Literature DB >> 12063241

Cranial MR spectroscopy of tetrahydrobiopterin deficiency.

Yin-Hsiu Chien1, Shiin-Feng Peng, Tso-Ren Wang, Wuh-Liang Hwu.   

Abstract

BACKGROUND AND
PURPOSE: Severe and progressive neurologic disease remains a problem for patients with hyperphenylalaninemia due to a deficiency of tetrahydrobiopterin (BH4), even with early diagnosis and despite treatment with BH4 and neurotransmitter precursors. Few reports have included the associated imaging characteristics. Our purpose was to describe the imaging features of BH4-deficient patients identified by neonatal screening in a Taiwanese population and to correlate the imaging features with the treatment.
METHODS: This study analyzed the cases of eight BH4-deficient patients who were examined by MR imaging and MR spectroscopy. Analysis of the findings was correlated with the clinical findings.
RESULTS: One patient whose intelligence quotient score was lower than those of the other seven patients experienced seizures in conjunction with central white matter signal changes on MR images and a lactate peak on MR spectroscopy. Lactate peak was revealed in another patient who had marked elevations of N-acetylaspartate:creatine and N-acetylaspartate:choline ratios. Although most patients had a higher than average N-acetylaspartate:creatine or N-acetylaspartate:choline ratio, the patient who had decreases of both ratios possessed the highest intelligence quotient scores among the eight patients. In addition, the myoinositol:choline ratio correlated positively with the average BH4 dosage (P =.027, r = 0.027) and the choline:creatine ratio correlated negatively with the average 5-hydroxytryptophan dosage (P =.035, r = -0.742).
CONCLUSION: Compared with classical phenylketonuria, patients with BH4 deficiency have fewer white matter changes revealed by MR imaging but more changes revealed by MR spectroscopy. MR spectroscopy is a potential method with which to monitor the dosages of supplements used to treat this disorder. In addition, MR spectroscopy may be helpful in gaining understanding of the neurophysiological changes that occur in association with this disease.

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Year:  2002        PMID: 12063241      PMCID: PMC7976926     

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  16 in total

1.  Brain CT and MR findings in hyperphenylalaninemia due to dihydropteridine reductase deficiency (variant of phenylketonuria).

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2.  Phenylketonuria: findings at MR imaging and localized in vivo H-1 MR spectroscopy of the brain in patients with early treatment.

Authors:  J Pietz; R Kreis; H Schmidt; U K Meyding-Lamadé; A Rupp; C Boesch
Journal:  Radiology       Date:  1996-11       Impact factor: 11.105

3.  Neuropathology of phenylketonuria.

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Journal:  J Neuropathol Exp Neurol       Date:  1966-04       Impact factor: 3.685

4.  Diagnosis and treatment of 6-pyruvoyl-tetrahydropterin synthase deficiency.

Authors:  H Shintaku; M Asada; Y Sawada
Journal:  Brain Dev       Date:  2000-09       Impact factor: 1.961

Review 5.  Proton MRS in neurological disorders.

Authors:  S Bonavita; F Di Salle; G Tedeschi
Journal:  Eur J Radiol       Date:  1999-05       Impact factor: 3.528

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Journal:  J Pediatr       Date:  1984-04       Impact factor: 4.406

7.  Localized brain proton NMR spectroscopy in young adult phenylketonuria patients.

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Journal:  Magn Reson Med       Date:  1994-01       Impact factor: 4.668

8.  Basal ganglion calcification in hyperphenylalaninemia due to deficiency of dihydropteridine reductase.

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Journal:  Pediatr Radiol       Date:  1988

9.  Cranial CT and MRI in malignant phenylketonuria.

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Journal:  Pediatr Radiol       Date:  1992

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Authors:  M A Cleary; J H Walter; J E Wraith; F White; K Tyler; J P Jenkins
Journal:  J Pediatr       Date:  1995-08       Impact factor: 4.406

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  5 in total

1.  Central tegmental tract involvement in an infant with 6-pyruvoyltetrahydropterin synthetase deficiency.

Authors:  J Takanashi; M Kanazawa; Y Kohno
Journal:  AJNR Am J Neuroradiol       Date:  2006-03       Impact factor: 3.825

2.  Diffusion tensor images in children with early-treated, chronic, malignant phenylketonuric: correlation with intelligence assessment.

Authors:  Steven Shinn-Forng Peng; Wen-Yih Isaac Tseng; Yin-Hsiu Chien; Wuh-Liang Hwu; Hon-Man Liu
Journal:  AJNR Am J Neuroradiol       Date:  2004-10       Impact factor: 3.825

3.  Long-term outcome and neuroradiological findings of 31 patients with 6-pyruvoyltetrahydropterin synthase deficiency.

Authors:  L Wang; W-M Yu; C He; M Chang; M Shen; Z Zhou; Z Zhang; S Shen; T-T Liu; K-J Hsiao
Journal:  J Inherit Metab Dis       Date:  2006-02       Impact factor: 4.982

4.  Tetrahydrobiopterin deficiencies: Lesson from clinical experience.

Authors:  Ayse Ergul Bozaci; Esra Er; Havva Yazici; Ebru Canda; Sema Kalkan Uçar; Merve Güvenc Saka; Cenk Eraslan; Hüseyin Onay; Sara Habif; Beat Thöny; Mahmut Coker
Journal:  JIMD Rep       Date:  2021-02-01

5.  GTP-Cyclohydrolase I deficiency presenting as malignant hyperphenylalaninemia, recurrent hyperthermia and progressive neurological dysfunction in a South Asian child - a case report.

Authors:  Kavinda Chandimal Dayasiri; Nayani Suraweera; Deepal Nawarathne; U E Senanayake; B K T P Dayanath; Eresha Jasinge; Kumudu Weerasekara
Journal:  BMC Pediatr       Date:  2019-06-15       Impact factor: 2.125

  5 in total

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