Literature DB >> 31745726

Novel NAXE variants as a cause for neurometabolic disorder: implications for treatment.

Joanne Trinh1, Sophie Imhoff1, Marija Dulovic-Mahlow1, Krishna Kumar Kandaswamy2, Vera Tadic1,3, Jochen Schäfer4, Valerija Dobricic1, Achim Nolte5, Martin Werber2, Arndt Rolfs2, Alexander Münchau1, Christine Klein6, Katja Lohmann1, Norbert Brüggemann1,3.   

Abstract

Neurometabolic disorders are often inherited and complex disorders that result from abnormalities of enzymes important for development and function of the nervous system. Recently, biallelic mutations in NAXE (APOA1BP) were found in patients with an infantile, lethal, neurometabolic disease. Here, exome sequencing was performed in two affected sisters and their healthy parents. The best candidate, NAXE, was tested for replication in exome sequencing data from 4351 patients with neurodevelopmental disorders. Quantitative RT-PCR, western blot and form factor analysis were performed to assess NAXE expression, protein levels and to analyze mitochondrial morphology in fibroblasts. Vitamin B3 was administered to one patient. Compound heterozygous missense (c.757G>A: p.Gly253Ser) and splicing (c.665-1G>A) variants in NAXE were identified in both affected sisters. In contrast to the previously reported patients with biallelic NAXE variants, our patients showed a milder phenotype with disease onset in early adulthood with psychosis, cognitive impairment, seizures, cerebellar ataxia and spasticity. The symptoms fluctuated. Additional screening of NAXE identified three novel homozygous missense variants (p.Lys245Gln, p.Asp218Asn, p.Ile214Val) in three patients with overlapping phenotype (fluctuating disease course, respiratory insufficiency, movement disorder). Lastly, patients with the c.665-1G>A splicing variant showed a significant reduction of NAXE expression compared to control fibroblasts and undetectable NAXE protein levels compared to control fibroblasts. Based on the metabolic pathway, vitamin B3 and coenzyme Q treatment was introduced in one patient in addition to antiepileptic treatment. This combination and avoidance of triggers was associated with continuous motor and cognitive improvement. The NAXE variants identified in this study suggest a loss-of-function mechanism leading to an insufficient NAD(P)HX repair system. Importantly, symptoms of patients with NAXE variants may improve with vitamin B3/coenzyme Q administration.

Entities:  

Keywords:  Apolipoprotein AI-binding protein; Energy metabolism; Metabolite repair; Mitochondria; NAD(P)H-hydrate epimerase

Mesh:

Substances:

Year:  2019        PMID: 31745726     DOI: 10.1007/s00415-019-09640-2

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  20 in total

1.  Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features.

Authors:  D N BARON; C E DENT; H HARRIS; E W HART; J B JEPSON
Journal:  Lancet       Date:  1956-09-01       Impact factor: 79.321

2.  NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses.

Authors:  Nicole J Van Bergen; Yiran Guo; Julia Rankin; Nicole Paczia; Julia Becker-Kettern; Laura S Kremer; Angela Pyle; Jean-François Conrotte; Carolyn Ellaway; Peter Procopis; Kristina Prelog; Tessa Homfray; Júlia Baptista; Emma Baple; Matthew Wakeling; Sean Massey; Daniel P Kay; Anju Shukla; Katta M Girisha; Leslie E S Lewis; Saikat Santra; Rachel Power; Piers Daubeney; Julio Montoya; Eduardo Ruiz-Pesini; Reka Kovacs-Nagy; Martin Pritsch; Uwe Ahting; David R Thorburn; Holger Prokisch; Robert W Taylor; John Christodoulou; Carole L Linster; Sian Ellard; Hakon Hakonarson
Journal:  Brain       Date:  2019-01-01       Impact factor: 13.501

3.  Lethal familial pellagra-like skin lesion associated with neurologic and developmental impairment and the development of cataracts.

Authors:  M A Salih; D A Bender; G M McCreanor
Journal:  Pediatrics       Date:  1985-11       Impact factor: 7.124

4.  Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation.

Authors:  Jennifer E Posey; Tamar Harel; Pengfei Liu; Jill A Rosenfeld; Regis A James; Zeynep H Coban Akdemir; Magdalena Walkiewicz; Weimin Bi; Rui Xiao; Yan Ding; Fan Xia; Arthur L Beaudet; Donna M Muzny; Richard A Gibbs; Eric Boerwinkle; Christine M Eng; V Reid Sutton; Chad A Shaw; Sharon E Plon; Yaping Yang; James R Lupski
Journal:  N Engl J Med       Date:  2016-12-07       Impact factor: 91.245

5.  Mutant Parkin impairs mitochondrial function and morphology in human fibroblasts.

Authors:  Anne Grünewald; Lisa Voges; Aleksandar Rakovic; Meike Kasten; Himesha Vandebona; Claudia Hemmelmann; Katja Lohmann; Slobodanka Orolicki; Alfredo Ramirez; Anthony H V Schapira; Peter P Pramstaller; Carolyn M Sue; Christine Klein
Journal:  PLoS One       Date:  2010-09-27       Impact factor: 3.240

Review 6.  The human NAD metabolome: Functions, metabolism and compartmentalization.

