Sökning: (WFRF:(Moat J.))
> (2020-2022) >
Thermo-sensitive mi...
Thermo-sensitive mitochondrial trifunctional protein deficiency presenting with episodic myopathy
-
Schwantje, M. (författare)
-
Ebberink, M. S. (författare)
-
Doolaard, M. (författare)
-
visa fler...
-
Ruiter, J. P. N. (författare)
-
Fuchs, S. A. (författare)
-
- Darin, Niklas, 1964 (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics
-
- Oldfors Hedberg, Carola, 1969 (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för laboratoriemedicin,Department of Laboratory Medicine
-
Regal, L. (författare)
-
Kaat, L. D. (författare)
-
Huidekoper, H. H. (författare)
-
Olpin, S. (författare)
-
Cole, D. (författare)
-
Moat, S. J. (författare)
-
Visser, G. (författare)
-
Ferdinandusse, S. (författare)
-
visa färre...
-
(creator_code:org_t)
- 2022-05-05
- 2022
- Engelska.
-
Ingår i: Journal of Inherited Metabolic Disease. - : Wiley. - 0141-8955 .- 1573-2665. ; 45:4, s. 819-831
- Relaterad länk:
-
https://gup.ub.gu.se...
-
visa fler...
-
https://doi.org/10.1...
-
visa färre...
Abstract
Ämnesord
Stäng
- Mitochondrial trifunctional protein (MTP) is involved in long-chain fatty acid beta-oxidation (lcFAO). Deficiency of one or more of the enzyme activities as catalyzed by MTP causes generalized MTP deficiency (MTPD), long-chain hydroxyacyl-CoA dehydrogenase deficiency (LCHADD), or long-chain ketoacyl-CoA thiolase deficiency (LCKATD). When genetic variants result in thermo-sensitive enzymes, increased body temperature (e.g. fever) can reduce enzyme activity and be a risk factor for clinical decompensation. This is the first description of five patients with a thermo-sensitive MTP deficiency. Clinical and genetic information was obtained from clinical files. Measurement of LCHAD and LCKAT activities, lcFAO-flux studies and palmitate loading tests were performed in skin fibroblasts cultured at 37 degrees C and 40 degrees C. In all patients (four MTPD, one LCKATD), disease manifested during childhood (manifestation age: 2-10 years) with myopathic symptoms triggered by fever or exercise. In four patients, signs of retinopathy or neuropathy were present. Plasma long-chain acylcarnitines were normal or slightly increased. HADHB variants were identified (at age: 6-18 years) by whole exome sequencing or gene panel analyses. At 37 degrees C, LCHAD and LCKAT activities were mildly impaired and lcFAO-fluxes were normal. Remarkably, enzyme activities and lcFAO-fluxes were markedly diminished at 40 degrees C. Preventive (dietary) measures improved symptoms for most. In conclusion, all patients with thermo-sensitive MTP deficiency had a long diagnostic trajectory and both genetic and enzymatic testing were required for diagnosis. The frequent absence of characteristic acylcarnitine abnormalities poses a risk for a diagnostic delay. Given the positive treatment effects, upfront genetic screening may be beneficial to enhance early recognition.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Neurologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Neurology (hsv//eng)
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Pediatrik (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Pediatrics (hsv//eng)
Nyckelord
- long-chain fatty acid oxidation disorders
- long-chain ketoacyl-CoA
- thiolase deficiency
- mitochondrial trifunctional protein complex
- mitochondrial trifunctional protein deficiency
- myopathy
- thermo-sensitivity
- fatty-acid oxidation
- beta-oxidation
- defects
- pathophysiology
- dehydrogenase
- disorders
- mutations
- enzyme
- Endocrinology & Metabolism
- Genetics & Heredity
- Research & Experimental
- Medicine
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
Hitta via bibliotek
Till lärosätets databas
- Av författaren/redakt...
-
Schwantje, M.
-
Ebberink, M. S.
-
Doolaard, M.
-
Ruiter, J. P. N.
-
Fuchs, S. A.
-
Darin, Niklas, 1 ...
-
visa fler...
-
Oldfors Hedberg, ...
-
Regal, L.
-
Kaat, L. D.
-
Huidekoper, H. H ...
-
Olpin, S.
-
Cole, D.
-
Moat, S. J.
-
Visser, G.
-
Ferdinandusse, S ...
-
visa färre...
- Om ämnet
-
- MEDICIN OCH HÄLSOVETENSKAP
-
MEDICIN OCH HÄLS ...
-
och Klinisk medicin
-
och Neurologi
-
- MEDICIN OCH HÄLSOVETENSKAP
-
MEDICIN OCH HÄLS ...
-
och Klinisk medicin
-
och Pediatrik
- Artiklar i publikationen
-
Journal of Inher ...
- Av lärosätet
-
Göteborgs universitet