Evidence map›Paper›PMID 39256734›Full record

ArticleLipids in health and disease2024

PCSK9 inhibitors on the management of primary and secondary cardiovascular prevention.

Victoria Marco-Benedí, Rosa M Sánchez-Hernández, José Luis Díaz, Estíbaliz Jarauta, Manuel Suárez-Tembra, Xavier Pintó, Carlos Morillas, Núria Plana, Juan Pedro-Botet, Fernando Civeira

Abstract read
In one paragraph

Article in Lipids in health and disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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. Review
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.

Victoria Marco-BenedíHospital Universitario Miguel Servet, IIS Aragón, CIBERCV, Saragossa, Spain. vmarcobenedi@gmail.com.
Rosa M Sánchez-HernándezSección de Endocrinología y Nutrición, Complejo Hospitalario Universitario Insular Materno-Infantil, Instituto Universitario de Investigaciones Biomédicas y Sanitarias de La Universidad de Las Palmas de Gran Canaria, de Las Palmas de Gran Canaria, Spain.
José Luis DíazUnidad de Lípidos y Riesgo Cardiovascular, Medicina Interna, Hospital Universitario A Coruña, A Coruña, Spain.
Estíbaliz JarautaHospital Universitario Miguel Servet, IIS Aragón, CIBERCV, Saragossa, Spain.
Manuel Suárez-TembraUnidad de Lípidos y Riesgo Cardiovascular Hospital San Rafael, A Coruña, Spain.
Xavier PintóUnidad de Lípidos y Riesgo Cardiovascular, Servicio de Medicina Interna, Hospital Universitario de Bellvitge, CIBEROBN, Barcelona, Spain.
Carlos MorillasUnidad de Lípidos Clínico-Epidemiológica, Hospital Universitario Dr. Peset, Valencia, Spain.
Núria PlanaUnitat de Medicina Vascular I Metabolisme, Hospital Sant Joan de Reus, IISPV, CIBERDEM, Universitat Rovira I Virgili, Reus, Spain.
Juan Pedro-BotetUnidad de Lípidos y Riesgo Vascular, Servicio de Endocrinología y Nutrición, Hospital del Mar, Universidad Autónoma de Barcelona, Barcelona, Spain.
Fernando CiveiraHospital Universitario Miguel Servet, IIS Aragón, CIBERCV, Saragossa, Spain. civeira@unizar.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) have represented an important change in the management of hypercholesterolemia, although, until now, they have barely been used. Without PCSK9i, many patients with atherosclerotic cardiovascular disease (CVD) or those at very high risk do not reach their therapeutic LDLc objectives.

objectiveThe analysis aimed to examine the clinical and biochemical characteristics of subjects receiving PCSK9i treatment in the Dyslipidemia Registry of the Spanish Atherosclerosis Society.

methodsAll consecutive subjects aged ≥ 18 years from different Lipid Units included in the Dyslipidemia Registry of the SEA were analyzed. Inclusion criteria consisted of unrelated patients aged ≥ 18 at the time of inclusion with hypercholesterolemia (LDL-C ≥ 130 mg/dL or non-HDL-C ≥ 160 mg/dL after the exclusion of secondary causes) who were studied for at least two years after inclusion. Participants' baseline and final visit clinical and biochemical characteristics were analyzed based on whether they were on primary or secondary prevention and whether they were taking PCSK9i at the end of follow-up.

resultsEight hundred twenty-nine patients were analyzed, 7014 patients in primary prevention and 1281 in secondary prevention at baseline. 4127 subjects completed the required follow-up for the final analysis. The median follow-up duration was 7 years (IQR 3.0-10.0). Five hundred patients (12.1%) were taking PCSK9i at the end of the follow-up. The percentage of PCSK9i use reached 35.6% (n = 201) and 8.7% (n = 318) in subjects with and without CVD, respectively. Subjects on PCSK9i and oral lipid-lowering agents with and without CVD achieved LDLc reductions of 80.3% and 75.1%, respectively, concerning concentrations without lipid-lowering drugs. Factors associated with PCSK9i use included increasing age, LDLc without lipid-lowering drugs and the Dutch Lipid Clinic Network (DLCN) score. However, hypertension, diabetes, smoking, and LDLc after oral lipid-lowering drugs were not independent factors associated with PCSK9i prescription. In subjects with CVD, the use of PCSK9i was higher in men than in women (an odds ratio of 1.613, P = 0.048).

conclusionsApproximately one-third of CVD patients received PCSK9i at the end of follow-up. The use of PCSK9i was more focused on baseline LDLc concentrations rather than on CVD risk. Women received less PCSK9i in secondary prevention compared to men.

Indexed as

Cardiovascular DiseasesCholesterol, LDLPCSK9 InhibitorsSecondary PreventionAgedAntibodies, Monoclonal, HumanizedAnticholesteremic AgentsFemaleHumansHypercholesterolemiaMaleMiddle AgedPrimary PreventionProprotein Convertase 9RegistriesAntibodies, Monoclonal, HumanizedAnticholesteremic AgentsCholesterol, LDLPCSK9 InhibitorsPCSK9 protein, humanProprotein Convertase 9Familial hypercholesterolemiaLDL-cholesterolPCSK9 inhibitorsPrimary preventionSecondary prevention

Identifiers

PMID39256734
PMCPMC11386113

What Socratic holds

Texttitle and abstract
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.