Literature DB >> 26915364

A New Approach for Fast Metabolic Diagnostics in CMAMMA.

Monique G M de Sain-van der Velden1, Maria van der Ham2, Judith J Jans2, Gepke Visser3, Hubertus C M T Prinsen2, Nanda M Verhoeven-Duif2, Koen L I van Gassen2, Peter M van Hasselt3.   

Abstract

BACKGROUND: The presence of increased urinary concentrations of both methylmalonic acid (MMA) and malonic acid (MA) is assumed to differentiate combined malonic and methylmalonic aciduria (CMAMMA), due to mutations in the ACSF3 gene, from other causes of methylmalonic aciduria (classic MMAemia). Detection of MA in urine, however, is challenging since excretion of MA can be easily missed. The objective of the study was to develop a method for quantification of MA in plasma to allow differentiation between CMAMMA and classic MMAemia.
METHODS: Compound heterozygosity for mutations in the ACSF3 gene was detected in two female siblings using diagnostic exome sequencing. Urine (MMA and MA) was analyzed with GC/MS, while plasma was analyzed with UPLC-MS/MS. MA/MMA ratios were calculated.
RESULTS: Both patients had a severe psychiatric presentation (at the age of 6 years and 5.5 years, respectively) after a viral infection. MA excretion in the patients was only just above the highest control value in several samples. MA concentrations in plasma from the two patients were clearly above the highest value observed in control subjects. However, MA concentrations in plasma from patients with classic MMAemia were also elevated. Additional, calculation of MA/MMA ratio in plasma allowed to fully differentiate between CMAMMA and classic MMAemia.
CONCLUSIONS: Calculating the MA/MMA ratio in plasma allows differentiation between CMAMMA and classic MMAemia. The full clinical spectrum of CMAMMA remains to be delineated.

Entities:  

Year:  2016        PMID: 26915364      PMCID: PMC5110436          DOI: 10.1007/8904_2016_531

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  8 in total

Review 1.  Development and validation of a quantitative assay based on tandem mass spectrometry.

Authors:  John W Honour
Journal:  Ann Clin Biochem       Date:  2011-02-08       Impact factor: 2.057

2.  Brain abnormalities in a case of malonyl-CoA decarboxylase deficiency.

Authors:  M C Y de Wit; I F M de Coo; E Verbeek; R Schot; G C Schoonderwoerd; M Duran; J B C de Klerk; J G M Huijmans; M H Lequin; F W Verheijen; G M S Mancini
Journal:  Mol Genet Metab       Date:  2005-11-04       Impact factor: 4.797

3.  Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype.

Authors:  Ahmed Alfares; Laura Dempsey Nunez; Khalid Al-Thihli; John Mitchell; Serge Melançon; Natascia Anastasio; Kevin C H Ha; Jacek Majewski; David S Rosenblatt; Nancy Braverman
Journal:  J Med Genet       Date:  2011-07-23       Impact factor: 6.318

4.  Suitability of methylmalonic acid and total homocysteine analysis in dried bloodspots.

Authors:  Monique G M de Sain-van der Velden; Maria van der Ham; Judith J Jans; Gepke Visser; Peter M van Hasselt; Hubertus C M T Prinsen; Nanda M Verhoeven-Duif
Journal:  Anal Chim Acta       Date:  2014-10-31       Impact factor: 6.558

5.  The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level.

Authors:  Christina B Pedersen; Steen Kølvraa; Agnete Kølvraa; Vibeke Stenbroen; Margrethe Kjeldsen; Regina Ensenauer; Ingrid Tein; Dietrich Matern; Piero Rinaldo; Christine Vianey-Saban; Antonia Ribes; Willy Lehnert; Ernst Christensen; Thomas J Corydon; Brage S Andresen; Søren Vang; Lars Bolund; Jerry Vockley; Peter Bross; Niels Gregersen
Journal:  Hum Genet       Date:  2008-06-04       Impact factor: 4.132

6.  Analysis of cases of 3-methylcrotonyl CoA carboxylase deficiency (3-MCCD) in the California newborn screening program reported in the state database.

Authors:  Christina Lam; Jennifer M Carter; Stephen D Cederbaum; Julie Neidich; Natalie M Gallant; Fred Lorey; Lisa Feuchtbaum; Derek A Wong
Journal:  Mol Genet Metab       Date:  2013-09-17       Impact factor: 4.797

7.  Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: a worldwide collaborative project.

