Literature DB >> 23653224

Carnitine levels in 26,462 individuals from the nationwide screening program for primary carnitine deficiency in the Faroe Islands.

Jan Rasmussen1, Olav W Nielsen, Nils Janzen, Morten Duno, Hannes Gislason, Lars Køber, Ulrike Steuerwald, Allan M Lund.   

Abstract

BACKGROUND: Primary carnitine deficiency (PCD) is an autosomal recessive disorder of fatty acid oxidation and has been associated to episodes of sudden death in the Faroe Islands. Data are presented from the nationwide population based Faroese screening program to find people with low carnitine levels indicating PCD.
METHODS: Whole blood samples from dried blood spots were analysed by tandem mass spectrometry with and without butylation. Genetic analyses were performed in all people with non-butylated free carnitine (fC0) below 7 μmol/L.
RESULTS: 55 % (n = 26,462) of the entire population was screened and 89 PCD patients were identified, yielding an overall prevalence of 1:297 of PCD in the Faroe Islands. Carnitine levels were positively correlated to age in both males and females (p < 0.003) although levels decreased in females when reaching fertile age. The gender difference in mean carnitine levels was significant during female fertile age (4.71 μmol/L fC0 in the age group 25-30 years, p < 0.01). A lower cut-off of 5 μmol/L in fC0 identified all homozygous for the severe genotype c.95A > G (p.N32S) (n = 20).
CONCLUSION: Carnitine levels differ by gender and age. A lower cut-off of 5 μmol/L in fC0 was appropriate to identify c.95A > G homozygotes. The prevalence of PCD in the Faroe Islands is the highest reported in the world (1:297).

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Year:  2013        PMID: 23653224     DOI: 10.1007/s10545-013-9606-2

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


  38 in total

1.  Age and sex dependency of carnitine concentration in human serum and skeletal muscle.

Authors:  J R Opalka; F N Gellerich; S Zierz
Journal:  Clin Chem       Date:  2001-12       Impact factor: 8.327

2.  Hereditary defect in carnitine membrane transport is expressed in skin fibroblasts.

Authors:  B O Eriksson; S Lindstedt; I Nordin
Journal:  Eur J Pediatr       Date:  1988-08       Impact factor: 3.183

3.  Increased serum carnitine concentration in renal insufficiency.

Authors:  S H Chen; S D Lincoln
Journal:  Clin Chem       Date:  1977-02       Impact factor: 8.327

4.  Carnitine transporter defect: diagnosis in asymptomatic adult women following analysis of acylcarnitines in their newborn infants.

Authors:  S Vijay; A Patterson; S Olpin; M J Henderson; S Clark; C Day; G Savill; J H Walter
Journal:  J Inherit Metab Dis       Date:  2006-07-23       Impact factor: 4.982

5.  Perturbation of serum carnitine levels in human adults by chronic renal disease and dialysis therapy.

Authors:  L L Bartel; J L Hussey; E Shrago
Journal:  Am J Clin Nutr       Date:  1981-07       Impact factor: 7.045

6.  Screening newborns for inborn errors of metabolism by tandem mass spectrometry.

Authors:  Bridget Wilcken; Veronica Wiley; Judith Hammond; Kevin Carpenter
Journal:  N Engl J Med       Date:  2003-06-05       Impact factor: 91.245

7.  Accurate measurement of free carnitine in dried blood spots by isotope-dilution electrospray tandem mass spectrometry without butylation.

Authors:  Andreas Schulze; Christiane Schmidt; Dirk Kohlmüller; Georg F Hoffmann; Ertan Mayatepek
Journal:  Clin Chim Acta       Date:  2003-09       Impact factor: 3.786

8.  Primary carnitine deficiency and pivalic acid exposure causing encephalopathy and fatal cardiac events.

Authors:  Jan Rasmussen; Olav W Nielsen; Allan M Lund; Lars Køber; Høgni Djurhuus
Journal:  J Inherit Metab Dis       Date:  2012-05-08       Impact factor: 4.982

9.  Biochemical screening of 504,049 newborns in Denmark, the Faroe Islands and Greenland--experience and development of a routine program for expanded newborn screening.

