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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Mol. Biosci.</journal-id>
<journal-title>Frontiers in Molecular Biosciences</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Mol. Biosci.</abbrev-journal-title>
<issn pub-type="epub">2296-889X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">1204985</article-id>
<article-id pub-id-type="doi">10.3389/fmolb.2023.1204985</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Molecular Biosciences</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Differences in the lipid metabolism profile and clinical characteristics between eosinophilic and non-eosinophilic acute exacerbation of chronic obstructive pulmonary disease</article-title>
<alt-title alt-title-type="left-running-head">Wang et al.</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmolb.2023.1204985">10.3389/fmolb.2023.1204985</ext-link>
</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Wang</surname>
<given-names>Yating</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="fn" rid="fn1">
<sup>&#x2020;</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Chang</surname>
<given-names>Chun</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="fn" rid="fn1">
<sup>&#x2020;</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1216649/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tian</surname>
<given-names>Sifan</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="fn" rid="fn1">
<sup>&#x2020;</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wang</surname>
<given-names>Juan</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/701417/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Gai</surname>
<given-names>Xiaoyan</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1171263/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Zhou</surname>
<given-names>Qiqiang</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Chen</surname>
<given-names>Yahong</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/455090/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Gao</surname>
<given-names>Xu</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1626733/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sun</surname>
<given-names>Yongchang</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/895259/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Liang</surname>
<given-names>Ying</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="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1265734/overview"/>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Department of Respiratory and Critical Care Medicine</institution>, <institution>Peking University Third Hospital</institution>, <addr-line>Beijing</addr-line>, <country>China</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Research Center for Chronic Airway Diseases</institution>, <institution>Peking University Health Science Center</institution>, <addr-line>Beijing</addr-line>, <country>China</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Department of Occupational and Environmental Health Sciences</institution>, <institution>School of Public Health</institution>, <institution>Peking University</institution>, <addr-line>Beijing</addr-line>, <country>China</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/176971/overview">Donghai Lin</ext-link>, Xiamen University, China</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2324429/overview">Yongxia Yang</ext-link>, Guangdong Pharmaceutical University, China</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1091578/overview">Xiaoxiao Ma</ext-link>, Tsinghua University, China</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Xu Gao, <email>xu.gao@pku.edu.cn</email>; Ying Liang, <email>bysyliangying@126.com</email>
</corresp>
<fn fn-type="equal" id="fn1">
<label>
<sup>&#x2020;</sup>
</label>
<p>These authors have contributed equally to this work</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>12</day>
<month>07</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>10</volume>
<elocation-id>1204985</elocation-id>
<history>
<date date-type="received">
<day>13</day>
<month>04</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>29</day>
<month>06</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2023 Wang, Chang, Tian, Wang, Gai, Zhou, Chen, Gao, Sun and Liang.</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Wang, Chang, Tian, Wang, Gai, Zhou, Chen, Gao, Sun and Liang</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>
<bold>Objective:</bold> In this study, we aimed to investigate the differences in serum lipid metabolite profiles and their relationship with clinical characteristics between patients with eosinophilic and non-eosinophilic AECOPD.</p>
<p>
<bold>Methods:</bold> A total of 71 AECOPD patients were enrolled. Eosinophilic AECOPD was defined as blood EOS% &#x2265; 2% (<italic>n</italic> &#x3d; 23), while non-eosinophilic AECOPD, as blood EOS&#x3c; 2% (<italic>n</italic> &#x3d; 48). Clinical data were collected, and serum lipid metabolism profiles were detected by liquid chromatography&#x2013;mass spectrometry (LC-MS). The XCMS software package was used to pre-process the raw data, and then, lipid metabolite identification was achieved through a spectral match using LipidBlast library. Differences in lipid profiles and clinical features between eosinophilic and non-eosinophilic groups were analyzed by generalized linear regression. The least absolute shrinkage and selection operator (LASSO) was applied to screen the most characteristic lipid markers for the eosinophilic phenotype.</p>
<p>
<bold>Results:</bold> Eosinophilic AECOPD patients had less hypercapnic respiratory failures, less ICU admissions, a shorter length of stay in the hospital, and a lower fibrinogen level. In the lipid metabolism profiles, 32 significantly different lipid metabolites were screened through a <italic>t</italic>-test adjusted by using FDR (FDR-adjusted <italic>p</italic> &#x3c; 0.05 and VIP&#x3e; 1). Nine differential lipid metabolites were found to be associated with the three clinical features, namely, hypercapnia respiratory failure, ICU admission, and fibrinogen in further integration analysis. The species of triacylglycerol (TAG), phosphatidylcholine (PC), lysophosphatidylcholine (LPC), and diacylglyceryl trimethylhomoserine (DGTS) were high in these eosinophilic AECOPD. The LASSO was applied, and three lipid metabolites were retained, namely, LPC (16:0), TAG (17:0/17:2/17:2), and LPC (20:2). The logistic regression model was fitted using these three markers, and the area under the ROC curve of the model was 0.834 (95% CI: 0.740&#x2013;0.929).</p>
<p>
<bold>Conclusion:</bold> Patients with eosinophilic AECOPD had a unique lipid metabolism status. Species of TAGs and LPCs were significantly increased in this phenotype and were associated with better clinical outcomes.</p>
</abstract>
<kwd-group>
<kwd>chronic obstructive pulmonary disease</kwd>
<kwd>acute exacerbation</kwd>
<kwd>eosinophils</kwd>
<kwd>lipidomics</kwd>
<kwd>LC-ESI-MS</kwd>
</kwd-group>
<contract-sponsor id="cn001">National Natural Science Foundation of China<named-content content-type="fundref-id">10.13039/501100001809</named-content>
</contract-sponsor>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Metabolomics</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1">
<title>1 Introduction</title>
<p>Chronic obstructive pulmonary disease (COPD) is a heterogeneous disease characterized by persistent respiratory symptoms and airflow limitations (<xref ref-type="bibr" rid="B14">Global Initiative for Chronic Obstructive Lung Disease, 2022</xref>). It is estimated that there are nearly 100 million patients with COPD in mainland China, with a prevalence of 13.7% among adults aged &#x2265; 40&#xa0;years (<xref ref-type="bibr" rid="B32">Wang et al., 2018</xref>). The prevalence of COPD will continue to rise, adding a heavy economic burden to individuals and society (<xref ref-type="bibr" rid="B14">Global Initiative for Chronic Obstructive Lung Disease, 2022</xref>). Additionally, acute exacerbations of COPD (AECOPD) have a significant impact on patients&#x2019; health (<xref ref-type="bibr" rid="B33">Wilkinson et al., 2004</xref>), contributing to hospitalization and readmission, disease progression, and increased risk of death.</p>
