Data Resource Profile: The Copenhagen Hospital Biobank (CHB)

Sørensen, Erik; Christiansen, Lene; Wilkowski, Bartłomiej; Larsen, Margit Hørup; Burgdorf, Kristoffer Sølvsten; Thørner, Lise Wegner; Nissen, Janna; Pedersen, Ole Birger; Banasik, Karina; Brunak, Søren; Bundgaard, Henning; Stefánsson, Hreinn; Stefánsson, Kāri; Melbye, Mads; Ullum, Henrik

doi:10.1093/ije/dyaa157

Cited by 34 publications

(37 citation statements)

References 13 publications

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“…National or regional surveys may also contain valuable data, such as self-reported physical and mental health, social relations, lifestyle and other factors not recorded in the registries. 7,113,117,[127][128][129][130] Lastly, researcher-initiated cohorts 7,117,128,[131][132][133][134][135][136][137][138][139] or biobanks 7,128,[131][132][133][134][135][136][137][138][139][140][141][142][143][144][145] are widely available.…”

Section: Other Registries and Databasesmentioning

confidence: 99%

Nordic Health Registry-Based Research: A Review of Health Care Systems and Key Registries

Laugesen

Ludvigsson

Schmidt

et al. 2021

CLEP

284

230

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The Nordic countries are Denmark, Finland, Iceland, Norway, and Sweden and comprise a total population of approximately 27 million. The countries provide unique opportunities for joint health registry-based research in large populations with long and complete follow-up, facilitated by shared features, such as the tax-funded and public health care systems, the similar population-based registries, and the personal identity number as unique identifier of all citizens. In this review, we provide an introduction to the health care systems, key registries, and how to navigate the practical and ethical aspects of setting up such studies. For each country, we provide an overview of population statistics and health care expenditures, and describe the operational and administrative organization of the health care system. The Nordic registries provide population-based, routine, and prospective data on individuals lives and health with virtually complete follow-up and exact censoring information. We briefly describe the total population registries, birth registries, patient registries, cancer registries, prescription registries, and causes of death registries with a focus on period of coverage, selected key variables, and potential limitations. Lastly, we discuss some practical and legal perspectives. The potential of joint research is not fully exploited, mainly due to legal and practical difficulties in, for example, cross-border sharing of data. Future tasks include clear and transparent legal pathways and a framework by which practical aspects are facilitated.

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Section: Other Registries and Databasesmentioning

confidence: 99%

Nordic Health Registry-Based Research: A Review of Health Care Systems and Key Registries

Laugesen

Ludvigsson

Schmidt

et al. 2021

CLEP

284

230

View full text Add to dashboard Cite

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“…ischemic heart disease, hypertension, cardiac arrhythmia, lipid metabolism disorders etc., registered in the Danish National Patient Registry [more information in Supplementary Methods ]). [17] Patients included in CHB have been informed about their right to refuse the use of their samples for research. Individuals registered in the national opt-out registry were excluded from analysis.…”

Section: Methodsmentioning

confidence: 99%

Common variants near the bradykinin receptor B₂gene are associated with angioedema induced by angiotensin-converting-enzyme inhibitor treatment - a genome wide association study

Ghouse

Ahlberg

Andreasen

et al. 2020

Preprint

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ObjectiveAngioedema is a rare, but potentially life-threatening adverse reaction, associated with angiotensin-converting-enzyme inhibitors (ACEi). Identification of potential genetic factors related to this adverse event may help identify at-risk patients.Design, Setting and ParticipantsA genome-wide association study (GWAS) involving patients of European descent, all taking ACEi was conducted in a discovery cohort (Copenhagen Hospital Biobank), and associations were confirmed in a replication cohort (Swedegene). Cases were defined as persons with an angioedema event and a filled prescription for an ACEi 180 days prior to the event. Controls were defined as persons with continuous treatment with ACEi without any history of angioedema. Odds ratios (ORs) and 95 % confidence intervals (95 % CI) were computed for angioedema risk by logistic mixed model regression analysis. Summary statistics from the discovery and the replication cohorts were analyzed with a fixed effects meta-analysis model.ExposureSingle-nucleotide polymorphisms associated with ACEi-associated angioedema.Main outcomeHospital record of angioedema.ResultsThe discovery cohort consisted of 462 cases and 53,391 ACEi-treated controls. The replication cohort consisted of 144 cases and 1,345 ACEi-treated controls. In the discovery cohort, we identified one locus, residing at chromosome 14q32.2, that was associated with angioedema at the genome-wide significance level of P <5 × 10−8. The lead variant at this locus, rs34485356, is an intergenic variant located 60 kb upstream of BDKRB2 (OR 1.62; 95 % CI 1.38 to 1.90; P = 4.3 × 10−9). This variant was validated in our replication cohort with similar direction and effect size (OR 1.60; 95 % CI 1.13 to 2.25; P = 7.2 × 10−3). We found that carriers of the risk allele had significantly lower systolic (−0.46 mmHg per T allele; 95 % CI −0.83 to −0.10; P = 0.013) and diastolic blood pressure (−0.26 mmHg per T allele; 95 % CI −0.46 to −0.05; P = 0.013).ConclusionIn this GWAS, involving individuals treated with ACEi, we found that common variants located in close proximity to the bradykinin receptor B2 gene were associated with ACEi-related angioedema. BDKRB2 genotype-directed therapy may aid in improving safety in evidence-based clinical decision-making.