Authors:  David M S McHugh; Cynthia A Cameron; Jose E Abdenur; Mahera Abdulrahman; Ona Adair; Shahira Ahmed Al Nuaimi; Henrik Åhlman; Jennifer J Allen; Italo Antonozzi; Shaina Archer; Sylvia Au; Christiane Auray-Blais; Mei Baker; Fiona Bamforth; Kinga Beckmann; Gessi Bentz Pino; Stanton L Berberich; Robert Binard; François Boemer; Jim Bonham; Nancy N Breen; Sandra C Bryant; Michele Caggana; S Graham Caldwell; Marta Camilot; Carlene Campbell; Claudia Carducci; Sandra C Bryant; Michele Caggana; S Graham Caldwell; Marta Camilot; Carlene Campbell; Claudia Carducci; Rohit Cariappa; Clover Carlisle; Ubaldo Caruso; Michela Cassanello; Ane Miren Castilla; Daisy E Castiñeiras Ramos; Pranesh Chakraborty; Ram Chandrasekar; Alfredo Chardon Ramos; David Cheillan; Yin-Hsiu Chien; Thomas A Childs; Petr Chrastina; Yuri Cleverthon Sica; Jose Angel Cocho de Juan; Maria Elena Colandre; Veronica Cornejo Espinoza; Gaetano Corso; Robert Currier; Denis Cyr; Noemi Czuczy; Oceania D'Apolito; Tim Davis; Monique G de Sain-Van der Velden; Carmen Delgado Pecellin; Iole Maria Di Gangi; Cristina Maria Di Stefano; Yannis Dotsikas; Melanie Downing; Stephen M Downs; Bonifacio Dy; Mark Dymerski; Inmaculada Rueda; Bert Elvers; Roger Eaton; Barbara M Eckerd; Fatma El Mougy; Sarah Eroh; Mercedes Espada; Catherine Evans; Sandy Fawbush; Kristel F Fijolek; Lawrence Fisher; Leifur Franzson; Dianne M Frazier; Luciana R C Garcia; Maria Sierra García-Valdecasas Bermejo; Dimitar Gavrilov; Rosemarie Gerace; Giuseppe Giordano; Yolanda González Irazabal; Lawrence C Greed; Robert Grier; Elyse Grycki; Xuefan Gu; Fizza Gulamali-Majid; Arthur F Hagar; Lianshu Han; W Harry Hannon; Christa Haslip; Fayza Abdelhamid Hassan; Miao He; Amy Hietala; Leslie Himstedt; Gary L Hoffman; William Hoffman; Philis Hoggatt; Patrick V Hopkins; David M Hougaard; Kerie Hughes; Patricia R Hunt; Wuh-Liang Hwu; June Hynes; Isabel Ibarra-González; Cindy A Ingham; Maria Ivanova; Ward B Jacox; Catharine John; John P Johnson; Jón J Jónsson; Eszter Karg; David Kasper; Brenda Klopper; Dimitris Katakouzinos; Issam Khneisser; Detlef Knoll; Hirinori Kobayashi; Ronald Koneski; Viktor Kozich; Rasoul Kouapei; Dirk Kohlmueller; Ivo Kremensky; Giancarlo la Marca; Marcia Lavochkin; Soo-Youn Lee; Denis C Lehotay; Aida Lemes; Joyce Lepage; Barbara Lesko; Barry Lewis; Carol Lim; Sharon Linard; Martin Lindner; Michele A Lloyd-Puryear; Fred Lorey; Yannis L Loukas; Julie Luedtke; Neil Maffitt; J Fergall Magee; Adrienne Manning; Shawn Manos; Sandrine Marie; Sônia Marchezi Hadachi; Gregg Marquardt; Stephen J Martin; Dietrich Matern; Stephanie K Mayfield Gibson; Philip Mayne; Tonya D McCallister; Mark McCann; Julie McClure; James J McGill; Christine D McKeever; Barbara McNeilly; Mark A Morrissey; Paraskevi Moutsatsou; Eleanor A Mulcahy; Dimitris Nikoloudis; Bent Norgaard-Pedersen; Devin Oglesbee; Mariusz Oltarzewski; Daniela Ombrone; Jelili Ojodu; Vagelis Papakonstantinou; Sherly Pardo Reoyo; Hyung-Doo Park; Marzia Pasquali; Elisabetta Pasquini; Pallavi Patel; Kenneth A Pass; Colleen Peterson; Rolf D Pettersen; James J Pitt; Sherry Poh; Arnold Pollak; Cory Porter; Philip A Poston; Ricky W Price; Cecilia Queijo; Jonessy Quesada; Edward Randell; Enzo Ranieri; Kimiyo Raymond; John E Reddic; Alejandra Reuben; Charla Ricciardi; Piero Rinaldo; Jeff D Rivera; Alicia Roberts; Hugo Rocha; Geraldine Roche; Cheryl Rochman Greenberg; José María Egea Mellado; María Jesús Juan-Fita; Consuelo Ruiz; Margherita Ruoppolo; S Lane Rutledge; Euijung Ryu; Christine Saban; Inderneel Sahai; Maria Isabel Salazar García-Blanco; Pedro Santiago-Borrero; Andrea Schenone; Roland Schoos; Barb Schweitzer; Patricia Scott; Margretta R Seashore; Mary A Seeterlin; David E Sesser; Darrin W Sevier; Scott M Shone; Graham Sinclair; Victor A Skrinska; Eleanor L Stanley; Erin T Strovel; April L Studinski Jones; Sherlykutty Sunny; Zoltan Takats; Tijen Tanyalcin; Francesca Teofoli; J Robert Thompson; Kathy Tomashitis; Mouseline Torquado Domingos; Jasmin Torres; Rosario Torres; Silvia Tortorelli; Sandor Turi; Kimberley Turner; Nick Tzanakos; Alf G Valiente; Hillary Vallance; Marcela Vela-Amieva; Laura Vilarinho; Ulrika von Döbeln; Marie-Francoise Vincent; B Chris Vorster; Michael S Watson; Dianne Webster; Sheila Weiss; Bridget Wilcken; Veronica Wiley; Sharon K Williams; Sharon A Willis; Michael Woontner; Katherine Wright; Raquel Yahyaoui; Seiji Yamaguchi; Melissa Yssel; Wendy M Zakowicz
Journal:  Genet Med       Date:  2011-03       Impact factor: 8.822

