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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Neurol.</journal-id>
<journal-title>Frontiers in Neurology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Neurol.</abbrev-journal-title>
<issn pub-type="epub">1664-2295</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fneur.2024.1381293</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Neurology</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Cardiac dysfunctions in children with drug-resistant epilepsy</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author"><name><surname>Sridech</surname> <given-names>Watthana</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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<contrib contrib-type="author"><name><surname>Intamul</surname> <given-names>Kamonchanok</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
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<contrib contrib-type="author"><name><surname>Saengsin</surname> <given-names>Kwannapas</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
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<contrib contrib-type="author"><name><surname>Wiwattanadittakul</surname> <given-names>Nattarujee</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
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<contrib contrib-type="author"><name><surname>Sittiwangkul</surname> <given-names>Rekwan</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
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<contrib contrib-type="author"><name><surname>Katanyuwong</surname> <given-names>Kamornwan</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
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<contrib contrib-type="author"><name><surname>Silvilairat</surname> <given-names>Suchaya</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
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<contrib contrib-type="author" corresp="yes"><name><surname>Sanguansermsri</surname> <given-names>Chinnuwat</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref><xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
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<aff id="aff1"><sup>1</sup><institution>Department of Pediatrics, Faculty of Medicine, Chiang Mai University</institution>, <addr-line>Chiang Mai</addr-line>, <country>Thailand</country></aff>
<aff id="aff2"><sup>2</sup><institution>Cardiology Division, Department of Pediatrics, Faculty of Medicine, Chiang Mai University</institution>, <addr-line>Chiang Mai</addr-line>, <country>Thailand</country></aff>
<aff id="aff3"><sup>3</sup><institution>Neurology Division, Department of Pediatrics, Faculty of Medicine, Chiang Mai University</institution>, <addr-line>Chiang Mai</addr-line>, <country>Thailand</country></aff>
<author-notes>
<fn fn-type="edited-by" id="fn0001">
<p>Edited by: Christopher Michael DeGiorgio MD, University of California, Los Angeles, United States</p>
</fn>
<fn fn-type="edited-by" id="fn0002">
<p>Reviewed by: Irena Dolezalova, St. Anne&#x2019;s University Hospital Brno, Czechia</p>
<p>Anca Adriana Arbune, Fundeni Clinical Institute, Romania</p>
</fn>
<corresp id="c001">&#x002A;Correspondence: Chinnuwat Sanguansermsri, <email>chinnuwat.s@cmu.ac.th</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>16</day>
<month>04</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="collection">
<year>2024</year>
</pub-date>
<volume>15</volume>
<elocation-id>1381293</elocation-id>
<history>
<date date-type="received">
<day>03</day>
<month>02</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>02</day>
<month>04</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2024 Sridech, Intamul, Saengsin, Wiwattanadittakul, Sittiwangkul, Katanyuwong, Silvilairat and Sanguansermsri.</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Sridech, Intamul, Saengsin, Wiwattanadittakul, Sittiwangkul, Katanyuwong, Silvilairat and Sanguansermsri</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<sec id="sec1">
<title>Objective</title>
<p>There were reports of cardiac dysfunction that led to sudden unexpected death in epilepsy (SUDEP) in patients with epilepsy. Early detection of cardiac dysfunction can lead to early management to prevent sudden cardiac death in these patients. The objective of our study is to assess cardiac functions in children with drug-resistant epilepsy (DRE) compared with the normal population by using a standard echocardiogram (SE), tissue Doppler imaging (TDI) and myocardial strain evaluations (MSE).</p>
</sec>
<sec id="sec2">
<title>Method</title>
<p>Twenty-seven children who have been diagnosed with DRE based on the International League against Epilepsy (ILAE) were included in the study, along with 27 children whose ages match those of the normal control group.</p>
</sec>
<sec id="sec3">
<title>Results</title>
<p>Seventeen children, median age 12&#x2009;years old, were using more than four anti-seizure medications. Structural brain lesions were the most common cause of epilepsy, 55.6% (15). Generalized tonic&#x2013;clonic seizures were the most common seizure type, 55.6% (15). Children with DRE had a lower early mitral valve E wave inflow velocity compared with the control group (<italic>p</italic>&#x2009;&#x003C;&#x2009;0.05). They also had lowered early diastolic velocities (e&#x2032;) and myocardial performance index (MPI) when compared with the control group (<italic>p</italic>&#x2009;&#x003C;&#x2009;0.05). There was a statistically significant difference in left ventricular myocardial strain in children with DRE, with an average of &#x2212;21.1 (IQR &#x2212;23.5 and &#x2212;19.4) and control, &#x2212;25.5 (IQR &#x2212;27.3 and &#x2212;24.2).</p>
</sec>
<sec id="sec4">
<title>Significance</title>
<p>Children with DRE have an impairment of left ventricular diastolic function and myocardial strain, which could indicate decreased myocardial deformation and contraction compared with controls. These cardiological assessments can be used to evaluate children with DRE for early diagnosis and management of their cardiac dysfunction.</p>
