Evidence map›Paper›PMID 37755635›Full record

ArticleCurrent medical science2023

Lipoprotein(a) and Benefit of PCSK9 Inhibition in Emergency Complex Higher-risk and Indicated Patients.

Zhi-Li Jin, Tao He, Li Peng, Xiao-Yan Wu, Di Fan, Ming Chen, Yong-Zhen Fan, Yuan-Lin Guo, Zhi-Bing Lu, Hai-Rong Wang

Abstract read
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In one paragraph

Article in Current medical science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 1 citations in OpenAlex.

  1. Pooled it
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Zhi-Li JinDepartment of Cardiovascular Medicine, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Tao HeDepartment of Cardiovascular Medicine, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Li PengDepartment of Cardiovascular Medicine, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Xiao-Yan WuDepartment of Cardiovascular Medicine, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Di FanDepartment of Cardiovascular Medicine, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Ming ChenDepartment of Cardiovascular Medicine, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Yong-Zhen FanDepartment of Cardiovascular Medicine, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Yuan-Lin GuoCardio-Metabolic Medicine Center, Fuwai Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100037, China.
Zhi-Bing LuDepartment of Cardiovascular Medicine, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China. Luzhibing222@163.com.
Hai-Rong WangDepartment of Cardiovascular Medicine, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China. wanghai2192@sina.com.
Wuhan University · CNZhongnan Hospital of Wuhan University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThere is a large population of patients classified as complex higher-risk and indicated patients (CHIPs) in China with a poor prognosis. The treatment of these patients is complex and challenging, especially when acute cardiac events occur, such as acute coronary syndrome (ACS) or heart failure. Pharmacotherapy and some mechanical circulatory support (MCS) therapeutic devices can provide stable hemodynamic support for CHIPs-percutaneous coronary intervention (PCI). LDL-C is an important pathogenic factor in atherosclerosis, and the target of blood lipid control. Recent studies have revealed that lipoprotein(a) [Lp(a)], which is formed when a covalent bond between apolipoprotein(a) and apolipoprotein B-100 is made, produces an LDL-like particle. This particle is an independent risk factor for the development of atherosclerosis, and is closely correlated to stent thrombosis and restenosis. Furthermore, this requires active intervention. PCSK9 inhibitors have been used in lipid-lowering treatment, and preventing atherosclerosis. The present study explores the efficacy of PCSK9 inhibitors in CHIPs-ACS, and the association between the change in Lp(a) and survival after 2 years of follow-up.

methodsThe present real-world, prospective control study enrolled 321 CHIPs-ACS who underwent emergency PCI from August 2019 to November 2020, and these patients were followed up for 2 years. These patients were divided into two groups: PCSK9 group (n=161) given the combined PCSK9 inhibitor (140 mg of evolocumab every 2 weeks) and statins-based therapy, and SOC group (n=160) treated with statin-based lipid-lowering therapy alone. Then, the change in lipid index was measured, and the cardiovascular (CV) event recurrence rate was evaluated after one month and 2 years. Afterwards, the contribution of serum lipid parameters, especially the Lp(a) alteration, in patients with earlier initiation of the PCSK9 inhibitor to the CV outcome was analyzed.

resultsThe LDL-C level was significantly reduced in both groups: 52.3% in the PCSK9 group and 32.3% (P<0.001) in the SOC group. It is noteworthy that the Lp(a) level decreased by 13.2% in the PCSK9 group, but increased by 30.3% in the SOC group (P<0.001). Furthermore, the number of CV events was not significantly different between the PCSK9 and SOC groups after the 2-year follow-up period. In the PCSK9 group, the Lp(a) reduction was associated with the baseline Lp(a) levels of the patients (r

conclusionThe early initiation of PCSK9 inhibitors can significantly reduce the LDL-C and Lp(a) levels in ACS CHIPs-PCI. However, further studies are needed to confirm whether PCSK9 inhibitors can reduce the incidence of CV disease in CHIPs.

Indexed as

Acute Coronary SyndromeAtherosclerosisHydroxymethylglutaryl-CoA Reductase InhibitorsPercutaneous Coronary InterventionCholesterol, LDLHumansLipidsLipoprotein(a)PCSK9 InhibitorsProprotein Convertase 9Prospective StudiesCholesterol, LDLHydroxymethylglutaryl-CoA Reductase InhibitorsLipidsLipoprotein(a)PCSK9 InhibitorsPCSK9 protein, humanProprotein Convertase 92-year cardiovascular event ratecomplex higher-risk and indicated patientslipoprotein(a) levellow-density lipoprotein cholesterol levelPCSK9 inhibitor

Identifiers

PMID37755635
OpenAlexW4387077699

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Texttitle and abstract
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.