Predictive value of lipoprotein(a) in coronary artery calcification among asymptomatic cardiovascular disease subjects: A systematic review and meta-analysis

Studies have indicated inconsistent results regarding the association between plasma levels of Lipoprotein(a) [Lp(a)] and coronary artery calcification (CAC). We performed a systematic review and meta-analysis to investigate the association between elevated levels of Lp(a) and risk of CAC in populat...

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Veröffentlicht in:Nutrition, metabolism, and cardiovascular diseases metabolism, and cardiovascular diseases, 2023-11, Vol.33 (11), p.2055-2066
Hauptverfasser: Vazirian, Fatemeh, Sadeghi, Masoumeh, Kelesidis, Theodoros, Budoff, Matthew J., Zandi, Zahra, Samadi, Sara, Mohammadpour, Amir Hooshang
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container_end_page 2066
container_issue 11
container_start_page 2055
container_title Nutrition, metabolism, and cardiovascular diseases
container_volume 33
creator Vazirian, Fatemeh
Sadeghi, Masoumeh
Kelesidis, Theodoros
Budoff, Matthew J.
Zandi, Zahra
Samadi, Sara
Mohammadpour, Amir Hooshang
description Studies have indicated inconsistent results regarding the association between plasma levels of Lipoprotein(a) [Lp(a)] and coronary artery calcification (CAC). We performed a systematic review and meta-analysis to investigate the association between elevated levels of Lp(a) and risk of CAC in populations free of cardiovascular disease (CVD) symptoms. PubMed, Web of Science, Embase, and Scopus were searched up to July 2022 and the methodological quality was assessed using Newcastle–Ottawa Scale (NOS) scale. Random-effects meta-analysis was used to estimate pooled odds ratio (OR) and 95% confidence interval. Out of 298 studies, data from 8 cross-sectional (n = 18,668) and 4 cohort (n = 15,355) studies were used in meta-analysis. Cohort studies demonstrated a positive significant association between Lp(a) and CAC, so that individuals with Lp(a)≥30–50 exposed to about 60% risk of CAC incidence compared to those with lower Lp(a) concentrations in asymptomatic CVD subjects (OR, 1.58; 95% CI, 1.38–1.80; l2, 0.0%; P, 0.483); Subgroup analysis showed that a cut-off level for Lp(a) measurement could not statistically affect the association, but race significantly affected the relationship between Lp(a) and CAC (OR,1.60; 95% CI, 1.41–1.81). Analyses also revealed that both men and women with higher Lp(a) concentrations are at the same risk for increased CAC. Blood Lp(a) level was significantly associated with CAC incidence in asymptomatic populations with CVD, indicating that measuring Lp(a) may be a useful biomarker for diagnosing subclinical atherosclerosis in individuals at higher risk of CAC score. CRD42022350297. [Display omitted] •Elevated Lp(a) level is an independent marker for identifying CVD asymptomatic individuals who are at risk of CAC incidence.•In populations free of CVD symptoms, individuals with Lp(a)≥30–50 exposed to about 60% risk of CAC incidence.•Race could potentially affect the relationship between Lp(a) and CAC.•Both men and women with higher Lp(a) concentrations are at the same risk for increased CAC.
