Familial hypercholesterolaemia: a study protocol for identification and investigation of potential causes and markers of subclinical coronary artery disease in the Faroe Islands

Introduction Familial hypercholesterolaemia (FH) is the most common monogenic autosomal dominant genetic disorder and is associated with a high risk of premature atherosclerotic cardiovascular disease. The prevalence of FH has been reported to be particularly high in certain founder populations. The...

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Published in:BMJ Open
Main Authors: Peter Søgaard, Albert Marni Joensen, Søren Lundbye-Christensen, Erik Berg Schmidt, Jan Jóanesarson, Christian Sørensen Bork, Tomas Zaremba, Sanna á Borg, Michael Rene Skjelbo Nielsen, Rudi Kollslíð
Format: Article in Journal/Newspaper
Language:English
Published: BMJ Publishing Group 2022
Subjects:
R
Online Access:https://doi.org/10.1136/bmjopen-2021-050857
https://doaj.org/article/237543fcde404810852f2a3fa0f2f139
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spelling ftdoajarticles:oai:doaj.org/article:237543fcde404810852f2a3fa0f2f139 2024-10-13T14:07:04+00:00 Familial hypercholesterolaemia: a study protocol for identification and investigation of potential causes and markers of subclinical coronary artery disease in the Faroe Islands Peter Søgaard Albert Marni Joensen Søren Lundbye-Christensen Erik Berg Schmidt Jan Jóanesarson Christian Sørensen Bork Tomas Zaremba Sanna á Borg Michael Rene Skjelbo Nielsen Rudi Kollslíð 2022-04-01T00:00:00Z https://doi.org/10.1136/bmjopen-2021-050857 https://doaj.org/article/237543fcde404810852f2a3fa0f2f139 EN eng BMJ Publishing Group https://bmjopen.bmj.com/content/12/4/e050857.full https://doaj.org/toc/2044-6055 https://doaj.org/article/237543fcde404810852f2a3fa0f2f139 BMJ Open, Vol 12, Iss 4 (2022) Medicine R article 2022 ftdoajarticles https://doi.org/10.1136/bmjopen-2021-050857 2024-09-25T15:39:13Z Introduction Familial hypercholesterolaemia (FH) is the most common monogenic autosomal dominant genetic disorder and is associated with a high risk of premature atherosclerotic cardiovascular disease. The prevalence of FH has been reported to be particularly high in certain founder populations. The population of the Faroe Islands is a founder population, but the prevalence of FH has never been investigated here. We aim to assess the prevalence of FH and to describe the genetic and clinical characteristics and potential causes of FH in the Faroe Islands. Furthermore, we aim to investigate whether indicators of subclinical coronary artery disease are associated with FH.Methods and analysis The prevalence of FH will be estimated based on an electronic nationwide laboratory database that includes all measurements of plasma lipid levels in the Faroe Islands since 2006. Subsequently, we will identify and invite subjects aged between 18 and 75 years registered with a plasma low-density lipoprotein cholesterol above 6.7 mmol/L for diagnostic evaluation. Eligible FH cases will be matched to controls on age and sex. We aim to include 120 FH cases and 120 controls.Detailed information will be collected using questionnaires and interviews, and a physical examination will be undertaken. An adipose tissue biopsy and blood samples for genetic testing, detailed lipid analyses and samples for storage in a biobank for future research will be collected. Furthermore, FH cases and controls will be invited to have a transthoracic echocardiography and a cardiac CT performed.Ethics and dissemination The project has been approved by the Ethical Committee and the Data Protection Agency of the Faroe Islands. The project is expected to provide important information, which will be published in international peer-reviewed journals. Article in Journal/Newspaper Faroe Islands Directory of Open Access Journals: DOAJ Articles Faroe Islands BMJ Open 12 4 e050857
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Medicine
R
spellingShingle Medicine
R
Peter Søgaard
Albert Marni Joensen
Søren Lundbye-Christensen
Erik Berg Schmidt
Jan Jóanesarson
Christian Sørensen Bork
Tomas Zaremba
Sanna á Borg
Michael Rene Skjelbo Nielsen
Rudi Kollslíð
