Literature DB >> 22669364

Maternal phenylketonuria: low phenylalaninemia might increase the risk of intra uterine growth retardation.

Raphaël Teissier1, Emmanuel Nowak, Murielle Assoun, Karine Mention, Aline Cano, Alain Fouilhoux, François Feillet, Hélène Ogier, Emmanuel Oger, Loïc de Parscau.   

Abstract

BACKGROUND: Malformations and mental retardation in the offspring of women with Phenylketonuria (PKU) can be prevented by maintaining maternal blood Phenylalanine (PHE) within a target range (120-300 μmol/L) through a PHE-restricted diet. In a former French study, a high and unexpected proportion of intra uterine growth retardation (IUGR) has been reported. Guidelines have been proposed to all French centres caring for maternal PKU since 2002.
OBJECTIVE: To confirm IUGR and investigate its causes. The other goals were to assess the follow-up of these pregnancies based on the new guidelines and the pertinence of these recommendations.
DESIGN: Clinical, biological and ultrasound data of all pregnancies in PKU women in France, from 2002 to 2007 were retrospectively analyzed.
RESULTS: Data from 115 pregnancies in 86 women with PKU were collected. Ninety percent of women had been informed of the risk of maternal PKU in the absence of a strict diet during pregnancy, 88 % of women had started a diet before conception, and 45 % of infants were born small for gestational age (birth length and/or weight ≤-2 SD). PHE intakes were lower in the group with IUGR from the fifth to the eighth month of pregnancy and duration of time spent at <120 μmol/L during pregnancy was associated with a higher risk of IUGR.
CONCLUSION: Hyperphenylalaninemia (HPA) is not the only risk factor for IUGR; PHE lower than 120 μmol/L could also be associated with the IUGR occurrence. Even if the monitoring of these pregnancies has been improved since the initiation of guidelines, we would like to stress on the importance of the dietary aspect of the disease.

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Year:  2012        PMID: 22669364     DOI: 10.1007/s10545-012-9491-0

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


  23 in total

1.  Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative Study.

Authors:  H L Levy; P Guldberg; F Güttler; W B Hanley; R Matalon; B M Rouse; F Trefz; C Azen; E N Allred; F de la Cruz; R Koch
Journal:  Pediatr Res       Date:  2001-05       Impact factor: 3.756

Review 2.  Tyrosine supplementation for phenylketonuria.

Authors:  Diana Webster; Joanne Wildgoose
Journal:  Cochrane Database Syst Rev       Date:  2010-08-04

Review 3.  Fetal nutrition and adult disease.

Authors:  K M Godfrey; D J Barker
Journal:  Am J Clin Nutr       Date:  2000-05       Impact factor: 7.045

4.  [Dietary recommendations for pregnant women affected with phenylketonuria].

Authors:  V Abadie; E Depondt; J L Bresson; M Vidailhet
Journal:  Arch Pediatr       Date:  2001-04       Impact factor: 1.180

5.  Large daily fluctuations in plasma tyrosine in treated patients with phenylketonuria.

Authors:  F J van Spronsen; T van Dijk; G P Smit; M van Rijn; D J Reijngoud; R Berger; H S Heymans
Journal:  Am J Clin Nutr       Date:  1996-12       Impact factor: 7.045

6.  Maternal phenylketonuria: the French survey.

Authors:  François Feillet; Véronique Abadie; Jacques Berthelot; Nicole Maurin; Hélène Ogier; Michel Vidailhet; Jean-Pierre Farriaux; Loic de Parscau
Journal:  Eur J Pediatr       Date:  2004-07-06       Impact factor: 3.183

7.  The Maternal Phenylketonuria International Study: 1984-2002.

Authors:  Richard Koch; William Hanley; Harvey Levy; Kim Matalon; Reuben Matalon; Bobbye Rouse; Frederick Trefz; Flemming Güttler; Colleen Azen; Larry Platt; Susan Waisbren; Keith Widaman; Jiaping Ning; Eva G Friedman; Felix de la Cruz
Journal:  Pediatrics       Date:  2003-12       Impact factor: 7.124

8.  Recommendations on the dietary management of phenylketonuria. Report of Medical Research Council Working Party on Phenylketonuria.

Authors: 
Journal:  Arch Dis Child       Date:  1993-03       Impact factor: 3.791

9.  Amino acids in plasma and CSF and monoamine metabolites in CSF: interrelationship in healthy subjects.

Authors:  L Hagenfeldt; L Bjerkenstedt; G Edman; G Sedvall; F A Wiesel
Journal:  J Neurochem       Date:  1984-03       Impact factor: 5.372

10.  Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies.