doi_str_mv 10.1016/j.numecd.2023.07.015
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We performed a systematic review and meta-analysis to investigate the association between elevated levels of Lp(a) and risk of CAC in populations free of cardiovascular disease (CVD) symptoms. PubMed, Web of Science, Embase, and Scopus were searched up to July 2022 and the methodological quality was assessed using Newcastle–Ottawa Scale (NOS) scale. Random-effects meta-analysis was used to estimate pooled odds ratio (OR) and 95% confidence interval. Out of 298 studies, data from 8 cross-sectional (n = 18,668) and 4 cohort (n = 15,355) studies were used in meta-analysis. Cohort studies demonstrated a positive significant association between Lp(a) and CAC, so that individuals with Lp(a)≥30–50 exposed to about 60% risk of CAC incidence compared to those with lower Lp(a) concentrations in asymptomatic CVD subjects (OR, 1.58; 95% CI, 1.38–1.80; l2, 0.0%; P, 0.483); Subgroup analysis showed that a cut-off level for Lp(a) measurement could not statistically affect the association, but race significantly affected the relationship between Lp(a) and CAC (OR,1.60; 95% CI, 1.41–1.81). Analyses also revealed that both men and women with higher Lp(a) concentrations are at the same risk for increased CAC. Blood Lp(a) level was significantly associated with CAC incidence in asymptomatic populations with CVD, indicating that measuring Lp(a) may be a useful biomarker for diagnosing subclinical atherosclerosis in individuals at higher risk of CAC score. CRD42022350297. 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Cohort studies demonstrated a positive significant association between Lp(a) and CAC, so that individuals with Lp(a)≥30–50 exposed to about 60% risk of CAC incidence compared to those with lower Lp(a) concentrations in asymptomatic CVD subjects (OR, 1.58; 95% CI, 1.38–1.80; l2, 0.0%; P, 0.483); Subgroup analysis showed that a cut-off level for Lp(a) measurement could not statistically affect the association, but race significantly affected the relationship between Lp(a) and CAC (OR,1.60; 95% CI, 1.41–1.81). Analyses also revealed that both men and women with higher Lp(a) concentrations are at the same risk for increased CAC. Blood Lp(a) level was significantly associated with CAC incidence in asymptomatic populations with CVD, indicating that measuring Lp(a) may be a useful biomarker for diagnosing subclinical atherosclerosis in individuals at higher risk of CAC score. CRD42022350297. [Display omitted] •Elevated Lp(a) level is an independent marker for identifying CVD asymptomatic individuals who are at risk of CAC incidence.•In populations free of CVD symptoms, individuals with Lp(a)≥30–50 exposed to about 60% risk of CAC incidence.•Race could potentially affect the relationship between Lp(a) and CAC.•Both men and women with higher Lp(a) concentrations are at the same risk for increased CAC.</description><subject>Adult</subject><subject>Aged</subject><subject>Asymptomatic Diseases</subject><subject>atherosclerosis</subject><subject>biomarkers</subject><subject>Biomarkers - blood</subject><subject>blood</subject><subject>CAC</subject><subject>calcification</subject><subject>cardiovascular disease</subject><subject>confidence interval</subject><subject>Coronary Artery Disease - blood</subject><subject>Coronary Artery Disease - diagnosis</subject><subject>Coronary Artery Disease - diagnostic imaging</subject><subject>Coronary Artery Disease - epidemiology</subject><subject>coronary vessels</subject><subject>Female</subject><subject>Humans</subject><subject>Incidence</subject><subject>lipoprotein(a)</subject><subject>Lipoprotein(a) - blood</subject><subject>lipoproteins</subject><subject>Male</subject><subject>meta-analysis</subject><subject>metabolism</subject><subject>Middle Aged</subject><subject>nutrition</subject><subject>odds ratio</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>risk</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>systematic review</subject><subject>Up-Regulation</subject><subject>Vascular Calcification - blood</subject><subject>Vascular Calcification - diagnosis</subject><subject>Vascular Calcification - diagnostic imaging</subject><subject>Vascular Calcification - epidemiology</subject><issn>0939-4753</issn><issn>1590-3729</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks9u1DAQxiMEotvCGyDkYzkk2LEdbzhQVVX5I1WCA5ytWXtSvErsxXaC9mF4V1ylVHBBnEby_OYbz8xXVS8YbRhl3et94-cJjW1a2vKGqoYy-ajaMNnTmqu2f1xtaM_7WijJT6rTlPaUckW5eFqdcCU7pXq2qX5-jmidyW5BssA4IwkDGd0hHGLI6Pw5vCLOExNi8BCPBGLGEgyMxg3OQHbBE5iCvyWQjtMhh6m8mQJE68ICycwjRGJdQkhI0rzbo8npDbkk6ZgyrnTExeEPAt6SCTPU4GE8JpeeVU8GGBM-v49n1dd311-uPtQ3n95_vLq8qY3oVa4Ns2boO5S2tdvBGIvtwBWHHjkV7cAkohTd0DJFFajeip0AKXbcinZn247xs-pi1T3MuwmtQZ8jjPoQ3VSG1gGc_jvj3Td9GxbNGFVcKlEUzu8VYvg-Y8p6csngOILHMCfdbreqox2V9D_QAlHZi66gYkVNDClFHB6-xKi-c4He69UF-s4FmipdXFDKXv45zkPR77MX4O0KYFlqWX3UyTj0plghlvNoG9y_O_wCnOHLGA</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Vazirian, Fatemeh</creator><creator>Sadeghi, Masoumeh</creator><creator>Kelesidis, Theodoros</creator><creator>Budoff, Matthew J.