</sec>
</abstract>
<kwd-group>
<kwd>epilepsy</kwd>
<kwd>drug-resistant</kwd>
<kwd>cardiac dysfunctions</kwd>
<kwd>myocardial strain</kwd>
<kwd>SUDEP</kwd>
<kwd>biomarkers</kwd>
</kwd-group>
<counts>
<fig-count count="1"/>
<table-count count="5"/>
<equation-count count="0"/>
<ref-count count="32"/>
<page-count count="7"/>
<word-count count="5072"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Epilepsy</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec5"><label>1</label>
<title>Introduction</title>
<p>Drug-resistant epilepsy (DRE) is defined by the inability of two well-tolerated and properly selected medications, whether used alone or in combination, to consistently achieve seizure independence despite sufficient trials (<xref ref-type="bibr" rid="ref1">1</xref>). Twenty-five percent of children with epilepsy have received the diagnosis of drug-resistant epilepsy (DRE), putting them at an increased risk for having sudden unexpected deaths in epilepsy patients (SUDEP) (<xref ref-type="bibr" rid="ref2">2</xref>). The incidence of SUDEP in children with DRE has been reported at approximately 1.2&#x2013;1.45 per persons year (<xref ref-type="bibr" rid="ref3 ref4 ref5">3&#x2013;5</xref>). While the precise mechanism of SUDEP remains incompletely comprehended, it is predominantly believed to be a multifactorial process (<xref ref-type="bibr" rid="ref6">6</xref>, <xref ref-type="bibr" rid="ref7">7</xref>). Cardiac dysfunction has been proposed as one of the leading causes of SUDEP. The reason to support this is due to postmortem findings: one-fourth of SUDEP patients have myocardial hypertrophy and fibrosis (<xref ref-type="bibr" rid="ref8">8</xref>). Additionally, evidence of myocardial injuries in adult patients with epilepsy and subclinical left ventricular dysfunction in children with DRE were reported (<xref ref-type="bibr" rid="ref9 ref10 ref11">9&#x2013;11</xref>). The correlation between epilepsy and cardiovascular injuries was defined as the epileptic heart, which is the heart and coronary vasculature that have been injured due to chronic epilepsy. This damage occurs as a result of repeated spikes in catecholamines and hypoxemia, leading to electrical and mechanical dysfunction (<xref ref-type="bibr" rid="ref12 ref13 ref14 ref15">12&#x2013;15</xref>). Currently, numerous studies are being conducted to avoid SUDEP by employing various methods and modern technology for prompt identification and intervention.</p>
<p>An echocardiogram is a non-invasive procedure that is used to evaluate heart functioning and detect myocardial damage. Nevertheless, the research conducted on individuals with epilepsy, particularly in pediatric populations, was scarce. The left ventricular ejection fraction (LVEF) has been widely employed as a biomarker to assess cardiac systolic function. But numerous data points indicate that the likelihood of it being abnormal in asymptomatic patients is low (<xref ref-type="bibr" rid="ref8">8</xref>, <xref ref-type="bibr" rid="ref16">16</xref>). Hence, relying just on LVEF may not provide for early detection of cardiac dysfunction, consequently exposing the patient to the risk of SUDEP. Additional echocardiography techniques, when combined with advanced multiple variables, have been investigated as indicators of myocardial dysfunction and injury. These include the measurement of mitral valve E wave inflow velocity and tissue Doppler lateral E&#x2032; wave (<xref ref-type="bibr" rid="ref8">8</xref>, <xref ref-type="bibr" rid="ref17">17</xref>). Speckle-tracking echocardiography is a non-invasive technique used to assess myocardial strain. Strain measurement has been employed as an early biomarker of cardiac injury in various diseases, including epilepsy (<xref ref-type="bibr" rid="ref8">8</xref>, <xref ref-type="bibr" rid="ref18">18</xref>). The strain value was different between epileptic patients and controls (<xref ref-type="bibr" rid="ref8">8</xref>, <xref ref-type="bibr" rid="ref19">19</xref>). It can provide early detection of subclinical myocardial dysfunctions (<xref ref-type="bibr" rid="ref8">8</xref>, <xref ref-type="bibr" rid="ref20">20</xref>). However, there is an abundance of data regarding children with DRE, and there is currently no definitive reference for strain value in pediatric populations with different age groups (<xref ref-type="bibr" rid="ref21">21</xref>).</p>
<p>Our study aims to identify cardiac dysfunctions in children with DRE by utilizing a standard echocardiogram, a tissue Doppler echocardiogram (TDI), and measuring myocardial strain. This will allow us to detect any initial signs of cardiac dysfunction in patients without cardiac symptoms.</p>
</sec>
<sec sec-type="materialandmethod" id="sec6"><label>2</label>
<title>Material and method</title>
<sec id="sec7"><label>2.1</label>
<title>Participants</title>
<p>The study comprised a total of 54 children and adolescents, ranging in age from 6 to 20&#x2009;years. They were categorized into two groups. The epilepsy group consisted of 27 children diagnosed with DRE according to the ILAE definition were selected from the outpatient Pediatric Neurology Clinic at Chiang Mai University Hospital. The recruitment took place between August 2022 and September 2023. The study excluded children who had underlying disorders or comorbidities that could potentially cause cardiac dysfunction, including known structural heart abnormalities, a history of post-cardiac arrest or acute myocarditis and endocrine problems. The control group consisted of 27 individuals who were healthy, of similar age and gender, and visited outpatient clinics for non-medical reasons. The parents of the children enrolled in the study were provided with comprehensive information about the study and acquired a written consent from them before enrolling their children. The data was obtained from all participants, including demographic information, seizure types and epilepsy syndromes [classified by using the ILAE 2017 classification (<xref ref-type="bibr" rid="ref22">22</xref>, <xref ref-type="bibr" rid="ref23">23</xref>)], seizure frequency, electroencephalography (EEG) results, number, and type of antiseizure medications. The study was approved by Chiang Mai University&#x2019;s Ethics Committee.</p>
