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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Cardiovasc. Med.</journal-id>
<journal-title>Frontiers in Cardiovascular Medicine</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Cardiovasc. Med.</abbrev-journal-title>
<issn pub-type="epub">2297-055X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fcvm.2022.973530</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Cardiovascular Medicine</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>The characteristics of thoracic aortic dissection in autopsy-diagnosed individuals: An autopsy study</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Zhao</surname> <given-names>Qianhao</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="author-notes" rid="fn002"><sup>&#x02020;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1003059/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Yin</surname> <given-names>Kun</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="author-notes" rid="fn002"><sup>&#x02020;</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Zhou</surname> <given-names>Nan</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="author-notes" rid="fn002"><sup>&#x02020;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1968320/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Wu</surname> <given-names>Qiuping</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<xref ref-type="author-notes" rid="fn002"><sup>&#x02020;</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Xiao</surname> <given-names>Yuxi</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Zheng</surname> <given-names>Jinxiang</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
<xref ref-type="aff" rid="aff5"><sup>5</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Zheng</surname> <given-names>Da</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Bi</surname> <given-names>Qiming</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Quan</surname> <given-names>Li</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Hu</surname> <given-names>Bingjie</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x0002A;</sup></xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Cheng</surname> <given-names>Jianding</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="corresp" rid="c002"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1795519/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Faculty of Forensic Medicine, Zhongshan School of Medicine, Sun Yat-sen University</institution>, <addr-line>Guangzhou</addr-line>, <country>China</country></aff>
<aff id="aff2"><sup>2</sup><institution>Guangdong Province Translational Forensic Medicine Engineering Technology Research Center, Sun Yat-Sen University</institution>, <addr-line>Guangzhou</addr-line>, <country>China</country></aff>
<aff id="aff3"><sup>3</sup><institution>Division of Forensic Medicine, Department of Pathology, School of Basic Medical Sciences, Guangzhou Medical University</institution>, <addr-line>Guangzhou</addr-line>, <country>China</country></aff>
<aff id="aff4"><sup>4</sup><institution>Department of Molecular Pathology, The Affiliated Cancer Hospital of Zhengzhou University</institution>, <addr-line>Zhengzhou</addr-line>, <country>China</country></aff>
<aff id="aff5"><sup>5</sup><institution>Henan Key Laboratory of Molecular Pathology</institution>, <addr-line>Zhengzhou</addr-line>, <country>China</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited by: Pasqualino Sirignano, Sapienza University of Rome, Italy</p></fn>
<fn fn-type="edited-by"><p>Reviewed by: Jia Hu, Sichuan University, China; Cristoforo Pomara, University of Catania, Italy</p></fn>
<corresp id="c001">&#x0002A;Correspondence: Bingjie Hu <email>hubingjie&#x00040;126.com</email></corresp>
<corresp id="c002">Jianding Cheng <email>chengjd&#x00040;mail.sysu.edu.cn</email></corresp>
<fn fn-type="other" id="fn001"><p>This article was submitted to Atherosclerosis and Vascular Medicine, a section of the journal Frontiers in Cardiovascular Medicine</p></fn>
<fn fn-type="equal" id="fn002"><p>&#x02020;These authors have contributed equally to this work and share first authorship</p></fn></author-notes>
<pub-date pub-type="epub">
<day>11</day>
<month>10</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="collection">
<year>2022</year>
</pub-date>
<volume>9</volume>
<elocation-id>973530</elocation-id>
<history>
<date date-type="received">
<day>20</day>
<month>06</month>
<year>2022</year>
</date>
<date date-type="accepted">
<day>20</day>
<month>09</month>
<year>2022</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2022 Zhao, Yin, Zhou, Wu, Xiao, Zheng, Zheng, Bi, Quan, Hu and Cheng.</copyright-statement>
<copyright-year>2022</copyright-year>
<copyright-holder>Zhao, Yin, Zhou, Wu, Xiao, Zheng, Zheng, Bi, Quan, Hu and Cheng</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>
<p>Thoracic aortic dissection (TAD) is the most common cause of sudden cardiac death associated with aortic diseases. The age of TAD victims in forensic studies is significantly younger than hospitalized patients with TAD, while only a few studies have been conducted on autopsy-diagnosed TAD deceased. A retrospective study was conducted at the Medicolegal Center of Sun Yat-sen University from 1999 to 2019 to address the characteristics of TAD victims. A total of 200 deceased from spontaneous rupture of TAD were assessed, with 165 (82.5%) males and 175 (87.5%) Stanford type A deceased. Our main results showed that compared with patients with TAD diagnosed during their lifetime, individuals diagnosed with TAD until an autopsy showed an earlier onset (43.80 years old) and less accompanied hypertension (&#x0003C;50%). Sudden death was the initial symptom of 32 decedents. Instead of chest/back pain (40 decedents), abdominal pain (59 decedents) was the most common initial symptom, and 42 decedents presented with no accompanying pain. A higher proportion of abdominal pain and the painless symptom was associated with a higher risk of misdiagnosis. Women showed a more atypical clinical presentation and rapid progression than men. Younger decedents showed more pronounced left heart changes. The present study implicated the TAD individuals diagnosed until an autopsy as a particular entity, indicating the urgent need for further investigation on early diagnosis and pathogenesis of patients with TAD with atypical pain and painless or with younger age to reduce the burden of TAD-related sudden death.</p></abstract>
