Literature DB >> 1861462

Neonatal cardiomyopathy and lactic acidosis responsive to thiamine.

H D Bakker1, H R Scholte, I E Luyt-Houwen, A H van Gennip, N G Abeling, J Lam.   

Abstract

A congestive cardiomyopathy was diagnosed in a girl at the age of 4 weeks. In the weeks following she developed general muscle hypotonia and plasma lactate increased to 8.5 mmol/L. Biochemical investigations of a muscle biopsy at the age of 3 months showed a deficiency in the oxidation of all substrates tested: pyruvate plus malate, 2-ketoglutarate and palmitate plus malate. After freezing and thawing of the homogenate and the addition of essential cofactors, the oxidation of the ketoacids normalized. The oxidation defect in the untreated homogenate can be explained by a deficiency in one of the cofactors (such as thiamine pyrophosphate, NAD+ or CoASH), or by a defect in the oxidative phosphorylation. Treatment with thiamine and carnitine resulted in a decrease in blood lactate to normal levels and a dramatic clinical improvement. Suspension of thiamine caused deterioration of her clinical condition and lactic acidaemia. The thiamine therapy was then continued. The girl is now 6 years old and in perfect health.

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Year:  1991        PMID: 1861462     DOI: 10.1007/bf01804393

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


  11 in total

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Review 4.  The role of the carnitine system in myocardial fatty acid oxidation: carnitine deficiency, failing mitochondria and cardiomyopathy.

Authors:  H R Scholte; I E Luyt-Houwen; M H Vaandrager-Verduin
Journal:  Basic Res Cardiol       Date:  1987       Impact factor: 17.165

5.  Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidase.

Authors:  A M Roodhooft; K J Van Acker; J J Martin; C Ceuterick; H R Scholte; I E Luyt-Houwen
Journal:  Neuropediatrics       Date:  1986-11       Impact factor: 1.947

6.  Oxygen electrode studies with human skeletal muscle mitochondria in vitro. A re-appraisal.

Authors:  E Byrne; I Trounce
Journal:  J Neurol Sci       Date:  1985-07       Impact factor: 3.181

7.  An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes.

Authors:  P G Barth; H R Scholte; J A Berden; J M Van der Klei-Van Moorsel; I E Luyt-Houwen; E T Van 't Veer-Korthof; J J Van der Harten; M A Sobotka-Plojhar
Journal:  J Neurol Sci       Date:  1983-12       Impact factor: 3.181

Review 8.  Primary (genetic) cardiomyopathies in infancy. A survey of possible disorders and guidelines for diagnosis.

Authors:  A Kohlschütter; G Hausdorf
Journal:  Eur J Pediatr       Date:  1986-12       Impact factor: 3.183

9.  [Apparently idiopathic primary myocardiopathies in children. The role of metabolic etiology].

Authors:  A Lombes; F Hervé; H Ogier; A Pellet; D Sidi; E Villain; J Kachaner; C Charpentier; M Paturneau-Jouas; M Fardeau
Journal:  Arch Fr Pediatr       Date:  1987-10

10.  Congestive cardiomyopathy of childhood.

Authors:  M E Tripp
Journal:  Adv Pediatr       Date:  1984
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