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Ancestry, Lipoprotein(a), and Cardiovascular Risk Thresholds JACC Review Topic of the Week
被引:31
|作者:
Tsimikas, Sotirios
[1
,3
]
Marcovina, Santica M.
[2
]
机构:
[1] Univ Calif San Diego, Sulpizio Cardiovasc Ctr, Div Cardiovasc Med, La Jolla, CA USA
[2] Medpace Reference Labs, Cincinnati, OH USA
[3] Univ Calif San Diego, Sulpizio Cardiovasc Ctr, Vasc Med Program, 9500 Gilman Dr, BSB 1080, La Jolla, CA 92093 USA
基金:
美国国家卫生研究院;
关键词:
ancestry;
aortic stenosis;
atherosclerosis;
lipoprotein(a);
threshold;
GENOME-WIDE ASSOCIATION;
CORONARY-HEART-DISEASE;
OXIDIZED PHOSPHOLIPIDS;
CONSENSUS STATEMENT;
SIZE POLYMORPHISM;
LP(A) LIPOPROTEIN;
APOLIPOPROTEIN(A);
OUTCOMES;
DYSLIPIDEMIA;
METAANALYSIS;
D O I:
10.1016/j.jacc.2022.06.019
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
This study reviews ancestral differences in the genetics of the LPA gene, risk categories of elevated lipoprotein(a) [Lp(a)] as defined by guidelines, ancestry-specific Lp(a) risk, absolute and proportional risk, predictive value of risk thresholds among different ancestries, and differences between laboratory vs clinical accuracy in Lp(a) assays. For clinical decision -making, the preponderance of evidence suggests that the predictive value of Lp(a) does not vary sufficiently to mandate the use of ancestry-specific risk thresholds. This paper interprets the literature on Lp(a) and ancestral risk to support: 1) clinicians on understanding cardiovascular disease risk in different ancestral groups; 2) trialists for the design of clinical trials to ensure adequate ancestral diversity to support broad conclusions of drug effects; 3) regulators in the evaluation of the design and interpretation of results of Lp(a)-lowering trials with different Lp(a) inclusion thresholds; and 4) clinical laboratories to measure Lp(a) by assays that discriminate risk thresholds appropriately. (J Am Coll Cardiol 2022;80:934-946)(c) 2022 by the American College of Cardiology Foundation.
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页码:934 / 946
页数:13
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