Loading…

Longitudinal changes in high-density lipoprotein cholesterol and cardiovascular events in older adults

Summary Objective While low high‐density lipoprotein cholesterol (HDL‐C) is associated with increased risk of cardiovascular (CV) events, there are limited data evaluating the association of longitudinal change in HDL‐C with CV event risk in older populations. The aim of this study was to examine th...

Full description

Saved in:
Bibliographic Details
Published in:Clinical endocrinology (Oxford) 2014-05, Vol.80 (5), p.662-670
Main Authors: Araujo, Andre B., Chiu, Gretchen R., Christian, Jennifer B., Kim, Hae Young, Evans, William J., Clark, Richard V.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c4212-c9e40bf1ef0c24a20e817a282611855e26e2f2c9b6dfc5fdb104cae00aaa4dc73
cites cdi_FETCH-LOGICAL-c4212-c9e40bf1ef0c24a20e817a282611855e26e2f2c9b6dfc5fdb104cae00aaa4dc73
container_end_page 670
container_issue 5
container_start_page 662
container_title Clinical endocrinology (Oxford)
container_volume 80
creator Araujo, Andre B.
Chiu, Gretchen R.
Christian, Jennifer B.
Kim, Hae Young
Evans, William J.
Clark, Richard V.
description Summary Objective While low high‐density lipoprotein cholesterol (HDL‐C) is associated with increased risk of cardiovascular (CV) events, there are limited data evaluating the association of longitudinal change in HDL‐C with CV event risk in older populations. The aim of this study was to examine the association between within‐subject changes in HDL‐C levels and CV events in an older population. Design Observational cohort study. Patients 1293 men and 1422 women age ≥50 years, with ≥2 consecutive HDL measurements, and no prior CVD as part of Framingham Offspring Study. Measurements A clinical CV event was defined as the first occurrence of any of the following: coronary heart disease (coronary death, myocardial infarction, coronary insufficiency and angina), cerebrovascular event, peripheral artery disease or heart failure. Results Median total follow‐up time across subjects was 9·6 years. Change in HDL‐C was evaluated as between‐exam (approximately 3·5 years) percentage change in HDL‐C, categorized as ≥10% decrease,
doi_str_mv 10.1111/cen.12212
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1514428477</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1514428477</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4212-c9e40bf1ef0c24a20e817a282611855e26e2f2c9b6dfc5fdb104cae00aaa4dc73</originalsourceid><addsrcrecordid>eNp1kc1uEzEURi0EoqGw4AXQSAipLKa1Pf6ZWULUBqSoZAFiaTn2ncTFsVN7pjRvj9OkRULCGy987nc_HSP0luBzUs6FgXBOKCX0GZqQRvCaUsGfowluMK6xEOwEvcr5BmPMWyxfohPacI7bjk1QP49h5YbRuqB9ZdY6rCBXLlRrt1rXFkJ2w67ybhu3KQ5QHsw6esgDpOgrHWxldLIu3ulsRq9TBXcQhoeE6C2kStvRD_k1etFrn-HN8T5FP64uv0-_1PNvs6_TT_PasFK_Nh0wvOwJ9NhQpimGlkhNWyoIaTkHKoD21HRLYXvDe7skmBkNGGutmTWyOUVnh9zS9nYsNdXGZQPe6wBxzIpwwhhtmdyj7_9Bb-KYioU9RQWVTEhaqI8HyqSYc4JebZPb6LRTBKu9fFXkqwf5hX13TByXG7BP5KPtAnw4AsWW9n3Swbj8l2ubrsGEF-7iwP12Hnb_36iml9ePq-vDhCs_c_80odMvJWQjufp5PVOfF7NusZBXat78Ada6qyE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1526274672</pqid></control><display><type>article</type><title>Longitudinal changes in high-density lipoprotein cholesterol and cardiovascular events in older adults</title><source>Wiley:Jisc Collections:Wiley Read and Publish Open Access 2024-2025 (reading list)</source><creator>Araujo, Andre B. ; Chiu, Gretchen R. ; Christian, Jennifer B. ; Kim, Hae Young ; Evans, William J. ; Clark, Richard V.</creator><creatorcontrib>Araujo, Andre B. ; Chiu, Gretchen R. ; Christian, Jennifer B. ; Kim, Hae Young ; Evans, William J. ; Clark, Richard V.