</creator><creator>Zandi, Zahra</creator><creator>Samadi, Sara</creator><creator>Mohammadpour, Amir Hooshang</creator><general>Elsevier B.V</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>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0132-4491</orcidid><orcidid>https://orcid.org/0000-0002-8463-3811</orcidid><orcidid>https://orcid.org/0000-0002-1357-7605</orcidid></search><sort><creationdate>20231101</creationdate><title>Predictive value of lipoprotein(a) in coronary artery calcification among asymptomatic cardiovascular disease subjects: A systematic review and meta-analysis</title><author>Vazirian, Fatemeh ; 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We performed a systematic review and meta-analysis to investigate the association between elevated levels of Lp(a) and risk of CAC in populations free of cardiovascular disease (CVD) symptoms. PubMed, Web of Science, Embase, and Scopus were searched up to July 2022 and the methodological quality was assessed using Newcastle–Ottawa Scale (NOS) scale. Random-effects meta-analysis was used to estimate pooled odds ratio (OR) and 95% confidence interval. Out of 298 studies, data from 8 cross-sectional (n = 18,668) and 4 cohort (n = 15,355) studies were used in meta-analysis. Cohort studies demonstrated a positive significant association between Lp(a) and CAC, so that individuals with Lp(a)≥30–50 exposed to about 60% risk of CAC incidence compared to those with lower Lp(a) concentrations in asymptomatic CVD subjects (OR, 1.58; 95% CI, 1.38–1.80; l2, 0.0%; P, 0.483); Subgroup analysis showed that a cut-off level for Lp(a) measurement could not statistically affect the association, but race significantly affected the relationship between Lp(a) and CAC (OR,1.60; 95% CI, 1.41–1.81). Analyses also revealed that both men and women with higher Lp(a) concentrations are at the same risk for increased CAC. Blood Lp(a) level was significantly associated with CAC incidence in asymptomatic populations with CVD, indicating that measuring Lp(a) may be a useful biomarker for diagnosing subclinical atherosclerosis in individuals at higher risk of CAC score. CRD42022350297. [Display omitted] •Elevated Lp(a) level is an independent marker for identifying CVD asymptomatic individuals who are at risk of CAC incidence.•In populations free of CVD symptoms, individuals with Lp(a)≥30–50 exposed to about 60% risk of CAC incidence.•Race could potentially affect the relationship between Lp(a) and CAC.•Both men and women with higher Lp(a) concentrations are at the same risk for increased CAC.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>37567791</pmid><doi>10.1016/j.numecd.2023.07.015</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-0132-4491</orcidid><orcidid>https://orcid.org/0000-0002-8463-3811</orcidid><orcidid>https://orcid.org/0000-0002-1357-7605</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Adult
Aged
Asymptomatic Diseases
atherosclerosis
biomarkers
Biomarkers - blood
blood
CAC
calcification
cardiovascular disease
confidence interval
Coronary Artery Disease - blood
Coronary Artery Disease - diagnosis
Coronary Artery Disease - diagnostic imaging
Coronary Artery Disease - epidemiology
coronary vessels
Female
Humans
Incidence
lipoprotein(a)
Lipoprotein(a) - blood
lipoproteins
Male
meta-analysis
metabolism
Middle Aged
nutrition
odds ratio
Predictive Value of Tests
Prognosis
risk
Risk Assessment
Risk Factors
systematic review
Up-Regulation
Vascular Calcification - blood
Vascular Calcification - diagnosis
Vascular Calcification - diagnostic imaging
Vascular Calcification - epidemiology
title Predictive value of lipoprotein(a) in coronary artery calcification among asymptomatic cardiovascular disease subjects: A systematic review and meta-analysis
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