</sec>
<sec id="sec8"><label>2.2</label>
<title>Echocardiogram measurement</title>
<sec id="sec9"><label>2.2.1</label>
<title>Standard echocardiogram</title>
<p>Both patients and controls underwent an electrocardiogram (ECG) followed by a standard echocardiogram according to the study&#x2019;s protocol in the outpatient Pediatric Cardiology clinic at Chiang Mai University Hospital with a standard ultrasound machine (Philips EPIQ CVx Ultrasonography). Two-dimensional echocardiography (M-mode) for parasternal long-axis view was used to measure the ejection fraction (EF) and fraction shortening (FS). An apical four-chamber view with Pulse-wave Doppler was used to evaluate early mitral inflow velocity (E), late mitral inflow velocity (A) and the E/A ratio.</p>
</sec>
<sec id="sec10"><label>2.2.2</label>
<title>Tissue Doppler imaging echocardiogram (TDI)</title>
<p>An echocardiogram using Tissue Doppler Imaging (TDI) was employed to evaluate the diastolic function of the heart at the level of the mitral septal annular plane and lateral wall plane. Measurements are taken for the early diastolic velocity (e&#x2032;), late diastolic velocity (a&#x2032;), peak systolic velocity (S), ratio between the early mitral flow velocity (E) and early diastolic mitral velocity (e&#x2032;) (E/e&#x2032;), and myocardial performance index (MPI).</p>
</sec>
<sec id="sec11"><label>2.2.3</label>
<title>Myocardial strain</title>
<p>The measurement of global longitudinal strain was performed using vendor-specific software in a semi-automated manner. The cardiologist, who was unaware of the patient&#x2019;s medical history, chose the end-systolic and end-diastolic strains. The longitudinal and circumferential systolic strains are displayed as negative numbers during the contraction of the heart. The segmental strain is illustrated by three apical images: apical two chamber (A2C), apical three chamber (A3C), and apical four chamber (A4C). Additionally, a thorough visualization of the entire left ventricle is presented in a Bull&#x2019;s eye view, as depicted in <xref ref-type="fig" rid="fig1">Figure 1</xref>.</p>
<fig position="float" id="fig1"><label>Figure 1</label>
<caption>
<p>Example of left ventricular strain of a child with DRE including apical four chamber (A4C), apical two chamber (A2C), apical three chamber (A3C) and average strain (Avg) strain in Bull&#x2019;s eye view.</p>
</caption>
<graphic xlink:href="fneur-15-1381293-g001.tif"/>
</fig>
</sec>
</sec>
<sec id="sec12"><label>2.3</label>
<title>Statistical analysis</title>
<p>The statistical analysis was performed using Stata MP version 14.1 (StataCorp LLC, Texas, United States). The categorical variables were summarized by calculating the frequency counts and percentages. The statistical tests used to calculate these values were the Chi-square test and Fisher&#x2019;s exact test. The median and interquartile range (IQR) were used to summarize continuous variables. The cardiac function measurements of patients and controls were compared using an independent Mann&#x2013;Whitney U test to assess the difference between the observations in the two groups. There was no additional missing data. The statistical significance was established with a <italic>p</italic>-value of less than 0.05.</p>
</sec>
</sec>
<sec sec-type="results" id="sec13"><label>3</label>
<title>Results</title>
<p>For the baseline clinical characteristics as demonstrated in <xref ref-type="table" rid="tab1">Table 1</xref>, the gender and age distribution of the 27 patients and 27 controls included 16 males and 11 females, with a median age of 12&#x2009;years (IQR 8&#x2013;14&#x2009;years). Seven children (26%) in the epilepsy group were non-ambulatory. Fourteen children (51.8%) had other medical conditions such as malnutrition (29.6%), central adrenal insufficiency (3.7%), autism spectrum disorder (11.1%) and obesity (7.4%). Only three patients (11%) were found to be currently using additional medications, namely aspirin, risperidone, and prednisolone. There was no family history of cardiac disease in any of the patients.</p>
<table-wrap position="float" id="tab1"><label>Table 1</label>
<caption>
<p>Baseline clinical characteristic of children with DRE.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th/>
<th align="center" valign="top">Number (<italic>N</italic>)</th>
<th align="center" valign="top">Percentage</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" colspan="3">Gender</td>
</tr>
<tr>
<td align="left" valign="top">Male</td>
<td align="center" valign="top">16</td>
<td align="center" valign="top">59.3</td>
</tr>
<tr>
<td align="left" valign="top">Female</td>
<td align="center" valign="top">11</td>
<td align="center" valign="top">40.7</td>
</tr>
<tr>
<td align="left" valign="top" colspan="3">Age</td>
</tr>
<tr>
<td align="left" valign="top">6&#x2013;10&#x2009;years</td>
<td align="center" valign="top">11</td>
<td align="center" valign="top">40.7</td>
</tr>
<tr>
<td align="left" valign="top">11&#x2013;15&#x2009;years</td>
<td align="center" valign="top">11</td>
<td align="center" valign="top">40.7</td>
</tr>
<tr>
<td align="left" valign="top">16&#x2013;20&#x2009;years</td>
<td align="center" valign="top">5</td>
<td align="center" valign="top">18.6</td>
</tr>
<tr>
<td align="left" valign="top" colspan="3">Ambulatory status</td>
</tr>
<tr>
<td align="left" valign="top">Walk</td>
<td align="center" valign="top">20</td>
<td align="center" valign="top">74</td>
</tr>
<tr>
<td align="left" valign="top">Non-ambulatory</td>
<td align="center" valign="top">7</td>
<td align="center" valign="top">26</td>
</tr>
<tr>
<td align="left" valign="top" colspan="3">Comorbid disease</td>
</tr>
<tr>
<td align="left" valign="top">None</td>
<td align="center" valign="top">13</td>
<td align="center" valign="top">48.2</td>
</tr>
<tr>
<td align="left" valign="top">Comorbidity<break/>-Malnutrition<break/>-Central adrenal insufficiency<break/>-Autistic spectrum disorder<break/>-Obesity</td>
