Impact of lipoprotein(a) level on cardiometabolic disease in the Chinese population: The CHCN‐BTH Study
Background The emergence of promising compounds to lower lipoprotein(a) [Lp(a)] has increased the need for a precise characterisation and comparability assessment of Lp(a)‐associated cardiometabolic disease risk. This study aimed to evaluate the distribution of Lp(a) levels in a Chinese population a...
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Veröffentlicht in: | European journal of clinical investigation 2022-02, Vol.52 (2), p.e13689-n/a |
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creator | Xia, Juan Guo, Chunyue Cao, Han Liu, Kuo Peng, Wenjuan Sun, Yanyan Xie, Yunyi Li, Bingxiao Zhang, Fengxu Wen, Fuyuan Zhang, Ling |
description | Background
The emergence of promising compounds to lower lipoprotein(a) [Lp(a)] has increased the need for a precise characterisation and comparability assessment of Lp(a)‐associated cardiometabolic disease risk. This study aimed to evaluate the distribution of Lp(a) levels in a Chinese population and characterise the association with cardiometabolic diseases.
Methods
We assessed data from individuals from the Cohort Study on Chronic Diseases of the General Community Population in the Beijing‐Tianjin‐Hebei Region project. All Lp(a) measurements were performed in the same hospital. The cardiometabolic diseases considered were coronary heart disease (CHD), stroke, hypertension and type 2 diabetes (T2DM).
Results
A total of 25343 individuals were included in the study. The median level of Lp(a) was 11.9 mg/dl (IQR 5.9 to 23.7 mg/dl), and higher Lp(a) levels showed a significant concentration‐dependent association with CHD risk. Individuals with Lp(a) levels lower than the 25th percentile were at increased risk of hypertension (OR: 1.15, 95% CI: 1.06–1.25) and T2DM (OR: 1.15, 95% CI: 1.03–1.28); however, Lp(a) levels were not significantly associated with stroke. The addition of Lp(a) levels to the prognostic model led to a marginal but significant C‐index, integrated discrimination improvement and net reclassification improvement.
Conclusions
In this large sample size study, we observed that elevated Lp(a) levels were significantly associated with CHD. Furthermore, we found that the lowest Lp(a) levels were also significantly associated with hypertension and T2DM. These results provide evidence for differential approaches to higher levels of Lp(a) in individuals with different cardiometabolic diseases. |
doi_str_mv | 10.1111/eci.13689 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2580939483</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2618160001</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3539-ee254e730b6b76b96106c2aaa2d9d7366543178218eadf7779d567a7f888e1003</originalsourceid><addsrcrecordid>eNp1kM9O3DAQh60K1F22PfQFKktc2EPAfxLb4QbR0l0J0UO3Z8tJJsIrJ97GSau98Qg8I0-CYbcckPBl5NE3P818CH2j5JzGdwGVPadcqPwTmsaaJYwLdoSmhNA0YblkE3QSwoYQoihnn9GEp4KzTNEpsqt2a6oB-wY7u_Xb3g9guzMzxw7-gsO-w5Xpa-tbGEzpna1wbQOYANh2eLgHXNzbDuI3Do_ODNZ3l3j90l8Wd08Pj9frJf41jPXuCzpujAvw9VBn6PfNYl0sk9ufP1bF1W1S8YznCQDLUpCclKKUoswFJaJixhhW57XkQmQpp1IxqsDUjZQyrzMhjWyUUkAJ4TN0ts-Nt_wZIQy6taEC50wHfgw63k1ynqeKR_T0HbrxY9_F7TQTVFERjdFIzfdU1fsQemj0tret6XeaEv3iX0f_-tV_ZL8fEseyhfqN_C88Ahd74J91sPs4SS-K1T7yGf6mjYY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2618160001</pqid></control><display><type>article</type><title>Impact of lipoprotein(a) level on cardiometabolic disease in the Chinese population: The CHCN‐BTH Study</title><source>Wiley-Blackwell Journals</source><source>MEDLINE</source><creator>Xia, Juan ; Guo, Chunyue ; Cao, Han ; Liu, Kuo ; Peng, Wenjuan ; Sun, Yanyan ; Xie, Yunyi ; Li, Bingxiao ; Zhang, Fengxu ; Wen, Fuyuan ; Zhang, Ling</creator><creatorcontrib>Xia, Juan ; Guo, Chunyue ; Cao, Han ; Liu, Kuo ; Peng, Wenjuan ; Sun, Yanyan ; Xie, Yunyi ; Li, Bingxiao ; Zhang, Fengxu ; Wen, Fuyuan ; Zhang, Ling</creatorcontrib><description>Background
The emergence of promising compounds to lower lipoprotein(a) [Lp(a)] has increased the need for a precise characterisation and comparability assessment of Lp(a)‐associated cardiometabolic disease risk. This study aimed to evaluate the distribution of Lp(a) levels in a Chinese population and characterise the association with cardiometabolic diseases.