8.  Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria.

Authors:  Jennifer L Sloan; Jennifer J Johnston; Irini Manoli; Randy J Chandler; Caitlin Krause; Nuria Carrillo-Carrasco; Suma D Chandrasekaran; Justin R Sysol; Kevin O'Brien; Natalie S Hauser; Julie C Sapp; Heidi M Dorward; Marjan Huizing; Bruce A Barshop; Susan A Berry; Philip M James; Neena L Champaigne; Pascale de Lonlay; Vassilli Valayannopoulos; Michael D Geschwind; Dimitar K Gavrilov; William L Nyhan; Leslie G Biesecker; Charles P Venditti
Journal:  Nat Genet       Date:  2011-08-14       Impact factor: 38.330

  8 in total
  3 in total

1.  Combined Malonic and Methylmalonic Aciduria Due to ACSF3 Variants Results in Benign Clinical Course in Three Chinese Patients.

Authors:  Ping Wang; Jianbo Shu; Chunyu Gu; Xiaoli Yu; Jie Zheng; Chunhua Zhang; Chunquan Cai
Journal:  Front Pediatr       Date:  2021-11-25       Impact factor: 3.418

2.  Improving the diagnosis of cobalamin and related defects by genomic analysis, plus functional and structural assessment of novel variants.

Authors:  Sandra Brasil; Fátima Leal; Ana Vega; Rosa Navarrete; María Jesús Ecay; Lourdes R Desviat; Casandra Riera; Natàlia Padilla; Xavier de la Cruz; Mari Luz Couce; Elena Martin-Hernández; Ana Morais; Consuelo Pedrón; Luis Peña-Quintana; Miriam Rigoldi; Norma Specola; Isabel Tavares de Almeida; Inmaculada Vives; Raquel Yahyaoui; Pilar Rodríguez-Pombo; Magdalena Ugarte; Celia Pérez-Cerda; Begoña Merinero; Belén Pérez
Journal:  Orphanet J Rare Dis       Date:  2018-07-24       Impact factor: 4.123

3.  Brain metabolism and neurological symptoms in combined malonic and methylmalonic aciduria.

Authors:  Sara Tucci
Journal:  Orphanet J Rare Dis       Date:  2020-01-22       Impact factor: 4.123

  3 in total

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