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JIMD Reports, Volume 32

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Cover of 'JIMD Reports, Volume 32'

Table of Contents

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    Book Overview
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    Chapter 537 Newborn Screening Programmes in Europe, Arguments and Efforts Regarding Harmonisation: Focus on Organic Acidurias
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    Chapter 541 Whole Exome Sequencing Identifies the Genetic Basis of Late-Onset Leigh Syndrome in a Patient with MRI but Little Biochemical Evidence of a Mitochondrial Disorder
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    Chapter 547 Hydroxysteroid 17-Beta Dehydrogenase Type 10 Disease in Siblings
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    Chapter 553 Endurance Exercise Training in Young Adults with Barth Syndrome: A Pilot Study
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    Chapter 556 Newborn Screening for Vitamin B6 Non-responsive Classical Homocystinuria: Systematical Evaluation of a Two-Tier Strategy
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    Chapter 560 Establishing New Cut-Off Limits for Galactose 1-Phosphate-Uridyltransferase Deficiency for the Dutch Newborn Screening Programme
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    Chapter 561 Management of an LCHADD Patient During Pregnancy and High Intensity Exercise
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    Chapter 562 Rare Case of Hepatic Gaucheroma in a Child on Enzyme Replacement Therapy
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    Chapter 564 Reliable Diagnosis of Carnitine Palmitoyltransferase Type IA Deficiency by Analysis of Plasma Acylcarnitine Profiles
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    Chapter 566 Low Protein Formula: Consequences of Quantitative Effects of Pre-analytical Factors on Amino Acid Concentrations in Plasma of Healthy Infants
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    Chapter 567 Relationships Between Childhood Experiences and Adulthood Outcomes in Women with PKU: A Qualitative Analysis
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    Chapter 568 A Multiplatform Metabolomics Approach to Characterize Plasma Levels of Phenylalanine and Tyrosine in Phenylketonuria
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    Chapter 570 Japanese Male Siblings with 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency (HSD10 Disease) Without Neurological Regression
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    Chapter 571 The Effect of S-Adenosylmethionine on Self-Mutilation in a Patient with Lesch–Nyhan Disease
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    Chapter 572 Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian Patients
Attention for Chapter 564: Reliable Diagnosis of Carnitine Palmitoyltransferase Type IA Deficiency by Analysis of Plasma Acylcarnitine Profiles
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Chapter title
Reliable Diagnosis of Carnitine Palmitoyltransferase Type IA Deficiency by Analysis of Plasma Acylcarnitine Profiles
Chapter number 564
Book title
JIMD Reports, Volume 32
Published in
JIMD Reports, June 2016
DOI 10.1007/8904_2016_564
Pubmed ID
Book ISBNs
978-3-66-254384-9, 978-3-66-254385-6
Authors

Heiner-Fokkema, M Rebecca, Vaz, Frédéric M, Maatman, Ronald, Kluijtmans, Leo A J, van Spronsen, Francjan J, Reijngoud, Dirk-Jan, Heiner-Fokkema, M. Rebecca, Vaz, Frédéric M., Kluijtmans, Leo A. J., van Spronsen, Francjan J., M. Rebecca Heiner-Fokkema, Frédéric M. Vaz, Ronald Maatman, Leo A. J. Kluijtmans, Francjan J. van Spronsen, Dirk-Jan Reijngoud, Spronsen, Francjan J.

Editors

Eva Morava, Matthias Baumgartner, Marc Patterson, Shamima Rahman, Johannes Zschocke, Verena Peters

Abstract

Carnitine palmitoyltransferase IA (CPT-IA) deficiency is an inherited disorder of the carnitine cycle (MIM #255120). Patients affected by this deficiency might be missed easily because of lack of specific and sensitive biochemical markers. In this study, sensitivity and specificity of plasma free carnitine (C0) and long-chain acylcarnitines (lc-ac: C16:0-, C16:1-, C18:0-, C18:1- and C18:2-ac) was evaluated, including the sum of lc-ac (∑lc-ac) and the molar ratios C0/(C16:0-ac+C18:0-ac) and C0/∑lc-ac. Nine plasma acylcarnitine profiles of 4 CPT-IA deficient patients were compared with profiles of 2,190 subjects suspected of or diagnosed with an inherited disorder of metabolism. Age-dependent reference values were calculated based on the patient population without a definite diagnosis of an inborn error of metabolism (n = 1,600). Sensitivity, specificity, and Receiver Operating Characteristic (ROC) curves were calculated based on samples of the whole patient population. Concentrations of C0 in plasma were normal in all CPT-IA deficient patient samples. ROC analyses showed highest diagnostic values for C18:0-ac, C18:1-ac, and ∑lc-ac (AUC 1.000) and lowest for C0 (AUC 0.738). Combining two markers, i.e., a plasma C18:1-ac concentration <0.05 μmol/L and a molar ratio of C0/(C16:0-ac+C18:0-ac) >587, specificity to diagnose CPT-IA deficiency increased to 99.3% compared with either C18:1-ac (97.4%) or C0/(C16:0-ac+C18:0-ac) (96.9%) alone, all at a sensitivity of 100%. Combination of a low concentration of C18:1-ac with a high molar ratio of C0/(C16:0-ac+C18:0-ac) ratio in plasma has high diagnostic value for CPT-IA deficiency. Patients with a clinical suspicion of CPT-IA deficiency can be diagnosed with this test combination.

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Mendeley readers

The data shown below were compiled from readership statistics for 10 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 10 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 2 20%
Student > Master 2 20%
Researcher 1 10%
Student > Ph. D. Student 1 10%
Unknown 4 40%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 20%
Medicine and Dentistry 2 20%
Agricultural and Biological Sciences 1 10%
Pharmacology, Toxicology and Pharmaceutical Science 1 10%
Unknown 4 40%