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Achieving low-density lipoprotein cholesterol targets as assessed by different methods in patients with familial hypercholesterolemia: an analysis from the HELLAS-FH registry

BACKGROUND: Familial hypercholesterolemia (FH) is characterized by elevated low-density lipoprotein cholesterol (LDL-C) levels and increased cardiovascular disease (CVD) risk. FH patients often have increased lipoprotein(a) [Lp(a)] levels, which further increase CVD risk. Novel methods for accuratel...

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Autores principales: Rizos, Christos V., Florentin, Matilda, Skoumas, Ioannis, Tziomalos, Konstantinos, Rallidis, Loukianos, Kotsis, Vasileios, Athyros, Vasileios, Skalidis, Emmanouil, Kolovou, Genovefa, Garoufi, Anastasia, Bilianou, Eleni, Koutagiar, Iosif, Agapakis, Dimitrios, Kiouri, Estela, Antza, Christina, Katsiki, Niki, Zacharis, Evangelos, Attilakos, Achilleas, Sfikas, George, Anagnostis, Panagiotis, Panagiotakos, Demosthenes B., Liberopoulos, Evangelos N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7257219/
https://www.ncbi.nlm.nih.gov/pubmed/32466791
http://dx.doi.org/10.1186/s12944-020-01289-5
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author Rizos, Christos V.
Florentin, Matilda
Skoumas, Ioannis
Tziomalos, Konstantinos
Rallidis, Loukianos
Kotsis, Vasileios
Athyros, Vasileios
Skalidis, Emmanouil
Kolovou, Genovefa
Garoufi, Anastasia
Bilianou, Eleni
Koutagiar, Iosif
Agapakis, Dimitrios
Kiouri, Estela
Antza, Christina
Katsiki, Niki
Zacharis, Evangelos
Attilakos, Achilleas
Sfikas, George
Anagnostis, Panagiotis
Panagiotakos, Demosthenes B.
Liberopoulos, Evangelos N.
author_facet Rizos, Christos V.
Florentin, Matilda
Skoumas, Ioannis
Tziomalos, Konstantinos
Rallidis, Loukianos
Kotsis, Vasileios
Athyros, Vasileios
Skalidis, Emmanouil
Kolovou, Genovefa
Garoufi, Anastasia
Bilianou, Eleni
Koutagiar, Iosif
Agapakis, Dimitrios
Kiouri, Estela
Antza, Christina
Katsiki, Niki
Zacharis, Evangelos
Attilakos, Achilleas
Sfikas, George
Anagnostis, Panagiotis
Panagiotakos, Demosthenes B.
Liberopoulos, Evangelos N.
author_sort Rizos, Christos V.
collection PubMed
description BACKGROUND: Familial hypercholesterolemia (FH) is characterized by elevated low-density lipoprotein cholesterol (LDL-C) levels and increased cardiovascular disease (CVD) risk. FH patients often have increased lipoprotein(a) [Lp(a)] levels, which further increase CVD risk. Novel methods for accurately calculating LDL-C have been proposed. METHODS: Patients with FH were recruited by a network of Greek sites participating in the HELLAS-FH registry. LDL-C levels were calculated using the Friedewald (LDL-C(F)) and the Martin/Hopkins (LDL-C(M/H)) equations as well as after correcting LDL-C(M/H) for Lp(a) levels [LDL-C(Lp(a)corM/H)]. The objective was to compare LDL-C levels and target achievement as estimated by different methods in FH patients. RESULTS: This analysis included 1620 patients (1423 adults and 197 children). In adults at diagnosis, LDL-C(F) and LDL-C(M/H) levels were similar [235 ± 70 mg/dL (6.1 ± 1.8 mmol/L) vs 235 ± 69 mg/dL (6.1 ± 1.8 mmol/L), respectively; P = NS], while LDL-C(Lp(a)corM/H) levels were non-significantly lower than LDL-C(F) [211 ± 61 mg/dL (5.5 ± 1.6 mmol/L); P = 0.432]. In treated adults (n = 966) both LDL-C(F) [150 ± 71 mg/dL (3.9 ± 1.8 mmol/L)] and LDL-C(M/H) levels [151 ± 70 mg/dL (6.1 ± 1.8 mmol/L); P = 0.746] were similar, whereas LDL-C(Lp(a)corM/H) levels were significantly lower than LDL-C(F) [121 ± 62 mg/dL (3.1 ± 1.6 mmol/L); P < 0.001]. Target achievement as per latest guidelines in treated patients using the LDL-C(M/H) (2.5%) and especially LDL-C(Lp(a)corM/H) methods (10.7%) were significantly different than LDL-C(F) (2.9%; P < 0.001). In children, all 3 formulas resulted in similar LDL-C levels, both at diagnosis and in treated patients. However, target achievement by LDL-C(F) was lower compared with LDL-C(M/H) and LDL-C(Lp(a)corM/H) methods (22.1 vs 24.8 vs 33.3%; P < 0.001 for both comparisons). CONCLUSION: LDL-C(Lp(a)corM/H) results in significantly lower values and higher target achievement rate in both treated adults and children. If validated in clinical trials, LDL-C(Lp(a)corM/H) may become the method of choice to more accurately estimate ‘true’ LDL-C levels in FH patients.
