Assessment of intellectual impairment, health‐related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: Data from the iNTD registry. Issue 6 (2nd August 2021)
- Record Type:
- Journal Article
- Title:
- Assessment of intellectual impairment, health‐related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: Data from the iNTD registry. Issue 6 (2nd August 2021)
- Main Title:
- Assessment of intellectual impairment, health‐related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: Data from the iNTD registry
- Authors:
- Keller, Mareike
Brennenstuhl, Heiko
Kuseyri Hübschmann, Oya
Manti, Filippo
Julia Palacios, Natalia Alexandra
Friedman, Jennifer
Yıldız, Yılmaz
Koht, Jeanette Aimee
Wong, Suet‐Na
Zafeiriou, Dimitrios I.
López‐Laso, Eduardo
Pons, Roser
Kulhánek, Jan
Jeltsch, Kathrin
Serrano‐Lomelin, Jesus
Garbade, Sven F.
Opladen, Thomas
Goez, Helly
Burlina, Alberto
Cortès‐Saladelafont, Elisenda
Fernández Ramos, Joaquín Alejandro
García‐Cazorla, Angeles
Hoffmann, Georg F.
Kiat Hong, Stacey Tay
Honzík, Tomáš
Kavecan, Ivana
Kurian, Manju A.
Leuzzi, Vincenzo
Lücke, Thomas
Manzoni, Francesca
Mastrangelo, Mario
Mercimek‐Andrews, Saadet
Mir, Pablo
Oppebøen, Mari
Pearson, Toni S.
Sivri, H. Serap
Steel, Dora
Stevanović, Galina
Fung, Cheuk‐Wing
… (more) - Abstract:
- Abstract: Inherited disorders of neurotransmitter metabolism are a group of rare diseases, which are caused by impaired synthesis, transport, or degradation of neurotransmitters or cofactors and result in various degrees of delayed or impaired psychomotor development. To assess the effect of neurotransmitter deficiencies on intelligence, quality of life, and behavior, the data of 148 patients in the registry of the International Working Group on Neurotransmitter Related Disorders (iNTD) was evaluated using results from standardized age‐adjusted tests and questionnaires. Patients with a primary disorder of monoamine metabolism had lower IQ scores (mean IQ 58, range 40‐100) within the range of cognitive impairment (<70) compared to patients with a BH4 deficiency (mean IQ 84, range 40‐129). Short attention span and distractibility were most frequently mentioned by parents, while patients reported most frequently anxiety and distractibility when asked for behavioral traits. In individuals with succinic semialdehyde dehydrogenase deficiency, self‐stimulatory behaviors were commonly reported by parents, whereas in patients with dopamine transporter deficiency, DNAJC12 deficiency, and monoamine oxidase A deficiency, self‐injurious or mutilating behaviors have commonly been observed. Phobic fears were increased in patients with 6‐pyruvoyltetrahydropterin synthase deficiency, while individuals with sepiapterin reductase deficiency frequently experienced communication and sleepAbstract: Inherited disorders of neurotransmitter metabolism are a group of rare diseases, which are caused by impaired synthesis, transport, or degradation of neurotransmitters or cofactors and result in various degrees of delayed or impaired psychomotor development. To assess the effect of neurotransmitter deficiencies on intelligence, quality of life, and behavior, the data of 148 patients in the registry of the International Working Group on Neurotransmitter Related Disorders (iNTD) was evaluated using results from standardized age‐adjusted tests and questionnaires. Patients with a primary disorder of monoamine metabolism had lower IQ scores (mean IQ 58, range 40‐100) within the range of cognitive impairment (<70) compared to patients with a BH4 deficiency (mean IQ 84, range 40‐129). Short attention span and distractibility were most frequently mentioned by parents, while patients reported most frequently anxiety and distractibility when asked for behavioral traits. In individuals with succinic semialdehyde dehydrogenase deficiency, self‐stimulatory behaviors were commonly reported by parents, whereas in patients with dopamine transporter deficiency, DNAJC12 deficiency, and monoamine oxidase A deficiency, self‐injurious or mutilating behaviors have commonly been observed. Phobic fears were increased in patients with 6‐pyruvoyltetrahydropterin synthase deficiency, while individuals with sepiapterin reductase deficiency frequently experienced communication and sleep difficulties. Patients with BH4 deficiencies achieved significantly higher quality of life as compared to other groups. This analysis of the iNTD registry data highlights: (a) difference in IQ and subdomains of quality of life between BH4 deficiencies and primary neurotransmitter‐related disorders and (b) previously underreported behavioral traits. … (more)
- Is Part Of:
- Journal of inherited metabolic disease. Volume 44:Issue 6(2021)
- Journal:
- Journal of inherited metabolic disease
- Issue:
- Volume 44:Issue 6(2021)
- Issue Display:
- Volume 44, Issue 6 (2021)
- Year:
- 2021
- Volume:
- 44
- Issue:
- 6
- Issue Sort Value:
- 2021-0044-0006-0000
- Page Start:
- 1489
- Page End:
- 1502
- Publication Date:
- 2021-08-02
- Subjects:
- behavioral phenotype -- cognitive impairment -- iNTD -- intelligence -- neurotransmitter deficiencies -- quality of life
Metabolism, Inborn errors of -- Periodicals
Metabolism -- Disorders -- Periodicals
616.39042 - Journal URLs:
- http://www.springer.com/gb/ ↗
- DOI:
- 10.1002/jimd.12416 ↗
- 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:
- 26254.xml