<p>Eosinophilic COPD is a phenotype of airway inflammation characterized by the presence of eosinophilic inflammation in the airways, manifested by elevated peripheral blood and/or sputum eosinophil counts (<xref ref-type="bibr" rid="B2">Barnes, 2019</xref>). Some patients with COPD during exacerbation also have a peripheral blood eosinophilia &#x2265; 2% or sputum eosinophilia &#x2265; 3%, who are classified as eosinophilic AECOPD phenotypes (<xref ref-type="bibr" rid="B30">Singh et al., 2014</xref>; <xref ref-type="bibr" rid="B25">Pascoe et al., 2015</xref>; <xref ref-type="bibr" rid="B10">Dai et al., 2020</xref>). These patients have specific characteristics in terms of clinical characteristics, laboratory test results, treatment, and prognosis. For instance, the risk of in-hospital mortality is lower among eosinophilic AECOPD patients, and the hospital stay is shorter (<xref ref-type="bibr" rid="B35">You and Shi, 2021</xref>), with better response to systemic glucocorticoid treatment (<xref ref-type="bibr" rid="B1">Bafadhel et al., 2014</xref>). However, the pathogenesis of the eosinophilic phenotype of COPD exacerbation is still not clear. Novel biomarkers can help clinicians recognize this phenotype and develop potential new therapeutic targets.</p>
<p>Lipids are important cellular components. They participate in the formation of cell membranes and are important energy storage substances, components of various hormones, and important mediators in cell signal transduction pathways. Accumulating studies have demonstrated that lipid metabolism disorders are closely related to the pathogenesis of COPD by affecting occurrence and development of the disease (<xref ref-type="bibr" rid="B11">Fahy et al., 2005</xref>; <xref ref-type="bibr" rid="B9">Chen et al., 2019</xref>; <xref ref-type="bibr" rid="B17">Kotlyarov and Bulgakov, 2021</xref>). For example, obesity with high amounts of triglyceride and cholesterol was associated with poorer COPD-related outcomes (lower quality of life, more dyspnea, and more severe COPD exacerbations) (<xref ref-type="bibr" rid="B18">Lambert et al., 2017</xref>). In addition, some species of sphingolipids were inversely associated with emphysema, while sphingosine 1-phosphate showed negative association with COPD exacerbation (<xref ref-type="bibr" rid="B6">Bowler et al., 2015</xref>). Phospholipids, accounting for forming cell membranes and pulmonary surfactants, were found to be decreased in patients with COPD, which may correlate with pulmonary functions (<xref ref-type="bibr" rid="B23">Lusuardi et al., 1992</xref>).</p>
<p>Lipidomics is an &#x201c;omics&#x201d; approach, which comprehensively analyzes the full lipid components in various biological samples and can provide significant insights into the understanding of disease pathogenesis. With this technology, fatty acid metabolism was identified to be altered in bronchial epithelial cells of asthmatic patients, leading to an increase in levels of some lipid species [phosphatidylcholine, lysophosphatidylcholine, and bis (monoacylglycero) phosphate] (<xref ref-type="bibr" rid="B27">Ravi et al., 2021</xref>). Our previous study found that the levels of lysophosphatidylcholine (LPC) 18:3, lysophosphatidylethanolamine (LPE) 16:1, and phosphatidylinositol (PI) 32:1 significantly dropped in the acute stage compared to the recovery stage in hospitalized patients with COPD exacerbation (<xref ref-type="bibr" rid="B13">Gai et al., 2021</xref>). In our study, we aimed to compare the serum lipid metabolite profiles between eosinophilic and non-eosinophilic AECOPD patients, and to explore the association between differential lipid metabolites and patients&#x2019; clinical and prognostic features, based on the untargeted liquid chromatography&#x2013;mass spectrometry (LC-MS) lipidomics technology. We hypothesized that lipid metabolic profiles were different between these two phenotypes of AECOPD, and lipidomics analysis may help elucidate the underlying pathogenesis.</p>
</sec>
<sec sec-type="materials|methods" id="s2">
<title>2. Materials and methods</title>
<sec id="s2-1">
<title>2.1 Study subjects and data collection</title>
<p>Data were collected from 71 AECOPD patients hospitalized in the Department of Respiratory Medicine and Critical Care Medicine of Peking University Third Hospital from April 2017 to March 2018. These patients met the criteria for the diagnosis of acute exacerbation of COPD, according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) guidelines (<xref ref-type="bibr" rid="B14">Global Initiative for Chronic Obstructive Lung Disease, 2022</xref>). The exclusion criteria were as follows: subjects with other airflow limitation diseases rather than COPD, combination of pneumonia and active pulmonary tuberculosis, severe liver and kidney insufficiency, malignancies, an immunosuppressive condition due to chemotherapy or HIV infection, receiving systemic glucocorticoids due to COPD exacerbation in the past 1&#xa0;month, and severe trauma or stress reaction.</p>
<p>The clinical data included demographic characteristics, smoking status, comorbidities, presence or absence of hypercapnic respiratory failure [arterial carbon dioxide partial pressure (PaCO<sub>2</sub>) &#x2265; 50&#xa0;mmHg], the length of stay (LOS) in the hospital, and requirement for an intensive care unit (ICU) stay or not. The time taken for the next exacerbation was also collected.</p>
<p>A blood routine test and blood biochemical examination were performed in the clinical laboratory of our hospital. The peripheral blood cell count and classification, fibrinogen, D-dimer, total cholesterol, total triglyceride, and other laboratory parameters were recorded. Our patients were grouped according to the percentage of eosinophils (EOS) in peripheral blood. Non-eosinophilic AECOPD was defined as having blood EOS%&#x3c; 2% and eosinophilic AECOPD as having blood EOS &#x2265; 2%.</p>
<p>All subjects or their close relatives participating in this study signed an informed consent before data collection. The study procedures were performed in compliance with the Declaration of Helsinki (1964), and the study protocol was approved by the Ethics Committee of Peking University Third Hospital (M2017410).</p>
</sec>
<sec id="s2-2">
<title>2.2 LC-MS analysis</title>
<sec id="s2-2-1">
<title>2.2.1 Serum sample collection and preparation</title>
<p>Fasting (after at least 8&#xa0;h) peripheral blood samples were collected from patients using vacuum blood collection tubes. The blood samples were left at room temperature for approximately 30&#xa0;min until complete clotting, and then, the samples were centrifuged at 4&#xb0;C at 2,500 &#xd7; g for 15&#xa0;min. The upper serum samples were extracted and then placed in frozen storage at &#x2212;80&#xb0;C.</p>
</sec>
<sec id="s2-2-2">
<title>2.2.2 Lipid metabolite extraction</title>
<p>After being reheated and dissolved, 100&#xa0;&#x3bc;L of the serum sample was transferred into an EP tube, and then, 480&#xa0;&#x3bc;L of the extract solution (methyltert-butylether: methanol &#x3d; 5:1) was added to the sample. After vortexing and mixing for 30&#xa0;s, the samples were sonicated in an ice water bath for 10&#xa0;min. After incubating at &#x2212;40&#xb0;C for 1&#xa0;h, the sample was centrifuged at 3,000&#xa0;rpm for 15&#xa0;min at 4&#xb0;C. Then, 350&#xa0;&#x3bc;L of the supernatant was transferred to a fresh EP tube and vacuum dried. A measure of 200&#xa0;&#x3bc;L of the solution (DCM: MeOH &#x3d; 1:1) was added to reconstitute the dried samples. Then, the solution was vortexed for 30&#xa0;s and sonicated in an ice water bath for 10&#xa0;min. A measure of 75&#xa0;&#x3bc;L of the supernatant was placed in a fresh glass vial for LC-MS analysis. A quality control (QC) sample was prepared by mixing an equal aliquot (10&#xa0;&#x3bc;L) of the supernatants from each subject&#x2019;s sample.</p>
</sec>
<sec id="s2-2-3">