Authors:  Andrey Nikiforov; Veronika Kulikova; Mathias Ziegler
Journal:  Crit Rev Biochem Mol Biol       Date:  2015-04-02       Impact factor: 8.250

7.  Clinical exome sequencing: results from 2819 samples reflecting 1000 families.

Authors:  Daniel Trujillano; Aida M Bertoli-Avella; Krishna Kumar Kandaswamy; Maximilian Er Weiss; Julia Köster; Anett Marais; Omid Paknia; Rolf Schröder; Jose Maria Garcia-Aznar; Martin Werber; Oliver Brandau; Maria Calvo Del Castillo; Caterina Baldi; Karen Wessel; Shivendra Kishore; Nahid Nahavandi; Wafaa Eyaid; Muhammad Talal Al Rifai; Ahmed Al-Rumayyan; Waleed Al-Twaijri; Ali Alothaim; Amal Alhashem; Nouriya Al-Sannaa; Mohammed Al-Balwi; Majid Alfadhel; Arndt Rolfs; Rami Abou Jamra
Journal:  Eur J Hum Genet       Date:  2016-11-16       Impact factor: 4.246

8.  Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders.

Authors:  Joanne Trinh; Krishna Kumar Kandaswamy; Martin Werber; Maximilian E R Weiss; Gabriela Oprea; Shivendra Kishore; Katja Lohmann; Arndt Rolfs
Journal:  J Neurodev Disord       Date:  2019-06-25       Impact factor: 4.025

Review 9.  Mitochondrial disease: genetics and management.

Authors:  Yi Shiau Ng; Doug M Turnbull
Journal:  J Neurol       Date:  2015-08-28       Impact factor: 4.849

Review 10.  Targeting NAD+ in Metabolic Disease: New Insights Into an Old Molecule.

Authors:  Yasir S Elhassan; Andrew A Philp; Gareth G Lavery
Journal:  J Endocr Soc       Date:  2017-05-15
View more
  10 in total

Review 1.  Skin Conditions and Movement Disorders: Hiding in Plain Sight.

Authors:  Kristina Kulcsarova; Janette Baloghova; Jan Necpal; Matej Skorvanek
Journal:  Mov Disord Clin Pract       Date:  2022-03-24

2.  Identification of a novel homozygous mutation in NAXE gene associated with early-onset progressive encephalopathy by whole-exome sequencing: in silico protein structure characterization, molecular docking, and dynamic simulation.

Authors:  Marwa Maalej; Lamia Sfaihi; Marwa Ammar; Fakher Frikha; Marwa Kharrat; Olfa Alila-Fersi; Emna Mkaouar-Rebai; Abdelaziz Tlili; Thouraya Kammoun; Faiza Fakhfakh
Journal:  Neurogenetics       Date:  2022-07-11       Impact factor: 3.017

3.  Intracellular AIBP (Apolipoprotein A-I Binding Protein) Regulates Oxidized LDL (Low-Density Lipoprotein)-Induced Mitophagy in Macrophages.

Authors:  Soo-Ho Choi; Colin Agatisa-Boyle; Ayelet Gonen; Alisa Kim; Jungsu Kim; Elena Alekseeva; Sotirios Tsimikas; Yury I Miller
Journal:  Arterioscler Thromb Vasc Biol       Date:  2020-12-24       Impact factor: 8.311

4.  Current progress in the therapeutic options for mitochondrial disorders.

Authors:  E Koňaříková; A Marković; Z Korandová; J Houštěk; T Mráček
Journal:  Physiol Res       Date:  2020-11-02       Impact factor: 1.881

Review 5.  A Proposed Diagnostic Algorithm for Inborn Errors of Metabolism Presenting With Movements Disorders.

Authors:  Juan Darío Ortigoza-Escobar
Journal:  Front Neurol       Date:  2020-11-13       Impact factor: 4.003

Review 6.  Treatable inherited metabolic disorders causing intellectual disability: 2021 review and digital app.

Authors:  Eva M M Hoytema van Konijnenburg; Saskia B Wortmann; Marina J Koelewijn; Laura A Tseng; Roderick Houben; Sylvia Stöckler-Ipsiroglu; Carlos R Ferreira; Clara D M van Karnebeek
Journal:  Orphanet J Rare Dis       Date:  2021-04-12       Impact factor: 4.123

7.  NAXE gene mutation-related progressive encephalopathy: A case report and literature review.

Authors:  Li-Wei Chiu; Sheng-Shing Lin; Chieh-Ho Chen; Chien-Heng Lin; Ni-Chung Lee; Syuan-Yu Hong; I-Ching Chou; Chien-Lin Lin; Pei-Yu Yang
Journal:  Medicine (Baltimore)       Date:  2021-10-22       Impact factor: 1.817

8.  Progressive Myoclonus Epilepsies: Diagnostic Yield With Next-Generation Sequencing in Previously Unsolved Cases.

Authors:  Laura Canafoglia; Silvana Franceschetti; Antonio Gambardella; Pasquale Striano; Anna Teresa Giallonardo; Paolo Tinuper; Carlo Di Bonaventura; Roberto Michelucci; Edoardo Ferlazzo; Tiziana Granata; Adriana Magaudda; Laura Licchetta; Alessandro Filla; Angela La Neve; Patrizia Riguzzi; Teresa Anna Cantisani; Martina Fanella; Barbara Castellotti; Cinzia Gellera; Melanie Bahlo; Federico Zara; Carolina Courage; Anna-Elina Lehesjoki; Karen L Oliver; Samuel F Berkovic
Journal:  Neurol Genet       Date:  2021-11-12

9.  NAD(P)HX epimerase downregulation promotes tumor progression through ROS/HIF-1α signaling in hepatocellular carcinoma.

Authors:  Bo Sun; Lei Yu; Cong Xu; Yi-Ming Li; Yan-Rong Zhao; Mo-Mo Cao; Lian-Yue Yang
Journal:  Cancer Sci       Date:  2021-05-04       Impact factor: 6.716

10.  Systemic metabolite profiling reveals sexual dimorphism of AIBP control of metabolism in mice.

Authors:  Jun-Dae Kim; Lingping Zhu; Quan Sun; Longhou Fang
Journal:  PLoS One       Date:  2021-04-01       Impact factor: 3.240

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.