<td align="center" valign="top">14<break/>8<break/>1<break/><break/>3<break/>2</td>
<td align="center" valign="top">51.8<break/>29.6<break/>3.7<break/><break/>11.1<break/>7.4</td>
</tr>
<tr>
<td align="left" valign="top" colspan="3">Number of additional medications</td>
</tr>
<tr>
<td align="left" valign="top">None</td>
<td align="center" valign="top">24</td>
<td align="center" valign="top">89</td>
</tr>
<tr>
<td align="left" valign="top">Current medication</td>
<td align="center" valign="top">3</td>
<td align="center" valign="top">11</td>
</tr>
<tr>
<td align="left" valign="top" colspan="3">Familial cardiac disease</td>
</tr>
<tr>
<td align="left" valign="top">None</td>
<td align="center" valign="top">27</td>
<td align="center" valign="top">100</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>The seizure characteristics of the children with DRE are presented in <xref ref-type="table" rid="tab2">Table 2</xref>. The main etiologies of epilepsy were structural brain lesions (15, 55.6%), genetic (5, 18.5%), and a combination of genetic and structural brain lesions (3, 11%). Focal cortical dysplasia (n&#x2009;=&#x2009;2) was the most common in patients with structural brain lesions and Dravet syndrome with <italic>SCN1A</italic> mutations (<italic>n</italic>&#x2009;=&#x2009;2) was the most common epilepsy syndrome in the genetic group. A majority of patients (63%) experienced seizures for a duration exceeding 10&#x2009;years. At the time of the investigation, there was one patient who had been diagnosed with DRE within the past two years. For seizure types, 15 patients (55.6%) had generalized seizures and all of them were generalized tonic&#x2013;clonic seizures. Seven (25.9%) had focal seizures based on their seizure semiology and EEG findings. Daily seizures were seen in 12 patients (44.4%). Seventeen patients (63%) had been using four or more current ASMs. Levetiracetam was the most common ASM used (n&#x2009;=&#x2009;24), followed by valproic acid (n&#x2009;=&#x2009;17) and topiramate (n&#x2009;=&#x2009;13). None of the patients used only one ASM. Fourteen patients (51.8%) had failed at least four ASMs. There were two patients who failed only two ASMs at the time they were enrolled in the study. Twenty-five patients (92.5%) underwent to have an EEG and all of them had abnormal EEG results. Neurological imaging was performed by either computed tomography (CT) or magnetic resonance imaging (MRI) in all patients. Out of the total, 19 (70.4%) showed a structural brain abnormality.</p>
<table-wrap position="float" id="tab2"><label>Table 2</label>
<caption>
<p>Seizure characteristics.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th/>
<th align="center" valign="top">Number (<italic>N</italic>)</th>
<th align="center" valign="top">Percentage</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" colspan="3">Etiology</td>
</tr>
<tr>
<td align="left" valign="top">Genetic</td>
<td align="center" valign="top">5</td>
<td align="center" valign="top">18.5</td>
</tr>
<tr>
<td align="left" valign="top">Structure</td>
<td align="center" valign="top">15</td>
<td align="center" valign="top">55.6</td>
</tr>
<tr>
<td align="left" valign="top">Genetic and structure</td>
<td align="center" valign="top">3</td>
<td align="center" valign="top">11</td>
</tr>
<tr>
<td align="left" valign="top">Infection</td>
<td align="center" valign="top">1</td>
<td align="center" valign="top">3.7</td>
</tr>
<tr>
<td align="left" valign="top">Unknown</td>
<td align="center" valign="top">3</td>
<td align="center" valign="top">11</td>
</tr>
<tr>
<td align="left" valign="top" colspan="3">Duration of seizure</td>
</tr>
<tr>
<td align="left" valign="top">Less than two years</td>
<td align="center" valign="top">1</td>
<td align="center" valign="top">3.7</td>
</tr>
<tr>
<td align="left" valign="top">Three years</td>
<td align="center" valign="top">1</td>
<td align="center" valign="top">3.7</td>
</tr>
<tr>
<td align="left" valign="top">More than five years</td>
<td align="center" valign="top">8</td>
<td align="center" valign="top">29.6</td>
</tr>
<tr>
<td align="left" valign="top">More than ten years</td>
<td align="center" valign="top">17</td>
<td align="center" valign="top">63</td>
</tr>
<tr>
<td align="left" valign="top" colspan="3">Seizure type</td>
</tr>
<tr>
<td align="left" valign="top">Generalized</td>
<td align="center" valign="top">15</td>
<td align="center" valign="top">55.6</td>
</tr>
<tr>
<td align="left" valign="top">Focal</td>
<td align="center" valign="top">7</td>
<td align="center" valign="top">25.9</td>
</tr>
<tr>
<td align="left" valign="top">Focal and generalized</td>
<td align="center" valign="top">5</td>
<td align="center" valign="top">18.5</td>
</tr>
<tr>
<td align="left" valign="top" colspan="3">Seizure frequency</td>
</tr>
<tr>
<td align="left" valign="top">Daily</td>
<td align="center" valign="top">12</td>
<td align="center" valign="top">44.4</td>
</tr>
<tr>
<td align="left" valign="top">Weekly</td>
<td align="center" valign="top">8</td>
<td align="center" valign="top">29.6</td>
</tr>
<tr>
<td align="left" valign="top">Monthly</td>
<td align="center" valign="top">5</td>
<td align="center" valign="top">18.5</td>
</tr>
<tr>
<td align="left" valign="top">Yearly</td>
<td align="center" valign="top">2</td>
<td align="center" valign="top">7.5</td>
</tr>
<tr>
<td align="left" valign="top" colspan="3">Current ASM</td>
</tr>
<tr>
<td align="left" valign="top">Two</td>
<td align="center" valign="top">3</td>
<td align="center" valign="top">11.1</td>
</tr>
<tr>
<td align="left" valign="top">Three</td>
<td align="center" valign="top">7</td>
<td align="center" valign="top">25.9</td>
</tr>
<tr>
<td align="left" valign="top">Four</td>
<td align="center" valign="top">10</td>
<td align="center" valign="top">37.1</td>
</tr>
<tr>
<td align="left" valign="top">More than four</td>
<td align="center" valign="top">7</td>
<td align="center" valign="top">25.9</td>
</tr>
<tr>
<td align="left" valign="top" colspan="3">Previous ASM</td>
</tr>
<tr>
<td align="left" valign="top">None</td>
<td align="center" valign="top">2</td>