<title>2.2.3 LC-MS analysis procedure</title>
<p>After lipid metabolite extraction was carried out, an ultra-high-performance liquid chromatograph (ExionLC, AB SCIEX, United States) was used to separate the target compounds using a Phenomenex Kinetex C18 (2.1&#xa0;mm &#xd7; 100&#xa0;mm, 1.7&#xa0;&#x3bc;m, Phenomenex, United States) liquid chromatography column. High-resolution mass spectrometry data acquisition was performed in information-dependent acquisition (IDA) mode, utilizing a triple TOF 5600 mass spectrometer (AB SCIEX, United States). The data acquisition software application (Analyst TF 1.7, AB Sciex) conducts primary acquisition, followed by automated ion selection and secondary mass spectrometry data collection based on predetermined criteria derived from primary mass spectrometry data. In each cycle, the most intensive 12 precursor ions with intensities over 100 were selected for secondary mass spectrometry scanning. The energy of collision-induced dissociation was 45&#xa0;eV, and the accumulation time of each secondary spectrum was 50&#xa0;ms. The ion source parameters are as follows: GS1 60 psi, GS2 60 psi, CUR 30 psi, TEM 600&#xb0;C, DP 100&#xa0;V, ISVF 5,000&#xa0;V (ESI &#x2b; mode), and &#x2212;3800&#xa0;V (ESI &#x2212; mode).</p>
</sec>
<sec id="s2-2-4">
<title>2.2.4 Data preprocessing and annotation</title>
<p>The mass-to-charge ratio (m/z) and retention time (RT) information of the test samples were determined by liquid chromatography&#x2013;mass spectrometry (LC-MS), and then, XCMS was used for retention time correction, peak identification, peak extraction, peak integration, and peak alignment. Minfrac was set as 0.5, and the cutoff was set as 0.3. The m/z of the substances in the LipidBlast database was matched with RT. In the qualitative process, the score value of the secondary qualitative metabolites was calculated based on the Euclidean distance and the dot product algorithm, which improved the accuracy of the mass spectrum annotation. XCMS parameters were set as follows: centWave, ppm 10, peak width 5&#x2013;20, and SN 3; prefiltering step: the metabolites could be retained only if it contained at least three peaks of intensity &#x2265; 1,000. The function used to calculate the m/z center of the chromatographic peak was wMean, which was the intensity weighted average of the m/z values of the peak. The minimum m/z dimension difference required for peaks with overlapping retention times was &#x2212;0.001. Then, lipid metabolite identification was achieved through a spectral match using the LipidBlast library. Finally, a total of 2,431 lipid metabolites in the ESI &#x2b; mode and 1,821 lipid metabolites in the ESI &#x2212; mode were detected for further multivariate analysis.</p>
</sec>
</sec>
<sec id="s2-3">
<title>2.3 Statistical analysis</title>
<p>The baseline data were compared between the patients with the percentage of peripheral eosinophils &#x2265; 2% and &#x3c;2% using Student&#x2019;s <italic>t</italic>-test for continuous and Pearson&#x2019;s chi-squared test or Fisher&#x2019;s exact test for categorical variables. The numerical variables were presented as the mean value and standard deviation (SD), while the categorical variables were expressed as numbers and percentages.</p>
<p>Significance of the difference between the two groups was analyzed for each lipid using Student&#x2019;s <italic>t</italic>-test, and an FDR-adjusted <italic>p</italic>-value &#x3c; 0.05 was considered significant. The fold changes of each lipid were calculated on the basis of the average in each group. Orthogonal projections to latent structure discriminant analysis (OPLS-DA) was applied to obtain a high level of group separation and a good understanding of the variables responsible for classification, and the first principal component of the variable importance projection (VIP) was obtained. VIP values exceeding 1.0 with an adjusted <italic>p</italic>-value &#x3c; 0.05 in the Student&#x2019;s <italic>t</italic>-test were selected to correspond to potential lipid biomarker candidates. To control the possible influences of some factors, such as age, sex, BMI, smoking status, serum total cholesterol, and triglyceride, linear regression was performed for each lipid. The lipids with an FDR-adjusted <italic>p</italic>-value &#x3c; 0.05 from the Wald statistic were retained as potential lipid biomarkers.</p>
<p>We also checked the associations between the percentage of peripheral eosinophils and other clinical features. Linear regression or generalized linear regression was performed for each potential lipid biomarker and clinical features significantly associated with the percentage of peripheral eosinophils to determine more characteristic lipid metabolites. Then, the least absolute shrinkage and selection operator (LASSO) was applied to downsize these lipid metabolites for discriminating eosinophilic and non-eosinophilic AECOPD, while the largest value of lambda, whose corresponding misclassification error was within one standard error of the minimum misclassification error, known as &#x201c;1-se&#x201d; lambda, was defined as the optimal value. A logistic regression model was fitted using these selected markers as the covariates to obtain a combined screening score. The predictability of the model was evaluated by using the area under receiver operation characteristic curve (ROC).</p>
<p>All the analyses were conducted using R version 4.0.5, with the following packages being used: &#x201c;ropls,&#x201d; &#x201c;glmnet,&#x201d; and &#x201c;pROC&#x201d;. A two-sided <italic>p</italic>-value of &#x3c; 0.05 was considered statistically significant. All data were analyzed anonymously.</p>
</sec>
</sec>
<sec sec-type="results" id="s3">
<title>3 Results</title>
<sec id="s3-1">
<title>3.1 Clinical characteristics</title>
<p>As shown in <xref ref-type="table" rid="T1">Table 1</xref>, the mean age of our patients was 74.1 &#xb1; 9.6&#xa0;years, and 87.3% of these patients were male, where 59.2% and 31.0% were former and current smokers, respectively. The age, sex proportion, body mass index, tobacco exposure, and comorbidities were not different between eosinophilic and non-eosinophilic AECOPD patients. Serum triglyceride and cholesterol levels were similar between the groups. Eosinophilic AECOPD patients had less hypercapnic respiratory failure, less ICU admission, and shorter LOS in the hospital, as well as a lower fibrinogen level. The time taken for the next exacerbation was not statistically different.</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Demographic and clinical characteristics of the study subjects.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">Characteristic</th>
<th align="center">Total (<italic>n</italic> &#x3d; 71)</th>
<th align="center">Non-eosinophilic (<italic>n</italic> &#x3d; 48)</th>
<th align="center">Eosinophilic (<italic>n</italic> &#x3d; 23)</th>
<th align="center">
<italic>p</italic>-value<sup>a</sup>
</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Age (years)</td>
<td align="center">74.1 (9.6)</td>
<td align="center">73.7 (10.3)</td>
<td align="center">75.0 (8.0)</td>
<td align="center">0.566</td>
</tr>
<tr>
<td align="left">Male</td>
<td align="center">62 (87.3%)</td>
<td align="center">42 (87.5%)</td>
<td align="center">20 (87.0%)</td>
<td align="center">1.000</td>
</tr>
<tr>
<td align="left">BMI (kg/m<sup>2</sup>)</td>
<td align="center">22.0 (5.2)</td>
<td align="center">22.0 (5.8)</td>
<td align="center">22.1 (3.7)</td>
<td align="center">0.910</td>
</tr>
<tr>
<td colspan="5" align="left">Smoking status</td>
</tr>
<tr>
<td align="left">Never</td>
<td align="center">7 (9.9%)</td>
<td align="center">5 (10.4%)</td>
<td align="center">2 (8.7%)</td>
<td align="center">0.303</td>
</tr>
<tr>
<td align="left">Former</td>
<td align="center">42 (59.2%)</td>
<td align="center">31 (64.6%)</td>
<td align="center">11 (47.8%)</td>
<td align="left"/>
</tr>
<tr>
<td align="left">Current</td>
<td align="center">22 (31.0%)</td>
<td align="center">12 (25.0%)</td>
<td align="center">10 (43.5%)</td>
<td align="left"/>
</tr>
<tr>
<td align="left">Smoking index (packs per year)</td>
