Cerebrospinal fluid biogenic amines depletion and brain atrophy in adult patients with phenylketonuria. Issue 3 (1st February 2019)
- Record Type:
- Journal Article
- Title:
- Cerebrospinal fluid biogenic amines depletion and brain atrophy in adult patients with phenylketonuria. Issue 3 (1st February 2019)
- Main Title:
- Cerebrospinal fluid biogenic amines depletion and brain atrophy in adult patients with phenylketonuria
- Authors:
- Pilotto, Andrea
Blau, Nenad
Leks, Edytha
Schulte, Claudia
Deuschl, Christian
Zipser, Carl
Piel, David
Freisinger, Peter
Gramer, Gwendolyn
Kölker, Stefan
Haas, Dorothea
Burgard, Peter
Nawroth, Peter
Georg, Hoffmann
Scheffler, Klaus
Berg, Daniela
Trefz, Friedrich - Abstract:
- Abstract: Biogenic amines synthesis in phenylketonuria (PKU) patients with high phenylalanine (Phe) concentration is thought to be impaired due to inhibition of tyrosine and tryptophan hydroxylases and competition with amino acids at the blood‐brain barrier. Dopamine and serotonin deficits might explain brain damage and progressive neuropsychiatric impairment in adult PKU patients. Ten early treated adult PKU patients (mean age 38.2 years) and 15 age‐matched controls entered the study. Plasma and cerebrospinal fluid (CSF) Phe, 5‐hydroxyindoleacetic acid (5‐HIAA), 5‐hydroxytryptophan (5‐HTP), 3, 4‐dihydroxy‐l ‐phenylalanine (l ‐DOPA) and homovanillic acid (HVA) were analyzed. Voxel‐based morphometry statistical nonparametric mapping was used to test the age‐corrected correlation between gray matter atrophy and CSF biogenic amines levels. 5‐HIAA and 5‐HTP were significantly reduced in PKU patients compared to controls. Significant negative correlations were found between CSF 5‐HIAA, HVA, and 5‐HTP and Phe levels. A decrease in 5‐HIAA and 5‐HTP concentrations correlated with precuneus and frontal atrophy, respectively. Lower HVA levels correlated with occipital atrophy. Biogenic amines deficits correlate with specific brain atrophy patterns in adult PKU patients, in line with serotonin and dopamine projections. These findings may support a more rigorous Phe control in adult PKU to prevent neurotransmitter depletion and accelerated brain damage due to aging.
- Is Part Of:
- Journal of inherited metabolic disease. Volume 42:Issue 3(2019)
- Journal:
- Journal of inherited metabolic disease
- Issue:
- Volume 42:Issue 3(2019)
- Issue Display:
- Volume 42, Issue 3 (2019)
- Year:
- 2019
- Volume:
- 42
- Issue:
- 3
- Issue Sort Value:
- 2019-0042-0003-0000
- Page Start:
- 398
- Page End:
- 406
- Publication Date:
- 2019-02-01
- Subjects:
- adult -- cerebrospinal fluid -- dopamine -- phenylketonuria -- serotonin
Metabolism, Inborn errors of -- Periodicals
Metabolism -- Disorders -- Periodicals
616.39042 - Journal URLs:
- http://www.springer.com/gb/ ↗
- DOI:
- 10.1002/jimd.12049 ↗
- Languages:
- English
- ISSNs:
- 0141-8955
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5006.950000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 10086.xml