<kwd-group>
<kwd>thoracic aortic dissection</kwd>
<kwd>sudden death</kwd>
<kwd>forensic autopsy</kwd>
<kwd>epidemiology</kwd>
<kwd>retrospective study</kwd>
</kwd-group>
<contract-num rid="cn001">81901919</contract-num>
<contract-num rid="cn001">81920108021</contract-num>
<contract-sponsor id="cn001">National Natural Science Foundation of China<named-content content-type="fundref-id">10.13039/501100001809</named-content></contract-sponsor>
<contract-sponsor id="cn002">Guangzhou Municipal Science and Technology Project<named-content content-type="fundref-id">10.13039/501100010256</named-content></contract-sponsor>
<contract-sponsor id="cn003">Natural Science Foundation of Guangdong Province<named-content content-type="fundref-id">10.13039/501100003453</named-content></contract-sponsor>
<counts>
<fig-count count="2"/>
<table-count count="6"/>
<equation-count count="0"/>
<ref-count count="43"/>
<page-count count="10"/>
<word-count count="6090"/>
</counts>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="s1">
<title>Introduction</title>
<p>Thoracic aortic dissection (TAD) is an emergent and life-threatening cardiovascular disease resulting in sudden cardiac death (SCD). Hospital studies have ascertained the annual incidence of acute aortic dissection (AAD) of about three cases per 100,000 (<xref ref-type="bibr" rid="B1">1</xref>), which may underestimate the incidence of aortic dissection as hospital-based reports do not account for preadmission deaths (<xref ref-type="bibr" rid="B2">2</xref>&#x02013;<xref ref-type="bibr" rid="B5">5</xref>). Thus, these deaths are not accounted for unless an autopsy is performed. Systematic and standardized autopsy investigation is crucial for forensic pathologists to determine the cause of death of SCD victims (<xref ref-type="bibr" rid="B6">6</xref>). Our previous study reported that rupture of aortic dissection accounts for 5.2% of SCD victims (<xref ref-type="bibr" rid="B7">7</xref>). Prakash et al. (<xref ref-type="bibr" rid="B8">8</xref>) found that the age of TAD decedents was significantly younger than hospitalized patients with TAD, which indicated that autopsy-diagnosed TAD decedents might be a particular entity in TAD cases. However, only a few studies have been conducted on TAD deceased, and the sample size was too small to further investigate. Large sample size study of TAD deceased who were diagnosed until an autopsy could help us to uncover the nature of the particular TAD entity.</p>
<p>Our study recruiting 200 autopsy cases of TAD showed the characteristics of TAD deceased and identified that forensic autopsy is essential for determining the cause of death in sudden death cases and provides valuable additional information for physicians to further understand TAD. The prompt investigation of forensic autopsy data is indispensable to revealing pivotal information about TAD.</p>
</sec>
<sec sec-type="methods" id="s2">
<title>Methods</title>
<sec>
<title>Study subjects</title>
<p>A retrospective study of forensic autopsy cases at the Medicolegal Center of Sun Yat-sen University was conducted. Autopsy reports that listed the primary cause of death as spontaneous rupture of TAD from 1999 to 2019 were reviewed. Decedents who died due to traumatic, iatrogenic TAD, or for who without a complete autopsy were excluded. Thus, 200 adult cases (&#x02265;18 years old) who met the study inclusion criteria formed the TAD group. As for control cases, each decedent from the TAD group was sex- and age-matched (same sex, with an age difference of no more than 3 years, with a death time difference of no more than 2 years) with three separate cases and decedents with aorta-related disease (intramural hematoma, penetrating aortic ulcer, aortic pseudoaneurysm, thoracic aortic aneurysms, abdominal aortic aneurysm/dissection, and aortic tumors) were excluded. All the control cases, aggregate up to 600, were classified into the control group. All the procedures followed were in accordance with the ethical standards of Sun Yat-sen University (approval no. 2019-004).</p>
</sec>
<sec>
<title>Data collection</title>
<p>We retrospectively collected the index event&#x00027;s circumstances, including demographic data and medical history. Pathological data, including the location and extent of TAD, myocardial characteristics and dimensions, aortic and epicardial atherosclerotic diseases, and other congenital disabilities, was obtained from autopsy reports.</p>
</sec>
<sec>
<title>Statistical analysis</title>
<p>Continuous variables were presented as mean &#x000B1; SEM or median (interquartile range) and analyzed using the unpaired Student&#x00027;s <italic>t</italic>-test or Mann&#x02013;Whitney <italic>U</italic>-test. Categorical variables were expressed as the count (percent) and analyzed using the Pearson&#x00027;s chi-squared test and Fisher&#x00027;s exact test. A measure probability value of <italic>P</italic> &#x0003C;.05 was considered significant. Statistical evaluation was performed using SPSS Statistics version 22.0 (IBM Incorporation, Chicago, Illinois, USA).</p>
</sec>
</sec>
<sec sec-type="results" id="s3">
<title>Results</title>
<sec>
<title>Demographics</title>
<p>Overall, 200 deaths from spontaneous rupture of TAD were identified in a population aged from 19 to 73 years old, and the average age was 43.80 &#x000B1; 0.75 years old; a total of 165 cases (82.5%) were male (<xref ref-type="table" rid="T1">Table 1</xref>). The TAD decedents in this study spanned more than 20 years, with significantly more decedents in the latter decade (149 decedents, 2010&#x02013;2009) than in the first decade (51 decedents, 1999&#x02013;2009). Still, there were no significant differences in the mean age at death, age distribution, and sex distribution between the two decades.</p>
<table-wrap position="float" id="T1">
<label>Table 1</label>
<caption><p>Demographic characteristics of TAD cases.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th/>
<th valign="top" align="center"><bold>Total (<italic>n</italic> = 200)</bold></th>
<th valign="top" align="center"><bold>Male (<italic>n</italic> = 165)</bold></th>
<th valign="top" align="center"><bold>Female (<italic>n</italic> = 35)</bold></th>
