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Early severe coronary heart disease and ischemic heart failure in homozygous familial hypercholesterolemia: A case report

RATIONALE: Familial hypercholesterolemia (FH) is a common inherited cause of coronary heart disease (CHD) and premature death in an early age. Nevertheless, an ischemic heart failure (IHF) associated with FH seems to be rare, and an early diagnosis and therapy could influence the prognosis. PATIENT...

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Autores principales: Kuang, Hongyu, Zhou, Xue, Li, Li, Yi, Qijian, Shou, Weinian, Lu, Tiewei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211926/
https://www.ncbi.nlm.nih.gov/pubmed/30335000
http://dx.doi.org/10.1097/MD.0000000000012869
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author Kuang, Hongyu
Zhou, Xue
Li, Li
Yi, Qijian
Shou, Weinian
Lu, Tiewei
author_facet Kuang, Hongyu
Zhou, Xue
Li, Li
Yi, Qijian
Shou, Weinian
Lu, Tiewei
author_sort Kuang, Hongyu
collection PubMed
description RATIONALE: Familial hypercholesterolemia (FH) is a common inherited cause of coronary heart disease (CHD) and premature death in an early age. Nevertheless, an ischemic heart failure (IHF) associated with FH seems to be rare, and an early diagnosis and therapy could influence the prognosis. PATIENT CONCERNS: In this 13-year-old girl, multiple xanthomas began to develop from the first day of birth. Until June, 2017, she was admitted to our center due to edema, oliguria, and dyspnea during exertion, which was attributed to a recent respiratory infection. DIAGNOSIS: Homozygous FH (HoFH), CHD, and IHF. INTERVENTIONS: The patient has been treated with statin, ezetimibe, aspirin, and traditional heart failure (HF) medications. In addition, the beta-blocker was simultaneously administered. OUTCOMES: Genotypes of this proband indicated homozygous mutations of low-density lipoprotein receptor (LDLR) and some co-segregated mutations, such as von Willebrand factor (VWF) and fibroblast growth factor receptors. At 6-month follow-up, we found a decreased level of plasma lipid profile, in addition to a significant improvement in 6-minute walk distance and functional class. Echocardiography indicated nonsignificant improvements in the structure and function of the heart. LESSONS: This case report indicates that HoFH can lead to dramatically progressive endothelial damages and ventricular remodeling, severe atherosclerosis, even IHF. Genetic outcomes indicate IHF with HoFH could possibly result from LDLR mutations and some co-segregated mutations influencing endothelial function and cardiovascular remodeling. In a short-term follow-up, a combination of statins, ezetimibe, aspirin, and traditional HF agents is safe and effective for IHF with HoFH, and there is a need for further identification of drugs to ameliorate endothelial function and cardiovascular remodeling which may play an important role in long-term treatment.
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spelling pubmed-62119262018-11-27 Early severe coronary heart disease and ischemic heart failure in homozygous familial hypercholesterolemia: A case report Kuang, Hongyu Zhou, Xue Li, Li Yi, Qijian Shou, Weinian Lu, Tiewei Medicine (Baltimore) Research Article RATIONALE: Familial hypercholesterolemia (FH) is a common inherited cause of coronary heart disease (CHD) and premature death in an early age. Nevertheless, an ischemic heart failure (IHF) associated with FH seems to be rare, and an early diagnosis and therapy could influence the prognosis. PATIENT CONCERNS: In this 13-year-old girl, multiple xanthomas began to develop from the first day of birth. Until June, 2017, she was admitted to our center due to edema, oliguria, and dyspnea during exertion, which was attributed to a recent respiratory infection. DIAGNOSIS: Homozygous FH (HoFH), CHD, and IHF. INTERVENTIONS: The patient has been treated with statin, ezetimibe, aspirin, and traditional heart failure (HF) medications. In addition, the beta-blocker was simultaneously administered. OUTCOMES: Genotypes of this proband indicated homozygous mutations of low-density lipoprotein receptor (LDLR) and some co-segregated mutations, such as von Willebrand factor (VWF) and fibroblast growth factor receptors. At 6-month follow-up, we found a decreased level of plasma lipid profile, in addition to a significant improvement in 6-minute walk distance and functional class. Echocardiography indicated nonsignificant improvements in the structure and function of the heart. LESSONS: This case report indicates that HoFH can lead to dramatically progressive endothelial damages and ventricular remodeling, severe atherosclerosis, even IHF. Genetic outcomes indicate IHF with HoFH could possibly result from LDLR mutations and some co-segregated mutations influencing endothelial function and cardiovascular remodeling. In a short-term follow-up, a combination of statins, ezetimibe, aspirin, and traditional HF agents is safe and effective for IHF with HoFH, and there is a need for further identification of drugs to ameliorate endothelial function and cardiovascular remodeling which may play an important role in long-term treatment. Wolters Kluwer Health 2018-10-19 /pmc/articles/PMC6211926/ /pubmed/30335000 http://dx.doi.org/10.1097/MD.0000000000012869 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0
spellingShingle Research Article
Kuang, Hongyu
Zhou, Xue
Li, Li
Yi, Qijian
Shou, Weinian
Lu, Tiewei
Early severe coronary heart disease and ischemic heart failure in homozygous familial hypercholesterolemia: A case report
title Early severe coronary heart disease and ischemic heart failure in homozygous familial hypercholesterolemia: A case report
title_full Early severe coronary heart disease and ischemic heart failure in homozygous familial hypercholesterolemia: A case report
title_fullStr Early severe coronary heart disease and ischemic heart failure in homozygous familial hypercholesterolemia: A case report
title_full_unstemmed Early severe coronary heart disease and ischemic heart failure in homozygous familial hypercholesterolemia: A case report
title_short Early severe coronary heart disease and ischemic heart failure in homozygous familial hypercholesterolemia: A case report
title_sort early severe coronary heart disease and ischemic heart failure in homozygous familial hypercholesterolemia: a case report
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211926/
https://www.ncbi.nlm.nih.gov/pubmed/30335000
http://dx.doi.org/10.1097/MD.0000000000012869
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