Cardiovascular risk categories in patients with nonalcoholic fatty liver disease and the role of low-density lipoprotein cholesterol

dc.contributor.authorLabenz, Christian
dc.contributor.authorProchaska, Jürgen H.
dc.contributor.authorHuber, Yvonne
dc.contributor.authorNagel, Michael
dc.contributor.authorStraub, Beate
dc.contributor.authorWild, Philipp
dc.contributor.authorGalle, Peter R.
dc.contributor.authorSchattenberg, Jörn
dc.date.accessioned2019-11-11T15:06:07Z
dc.date.available2019-11-11T16:06:07Z
dc.date.issued2019
dc.description.abstractCardiovascular disease (CVD) is the leading cause of death in patients with nonalcoholic fatty liver disease (NAFLD). The current analysis expands the knowledge on atherogenic lipid profiles in NAFLD by modeling changes in low-density lipoprotein cholesterol (LDL-C) and total cholesterol (TC) in a prospectively enrolling real-life study cohort to inform physicians on the cardiovascular (CV) event risk based on these changes. A total of 304 patients with histologically confirmed NAFLD were included (mean age, 52 years; equal sex distribution). Of these, 129 (42.4%) patients exhibited a NAFLD activity score ≥4 and 186 (61.2%) had at least intermediate fibrosis ≥F2. The median TC levels were 209 mg/dL (interquartile range [IQR], 183, 239), LDL-C 131 mg/dL (IQR, 103, 152), and high density lipoprotein cholesterol (HDL-C) 45 mg/dL (IQR, 38, 52). Only 16.9% of patients received lipid-lowering therapy. According to the LDL/HDL ratio, 69 (23.7%) patients exhibited a high CV risk. The 10-year CV event risk according to the Framingham risk score (FRS) was low in 91 (41.2%), intermediate in 59 (26.7%), and high in 71 (32.1%) patients and higher in the ≥F2 NAFLD population. A moderate increase in LDL-C levels by 20 mg/dL led to a transition of 20% of patients into the high-risk group when assessing the LDL/HDL ratio. According to the FRS, 6 (2.7%) patients moved from low to intermediate and 11 (4.9%) from intermediate to high CV risk. Conclusion: Patients with NAFLD exhibit a substantial CV event risk and are frequently undertreated with lipid-lowering medication. Moderate increases in LDL-C would result in worsening of the CV event risk in approximately 7.8% of all patients without a history of CVD. ERen_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizin
dc.identifier.doihttp://doi.org/10.25358/openscience-230
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/232
dc.identifier.urnurn:nbn:de:hebis:77-publ-594153
dc.language.isoeng
dc.rightsCC-BY-NC-ND-4.0
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleCardiovascular risk categories in patients with nonalcoholic fatty liver disease and the role of low-density lipoprotein cholesterolen_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.apc.price1608,88
jgu.journal.issue11
jgu.journal.titleHepatology communications
jgu.journal.volume3
jgu.organisation.departmentFB 04 Medizinde_DE
jgu.organisation.nameJohannes Gutenberg-Universität Mainzde_DE
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.end1481
jgu.pages.start1472
jgu.publisher.doi10.1002/hep4.1428
jgu.publisher.issn2471-254X
jgu.publisher.nameWiley
jgu.publisher.placeHoboken, NJ
jgu.publisher.urihttp://dx.doi.org/10.1002/hep4.1428
jgu.publisher.year2019
jgu.rights.accessrightsopenAccessen_GB
jgu.subject.ddccode610
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTexten_GB
jgu.type.versionPublished versionen_GB
opus.affiliatedLabenz, Christian
opus.affiliatedHuber, Yvonne
opus.affiliatedNagel, Michael
opus.affiliatedStraub, Beate
opus.affiliatedWild, Philipp
opus.affiliatedGalle, Peter R.
opus.affiliatedSchattenberg, Jörn
opus.date.accessioned2019-11-11T15:06:07Z
opus.date.available2019-11-11T16:06:07
opus.date.modified2019-11-15T09:59:59Z
opus.identifier.opusid59415
opus.institute.number0423
opus.institute.number0425
opus.institute.number0463
opus.institute.number0466
opus.metadataonlyfalse
opus.organisation.stringFB 04: Medizin: Institut für Pathologie
opus.organisation.stringFB 04: Medizin: I. Medizinische Klinik und Poliklinik
opus.organisation.stringFB 04: Medizin: Centrum für Thrombose und Hämostase (CTH)
opus.organisation.stringFB 04: Medizin: Zentrum für Kardiologie
opus.subject.dfgcode00-000
opus.type.contenttypeKeine
opus.type.contenttypeNone

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