<th valign="top" align="center"><bold><italic>p</italic>-value</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Age (Mean &#x000B1; SD)</td>
<td valign="top" align="center">43.80 &#x000B1; 0.75</td>
<td valign="top" align="center">43.75 &#x000B1; 0.82</td>
<td valign="top" align="center">44.11 &#x000B1; 10.67</td>
<td valign="top" align="center">0.8539</td>
</tr>
<tr>
<td valign="top" align="left">Age distribution [<italic>n</italic> (%)]</td>
<td/>
<td/>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;19&#x02013;30</td>
<td valign="top" align="center">22 (11)</td>
<td valign="top" align="center">18 (10.91)</td>
<td valign="top" align="center">4 (11.43)</td>
<td valign="top" align="center">0.941</td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;31&#x02013;40</td>
<td valign="top" align="center">55 (27.5)</td>
<td valign="top" align="center">47 (28.48)</td>
<td valign="top" align="center">8 (22.86)</td>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;41&#x02013;50</td>
<td valign="top" align="center">74 (37)</td>
<td valign="top" align="center">59 (35.76)</td>
<td valign="top" align="center">15 (42.86)</td>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;51&#x02013;60</td>
<td valign="top" align="center">37 (18.5)</td>
<td valign="top" align="center">31 (18.79)</td>
<td valign="top" align="center">6 (17.14)</td>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;61&#x02013;73</td>
<td valign="top" align="center">12 (6)</td>
<td valign="top" align="center">10 (6.06)</td>
<td valign="top" align="center">2 (5.71)</td>
<td/>
</tr>
<tr>
<td valign="top" align="left">Stanford type [<italic>n</italic> (%)]</td>
<td/>
<td/>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Stanford A</td>
<td valign="top" align="center">175 (87.5)</td>
<td valign="top" align="center">142 (86.06)</td>
<td valign="top" align="center">33 (94.29)</td>
<td valign="top" align="center">0.2622</td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Stanford B</td>
<td valign="top" align="center">25 (12.5)</td>
<td valign="top" align="center">23 (13.94)</td>
<td valign="top" align="center">2 (5.71)</td>
<td/>
</tr>
</tbody>
</table>
</table-wrap>
<p>The TAD decedent number during the warmer period (85 decedents, May to October) in Southern China was less than that during the colder period (115 decedents, November to April) in our study. However, 60% (21 decedents) of female TAD died during the warm period, compared with only 38.32% (64 decedents, <italic>P</italic> = 0.0211) of the total male TAD deaths during the same period.</p>
</sec>
<sec>
<title>Clinical data</title>
<p>Unfortunately, thirty-two victims (16%) have not been able to get to the hospital, and sudden death was their initial symptom (female: 8 in 35, 22.86%; male: 24 in 165, 14.55%). Meanwhile, the rest victims died very soon after admission to the emergency room. A total of 168 (84%) intervals from hospital admission to clinical death of TAD deaths were recorded. Seventy-one decedents (42.26%) died within 12 h, and 102 decedents (60.71%) died within 24 h. The interval from hospitalization to clinical death (IHD), with 17.5 (5.84, 41.21) h in men and 10.17 (3.33, 32) h in women, revealed a trend (<italic>P</italic> = 0.1966) in favor of men, and the median absolute difference of 7.33 h was likely to reveal the more urgent situation for women.</p>
<p>Excluding the TAD cases with sudden death as the initial symptom, abdominal pain was the most common symptom [59 decedents, 35.12% (<xref ref-type="table" rid="T2">Table 2</xref>)]. Rightfully, the most common misdiagnosis was acute abdomen. The acute onset of severe chest/back pain was the second most common initial complaint (40 decedents, 23.81%). In addition, the TAD deceased with headache or low back pain as their initial symptom showed a lower TAD suspected diagnosis ratio and a shorter IHD than those initially with chest/back pain or abdominal pain (<xref ref-type="table" rid="T2">Table 2</xref>). Meanwhile, 42 decedents (25%) presented with no accompanying pain in the present study. Syncope, chest distress, distention, and hemiplegia or paresis were the primary manifestations among these painless TAD deceased (<xref ref-type="table" rid="T2">Table 2</xref>). Painless TAD deceased showed a lower TAD suspected diagnosis ratio [4.76 vs. 12.70% (<xref ref-type="table" rid="T2">Table 2</xref>)] and a shorter IHD [10.98 (3.20, 30.00) vs. 18.67 (6, 42.09) (<xref ref-type="table" rid="T2">Table 2</xref>)] than the painful TAD deceased. Surprisingly, the proportion of painless victims was slightly higher among females than males (40.74 vs. 21.99%, <italic>P</italic> = 0.0519).</p>
<table-wrap position="float" id="T2">
<label>Table 2</label>
<caption><p>Initial symptoms of TAD deceased whose prior symptom was not sudden death.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th valign="top" align="left"><bold>Initial symptoms</bold></th>
<th valign="top" align="center"><bold>Total (<italic>n</italic> = 168)</bold><break/> <bold>n (%)</bold></th>
<th valign="top" align="center"><bold>Suspected TAD (<italic>n</italic> = 18)</bold><break/> <bold><italic>n</italic> (%)</bold></th>
<th valign="top" align="center"><bold>IHD<xref ref-type="table-fn" rid="TN1"><sup>$</sup></xref> (hours) Median (IQR)</bold></th>
<th valign="top" align="center"><bold><italic>p</italic>-value</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Pain</td>
<td valign="top" align="center">126 (75)</td>
<td valign="top" align="center">16 (12.70)</td>
<td valign="top" align="center">18.67 (6, 42.09)</td>
<td valign="top" align="center">0.0716<xref ref-type="table-fn" rid="TN2"><sup>&#x0002A;</sup></xref></td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Headache</td>
<td valign="top" align="center">9 (5.36)</td>
<td valign="top" align="center">0</td>
<td valign="top" align="center">9 (3.20, 11.84)</td>
<td valign="top" align="center">0.0114<xref ref-type="table-fn" rid="TN3"><sup>&#x00023;</sup></xref></td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Chest pain or back pain</td>
<td valign="top" align="center">40 (23.81)</td>
<td valign="top" align="center">9 (22.5)</td>
<td valign="top" align="center">24.93 (10.72, 69.93)</td>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Abdominal pain</td>
<td valign="top" align="center">59 (35.12)</td>
<td valign="top" align="center">7 (11.86)</td>
