Loading…
Cumulative residual cholesterol predicts the risk of cardiovascular disease in the general population aged 45 years and older
Numerous studies have affirmed a robust correlation between residual cholesterol (RC) and the occurrence of cardiovascular disease (CVD). However, the current body of literature fails to adequately address the link between alterations in RC and the occurrence of CVD. Existing studies have focused ma...
Saved in:
Published in: | Lipids in health and disease 2024-01, Vol.23 (1), p.19-19, Article 19 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c459t-324d5656b562fcab2c1c40b4929640ebc7ca60e177de93261a1e9b76940b41b33 |
container_end_page | 19 |
container_issue | 1 |
container_start_page | 19 |
container_title | Lipids in health and disease |
container_volume | 23 |
creator | Zhao, Mengjie Xiao, Mengli Tan, Qin Ji, Jinjin Lu, Fang |
description | Numerous studies have affirmed a robust correlation between residual cholesterol (RC) and the occurrence of cardiovascular disease (CVD). However, the current body of literature fails to adequately address the link between alterations in RC and the occurrence of CVD. Existing studies have focused mainly on individual RC values. Hence, the primary objective of this study is to elucidate the association between the cumulative RC (Cum-RC) and the morbidity of CVD.
The changes in RC were categorized into a high-level fast-growth group (Class 1) and a low-level slow-growth group (Class 2) by K-means cluster analysis. To investigate the relationship between combined exposure to multiple lipids and CVD risk, a weighted quantile sum (WQS) regression analysis was employed. This analysis involved the calculation of weights for total cholesterol (TC), low-density lipoprotein (LDL), and high-density lipoprotein (HDL), which were used to effectively elucidate the RC.
Among the cohort of 5,372 research participants, a considerable proportion of 45.94% consisted of males, with a median age of 58. In the three years of follow-up, 669 participants (12.45%) had CVD. Logistic regression analysis revealed that Class 2 individuals had a significantly reduced risk of developing CVD compared to Class 1. The probability of having CVD increased by 13% for every 1-unit increase in the Cum-RC according to the analysis of continuous variables. The restricted cubic spline (RCS) analysis showed that Cum-RC and CVD risk were linearly related (P for nonlinearity = 0.679). The WQS regression results showed a nonsignificant trend toward an association between the WQS index and CVD incidence but an overall positive trend, with the greatest contribution from TC (weight = 0.652), followed by LDL (weight = 0.348).
Cum-RC was positively and strongly related to CVD risk, suggesting that in addition to focusing on traditional lipid markers, early intervention in patients with increased RC may further reduce the incidence of CVD. |
doi_str_mv | 10.1186/s12944-023-02000-0 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_e7104d2bb2b64110b22abf3c1e47bb34</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A782195954</galeid><doaj_id>oai_doaj_org_article_e7104d2bb2b64110b22abf3c1e47bb34</doaj_id><sourcerecordid>A782195954</sourcerecordid><originalsourceid>FETCH-LOGICAL-c459t-324d5656b562fcab2c1c40b4929640ebc7ca60e177de93261a1e9b76940b41b33</originalsourceid><addsrcrecordid>eNptkkuLFDEUhQtRnHH0D7iQgBs3NeYmqaSzHBofAwNuFNyFPG71pK2qtEnVwCz876a756EiISRcvnNubjhN8xroOcBKvi_AtBAtZbxuSmlLnzSnIJRsO4DvT_-4nzQvStnSSikpnzcnfMUEZ0yeNr_Wy7gMdo43SDKWGBY7EH-dBiwz5jSQXcYQ_VzIfF2JWH6Q1BNvc4jpxhZftZmEWNAWJHE6UBucMFebXdodrNNE7AYDER25RZsLsVMgaQiYXzbPejsUfHV3njXfPn74uv7cXn35dLm-uGq96PTcciZCJzvpOsl6bx3z4AV1QjMtBUXnlbeSIigVUHMmwQJqp6TeQ-A4P2suj74h2a3Z5TjafGuSjeZQSHljbJ6jH9CgAioCc445KQCoY8y6nntAoZzjonq9O3rtcvq51G8yYyweh8FOmJZimAbVdQo4q-jbf9BtWvJUJ60UqxOthIRHamNr_zj1ac7W703NhVox0J3u9m3P_0PVFXCMPk3Yx1r_S8COAp9TKRn7h7mBmn1-zDE_pubHHPJjaBW9uXvx4kYMD5L7wPDfHs6_GQ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2925658461</pqid></control><display><type>article</type><title>Cumulative residual cholesterol predicts the risk of cardiovascular disease in the general population aged 45 years and older</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>PubMed Central</source><creator>Zhao, Mengjie ; Xiao, Mengli ; Tan, Qin ; Ji, Jinjin ; Lu, Fang</creator><creatorcontrib>Zhao, Mengjie ; Xiao, Mengli ; Tan, Qin ; Ji, Jinjin ; Lu, Fang</creatorcontrib><description>Numerous studies have affirmed a robust correlation between residual cholesterol (RC) and the occurrence of cardiovascular disease (CVD). However, the current body of literature fails to adequately address the link between alterations in RC and the occurrence of CVD. Existing studies have focused mainly on individual RC values. Hence, the primary objective of this study is to elucidate the association between the cumulative RC (Cum-RC) and the morbidity of CVD.