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“…The data foundation of CHB is a collection of leftover EDTA blood samples from patients hospitalised in the Capital Region of Denmark, who were subject to blood typing or red blood cell antibody screening. Details about data collection, quality assessment and storage can be found in Sørensen et al 16 Presently, CHB contains samples from more than 450 000 individuals. 16 Each patient is identified by a Central Person Registry (CPR) number, which facilitates linkage to nationwide registries and electronic patient records.…”

Section: Strengths and Limitations Of This Studymentioning

confidence: 99%

“…Details about data collection, quality assessment and storage can be found in Sørensen et al 16 Presently, CHB contains samples from more than 450 000 individuals. 16 Each patient is identified by a Central Person Registry (CPR) number, which facilitates linkage to nationwide registries and electronic patient records. Nationwide registries and electronic patient records are updated continuously.…”

Section: Strengths and Limitations Of This Studymentioning

confidence: 99%

“…Patients in CHB are over 18 years old and only included once. 16 The aim of the CHB-CVDC is to provide a platform for studying genetic, environmental, medical and other factors to further our knowledge of initiation, progression and manifestation of CVDs. CHB-CVDC facilitate studies of individual diseases as well as the shared risk factors, pathophysiology and disease trajectories.…”

Section: Strengths and Limitations Of This Studymentioning

confidence: 99%

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Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases

et al. 2021

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PurposeThe aim of Copenhagen Hospital Biobank-Cardiovascular Disease Cohort (CHB-CVDC) is to establish a cohort that can accelerate our understanding of CVD initiation and progression by jointly studying genetics, diagnoses, treatments and risk factors.ParticipantsThe CHB-CVDC is a large genomic cohort of patients with CVD. CHB-CVDC currently includes 96 308 patients. The cohort is part of CHB initiated in 2009 in the Capital Region of Denmark. CHB is continuously growing with ~40 000 samples/year. Patients in CHB were included in CHB-CVDC if they were above 18 years of age and assigned at least one cardiovascular diagnosis. Additionally, up-to 110 000 blood donors can be analysed jointly with CHB-CVDC. Linkage with the Danish National Health Registries, Electronic Patient Records, and Clinical Quality Databases allow up-to 41 years of medical history. All individuals are genotyped using the Infinium Global Screening Array from Illumina and imputed using a reference panel consisting of whole-genome sequence data from 8429 Danes along with 7146 samples from North-Western Europe. Currently, 39 539 of the patients are deceased.Findings to dateHere, we demonstrate the utility of the cohort by showing concordant effects between known variants and selected CVDs, that is, >93% concordance for coronary artery disease, atrial fibrillation, heart failure and cholesterol measurements and 85% concordance for hypertension. Furthermore, we evaluated multiple study designs and the validity of using Danish blood donors as part of CHB-CVDC. Lastly, CHB-CVDC has already made major contributions to studies of sick sinus syndrome and the role of phytosterols in development of atherosclerosis.Future plansIn addition to genetics, electronic patient records, national socioeconomic and health registries extensively characterise each patient in CHB-CVDC and provides a promising framework for improved understanding of risk and protective variants. We aim to include other measurable biomarkers for example, proteins in CHB-CVDC making it a platform for multiomics cardiovascular studies.

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Data Resource Profile: The Copenhagen Hospital Biobank (CHB)

Cited by 34 publications

References 13 publications

Nordic Health Registry-Based Research: A Review of Health Care Systems and Key Registries

Nordic Health Registry-Based Research: A Review of Health Care Systems and Key Registries

Common variants near the bradykinin receptor B₂gene are associated with angioedema induced by angiotensin-converting-enzyme inhibitor treatment - a genome wide association study

Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases

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Data Resource Profile: The Copenhagen Hospital Biobank (CHB)

Cited by 34 publications

References 13 publications

Nordic Health Registry-Based Research: A Review of Health Care Systems and Key Registries

Nordic Health Registry-Based Research: A Review of Health Care Systems and Key Registries

Common variants near the bradykinin receptor B2gene are associated with angioedema induced by angiotensin-converting-enzyme inhibitor treatment - a genome wide association study

Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases

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Common variants near the bradykinin receptor B₂gene are associated with angioedema induced by angiotensin-converting-enzyme inhibitor treatment - a genome wide association study