Evidence map›Paper›PMID 42756755›Full record

ArticleCJC open2026

Rationale and Design of the Canadian Lipoprotein(a) Registry.

Adam I Kramer, Husam Abdel-Qadir, Beth L Abramson, Alexis Baass, Jean Bergeron, Apoorva Bollu, Lubomira Cermakova, Patrick Couture, Christopher B Fordyce, Milan Gupta and 15 more

Abstract read
In one paragraph

Article in CJC open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

25 authors.

Adam I KramerDivision of General Internal Medicine, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Husam Abdel-QadirDivision of Cardiology, Department of Medicine, Women's College Hospital, Toronto, Canada.
Beth L AbramsonDivision of Cardiology, St Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
Alexis BaassGenetic Dyslipidemias Clinic of the Montréal Clinical Research Institute, Montréal, Québec, Canada.
Jean BergeronDepartment of Laboratory Medicine, Centre Hospitalier Universitaire de Québec, Université Laval, Québec City, Québec, Canada.
Apoorva BolluDivision of General Internal Medicine, Surrey Memorial Hospital, Surrey, British Columbia, Canada.
Lubomira CermakovaHealthy Heart Program Prevention Clinic, St Paul's Hospital, Vancouver, British Columbia, Canada.
Patrick CoutureDepartment of Laboratory Medicine, Centre Hospitalier Universitaire de Québec, Université Laval, Québec City, Québec, Canada.
Christopher B FordyceDivision of Cardiology, Department of Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Milan GuptaDepartment of Medicine, University of Toronto, Toronto, Ontario, Canada.
Robert A HegeleRobarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.
G B John ManciniDivision of Cardiology, Department of Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Ruth McPhersonLipid Clinic & Atherogenomics Laboratory, University of Ottawa Heart Institute, Ottawa, Ontario, Canada.
Nathaniel MoulsonDivision of Cardiology, Department of Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Glen J PearsonFaculty of Medicine & Dentistry, Division of Cardiology, Department of Medicine, University of Alberta, Mazankowski Alberta Heart Institute, Edmonton, Alberta, Canada.
Thomas RostonDivision of Cardiology, Department of Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Isabelle RuelResearch Institute of the McGill University Health Centre, Montréal, Québec, Canada.
Tara SedlakDivision of Cardiology, Department of Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Mark H ShermanDepartment of Endocrinology, McGill University Health Centre, Montréal, Québec, Canada.
George ThanassoulisMike and Valeria Rosenbloom Centre for Cardiovascular Prevention, Department of Medicine, McGill University Health Centre-Royal Victoria Hospital, Montréal, Québec, Canada.
Jacob A UdellDivision of Cardiology, Department of Medicine, Women's College Hospital, Toronto, Canada.
Subodh VermaDivision of Cardiac Surgery, St Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
Darryl WanDivision of Cardiology, Department of Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Iulia IatanDivision of General Internal Medicine, Department of Medicine, McGill University Health Centre, Montréal, Québec, Canada.
Liam R BrunhamDivision of General Internal Medicine, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipoprotein(a) [Lp(a)] is an independent, heritable risk factor for atherosclerotic cardiovascular disease. Guidelines recommend Lp(a) testing once in a lifetime and recognize it as a risk-enhancing factor. However, management of elevated Lp(a) in real-world clinical practice is not well described. Here we describe the rationale, design, and preliminary baseline characteristics of the Canadian Lp(a) Registry, a prospective, longitudinal observational study of patients with Lp(a) ≥ 100 nmol/L (≥ 50 mg/dL). Patient demographics, cardiovascular risk factors, laboratory results, and clinical outcomes are collected at baseline and at annual follow-up. The primary objective is to evaluate the clinical management and outcomes of patients with elevated Lp(a). From April 2024 to April 2025, 127 patients (mean age 57.5 ± 12.7 years, 48.8% female) were enrolled with a median Lp(a) level of 225 nmol/L (interquartile range 186-346 nmol/L), and 51.2% had multiple Lp(a) levels obtained. The most recent mean low-density lipoprotein cholesterol (LDL-C) was 2.49 ± 1.74 mmol/L. At the time of registry entry, 104 (81.9%) patients were receiving lipid-lowering therapies, including statins (74.8%), ezetimibe (48.0%), and proprotein convertase subtilisin/kexin type 9 inhibitors (27.6%), whereas 18.1% were not taking prescription lipid-lowering therapy. There were 66 (52.0%) patients with an LDL-C < 2.0 mmol/L. The Canadian Lp(a) Registry is an ongoing prospective, observational study designed to evaluate the clinical management, cardiovascular risk profile, and outcomes for patients with elevated Lp(a). It is expected to improve our understanding of how elevated Lp(a) is managed in contemporary clinical practice and to identify opportunities to improve care.

Indexed as

atherosclerotic cardiovascular diseaselipoprotein(a)low-density lipoprotein cholesterolregistry

Identifiers

PMID42756755
PMCPMC13583562

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.