The changes in RC were categorized into a high-level fast-growth group (Class 1) and a low-level slow-growth group (Class 2) by K-means cluster analysis. To investigate the relationship between combined exposure to multiple lipids and CVD risk, a weighted quantile sum (WQS) regression analysis was employed. This analysis involved the calculation of weights for total cholesterol (TC), low-density lipoprotein (LDL), and high-density lipoprotein (HDL), which were used to effectively elucidate the RC.
Among the cohort of 5,372 research participants, a considerable proportion of 45.94% consisted of males, with a median age of 58. In the three years of follow-up, 669 participants (12.45%) had CVD. Logistic regression analysis revealed that Class 2 individuals had a significantly reduced risk of developing CVD compared to Class 1. The probability of having CVD increased by 13% for every 1-unit increase in the Cum-RC according to the analysis of continuous variables. The restricted cubic spline (RCS) analysis showed that Cum-RC and CVD risk were linearly related (P for nonlinearity = 0.679). The WQS regression results showed a nonsignificant trend toward an association between the WQS index and CVD incidence but an overall positive trend, with the greatest contribution from TC (weight = 0.652), followed by LDL (weight = 0.348).
Cum-RC was positively and strongly related to CVD risk, suggesting that in addition to focusing on traditional lipid markers, early intervention in patients with increased RC may further reduce the incidence of CVD.</description><identifier>ISSN: 1476-511X</identifier><identifier>EISSN: 1476-511X</identifier><identifier>DOI: 10.1186/s12944-023-02000-0</identifier><identifier>PMID: 38243226</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Cardiovascular disease ; Cardiovascular diseases ; Cardiovascular Diseases - epidemiology ; CHARLS ; Cholesterol ; Cholesterol, HDL ; Cholesterol, LDL ; Clustering ; Datasets ; Diabetes ; Education ; Health aspects ; Heart ; High density lipoprotein ; Humans ; Hypertension ; Incidence ; K-means clustering ; Lipids ; Lipoproteins ; Low density lipoprotein ; Male ; Measurement ; Metabolic disorders ; Middle aged persons ; Missing data ; Morbidity ; Nonlinear systems ; Population ; Questionnaires ; Regression analysis ; Residual cholesterol ; Risk Factors ; Trends ; Weighted quantile sum</subject><ispartof>Lipids in health and disease, 2024-01, Vol.23 (1), p.19-19, Article 19</ispartof><rights>2024. The Author(s).</rights><rights>COPYRIGHT 2024 BioMed Central Ltd.</rights><rights>2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c459t-324d5656b562fcab2c1c40b4929640ebc7ca60e177de93261a1e9b76940b41b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2925658461?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38243226$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhao, Mengjie</creatorcontrib><creatorcontrib>Xiao, Mengli</creatorcontrib><creatorcontrib>Tan, Qin</creatorcontrib><creatorcontrib>Ji, Jinjin</creatorcontrib><creatorcontrib>Lu, Fang</creatorcontrib><title>Cumulative residual cholesterol predicts the risk of cardiovascular disease in the general population aged 45 years and older</title><title>Lipids in health and disease</title><addtitle>Lipids Health Dis</addtitle><description>Numerous studies have affirmed a robust correlation between residual cholesterol (RC) and the occurrence of cardiovascular disease (CVD). However, the current body of literature fails to adequately address the link between alterations in RC and the occurrence of CVD. Existing studies have focused mainly on individual RC values. Hence, the primary objective of this study is to elucidate the association between the cumulative RC (Cum-RC) and the morbidity of CVD.
The changes in RC were categorized into a high-level fast-growth group (Class 1) and a low-level slow-growth group (Class 2) by K-means cluster analysis. To investigate the relationship between combined exposure to multiple lipids and CVD risk, a weighted quantile sum (WQS) regression analysis was employed. This analysis involved the calculation of weights for total cholesterol (TC), low-density lipoprotein (LDL), and high-density lipoprotein (HDL), which were used to effectively elucidate the RC.
