Literature DB >> 11596648

The intellectual abilities of early-treated individuals with pyridoxine-nonresponsive homocystinuria due to cystathionine beta-synthase deficiency.

S Yap1, H Rushe, P M Howard, E R Naughten.   

Abstract

The pathological sequelae of untreated homocystinuria due to cystathionine beta-synthase deficiency include ectopia lentis, osteoporosis, thromboembolic events and mental retardation. They occur at a significantly higher rate with poorer mental capabilities (mean IQ = 57) in the untreated pyridoxine-nonresponsive individuals. The mental capabilities of 23 pyridoxine-nonresponsive individuals with 339 patient-years of treatment were assessed using age-appropriate psychometric tests and were compared to those of 10 unaffected siblings (controls). Of the 23 individuals, 19 were diagnosed through newborn screening with early treatment, two were late-detected and two were untreated at the time of assessment. Thirteen of the newborn, screened group who were compliant with treatment had no complications, while the remaining 6, who had poor compliance, developed complications. Good compliance was defined by a lifetime plasma free homocystine median < 11 micromol/L. The newborn screened, good compliance group (n = 13) with a mean age of 14.4 years (range 4.4-24.9) had mean full-scale IQ (FIQ) of 105.8 (range 84-120), while the poorly compliant group (n = 6) with a mean age of 19.9 years (range 13.8-25.5) had a mean FIQ of 80.8 (range 40-103). The control group (n = 10) with mean age of 19.4 years (range 9.7-32.9) years had a mean FIQ of 102 (range 76-116). The two late-detected patients aged 18.9 and 18.8 years had FIQ of 80 and 102, while the two untreated patients aged 22.4 and 11.7 years had FIQ of 52 and 53, respectively. There was no statistical evidence of significant differences between the compliant, early-treated individuals and their unaffected siblings (controls) except for the FIQ, which was significantly higher than that of the unaffected siblings (p = 0.0397). These data, despite the relatively small numbers, suggest that early treatment with good biochemical control (lifetime plasma free homocystine median < 11 micromol/L) seems to prevent mental retardation.

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Year:  2001        PMID: 11596648     DOI: 10.1023/a:1010525528842

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


  7 in total

1.  Newborn screening for homocystinuria: Irish and world experience.

Authors:  E R Naughten; S Yap; P D Mayne
Journal:  Eur J Pediatr       Date:  1998-04       Impact factor: 3.183

2.  Strategies for the treatment of cystathionine beta-synthase deficiency: the experience of the Willink Biochemical Genetics Unit over the past 30 years.

Authors:  J H Walter; J E Wraith; F J White; C Bridge; J Till
Journal:  Eur J Pediatr       Date:  1998-04       Impact factor: 3.183

Review 3.  Psychological testing for child and adolescent psychiatrists: a review of the past 10 years.

Authors:  J M Halperin; K E McKay
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  1998-06       Impact factor: 8.829

4.  Homocystinuria (cystathionine synthase deficiency). Results of treatment in late-diagnosed patients.

Authors:  H Gröbe
Journal:  Eur J Pediatr       Date:  1980-12       Impact factor: 3.183

5.  Psychiatric manifestations of homocystinuria due to cystathionine beta-synthase deficiency: prevalence, natural history, and relationship to neurologic impairment and vitamin B6-responsiveness.

Authors:  M H Abbott; S E Folstein; H Abbey; R E Pyeritz
Journal:  Am J Med Genet       Date:  1987-04

6.  The natural history of homocystinuria due to cystathionine beta-synthase deficiency.

Authors:  S H Mudd; F Skovby; H L Levy; K D Pettigrew; B Wilcken; R E Pyeritz; G Andria; G H Boers; I L Bromberg; R Cerone
Journal:  Am J Hum Genet       Date:  1985-01       Impact factor: 11.025

7.  Homocystinuria due to cystathionine beta-synthase deficiency in Ireland: 25 years' experience of a newborn screened and treated population with reference to clinical outcome and biochemical control.

Authors:  S Yap; E Naughten
Journal:  J Inherit Metab Dis       Date:  1998-10       Impact factor: 4.982

  7 in total
  14 in total

Review 1.  The consequences of extended newborn screening programmes: do we know who needs treatment?

Authors:  B Wilcken
Journal:  J Inherit Metab Dis       Date:  2008-02-22       Impact factor: 4.982

Review 2.  Cystathionine β-synthase deficiency: Of mice and men.

Authors:  Warren D Kruger
Journal:  Mol Genet Metab       Date:  2017-05-19       Impact factor: 4.797

Review 3.  Oxidative Stress in Homocystinuria Due to Cystathionine ß-Synthase Deficiency: Findings in Patients and in Animal Models.

Authors:  Jéssica Lamberty Faverzani; Tatiane Grazieli Hammerschmidt; Angela Sitta; Marion Deon; Moacir Wajner; Carmen Regla Vargas
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4.  Neurodevelopmental and Cognitive Outcomes of Classical Homocystinuria: Experience from Qatar.

Authors:  Haitham El Bashir; Lubna Dekair; Yasmeen Mahmoud; Tawfeg Ben-Omran
Journal:  JIMD Rep       Date:  2015-02-25

5.  Cognitive functioning and psychiatric disorders in children with a metabolic disease.

Authors:  Annik Simons; François Eyskens; Ann De Groof; Ellen Van Diest; Dirk Deboutte; Robert Vermeiren
Journal:  Eur Child Adolesc Psychiatry       Date:  2006-03-10       Impact factor: 4.785

6.  Neonatal screening of inborn errors of metabolism using tandem mass spectrometry: an evidence-based analysis.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2003-05-01

7.  Changes in bone mineral density and body composition of children with well-controlled homocystinuria caused by CBS deficiency.

Authors:  J S Lim; D H Lee
Journal:  Osteoporos Int       Date:  2013-05-18       Impact factor: 4.507

8.  Social outcome in treated individuals with inherited metabolic disorders: UK study.

Authors:  M Bhat; C Haase; P J Lee
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.750

9.  Analysis of differential neonatal lethality in cystathionine β-synthase deficient mouse models using metabolic profiling.

Authors:  Sapna Gupta; Liqun Wang; Michael J Slifker; Kathy Q Cai; Kenneth N Maclean; Brandi Wasek; Teodoro Bottiglieri; Warren D Kruger
Journal:  FASEB J       Date:  2021-06       Impact factor: 5.834

Review 10.  Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes.

Authors:  Yin-Hsiu Chien; Jose E Abdenur; Federico Baronio; Allison Anne Bannick; Fernando Corrales; Maria Couce; Markus G Donner; Can Ficicioglu; Cynthia Freehauf; Deborah Frithiof; Garrett Gotway; Koichi Hirabayashi; Floris Hofstede; George Hoganson; Wuh-Liang Hwu; Philip James; Sook Kim; Stanley H Korman; Robin Lachmann; Harvey Levy; Martin Lindner; Lilia Lykopoulou; Ertan Mayatepek; Ania Muntau; Yoshiyuki Okano; Kimiyo Raymond; Estela Rubio-Gozalbo; Sabine Scholl-Bürgi; Andreas Schulze; Rani Singh; Sally Stabler; Mary Stuy; Janet Thomas; Conrad Wagner; William G Wilson; Saskia Wortmann; Shigenori Yamamoto; Maryland Pao; Henk J Blom
Journal:  Orphanet J Rare Dis       Date:  2015-08-20       Impact factor: 4.123

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