Authors:  R R Lenke; H L Levy
Journal:  N Engl J Med       Date:  1980-11-20       Impact factor: 91.245

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  13 in total

1.  Infants with Tyrosinemia Type 1: Should phenylalanine be supplemented?

Authors:  Danique van Vliet; Esther van Dam; Margreet van Rijn; Terry G J Derks; Gineke Venema-Liefaard; Marrit M Hitzert; Roelineke J Lunsing; M Rebecca Heiner-Fokkema; Francjan J van Spronsen
Journal:  JIMD Rep       Date:  2014-09-26

2.  Use of sapropterin dihydrochloride in maternal phenylketonuria. A European experience of eight cases.

Authors:  François Feillet; Ania C Muntau; François-Guillaume Debray; Amelie S Lotz-Havla; Alexandra Puchwein-Schwepcke; Ma'atem Béatrice Fofou-Caillierez; Francjan van Spronsen; Fritz Friedrich Trefz
Journal:  J Inherit Metab Dis       Date:  2014-05-01       Impact factor: 4.982

3.  What Is the Best Blood Sampling Time for Metabolic Control of Phenylalanine and Tyrosine Concentrations in Tyrosinemia Type 1 Patients?

Authors:  Esther van Dam; Anne Daly; Gineke Venema-Liefaard; Margreet van Rijn; Terry G J Derks; Patrick J McKiernan; M Rebecca Heiner-Fokkema; Anita MacDonald; Francjan J van Spronsen
Journal:  JIMD Rep       Date:  2017-01-25

Review 4.  Genetic etiology and clinical challenges of phenylketonuria.

Authors:  Nasser A Elhawary; Imad A AlJahdali; Iman S Abumansour; Ezzeldin N Elhawary; Nagwa Gaboon; Mohammed Dandini; Abdulelah Madkhali; Wafaa Alosaimi; Abdulmajeed Alzahrani; Fawzia Aljohani; Ehab M Melibary; Osama A Kensara
Journal:  Hum Genomics       Date:  2022-07-19       Impact factor: 6.481

5.  Maternal phenylketonuria in Turkey: outcomes of 71 pregnancies and issues in management.

Authors:  Yılmaz Yıldız; Hatice Serap Sivri
Journal:  Eur J Pediatr       Date:  2019-05-03       Impact factor: 3.183

Review 6.  The complete European guidelines on phenylketonuria: diagnosis and treatment.

Authors:  A M J van Wegberg; A MacDonald; K Ahring; A Bélanger-Quintana; N Blau; A M Bosch; A Burlina; J Campistol; F Feillet; M Giżewska; S C Huijbregts; S Kearney; V Leuzzi; F Maillot; A C Muntau; M van Rijn; F Trefz; J H Walter; F J van Spronsen
Journal:  Orphanet J Rare Dis       Date:  2017-10-12       Impact factor: 4.123

Review 7.  Phenylketonuria.

Authors:  Francjan J van Spronsen; Nenad Blau; Cary Harding; Alberto Burlina; Nicola Longo; Annet M Bosch
Journal:  Nat Rev Dis Primers       Date:  2021-05-20       Impact factor: 52.329

8.  Diagnostic and management practices for phenylketonuria in 19 countries of the South and Eastern European Region: survey results.

Authors:  Maria Giżewska; Anita MacDonald; Amaya Bélanger-Quintana; Alberto Burlina; Maureen Cleary; Turgay Coşkun; François Feillet; Ania C Muntau; Friedrich K Trefz; Francjan J van Spronsen; Nenad Blau
Journal:  Eur J Pediatr       Date:  2015-09-08       Impact factor: 3.183

9.  Dietary management of maternal phenylketonuria with glycomacropeptide and amino acids supplements: A case report.

Authors:  A Pinto; M F Almeida; A Cunha; C Carmona; S Rocha; A Guimas; R Ribeiro; C R Mota; E Martins; A MacDonald; J C Rocha
Journal:  Mol Genet Metab Rep       Date:  2017-10-18

10.  Maternal Phenylketonuria International Collaborative Study revisited: evaluation of maternal nutritional risk factors besides phenylalanine for fetal congenital heart defects.

Authors:  Shoji Yano; Kathryn Moseley; Teodoro Bottiglieri; Erland Arning; Colleen Azen
Journal:  J Inherit Metab Dis       Date:  2013-06-20       Impact factor: 4.982

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