<td align="center">39.2 (29.7)</td>
<td align="center">37.7 (28.1)</td>
<td align="center">42.2 (33.3)</td>
<td align="center">0.578</td>
</tr>
<tr>
<td colspan="5" align="left">Comorbidities</td>
</tr>
<tr>
<td align="left">Hypertension</td>
<td align="center">37 (52.1%)</td>
<td align="center">27 (56.3%)</td>
<td align="center">10 (43.5%)</td>
<td align="center">0.451</td>
</tr>
<tr>
<td align="left">Coronary heart disease</td>
<td align="center">11 (15.5%)</td>
<td align="center">8 (16.7%)</td>
<td align="center">3 (13.0%)</td>
<td align="center">1.000</td>
</tr>
<tr>
<td align="left">Heart failure</td>
<td align="center">4 (5.6%)</td>
<td align="center">3 (6.3%)</td>
<td align="center">1 (4.3%)</td>
<td align="center">1.000</td>
</tr>
<tr>
<td align="left">Diabetes</td>
<td align="center">11 (15.5%)</td>
<td align="center">8 (16.7%)</td>
<td align="center">3 (13.0%)</td>
<td align="center">1.000</td>
</tr>
<tr>
<td align="left">Hyperlipidemia</td>
<td align="center">8 (11.3%)</td>
<td align="center">5 (10.4%)</td>
<td align="center">3 (13.0%)</td>
<td align="center">0.708</td>
</tr>
<tr>
<td align="left">Eosinophil count (cells/&#x3bc;L)</td>
<td align="center">115 (176)</td>
<td align="center">33 (44)</td>
<td align="center">287 (220)</td>
<td align="center">&#x3c;0.001</td>
</tr>
<tr>
<td align="left">Eosinophil %</td>
<td align="center">1.65 (2.23)</td>
<td align="center">0.43 (0.50)</td>
<td align="center">4.19 (2.29)</td>
<td align="center">&#x3c;0.001</td>
</tr>
<tr>
<td align="left">D-dimer (&#x3bc;g/mL)</td>
<td align="center">0.26 (0.19)</td>
<td align="center">0.28 (0.21)</td>
<td align="center">0.21 (0.13)</td>
<td align="center">0.106</td>
</tr>
<tr>
<td align="left">Fibrinogen (g/L)</td>
<td align="center">3.97 (1.29)</td>
<td align="center">4.20 (1.41)</td>
<td align="center">3.48 (0.82)</td>
<td align="center">0.008</td>
</tr>
<tr>
<td align="left">Total cholesterol (mmol/L)</td>
<td align="center">3.98 (0.85)</td>
<td align="center">3.95 (0.89)</td>
<td align="center">4.04 (0.80)</td>
<td align="center">0.668</td>
</tr>
<tr>
<td align="left">Triglyceride (mmol/L)</td>
<td align="center">1.02 (0.46)</td>
<td align="center">0.96 (0.40)</td>
<td align="center">1.14 (0.55)</td>
<td align="center">0.156</td>
</tr>
<tr>
<td align="left">Hypercapinic respiratory failure</td>
<td align="center">24 (36.9%)</td>
<td align="center">22 (45.8%)</td>
<td align="center">2 (8.7%)</td>
<td align="center">0.004</td>
</tr>
<tr>
<td align="left">Need for ICU admission</td>
<td align="center">14 (19.7%)</td>
<td align="center">13 (27.1%)</td>
<td align="center">1 (4.3%)</td>
<td align="center">0.027</td>
</tr>
<tr>
<td align="left">Time to next exacerbation (months)</td>
<td align="center">27.1 (13.6)</td>
<td align="center">27.1 (13.6)</td>
<td align="center">27.1 (13.9)</td>
<td align="center">0.994</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>Data are presented as mean (SD) or n (%).</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3-2">
<title>3.2 Lipid metabolite profiling difference between eosinophilic and non-eosinophilic AECOPD</title>
<p>Log2 transformation was performed before statistics analysis. First, OPLS-DA was performed. As shown in <xref ref-type="fig" rid="F1">Figure 1</xref>, OPLS-DA plots both demonstrated a barely clear separation between eosinophilic and non-eosinophilic AECOPD, with most samples being within the 95% confidential interval with the exception of one non-eosinophilic sample. The R2Y values of the OPLS-DA model in ESI &#x2b; and ESI &#x2212; modes were 0.562 and 0.688, respectively, and the Q2Y values were 0.076 and 0.057, respectively. A total of 838 and 616 lipids had a VIP score &#x3e; 1 in ESI &#x2b; and ESI &#x2212; modes, respectively. Subsequently, a <italic>t</italic>-test with FDR-adjusting values and fold changes was conducted to compare the difference between the mean concentrations of lipid species between the two groups. In this process, a total of 32 lipid metabolites (26 in ESI &#x2b; and 6 in ESI &#x2212; modes) met both FDR-adjusted <italic>p</italic> &#x3c; 0.05 and VIP &#x3e; 1, and were selected as potential candidate metabolites.</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>OPLS-DA of LC-MS metabolite profiles between eosinophilic AECOPD and non-eosinophilic AECOPD subjects in electrospray positive ion (ESI&#x2b;) mode and electrospray negative ion (ESI&#x2212;) mode, respectively. Red points represented eosinophilic AECOPD subjects, while blue points represented non-eosinophilic AECOPD subjects. OPLS-DA, orthogonal projections to latent structures-discriminate analysis; LC-MS, liquid chromatography-mass spectrometry; AECOPD, acute exacerbation of chronic obstructive pulmonary disease; POS, electrospray positive ion mode; NEG, electrospray negative ion mode.</p>
</caption>
<graphic xlink:href="fmolb-10-1204985-g001.tif"/>
</fig>
<p>To further control the possible influencing factors, such as age, sex, BMI, smoking status, serum total cholesterol, and triglyceride, a linear regression model was structured for each candidate, and lipids with an FDR-adjusted <italic>p</italic>-value &#x3c; 0.05 from the Wald statistic were retained in this model. It turned out that all the 32 candidate metabolites were retained. Therefore, a total of 32 lipid metabolites (<xref ref-type="table" rid="T2">Table 2</xref>) were selected as potential biomarkers, and they were mapped to show the clear difference between the two groups (<xref ref-type="fig" rid="F2">Figure 2</xref>).</p>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Differentially expressed metabolites between eosinophilic and non-eosinophilic patients.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Metabolite</th>
<th align="center">Median m/z</th>
<th align="center">Median RT (s)</th>
<th align="center">MS2. score</th>
<th align="center">Mean non-eosinophilic</th>
<th align="center">Mean eosinophilic</th>
<th align="center">log2fc</th>
<th align="center">p.<italic>t</italic>-test</th>
<th align="center">p.t.adj</th>
<th align="center">VIP</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td colspan="10" align="left">Positive-ion mode (ESI &#x2b;)</td>
</tr>
<tr>
<td align="left">TAG (12:0/12:0/22:3)</td>
<td align="center">795.611</td>
<td align="center">424.092</td>
<td align="center">0.876</td>
<td align="center">2.24 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">1.69 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">&#x2212;0.405</td>
<td align="center">5.60 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.040</td>
<td align="center">2.147</td>
</tr>
<tr>
<td align="left">TAG (12:1/12:3/12:3)</td>
<td align="center">647.423</td>
<td align="center">155.660</td>
<td align="center">0.876</td>
<td align="center">3.27 &#xd7; 10<sup>&#x2212;6</sup>
</td>
<td align="center">1.93 &#xd7; 10<sup>&#x2212;6</sup>
</td>
<td align="center">&#x2212;0.756</td>
<td align="center">6.50 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.042</td>
<td align="center">2.088</td>
</tr>
<tr>
<td align="left">TAG (13:1/22:5/22:5)</td>
<td align="center">933.671</td>
<td align="center">660.639</td>
<td align="center">0.880</td>
<td align="center">1.54 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">2.30 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.576</td>
<td align="center">1.23 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.022</td>
<td align="center">2.469</td>
</tr>
<tr>
<td align="left">TAG (14:0/18:2/18:2)</td>
<td align="center">849.695</td>
<td align="center">655.631</td>
<td align="center">0.976</td>
<td align="center">4.48 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">6.61 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.559</td>
<td align="center">6.20 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.042</td>
<td align="center">2.258</td>
</tr>
<tr>
<td align="left">TAG (14:3/21:5/22:0)</td>
<td align="center">934.675</td>
<td align="center">659.682</td>
<td align="center">0.975</td>
<td align="center">1.26 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">1.93 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.615</td>