Familial hypercholesterolaemia: a study protocol for identification and investigation of potential causes and markers of subclinical coronary artery disease in the Faroe Islands
topic_facet Medicine
R
description Introduction Familial hypercholesterolaemia (FH) is the most common monogenic autosomal dominant genetic disorder and is associated with a high risk of premature atherosclerotic cardiovascular disease. The prevalence of FH has been reported to be particularly high in certain founder populations. The population of the Faroe Islands is a founder population, but the prevalence of FH has never been investigated here. We aim to assess the prevalence of FH and to describe the genetic and clinical characteristics and potential causes of FH in the Faroe Islands. Furthermore, we aim to investigate whether indicators of subclinical coronary artery disease are associated with FH.Methods and analysis The prevalence of FH will be estimated based on an electronic nationwide laboratory database that includes all measurements of plasma lipid levels in the Faroe Islands since 2006. Subsequently, we will identify and invite subjects aged between 18 and 75 years registered with a plasma low-density lipoprotein cholesterol above 6.7 mmol/L for diagnostic evaluation. Eligible FH cases will be matched to controls on age and sex. We aim to include 120 FH cases and 120 controls.Detailed information will be collected using questionnaires and interviews, and a physical examination will be undertaken. An adipose tissue biopsy and blood samples for genetic testing, detailed lipid analyses and samples for storage in a biobank for future research will be collected. Furthermore, FH cases and controls will be invited to have a transthoracic echocardiography and a cardiac CT performed.Ethics and dissemination The project has been approved by the Ethical Committee and the Data Protection Agency of the Faroe Islands. The project is expected to provide important information, which will be published in international peer-reviewed journals.
format Article in Journal/Newspaper
author Peter Søgaard
Albert Marni Joensen
Søren Lundbye-Christensen
Erik Berg Schmidt
Jan Jóanesarson
Christian Sørensen Bork
Tomas Zaremba
Sanna á Borg
Michael Rene Skjelbo Nielsen
Rudi Kollslíð
author_facet Peter Søgaard
Albert Marni Joensen
Søren Lundbye-Christensen
Erik Berg Schmidt
Jan Jóanesarson
Christian Sørensen Bork
Tomas Zaremba
Sanna á Borg
Michael Rene Skjelbo Nielsen
Rudi Kollslíð
author_sort Peter Søgaard
title Familial hypercholesterolaemia: a study protocol for identification and investigation of potential causes and markers of subclinical coronary artery disease in the Faroe Islands
title_short Familial hypercholesterolaemia: a study protocol for identification and investigation of potential causes and markers of subclinical coronary artery disease in the Faroe Islands
title_full Familial hypercholesterolaemia: a study protocol for identification and investigation of potential causes and markers of subclinical coronary artery disease in the Faroe Islands
title_fullStr Familial hypercholesterolaemia: a study protocol for identification and investigation of potential causes and markers of subclinical coronary artery disease in the Faroe Islands
title_full_unstemmed Familial hypercholesterolaemia: a study protocol for identification and investigation of potential causes and markers of subclinical coronary artery disease in the Faroe Islands
title_sort familial hypercholesterolaemia: a study protocol for identification and investigation of potential causes and markers of subclinical coronary artery disease in the faroe islands
publisher BMJ Publishing Group
publishDate 2022
url https://doi.org/10.1136/bmjopen-2021-050857
https://doaj.org/article/237543fcde404810852f2a3fa0f2f139
geographic Faroe Islands
geographic_facet Faroe Islands
genre Faroe Islands
genre_facet Faroe Islands
op_source BMJ Open, Vol 12, Iss 4 (2022)
op_relation https://bmjopen.bmj.com/content/12/4/e050857.full
https://doaj.org/toc/2044-6055
https://doaj.org/article/237543fcde404810852f2a3fa0f2f139
op_doi https://doi.org/10.1136/bmjopen-2021-050857
container_title BMJ Open
container_volume 12
container_issue 4
container_start_page e050857
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