Authors:  Allan Meldgaard Lund; David Michael Hougaard; Henrik Simonsen; Brage Storstein Andresen; Mette Christensen; Morten Dunø; Kristin Skogstrand; Rikke K J Olsen; Ulrich Glümer Jensen; Arieh Cohen; Nanna Larsen; Peter Saugmann-Jensen; Niels Gregersen; Niels Jacob Brandt; Ernst Christensen; Flemming Skovby; Bent Nørgaard-Pedersen
Journal:  Mol Genet Metab       Date:  2012-06-21       Impact factor: 4.797

10.  Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency.

Authors:  F Scaglia; Y Wang; R H Singh; P P Dembure; M Pasquali; P M Fernhoff; N Longo
Journal:  Genet Med       Date:  1998 Nov-Dec       Impact factor: 8.822

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  26 in total

1.  Carnitine levels in skeletal muscle, blood, and urine in patients with primary carnitine deficiency during intermission of L-carnitine supplementation.

Authors:  J Rasmussen; J A Thomsen; J H Olesen; T M Lund; M Mohr; J Clementsen; O W Nielsen; A M Lund
Journal:  JIMD Rep       Date:  2015-02-10

2.  Primary Carnitine Deficiency - A Rare Treatable Cause of Cardiomyopathy and Massive Hepatomegaly.

Authors:  Shivani Deswal; Sunita Bijarnia-Mahay; Vinamr Manocha; Keiichi Hara; Yosuke Shigematsu; Renu Saxena; Ishwar C Verma
Journal:  Indian J Pediatr       Date:  2016-09-01       Impact factor: 1.967

3.  Functional and molecular studies in primary carnitine deficiency.

Authors:  Marta Frigeni; Bijina Balakrishnan; Xue Yin; Fernanda R O Calderon; Rong Mao; Marzia Pasquali; Nicola Longo
Journal:  Hum Mutat       Date:  2017-09-14       Impact factor: 4.878

4.  Primary Carnitine Deficiency: Is Foetal Development Affected and Can Newborn Screening Be Improved?

Authors:  Jan Rasmussen; David M Hougaard; Noreen Sandhu; Katrine Fjællegaard; Poula R Petersen; Ulrike Steuerwald; Allan M Lund
Journal:  JIMD Rep       Date:  2017-01-20

5.  Is L-Carnitine Supplementation Beneficial in 3-Methylcrotonyl-CoA Carboxylase Deficiency?

Authors:  Jákup Andreas Thomsen; Allan Meldgaard Lund; Jess Have Olesen; Magni Mohr; Jan Rasmussen
Journal:  JIMD Rep       Date:  2015-03-03

6.  Application of the Artificial Intelligence Algorithm Model for Screening of Inborn Errors of Metabolism.

Authors:  Muping Zhou; Liyuan Deng; Yan Huang; Ying Xiao; Jun Wen; Na Liu; Yingchao Zeng; Hua Zhang
Journal:  Front Pediatr       Date:  2022-05-19       Impact factor: 3.569

7.  FarGen - participants in the genetic research infrastructure of the Faroe Islands.

Authors:  Katrin D Apol; Leivur N Lydersen; Ólavur Mortensen; Pál Weihe; Bjarni Á Steig; Guðrið Andorsdóttir; Noomi O Gregersen
Journal:  Scand J Public Health       Date:  2021-10-05       Impact factor: 3.199

8.  Primary Carnitine deficiency in the Faroe Islands: health and cardiac status in 76 adult patients diagnosed by screening.

Authors:  Jan Rasmussen; Lars Køber; Allan M Lund; Olav W Nielsen
Journal:  J Inherit Metab Dis       Date:  2013-08-21       Impact factor: 4.982

Review 9.  Carnitine transport and fatty acid oxidation.

Authors:  Nicola Longo; Marta Frigeni; Marzia Pasquali
Journal:  Biochim Biophys Acta       Date:  2016-01-29

10.  Similar Gut Bacterial Composition Between Patients With Ulcerative Colitis and Healthy Controls in a High Incidence Population: A Cross-sectional Study of the Faroe Islands IBD Cohort.

Authors:  Marjun Á Fríðirksmørk Berbisá; Kári Rubek Nielsen; Anna Cäcilia Ingham; Jóngerð Midjord; Turið Hammer; Poula Patursson; Nicolina M O Vest; Noomi O Gregersen; Johan Burisch; Amanda Vang
Journal:  Inflamm Bowel Dis       Date:  2022-07-01       Impact factor: 7.290

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