<td align="center">2.59 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.033</td>
<td align="center">2.167</td>
</tr>
<tr>
<td align="left">TAG (15:0/20:5/20:5)</td>
<td align="center">907.657</td>
<td align="center">656.299</td>
<td align="center">0.882</td>
<td align="center">5.00 &#xd7; 10<sup>&#x2212;6</sup>
</td>
<td align="center">8.04 &#xd7; 10<sup>&#x2212;6</sup>
</td>
<td align="center">0.685</td>
<td align="center">6.48 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.042</td>
<td align="center">2.101</td>
</tr>
<tr>
<td align="left">TAG (15:0/21:3/21:3)</td>
<td align="center">938.819</td>
<td align="center">643.019</td>
<td align="center">0.515</td>
<td align="center">9.23 &#xd7; 10<sup>&#x2212;6</sup>
</td>
<td align="center">1.70 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.878</td>
<td align="center">5.78 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.040</td>
<td align="center">2.092</td>
</tr>
<tr>
<td align="left">TAG (16:0/18:1/18:2)</td>
<td align="center">874.699</td>
<td align="center">643.315</td>
<td align="center">0.958</td>
<td align="center">1.50 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">2.48 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.723</td>
<td align="center">4.96 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.038</td>
<td align="center">2.452</td>
</tr>
<tr>
<td align="left">TAG (16:0/18:2/18:3)</td>
<td align="center">870.756</td>
<td align="center">660.559</td>
<td align="center">0.834</td>
<td align="center">9.80 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">1.65 &#xd7; 10<sup>&#x2212;3</sup>
</td>
<td align="center">0.752</td>
<td align="center">5.56 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.040</td>
<td align="center">2.148</td>
</tr>
<tr>
<td align="left">TAG (16:1/16:1/18:3)</td>
<td align="center">847.680</td>
<td align="center">637.878</td>
<td align="center">0.903</td>
<td align="center">1.17 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">2.03 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.794</td>
<td align="center">3.54 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.037</td>
<td align="center">2.341</td>
</tr>
<tr>
<td align="left">TAG (16:2/18:2/18:3)</td>
<td align="center">866.673</td>
<td align="center">655.307</td>
<td align="center">0.577</td>
<td align="center">3.17 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">4.09 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.369</td>
<td align="center">6.43 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.042</td>
<td align="center">2.306</td>
</tr>
<tr>
<td align="left">TAG (17:0/17:2/17:2)</td>
<td align="center">863.676</td>
<td align="center">639.317</td>
<td align="center">0.910</td>
<td align="center">2.04 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">3.32 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.703</td>
<td align="center">3.13 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.015</td>
<td align="center">2.632</td>
</tr>
<tr>
<td align="left">TAG (18:1/18:1/21:5)</td>
<td align="center">941.703</td>
<td align="center">660.805</td>
<td align="center">0.885</td>
<td align="center">4.19 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">6.54 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.644</td>
<td align="center">4.18 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.037</td>
<td align="center">2.081</td>
</tr>
<tr>
<td align="left">TAG (20:4/22:7/22:7)</td>
<td align="center">1,017.690</td>
<td align="center">84.972</td>
<td align="center">0.876</td>
<td align="center">2.21 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">3.64 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.725</td>
<td align="center">4.10 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.037</td>
<td align="center">2.529</td>
</tr>
<tr>
<td align="left">TAG (20:5/22:7/22:7)</td>
<td align="center">1,015.664</td>
<td align="center">83.199</td>
<td align="center">0.876</td>
<td align="center">4.07 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">5.96 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.552</td>
<td align="center">8.86 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.021</td>
<td align="center">2.903</td>
</tr>
<tr>
<td align="left">TAG (20:6/20:6/22:5)</td>
<td align="center">991.674</td>
<td align="center">83.242</td>
<td align="center">0.876</td>
<td align="center">6.68 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">1.20 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.849</td>
<td align="center">9.28 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.021</td>
<td align="center">2.640</td>
</tr>
<tr>
<td align="left">TAG (20:6/22:7/22:7)</td>
<td align="center">1,013.656</td>
<td align="center">83.220</td>
<td align="center">0.876</td>
<td align="center">1.79 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">2.74 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.610</td>
<td align="center">3.01 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.015</td>
<td align="center">2.962</td>
</tr>
<tr>
<td align="left">LPC (16:0)</td>
<td align="center">496.340</td>
<td align="center">83.237</td>
<td align="center">0.982</td>
<td align="center">9.99 &#xd7; 10<sup>&#x2212;3</sup>
</td>
<td align="center">1.36 &#xd7; 10<sup>&#x2212;2</sup>
</td>
<td align="center">0.448</td>
<td align="center">3.75 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.016</td>
<td align="center">3.021</td>
</tr>
<tr>
<td align="left">LPC (20:2)</td>
<td align="center">548.359</td>
<td align="center">112.762</td>
<td align="center">0.852</td>
<td align="center">4.67 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">6.71 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.523</td>
<td align="center">9.73 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.021</td>
<td align="center">2.740</td>
</tr>
<tr>
<td align="left">PC (14:1e/22:6)</td>
<td align="center">762.564</td>
<td align="center">315.218</td>
<td align="center">0.811</td>
<td align="center">4.35 &#xd7; 10<sup>&#x2212;6</sup>
</td>
<td align="center">5.89 &#xd7; 10<sup>&#x2212;6</sup>
</td>
<td align="center">0.436</td>
<td align="center">4.74 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.038</td>
<td align="center">1.110</td>
</tr>
<tr>
<td align="left">DGTS (21:1/21:1)</td>
<td align="center">848.683</td>
<td align="center">637.876</td>
<td align="center">0.641</td>
<td align="center">6.72 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">1.20 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.838</td>
<td align="center">1.25 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.022</td>
<td align="center">2.380</td>
</tr>
<tr>
<td align="left">DGTS (26:0/16:1)</td>
<td align="center">850.699</td>
<td align="center">655.426</td>
<td align="center">0.515</td>
<td align="center">2.63 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">3.83 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.542</td>
<td align="center">4.42 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.037</td>
<td align="center">2.297</td>
</tr>
<tr>
<td align="left">DGTS (3:0/21:0)</td>
<td align="center">600.467</td>
<td align="center">83.235</td>
<td align="center">0.620</td>
<td align="center">1.74 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">2.53 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.543</td>
<td align="center">7.55 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.044</td>
<td align="center">2.356</td>
</tr>
<tr>
<td align="left">ACar (26:7)</td>
<td align="center">526.377</td>
<td align="center">112.711</td>
<td align="center">0.587</td>
<td align="center">1.74 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">2.26 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.374</td>
<td align="center">3.84 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.037</td>
<td align="center">2.866</td>
</tr>
<tr>
<td align="left">PEtOH (22:0/26:0)</td>
<td align="center">918.755</td>
<td align="center">640.810</td>
<td align="center">0.796</td>
<td align="center">6.16 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">1.03 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.747</td>
