TY - JOUR
T1 - Assessment of intellectual impairment, health-related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders
T2 - Data from the iNTD registry
AU - International Working Group on Neurotransmitter related Disorders (iNTD)
AU - Keller, Mareike
AU - Brennenstuhl, Heiko
AU - Kuseyri Hübschmann, Oya
AU - Manti, Filippo
AU - Julia Palacios, Natalia Alexandra
AU - Friedman, Jennifer
AU - Yıldız, Yılmaz
AU - Koht, Jeanette Aimee
AU - Wong, Suet Na
AU - Zafeiriou, Dimitrios I.
AU - López-Laso, Eduardo
AU - Pons, Roser
AU - Kulhánek, Jan
AU - Jeltsch, Kathrin
AU - Serrano-Lomelin, Jesus
AU - Garbade, Sven F.
AU - Opladen, Thomas
AU - Goez, Helly
AU - Burlina, Alberto
AU - Cortès-Saladelafont, Elisenda
AU - Fernández Ramos, Joaquín Alejandro
AU - García-Cazorla, Angeles
AU - Hoffmann, Georg F.
AU - Kiat Hong, Stacey Tay
AU - Honzík, Tomáš
AU - Kavecan, Ivana
AU - Kurian, Manju A.
AU - Leuzzi, Vincenzo
AU - Lücke, Thomas
AU - Manzoni, Francesca
AU - Mastrangelo, Mario
AU - Mercimek-Andrews, Saadet
AU - Mir, Pablo
AU - Oppebøen, Mari
AU - Pearson, Toni S.
AU - Sivri, H. Serap
AU - Steel, Dora
AU - Stevanović, Galina
AU - Fung, Cheuk Wing
N1 - Funding Information:
We thank the patients and their parents for participation in the iNTD patient registry. We also thank the Women and Children's Health Research Institute (Canada) to facilitate statistical services. Heiko Brennenstuhl received financial support from the physician scientist program of the Medical Faculty of the University of Heidelberg. This study was in parts funded by the Dietmar Hopp Foundation, St. Leon-Rot, Germany.
Funding Information:
We thank the patients and their parents for participation in the iNTD patient registry. We also thank the Women and Children's Health Research Institute (Canada) to facilitate statistical services. Heiko Brennenstuhl received financial support from the physician scientist program of the Medical Faculty of the University of Heidelberg. This study was in parts funded by the Dietmar Hopp Foundation, St. Leon‐Rot, Germany.
Publisher Copyright:
© 2021 The Authors. Journal of Inherited Metabolic Disease published by John Wiley & Sons Ltd on behalf of SSIEM.
PY - 2021/11
Y1 - 2021/11
N2 - 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.
AB - 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.
KW - behavioral phenotype
KW - cognitive impairment
KW - iNTD
KW - intelligence
KW - neurotransmitter deficiencies
KW - quality of life
UR - http://www.scopus.com/inward/record.url?scp=85111968071&partnerID=8YFLogxK
U2 - 10.1002/jimd.12416
DO - 10.1002/jimd.12416
M3 - Article
C2 - 34245036
AN - SCOPUS:85111968071
SN - 0141-8955
VL - 44
SP - 1489
EP - 1502
JO - Journal of Inherited Metabolic Disease
JF - Journal of Inherited Metabolic Disease
IS - 6
ER -