<td align="center" valign="top">7.5</td>
</tr>
<tr>
<td align="left" valign="top">One</td>
<td align="center" valign="top">3</td>
<td align="center" valign="top">11.1</td>
</tr>
<tr>
<td align="left" valign="top">Two</td>
<td align="center" valign="top">3</td>
<td align="center" valign="top">11.1</td>
</tr>
<tr>
<td align="left" valign="top">Three</td>
<td align="center" valign="top">5</td>
<td align="center" valign="top">18.5</td>
</tr>
<tr>
<td align="left" valign="top">Four</td>
<td align="center" valign="top">2</td>
<td align="center" valign="top">7.5</td>
</tr>
<tr>
<td align="left" valign="top">More than four</td>
<td align="center" valign="top">12</td>
<td align="center" valign="top">44.3</td>
</tr>
<tr>
<td align="left" valign="top" colspan="3">EEG</td>
</tr>
<tr>
<td align="left" valign="top">Not done</td>
<td align="center" valign="top">2</td>
<td align="center" valign="top">7.5</td>
</tr>
<tr>
<td align="left" valign="top">Done<break/>Abnormal</td>
<td align="center" valign="top">25<break/>25</td>
<td align="center" valign="top">92.5<break/>92.5</td>
</tr>
<tr>
<td align="left" valign="top" colspan="3">Neuroimaging</td>
</tr>
<tr>
<td align="left" valign="top">Normal</td>
<td align="center" valign="top">8</td>
<td align="center" valign="top">29.6</td>
</tr>
<tr>
<td align="left" valign="top">Abnormal</td>
<td align="center" valign="top">19</td>
<td align="center" valign="top">70.4</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Standard echocardiogram measurements for patients and controls are shown in <xref ref-type="table" rid="tab3">Table 3</xref>. There were no structural cardiac abnormalities identified in both groups. All of the participants had normal sinus rhythms in their ECG results. There was a statistically significant difference in the lower left ventricular internal diameter end diastole (LVIDd) in patients in the epilepsy group compared to the control group (median 3.6&#x2009;mm [IQR&#x2009;=&#x2009;2.9&#x2013;3.9] vs. 4.0&#x2009;mm [IQR&#x2009;=&#x2009;3.8&#x2013;4.4], <italic>p</italic>&#x2009;=&#x2009;0.001). The left ventricular internal diameter end systole (LVIDs) was lower in patients compared to controls (median 2.3&#x2009;mm [IQR&#x2009;=&#x2009;1.9&#x2013;2.6] vs. 2.6&#x2009;mm [IQR&#x2009;=&#x2009;2.5&#x2013;2.9], p&#x2009;=&#x2009;0.001). The difference was statistically significant. There was no significant difference in the ejection fraction (EF) and fractional shortening (FS) of patients, which were used for cardiac systolic function assessment, compared to controls. Pulse wave standard echocardiogram revealed a significant difference in the low early mitral inflow velocity (E) (median 89.5&#x2009;cm/s [IQR&#x2009;=&#x2009;71.9&#x2013;105.8] vs. 102&#x2009;cm/s [IQR&#x2009;=&#x2009;92.1&#x2013;106.3], <italic>p</italic>&#x2009;=&#x2009;0.027), late mitral inflow velocity (A) (median 63.4&#x2009;cm/s [IQR&#x2009;=&#x2009;51.8&#x2013;71.9] vs. 54.2&#x2009;cm/s [IQR&#x2009;=&#x2009;50.5&#x2013;59.1], <italic>p</italic>&#x2009;=&#x2009;0.023) and E/A ratio (median 1.4 [IQR&#x2009;=&#x2009;1.3&#x2013;1.5] vs. 1.8 [IQR&#x2009;=&#x2009;1.6&#x2013;2.1], <italic>p</italic>&#x2009;&#x003C;&#x2009;0.001) between the patients and the control group.</p>
<table-wrap position="float" id="tab3"><label>Table 3</label>
<caption>
<p>Standard echocardiogram.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th/>
<th align="center" valign="middle">Patient median, (IQR)</th>
<th align="center" valign="middle">Control median, (IQR)</th>
<th align="center" valign="middle"><italic>p</italic>-value</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">
<italic>N</italic>
</td>
<td align="center" valign="top">27</td>
<td align="center" valign="top">27</td>
<td/>
</tr>
<tr>
<td align="left" valign="top">LVIDd(cm)</td>
<td align="center" valign="top">3.6 (2.9&#x2013;3.9)</td>
<td align="center" valign="top">4.0 (3.8&#x2013;4.4)</td>
<td align="center" valign="top">0.001</td>
</tr>
<tr>
<td align="left" valign="top">LVIDs(cm)</td>
<td align="center" valign="top">2.3 (1.9&#x2013;2.6)</td>
<td align="center" valign="top">2.6 (2.5&#x2013;2.9)</td>
<td align="center" valign="top">0.001</td>
</tr>
<tr>
<td align="left" valign="top">IVSd(cm)</td>
<td align="center" valign="top">0.8 (0.7&#x2013;1.1)</td>
<td align="center" valign="top">0.84 (0.7&#x2013;1.0)</td>
<td align="center" valign="top">0.465</td>
</tr>
<tr>
<td align="left" valign="top">IVSs(cm)</td>
<td align="center" valign="top">1.12 (0.98&#x2013;1.26)</td>
<td align="center" valign="top">1.12 (0.98&#x2013;1.26)</td>
<td align="center" valign="top">0.825</td>
</tr>
<tr>
<td align="left" valign="top">LVPWd(cm)</td>
<td align="center" valign="top">0.81 (0.63&#x2013;1.04)</td>
<td align="center" valign="top">0.80 (0.71&#x2013;0.93)</td>
<td align="center" valign="top">0.806</td>
</tr>
<tr>
<td align="left" valign="top">LVPWs(cm)</td>
<td align="center" valign="top">0.98 (0.77&#x2013;1.13)</td>
<td align="center" valign="top">1.11 (0.95&#x2013;1.24)</td>
<td align="center" valign="top">0.093</td>
</tr>
<tr>
<td align="left" valign="top">EF (%)</td>
<td align="center" valign="top">65.3 (61&#x2013;71.3)</td>
<td align="center" valign="top">65.7 (60.7&#x2013;68.2)</td>
<td align="center" valign="top">0.870</td>
</tr>
<tr>
<td align="left" valign="top">FS (%)</td>
<td align="center" valign="top">35.1 (32.1&#x2013;39.1)</td>
<td align="center" valign="top">36 (32.4&#x2013;38.2)</td>
<td align="center" valign="top">0.974</td>
</tr>
<tr>
<td align="left" valign="top">MAPSE</td>
<td align="center" valign="top">1.27 (1.13&#x2013;1.68)</td>
<td align="center" valign="top">1.46 (1.23&#x2013;1.71)</td>
<td align="center" valign="top">0.294</td>
</tr>
<tr>
<td align="left" valign="top">Pulse wave Doppler</td>
<td/>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Early mitral inflow velocity (E) (cm/s)</td>
<td align="center" valign="top">89.5 (71.9&#x2013;105.8)</td>
<td align="center" valign="top">102 (92.1&#x2013;106.3)</td>
<td align="center" valign="top">0.027</td>
</tr>
<tr>
<td align="left" valign="top">Late mitral inflow velocity (A) (cm/s)</td>