<td valign="top" align="center">19 (5.63, 39.98)</td>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Low back pain</td>
<td valign="top" align="center">18 (10.71)</td>
<td valign="top" align="center">0</td>
<td valign="top" align="center">9.71 (5.08, 26.00)</td>
<td/>
</tr>
<tr>
<td valign="top" align="left">Painless</td>
<td valign="top" align="center">42 (25)</td>
<td valign="top" align="center">2 (4.76)</td>
<td valign="top" align="center">10.98 (3.20, 30.00)</td>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Dizziness or syncope</td>
<td valign="top" align="center">13 (7.74)</td>
<td valign="top" align="center">1 (7.69)</td>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Chest distress</td>
<td valign="top" align="center">8 (4.76)</td>
<td valign="top" align="center">0</td>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Distention or emesis</td>
<td valign="top" align="center">7 (4.17)</td>
<td valign="top" align="center">0</td>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Hemiplegia or paresis</td>
<td valign="top" align="center">6 (3.57)</td>
<td valign="top" align="center">1 (16.67)</td>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Cold</td>
<td valign="top" align="center">8 (4.76)</td>
<td valign="top" align="center">0</td>
<td/>
<td/>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="TN1"><label>$</label><p>Interval from hospitalization to clinical death.</p></fn>
<fn id="TN2"><label>&#x0002A;</label><p>p-value of intervals between painful deceased and painless deceased.</p></fn>
<fn id="TN3"><label>&#x00023;</label><p>p-value of intervals within painful deceased.</p></fn>
</table-wrap-foot>
</table-wrap>
<p>The clinical characteristics and outcomes in deceased with TAD vary with age. Compared with the older TAD deceased [&#x0003E;35 years old, 157 decedents, 47 (41, 52) years old], the incidence of sudden death as the initial symptom in youngers [&#x02264;35 years old, 43 decedents, 30 (26, 33) years old] was significantly higher (27.91 vs. 12.74%, <italic>P</italic> = 0.0319), while the incidence of painless TAD deceased was significantly lower among younger victims than older victims (6.45 vs. 29.20%, <italic>P</italic> = 0.0061).</p>
<p>Hypertension is an independent risk factor for TAD. In the present study, only 55.17% (32 in 58 available cases) of TAD deceased had a history of hypertension, and 48.74% (58 in 119 available cases) of TAD deceased with systolic blood pressure (SBP) &#x02265;140 mm Hg.</p>
</sec>
<sec>
<title>Autopsy findings</title>
<p>Autopsy findings are shown in <xref ref-type="table" rid="T3">Table 3</xref>. According to Stanford classification, Stanford type A (175 cases, 87.5%) deceased was much more common than Stanford type B (25 cases, 12.5%). Dissection extended to the abdominal aorta in 41 victims (type A: 35). The intimal tear was most often single. Only in 8 cases, there were two tears, and in 1 case, there were three tears. The intimal tear was mainly found at ascending aorta in type A decedents, while at descending aorta in type B decedents, which was the same with the adventitial tear. Therefore, cardiac tamponade due to a rupture of the dissected channel into the pericardial sac was the most common cause of death for type A TAD decedents (167 of 175, 95.43%).</p>
<table-wrap position="float" id="T3">
<label>Table 3</label>
<caption><p>Postmortem findings in TAD deceased.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th valign="top" align="left"><bold>Postmortem findings</bold></th>
<th valign="top" align="center"><bold>Total <italic>n</italic> = 200</bold><break/> <bold><italic>n</italic> (%)</bold></th>
<th valign="top" align="center"><bold>Type A <italic>n</italic> = 175</bold><break/> <bold><italic>n</italic> (%)</bold></th>
<th valign="top" align="center"><bold>Type B <italic>n</italic> = 25</bold><break/> <bold><italic>n</italic> (%)</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Entry tear</td>
<td/>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Ascending aorta</td>
<td valign="top" align="center">145 (72.5)</td>
<td valign="top" align="center">145 (82.86)</td>
<td valign="top" align="center">0 (0)</td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Arch of aorta</td>
<td valign="top" align="center">37 (18.5)</td>
<td valign="top" align="center">25 (14.29)</td>
<td valign="top" align="center">12 (48)</td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Descending aorta</td>
<td valign="top" align="center">24 (12)</td>
<td valign="top" align="center">10 (5.71)</td>
<td valign="top" align="center">14 (56)</td>
</tr>
<tr>
<td valign="top" align="left">Exit tear</td>
<td/>
<td/>
<td/>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Ascending aorta</td>
<td valign="top" align="center">165 (82.5)</td>
<td valign="top" align="center">165 (94.29)</td>
<td valign="top" align="center">0 (0)</td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Arch of aorta</td>
<td valign="top" align="center">13 (6.5)</td>
<td valign="top" align="center">4 (2.29)</td>
<td valign="top" align="center">9 (36)</td>
</tr>
<tr>
<td valign="top" align="left">&#x000A0;&#x000A0;&#x000A0;Descending aorta</td>
<td valign="top" align="center">24 (12)</td>
<td valign="top" align="center">7 (4)</td>
<td valign="top" align="center">17 (68)</td>
</tr>
<tr>
<td valign="top" align="left">Cardiac tamponade</td>
<td valign="top" align="center">167 (83.5)</td>
<td valign="top" align="center">167 (95.43)</td>
<td valign="top" align="center">0 (0)</td>
</tr>
<tr>
<td valign="top" align="left">Thoracic hemorrhage</td>
<td valign="top" align="center">56 (28)</td>
<td valign="top" align="center">32 (18.29)</td>
<td valign="top" align="center">24 (96)</td>
</tr>
<tr>
<td valign="top" align="left">MFS</td>
<td valign="top" align="center">1 (0.5)</td>
<td valign="top" align="center">1 (0.57)</td>
<td valign="top" align="center">0 (0)</td>
</tr>
<tr>
<td valign="top" align="left">BAV</td>
<td valign="top" align="center">8 (4)</td>
<td valign="top" align="center">8 (4.57)</td>
<td valign="top" align="center">0 (0)</td>
</tr>
<tr>
<td valign="top" align="left">Coronary atherosclerosis</td>
<td valign="top" align="center">45 (22.5)</td>
<td valign="top" align="center">42 (24)</td>
<td valign="top" align="center">3 (12)</td>
</tr>
<tr>
<td valign="top" align="left">Renal cyst</td>
<td valign="top" align="center">16 (8)</td>