Methods
We assessed data from individuals from the Cohort Study on Chronic Diseases of the General Community Population in the Beijing‐Tianjin‐Hebei Region project. All Lp(a) measurements were performed in the same hospital. The cardiometabolic diseases considered were coronary heart disease (CHD), stroke, hypertension and type 2 diabetes (T2DM).
Results
A total of 25343 individuals were included in the study. The median level of Lp(a) was 11.9 mg/dl (IQR 5.9 to 23.7 mg/dl), and higher Lp(a) levels showed a significant concentration‐dependent association with CHD risk. Individuals with Lp(a) levels lower than the 25th percentile were at increased risk of hypertension (OR: 1.15, 95% CI: 1.06–1.25) and T2DM (OR: 1.15, 95% CI: 1.03–1.28); however, Lp(a) levels were not significantly associated with stroke. The addition of Lp(a) levels to the prognostic model led to a marginal but significant C‐index, integrated discrimination improvement and net reclassification improvement.
Conclusions
In this large sample size study, we observed that elevated Lp(a) levels were significantly associated with CHD. Furthermore, we found that the lowest Lp(a) levels were also significantly associated with hypertension and T2DM. These results provide evidence for differential approaches to higher levels of Lp(a) in individuals with different cardiometabolic diseases.</description><identifier>ISSN: 0014-2972</identifier><identifier>EISSN: 1365-2362</identifier><identifier>DOI: 10.1111/eci.13689</identifier><identifier>PMID: 34632581</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adult ; cardiometabolic disease ; Cardiovascular disease ; Cardiovascular diseases ; CHCN‐BTH ; China ; Coronary artery disease ; Diabetes mellitus (non-insulin dependent) ; Female ; Health risks ; Heart diseases ; Heart Diseases - blood ; Heart Diseases - complications ; Humans ; Hypertension ; Lipoprotein(a) ; Lipoprotein(a) - blood ; Male ; Metabolic Diseases - blood ; Metabolic Diseases - complications ; Middle Aged ; Population studies ; Prospective Studies ; Reclassification ; Risk ; Stroke</subject><ispartof>European journal of clinical investigation, 2022-02, Vol.52 (2), p.e13689-n/a</ispartof><rights>2021 Stichting European Society for Clinical Investigation Journal Foundation. Published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2022 Stichting European Society for Clinical Investigation Journal Foundation</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3539-ee254e730b6b76b96106c2aaa2d9d7366543178218eadf7779d567a7f888e1003</citedby><cites>FETCH-LOGICAL-c3539-ee254e730b6b76b96106c2aaa2d9d7366543178218eadf7779d567a7f888e1003</cites><orcidid>0000-0003-2468-864X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Feci.13689$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Feci.13689$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34632581$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xia, Juan</creatorcontrib><creatorcontrib>Guo, Chunyue</creatorcontrib><creatorcontrib>Cao, Han</creatorcontrib><creatorcontrib>Liu, Kuo</creatorcontrib><creatorcontrib>Peng, Wenjuan</creatorcontrib><creatorcontrib>Sun, Yanyan</creatorcontrib><creatorcontrib>Xie, Yunyi</creatorcontrib><creatorcontrib>Li, Bingxiao</creatorcontrib><creatorcontrib>Zhang, Fengxu</creatorcontrib><creatorcontrib>Wen, Fuyuan</creatorcontrib><creatorcontrib>Zhang, Ling</creatorcontrib><title>Impact of lipoprotein(a) level on cardiometabolic disease in the Chinese population: The CHCN‐BTH Study</title><title>European journal of clinical investigation</title><addtitle>Eur J Clin Invest</addtitle><description>Background
The emergence of promising compounds to lower lipoprotein(a) [Lp(a)] has increased the need for a precise characterisation and comparability assessment of Lp(a)‐associated cardiometabolic disease risk. This study aimed to evaluate the distribution of Lp(a) levels in a Chinese population and characterise the association with cardiometabolic diseases.
