Lp(a) lipoprotein is a major risk factor for cardiovascular disease: pathogenic mechanisms and clinical significance
The results of two previous and two recent studies of middle‐aged males and females are presented to exemplify the clinical importance of lipoprotein (a) (Lp(a)) as a risk factor for atherosclerosis and coronary heart disease. In these studies various conventional and recently suggested risk factors...
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Veröffentlicht in: | Clinical genetics 1997-11, Vol.52 (5), p.272-280 |
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description | The results of two previous and two recent studies of middle‐aged males and females are presented to exemplify the clinical importance of lipoprotein (a) (Lp(a)) as a risk factor for atherosclerosis and coronary heart disease. In these studies various conventional and recently suggested risk factors were included and different methods for Lp(a) quantification were used. Lp(a) was a significant risk factor in all four studies. In the recent prospective case‐control study, Lp(a) and cholesterol were found to act synergistically and predict primary acute myocardial infarction in Swedish males. A cholesterol level above 6.5 mmol/1 increased the risk of acute myocardial infarction if the Lp(a) level was above 200 mg/1. The plasma apo A‐I level was a protective factor. In the other recent case‐control study, an Lp(a) level above 500 mg/1 was a highly significant risk factor in Black and White US women with myocardial infarction or advanced coronary artery disease in addition to low density lipoprotein cholesterol levels above 130 mg/dl. A high apo A‐I level was a protective factor. In these studies no other factors tested reached significance in multivariate logistic regression analysis. A hypothetical association between high Lp(a) levels and intracellular infection with Chlamydia pneumoniae is discussed. The results suggest that the Lp(a) level is useful in identifying high‐risk individuals. Lowering low density lipoprotein cholesterol below 100 mg/dl (7lt;2.6 mmol/1) seems to be most important in both males and females with high‐risk Lp(a) levels. |
doi_str_mv | 10.1111/j.1399-0004.1997.tb04344.x |
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In these studies various conventional and recently suggested risk factors were included and different methods for Lp(a) quantification were used. Lp(a) was a significant risk factor in all four studies. In the recent prospective case‐control study, Lp(a) and cholesterol were found to act synergistically and predict primary acute myocardial infarction in Swedish males. A cholesterol level above 6.5 mmol/1 increased the risk of acute myocardial infarction if the Lp(a) level was above 200 mg/1. The plasma apo A‐I level was a protective factor. In the other recent case‐control study, an Lp(a) level above 500 mg/1 was a highly significant risk factor in Black and White US women with myocardial infarction or advanced coronary artery disease in addition to low density lipoprotein cholesterol levels above 130 mg/dl. A high apo A‐I level was a protective factor. In these studies no other factors tested reached significance in multivariate logistic regression analysis. A hypothetical association between high Lp(a) levels and intracellular infection with Chlamydia pneumoniae is discussed. The results suggest that the Lp(a) level is useful in identifying high‐risk individuals. Lowering low density lipoprotein cholesterol below 100 mg/dl (7lt;2.6 mmol/1) seems to be most important in both males and females with high‐risk Lp(a) levels.</description><identifier>ISSN: 0009-9163</identifier><identifier>EISSN: 1399-0004</identifier><identifier>DOI: 10.1111/j.1399-0004.1997.tb04344.x</identifier><identifier>PMID: 9520117</identifier><identifier>CODEN: CLGNAY</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; apolipoprotein A-I ; Arteriosclerosis - etiology ; atherosclerosis ; Biological and medical sciences ; Black or African American ; Black People ; Cardiology. Vascular system ; Cardiovascular Diseases - etiology ; Cardiovascular Diseases - physiopathology ; Case-Control Studies ; Chlamydophila pneumoniae - pathogenicity ; Cholesterol, LDL - blood ; Coronary heart disease ; cytokines ; Female ; Heart ; HLA antigens ; Humans ; Lipids - blood ; lipoprotein(a) (Lp(a)) ; Lipoprotein(a) - blood ; low density lipoprotein (LDL) cholesterol ; Male ; Medical sciences ; Middle Aged ; Models, Biological ; Myocardial Infarction - physiopathology ; Prospective Studies ; Regression Analysis ; Risk Factors ; Sweden ; United States ; White People</subject><ispartof>Clinical genetics, 1997-11, Vol.52 (5), p.272-280</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4362-6d8001dc4b9750411f6d664d237c2b4bffc1ac4eb4ec8b382eed12918cbfbdf13</citedby><cites>FETCH-LOGICAL-c4362-6d8001dc4b9750411f6d664d237c2b4bffc1ac4eb4ec8b382eed12918cbfbdf13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1399-0004.1997.tb04344.