</creatorcontrib><description>Summary Objective While low high‐density lipoprotein cholesterol (HDL‐C) is associated with increased risk of cardiovascular (CV) events, there are limited data evaluating the association of longitudinal change in HDL‐C with CV event risk in older populations. The aim of this study was to examine the association between within‐subject changes in HDL‐C levels and CV events in an older population. Design Observational cohort study. Patients 1293 men and 1422 women age ≥50 years, with ≥2 consecutive HDL measurements, and no prior CVD as part of Framingham Offspring Study. Measurements A clinical CV event was defined as the first occurrence of any of the following: coronary heart disease (coronary death, myocardial infarction, coronary insufficiency and angina), cerebrovascular event, peripheral artery disease or heart failure. Results Median total follow‐up time across subjects was 9·6 years. Change in HDL‐C was evaluated as between‐exam (approximately 3·5 years) percentage change in HDL‐C, categorized as ≥10% decrease, &lt;10% change (stable) and ≥10% increase. Crude and adjusted sex‐specific Cox hazards regression models with change in HDL‐C as a time‐dependent covariate quantified the association with CV events. Mean baseline age of the analysis sample was 53 years. There were 233 and 111 CV events among men and women, respectively. Change in HDL‐C was not significantly associated with CVD incidence in men or women, without or with adjustment for confounders including baseline HDL‐C or use of relevant medications. Conclusion In conclusion, relatively short‐term (3·5 years) changes in HDL‐C levels do not affect CV events in men and women.</description><identifier>ISSN: 0300-0664</identifier><identifier>EISSN: 1365-2265</identifier><identifier>DOI: 10.1111/cen.12212</identifier><identifier>PMID: 23550894</identifier><identifier>CODEN: CLECAP</identifier><language>eng</language><publisher>Oxford: Blackwell Publishing Ltd</publisher><subject>Aged ; Aging ; Biological and medical sciences ; Cardiovascular disease ; Cardiovascular Diseases - blood ; Cholesterol ; Cholesterol, HDL - blood ; Disorders of blood lipids. Hyperlipoproteinemia ; Endocrinopathies ; Female ; Fundamental and applied biological sciences. Psychology ; Heart attacks ; Humans ; Longitudinal Studies ; Male ; Medical sciences ; Metabolic diseases ; Middle Aged ; Multivariate Analysis ; Peripheral Arterial Disease - blood ; Proportional Hazards Models ; Risk Factors ; Treatment Outcome ; Vertebrates: endocrinology</subject><ispartof>Clinical endocrinology (Oxford), 2014-05, Vol.80 (5), p.662-670</ispartof><rights>2013 John Wiley &amp; Sons Ltd</rights><rights>2015 INIST-CNRS</rights><rights>2013 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2014 John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4212-c9e40bf1ef0c24a20e817a282611855e26e2f2c9b6dfc5fdb104cae00aaa4dc73</citedby><cites>FETCH-LOGICAL-c4212-c9e40bf1ef0c24a20e817a282611855e26e2f2c9b6dfc5fdb104cae00aaa4dc73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28393015$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23550894$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Araujo, Andre B.</creatorcontrib><creatorcontrib>Chiu, Gretchen R.</creatorcontrib><creatorcontrib>Christian, Jennifer B.</creatorcontrib><creatorcontrib>Kim, Hae Young</creatorcontrib><creatorcontrib>Evans, William J.</creatorcontrib><creatorcontrib>Clark, Richard V.</creatorcontrib><title>Longitudinal changes in high-density lipoprotein cholesterol and cardiovascular events in older adults</title><title>Clinical endocrinology (Oxford)</title><addtitle>Clin Endocrinol</addtitle><description>Summary Objective While low high‐density lipoprotein cholesterol (HDL‐C) is associated with increased risk of cardiovascular (CV) events, there are limited data evaluating the association of longitudinal change in HDL‐C with CV event risk in older populations. The aim of this study was to examine the association between within‐subject changes in HDL‐C levels and CV events in an older population. Design Observational cohort study. Patients 1293 men and 1422 women age ≥50 years, with ≥2 consecutive HDL measurements, and no prior CVD as part of Framingham Offspring Study. Measurements A clinical CV event was defined as the first occurrence of any of the following: coronary heart disease (coronary death, myocardial infarction, coronary insufficiency