<td align="center" valign="top">63.4 (51.8&#x2013;71.9)</td>
<td align="center" valign="top">54.2 (50.5&#x2013;59.1)</td>
<td align="center" valign="top">0.023</td>
</tr>
<tr>
<td align="left" valign="top">E/A ratio</td>
<td align="center" valign="top">1.4 (1.3&#x2013;1.5)</td>
<td align="center" valign="top">1.8 (1.6&#x2013;2.1)</td>
<td align="center" valign="top">&#x003C;0.001</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>LVIDd, Left ventricular internal diameter end diastole; LVIDs, Left ventricular internal diameter end systole; IVSd, Interventricular septal end diastole; IVSs, Interventricular septal end systole; LVPWd, Left ventricular posterior wall end diastole; LVPWs, Left ventricular posterior wall end systole; EF, Ejection fraction; FS, Fractional shortening; MAPSE, Mitral annular plane systolic excursion.</p>
</table-wrap-foot>
</table-wrap>
<p>In the TDI echocardiography (<xref ref-type="table" rid="tab4">Table 4</xref>), patients exhibited a significant reduction in lateral left ventricular early diastolic velocity (e&#x2032;) (median 15.4&#x2009;cm/s [IQR&#x2009;=&#x2009;12.9&#x2013;17.2] vs. 18.7&#x2009;cm/s [IQR&#x2009;=&#x2009;16.7&#x2013;22.0], p&#x2009;&#x003C;&#x2009;0.001) and medial ventricular early diastolic velocity (e&#x2032;) (median 12.7&#x2009;cm/s [IQR&#x2009;=&#x2009;10.7&#x2013;13.9] vs. 14.3&#x2009;cm/s [IQR&#x2009;=&#x2009;12.8&#x2013;15.9], <italic>p</italic>&#x2009;=&#x2009;0.006) compared to the control group. The myocardial performance index showed a significant elevation in patients compared with controls in both the lateral and medial walls of the left ventricles.</p>
<table-wrap position="float" id="tab4"><label>Table 4</label>
<caption>
<p>Tissue Doppler imaging (TDI) echocardiogram.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th/>
<th align="center" valign="top">Patient median, (IQR)</th>
<th align="center" valign="top">Control median, (IQR)</th>
<th align="center" valign="top"><italic>p</italic>-value</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">
<italic>N</italic>
</td>
<td align="center" valign="top">27</td>
<td align="center" valign="top">27</td>
<td/>
</tr>
<tr>
<td align="left" valign="top" colspan="4">Lateral left ventricle</td>
</tr>
<tr>
<td align="left" valign="top">Early diastolic velocity (e&#x2032;) (cm/s)</td>
<td align="center" valign="top">15.4 (12.9&#x2013;17.2)</td>
<td align="center" valign="top">18.7 (16.7&#x2013;22.0)</td>
<td align="center" valign="top">&#x003C;0.001</td>
</tr>
<tr>
<td align="left" valign="top">Late diastolic velocity (a&#x2032;) (cm/s)</td>
<td align="center" valign="top">7.6 (6.4&#x2013;9.1)</td>
<td align="center" valign="top">7.6 (6.1&#x2013;8.9)</td>
<td align="center" valign="top">0.652</td>
</tr>
<tr>
<td align="left" valign="top">E&#x2032;/a&#x2032; ratio</td>
<td align="center" valign="top">2.0 (1.7&#x2013;2.3)</td>
<td align="center" valign="top">2.5 (2.0&#x2013;3.21)</td>
<td align="center" valign="top">0.009</td>
</tr>
<tr>
<td align="left" valign="top">Peak systolic velocity (S) (cm/s)</td>
<td align="center" valign="top">9.2 (7.2&#x2013;11.1)</td>
<td align="center" valign="top">11.0 (8.9&#x2013;12.8)</td>
<td align="center" valign="top">0.045</td>
</tr>
<tr>
<td align="left" valign="top">Ratio between the early mitral flow velocity (E) and early diastolic mitral velocity (e&#x2032;) E/e&#x2032;</td>
<td align="center" valign="top">5.7 (4.9&#x2013;7.1)</td>
<td align="center" valign="top">5.2 (4.7&#x2013;6.1)</td>
<td align="center" valign="top">0.058</td>
</tr>
<tr>
<td align="left" valign="top">Myocardial performance index (MPI)</td>
<td align="center" valign="top">0.51 (0.43&#x2013;0.63)</td>
<td align="center" valign="top">0.41 (0.38&#x2013;0.47)</td>
<td align="center" valign="top">0.008</td>
</tr>
<tr>
<td align="left" valign="top" colspan="4">Medium left ventricle</td>
</tr>
<tr>
<td align="left" valign="top">Early diastolic velocity (e&#x2032;) (cm/s)</td>
<td align="center" valign="top">12.7 (10.7&#x2013;13.9)</td>
<td align="center" valign="top">14.3 (12.8&#x2013;15.9)</td>
<td align="center" valign="top">0.006</td>
</tr>
<tr>
<td align="left" valign="top">Late diastolic velocity (a&#x2032;) (cm/s)</td>
<td align="center" valign="top">7.8 (6.5&#x2013;8.9)</td>
<td align="center" valign="top">6.4 (6.0&#x2013;7.5)</td>
<td align="center" valign="top">0.004</td>
</tr>
<tr>
<td align="left" valign="top">E&#x2032;/a&#x2032; ratio</td>
<td align="center" valign="top">1.5 (1.3&#x2013;1.8)</td>
<td align="center" valign="top">2.1 (1.8&#x2013;2.6)</td>
<td align="center" valign="top">&#x003C;0.001</td>
</tr>
<tr>
<td align="left" valign="top">Peak systolic velocity (S) (cm/s)</td>
<td align="center" valign="top">8.5 (7.4&#x2013;8.8)</td>
<td align="center" valign="top">8.1 (7.1&#x2013;8.9)</td>
<td align="center" valign="top">0.724</td>
</tr>
<tr>
<td align="left" valign="top">Ratio between the early mitral flow velocity (E) and early diastolic mitral velocity (e&#x2032;) E/e&#x2032;</td>
<td align="center" valign="top">7.2 (6.3&#x2013;8.4)</td>
<td align="center" valign="top">7.0 (6.5&#x2013;7.9)</td>
<td align="center" valign="top">0.825</td>
</tr>
<tr>
<td align="left" valign="top">Myocardial performance index (MPI)</td>
<td align="center" valign="top">0.50 (0.41&#x2013;0.62)</td>
<td align="center" valign="top">0.41 (0.33&#x2013;0.51)</td>
<td align="center" valign="top">0.011</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Myocardial strains were measured for both the left ventricular (LV) and right ventricular (RV) myocardium, as shown in <xref ref-type="table" rid="tab5">Table 5</xref>. The average strains in the left ventricle (LV) were substantially greater in patients compared to controls. The median strain in patients was &#x2212;21.1% (IQR &#x2212;23.5 to &#x2212;19.4), whereas in controls it was &#x2212;25.5% (IQR &#x2212;27.3 to &#x2212;24.2). The right ventricular free wall longitudinal strains (RVFWLS) were greater in patients than in controls, with a median of &#x2212;24.5% (IQR &#x2212;26.6 to &#x2212;20.5%) compared to &#x2212;25.5% (IQR &#x2212;28.5 to &#x2212;22.7%). Similarly, the right ventricular four chamber longitudinal strains (RV4CLS) were higher in patients than in controls, with a median of &#x2212;20.6% (IQR &#x2212;23.0 to &#x2212;18.7%) compared to &#x2212;23.3% (IQR &#x2212;25.8 to &#x2212;21.4%). <xref ref-type="fig" rid="fig1">Figure 1</xref> shows an example of the myocardial strain evaluation of a child with DRE.</p>