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1399-0004.1997.tb04344.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>309,310,314,780,784,789,790,1417,23930,23931,25140,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2175209$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9520117$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dahlén, Gösta H.</creatorcontrib><creatorcontrib>Stenlund, Hans</creatorcontrib><title>Lp(a) lipoprotein is a major risk factor for cardiovascular disease: pathogenic mechanisms and clinical significance</title><title>Clinical genetics</title><addtitle>Clin Genet</addtitle><description>The results of two previous and two recent studies of middle‐aged males and females are presented to exemplify the clinical importance of lipoprotein (a) (Lp(a)) as a risk factor for atherosclerosis and coronary heart disease. In these studies various conventional and recently suggested risk factors were included and different methods for Lp(a) quantification were used. Lp(a) was a significant risk factor in all four studies. In the recent prospective case‐control study, Lp(a) and cholesterol were found to act synergistically and predict primary acute myocardial infarction in Swedish males. A cholesterol level above 6.5 mmol/1 increased the risk of acute myocardial infarction if the Lp(a) level was above 200 mg/1. The plasma apo A‐I level was a protective factor. In the other recent case‐control study, an Lp(a) level above 500 mg/1 was a highly significant risk factor in Black and White US women with myocardial infarction or advanced coronary artery disease in addition to low density lipoprotein cholesterol levels above 130 mg/dl. A high apo A‐I level was a protective factor. In these studies no other factors tested reached significance in multivariate logistic regression analysis. A hypothetical association between high Lp(a) levels and intracellular infection with Chlamydia pneumoniae is discussed. The results suggest that the Lp(a) level is useful in identifying high‐risk individuals. Lowering low density lipoprotein cholesterol below 100 mg/dl (7lt;2.6 mmol/1) seems to be most important in both males and females with high‐risk Lp(a) levels.</description><subject>Adult</subject><subject>Aged</subject><subject>apolipoprotein A-I</subject><subject>Arteriosclerosis - etiology</subject><subject>atherosclerosis</subject><subject>Biological and medical sciences</subject><subject>Black or African American</subject><subject>Black People</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular Diseases - etiology</subject><subject>Cardiovascular Diseases - physiopathology</subject><subject>Case-Control Studies</subject><subject>Chlamydophila pneumoniae - pathogenicity</subject><subject>Cholesterol, LDL - blood</subject><subject>Coronary heart disease</subject><subject>cytokines</subject><subject>Female</subject><subject>Heart</subject><subject>HLA antigens</subject><subject>Humans</subject><subject>Lipids - blood</subject><subject>lipoprotein(a) (Lp(a))</subject><subject>Lipoprotein(a) - blood</subject><subject>low density lipoprotein (LDL) cholesterol</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Models, Biological</subject><subject>Myocardial Infarction - physiopathology</subject><subject>Prospective Studies</subject><subject>Regression Analysis</subject><subject>Risk Factors</subject><subject>Sweden</subject><subject>United States</subject><subject>White People</subject><issn>0009-9163</issn><issn>1399-0004</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkVtrFDEUx4NY6tr6EYQgIvowY24zmfShIEvdFteKN3wMmVzabDMXk1ndfnuz7LDvBsI5yfmff5JfAHiFUYnzeL8pMRWiQAixEgvBy6lFjDJW7p6AxbH0FCxyEIXANX0Gnqe0yUvKK3EKTkVFEMZ8Aab1-Fa9g8GPwxiHyfoe-gQV7NRmiDD69ACd0lPOXZ5aReOHPyrpbVARGp-sSvYCjmq6H-5s7zXsrL5XvU9ddukN1MHnXRVg8ne9dznttT0HJ06FZF_M8Qz8_Hj1Y3ldrL-sbpYf1oVmtCZFbRqEsNGsFbxCDGNXm7pmhlCuScta5zRWmtmWWd20tCHWGkwEbnTrWuMwPQNvDr75ab-3Nk2y80nbEFRvh22SXFS8Zk2ThRcHoY5DStE6OUbfqfgoMZJ75HIj91zlnqvcI5czcrnLzS_nU7ZtZ82xdWac66_neuamgosZgU9HGcE8C0WWXR5kf32wj_9xAblcXRFOskFxMPBpsrujgYoPsub53-Wv25X8_Okbq75-v5ZL-g_afa8i</recordid><startdate>199711</startdate><enddate>199711</enddate><creator>Dahlén, Gösta H.