and angina), cerebrovascular event, peripheral artery disease or heart failure. Results Median total follow‐up time across subjects was 9·6 years. Change in HDL‐C was evaluated as between‐exam (approximately 3·5 years) percentage change in HDL‐C, categorized as ≥10% decrease, &lt;10% change (stable) and ≥10% increase. Crude and adjusted sex‐specific Cox hazards regression models with change in HDL‐C as a time‐dependent covariate quantified the association with CV events. Mean baseline age of the analysis sample was 53 years. There were 233 and 111 CV events among men and women, respectively. Change in HDL‐C was not significantly associated with CVD incidence in men or women, without or with adjustment for confounders including baseline HDL‐C or use of relevant medications. Conclusion In conclusion, relatively short‐term (3·5 years) changes in HDL‐C levels do not affect CV events in men and women.</description><subject>Aged</subject><subject>Aging</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular Diseases - blood</subject><subject>Cholesterol</subject><subject>Cholesterol, HDL - blood</subject><subject>Disorders of blood lipids. Hyperlipoproteinemia</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Heart attacks</subject><subject>Humans</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Peripheral Arterial Disease - blood</subject><subject>Proportional Hazards Models</subject><subject>Risk Factors</subject><subject>Treatment Outcome</subject><subject>Vertebrates: endocrinology</subject><issn>0300-0664</issn><issn>1365-2265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp1kc1uEzEURi0EoqGw4AXQSAipLKa1Pf6ZWULUBqSoZAFiaTn2ncTFsVN7pjRvj9OkRULCGy987nc_HSP0luBzUs6FgXBOKCX0GZqQRvCaUsGfowluMK6xEOwEvcr5BmPMWyxfohPacI7bjk1QP49h5YbRuqB9ZdY6rCBXLlRrt1rXFkJ2w67ybhu3KQ5QHsw6esgDpOgrHWxldLIu3ulsRq9TBXcQhoeE6C2kStvRD_k1etFrn-HN8T5FP64uv0-_1PNvs6_TT_PasFK_Nh0wvOwJ9NhQpimGlkhNWyoIaTkHKoD21HRLYXvDe7skmBkNGGutmTWyOUVnh9zS9nYsNdXGZQPe6wBxzIpwwhhtmdyj7_9Bb-KYioU9RQWVTEhaqI8HyqSYc4JebZPb6LRTBKu9fFXkqwf5hX13TByXG7BP5KPtAnw4AsWW9n3Swbj8l2ubrsGEF-7iwP12Hnb_36iml9ePq-vDhCs_c_80odMvJWQjufp5PVOfF7NusZBXat78Ada6qyE</recordid><startdate>201405</startdate><enddate>201405</enddate><creator>Araujo, Andre B.</creator><creator>Chiu, Gretchen R.</creator><creator>Christian, Jennifer B.</creator><creator>Kim, Hae Young</creator><creator>Evans, William J.</creator><creator>Clark, Richard V.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><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>7QP</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>201405</creationdate><title>Longitudinal changes in high-density lipoprotein cholesterol and cardiovascular events in older adults</title><author>Araujo, Andre B. ; Chiu, Gretchen R. ; Christian, Jennifer B. ; Kim, Hae Young ; Evans, William J. ; Clark, Richard V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4212-c9e40bf1ef0c24a20e817a282611855e26e2f2c9b6dfc5fdb104cae00aaa4dc73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Aging</topic><topic>Biological and medical sciences</topic><topic>Cardiovascular disease</topic><topic>Cardiovascular Diseases - blood</topic><topic>Cholesterol</topic><topic>Cholesterol, HDL - blood</topic><topic>Disorders of blood lipids. Hyperlipoproteinemia</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Heart attacks</topic><topic>Humans</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Peripheral Arterial Disease - blood</topic><topic>Proportional Hazards Models</topic><topic>Risk Factors</topic><topic>Treatment Outcome</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Araujo, Andre B.</creatorcontrib><creatorcontrib>Chiu, Gretchen R.</creatorcontrib><creatorcontrib>Christian, Jennifer B.</creatorcontrib><creatorcontrib>Kim, Hae Young</creatorcontrib><creatorcontrib>Evans, William J.</creatorcontrib><creatorcontrib>Clark, Richard V.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical endocrinology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Araujo, Andre B.</au><au>Chiu, Gretchen R.