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Quantifying atherog...
Quantifying atherogenic lipoproteins for lipid-lowering strategies: Consensus-based recommendations from EAS and EFLM
- Article/chapterEnglish2020
Publisher, publication year, extent ...
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2019-12-19
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Walter de Gruyter GmbH,2020
Numbers
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LIBRIS-ID:oai:gup.ub.gu.se/293403
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https://gup.ub.gu.se/publication/293403URI
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https://doi.org/10.1515/cclm-2019-1253DOI
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
Notes
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The joint consensus panel of the European Atherosclerosis Society (EAS) and the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) recently addressed present and future challenges in the laboratory diagnostics of atherogenic lipoproteins. Total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDLC), LDL cholesterol (LDLC), and calculated non-HDLC (=total - HDLC) constitute the primary lipid panel for estimating risk of atherosclerotic cardiovascular disease (ASCVD) and can be measured in the nonfasting state. LDLC is the primary target of lipid-lowering therapies. For on-treatment follow-up, LDLC shall be measured or calculated by the same method to attenuate errors in treatment decisions due to marked between-method variations. Lipoprotein(a) [Lp(a)]-cholesterol is part of measured or calculated LDLC and should be estimated at least once in all patients at risk of ASCVD, especially in those whose LDLC declines poorly upon statin treatment. Residual risk of ASCVD even under optimal LDL-lowering treatment should be also assessed by non-HDLC or apolipoprotein B (apoB), especially in patients with mild-to-moderate hypertriglyceridemia (2-10 mmol/L). Non-HDLC includes the assessment of remnant lipoprotein cholesterol and shall be reported in all standard lipid panels. Additional apoB measurement can detect elevated LDL particle (LDLP) numbers often unidentified on the basis of LDLC alone. Reference intervals of lipids, lipoproteins, and apolipoproteins are reported for European men and women aged 20-100 years. However, laboratories shall flag abnormal lipid values with reference to therapeutic decision thresholds. © 2019 Walter de Gruyter GmbH, Berlin/Boston 2019.
Subject headings and genre
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Nordestgaard, Bø G.
(author)
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Langsted, A.
(author)
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Chapman, M. J.
(author)
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Aakre, K. M.
(author)
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Baum, H.
(author)
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Borén, Jan,1963Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Institutionen för medicin,Wallenberg Laboratory,Institute of Medicine(Swepub:gu)xborej
(author)
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Bruckert, E.
(author)
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Catapano, A.
(author)
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Cobbaert, C.
(author)
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Collinson, P.
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Descamps, O. S.
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Duff, C. J.
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Von Eckardstein, A.
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Hammerer-Lercher, A.
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Kamstrup, P. R.
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Kolovou, G.
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Kronenberg, F.
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Mora, S.
(author)
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Pulkki, K.
(author)
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Remaley, A. T.
(author)
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Rifai, N.
(author)
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Ros, E.
(author)
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Stankovic, S.
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Stavljenic-Rukavina, A.
(author)
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Sypniewska, G.
(author)
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Watts, G. F.
(author)
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Wiklund, Olov,1943Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Institutionen för medicin,Wallenberg Laboratory,Institute of Medicine(Swepub:gu)xwikol
(author)
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Laitinen, P.
(author)
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Göteborgs universitetWallenberglaboratoriet
(creator_code:org_t)
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In:Clinical Chemistry and Laboratory Medicine: Walter de Gruyter GmbH58:4, s. 496-5171434-66211437-4331
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Langlois, M. R.
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Nordestgaard, Bø ...
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Langsted, A.
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Chapman, M. J.
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Aakre, K. M.
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Baum, H.
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show more...
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Borén, Jan, 1963
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Bruckert, E.
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Catapano, A.
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Cobbaert, C.
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Collinson, P.
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Descamps, O. S.
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Duff, C. J.
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Von Eckardstein, ...
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Hammerer-Lercher ...
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Kamstrup, P. R.
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Kolovou, G.
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Kronenberg, F.
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Mora, S.
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Pulkki, K.
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Remaley, A. T.
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Rifai, N.
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Ros, E.
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Stankovic, S.
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Stavljenic-Rukav ...
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Sypniewska, G.
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Watts, G. F.
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Wiklund, Olov, 1 ...
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Laitinen, P.
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Clinical Chemist ...
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University of Gothenburg