Among the cohort of 5,372 research participants, a considerable proportion of 45.94% consisted of males, with a median age of 58. In the three years of follow-up, 669 participants (12.45%) had CVD. Logistic regression analysis revealed that Class 2 individuals had a significantly reduced risk of developing CVD compared to Class 1. The probability of having CVD increased by 13% for every 1-unit increase in the Cum-RC according to the analysis of continuous variables. The restricted cubic spline (RCS) analysis showed that Cum-RC and CVD risk were linearly related (P for nonlinearity = 0.679). The WQS regression results showed a nonsignificant trend toward an association between the WQS index and CVD incidence but an overall positive trend, with the greatest contribution from TC (weight = 0.652), followed by LDL (weight = 0.348).
Cum-RC was positively and strongly related to CVD risk, suggesting that in addition to focusing on traditional lipid markers, early intervention in patients with increased RC may further reduce the incidence of CVD.</description><subject>Cardiovascular disease</subject><subject>Cardiovascular diseases</subject><subject>Cardiovascular Diseases - epidemiology</subject><subject>CHARLS</subject><subject>Cholesterol</subject><subject>Cholesterol, HDL</subject><subject>Cholesterol, LDL</subject><subject>Clustering</subject><subject>Datasets</subject><subject>Diabetes</subject><subject>Education</subject><subject>Health aspects</subject><subject>Heart</subject><subject>High density lipoprotein</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Incidence</subject><subject>K-means clustering</subject><subject>Lipids</subject><subject>Lipoproteins</subject><subject>Low density lipoprotein</subject><subject>Male</subject><subject>Measurement</subject><subject>Metabolic disorders</subject><subject>Middle aged persons</subject><subject>Missing data</subject><subject>Morbidity</subject><subject>Nonlinear systems</subject><subject>Population</subject><subject>Questionnaires</subject><subject>Regression analysis</subject><subject>Residual cholesterol</subject><subject>Risk Factors</subject><subject>Trends</subject><subject>Weighted quantile sum</subject><issn>1476-511X</issn><issn>1476-511X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkkuLFDEUhQtRnHH0D7iQgBs3NeYmqaSzHBofAwNuFNyFPG71pK2qtEnVwCz876a756EiISRcvnNubjhN8xroOcBKvi_AtBAtZbxuSmlLnzSnIJRsO4DvT_-4nzQvStnSSikpnzcnfMUEZ0yeNr_Wy7gMdo43SDKWGBY7EH-dBiwz5jSQXcYQ_VzIfF2JWH6Q1BNvc4jpxhZftZmEWNAWJHE6UBucMFebXdodrNNE7AYDER25RZsLsVMgaQiYXzbPejsUfHV3njXfPn74uv7cXn35dLm-uGq96PTcciZCJzvpOsl6bx3z4AV1QjMtBUXnlbeSIigVUHMmwQJqp6TeQ-A4P2suj74h2a3Z5TjafGuSjeZQSHljbJ6jH9CgAioCc445KQCoY8y6nntAoZzjonq9O3rtcvq51G8yYyweh8FOmJZimAbVdQo4q-jbf9BtWvJUJ60UqxOthIRHamNr_zj1ac7W703NhVox0J3u9m3P_0PVFXCMPk3Yx1r_S8COAp9TKRn7h7mBmn1-zDE_pubHHPJjaBW9uXvx4kYMD5L7wPDfHs6_GQ</recordid><startdate>20240119</startdate><enddate>20240119</enddate><creator>Zhao, Mengjie</creator><creator>Xiao, Mengli</creator><creator>Tan, Qin</creator><creator>Ji, Jinjin</creator><creator>Lu, Fang</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>20240119</creationdate><title>Cumulative residual cholesterol predicts the risk of cardiovascular disease in the general population aged 45 years and older</title><author>Zhao, Mengjie ; Xiao, Mengli ; Tan, Qin ; Ji, Jinjin ; Lu, Fang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-324d5656b562fcab2c1c40b4929640ebc7ca60e177de93261a1e9b76940b41b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Cardiovascular disease</topic><topic>Cardiovascular diseases</topic><topic>Cardiovascular Diseases - epidemiology</topic><topic>CHARLS</topic><topic>Cholesterol</topic><topic>Cholesterol, HDL</topic><topic>Cholesterol, LDL</topic><topic>Clustering</topic><topic>Datasets</topic><topic>Diabetes</topic><topic>Education</topic><topic>Health aspects</topic><topic>Heart</topic><topic>High density lipoprotein</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Incidence</topic><topic>K-means clustering</topic><topic>Lipids</topic><topic>Lipoproteins</topic><topic>Low density lipoprotein</topic><topic>Male</topic><topic>Measurement</topic><topic>Metabolic disorders</topic><topic>Middle aged persons</topic><topic>Missing data</topic><topic>Morbidity</topic><topic>Nonlinear systems</topic><topic>Population</topic><topic>Questionnaires</topic><topic>Regression analysis</topic><topic>Residual cholesterol</topic><topic>Risk Factors</topic><topic>Trends</topic><topic>Weighted quantile sum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Mengjie</creatorcontrib><creatorcontrib>Xiao, Mengli</creatorcontrib><creatorcontrib>Tan, Qin</creatorcontrib><creatorcontrib>Ji, Jinjin</creatorcontrib><creatorcontrib>Lu, Fang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Directory