<table-wrap position="float" id="tab5"><label>Table 5</label>
<caption>
<p>Myocardial strain.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th/>
<th align="center" valign="middle">Patient median, (IQR)</th>
<th align="center" valign="middle">Control median, (IQR)</th>
<th align="center" valign="middle"><italic>p</italic>- value</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">
<italic>N</italic>
</td>
<td align="center" valign="top">27</td>
<td align="center" valign="top">27</td>
<td/>
</tr>
<tr>
<td align="left" valign="top">Strain</td>
<td colspan="3"/>
</tr>
<tr>
<td align="left" valign="top" colspan="4">Left ventricle</td>
</tr>
<tr>
<td align="left" valign="top">A4C</td>
<td align="center" valign="top">&#x2212;21.2 (&#x2212;23.9 to &#x2212;18.48)</td>
<td align="center" valign="top">&#x2212;25.5 (&#x2212;27.3 to &#x2212;24.2)</td>
<td align="center" valign="top">&#x003C;0.001</td>
</tr>
<tr>
<td align="left" valign="top">A2C</td>
<td align="center" valign="top">&#x2212;21.3 (&#x2212;25.2 to &#x2212;19.3)</td>
<td align="center" valign="top">&#x2212;25.0 (&#x2212;27.3 to &#x2212;23.3)</td>
<td align="center" valign="top">0.005</td>
</tr>
<tr>
<td align="left" valign="top">A3C</td>
<td align="center" valign="top">&#x2212;19.9 (&#x2212;23.6 to &#x2212;16.9)</td>
<td align="center" valign="top">&#x2212;24.5 (&#x2212;26.8 to &#x2212;23.2)</td>
<td align="center" valign="top">&#x003C;0.001</td>
</tr>
<tr>
<td align="left" valign="top">Average</td>
<td align="center" valign="top">&#x2212;21.1 (&#x2212;23.5 to &#x2212;19.4)</td>
<td align="center" valign="top">&#x2212;25.5 (&#x2212;27.3 to &#x2212;24.2)</td>
<td align="center" valign="top">&#x003C;0.001</td>
</tr>
<tr>
<td align="left" valign="top" colspan="4">Right ventricle</td>
</tr>
<tr>
<td align="left" valign="top">RVFWLS</td>
<td align="center" valign="top">&#x2212;24.5 (&#x2212;26.6 to &#x2212;20.5)</td>
<td align="center" valign="top">&#x2212;25.5(&#x2212;28.5 to &#x2212;22.7)</td>
<td align="center" valign="top">0.110</td>
</tr>
<tr>
<td align="left" valign="top">RV4CLS</td>
<td align="center" valign="top">&#x2212;20.6 (&#x2212;23.0 to &#x2212;18.7)</td>
<td align="center" valign="top">&#x2212;23.3 (&#x2212;25.8 to &#x2212;21.4)</td>
<td align="center" valign="top">0.014</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>A4C, apical four chamber; A2C, apical two chamber; A3C, apical three chamber; RVFWLS, right ventricular free wall longitudinal strain; RV4CLS, right ventricular four chamber longitudinal strain.</p>
</table-wrap-foot>
</table-wrap>
<p>Our study attempted to evaluate the association between patient characteristics that may significantly impact cardiac function and myocardial strain. These attributes include seizure types, duration of epilepsy, frequency of seizures, and the number of antiseizure medications (ASMs). The corresponding data can be found in <xref ref-type="supplementary-material" rid="SM1">Supplementary Tables S1&#x2013;S4</xref>. However, our subgroup analysis did not reveal significant changes in relationships.</p>
</sec>
<sec sec-type="discussion" id="sec14"><label>4</label>
<title>Discussion</title>
<p>Our study demonstrates that children with DRE have early signs of cardiac dysfunction and myocardial injuries, specifically left ventricular diastolic dysfunctions and abnormal myocardial strains in both ventricles. This is evidenced by a significant decrease in left ventricular diastolic velocity (e&#x2032;) and early mitral E wave inflow velocity and an increase in myocardial strain value in patients when compared to controls of the same age and gender. Our findings further validate the existence of the epileptic heart and enhance the comprehension of SUDEP.</p>
<p>Cardiac dysfunctions have been proposed and recognized as a primary factor contributing to SUDEP in both the pediatric and adult populations with epilepsy, while the supporting evidence has some limitations. Individuals diagnosed with DRE exhibited subclinical impairments in the functioning of the left ventricle of their heart (<xref ref-type="bibr" rid="ref9">9</xref>, <xref ref-type="bibr" rid="ref11">11</xref>, <xref ref-type="bibr" rid="ref24">24</xref>). These impairments were not associated with the length of time patients had epilepsy, the type of seizures they experienced, or how often they had seizures (<xref ref-type="bibr" rid="ref9">9</xref>). Our work provides more evidence for these findings through the utilization of both standard and TDI echocardiograms. However, our investigation did not provide evidence of the impairment of heart systolic functions, as previously recorded in the comprehensive review (<xref ref-type="bibr" rid="ref25">25</xref>). The use of various assessment techniques for evaluating echocardiograms, the disparity in populations, and the small number of patients in each study may all have made it difficult for us to compare differences between our study and others.</p>
<p>Utilizing LVEF alone as an indicator of cardiac dysfunction in DRE patients may result in a delayed diagnosis since it primarily reflects cardiac systolic function. Our work, along with other reports, has demonstrated that EF does not exhibit a substantial change during the early stages of cardiac impairment (<xref ref-type="bibr" rid="ref8">8</xref>, <xref ref-type="bibr" rid="ref9">9</xref>, <xref ref-type="bibr" rid="ref19">19</xref>). Our study proposes the utilization of pulse wave Doppler and TDI echocardiograms to evaluate the decrease in early mitral valve E wave inflow velocity, early diastolic velocity (e&#x2032;) and MPI as indicators of cardiac diastolic dysfunctions in this specific group of patients. These findings were corroborated by other investigations that yielded comparable outcomes (<xref ref-type="bibr" rid="ref8">8</xref>, <xref ref-type="bibr" rid="ref16">16</xref>, <xref ref-type="bibr" rid="ref17">17</xref>, <xref ref-type="bibr" rid="ref19">19</xref>).</p>