Methods
We assessed data from individuals from the Cohort Study on Chronic Diseases of the General Community Population in the Beijing‐Tianjin‐Hebei Region project. All Lp(a) measurements were performed in the same hospital. The cardiometabolic diseases considered were coronary heart disease (CHD), stroke, hypertension and type 2 diabetes (T2DM).
Results
A total of 25343 individuals were included in the study. The median level of Lp(a) was 11.9 mg/dl (IQR 5.9 to 23.7 mg/dl), and higher Lp(a) levels showed a significant concentration‐dependent association with CHD risk. Individuals with Lp(a) levels lower than the 25th percentile were at increased risk of hypertension (OR: 1.15, 95% CI: 1.06–1.25) and T2DM (OR: 1.15, 95% CI: 1.03–1.28); however, Lp(a) levels were not significantly associated with stroke. The addition of Lp(a) levels to the prognostic model led to a marginal but significant C‐index, integrated discrimination improvement and net reclassification improvement.
Conclusions
In this large sample size study, we observed that elevated Lp(a) levels were significantly associated with CHD. Furthermore, we found that the lowest Lp(a) levels were also significantly associated with hypertension and T2DM. These results provide evidence for differential approaches to higher levels of Lp(a) in individuals with different cardiometabolic diseases.</description><subject>Adult</subject><subject>cardiometabolic disease</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular diseases</subject><subject>CHCN‐BTH</subject><subject>China</subject><subject>Coronary artery disease</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Female</subject><subject>Health risks</subject><subject>Heart diseases</subject><subject>Heart Diseases - blood</subject><subject>Heart Diseases - complications</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Lipoprotein(a)</subject><subject>Lipoprotein(a) - blood</subject><subject>Male</subject><subject>Metabolic Diseases - blood</subject><subject>Metabolic Diseases - complications</subject><subject>Middle Aged</subject><subject>Population studies</subject><subject>Prospective Studies</subject><subject>Reclassification</subject><subject>Risk</subject><subject>Stroke</subject><issn>0014-2972</issn><issn>1365-2362</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM9O3DAQh60K1F22PfQFKktc2EPAfxLb4QbR0l0J0UO3Z8tJJsIrJ97GSau98Qg8I0-CYbcckPBl5NE3P818CH2j5JzGdwGVPadcqPwTmsaaJYwLdoSmhNA0YblkE3QSwoYQoihnn9GEp4KzTNEpsqt2a6oB-wY7u_Xb3g9guzMzxw7-gsO-w5Xpa-tbGEzpna1wbQOYANh2eLgHXNzbDuI3Do_ODNZ3l3j90l8Wd08Pj9frJf41jPXuCzpujAvw9VBn6PfNYl0sk9ufP1bF1W1S8YznCQDLUpCclKKUoswFJaJixhhW57XkQmQpp1IxqsDUjZQyrzMhjWyUUkAJ4TN0ts-Nt_wZIQy6taEC50wHfgw63k1ynqeKR_T0HbrxY9_F7TQTVFERjdFIzfdU1fsQemj0tret6XeaEv3iX0f_-tV_ZL8fEseyhfqN_C88Ahd74J91sPs4SS-K1T7yGf6mjYY</recordid><startdate>202202</startdate><enddate>202202</enddate><creator>Xia, Juan</creator><creator>Guo, Chunyue</creator><creator>Cao, Han</creator><creator>Liu, Kuo</creator><creator>Peng, Wenjuan</creator><creator>Sun, Yanyan</creator><creator>Xie, Yunyi</creator><creator>Li, Bingxiao</creator><creator>Zhang, Fengxu</creator><creator>Wen, Fuyuan</creator><creator>Zhang, Ling</creator><general>Blackwell Publishing Ltd</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>7QO</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2468-864X</orcidid></search><sort><creationdate>202202</creationdate><title>Impact of lipoprotein(a) level on cardiometabolic disease in the Chinese population: The CHCN‐BTH Study</title><author>Xia, Juan ; Guo, Chunyue ; Cao, Han ; Liu, Kuo ; Peng, Wenjuan ; Sun, Yanyan ; Xie, Yunyi ; Li, Bingxiao ; Zhang, Fengxu ; Wen, Fuyuan ; Zhang, Ling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3539-ee254e730b6b76b96106c2aaa2d9d7366543178218eadf7779d567a7f888e1003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adult</topic><topic>cardiometabolic disease</topic><topic>Cardiovascular disease</topic><topic>Cardiovascular diseases</topic><topic>CHCN‐BTH</topic><topic>China</topic><topic>Coronary artery disease</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Female</topic><topic>Health risks</topic><topic>Heart diseases</topic><topic>Heart Diseases - blood</topic><topic>Heart Diseases - complications</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Lipoprotein(a)</topic><topic>Lipoprotein(a) - blood</topic><topic>Male</topic><topic>Metabolic Diseases - blood</topic><topic>Metabolic Diseases - complications</topic><topic>Middle Aged</topic><topic>Population studies</topic><topic>Prospective Studies</topic><topic>Reclassification</topic><topic>Risk</topic><topic>Stroke</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xia, Juan</creatorcontrib><creatorcontrib>Guo, Chunyue</creatorcontrib><creatorcontrib>Cao, Han</creatorcontrib><creatorcontrib>Liu, Kuo</creatorcontrib><creatorcontrib>Peng, Wenjuan</creatorcontrib><creatorcontrib>Sun, Yanyan</creatorcontrib><creatorcontrib>Xie, Yunyi</creatorcontrib><creatorcontrib>Li, Bingxiao</creatorcontrib><creatorcontrib>Zhang, Fengxu</creatorcontrib><creatorcontrib>Wen, Fuyuan</creatorcontrib><creatorcontrib>Zhang, Ling</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of clinical investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xia, Juan</au><au>Guo, Chunyue</au><au>Cao, Han</au><au>Liu, Kuo</au><au>Peng, Wenjuan</au><au>Sun, Yanyan</au><au>Xie, Yunyi</au><au>Li, Bingxiao</au><au>Zhang, Fengxu</au><au>Wen, Fuyuan</au><au>Zhang, Ling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of lipoprotein(a) level on cardiometabolic disease in the Chinese population: The CHCN‐BTH Study</atitle><jtitle>European journal of clinical investigation</jtitle><addtitle>Eur J Clin Invest</addtitle><date>2022-02</date><risdate>2022</risdate><volume>52</volume><issue>2</issue><spage>e13689</spage><epage>n/a</epage><pages>e13689-n/a</pages><issn>0014-2972</issn><eissn>1365-2362</eissn><abstract>Background
The emergence of promising compounds to lower lipoprotein(a) [Lp(a)] has increased the need for a precise characterisation and comparability assessment of Lp(a)‐associated cardiometabolic disease risk. This study aimed to evaluate the distribution of Lp(a) levels in a Chinese population and characterise the association with cardiometabolic diseases.
Methods
We assessed data from individuals from the Cohort Study on Chronic Diseases of the General Community Population in the Beijing‐Tianjin‐Hebei Region project. All Lp(a) measurements were performed in the same hospital. The cardiometabolic diseases considered were coronary heart disease (CHD), stroke, hypertension and type 2 diabetes (T2DM).
Results
A total of 25343 individuals were included in the study. The median level of Lp(a) was 11.9 mg/dl (IQR 5.9 to 23.7 mg/dl), and higher Lp(a) levels showed a significant concentration‐dependent association with CHD risk. Individuals with Lp(a) levels lower than the 25th percentile were at increased risk of hypertension (OR: 1.15, 95% CI: 1.06–1.25) and T2DM (OR: 1.15, 95% CI: 1.03–1.28); however, Lp(a) levels were not significantly associated with stroke. The addition of Lp(a) levels to the prognostic model led to a marginal but significant C‐index, integrated discrimination improvement and net reclassification improvement.
Conclusions
In this large sample size study, we observed that elevated Lp(a) levels were significantly associated with CHD. Furthermore, we found that the lowest Lp(a) levels were also significantly associated with hypertension and T2DM. These results provide evidence for differential approaches to higher levels of Lp(a) in individuals with different cardiometabolic diseases.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>34632581</pmid><doi>10.1111/eci.13689</doi><tpages>0</tpages><orcidid>https://orcid.org/0000-0003-2468-864X</orcidid></addata></record> |
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subjects | Adult cardiometabolic disease Cardiovascular disease Cardiovascular diseases CHCN‐BTH China Coronary artery disease Diabetes mellitus (non-insulin dependent) Female Health risks Heart diseases Heart Diseases - blood Heart Diseases - complications Humans Hypertension Lipoprotein(a) Lipoprotein(a) - blood Male Metabolic Diseases - blood Metabolic Diseases - complications Middle Aged Population studies Prospective Studies Reclassification Risk Stroke |
title | Impact of lipoprotein(a) level on cardiometabolic disease in the Chinese population: The CHCN‐BTH Study |
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