<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chang KC</submitter><funding>China Medical University hospital</funding><funding>Taiwan Ministry of Science and Technology</funding><funding>China Medical University Hospital</funding><pagination>835</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9143734</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(5)</volume><pubmed_abstract>Background: The effects of methadone-induced severe prolongation of the corrected QT interval (QTc) and sudden cardiac death appear unpredictable and sex-dependent. Genetic polymorphisms in the nitric oxide synthase 1 adaptor protein (NOS1AP) have been implicated in QTc prolongation in general populations. We investigated whether common NOS1AP variants interact with methadone in relation to QTc prolongation in patients with heroin dependence. Methods: We genotyped 17 NOS1AP variants spanning the entire gene in heroin-dependent patients who received a 12-lead electrocardiography (ECG) examination both at baseline and during maintenance methadone treatment in Cohort 1 and only during maintenance methadone treatment in Cohort 2. The QT interval was measured automatically by the Marquette 12SL</pubmed_abstract><journal>Journal of personalized medicine</journal><pubmed_title>Association of a Common &lt;i>NOS1AP&lt;/i> Variant with Attenuation of QTc Prolongation in Men with Heroin Dependence Undergoing Methadone Treatment.</pubmed_title><pmcid>PMC9143734</pmcid><funding_grant_id>DMR-111-020</funding_grant_id><funding_grant_id>MOST 110-2314-B-039-050 and MOST 109-2314-B-039-045</funding_grant_id><funding_grant_id>DMR-111-020 and DMR-110-012</funding_grant_id><funding_grant_id>MOST 109-2314-B-039-045</funding_grant_id><funding_grant_id>MOST 110-2314-B-039-050</funding_grant_id><funding_grant_id>DMR-110-012</funding_grant_id><pubmed_authors>Wu MY</pubmed_authors><pubmed_authors>Chung WH</pubmed_authors><pubmed_authors>Chen KW</pubmed_authors><pubmed_authors>Chang KC</pubmed_authors><pubmed_authors>Shiao YT</pubmed_authors><pubmed_authors>Lane HY</pubmed_authors><pubmed_authors>Liao WL</pubmed_authors><pubmed_authors>Lin YK</pubmed_authors><pubmed_authors>Huang CL</pubmed_authors><pubmed_authors>Lin YN</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association of a Common &lt;i>NOS1AP&lt;/i> Variant with Attenuation of QTc Prolongation in Men with Heroin Dependence Undergoing Methadone Treatment.</name><description>Background: The effects of methadone-induced severe prolongation of the corrected QT interval (QTc) and sudden cardiac death appear unpredictable and sex-dependent. Genetic polymorphisms in the nitric oxide synthase 1 adaptor protein (NOS1AP) have been implicated in QTc prolongation in general populations. We investigated whether common NOS1AP variants interact with methadone in relation to QTc prolongation in patients with heroin dependence. Methods: We genotyped 17 NOS1AP variants spanning the entire gene in heroin-dependent patients who received a 12-lead electrocardiography (ECG) examination both at baseline and during maintenance methadone treatment in Cohort 1 and only during maintenance methadone treatment in Cohort 2. The QT interval was measured automatically by the Marquette 12SL</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-05-07T03:16:46.597Z</modification><creation>2025-02-19T02:58:39.48Z</creation></dates><accession>S-EPMC9143734</accession><cross_references><pubmed>35629257</pubmed><doi>10.3390/jpm12050835</doi></cross_references></HashMap>