<td align="center">2.14 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.029</td>
<td align="center">2.037</td>
</tr>
<tr>
<td align="left">PMeOH (24:4/24:4)</td>
<td align="center">888.656</td>
<td align="center">628.171</td>
<td align="center">0.947</td>
<td align="center">7.93 &#xd7; 10<sup>&#x2212;6</sup>
</td>
<td align="center">1.21 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.607</td>
<td align="center">3.80 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.037</td>
<td align="center">1.982</td>
</tr>
<tr>
<td colspan="10" align="left">Negative-ion mode (ESI -)</td>
</tr>
<tr>
<td align="left">HexCer/NS (d14:2/40:2)</td>
<td align="center">972.837</td>
<td align="center">692.336</td>
<td align="center">0.567</td>
<td align="center">1.35 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">1.06 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">&#x2212;0.353</td>
<td align="center">5.87 &#xd7; 10<sup>&#x2212;3</sup>
</td>
<td align="center">0.123</td>
<td align="center">2.412</td>
</tr>
<tr>
<td align="left">PI (16:0/18:1)</td>
<td align="center">835.519</td>
<td align="center">273.846</td>
<td align="center">0.815</td>
<td align="center">1.81 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">2.48 &#xd7; 10<sup>&#x2212;4</sup>
</td>
<td align="center">0.452</td>
<td align="center">2.46 &#xd7; 10<sup>&#x2212;3</sup>
</td>
<td align="center">0.077</td>
<td align="center">1.965</td>
</tr>
<tr>
<td align="left">SQDG (18:3/26:4)</td>
<td align="center">947.607</td>
<td align="center">85.781</td>
<td align="center">0.826</td>
<td align="center">2.70 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">4.12 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">0.611</td>
<td align="center">9.92 &#xd7; 10<sup>&#x2212;3</sup>
</td>
<td align="center">0.156</td>
<td align="center">1.799</td>
</tr>
<tr>
<td align="left">SQDG (23:0/22:5)</td>
<td align="center">965.616</td>
<td align="center">449.079</td>
<td align="center">0.876</td>
<td align="center">2.63 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">2.19 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">&#x2212;0.264</td>
<td align="center">5.88 &#xd7; 10<sup>&#x2212;2</sup>
</td>
<td align="center">0.311</td>
<td align="center">1.559</td>
</tr>
<tr>
<td align="center">TAG [17:0/22:1 (13Z)/22:3 (10Z,13Z,16Z)] [iso6]</td>
<td align="center">979.846</td>
<td align="center">688.173</td>
<td align="center">0.898</td>
<td align="center">1.43 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">1.08 &#xd7; 10<sup>&#x2212;5</sup>
</td>
<td align="center">&#x2212;0.400</td>
<td align="center">2.68 &#xd7; 10<sup>&#x2212;2</sup>
</td>
<td align="center">0.229</td>
<td align="center">2.192</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>RT, retention time; log2fc, log2 transformed fold change; p. <italic>t</italic>-test, <italic>p</italic>-value of the <italic>t</italic>-test; p.t.adj, FDR-adjusted <italic>p</italic>-value of the <italic>t</italic>-test; VIP, variable importance projection.</p>
</fn>
<fn>
<p>Lipid metabolites: TAG, triacylglycerol; LPC, lysophosphatidylcholine; PC, phosphatidylcholine; DGTS, diacylglyceryl trimethylhomoserine; ACar, acylcarnitine; PEtOH, phosphatidylethanol; PMeOH, phosphatidylmethanol; HexCer/NS, hexosylceramide non-hydroxyfatty acid-sphingosine; PI, phosphatidylinositol; SQDG, sulfoquinovosyl diacylglycerol.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>Heat map presenting 32 differential lipid metabolites between eosinophilic AECOPD and non-eosinophilic AECOPD subjects.</p>
</caption>
<graphic xlink:href="fmolb-10-1204985-g002.tif"/>
</fig>
<p>In the ESI &#x2b; mode, the levels of most of triacylglycerols (TAGs), lysophophatidylcholines (LPCs), and diacylglyceryl trimethylhomoserine (DGTSs) were significantly higher in the eosinophilic AECOPD patients than those in the non-eosinophilic patients, except TAG (12:0/12:0/22:3) and TAG (12:1/12:3/12:3). In the ESI &#x2212; mode, the levels of PI (16:0/18:1), PIM1 (18:0/18:0), and SQDG (18:3/26:4) were significantly higher in the eosinophilic AECOPD patients.</p>
</sec>
<sec id="s3-3">
<title>3.3 Integration analysis between clinical characteristics and differential lipid metabolites</title>
<p>The correlation analysis between the 32 lipid metabolites and the clinical characteristics of all the AECOPD patients is shown in <xref ref-type="sec" rid="s11">Supplementary Figure 1</xref>. The most significant clinical characteristics correlated with lipid metabolites were body mass index, D-dimer, fibrinogen, total cholesterol, hypercapnic respiratory failure, and ICU admission. We further analyzed the associations between each of these 32 metabolites and the clinical features which were different between the eosinophilic and non-eosinophilic AECOPD, including hypercapnia respiratory failure, need for ICU admission, and fibrinogen. There were nine differential lipid metabolites associated with each of the three features (<xref ref-type="table" rid="T3">Table 3</xref>). Most of them have a negative association with these three features.</p>
<table-wrap id="T3" position="float">
<label>TABLE 3</label>
<caption>
<p>Nine lipid metabolites and their association with clinical features<sup>a</sup>.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th rowspan="2" align="center">Metabolite</th>
<th colspan="3" align="center">Preliminary screening</th>
<th colspan="2" align="center">Eosinophil</th>
<th colspan="2" align="center">Hypercapnic respiratory failure</th>
<th colspan="2" align="center">Need for ICU</th>
<th colspan="2" align="center">Fibrinogen</th>
</tr>
<tr>
<th align="center">log2fc</th>
<th align="center">p.t.adj</th>
<th align="center">VIP</th>
<th align="center">&#x3b2;</th>
<th align="center">p.adj</th>
<th align="center">OR (95% CI)</th>
<th align="center">p.adj</th>
<th align="center">OR (95% CI)</th>
<th align="center">p.adj</th>
<th align="center">&#x3b2;</th>
<th align="center">p.adj</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">TAG (20:6/20:6/22:5)</td>
<td align="center">0.849</td>
<td align="center">0.021</td>
<td align="center">2.640</td>
<td align="center">1.186</td>
<td align="center">0.001</td>
<td align="center">0.377 (0.211, 0.675)</td>
<td align="center">0.011</td>
<td align="center">0.433 (0.236, 0.792)</td>
<td align="center">0.028</td>
<td align="center">&#x2212;0.426</td>
<td align="center">0.004</td>
</tr>
<tr>
<td align="left">TAG (20:6/22:7/22:7)</td>
<td align="center">0.610</td>
<td align="center">0.015</td>
<td align="center">2.962</td>
<td align="center">0.807</td>
<td align="center">0.001</td>
<td align="center">0.230 (0.095, 0.554)</td>
<td align="center">0.011</td>
<td align="center">0.224 (0.088, 0.575)</td>
<td align="center">0.023</td>
<td align="center">&#x2212;0.618</td>
<td align="center">0.005</td>
</tr>
<tr>
<td align="left">TAG (20:5/22:7/22:7)</td>
<td align="center">0.552</td>
<td align="center">0.021</td>
<td align="center">2.903</td>
<td align="center">0.731</td>
<td align="center">0.001</td>
<td align="center">0.228 (0.090, 0.578)</td>
<td align="center">0.012</td>
<td align="center">0.198 (0.071, 0.554)</td>
<td align="center">0.023</td>
<td align="center">&#x2212;0.694</td>
<td align="center">0.004</td>
</tr>
<tr>
<td align="left">LPC (20:2)</td>
<td align="center">0.523</td>
<td align="center">0.021</td>
<td align="center">2.740</td>
<td align="center">0.663</td>
<td align="center">0.001</td>
<td align="center">0.259 (0.098, 0.685)</td>
<td align="center">0.024</td>
<td align="center">0.204 (0.064, 0.649)</td>
<td align="center">0.028</td>
<td align="center">&#x2212;0.771</td>
<td align="center">0.004</td>
</tr>
<tr>
<td align="left">TAG (17:0/17:2/17:2)</td>
<td align="center">0.703</td>
<td align="center">0.015</td>
<td align="center">2.632</td>
<td align="center">0.637</td>
<td align="center">0.003</td>
<td align="center">0.264 (0.099, 0.703)</td>
<td align="center">0.024</td>
<td align="center">0.203 (0.059, 0.698)</td>
<td align="center">0.036</td>
<td align="center">&#x2212;0.689</td>
<td align="center">0.005</td>
</tr>
<tr>
<td align="left">DGTS (3:0/21:0)</td>
