newborn screening, enzyme activity, and genetics. JIMD Rep. 63(2): 181-190.
Fulltext (DOI)
Pubmed
II. Stenlid, R., D. Olsson, J. Cen, H. Manell, C. Haglind, A. I. Chowdhury, P. Bergsten, A. Nordenström and M. Halldin (2022). Altered mitochondrial metabolism in peripheral blood cells from patients with inborn errors of β-oxidation. Clin Transl Sci. 15(1): 182-194.
Fulltext (DOI)
Pubmed
View record in Web of Science®
III. Olsson, D., C. Haglind, M. Halldin, S. Lajic and A. Nordenström. Assessment of fasting metabolism with microdialysis indicates earlier lipolysis in children with VLCADD compared to MCADD. [Submitted]
IV. Olsson, D., M. Halldin, C. Haglind, T. Gustafsson, S. Lajic and A. Nordenström. Hormonal responses to a short daytime fast in children with beta-oxidation disorders. [Manuscript]
Institution: Karolinska Institutet
Supervisor: Nordenström, Anna
Co-supervisor: Halldin-Stenlid, Maria; Lajic, Svetlana; Bieneck Haglind, Charlotte
Issue date: 2024-08-29
Rights:
Publication year: 2024
ISBN: 978-91-8017-735-1
Statistics
Total Visits
Views | |
---|---|
Mitochondrial ... | 99 |
Total Visits Per Month
March 2024 | April 2024 | May 2024 | June 2024 | July 2024 | August 2024 | September 2024 | |
---|---|---|---|---|---|---|---|
Mitochondrial ... | 0 | 0 | 0 | 0 | 0 | 46 | 53 |
File Visits
Views | |
---|---|
Thesis_David_Olsson.pdf | 158 |
Top country views
Views | |
---|---|
United States | 29 |
China | 23 |
Sweden | 17 |
Ireland | 7 |
Austria | 2 |
Iran | 2 |
Netherlands | 2 |
Portugal | 2 |
Czech Republic | 1 |
Germany | 1 |
Top cities views
Views | |
---|---|
Zhengzhou | 6 |
Stockholm | 5 |
Dublin | 4 |
Norrköping | 4 |
Ashburn | 3 |
Hangzhou | 3 |
Faerjestaden | 2 |
Lisbon | 2 |
Lund | 2 |
Shenzhen | 2 |