<td valign="top" align="center">14 (8)</td>
<td valign="top" align="center">2 (8)</td>
</tr>
<tr>
<td valign="top" align="left">Heart weight (g)</td>
<td valign="top" align="center">450 (400, 500)</td>
<td valign="top" align="center">450 (400, 510)</td>
<td valign="top" align="center">400 (355, 485)</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Pathological examination of the hearts from most TAD autopsy cases showed severe ventricular hypertrophy with an average cardiac mass of 450 (400, 500) g [control: 360 (300, 410) g, <italic>P</italic> &#x0003C; 0.0001 (<xref ref-type="table" rid="T4">Table 4</xref>)] and an average left ventricular-free wall thickness of 1.4 (1.2, 1.5) cm [control: 1.2 (1.1, 1.4) cm, <italic>P</italic> &#x0003C; 0.0001 (<xref ref-type="table" rid="T4">Table 4</xref>)]. As for the circumference of the cardiac valve annulus, except for the tricuspid annulus, the circumferences of the mitral/aortic/pulmonary annulus in the TAD group were significantly longer than those in the control group. Furthermore, we found that younger TAD decedents showed more pronounced changes in the left heart than their control counterparts. Compared with their control counterparts, younger TAD decedents not only had thicker left ventricular free wall [1.4 (1.2, 1.5) vs. 1.2 (1.0, 1.3) cm, <italic>P</italic> &#x0003C; 0.0001 (<xref ref-type="table" rid="T5">Table 5</xref>)] and longer circumference of the aortic annulus (CAA) [7.8 (7, 8.5) vs. 6.5 (6, 7) cm, <italic>P</italic> &#x0003C; 0.0001 (<xref ref-type="table" rid="T5">Table 5</xref>)], but also had a longer circumference of the mitral annulus (CMA) [9.7 (9, 10.5) vs. 9 (8.5, 9.5) cm, <italic>P</italic> = 0.0007 (<xref ref-type="table" rid="T5">Table 5</xref>)]. In addition, the differences in heart weight, CMA, and CAA between younger TAD and their control counterparts were more significant than those between older TAD and their control counterparts [heart weight: 90 vs. 70 g, CMA: 0.7 vs. 0 cm, and CAA: 1.3 vs. 0.5 cm (<xref ref-type="table" rid="T5">Table 5</xref>)].</p>
<table-wrap position="float" id="T4">
<label>Table 4</label>
<caption><p>Postmortem finding differences between TAD deceased and control counterparts.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th/>
<th valign="top" align="center"><bold>TAD (<italic>n</italic> = 200)</bold></th>
<th valign="top" align="center"><bold>Control (<italic>n</italic> = 600)</bold></th>
<th valign="top" align="center"><bold><italic>p</italic>-value</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Height (cm)</td>
<td valign="top" align="center">169 (163, 173)</td>
<td valign="top" align="center">165 (160, 170)</td>
<td valign="top" align="center">&#x0003C;0.0001</td>
</tr>
<tr>
<td valign="top" align="left">Heart weight (g)</td>
<td valign="top" align="center">450 (400, 500)</td>
<td valign="top" align="center">360 (300, 410)</td>
<td valign="top" align="center">&#x0003C;0.0001</td>
</tr>
<tr>
<td valign="top" align="left">TLV (cm)</td>
<td valign="top" align="center">1.4 (1.2, 1.5)</td>
<td valign="top" align="center">1.2 (1.1, 1.4)</td>
<td valign="top" align="center">&#x0003C;0.0001</td>
</tr>
<tr>
<td valign="top" align="left">TRV (cm)</td>
<td valign="top" align="center">0.3 (0.3, 0.4)</td>
<td valign="top" align="center">0.3 (0.3, 0.3)</td>
<td valign="top" align="center">&#x0003C;0.0001</td>
</tr>
<tr>
<td valign="top" align="left">CMA (cm)</td>
<td valign="top" align="center">9.5 (9, 10)</td>
<td valign="top" align="center">9.2 (8.5, 10)</td>
<td valign="top" align="center">0.0107</td>
</tr>
<tr>
<td valign="top" align="left">CTA (cm)</td>
<td valign="top" align="center">11.5 (11, 12)</td>
<td valign="top" align="center">11.5 (11, 12.23)</td>
<td valign="top" align="center">0.9304</td>
</tr>
<tr>
<td valign="top" align="left">CAA (cm)</td>
<td valign="top" align="center">7.5 (7, 8)</td>
<td valign="top" align="center">7 (6.5, 7.5)</td>
<td valign="top" align="center">&#x0003C;0.0001</td>
</tr>
<tr>
<td valign="top" align="left">CPA (cm)</td>
<td valign="top" align="center">8 (7.5, 8.5)</td>
<td valign="top" align="center">7.55 (7, 8)</td>
<td valign="top" align="center">0.0208</td>
</tr>
<tr>
<td valign="top" align="left">Coronary atherosclerosis (%)</td>
<td valign="top" align="center">45 (22.5)</td>
<td valign="top" align="center">99 (16.5)</td>
<td valign="top" align="center">0.0703</td>
</tr>
<tr>
<td valign="top" align="left">Renal cyst (%)</td>
<td valign="top" align="center">16 (8)</td>
<td valign="top" align="center">22 (3.67)</td>
<td valign="top" align="center">0.0197</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>TLV, Thickness of left ventricular wall; TRV, Thickness of right ventricular wall; CTA, Circumference of tricuspid annulus; CPA, Circumference of pulmonary annulus; CMA, Circumference of mitral annulus; CAA, Circumference of aortic annulus.</p>
</table-wrap-foot>
</table-wrap>
<table-wrap position="float" id="T5">
<label>Table 5</label>
<caption><p>Differences of postmortem findings between different age groups and their control counterparts.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th valign="top" align="left"><bold>Age&#x02264;35</bold></th>
<th valign="top" align="center"><bold>TAD</bold><break/> <bold>(<italic>n</italic> = 43)</bold></th>
<th valign="top" align="center"><bold>CTR</bold><break/> <bold>(<italic>n</italic> = 129)</bold></th>
<th valign="top" align="center"><bold><italic>p</italic>-value</bold></th>
<th valign="top" align="center"><bold>Age&#x0003E;35</bold></th>
<th valign="top" align="center"><bold>TAD</bold><break/> <bold>(<italic>n</italic> = 157)</bold></th>
<th valign="top" align="center"><bold>CTR</bold><break/> <bold>(<italic>n</italic> = 471)</bold></th>
<th valign="top" align="center"><bold><italic>p</italic>-value</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Height (cm)</td>
<td valign="top" align="center">172.57 &#x000B1; 1.37</td>
<td valign="top" align="center">167.03 &#x000B1; 0.63</td>
<td valign="top" align="center">0.0005</td>
<td valign="top" align="center">Height (cm)</td>
<td valign="top" align="center">168 (161, 172)</td>
<td valign="top" align="center">165 (160, 170)</td>
<td valign="top" align="center">0.003</td>
</tr>
<tr>
<td valign="top" align="left">Heart weight (g)</td>
<td valign="top" align="center">400 (360, 460)</td>
