dc.contributor.author
König, Maximilian
dc.contributor.author
Joshi, Samita
dc.contributor.author
Leistner, David M.
dc.contributor.author
Landmesser, Ulf
dc.contributor.author
Sinning, David
dc.contributor.author
Steinhagen-Thiessen, Elisabeth
dc.contributor.author
Demuth, Ilja
dc.date.accessioned
2019-11-27T12:00:46Z
dc.date.available
2019-11-27T12:00:46Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/26006
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-25764
dc.description.abstract
PURPOSE:
The LipidCardio Study was established for in-depth analyses of cardiovascular risk factors, providing well-defined cardiovascular and metabolic phenotypes. In particular, the role of lipoproteins in the pathobiological process and treatment of cardiovascular disease (CVD) will be a main focus.
PARTICIPANTS:
1005 individuals aged 21 years and older undergoing cardiac catheterisation during 17 months at a tertiary academic cardiology centre were enrolled (troponin-positive acute coronary syndrome was exclusion criterion). The baseline data not only contain detailed phenotyping, broad biochemical parameters, genetic data, but also standardised personal and family history, a screening test for cognitive impairment, pulse wave analysis and measurements of hand grip strength, among others. Blood samples were stored in a biobank for future analyses.
FINDINGS TO DATE:
The mean age of the participants at enrolment was 70.9±11.1 years (70% male). Coronary angiography provided evidence of obstructive coronary artery disease (CAD) in 69.9% of participants. Those with evidence of CAD were significantly more likely to be male, inactive, diabetic and with a family history of CVD than participants without CAD.About 20% of patients had lipoprotein(a) (Lp(a)) concentrations above 106.9 nmol/L (fifth quintile). These patients had significantly increased odds of obstructive CAD compared with participants in quintiles 1-4 (crude OR 1.70, 95% CI 1.17 to 2.48, p=0.005). There was reasonable evidence that with increasing severity of CAD the odds of having elevated Lp(a) increased. We were able to replicate the established strong association between specified single nucleotide polymorphisms (SNPs) in the LPA gene (rs10455872, rs3798220 and rs186696265) and the APOE gene (rs7412), and the concentration of Lp(a), validating our phenotype database and biobank.
FUTURE PLANS:
Mortality information will be obtained in 2 year intervals. Follow-up phone interviews will be conducted at 3 and 6 years after enrolment. We seek to cooperate with other researchers, for example, by sharing data and biobank samples.
en
dc.rights.uri
https://creativecommons.org/licenses/by-nc/4.0/
dc.subject
Coronary heart disease
en
dc.subject
Lipoprotein a
en
dc.subject
cohort studies
en
dc.subject
Lipid disorders
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Cohort profile: role of lipoproteins in cardiovascular disease-the LipidCardio study
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
e030097
dcterms.bibliographicCitation.doi
10.1136/bmjopen-2019-030097
dcterms.bibliographicCitation.journaltitle
BMJ Open
dcterms.bibliographicCitation.number
9
dcterms.bibliographicCitation.originalpublishername
BMJ Publishing Group
dcterms.bibliographicCitation.volume
9
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
31481563
dcterms.isPartOf.eissn
2044-6055