2022
DOI: 10.18332/pht/145601
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Lipoprotein a: An emerging risk identifier and evolving clinical target

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Cited by 2 publications
(2 citation statements)
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“…From a pathogenic perspective, the results are also consistent with those from several Mendelian randomization studies which have unveiled a polygenic relationship between Lp(a) levels and BP. Furthermore, these findings harmonize with data from other basic research that associate Lp(a) levels with oxidative stress, inflammation and atherosclerotic vascular damage 35 , 36 . Despite this, clinical understanding of the Lp(a)-BP relationship, especially during night-time, remains somewhat underexplored.…”
Section: Discussionsupporting
confidence: 86%
“…From a pathogenic perspective, the results are also consistent with those from several Mendelian randomization studies which have unveiled a polygenic relationship between Lp(a) levels and BP. Furthermore, these findings harmonize with data from other basic research that associate Lp(a) levels with oxidative stress, inflammation and atherosclerotic vascular damage 35 , 36 . Despite this, clinical understanding of the Lp(a)-BP relationship, especially during night-time, remains somewhat underexplored.…”
Section: Discussionsupporting
confidence: 86%
“…Small isoforms of Lp(a) are linked to elevated serum Lp(a) levels, and thus, to an increased risk of coronary artery disease. Thus, screening for genetic factors of Lp(a) is expected to have added value and proves to be cost-effective in primary prevention, whereas the monitoring of serum Lp(a) levels could improve the prediction of the clinical risk of atherosclerotic damage in patients with ASCVD [36,37]. The five plasminogen kringle domains are numbered from 1 to 5 (i.e., KI, KII, KIII, KIV, and KV).…”
Section: Fractional Clearance Ramentioning
confidence: 99%