Should metabolic diseases be systematically screened in nonsyndromic autism spectrum disorders?

<h4>Background</h4>In the investigation of autism spectrum disorders (ASD), a genetic cause is found in approximately 10-20%. Among these cases, the prevalence of the rare inherited metabolic disorders (IMD) is unknown and poorly evaluated. An IMD responsible for ASD is usually identifie...

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Main Authors: Manuel Schiff, Jean-François Benoist, Sofiane Aïssaoui, Odile Boespflug-Tanguy, Marie-Christine Mouren, Hélène Ogier de Baulny, Richard Delorme
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21760924/pdf/?tool=EBI
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spelling doaj-1611c12f2bfa4000b6c5823b18e6e0552021-03-04T01:46:32ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0167e2193210.1371/journal.pone.0021932Should metabolic diseases be systematically screened in nonsyndromic autism spectrum disorders?Manuel SchiffJean-François BenoistSofiane AïssaouiOdile Boespflug-TanguyMarie-Christine MourenHélène Ogier de BaulnyRichard Delorme<h4>Background</h4>In the investigation of autism spectrum disorders (ASD), a genetic cause is found in approximately 10-20%. Among these cases, the prevalence of the rare inherited metabolic disorders (IMD) is unknown and poorly evaluated. An IMD responsible for ASD is usually identified by the associated clinical phenotype such as dysmorphic features, ataxia, microcephaly, epilepsy, and severe intellectual disability (ID). In rare cases, however, ASD may be considered as nonsyndromic at the onset of a related IMD.<h4>Objectives</h4>To evaluate the utility of routine metabolic investigations in nonsyndromic ASD.<h4>Patients and methods</h4>We retrospectively analyzed the results of a metabolic workup (urinary mucopolysaccharides, urinary purines and pyrimidines, urinary creatine and guanidinoacetate, urinary organic acids, plasma and urinary amino acids) routinely performed in 274 nonsyndromic ASD children.<h4>Results</h4>The metabolic parameters were in the normal range for all but 2 patients: one with unspecific creatine urinary excretion and the other with persistent 3-methylglutaconic aciduria.<h4>Conclusions</h4>These data provide the largest ever reported cohort of ASD patients for whom a systematic metabolic workup has been performed; they suggest that such a routine metabolic screening does not contribute to the causative diagnosis of nonsyndromic ASD. They also emphasize that the prevalence of screened IMD in nonsyndromic ASD is probably not higher than in the general population (<0.5%). A careful clinical evaluation is probably more reasonable and of better medical practice than a costly systematic workup.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21760924/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Manuel Schiff
Jean-François Benoist
Sofiane Aïssaoui
Odile Boespflug-Tanguy
Marie-Christine Mouren
Hélène Ogier de Baulny
Richard Delorme
spellingShingle Manuel Schiff
Jean-François Benoist
Sofiane Aïssaoui
Odile Boespflug-Tanguy
Marie-Christine Mouren
Hélène Ogier de Baulny
Richard Delorme
Should metabolic diseases be systematically screened in nonsyndromic autism spectrum disorders?
PLoS ONE
author_facet Manuel Schiff
Jean-François Benoist
Sofiane Aïssaoui
Odile Boespflug-Tanguy
Marie-Christine Mouren
Hélène Ogier de Baulny
Richard Delorme
author_sort Manuel Schiff
title Should metabolic diseases be systematically screened in nonsyndromic autism spectrum disorders?
title_short Should metabolic diseases be systematically screened in nonsyndromic autism spectrum disorders?
title_full Should metabolic diseases be systematically screened in nonsyndromic autism spectrum disorders?
title_fullStr Should metabolic diseases be systematically screened in nonsyndromic autism spectrum disorders?
title_full_unstemmed Should metabolic diseases be systematically screened in nonsyndromic autism spectrum disorders?
title_sort should metabolic diseases be systematically screened in nonsyndromic autism spectrum disorders?
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description <h4>Background</h4>In the investigation of autism spectrum disorders (ASD), a genetic cause is found in approximately 10-20%. Among these cases, the prevalence of the rare inherited metabolic disorders (IMD) is unknown and poorly evaluated. An IMD responsible for ASD is usually identified by the associated clinical phenotype such as dysmorphic features, ataxia, microcephaly, epilepsy, and severe intellectual disability (ID). In rare cases, however, ASD may be considered as nonsyndromic at the onset of a related IMD.<h4>Objectives</h4>To evaluate the utility of routine metabolic investigations in nonsyndromic ASD.<h4>Patients and methods</h4>We retrospectively analyzed the results of a metabolic workup (urinary mucopolysaccharides, urinary purines and pyrimidines, urinary creatine and guanidinoacetate, urinary organic acids, plasma and urinary amino acids) routinely performed in 274 nonsyndromic ASD children.<h4>Results</h4>The metabolic parameters were in the normal range for all but 2 patients: one with unspecific creatine urinary excretion and the other with persistent 3-methylglutaconic aciduria.<h4>Conclusions</h4>These data provide the largest ever reported cohort of ASD patients for whom a systematic metabolic workup has been performed; they suggest that such a routine metabolic screening does not contribute to the causative diagnosis of nonsyndromic ASD. They also emphasize that the prevalence of screened IMD in nonsyndromic ASD is probably not higher than in the general population (<0.5%). A careful clinical evaluation is probably more reasonable and of better medical practice than a costly systematic workup.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21760924/pdf/?tool=EBI
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