of Open Access Journals (DOAJ)</collection><jtitle>Lipids in health and disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Mengjie</au><au>Xiao, Mengli</au><au>Tan, Qin</au><au>Ji, Jinjin</au><au>Lu, Fang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cumulative residual cholesterol predicts the risk of cardiovascular disease in the general population aged 45 years and older</atitle><jtitle>Lipids in health and disease</jtitle><addtitle>Lipids Health Dis</addtitle><date>2024-01-19</date><risdate>2024</risdate><volume>23</volume><issue>1</issue><spage>19</spage><epage>19</epage><pages>19-19</pages><artnum>19</artnum><issn>1476-511X</issn><eissn>1476-511X</eissn><abstract>Numerous studies have affirmed a robust correlation between residual cholesterol (RC) and the occurrence of cardiovascular disease (CVD). However, the current body of literature fails to adequately address the link between alterations in RC and the occurrence of CVD. Existing studies have focused mainly on individual RC values. Hence, the primary objective of this study is to elucidate the association between the cumulative RC (Cum-RC) and the morbidity of CVD.
The changes in RC were categorized into a high-level fast-growth group (Class 1) and a low-level slow-growth group (Class 2) by K-means cluster analysis. To investigate the relationship between combined exposure to multiple lipids and CVD risk, a weighted quantile sum (WQS) regression analysis was employed. This analysis involved the calculation of weights for total cholesterol (TC), low-density lipoprotein (LDL), and high-density lipoprotein (HDL), which were used to effectively elucidate the RC.
Among the cohort of 5,372 research participants, a considerable proportion of 45.94% consisted of males, with a median age of 58. In the three years of follow-up, 669 participants (12.45%) had CVD. Logistic regression analysis revealed that Class 2 individuals had a significantly reduced risk of developing CVD compared to Class 1. The probability of having CVD increased by 13% for every 1-unit increase in the Cum-RC according to the analysis of continuous variables. The restricted cubic spline (RCS) analysis showed that Cum-RC and CVD risk were linearly related (P for nonlinearity = 0.679). The WQS regression results showed a nonsignificant trend toward an association between the WQS index and CVD incidence but an overall positive trend, with the greatest contribution from TC (weight = 0.652), followed by LDL (weight = 0.348).
Cum-RC was positively and strongly related to CVD risk, suggesting that in addition to focusing on traditional lipid markers, early intervention in patients with increased RC may further reduce the incidence of CVD.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>38243226</pmid><doi>10.1186/s12944-023-02000-0</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1476-511X |
ispartof | Lipids in health and disease, 2024-01, Vol.23 (1), p.19-19, Article 19 |
issn | 1476-511X 1476-511X |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_e7104d2bb2b64110b22abf3c1e47bb34 |
source | Publicly Available Content Database (Proquest) (PQ_SDU_P3); PubMed Central |
subjects | Cardiovascular disease Cardiovascular diseases Cardiovascular Diseases - epidemiology CHARLS Cholesterol Cholesterol, HDL Cholesterol, LDL Clustering Datasets Diabetes Education Health aspects Heart High density lipoprotein Humans Hypertension Incidence K-means clustering Lipids Lipoproteins Low density lipoprotein Male Measurement Metabolic disorders Middle aged persons Missing data Morbidity Nonlinear systems Population Questionnaires Regression analysis Residual cholesterol Risk Factors Trends Weighted quantile sum |
title | Cumulative residual cholesterol predicts the risk of cardiovascular disease in the general population aged 45 years and older |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T11%3A31%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cumulative%20residual%20cholesterol%20predicts%20the%20risk%20of%20cardiovascular%20disease%20in%20the%20general%20population%20aged%2045%20years%20and%20older&rft.jtitle=Lipids%20in%20health%20and%20disease&rft.au=Zhao,%20Mengjie&rft.date=2024-01-19&rft.volume=23&rft.issue=1&rft.spage=19&rft.epage=19&rft.pages=19-19&rft.artnum=19&rft.issn=1476-511X&rft.eissn=1476-511X&rft_id=info:doi/10.1186/s12944-023-02000-0&rft_dat=%3Cgale_doaj_%3EA782195954%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c459t-324d5656b562fcab2c1c40b4929640ebc7ca60e177de93261a1e9b76940b41b33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2925658461&rft_id=info:pmid/38243226&rft_galeid=A782195954&rfr_iscdi=true |