Literature DB >> 33473339

Long-term follow-up with filter paper samples in patients with propionic acidemia.

Sinziana Stanescu1, Amaya Belanger-Quintana1, Borja Manuel Fernández-Felix2, Celia Pérez-Cerdá3, Begoña Merinero3, Pedro Ruiz-Sala3, Francisco Arrieta1, Mercedes Martínez-Pardo1.   

Abstract

BACKGROUND: Propionic acidemia (PA) is an inherited disorder caused by deficiency of propionyl CoA carboxylase. Most patients with this disorder are diagnosed during the neonatal period because of severe metabolic acidosis and hyperammonemia. Patients are required to undergo blood and urine analysis at least 3 to 4 times per year, depending on age and metabolic control.
METHODS: We designed a prospective study in which we investigated the results from blood and urinary samples collected monthly in filter paper from 10 PA patients followed in a single metabolic reference center from January 2015 to September 2017. The aim of this study was to evaluate the usefulness of filter paper samples in the follow-up of the PA patients.
RESULTS: During the follow-up period, 163 dried blood spot (DBS) and 119 urine dried spot samples were analyzed and compared with 160 plasma and 103 liquid urine specimens; 64 specimens of plasma were analyzed for odd-numbered long-chain fatty acids (OLCFAs). A total of 40 metabolic crises, 18 of them with hyperammonemia were documented. We observed a strong correlation between the filter paper and the urine/plasma samples for the main PA parameters both in stable metabolic conditions as well as in acute decompensations. Also, there was a strong correlation between OLCFAs measured in plasma and quantification of odd number acylcarnitines in DBS.
CONCLUSIONS: We conclude that filter paper blood and urinary samples can be used for the follow-up of the patients with PA, correctly reflecting their metabolic situation.
© 2020 The Authors. JIMD Reports published by John Wiley & Sons Ltd on behalf of SSIEM.

Entities:  

Keywords:  filter paper samples; follow‐up; propionic acidemia

Year:  2020        PMID: 33473339      PMCID: PMC7802619          DOI: 10.1002/jmd2.12166

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  15 in total

1.  Odd-numbered long-chain fatty acids in propionic acidaemia.

Authors:  W Sperl; C Murr; D Skladal; J O Sass; T Suormala; R Baumgartner; U Wendel
Journal:  Eur J Pediatr       Date:  2000 Jan-Feb       Impact factor: 3.183

Review 2.  Chronic management and health supervision of individuals with propionic acidemia.

Authors:  V Reid Sutton; Kimberly A Chapman; Andrea L Gropman; Erin MacLeod; Kathy Stagni; Marshall L Summar; Keiko Ueda; Nicholas Ah Mew; Jill Franks; Eddie Island; Dietrich Matern; Loren Peña; Brittany Smith; Tina Urv; Charles Venditti; Anupam Chakarapani
Journal:  Mol Genet Metab       Date:  2011-09-10       Impact factor: 4.797

3.  Separation and identification of plasma short-chain acylcarnitine isomers by HPLC/MS/MS for the differential diagnosis of fatty acid oxidation defects and organic acidemias.

Authors:  Isaac Ferrer; Pedro Ruiz-Sala; Yolanda Vicente; Begoña Merinero; Celia Pérez-Cerdá; Magdalena Ugarte
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2007-10-22       Impact factor: 3.205

Review 4.  Pathophysiology of propionic and methylmalonic acidemias. Part 2: Treatment strategies.

Authors:  Hanneke A Haijes; Peter M van Hasselt; Judith J M Jans; Nanda M Verhoeven-Duif
Journal:  J Inherit Metab Dis       Date:  2019-07-09       Impact factor: 4.982

5.  Propionic acidaemia: clinical, biochemical and therapeutic aspects. Experience in 30 patients.

Authors:  W Lehnert; W Sperl; T Suormala; E R Baumgartner
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

6.  Usefulness of biochemical parameters in decision-making on the start of emergency treatment in patients with propionic acidemia.

Authors:  Tamaris Zwickler; Alina Riderer; Gisela Haege; Georg F Hoffmann; Stefan Kölker; Peter Burgard
Journal:  J Inherit Metab Dis       Date:  2013-06-25       Impact factor: 4.982

7.  Metabolic changes associated with hyperammonemia in patients with propionic acidemia.

Authors:  Heather R Filipowicz; Sharon L Ernst; Carrie L Ashurst; Marzia Pasquali; Nicola Longo
Journal:  Mol Genet Metab       Date:  2006-01-10       Impact factor: 4.797

8.  Methylmalonic acidaemia: examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation group.

Authors:  B Merinero; B Pérez; C Pérez-Cerdá; A Rincón; L R Desviat; M A Martínez; P Ruiz Sala; M J García; L Aldamiz-Echevarría; J Campos; V Cornejo; M Del Toro; A Mahfoud; M Martínez-Pardo; R Parini; C Pedrón; L Peña-Quintana; M Pérez; M Pourfarzam; M Ugarte
Journal:  J Inherit Metab Dis       Date:  2007-10-22       Impact factor: 4.982

9.  Development of electrospray ionization tandem mass spectrometry methods for the study of a high number of urine markers of inborn errors of metabolism.

Authors:  M Maira Rebollido-Fernandez; Daisy E Castiñeiras; M Dolores Bóveda; M Luz Couce; José A Cocho; Jose M Fraga
Journal:  Rapid Commun Mass Spectrom       Date:  2012-09-30       Impact factor: 2.419

10.  Accumulation of odd-numbered long-chain fatty acids in fetuses and neonates with inherited disorders of propionate metabolism.

Authors:  U Wendel; R Baumgartner; S B van der Meer; L J Spaapen
Journal:  Pediatr Res       Date:  1991-04       Impact factor: 3.756

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  1 in total

1.  O-GlcNAcylation enhances CPS1 catalytic efficiency for ammonia and promotes ureagenesis.

Authors:  Leandro R Soria; Georgios Makris; Alfonso M D'Alessio; Angela De Angelis; Iolanda Boffa; Veronica M Pravata; Véronique Rüfenacht; Sergio Attanasio; Edoardo Nusco; Paola Arena; Andrew T Ferenbach; Debora Paris; Paola Cuomo; Andrea Motta; Matthew Nitzahn; Gerald S Lipshutz; Ainhoa Martínez-Pizarro; Eva Richard; Lourdes R Desviat; Johannes Häberle; Daan M F van Aalten; Nicola Brunetti-Pierri
Journal:  Nat Commun       Date:  2022-09-05       Impact factor: 17.694

  1 in total

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