<p>Our investigation reveals a notable disparity in myocardial strain between the DRE group and the control group. We confirm that myocardial strain is a reliable method for non-invasively assessing early myocardial injury in children and adolescents with DRE who have normal standard echocardiogram findings. Compared to the conventional evaluation of heart systolic and diastolic functions, it is a more precise measurement for detecting myocardial injury (<xref ref-type="bibr" rid="ref8">8</xref>, <xref ref-type="bibr" rid="ref19">19</xref>). According to the reference range of the Global Longitudinal Strain (GLS) result for the Philips analysis instrument, any value close to zero is considered abnormal (<xref ref-type="bibr" rid="ref21">21</xref>, <xref ref-type="bibr" rid="ref26">26</xref>, <xref ref-type="bibr" rid="ref27">27</xref>). Nevertheless, it is important to utilize caution when interpreting the strain result, as the reference range for pediatrics and adolescents spans a large age range of 0 to 19&#x2009;years old. Merely relying on the absolute value will deem the findings of diastolic function abnormalities from the Doppler and TDI echocardiograms as not clinically relevant. The disparity in strain value has the ability to elucidate the fundamental causes of myocardial injury, which may result in cardiac dysfunction in patients with DRE.</p>
<p>Caution should be taken when interpreting our results, as the study had a small sample size. No further support was found to suggest that anti-seizure medication has any impact on cardiovascular dysfunction. According to previous reports, adverse effects associated with the administration of anti-seizure medication on cardiac function and conduction have been documented (<xref ref-type="bibr" rid="ref28 ref29 ref30">28&#x2013;30</xref>). However, our research was unable to find a connection between the various types, quantities, and duration of anti-seizure medication and cardiac dysfunction. Furthermore, it is conceivable that cardiac dysfunction may result from several reasons, including channelopathy in genetic epilepsy syndromes such as <italic>SCN1A</italic> and <italic>SCN8A</italic>. These genetic variations have been recognized as causal factors in cardiac conduction anomalies and SUDEP (<xref ref-type="bibr" rid="ref28">28</xref>, <xref ref-type="bibr" rid="ref31">31</xref>, <xref ref-type="bibr" rid="ref32">32</xref>). Increasing patient enrollment could improve the statistical power of the study in identifying this relationship between variables.</p>
</sec>
<sec sec-type="conclusions" id="sec15"><label>5</label>
<title>Conclusion</title>
<p>Children diagnosed with DRE exhibit compromised subclinical cardiac function, specifically in terms of left ventricular diastolic function and myocardial strain. This suggests a reduction in myocardial deformation and contraction when compared to a control group. Employing conventional echocardiography to identify noticeable structural abnormalities and reduce LVEF may result in a delay in diagnosing cardiac dysfunction in these individuals. Further research using a more extensive cohort of patients and extended follow-up assessments is necessary to evaluate the clinical result. Pulse Doppler and TDI echocardiograms in combination with MSE can be utilized to screen children with DRE for prompt identification and treatment of their cardiac dysfunction, hence mitigating the risk of SUDEP.</p>
</sec>
<sec sec-type="data-availability" id="sec16">
<title>Data availability statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p>
</sec>
<sec sec-type="ethics-statement" id="sec17">
<title>Ethics statement</title>
<p>The studies involving humans were approved by Chiang Mai University&#x2019;s Ethics Committee. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation in this study was provided by the participants&#x2019; legal guardians/next of kin. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.</p>
</sec>
<sec sec-type="author-contributions" id="sec18">
<title>Author contributions</title>
<p>WS: Data curation, Formal analysis, Investigation, Writing &#x2013; original draft. KI: Investigation, Writing &#x2013; review &#x0026; editing. KS: Data curation, Validation, Writing &#x2013; review &#x0026; editing. NW: Resources, Writing &#x2013; review &#x0026; editing. RS: Investigation, Writing &#x2013; review &#x0026; editing. KK: Resources, Writing &#x2013; review &#x0026; editing. SS: Writing &#x2013; review &#x0026; editing. CS: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Supervision, Validation, Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing.</p>
</sec>
</body>
<back>
<sec sec-type="funding-information" id="sec19">
<title>Funding</title>
<p>The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The research was financially supported by the Research Affairs of the Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand with a grant number 42&#x2013;66.</p>
</sec>
<ack>
<p>We extend our gratitude to all the participants and their families for being involved in this research project.</p>
</ack>
<sec sec-type="COI-statement" id="sec20">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="sec100" sec-type="disclaimer">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<sec sec-type="supplementary-material" id="sec21">
<title>Supplementary material</title>
<p>The Supplementary material for this article can be found online at: <ext-link xlink:href="https://www.frontiersin.org/articles/10.3389/fneur.2024.1381293/full#supplementary-material" ext-link-type="uri">https://www.frontiersin.org/articles/10.3389/fneur.2024.1381293/full#supplementary-material</ext-link></p>
<supplementary-material xlink:href="Table_1.docx" id="SM1" mimetype="application/vnd.openxmlformats-officedocument.wordprocessingml.document" xmlns:xlink="http://www.w3.org/1999/xlink"/>
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