<td valign="top" align="center">310 (280, 380)</td>
<td valign="top" align="center">&#x0003C;0.0001</td>
<td valign="top" align="center">Heart weight (g)</td>
<td valign="top" align="center">450 (400, 515)</td>
<td valign="top" align="center">380 (300, 420)</td>
<td valign="top" align="center">&#x0003C;0.0001</td>
</tr>
<tr>
<td valign="top" align="left">TLV (cm)</td>
<td valign="top" align="center">1.4 (1.2, 1.5)</td>
<td valign="top" align="center">1.2 (1.0, 1.3)</td>
<td valign="top" align="center">&#x0003C;0.0001</td>
<td valign="top" align="center">TLV (cm)</td>
<td valign="top" align="center">1.4 (1.2, 1.55)</td>
<td valign="top" align="center">1.3 (1.1, 1.4)</td>
<td valign="top" align="center">&#x0003C;0.0001</td>
</tr>
<tr>
<td valign="top" align="left">TRV (cm)</td>
<td valign="top" align="center">0.3 (0.3, 0.4)</td>
<td valign="top" align="center">0.3 (0.3, 0.3)</td>
<td valign="top" align="center">0.0089</td>
<td valign="top" align="center">TRV (cm)</td>
<td valign="top" align="center">0.3 (0.3, 0.4)</td>
<td valign="top" align="center">0.3 (0.3, 0.4)</td>
<td valign="top" align="center">0.0003</td>
</tr>
<tr>
<td valign="top" align="left">CMA (cm)</td>
<td valign="top" align="center">9.7 (9, 10.5)</td>
<td valign="top" align="center">9 (8.5, 9.5)</td>
<td valign="top" align="center">0.0007</td>
<td valign="top" align="center">CMA (cm)</td>
<td valign="top" align="center">9.5 (9, 10)</td>
<td valign="top" align="center">9.5 (9, 10)</td>
<td valign="top" align="center">0.332</td>
</tr>
<tr>
<td valign="top" align="left">CTA (cm)</td>
<td valign="top" align="center">11.5 (11, 13)</td>
<td valign="top" align="center">11.5 (11, 12)</td>
<td valign="top" align="center">0.2391</td>
<td valign="top" align="center">CTA (cm)</td>
<td valign="top" align="center">11.5 (11, 12)</td>
<td valign="top" align="center">11.8 (11, 12.5)</td>
<td valign="top" align="center">0.4046</td>
</tr>
<tr>
<td valign="top" align="left">CAA (cm)</td>
<td valign="top" align="center">7.8 (7, 8.5)</td>
<td valign="top" align="center">6.5 (6, 7)</td>
<td valign="top" align="center">&#x0003C;0.0001</td>
<td valign="top" align="center">CAA (cm)</td>
<td valign="top" align="center">7.5 (7, 8)</td>
<td valign="top" align="center">7 (6.5, 7.5)</td>
<td valign="top" align="center">&#x0003C;0.0001</td>
</tr>
<tr>
<td valign="top" align="left">CPA (cm)</td>
<td valign="top" align="center">8 (7, 8.5)</td>
<td valign="top" align="center">7.5 (7, 8)</td>
<td valign="top" align="center">0.0151</td>
<td valign="top" align="center">CPA (cm)</td>
<td valign="top" align="center">8 (7.5, 8.5)</td>
<td valign="top" align="center">8 (7.2, 8.5)</td>
<td valign="top" align="center">0.2147</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>The most common congenital disorder found in this study was bicuspid aortic valves (BAV) [eight cases, 4%, all Stanford A (<xref ref-type="table" rid="T3">Table 3</xref>, <xref ref-type="fig" rid="F1">Figure 1</xref>)], classified by autopsy. Only one deceased was found with Marfan syndrome (MFS). The prevalence of coronary atherosclerosis in the TAD group was slightly higher than in controls (22.5 vs. 16.5%, <italic>P</italic> = 0.0703), but generally, there is no association of coronary atherosclerosis with TAD. Patients with TAD were reported to have a greater prevalence of renal cysts on CT than healthy controls. Our findings regarding the detection rate of renal cysts in TAD deceased were consistent with this [8 vs. 3.67%, <italic>P</italic> = 0.0197 (<xref ref-type="table" rid="T3">Table 3</xref>)]. As to microscopic examination of medial alteration, the mucoid extracellular matrix accumulation (MEMA) was confirmed in all the available cases to varying grades (<xref ref-type="fig" rid="F2">Figure 2</xref>).</p>
<fig id="F1" position="float">
<label>Figure 1</label>
<caption><p>Representative picture of bicuspid aortic valves.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fcvm-09-973530-g0001.tif"/>
</fig>
<fig id="F2" position="float">
<label>Figure 2</label>
<caption><p>Aorta of a TAD decedent.</p></caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fcvm-09-973530-g0002.tif"/>
</fig>
<p>In addition to clinical data, a forensic pathological autopsy could also find some anatomical features that might be related to hypertension, such as the thickness of the compact myocardium of the left ventricular &#x0003E;1.5 cm, heart weight &#x0003E;500 g, hyalinosis of the central splenic artery, and renal arteriosclerosis. However, none of the above indicators had a positive rate of more than 50% alone (<xref ref-type="table" rid="T6">Table 6</xref>).</p>
<table-wrap position="float" id="T6">
<label>Table 6</label>
<caption><p>Hypertensive indicators in TAD deceased.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th valign="top" align="left"><bold>Indicator of hypertension</bold></th>
<th valign="top" align="center"><bold><italic>n</italic> (%)</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">History of hypertension<xref ref-type="table-fn" rid="TN4"><sup>&#x0002A;</sup></xref></td>
<td valign="top" align="center">32 (55.17)</td>
</tr>
<tr>
<td valign="top" align="left">SBP &#x02265;140 mmHg<xref ref-type="table-fn" rid="TN5"><sup>&#x00023;</sup></xref></td>
<td valign="top" align="center">58 (48.74)</td>
</tr>
<tr>
<td valign="top" align="left">Thickness of left ventricular wall &#x02265;1.5 cm</td>
<td valign="top" align="center">48 (24)</td>
</tr>
<tr>
<td valign="top" align="left">Heart weight &#x0003E;500 g</td>
<td valign="top" align="center">47 (23.5)</td>
</tr>
<tr>
<td valign="top" align="left">Hyalinosis of central splenic artery</td>
<td valign="top" align="center">86 (43)</td>
</tr>
<tr>
<td valign="top" align="left">Renal arteriolosclerosis</td>
<td valign="top" align="center">54 (27)</td>
</tr>
<tr>
<td valign="top" align="left">All negative</td>
<td valign="top" align="center">39 (19.5)</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="TN4"><label>&#x0002A;</label><p>Only 58 cases with available record of hypertension.</p></fn>
<fn id="TN5"><label>&#x00023;</label><p>Only 119 cases with available records of blood pressure.</p></fn>
</table-wrap-foot>
</table-wrap>
</sec>
</sec>
<sec sec-type="discussion" id="s4">
<title>Discussion</title>
