<?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>2026-04-13T14:21:37Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:20.500.14342/3725" metadataPrefix="marc">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><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Arranz, Maria J</subfield>
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      <subfield code="a">Salazar, Juliana</subfield>
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      <subfield code="a">Bote, Valentin</subfield>
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      <subfield code="a">Artigas-Baleri, Alícia</subfield>
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      <subfield code="a">Serra-Llovich, Alexandre</subfield>
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      <subfield code="a">Triviño, Emma</subfield>
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      <subfield code="a">Roige, Jordi</subfield>
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      <subfield code="a">Lombardia, Carlos</subfield>
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      <subfield code="a">Cancino, Martha</subfield>
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      <subfield code="a">Hernández Hernández, Marta</subfield>
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      <subfield code="a">Cendros, Marc</subfield>
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      <subfield code="a">Duran-Tauleria, Enric</subfield>
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      <subfield code="a">Maraver, Natalia</subfield>
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      <subfield code="a">Hervas, Amaia</subfield>
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      <subfield code="c">2022-05</subfield>
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      <subfield code="a">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.</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.14342/3725</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">https://doi.org/10.3390/pharmaceutics14050999</subfield>
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      <subfield code="a">Infants autistes</subfield>
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      <subfield code="a">Autisme</subfield>
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      <subfield code="a">ASD</subfield>
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      <subfield code="a">Farmacogenètica</subfield>
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      <subfield code="a">Farmacologia</subfield>
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      <subfield code="a">Antipsicòtics</subfield>
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      <subfield code="a">Antidepressius</subfield>
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      <subfield code="a">Tranquil·lizants</subfield>
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      <subfield code="a">Pharmacogenetic interventions improve the clinical outcome of treatment-resistant autistic spectrum disorder sufferers</subfield>
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