</au><au>Christian, Jennifer B.</au><au>Kim, Hae Young</au><au>Evans, William J.</au><au>Clark, Richard V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Longitudinal changes in high-density lipoprotein cholesterol and cardiovascular events in older adults</atitle><jtitle>Clinical endocrinology (Oxford)</jtitle><addtitle>Clin Endocrinol</addtitle><date>2014-05</date><risdate>2014</risdate><volume>80</volume><issue>5</issue><spage>662</spage><epage>670</epage><pages>662-670</pages><issn>0300-0664</issn><eissn>1365-2265</eissn><coden>CLECAP</coden><abstract>Summary Objective While low high‐density lipoprotein cholesterol (HDL‐C) is associated with increased risk of cardiovascular (CV) events, there are limited data evaluating the association of longitudinal change in HDL‐C with CV event risk in older populations. The aim of this study was to examine the association between within‐subject changes in HDL‐C levels and CV events in an older population. Design Observational cohort study. Patients 1293 men and 1422 women age ≥50 years, with ≥2 consecutive HDL measurements, and no prior CVD as part of Framingham Offspring Study. Measurements A clinical CV event was defined as the first occurrence of any of the following: coronary heart disease (coronary death, myocardial infarction, coronary insufficiency and angina), cerebrovascular event, peripheral artery disease or heart failure. Results Median total follow‐up time across subjects was 9·6 years. Change in HDL‐C was evaluated as between‐exam (approximately 3·5 years) percentage change in HDL‐C, categorized as ≥10% decrease, &lt;10% change (stable) and ≥10% increase. Crude and adjusted sex‐specific Cox hazards regression models with change in HDL‐C as a time‐dependent covariate quantified the association with CV events. Mean baseline age of the analysis sample was 53 years. There were 233 and 111 CV events among men and women, respectively. Change in HDL‐C was not significantly associated with CVD incidence in men or women, without or with adjustment for confounders including baseline HDL‐C or use of relevant medications. Conclusion In conclusion, relatively short‐term (3·5 years) changes in HDL‐C levels do not affect CV events in men and women.</abstract><cop>Oxford</cop><pub>Blackwell Publishing Ltd</pub><pmid>23550894</pmid><doi>10.1111/cen.12212</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0300-0664
ispartof Clinical endocrinology (Oxford), 2014-05, Vol.80 (5), p.662-670
issn 0300-0664
1365-2265
language eng
recordid cdi_proquest_miscellaneous_1514428477
source Wiley:Jisc Collections:Wiley Read and Publish Open Access 2024-2025 (reading list)
subjects Aged
Aging
Biological and medical sciences
Cardiovascular disease
Cardiovascular Diseases - blood
Cholesterol
Cholesterol, HDL - blood
Disorders of blood lipids. Hyperlipoproteinemia
Endocrinopathies
Female
Fundamental and applied biological sciences. Psychology
Heart attacks
Humans
Longitudinal Studies
Male
Medical sciences
Metabolic diseases
Middle Aged
Multivariate Analysis
Peripheral Arterial Disease - blood
Proportional Hazards Models
Risk Factors
Treatment Outcome
Vertebrates: endocrinology
title Longitudinal changes in high-density lipoprotein cholesterol and cardiovascular events in older adults
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T02%3A59%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Longitudinal%20changes%20in%20high-density%20lipoprotein%20cholesterol%20and%20cardiovascular%20events%20in%20older%20adults&rft.jtitle=Clinical%20endocrinology%20(Oxford)&rft.au=Araujo,%20Andre%20B.&rft.date=2014-05&rft.volume=80&rft.issue=5&rft.spage=662&rft.epage=670&rft.pages=662-670&rft.issn=0300-0664&rft.eissn=1365-2265&rft.coden=CLECAP&rft_id=info:doi/10.1111/cen.12212&rft_dat=%3Cproquest_cross%3E1514428477%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4212-c9e40bf1ef0c24a20e817a282611855e26e2f2c9b6dfc5fdb104cae00aaa4dc73%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1526274672&rft_id=info:pmid/23550894&rfr_iscdi=true