<p>Thoracic aortic dissection still represented one of the most catastrophic cardiovascular diseases. Hitherto, many series of clinical studies have been conducted on hospitalized patients with TAD. Only reporting the incidence of hospitalized patients would introduce a serious underestimation of the incidence. A large number of patients with TAD remained undiagnosed until postmortem forensic autopsy and were not included in routine clinical studies of TAD (<xref ref-type="bibr" rid="B9">9</xref>&#x02013;<xref ref-type="bibr" rid="B11">11</xref>). TAD decedents diagnosed until autopsy generally experienced fewer medical interventions and had a more natural course and a more severe outcome than hospitalized patients with TAD. However, studies on the deceased with TAD are limited. Our study recruited 200 autopsy-diagnosed TAD decedents and found that the characteristics of TAD among individuals diagnosed until autopsy were significantly different among hospitalized patients with TAD.</p>
<sec>
<title>Early onset and low prevalence of hypertension</title>
<p>It has been shown in several studies that Chinese patients with AD are approximately 10 years younger than patients from western countries (<xref ref-type="bibr" rid="B12">12</xref>, <xref ref-type="bibr" rid="B13">13</xref>). Similarly, compared to the TAD victims in the west, the age of TAD victims in our study was significantly younger (<xref ref-type="bibr" rid="B8">8</xref>, <xref ref-type="bibr" rid="B14">14</xref>, <xref ref-type="bibr" rid="B15">15</xref>), which may be related to the inadequate control of hypertension in China. Furthermore, compared with the age of onset of clinical patients with TAD, the age of TAD victims in forensic TAD studies was significantly younger (<xref ref-type="bibr" rid="B12">12</xref>, <xref ref-type="bibr" rid="B13">13</xref>, <xref ref-type="bibr" rid="B15">15</xref>, <xref ref-type="bibr" rid="B16">16</xref>). Similar findings have been found in studies abroad between forensic and clinical TAD cases (<xref ref-type="bibr" rid="B8">8</xref>, <xref ref-type="bibr" rid="B17">17</xref>). One possible reason was that the older patients were more likely to seek medical care after the onset of symptoms and be admitted with higher blood pressure. However, advanced age was associated with less administration of forensic autopsy. Earlier onset of TAD deceased in our study brings up a lower incidence of comorbid hypertension. In addition to those well-known possible causes such as incomplete clinical data, poor health awareness, and fewer routine physical examinations, the high proportion of Stanford type A cases may be another reason for the low prevalence of hypertension in our study, for the reason that hypertension was more prevalent in those with type B AD than in those with type A AD (<xref ref-type="bibr" rid="B13">13</xref>, <xref ref-type="bibr" rid="B18">18</xref>, <xref ref-type="bibr" rid="B19">19</xref>).</p>
</sec>
<sec>
<title>Atypical pain and painless makes thoracic aortic dissection much more atypical</title>
<p>Aortic dissection has a myriad of clinical presentations and is for certain a diagnostic challenge. The symptoms of patients with TAD can vary and sometimes be very minimal. Symptoms of chest pain, abdominal pain, low back pain, limb ischemia, neurological dysfunction, and syncope have all been reported as potentially the sole presentation of TAD (<xref ref-type="bibr" rid="B20">20</xref>&#x02013;<xref ref-type="bibr" rid="B23">23</xref>). In common sense, the most common symptom of TAD is chest pain, which is usually sharp and sometimes reported as tearing or ripping, while often radiating to the back or the abdomen (<xref ref-type="bibr" rid="B18">18</xref>, <xref ref-type="bibr" rid="B24">24</xref>). Acute aortic chest pain can mimic pain from other more common acute conditions such as angina and acute coronary syndrome (ACS), which is more common than TAD and is, therefore, preferentially suspected by clinicians (<xref ref-type="bibr" rid="B20">20</xref>). The proportion of patients eventually diagnosed with TAD who receive a prior emergency diagnosis and management plan for ACS can be as high as 80% (<xref ref-type="bibr" rid="B25">25</xref>).</p>
<p>While the most common symptom in the present study was the sudden onset of abdominal pain rather than chest pain, regardless of Stanford type, which was different from that reported by the International Registry of Acute Aortic Dissection (IRAD) (chest pain) (<xref ref-type="bibr" rid="B24">24</xref>) and Sino-RAD (back pain) (<xref ref-type="bibr" rid="B13">13</xref>). Owe to lesion location, it is easy to understand that most Stanford type B patients with TAD presented with pain in the abdomen or low back. However, abdominal pain was also the initial symptom in Stanford type A deceased in the present study. Upchurch et al. found that patients who presented primarily with acute abdominal pain alone (4.6%) tended to have a delayed diagnosis and had higher mortality than those with more typical symptoms (<xref ref-type="bibr" rid="B26">26</xref>). In addition, our study found that TAD deceased present primarily with headache or low back pain showed a lower rate of suspected TAD diagnosis and a shorter IHD than those present with chest/back pain (<xref ref-type="table" rid="T2">Table 2</xref>). Atypical pain symptoms make correct diagnosis difficult.</p>
<p>Sudden onset of severe chest, back, or abdominal pain represents the most frequent symptom (<xref ref-type="bibr" rid="B13">13</xref>, <xref ref-type="bibr" rid="B24">24</xref>). However, atypical presentation is seen in &#x0007E;5% of AAD and is characterized by painless aortic dissection associated with higher mortality (<xref ref-type="bibr" rid="B27">27</xref>&#x02013;<xref ref-type="bibr" rid="B29">29</xref>). In our study, the figure was 25%, far more than that in other studies. The trend of lower TAD suspected diagnosis ratio and shorter IHD in painless TAD decedents implicated that TAD decedents with painless symptoms propagated more rapidly and were more vitally. The higher risk of misdiagnosis secondary to atypical manifestations might be a crucial cause of the death of patients with TAD.</p>
</sec>
<sec>
<title>Female: More atypical and critical</title>
