<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-13T00:58:34Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:20.500.14342/3725" metadataPrefix="mets">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:20.500.14342/3725</identifier><datestamp>2025-05-15T19:20:48Z</datestamp><setSpec>com_2072_482405</setSpec><setSpec>com_2072_183628</setSpec><setSpec>col_2072_482409</setSpec></header><metadata><mets xmlns="http://www.loc.gov/METS/" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" ID="&#xa;&#x9;&#x9;&#x9;&#x9;DSpace_ITEM_20.500.14342-3725" TYPE="DSpace ITEM" PROFILE="DSpace METS SIP Profile 1.0" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd" OBJID="&#xa;&#x9;&#x9;&#x9;&#x9;hdl:20.500.14342/3725">
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                  <mods:namePart>Arranz, Maria J</mods:namePart>
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                  <mods:namePart>Salazar, Juliana</mods:namePart>
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                  <mods:namePart>Bote, Valentin</mods:namePart>
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                  <mods:namePart>Artigas-Baleri, Alícia</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Serra-Llovich, Alexandre</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Triviño, Emma</mods:namePart>
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                  <mods:namePart>Roige, Jordi</mods:namePart>
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                  <mods:namePart>Lombardia, Carlos</mods:namePart>
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                  <mods:namePart>Cancino, Martha</mods:namePart>
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                  <mods:namePart>Hernández Hernández, Marta</mods:namePart>
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                  <mods:namePart>Cendros, Marc</mods:namePart>
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                  <mods:namePart>Duran-Tauleria, Enric</mods:namePart>
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                  <mods:namePart>Maraver, Natalia</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Hervas, Amaia</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2025-05-15T19:20:48Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2022-05</mods:dateIssued>
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               <mods:identifier type="uri">http://hdl.handle.net/20.500.14342/3725</mods:identifier>
               <mods:identifier type="doi">https://doi.org/10.3390/pharmaceutics14050999</mods:identifier>
               <mods:abstract>BACKGROUND: Autistic spectrum disorders (ASD) are severe neurodevelopmental alterations characterised by deficits in social communication and repetitive and restricted behaviours. About a third of patients receive pharmacological treatment for comorbid symptoms. However, 30–50% do not respond adequately and/or present severe and long-lasting side effects. METHODS: Genetic variants in CYP1A2, CYP2C19, CYP2D6 and SLC6A4 were investigated in N = 42 ASD sufferers resistant to pharmacological treatment. Clinical recommendations based on their pharmacogenetic profiles were provided within 24–48 h of receiving a biological sample. RESULTS: A total of 39 participants (93%) improved after the pharmacogenetic intervention according to their CGI scores (difference in basal-final scores: 2.26, SD 1.55) and 37 participants (88%) according to their CGAS scores (average improvement of 20.29, SD 11.85). Twenty-three of them (55%) achieved symptom stability (CGI ≤ 3 and CGAS improvement ≥ 20 points), requiring less frequent visits to their clinicians and hospital stays. Furthermore, the clinical improvement was higher than that observed in a control group (N = 62) with no pharmacogenetic interventions, in which 66% responded to treatment (difference in CGI scores: −0.87, SD 9.4, p = 1 × 10−5; difference in CGAS scores: 6.59, SD 7.76, p = 5 × 10−8). CONCLUSIONS: The implementation of pharmacogenetic interventions has the potential to significantly improve the clinical outcomes in severe comorbid ASD populations with drug treatment resistance and poor prognosis.</mods:abstract>
               <mods:language>
                  <mods:languageTerm authority="rfc3066">eng</mods:languageTerm>
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               <mods:accessCondition type="useAndReproduction">© L'autor/a Attribution 4.0 International</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Infants autistes</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Autisme</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>ASD</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Farmacogenètica</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Farmacologia</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Antipsicòtics</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Antidepressius</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Tranquil·lizants</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>Pharmacogenetic interventions improve the clinical outcome of treatment-resistant autistic spectrum disorder sufferers</mods:title>
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