</creator><creator>Stenlund, Hans</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</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>7X8</scope></search><sort><creationdate>199711</creationdate><title>Lp(a) lipoprotein is a major risk factor for cardiovascular disease: pathogenic mechanisms and clinical significance</title><author>Dahlén, Gösta H. ; Stenlund, Hans</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4362-6d8001dc4b9750411f6d664d237c2b4bffc1ac4eb4ec8b382eed12918cbfbdf13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adult</topic><topic>Aged</topic><topic>apolipoprotein A-I</topic><topic>Arteriosclerosis - etiology</topic><topic>atherosclerosis</topic><topic>Biological and medical sciences</topic><topic>Black or African American</topic><topic>Black People</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular Diseases - etiology</topic><topic>Cardiovascular Diseases - physiopathology</topic><topic>Case-Control Studies</topic><topic>Chlamydophila pneumoniae - pathogenicity</topic><topic>Cholesterol, LDL - blood</topic><topic>Coronary heart disease</topic><topic>cytokines</topic><topic>Female</topic><topic>Heart</topic><topic>HLA antigens</topic><topic>Humans</topic><topic>Lipids - blood</topic><topic>lipoprotein(a) (Lp(a))</topic><topic>Lipoprotein(a) - blood</topic><topic>low density lipoprotein (LDL) cholesterol</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Models, Biological</topic><topic>Myocardial Infarction - physiopathology</topic><topic>Prospective Studies</topic><topic>Regression Analysis</topic><topic>Risk Factors</topic><topic>Sweden</topic><topic>United States</topic><topic>White People</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dahlén, Gösta H.</creatorcontrib><creatorcontrib>Stenlund, Hans</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>MEDLINE - Academic</collection><jtitle>Clinical genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dahlén, Gösta H.</au><au>Stenlund, Hans</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lp(a) lipoprotein is a major risk factor for cardiovascular disease: pathogenic mechanisms and clinical significance</atitle><jtitle>Clinical genetics</jtitle><addtitle>Clin Genet</addtitle><date>1997-11</date><risdate>1997</risdate><volume>52</volume><issue>5</issue><spage>272</spage><epage>280</epage><pages>272-280</pages><issn>0009-9163</issn><eissn>1399-0004</eissn><coden>CLGNAY</coden><abstract>The results of two previous and two recent studies of middle‐aged males and females are presented to exemplify the clinical importance of lipoprotein (a) (Lp(a)) as a risk factor for atherosclerosis and coronary heart disease. In these studies various conventional and recently suggested risk factors were included and different methods for Lp(a) quantification were used. Lp(a) was a significant risk factor in all four studies. In the recent prospective case‐control study, Lp(a) and cholesterol were found to act synergistically and predict primary acute myocardial infarction in Swedish males. A cholesterol level above 6.5 mmol/1 increased the risk of acute myocardial infarction if the Lp(a) level was above 200 mg/1. The plasma apo A‐I level was a protective factor. In the other recent case‐control study, an Lp(a) level above 500 mg/1 was a highly significant risk factor in Black and White US women with myocardial infarction or advanced coronary artery disease in addition to low density lipoprotein cholesterol levels above 130 mg/dl. A high apo A‐I level was a protective factor. In these studies no other factors tested reached significance in multivariate logistic regression analysis. A hypothetical association between high Lp(a) levels and intracellular infection with Chlamydia pneumoniae is discussed. The results suggest that the Lp(a) level is useful in identifying high‐risk individuals. Lowering low density lipoprotein cholesterol below 100 mg/dl (7lt;2.6 mmol/1) seems to be most important in both males and females with high‐risk Lp(a) levels.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>9520117</pmid><doi>10.1111/j.1399-0004.1997.tb04344.x</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Aged apolipoprotein A-I Arteriosclerosis - etiology atherosclerosis Biological and medical sciences Black or African American Black People Cardiology. Vascular system Cardiovascular Diseases - etiology Cardiovascular Diseases - physiopathology Case-Control Studies Chlamydophila pneumoniae - pathogenicity Cholesterol, LDL - blood Coronary heart disease cytokines Female Heart HLA antigens Humans Lipids - blood lipoprotein(a) (Lp(a)) Lipoprotein(a) - blood low density lipoprotein (LDL) cholesterol Male Medical sciences Middle Aged Models, Biological Myocardial Infarction - physiopathology Prospective Studies Regression Analysis Risk Factors Sweden United States White People |
title | Lp(a) lipoprotein is a major risk factor for cardiovascular disease: pathogenic mechanisms and clinical significance |
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