Evidence map›Paper›PMID 36188622›Full record

ArticleFrontiers in pharmacology2022

Therapeutic potential of the Proprotein Convertase Subtilisin/Kexin family in vascular disease.

Bianca E Suur, Melody Chemaly, Moritz Lindquist Liljeqvist, Djordje Djordjevic, Markus Stenemo, Otto Bergman, Eva Karlöf, Mariette Lengquist, Jacob Odeberg, Eva Hurt-Camejo and 6 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

16 authors.

Bianca E SuurDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Melody ChemalyDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Moritz Lindquist LiljeqvistDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Djordje DjordjevicDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Markus StenemoDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Otto BergmanDepartment of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
Eva KarlöfDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Mariette LengquistDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Jacob OdebergDepartment of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
Eva Hurt-CamejoDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Per ErikssonDepartment of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
Daniel F J KetelhuthDepartment of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
Joy RoyDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Ulf HedinDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Michael NybergGlobal Drug Discovery, Novo Nordisk A/S, Maaloev, Denmark.
Ljubica MaticDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proprotein convertase subtilisin/kexins (PCSKs) constitute a family of nine related proteases: PCSK1-7, MBTPS1, and PCSK9. Apart from PCSK9, little is known about PCSKs in cardiovascular disease. Here, we aimed to investigate the expression landscape and druggability potential of the entire PCSK family for CVD. We applied an integrative approach, combining genetic, transcriptomic and proteomic data from three vascular biobanks comprising carotid atherosclerosis, thoracic and abdominal aneurysms, with patient clinical parameters and immunohistochemistry of vascular biopsies. Apart from

Indexed as

aortic aneurysmcarotid plaquePCSKtherapeutic targetingvascular disease

Identifiers

PMID36188622
PMCPMC9520287

What OpenQuestion holds

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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.