<td align="center">0.543</td>
<td align="center">0.044</td>
<td align="center">2.356</td>
<td align="center">0.628</td>
<td align="center">0.012</td>
<td align="center">0.200 (0.075, 0.534)</td>
<td align="center">0.011</td>
<td align="center">0.286 (0.121, 0.672)</td>
<td align="center">0.028</td>
<td align="center">&#x2212;0.686</td>
<td align="center">0.001</td>
</tr>
<tr>
<td align="left">LPC (16:0)</td>
<td align="center">0.448</td>
<td align="center">0.016</td>
<td align="center">3.021</td>
<td align="center">0.563</td>
<td align="center">0.001</td>
<td align="center">0.126 (0.036, 0.449)</td>
<td align="center">0.011</td>
<td align="center">0.103 (0.024, 0.439)</td>
<td align="center">0.023</td>
<td align="center">&#x2212;0.987</td>
<td align="center">0.004</td>
</tr>
<tr>
<td align="left">ACar (26:7)</td>
<td align="center">0.374</td>
<td align="center">0.037</td>
<td align="center">2.866</td>
<td align="center">0.498</td>
<td align="center">0.001</td>
<td align="center">0.174 (0.050, 0.607)</td>
<td align="center">0.024</td>
<td align="center">0.124 (0.028, 0.548)</td>
<td align="center">0.028</td>
<td align="center">&#x2212;1.162</td>
<td align="center">0.001</td>
</tr>
<tr>
<td align="left">TAG (16:2/18:2/18:3)</td>
<td align="center">0.369</td>
<td align="center">0.042</td>
<td align="center">2.306</td>
<td align="center">0.341</td>
<td align="center">0.012</td>
<td align="center">0.175 (0.043, 0.712)</td>
<td align="center">0.028</td>
<td align="center">0.104 (0.019, 0.570)</td>
<td align="center">0.033</td>
<td align="center">&#x2212;0.836</td>
<td align="center">0.025</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>a: Association of every one-fold increase of a marker with clinical features. Markers were considered the response variable for EOS, while the predictor variable for the other three clinical features.</p>
</fn>
<fn>
<p>Abbreviation: EOS, percentage of peripheral eosinophils; RF, respiratory failure; log2fc, log2 transformed fold change; p.t.adj, FDR-adjusted <italic>p</italic>-value for the <italic>t</italic>-test; VIP, variable importance projection; &#x3b2;, log2 transformed fold change after adjusting for age, sex, BMI, smoking status, serum total cholesterol, and triglyceride; p. adj, FDR-adjusted <italic>p</italic>-value.</p>
</fn>
<fn>
<p>Lipid metabolites: TAG, triacylglycerol; LPC, lysophosphatidylcholine; DGTS, diacylglyceryl trimethylhomoserine; ACar, acylcarnitine.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>In order to identify the most characteristic lipid biomarkers for the eosinophilic AECOPD phenotype, LASSO regression was applied to further screen the potential biomarkers. As shown in <xref ref-type="fig" rid="F3">Figure 3A</xref>, all the nine different lipid metabolites associated with the eosinophilic phenotype and clinical features were included in a 7-fold cross-validation (CV) and a CV plot was generated, in which the lambda.min and lambda.1se values were determined. Based on lambda.1se, three lipid metabolites were retained, which were LPC (16:0), TAG (17:0/17:2/17:2), and LPC (20:2) (<xref ref-type="fig" rid="F3">Figures 3A, B</xref>). All of these three lipid metabolites were high in patients with eosinophilic AECOPD. Next, logistic regression models were fitted by individually using each of the three selected markers as the covariate, as well as using them together to obtain the individual screening scores and a combined score, respectively. The predictability of the models was evaluated by the area under ROC curve. As shown in <xref ref-type="fig" rid="F4">Figure 4</xref>, the area under the ROC curve values of LPC (16:0), TAG (17:0/17:2/17:2), and LPC (20:2) were 0.790, 0.787, and 0.756, respectively. In addition, the AUC reached 0.834 (95% CI: 0.740&#x2013;0.929) when including all the three markers together, which meant this model had an excellent discriminative capacity to distinguish eosinophilic AECOPD and non-eosinophilic AECOPD.</p>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>LASSO analysis and cross-validation to identify the most characteristic lipid biomarkers. <bold>(A)</bold> Nine potential lipid biomarkers were included in the model for seven-fold cross-validation, in which lambda.min and lambda.1se were determined. Accordingly, lambda.1se was selected as the optimal value and there were three corresponding lipid metabolites at this optimal value. <bold>(B)</bold> Coefficient profiles of nine potential lipid biomarkers corresponding to different lambda values in LASSO analysis. LPC (16:0), TAG (17:0/17:2/17:2), and LPC (20:2) were retained in this model at lambda.1se &#x3d; 0.059.</p>
</caption>
<graphic xlink:href="fmolb-10-1204985-g003.tif"/>
</fig>
<fig id="F4" position="float">
<label>FIGURE 4</label>
<caption>
<p>Receiver operating characteristic (ROC) curve of the diagnostic prediction model with three LASSO-selected markers, namely, LPC (16:0), TAG (17:0/17:2/17:2), and LPC (20:2). The combined prediction performance of these three biomarkers was superior to the individual prediction performance of each biomarker.</p>
</caption>
<graphic xlink:href="fmolb-10-1204985-g004.tif"/>
</fig>
</sec>
</sec>
<sec sec-type="discussion" id="s4">
<title>4 Discussion</title>
<p>Our study demonstrated the unique characteristics of lipid profiles measured using LC-MS in a group of hospitalized AECOPD patients and indicated that alterations in lipid metabolism were involved in the pathogenesis of the eosinophilic phenotype. In our study, we observed that nine lipid metabolites were significantly associated with the difference in clinical features and prognosis between the eosinophilic and non-eosinophilic phenotypes, which were enriched in triglycerides and phospholipid metabolic pathways and were expected to be potential biomarkers for AECOPD patients and help explain the mechanisms of different clinical outcomes in the eosinophilic phenotype. Furthermore, three lipid metabolites were further screened using LASSO, including LPC (16:0), TAG (17:0/17:2/17:2), and LPC (20:2). Their combination was reliable to predict the clinical prognosis of AECOPD patients in different phenotypes.</p>
<p>Triglycerides are lipids containing three glyceryl groups (<xref ref-type="bibr" rid="B11">Fahy et al., 2005</xref>; <xref ref-type="bibr" rid="B21">Liebisch et al., 2020</xref>) and are mainly found in the adipose tissue (<xref ref-type="bibr" rid="B8">Chaurasia et al., 2016</xref>; <xref ref-type="bibr" rid="B34">Wu et al., 2020</xref>). Few studies have explored the characteristics and mechanisms of triglyceride metabolism of eosinophilic COPD. Our data showed that some species of TAGs were higher in those with eosinophilic AECOPD. In previous studies, high triglycerides and low HDL-C played an important role in type 2 inflammation in asthmatic patients (<xref ref-type="bibr" rid="B3">Barochia et al., 2017</xref>; <xref ref-type="bibr" rid="B7">Chanachon et al., 2022</xref>); the mechanism may be that free fatty acids released by triglycerides promoted inflammation by activating NF-&#x3ba;B signaling in mononuclear cells and enhancing reactive oxygen species generation (<xref ref-type="bibr" rid="B31">Tucker et al., 2020</xref>). Additionally, fatty acid synthesis or uptake and subsequent TAG synthesis were also significantly enhanced after inflammatory activation (<xref ref-type="bibr" rid="B31">Tucker et al., 2020</xref>). Airway inflammation in eosinophilic COPD and asthma were likely to share a similar mechanism, which could partly explain why some species of TAGs were increased in those with eosinophilic AECOPD. However, the increased levels of these species of TAGs in eosinophilic AECOPD were associated with better clinical outcomes and less systemic inflammation (a lower fibrinogen level) in our study, which seemed to contradict previous studies. A deficiency of lysosomal acid lipase could lead to disruption of triglyceride and cholesterol ester metabolism in alveolar macrophages, leading to respiratory inflammation, tissue remodeling, and emphysema (<xref ref-type="bibr" rid="B20">Lian et al., 2004</xref>; <xref ref-type="bibr" rid="B19">Lian et al., 2005</xref>). In addition, inflammation also increased the activity of angiopoietin-like protein, an inhibitor of lipoprotein lipase, which further prevented the metabolism of triglyceride-rich lipoproteins and led to elevated triglyceride levels (<xref ref-type="bibr" rid="B22">Lu et al., 2010</xref>). Triglycerides were associated with airflow obstruction and wheezing in asthma patients (<xref ref-type="bibr" rid="B12">Fenger et al., 2013</xref>; <xref ref-type="bibr" rid="B4">Barochia et al., 2015</xref>; <xref ref-type="bibr" rid="B7">Chanachon et al., 2022</xref>). However, inconsistent results between previous studies and ours may be related to different study population and disease statuses. In addition, very few studies elucidated the relevant mechanism of the effect of triglyceride species on eosinophil proliferation, activity, and function. The alteration of TAG metabolism and its role in the pathogenesis of eosinophilic COPD need to be further investigated.</p>