<p>Women were reported to be about 5 years older than men at presentation in hospitalized patients with TAD (<xref ref-type="bibr" rid="B10">10</xref>, <xref ref-type="bibr" rid="B30">30</xref>&#x02013;<xref ref-type="bibr" rid="B32">32</xref>). In the present autopsy-based study, women were of comparable age to men and did not show longer event-free survival (<xref ref-type="table" rid="T1">Table 1</xref>). Interestingly, we found that women were more frequently affected during the warmer period, which was not the higher risk season for TAD (<xref ref-type="bibr" rid="B33">33</xref>, <xref ref-type="bibr" rid="B34">34</xref>). Besides, women also showed a higher proportion of painless symptoms. These atypical features of TAD in women could mislead clinicians about the diagnosis. Further, our study found that women showed a higher proportion of sudden death as an initial symptom and shorter IHD. These results indicated that women die faster once the onset. Atypical clinical presentation and rapid progression made women with dissection die more often than men. Similar findings have been suggested in other hospitalized patient-based studies (<xref ref-type="bibr" rid="B10">10</xref>, <xref ref-type="bibr" rid="B31">31</xref>) and speculated that sex differences in aortic morphology and hidden coronary heart disease (CHD) in women were possible reasons (<xref ref-type="bibr" rid="B35">35</xref>). In our study, female and male TAD decedents showed a comparable proportion of CHD. Compared to their control counterparts, women were more frequently affected by CHD (women, TAD vs. control: 22.86 vs. 5.71%; men, TAD vs. control: 22.42 vs. 18.79%), which may provide a clue for the early diagnosis of TAD in women.</p>
</sec>
<sec>
<title>Younger thoracic aortic dissection decedents show more pronounced left ventricular hypertrophy</title>
<p>Left ventricular hypertrophy (LVH) was previously identified in AAD using echocardiography (<xref ref-type="bibr" rid="B36">36</xref>&#x02013;<xref ref-type="bibr" rid="B38">38</xref>), and LVH was also present in the youngest subjects with AAD and did not increase in relationship to age (<xref ref-type="bibr" rid="B8">8</xref>). Interestingly, in our study, younger TAD decedents with a higher prevalence of normotension showed more pronounced morphological changes in the left heart (<xref ref-type="table" rid="T5">Table 5</xref>). This result suggested that monitoring of cardiac volumes by echocardiography may be helpful in the early screening of TAD, especially in young patients. Further, familial TAD caused by several genetic mutations was also reported to be associated with disproportionate LVH in normotensive individuals (<xref ref-type="bibr" rid="B39">39</xref>), raising the possibility that some LVH (especially in youngers) may result from a genetic predisposition for both TAD and cardiac disease. In addition, our previous study found that the more genetic variants an individual carries, the earlier the onset of dissection (<xref ref-type="bibr" rid="B16">16</xref>). Genetic screening would help to anticipate prognosis and establish accurate risk stratification of any family member at risk of developing the same disease, especially for those of young TAD deceased.</p>
</sec>
<sec>
<title>Limitation</title>
<p>Due to the retrospective nature of the present autopsy study, the body mass index (BMI) data in some autopsies was inadequate, which is associated with mortality in patients with cardiovascular diseases (CVDs) (<xref ref-type="bibr" rid="B40">40</xref>, <xref ref-type="bibr" rid="B41">41</xref>) and is very important to evaluate the risks of CVD. Besides, as we do not routinely conduct toxicological analysis in decedents with a clear cause of death, cocaine use is not available in this study, which is associated with numerous CVDs and SCD (<xref ref-type="bibr" rid="B42">42</xref>, <xref ref-type="bibr" rid="B43">43</xref>). Furthermore, there was no adequate correlation between postmortem values and values obtained from living patients by imaging techniques. Last, our results relied on data from a single center that may not reflect nationwide trends.</p>
</sec>
</sec>
<sec sec-type="conclusions" id="s5">
<title>Conclusion</title>
<p>In summary, a significant number of patients remained undiagnosed until postmortem autopsy and were rarely reported compared to hospitalized patients. We conducted an autopsy-based study of TAD to detect the characteristics of the TAD deceased. Our results implicated the TAD individuals diagnosed until an autopsy was a particular entity. It showed an earlier onset and a low incidence of hypertension, a high incidence of painless and abdominal pain, more atypical and critical situation for women, and more pronounced left heart changes for young decedents. Our findings indicate the urgent need for studies on forensic TAD deaths to explore the early diagnosis of atypical TAD, as well as the pathogenesis and prevention of young patients with TAD to minimize the burden of TAD-related sudden death.</p>
</sec>
<sec sec-type="data-availability" id="s6">
<title>Data availability statement</title>
<p>The original contributions presented in the study are included in the article, further inquiries can be directed to the corresponding author/s.</p>
</sec>
<sec id="s7">
<title>Ethics statement</title>
<p>This project was approved by the Ethics Committee of Sun Yat-sen University (Approval No. 2019-004), and it was carried out in strict accordance with the ethical research principle of Sun Yat-sen University.</p>
</sec>
<sec id="s8">
<title>Author contributions</title>
<p>JC, BH, and QZ designed the project. QZ, NZ, QW, YX, and JZ collected all the data. DZ and QB managed the documents and tissue slides. KY managed the histopathological data. QZ, NZ, and QW analyzed the data. QZ, LQ, BH, and JC discussed the data. QZ, BH, and JC wrote the manuscript. All the authors have approved the final version of the manuscript.</p>
</sec>
<sec sec-type="funding-information" id="s9">
<title>Funding</title>
<p>This study was supported by the National Natural Science Foundation of China (grant nos. 81920108021 and 81901919), the Guangzhou Municipal Science and Technology Project (grant no. 202102080092), and the Natural Science Foundation of Guangdong Province (grant no. 2020A1515010078).</p>
</sec>
<sec sec-type="COI-statement" id="conf1">
<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 sec-type="disclaimer" id="s10">
<title>Publisher&#x00027;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>
</body>
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