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spelling pubmed-72572192020-06-07 Achieving low-density lipoprotein cholesterol targets as assessed by different methods in patients with familial hypercholesterolemia: an analysis from the HELLAS-FH registry Rizos, Christos V. Florentin, Matilda Skoumas, Ioannis Tziomalos, Konstantinos Rallidis, Loukianos Kotsis, Vasileios Athyros, Vasileios Skalidis, Emmanouil Kolovou, Genovefa Garoufi, Anastasia Bilianou, Eleni Koutagiar, Iosif Agapakis, Dimitrios Kiouri, Estela Antza, Christina Katsiki, Niki Zacharis, Evangelos Attilakos, Achilleas Sfikas, George Anagnostis, Panagiotis Panagiotakos, Demosthenes B. Liberopoulos, Evangelos N. Lipids Health Dis Research BACKGROUND: Familial hypercholesterolemia (FH) is characterized by elevated low-density lipoprotein cholesterol (LDL-C) levels and increased cardiovascular disease (CVD) risk. FH patients often have increased lipoprotein(a) [Lp(a)] levels, which further increase CVD risk. Novel methods for accurately calculating LDL-C have been proposed. METHODS: Patients with FH were recruited by a network of Greek sites participating in the HELLAS-FH registry. LDL-C levels were calculated using the Friedewald (LDL-C(F)) and the Martin/Hopkins (LDL-C(M/H)) equations as well as after correcting LDL-C(M/H) for Lp(a) levels [LDL-C(Lp(a)corM/H)]. The objective was to compare LDL-C levels and target achievement as estimated by different methods in FH patients. RESULTS: This analysis included 1620 patients (1423 adults and 197 children). In adults at diagnosis, LDL-C(F) and LDL-C(M/H) levels were similar [235 ± 70 mg/dL (6.1 ± 1.8 mmol/L) vs 235 ± 69 mg/dL (6.1 ± 1.8 mmol/L), respectively; P = NS], while LDL-C(Lp(a)corM/H) levels were non-significantly lower than LDL-C(F) [211 ± 61 mg/dL (5.5 ± 1.6 mmol/L); P = 0.432]. In treated adults (n = 966) both LDL-C(F) [150 ± 71 mg/dL (3.9 ± 1.8 mmol/L)] and LDL-C(M/H) levels [151 ± 70 mg/dL (6.1 ± 1.8 mmol/L); P = 0.746] were similar, whereas LDL-C(Lp(a)corM/H) levels were significantly lower than LDL-C(F) [121 ± 62 mg/dL (3.1 ± 1.6 mmol/L); P < 0.001]. Target achievement as per latest guidelines in treated patients using the LDL-C(M/H) (2.5%) and especially LDL-C(Lp(a)corM/H) methods (10.7%) were significantly different than LDL-C(F) (2.9%; P < 0.001). In children, all 3 formulas resulted in similar LDL-C levels, both at diagnosis and in treated patients. However, target achievement by LDL-C(F) was lower compared with LDL-C(M/H) and LDL-C(Lp(a)corM/H) methods (22.1 vs 24.8 vs 33.3%; P < 0.001 for both comparisons). CONCLUSION: LDL-C(Lp(a)corM/H) results in significantly lower values and higher target achievement rate in both treated adults and children. If validated in clinical trials, LDL-C(Lp(a)corM/H) may become the method of choice to more accurately estimate ‘true’ LDL-C levels in FH patients. BioMed Central 2020-05-28 /pmc/articles/PMC7257219/ /pubmed/32466791 http://dx.doi.org/10.1186/s12944-020-01289-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Rizos, Christos V.
Florentin, Matilda
Skoumas, Ioannis
Tziomalos, Konstantinos
Rallidis, Loukianos
Kotsis, Vasileios
Athyros, Vasileios
Skalidis, Emmanouil
Kolovou, Genovefa
Garoufi, Anastasia
Bilianou, Eleni
Koutagiar, Iosif
Agapakis, Dimitrios
Kiouri, Estela
Antza, Christina
Katsiki, Niki
Zacharis, Evangelos
Attilakos, Achilleas
Sfikas, George
Anagnostis, Panagiotis
Panagiotakos, Demosthenes B.
Liberopoulos, Evangelos N.
Achieving low-density lipoprotein cholesterol targets as assessed by different methods in patients with familial hypercholesterolemia: an analysis from the HELLAS-FH registry
title Achieving low-density lipoprotein cholesterol targets as assessed by different methods in patients with familial hypercholesterolemia: an analysis from the HELLAS-FH registry
title_full Achieving low-density lipoprotein cholesterol targets as assessed by different methods in patients with familial hypercholesterolemia: an analysis from the HELLAS-FH registry
title_fullStr Achieving low-density lipoprotein cholesterol targets as assessed by different methods in patients with familial hypercholesterolemia: an analysis from the HELLAS-FH registry
title_full_unstemmed Achieving low-density lipoprotein cholesterol targets as assessed by different methods in patients with familial hypercholesterolemia: an analysis from the HELLAS-FH registry
title_short Achieving low-density lipoprotein cholesterol targets as assessed by different methods in patients with familial hypercholesterolemia: an analysis from the HELLAS-FH registry
title_sort achieving low-density lipoprotein cholesterol targets as assessed by different methods in patients with familial hypercholesterolemia: an analysis from the hellas-fh registry
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7257219/
https://www.ncbi.nlm.nih.gov/pubmed/32466791
http://dx.doi.org/10.1186/s12944-020-01289-5
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