<p>Phospholipids are lipids containing phosphoric acid (<xref ref-type="bibr" rid="B11">Fahy et al., 2005</xref>; <xref ref-type="bibr" rid="B21">Liebisch et al., 2020</xref>) and are the main components of the biological membrane. Phospholipase A2 splits phospholipids into lysophospholipids (a kind of phospholipid containing a single fatty acid) and fatty acids. In our study, LPC (16:0) and LPC (20:2) were increased in eosinophilic AECOPD and associated with fewer hypercapnic respiratory failures, shorter ICU stay, and lower fibrinogen level. The physiological role of LPC in inflammation was complicated. In previous literature, LPCs could exhibit proinflammatory or anti-inflammatory activity under different conditions. Under certain pathophysiological conditions, LPC can be used as a proinflammatory substance. The mechanism may be that LPC-dependent NADPH oxidase can stimulate the production of reactive oxygen species, thus promoting the transformation of pro-cytokines into their mature bioactive forms (such as IL-1&#x3b2;, IL-18, and IL-33), promoting the occurrence of inflammation (<xref ref-type="bibr" rid="B29">Schilling and Eder, 2010</xref>). However, under other conditions, some polyunsaturated LPCs (such as LPC 20:4, LPC 20:5, and LPC 22:6) can exhibit anti-inflammatory effects. The mechanism may be to downregulate the formation of pro-inflammatory mediators (such as IL-5, IL-6, NO, 12-hydroxy eicosapentaenoic acid, and LPC16:0-induced PGE2) and upregulate the expression of anti-inflammatory mediators (IL-4 and IL-10) by reducing leukocyte exosmosis and plasma leakage (<xref ref-type="bibr" rid="B28">Riederer et al., 2010</xref>; <xref ref-type="bibr" rid="B15">Hung et al., 2011</xref>; <xref ref-type="bibr" rid="B16">Hung et al., 2012</xref>). In our study, elevated levels of several LPCs were found to have negative correlations with fibrinogen in eosinophilic AECOPD patients, suggesting that systemic inflammatory responses may be weaker and clinical outcomes may be better, and that LPC may have a protective effect in eosinophilic AECOPD patients. Regarding the association between LPC and eosinophilic AECOPD phenotypes, we speculated the mechanism as follows: eosinophils had been demonstrated to express high levels of phospholipase A2 (<xref ref-type="bibr" rid="B5">Blom et al., 1998</xref>), which can cleave phosphatidylcholine into LPC and a free fatty acid and increase the level of LPC. Additionally, LPC could induce eosinophils to adhere on and infiltrate into the airway wall (<xref ref-type="bibr" rid="B24">Nishiyama et al., 2004</xref>; <xref ref-type="bibr" rid="B36">Zhu et al., 2007</xref>). However, most previous studies were based on allergic diseases, such as asthma and allergic rhinitis. The saturated or unsaturated fatty acid chains on LPC species may exhibit different effects on inflammation. Therefore, these issues should be addressed in further studies.</p>
<p>In our study, we also found that eosinophilic AECOPD patients had better clinical outcomes, with shorter hospital stays, fewer cases of respiratory failure, and a lower rate of ICU admission during hospitalization. These results were similar to those found in a meta-analysis. In this analysis, eosinophilic AECOPD (blood eosinophilia &#x2265; 2% or 0.34 &#xd7; 10<sup>9</sup> cells/L) had a better prognosis (lower risk of in-hospital mortality, shorter stay in hospital, and lower risk of arrhythmia) (<xref ref-type="bibr" rid="B35">You and Shi, 2021</xref>). Although studies showed a higher risk of readmission (shorter first COPD-related readmissions and an increased number of 12-month COPD-related readmissions) in eosinophilic AECOPD patients, our study did not suggest an increase in the risk of acute exacerbations again (<xref ref-type="bibr" rid="B26">Peng et al., 2021</xref>).</p>
<p>This study included the following limitations: 1) since our study results were drawn from a small sample size, further studies are needed to elucidate the relation between lipid metabolism and phenotypes of AECOPD. 2) The Q2Y value in OPLS-DA was relatively low, which meant the estimates from the model were probably on the lower side. This may be due to a possible small difference between the whole lipid profiles of the two groups and the small sample size. However, a combination of several lipids could model well in the discrimination. In future, we would verify the relationship between these lipid metabolites and disease phenotypes in a prospective study. 3) In this study, we did not observe differences in serum lipid metabolic profiles between the two groups before and after the treatment, and it would be of great significance in elucidating the mechanism if we could observe the dynamic changes in lipid metabolites with the treatment time.</p>
<p>In conclusion, our LC-MS analysis demonstrated that patients with eosinophilic AECOPD had a unique serum lipid metabolite profile that could be used to differentiate them from non-eosinophilic AECOPD patients. TAGs and LPCs were significantly increased in eosinophilic phenotypes and associated with less hypercapnic respiratory failure and ICU admission, as well as a lower fibrinogen level, suggesting that these lipid species can serve as biomarkers and play an important role in the pathogenesis of COPD exacerbation. Further studies regarding the mechanisms around lipid metabolism and metabolic pathways will help develop potential therapeutic targets for patients with COPD.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="s5">
<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 id="s6">
<title>Ethics statement</title>
<p>The studies involving human participants were reviewed and approved by the Ethics Committee of Peking University Third Hospital (M2017410). The patients/participants provided their written informed consent to participate in this study.</p>
</sec>
<sec id="s7">
<title>Author contributions</title>
<p>YW, CC, XiG, YS, and YL contributed to the conception and design of the study. YW, CC, JW, YC, and YL organized the database. ST, XiG, and XuG performed the statistical analysis. YW, CC, ST, and YL wrote the first draft of the manuscript. JW, XiG, and QZ participated in writing the methods and results sections of the manuscript. YC participated in writing the discussion section of the manuscript. All authors contributed to the article and approved the submitted version.</p>
</sec>
<sec id="s8">
<title>Funding</title>
<p>This work was supported by the National Natural Science Foundation (project no. 81700039).</p>
</sec>
<sec sec-type="COI-statement" id="s9">
<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&#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 id="s11">
<title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fmolb.2023.1204985/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fmolb.2023.1204985/full&#x23;supplementary-material</ext-link>
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<supplementary-material xlink:href="DataSheet1.PDF" id="SM1" mimetype="application/PDF" xmlns:xlink="http://www.w3.org/1999/xlink"/>
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